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Surgeon General Reports, SAMHSA TIPs, SAMHSA PEPs Put Prevention Into Practice (Static collection) Clinician's Handbook of Preventive Services, 2nd Edition. PPIP

Adults and Older Adults ---Screening

27. Anemia and Hemoglobinopathies

Anemia in adults, defined as a hemoglobin level below the 5th percentile of the reference distribution range for age and gender, is most prevalent in young women (4.5%) and elderly men (4.8%). Anemia is also more common in individuals of low socioeconomic status and in African Americans. Common causes of anemia include iron and vitamin deficiencies (folate and vitamin B-12), occult blood loss, chronic illness, and hemoglobinopathies. Although most forms of anemia are treatable, the benefits of treating asymptomatic individuals are unclear. For this reason, most authorities either recommend against routine screening of adults for anemia or recommend screening only high-risk adults (eg, elderly men, pregnant women, adults with chronic disease).

The hemoglobinopathies are genetic disorders that affect the production and function of hemoglobin molecules. These disorders include sickle cell disease and trait, the thalassemias, and other rarer conditions. Hemoglobinopathies tend to occur in defined ethnic and racial groups, predominantly African Americans in this country. However, they are also found in individuals of Caribbean, Latin American, Asian, and Mediterranean descent. Approximately 50,000 African Americans are affected by sickle cell disease, and another 2million carry the trait. Fewer than 1000 Americans have betathalassemia major, but sizable numbers of Italian Americans, Greek Americans, and immigrants from Southeast Asia carry the genetic trait. In adult populations, screening is useful primarily for providing preconception and prenatal genetic counseling to carriers.

See chapters 1 and 8 for discussions about screening for anemia and hemoglobinopathies in children and adolescents.

Recommendations of Major Authorities

Screening for Anemia


American College of Physicians --
Routine screening for anemia is not recommended in adults without clinical indications.


American College of Obstetricians and Gynecologists --
Hemoglobin levels should be measured as part of routine preventive care for women with a history of excessive menstrual flow and for women 65 years of age or older at high risk.


US Preventive Services Task Force --
There is insufficient evidence to recommend for or against routine screening of asymptomatic, nonpregnant adults, although recommendations against can be made on the grounds of low prevalence, cost, and potential adverse effects of iron therapy.
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Screening for Hemoglobinopathies


American College of Obstetricians and Gynecologists --
Screening should be provided to women of reproductive age who are of Caribbean, Latin American, Asian, Mediterranean, or African descent.


Canadian Task Force on the Periodic Health Examination --
A family and genetic history should be obtained from all patients of Mediterranean, African, Middle Eastern, East Indian, Hispanic, or Asian ancestry who may become parents. Screening with hemoglobin electrophoresis or thin layer isoelectric focusing is recommended for pregnant, at-risk women but not for other adults.


US Preventive Services Task Force --
There is insufficient evidence to recommend for or against screening for hemoglobinopathies by hemoglobin electrophoresis in young adults from ethnic and racial groups known to be at increased risk for sickle cell disease, thalassemias, and other hemoglobinopathies in order for them to be able to make informed reproductive choices. Recommendations to offer such testing may be made on other grounds, including burden of suffering and patient preference. If provided, testing should be accompanied by counseling, which should include a description of the significance of the disease, how it is inherited, the availability of a screening test, and the implications to the individual and their offspring of a positive result.
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Basics of Screening for Anemia and Hemoglobinopathies

Anemia

1. The primary screening tests for anemia are measurements of hemoglobin (Hb) concentration and hematocrit (Hct), preferably measured from a venous blood specimen. Measuring venous samples yields more accurate and reliable results compared with analysis of a capillary sample by centrifuge or hemoglobinometer.

2. In men, anemia is defined as a hemoglobin level of less than 13 g/dL or a hematocrit of less than 41%. In nonpregnant women, the cut-off values are 12 g/dL for hemoglobin and 36% for hematocrit. Cigarette smokers and persons living at altitudes above 3000 feet (1000 meters) tend to have higher levels of hemoglobin and higher hematocrits. Adjust cut-off points for anemia in smokers and persons living at high altitudes by using the correction factors given in Tables 27.1 and 27.2.

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Hemoglobinopathies

1. Hemoglobin electrophoresis is the screening test of choice for hemoglobinopathies. This test is very accurate in identifying the types of hemoglobin in a blood sample. It can distinguish among affected homozygotes, heterozygous carriers, and persons who are unaffected by sickle cell disease, beta-thalassemia, and other hemoglobin disorders. Alphathalassemia trait may not be detectable. Sickle cell disease and trait can also be detected by using a sickle preparation that demonstrates red blood cell sickling under reduced oxygen concentration. After sickling is demonstrated, however, hemoglobin electrophoresis is still necessary to distinguish between the carrier and affected state and to determine if other hemoglobins are present. Measurement of mean corpuscular volume (MCV) can also be used to screen for thalassemia, but this method is much less sensitive than is hemoglobin electrophoresis.

2. Offer appropriate genetic counseling to adults who are screened for hemoglobinopathies, both before and after laboratory testing. At a minimum, this counseling should address: (1) a description of the disease process and its pattern of inheritance; (2) the availability and accuracy of screening and prenatal detection techniques; (3) the implications of possible results for the individual, partner, and potential offspring.

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Patient Resource


Sickle Cell Anemia (New Hope for People With). This and other publications are available from the FDA Office of Consumer Affairs, HFE 88 Room 1675, 5600 Fishers Ln, Rockville, MD 20857; (800)532-4440.
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Selected References

American College of Obstetricians and Gynecologists. . Hemoglobinopathies in Pregnancy: ACOG Technical Bulletin #220. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

Canadian Task Force on the Periodic Health Examination. . Screening for hemoglobinopathies in Canada. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 20.

Centers for Disease Control. . Reference criteria for anemia screening. MMWR. 1989. 38: 400-404.

Dallman P, Ray Y, Johnson C. . Prevalence and causes of anemia in the United States, 1976 to 1980. Am J Clin Nutr. 1984. 39: 437-445. (PubMed)

Lipkin M, Fisher L, Rowley PT, Loader S, Iker HP. . Genetic counseling of asymptomatic carriers in a primary care setting. Ann Intern Med. 1986. 105: 115-123. (PubMed)

Shapiro MF, Greenfield S. . The complete blood count and leukocyte differential count: an approach to their rational application. Ann Intern Med. 1987. 106: 65-74. (PubMed)

US Preventive Services Task Force. . Screening for hemoglobinopathies. In: Guide to Clinical Preventive Services. 2nd ed. Baltimore, Md: Williams & Wilkins; 1996: chap 22.

Tables

Table 27.1. Adjustments for Hemoglobin and Hematocrit Cut Points for Anemia in Smokers

Table 27.2. Altitude Adjustments for Hemoglobin and Hematocrit Cut Points for Anemia

28. Blood Pressure

Approximately 50 million Americans have blood pressure elevations that warrant monitoring or drug therapy. These persons are at increased risk for coronary artery disease, peripheral vascular disease, stroke, renal disease, and retinopathy. Treatment of hypertension is very effective. Use of antihypertensive therapy has contributed to a 59% reduction in age-adjusted stroke mortality and a 50% reduction in mortality from coronary artery disease since 1972. The benefits of antihypertensive therapy are greatest for persons with the most markedly elevated blood pressure; however, even patients with stage 1, or mild hypertension, benefit from treatment. Recent research has demonstrated the importance of treating "isolated" systolic hypertension, especially in older adults.

Recommendations of Major Authorities


American Academy of Family Physicians --
Blood pressure should be measured periodically in all patients over 21 years of age.


American College of Obstetrics and Gynecology --
Blood pressure should be measured as part of periodic evaluation visits, which should occur yearly or as appropriate.


American College of Physicians --
Blood pressure should be measured in adults every 1 to 2 years. Normotensive patients should have blood pressure measurements at least yearly if any of the following pertains: (1) diastolic blood pressure between 85 and 89 mm Hg; (2) African-American heritage; (3) moderate or extreme obesity; (4) a first-degree relative with hypertension; (5) a personal history of hypertension.


Canadian Task Force on the Periodic Health Examination --
Case-finding (screening patients seen for any reason) should be considered in all persons aged 21 to 84 years; individual clinical judgement should be exercised in all other cases except pregnant women (for whom blood pressure should be measured as part of prenatal care).


National High Blood Pressure Education Program (NHBPEP) of the National Heart, Lung, and Blood Institute --
Blood pressure measurements should be performed on adults at least every 2 years and at each patient visit if possible. Patients with diastolic blood pressures of 85 to 89 mm Hg should have their blood pressure rechecked within 1 year. See Tables 28.1 and 28.2 for classification of blood pressure and recommendations for follow-up.


US Preventive Services Task Force --
Adults should have blood pressure measured periodically, with the optimal interval left to clinical discretion.
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Basics of Blood Pressure Screening

1. Instruct patients not to use tobacco or caffeine for 30 minutes before the measurement is performed.

2. Seat the patient in a quiet environment, free from temperature extremes, for at least 5 minutes before the measurement is performed.

3. Perform the measurement with a mercury sphygmomanometer, if available. An aneroid manometer may be used if it is periodically calibrated according to manufacturer's recommendations. A validated electronic device meeting the requirements of the American National Standard for Electronic or Automated Sphygmomanometers set forth by the Association for the Advancement of Medical Instruments may also be used.

4. Position the manometer at eye level, if possible, to assure accuracy in reading the measurement.

5. Use an appropriately sized cuff. The bladder of the cuff should encircle 80% to 100% of the arm. The cuff width should be 40% of the circumference of the upper arm. Use of narrow cuffs leads to falsely elevated readings. Use of wide cuffs may falsely lower the reading.

6. The patient's arm should be bare; avoid constricting the upper arm with a rolled shirt sleeve. Support the arm horizontally so the cuff is positioned at heart level (the fourth intercostal space).

7. Apply the stethoscope lightly to the antecubital fossa. Excess pressure results in falsely low diastolic blood pressure readings.

8. Rapidly increase cuff pressure to about 30 mm Hg beyond the point at which the radial pulse is no longer palpable. Decrease pressure at a rate of no more than 2 to 3 mm Hg per second.

9. In adults, the measured systolic blood pressure (SBP) and the diastolic blood pressure (DBP) readings are the pressures corresponding to the first of two consecutive sounds and the disappearance of sound (not muffling), respectively. Confirm the disappearance of sound by continuing to listen while decreasing pressure 10 to 20 mm Hg below the last sound heard.

10. Use the average of at least two readings unless the first two differ by more than 5 mm Hg, in which case obtain additional readings. To permit blood to be released from arm veins, allow an interval of 1 to 2 minutes before repeating pressure measurements in the same arm.

11. Measure blood pressure in both arms initially; at subsequent visits, remeasure using the arm with the higher initial pressures.

12. Confirming the diagnosis of hypertension requires high blood pressure readings during at least two subsequent visits (unless SBP is 210 mm Hg or higher, DBP is 120 mm Hg or higher, or both). See Table 28.2 for recommendations for follow-up from the Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure.

13. Because blood pressure readings obtained in a medical setting may not be typical of a patient's usual blood pressure, monitoring at home or work by the patient, family, or friends may be valuable. Measurement devices must be calibrated initially and rechecked at least yearly. Instruct the person taking the blood pressure in proper technique, and recheck the technique periodically.

14. Lifestyle modifications can help prevent development of hypertension and should be the initial treatment modality for the first 3 to 4 months for patients with stage 1 (mild) hypertension. See Table 28.3 for a list of basic lifestyle modifications for controlling blood pressure.

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Patient Resources


High Blood Pressure: Treat it for Life; Check Your Healthy Heart IQ; High Blood Pressure and What You Can Do About It; Six Good Reasons to Control Your High Blood Pressure; Eat Right to Lower Your Blood Pressure. To order these and other materials, in both English and Spanish, contact the National Heart, Lung, and Blood Institute Information Center. PO Box 30105, Bethesda, MD 20824-0105; (301)251-1222. Internet address: http://www.nhlbi.nih.gov/nhlbi/nhlbi.htm.
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Provider Resources


The Fifth Report of the Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure. To order this report in either English or Spanish, contact the National Heart, Lung, and Blood Institute Information Center, PO Box 30105, Bethesda, MD 20824-0105; (301)251-1222. Internet address: http://www.nhlbi.nih.gov/nhlbi/nhlbi.htm.
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Physicians. . Guidelines. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991:396-397.

American College of Physicians. . Automated ambulatory blood pressure and self-measured blood pressure monitoring devices: their role in the diagnosis and management of hypertension (position paper). Ann Intern Med. 1993. 118: 889-892. (PubMed)

Appel LJ, Stason WB. . Ambulatory blood pressure monitoring and blood pressure self-measurement in the diagnosis and management of hypertension. Ann Intern Med. 1993. 118: 867-882. (PubMed)

Canadian Task Force on the Periodic Health Examination. . Hypertension in the elderly: case-finding and treatment to prevent vascular disease. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 79.

Canadian Task Force on the Periodic Health Examination. . Screening for hypertension in young and middle-aged adults. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 53.

Frohlich ED, Grim C, Labarthe DR, et al. . Recommendations for human blood pressure determination by sphygmomanometers: report of a special task force appointed by the Steering Committee, American Heart Association. Hypertension. 1988;11:209A-222A.

Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure. . The fifth report of the Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure. Arch Intern Med. 1993. 153: 154-188.

Littenberg B. . A practice guideline revisited: screening for hypertension. Ann Intern Med 1995. 122: 937-939. (PubMed)

National High Blood Pressure Education Program (NHBPEP) Working Group. . Report on ambulatory blood pressure monitoring. Arch Intern Med. 1990. 150: 2270-2280. (PubMed)

Systolic Hypertension in the Elderly Program (SHEP) Cooperative Research Group. . Prevention of stroke by antihypertensive drug treatment in older persons with isolated systolic hypertension. JAMA. 1991. 265: 3255-3264. (PubMed)

US Preventive Services Task Force. . Screening for hypertension. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 3.

Webster J, Newnham D, Petrie JC, Lovell HG. . Influence of arm position on measurement of blood pressure. Br Med J. 1984. 288: 1574-157.

Tables

Table 28.1. Classification of Blood Pressure for Adults Aged 18 Years and Older *

Table 28.2. Recommendations for Follow-Up Based on Initial Set of Blood Pressure Measurements for Adults Aged 18 and Over

Table 28.3. Life-style Modifications for Hypertension Control

29. Body Measurement

Obesity is a major public health concern in the United States. More than one-third of all American adults are overweight, and this proportion continues to increase. (NOTE: Obesity is an excess of body fat. Overweight refers to an excess of body weight relative to height. Because it is more readily quantified than obesity, overweight is often used as a proxy for obesity.) Overweight is associated with significantly increased mortality and multiple health risks, such as noninsulin-dependent diabetes mellitus (type 2), hypertension, hypercholesterolemia, stroke, and coronary heart disease, as well as several types of cancer. Abdominal adiposity, as measured by waist-to-hip circumference ratio (WHR) or absolute waist circumference, is associated with an increased risk of diabetes, hypertension, coronary heart disease, stroke, and death from all causes.

Even modest weight loss by overweight individuals, accomplished by changing the diet, increasing physical activity, and other interventions, can decrease the risk of most forms of morbidity associated with being overweight. The goal of any intervention should be making lifestyle changes that are permanent.

See chapter 3 for information on body measurement of children and adolescents. See chapters 56 and 57 for information on counseling adults about nutrition and physical activity.

Recommendations of Major Authorities


American Academy of Family Physicians --
All patients should be measured for height and weight periodically.


American College of Obstetricians and Gynecologists --
Height and weight should be measured as part of periodic evaluation visits, which should occur yearly or as appropriate.


Canadian Task Force on the Periodic Health Examination --
There is insufficient evidence to recommend the inclusion or exclusion of height and weight measurement and BMI calculation in the periodic health examination, given the lack of long-term effectiveness of weight reduction therapy in the large majority of obese individuals. Weight reduction can be cautiously recommended in persons with obesity and coexistent diabetes, hypertension, or hyperlipidemia.


US Department of Agriculture, US Department of Health and Human Services --
Calculation of the ratio of waist circumference to hip circumference can be used, in addition toheight and weight measurements, to help evaluate body weight.


US Preventive Services Task Force --
All adults should receive periodic measurement of height and weight. The optimal frequency for measuring height and weight in adults is a matter of clinical discretion. There is insufficient evidence to recommend for or against determination of the waist/hip ratio (WHR) as a routine screening test for obesity.
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Basics of Body Measurement Screening


1. To ensure accuracy, measure height while the patient is barefoot or in socks or stockings only. Make sure that the patient is standing as erect as possible, with feet flat on the floor. Height-measuring rods attached to scales should be regularly checked for accuracy, because they become inaccurate with use.


2. Use a balance beam or electronic scale (not a spring-type scale) to measure weight. The measurement will be most accurate if the patient is wearing minimal or no clothing. Calibrate scales on a regular basis.


3. Historically, the definition of "healthy" weight has been a subject of debate. Typically, two different methods have been used for evaluating weight: (1) comparison with the Metropolitan Life Insurance Tables, and (2) calculation of body mass index (BMI).


Clinicians have been most accustomed to using height-weight tables. Early tables were adapted from those developed in 1959 by the Metropolitan Life Insurance Company and were based on weights associated with minimal mortality. Although these tables were widely circulated and used, they had significant limitations: they included subjective estimates of body frame size and were based on an insured population, which may not be representative of the overall US population.


Today, most authorities endorse using BMI to evaluate healthy weight for adults. The formula for calculating BMI is:

Weight(kg)
Height(m)2


Although authorities previously suggested that the ranges of "healthy" BMI and weight should increase with age, most authorities now do not believe that such age adjustments are valid. Table 29.1 presents an easy way to calculate an individual's BMI based on the person's height and weight.


In 1995, the US Departments of Agriculture and Health and Human Services published new healthy weight ranges for adult men and women in Dietary Guidelines for Americans (see Selected References). These ranges, proposed by an expert committee and adopted by the Departments, are based on an extensive review of the literature pertaining to weight-related risk of morbidity and mortality over a range of BMI values. The weight ranges are presented in Table 29.2 and Figure 29.1. Note that the higher weights apply to people with more muscle and bone.


The upper boundary of healthy weight corresponds to a BMI of about 25, based on the significant increase in risk of mortality that occurs among persons with BMI values above this cutoff point. The lower boundary of healthy weight represents a BMI of 19, although whether a weight below this level is unhealthy remains unclear. BMI values above 28 to 29, the boundary between moderate and severe overweight, are associated with an increasingly higher risk of disease and death.


4. Research indicates that WHR or absolute weight circumference may be stronger predictors of mortality than are measures of general body adiposity. Determination of WHR is also useful for assessing patients, particularly those who have weight that is borderline-high and a personal or family medical history placing them at increased health risk. Determine the WHR by measuring the abdominal (waist) circumference and the hip circumference. Measure the abdominal circumference at the level of the umbilicus (or the level of greatest anterior extension of the abdomen) while the patient is standing. Determine the hip circumference by measuring the greatest circumference at the level of the buttocks. Obtain both measurements after a normal expiration by the patient and without indenting the skin. The formula for calculating WHR is:


Abdominal Circumference
Hip Circumference


WHR values above 1.0 for men and above 0.8 for women are associated with an increased risk of diabetes, hypertension, heart disease, and stroke. An absolute waist circumference measurement greater than 100 cm is also associated with an increased disease risk. However, evidence suggests that WHR or waist circumference and disease risk may not have as strong an association in some minority populations.


5. Bioelectric impedance analysis (BIA), a new technique for quickly estimating body composition, is currently used in many different practice settings. In theory, this technique measures the electrical impedance, or resistance, to the flow of electricity, in the body. From this measurement, an estimate of total body water (TBW) is calculated. An estimate of fat-free mass and body fat (adiposity) can then be determined. However, no industry standards for BIA currently exist, and a person's body fat measurement may vary by as much as 10% of body weight depending on the technique, machinery, conditions, and equations used. Variables that can affect the measurements include body position, hydration status, consumption of foods and beverages, ambient air and skin temperature, recent physical activity, and conductance of the examining table. Only when these variables become controlled and standardized may BIA prove to be a quick, accurate, and noninvasive way to determine body fat.
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Patient Resources


Nutrition and Health: Dietary Guidelines for Americans. 4th ed. US Dept of Agriculture and US Dept of Health and Human Services, 1995. This material is available from the Consumer Information Center  --- 3C, Dept 514-X, Pueblo, CO 81009.


Check Your Weight and Heart Disease I.Q. This information is available in both English and Spanish. National Heart, Lung, and Blood Institute Information Center, PO Box 30105, Bethesda, MD 20824-0105; (301)251-1222. Internet address: http://www.nhlbi.nih.gov/nhlbi/nhlbi.htm


Weight Control: Losing Weight and Keeping It Off. American Academy of Family Physicians, 8880 Ward Parkway, Kansas City, MO 64114-2797; (800)944-0000. Internet address: http://www.aafp.org


Bioelectric Impedance Analysis in Body Composition Measurement; Understanding Adult Obesity; Weight Cycling. The National Institute of Diabetes and Digestive and Kidney Disease, 1 WIN Way, Bethesda, MD 20892-3665; (800)946-8098.
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

Bjorntorp P. . Regional patterns of fat distribution. Ann Intern Med. 1985. 103: 994-995. (PubMed)

Bray GA, Gray DS. . Obesity: part 1  --- pathogenesis. West J Med. 1988. 149: 429-441. (PubMed)

Canadian Task Force on the Periodic Health Examination. . Prevention of obesity in adults. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 48.

Federation of American Societies for Experimental Biology, Life Sciences Research Office. . Third Report on Nutrition Monitoring in the United States. Washington, DC: US Government Printing Office; 1995.

Folsom AR, Kaye SA, Sellers TA, et al. . Body fat distribution and 5-year risk of death in older women. JAMA. 1993. 269: 483-487. (PubMed)

Hubert HB, Feinleib M, McNamara PM, Castelli WP. . Obesity as an independent risk factor for cardiovascular disease: a 26-year follow-up of participants in the Framingham Heart Study. Circulation. 1983. 67: 968-977. (PubMed)

Lissner L, Odell PM, D'Agostino RB, et al. . Variability of body weight and health outcomes in the Framingham population. N Engl J Med. 1991. 324: 1839-1844. (PubMed)

Lohman TG, Roche AF, Martorell R. . Anthropometric Standardization Reference Manual. Champaign, Ill: Human Kinetics Books; 1988.

Manson JE, Stampfer MJ, Hennekens CH, Willet WC. . Body weight and longevity: a reassessment. JAMA. 1987. 257: 353-358. (PubMed)

National Academy of Sciences, Committee on Diet and Health, Food and Nutrition Board, Commission on Life Sciences, National Research Council. . Diet and Health: Implications for Reducing Chronic Disease Risk. Washington, DC: National Academy Press; 1989:564-565.

National Institutes of Health. . National Institutes of Health Consensus Development Conference Statement: health implications of obesity. Ann Intern Med. 1985. 103: 1073-1077. (PubMed)

National Institutes of Health. . Bioelectric Impedance Analysis in Body Composition Measurement: Technology Assessment Conference Statement. Bethesda, Md.: National Institutes of Health; 1994.

Rowland ML. . A nomogram for computing body mass index. Dietetic Currents. 1989. 16: 5-12.

Simpoulos AP, Van Itallie TB. . Body weight, health and longevity. Ann Intern Med. 1984. 100: 285-295. (PubMed)

US Department of Agriculture, Agricultural Research Service; Dietary Guidelines Advisory Committee, 1995. . Report of the Dietary Guidelines Advisory Committee on the Dietary Guidelines for Americans, 1995. Washington, DC: US Department of Agriculture; 1995.

US Department of Agriculture, US Department of Health and Human Services. . Nutrition and Your Health: Dietary Guidelines for Americans. Washington DC: US Government Printing Office; 1995. Home and Garden Bulletin 232.

US Preventive Services Task Force. . Screening for obesity. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 21.

Van Itallie TB. . Health implications of overweight and obesity in the United States. Ann Intern Med. 1985. 103: 983-988. (PubMed)

Tables

Table 29.1. Body Weights in Pounds According to Height and Body Mass Index *

Table 29.2. Healthy Weight Ranges for Adult Men and Women

[Figures]

Figure 29.1. Weight Chart for Adult Men and Women*

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* The use of shading on the figure reflects the lack of consensus about exact cutoff points and emphasizes that disease risk varies with degree of overweight.top link


Note: To use this chart, find your height in feet and inches (without shoes) along the left side of the graph. Trace the line corresponding to your height across the figure until it intersects with the vertical line corresponding to your weight in pounds (without clothes). The point of intersection lies within a band that indicates whether your weight is healthy or is moderately or severely overweight. The higher weights apply mainly to men, who have more muscle and bone.top link


From: US Department of Agriculture, US Department of Health and Human Services. Nutrition and Your Health: Dietary Guidelines for Americans. Washington, DC: US Government Printing Office, 1995. Home and Garden Bulletin 232.top link

30. Cancer Detection By Physical Examination

Cancer will eventually develop in approximately 30% of Americans; three of every four families will be affected. Many cancers can be cured if they are detected early and treated in the early stages. See Table 30.1 for data on the incidence and mortality of major types of cancer.

This chapter presents information regarding detection of several cancers through physical examination. Screening tests for early detection of specific cancers are addressed in separate chapters.

Breast Examination

Cancer of the breast can manifest as visual and physical changes of the breast and axilla. Most clinical trials have evaluated the effectiveness of screening for breast cancer in women with either mammography alone or mammography combined with clinical breast examination (CBE). No direct evidence suggests superior effectiveness of CBE alone compared with no screening. When CBE is performed by a clinician, its sensitivity for detection of cancer is approximately 45%. The overall sensitivity of breast self-examination (BSE) is about 26%. The sensitivity of BSE decreases with advancing age: from 41% in women aged 35 to 39 years to only 21% for women aged 60 to 74 years. See chapter 36 for information on the epidemiology of breast cancer and screening mammography.

Recommendations of Major Authorities

Women Under 40 Years of Age


American Cancer Society --
Women should have clinical breast examinations every 3 years from age 20 to 39 years.


American College of Obstetricians and Gynecologists --
Women over age 18 years should have clinical breast examination during the periodic evaluation, yearly, or as appropriate.


Canadian Task Force on the Periodic Health Examination --
Clinical breast examination is not recommended for screening women less than 50 years of age.
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Women 40 Years of Age and Over


American Academy of Family Physicians --
Mammography and clinical breast examination should be offered to women aged 50 to 69 every 1 to 2 years.


American Cancer Society, American College of Obstetricians and Gynecologists, and American College of Physicians --
Annual clinical breast examination should be performed on women 40 years of age and older.


Canadian Task Force on the Periodic Health Examination --
Clinical breast examination screening should be performed annually on women 50 to 69 years of age. Clinical breast examination should be used in conjunction with mammography for screening.


US Preventive Services Task Force --
Breast cancer screening should be performed in women 50 to 69 years of age through mammography every one to two years with or without annual clinical breast examination. There is insufficient evidence to recommend for or against clinical breast examination alone in this age group or in any other age group. Although there is insufficient evidence, recommendations to screen high risk women beginning at age 40 and women over 70 may be made on other grounds.


There is no evidence specifically evaluating clinical breast examination in screening high-risk women under 50 years of age; recommendations for screening such women may be made on the basis of their high burden of suffering and the higher positive predictive value of screening. There is limited and conflicting evidence of the value of clinical breast examination screening in women 70 to 74 years of age and no evidence for women over 75; however, recommendations for screening women 70 years of age and older who have a reasonable life expectancy can be made on the basis of the high burden of suffering of this age group. There is insufficient evidence to recommend the use of clinical breast exam alone, without mammography, for screening.
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Basics of Breast Examination

1. General Considerations: Breast examination involves bilateral inspection and palpation of the breasts (and areolae) and the axillary and supraclavicular areas. Perform examination while the patient is in the upright position and again in the supine position.

2. Inspection: Visually examine the breasts under good lighting with the patient sitting or standing with her hands on her hips. Focus on the symmetry and contour of the breasts; position of the nipples; skin changes such as puckering, dimpling, or scaling of the skin; scars; nipple discharge; nipple retraction; and appearance of a mass. Note any bulging, discoloration, or edema of the lymphatic drainage areas (ie, the supraclavicular and axillary regions).

3. Screening for Retraction: Observe the breast tissue for signs of retraction while the patient lifts her arms slowly over her head. Both breasts should move symmetrically. With the patient's arms lowered and palms pressed together at waist level, observe the breast tissue again for signs of retraction. Ask patients with large breasts to lean forward, and note the symmetric forward movement of the breasts. No evidence of fixation to the chest wall should be evident.

4. Breast Palpation: Palpation must be systematic. Two commonly used patterns of palpation are to start with the nipple and move out radially to the periphery -- much like spokes on a wheel -- or to move outward from the nipple and around the breast in a spiral, or corkscrew, pattern. Regardless of the pattern used, be thorough, and do not miss any areas. A careful, thorough examination requires 5 to 10 minutes. Take care to palpate the tail of Spence, which extends from the upper outer quadrant to the axilla. Use the first three fingers to press firmly in a small circular motion. The amount of pressure should vary from firm, to detect deep masses, to light, to detect superficial ones. Palpate all of the breast tissue when the patient is upright and again while she is supine. First, with the woman in an upright position, palpate the breast using a bimanual technique. Support the inferior aspect of the breast with one hand while the other hand palpates the breast. Next, palpate each breast with the patient in a supine position; the arm on the side to be examined should be raised over her head.

5. Axillary and Supraclavicular Node Palpation: Palpate the axillary and supraclavicular areas for adenopathy while the patient is sitting. While lifting and supporting the woman's arm, place the fingers high into the axilla and move them down firmly to palpate in four directions: along the chest wall, along the anterior border of the axilla, along the posterior border of the axilla, and along the inner aspect of the upper arm. It may be helpful to move the patient's arm through the full range of motion to increase the surface area that can be reached. Palpate the supraclavicular nodes while the patient is sitting and relaxed, with neck flexed slightly forward. It mayhelp to have the patient's head turned slightly toward the side being examined. The supraclavicular nodes may be felt in the angle formed by the clavicle and the sternocleidomastoid muscle.

6. Areolae: Check the nipple for discharge by gently squeezing the nipple. Discharge is easier to elicit when the patient is in an upright position. Nipple inversion may be normal. However, changes in nipple inversion should not occur after puberty, and inverted nipples should not be fixed (ie, it should be possible to pull the nipple out).

7. Breast Self-Examination: The American Cancer Society and the American College of Obstetricians and Gynecologists recommend encouraging women to examine their breasts every month. Instructing female patients in breast self-examination may be desirable. See "Patient Resources" for information about ordering pamphlets on breast self-examination.

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Oral Cavity Examination

An estimated 30,750 new cases of oral cavity and pharyngeal cancer will be diagnosed in 1997, and approximately 8440 deaths are expected to occur during that period. Most deaths occur within 3 or 4 years of diagnosis. The incidence of oral cancer among men is more than twice that among women; the highest rates are seen among men over age 40 years. In the United States, 90% of oral cancer cases are attributable to the use of tobacco and to a lesser extent, alcohol.

Recommendations of Major Authorities


American Cancer Society --
Individuals 20 to 39 years of age should have a cancer checkup, including examination of the oral region, every 3 years; those 40 years of age and older should have one yearly.


American College of Obstetricians and Gynecologists --
Examinations of the oral cavity in women 40 years of age and older should be part of periodic health examinations performed annually, as appropriate.


Canadian Task Force on the Periodic Health Examination --
There is insufficient evidence for inclusion or exclusion of oral cancer screening in the periodic health examination. Annual examination by physicians and/or dentists should be considered for men and women over 60 years of age who have a known risk factor for oral premalignancy and invasive oral cancers, such as tobacco use in any form and regular alcohol consumption.


US Preventive Services Task Force --
There is insufficient evidence to recommend for or against routine screening of asymptomatic persons for oral cancer by primary care clinicians. Although direct evidence of a benefit is lacking, clinicians may wish to include an examination for cancerous and precancerous lesions of the oral cavity in the periodic health examination of persons who chew or smoke tobacco (or did so previously), older persons who drink regularly, and anyone with suspicious symptoms or lesions detected through self-examination. All patients, especially those over 65 years of age, should be advised to receive a complete dental examination on a regular basis.
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Basics of Oral Cavity Examination

1. General Considerations: Examination of the oral cavity is intended to identify the presence of lesions that are precancerous or may predispose to cancer. Lesions that have the potential for malignant transformation tend to be flat and white (leukoplakia), white-red (erythroleukoplakia), or red (erythroplakia). The examination should include inspection and palpation of the lips, gingivae, buccal mucosa, palate, floor of the mouth, tongue, and pharynx. If the patient is wearing dentures, these should be removed before examination. Work systematically from anterior to posterior, omitting no areas. Use a bright light for optimal visualization.

2. Lips: Inspect the lips closely, noting symmetry, color, moisture, and the presence of cracking and lesions.

3. Gingivae: Inspect the gums for bleeding, sponginess, and discoloration. Normal gums appear pink or coral with a stippled surface.

4. Buccal Mucosa: Ask the patient to hold his or her mouth open widely. Holding the cheek open with a wooden tongue blade, inspect the buccal mucosa, noting color and the presence of nodules and lesions. The normal buccal surface appears pink, smooth, and moist. Leukoplakia appears as white plaque on the mucous membranes of the cheeks, gums, and tongue. Squamous cell carcinoma in its earliest stages may present as an erythematous, indurated lesion.

5. Palate: Inspect the palate for plaques, ulceration, and masses. A normal variation is a torus palatinus, a nodular bony ridge down the middle of the hard palate.

6. Floor of the Mouth: Closely examine the entire U-shaped area under the patient's tongue; this is the most common location for oral malignancies. Inspect the mouth for white patches, nodules, and ulcerations. Palpate the floor of the mouth bimanually with one finger under the tongue and the other hand under the jaw to stabilize the tissue, feeling for induration, thickening, and masses.

7. Tongue: Note color, surface characteristics, and moisture. Ask the patient to touch the tongue to the roof of the mouth to permit examination of its undersurface. While the patient's tongue is protruded, gently grasp it with a piece of gauze, using the other hand to palpate the tongue. More than 85% of all lingual cancers arise in the lateral margins of the tongue. Neoplasms may limit a patient's ability to protrude the tongue. Induration and ulceration are suggestive of carcinoma.

8. Pharynx: Depress the middle third of the patient's tongue with a tongue blade to increase visualization of the posterior pharynx. Note any asymmetry, discharge, mass, or ulceration of the pharynx.

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Pelvic Examination And Ovarian Cancer

Pelvic examination is used to detect and identify cancers of the female genital tract. Use of the Pap smear testing during pelvic examination to identify cervical neoplasms and premalignant lesions (chapter 37) has been an unqualified success. Some authors have advocated performing bimanual examination during the pelvic examination to detect some pelvic neoplasms, including ovarian cancer, which has the highest mortality of all the gynecologic cancers. Approximately 26,800 new cases of ovarian cancer will occur in the United States in 1997, with an estimated 14,600 deaths occurring in that period. Ovarian cancer will develop in one of every 70 women. A woman's risk of ovarian cancer is increased by nulliparity; older age at the time of first pregnancy or live birth; fewer pregnancies; and a personal history of breast, endometrial, or colorectal cancer. Often, no signs or symptoms of ovarian cancer occur until late in the course of disease, and the cancer is often of considerable size by the time it is detectable by pelvic examination.

Recommendations of Major Authorities


American Cancer Society --
Pelvic examination should be performed every 1 to 3 years for women aged 18 to 39 and annually for women over age 40.


American College of Obstetricians and Gynecologists --
Women who have become sexually active or are 18 years of age and older should have annual pelvic examinations as part of a periodic health examination.


Canadian Task Force on the Periodic Health Examination (CTFPHE) and US Preventive Services Task Force --
Routine pelvic examination is not recommended for the detection of ovarian cancer. There is insufficient evidence to recommend for or against screening of asymptomatic women at increased risk for ovarian cancer. The CTFPHE states that it would be reasonable to examine the adnexa if a pelvic examination were being done for another reason, such as cervical inspection or Pap smear.
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Basics of Pelvic Examination

1. General Considerations: Use good lighting and proper examination procedure. Instruct the patient to empty her bladder and rectum before examination.

2. Inspection: Perform a general inspection of the external genitalia with the patient in the lithotomy position. Inspect the skin of the vulva for redness, excoriation, masses, leukoplakia, and pigmentation.

3. Femoral Nodes: Palpate the horizontal chain of nodes inferior to the inguinal ligament and the vertical chain along the upper inner thigh. Nodes in this area that are smaller than 1 cm in diameter may be normal if they are soft, discrete, and movable.

4. Vagina and Cervix: Use a speculum to inspect the vagina and cervix. Warm the speculum, and lubricate it with water, not a lubricating jelly, because the jelly may interfere with interpretation of cervical cytology. Separate the labia with two fingers, and apply pressure posteriorly in the introitus. Introduce the speculum at an oblique angle, avoiding pain-sensitive anterior structures, then rotate the speculum to the transverse position. Open the blades slowly, and lock the speculum open. Use a cotton-tipped applicator or swab to remove any discharge that obscures the vaginal walls or cervix. Visually inspect the vagina and cervix for erosion, ulceration, leukoplakia, and masses. At this point, obtain a specimen for Pap smear testing (chapter 37). As the speculum is removed, examine the vaginal sidewalls again for leukoplakia, masses, and other abnormalities.

5. Bimanual Palpation: Place the lubricated index and middle fingers of one hand into the vaginal vault; place the other hand on top of the abdomen. Use the fingers within the vaginal vault to palpate the cervix and sidewalls of the vagina for induration, masses, and tenderness. Next, use the fingers within the vagina to lift the reproductive organs out of the pelvis so they can be palpated with the hand on the abdomen. Note the size, location, contour, and mobility of the uterus, ovaries, and adnexa.

6. Rectovaginal Septum: Partially withdraw the hand from the vagina, moving the middle finger to insert it into the rectum. This maneuver allows for palpation of the rectovaginal septum to detect tumors, inflammatory or granulomatous masses, and for better evaluation of the uterus in obese individuals or in those in whom the uterus is retroverted.

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Digital Rectal Examination For Colorectal And Prostate Cancer

Digital rectal examination (DRE) can be used to identify colorectal and prostate cancers. The DRE is of limited value as a screening test for colorectal cancer, because fewer than 10% of colorectal cancers can be palpated. See chapter 34 for information on the epidemiology of colorectal cancer and screening with fecal occult blood testing.

Rectal examination does afford an opportunity for limited palpation of the prostate gland in men. See chapter 39 for information on the epidemiology of prostate cancer and screening with prostate-specific antigen (PSA). The sensitivity and specificity of digital rectal examination for detecting prostate cancer are 33% to 69% and 49% to 97%, respectively. Scant evidence exists suggesting that screening by digital rectal examination decreases mortality from prostate cancer. Some authorities believe that the limited effectiveness of DRE may be attributable to either its inability to detect tumors at an early, treatable stage or the fact that some tumors grow so rapidly that yearly screening cannot detect most of them at an early, treatable stage, or both.

Recommendations of Major Authorities


American Academy of Family Physicians --
Clinicians should counsel men age 50 to 65 about the known risks and uncertain benefits of screening for prostate cancer.


American Cancer Society --
Annual digital rectal examination should be performed for men aged 50 and over as part of prostate cancer screening (chapter 39). In men and women age 50 and over, a rectal examination should be done as part of colorectal cancer screening every 5 to 10 years, depending on the type of screening test used.


American College of Obstetricians and Gynecologists --
Digital rectal examination should be included in the periodic health examination of women 50 years of age and older as part of the pelvic exam.


American Society of Colon and Rectal Surgeons --
Annual digital rectal examination should be performed for asymptomatic, low-risk individuals 40 years of age and older and for asymptomatic individuals over 35 years of age with either a family history of colorectal adenomatous polyps or cancer in one or more first-degree relatives.


American Urological Association --
Annual digital rectal examination is recommended as part of prostate cancer screening for all men age 50 and over and for those at high risk starting at age 40 (chapter 39).


Canadian Task Force on the Periodic Health Examination(CTFPHE) --
There is insufficient evidence to recommend for or against the use of digital rectal examination to screen for prostate cancer. The CTFPHE has stated that evidence is insufficient to advise physicians who currently include digital rectal exam in examination on men 50 to 70 years of age to discontinue the practice.


US Preventive Services Task Force --
There is insufficient evidence to recommend for or against routine digital rectal examination as an effective screening test for prostate cancer in asymptomatic men. No recommendation has been made regarding the use of the examination for colorectal cancer screening.
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Basics of Rectum and Prostate Examination

1. General Considerations: Examine male and female patients while they are in the left lateral decubitus position or are standing, bent over the examination table. Female patients may also be examined while they are in the lithotomy position during a pelvic examination.

2. Inspection: Inspect the anal opening visually, noting any skin breakdown, fissures, and protrusions from the anal opening.

3. Palpation: To perform the examination, insert the lubricated, gloved index finger into the anal opening. Insert the gloved finger just past the rectal sphincter; do not advance it until the sphincter relaxes. The procedure can be uncomfortable for the patient but usually is not painful. Be sure to palpate all sides of the rectum for polyps, which may be sessile (attached by a base) or pedunculated (attached by a stalk). Intraperitoneal metastases may be felt anterior to the rectum as hard, shelf-like projections into the rectum. In men, thoroughly palpate the posterior and lateral lobes of the prostate gland. The normal prostate gland is approximately 2.5 cm by 4 cm and does not protrude into the rectum by more than 1 cm. It should feel smooth and rubbery throughout and have a palpable central groove. Asymmetry of the prostate gland or the presence of a hard, irregular nodule, or both, is typical of prostate cancer.

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Skin Examination

Skin cancer is the most common type of cancer in the United States. Approximately 900,000 new cases of basal and squamous cell carcinoma, as well as
40,300 cases of malignant melanoma, will be diagnosed in 1997. An estimated 7300 deaths from malignant melanoma and approximately 2190 deaths from other types of skin cancer will occur in 1997. The incidence of malignant melanoma is increasing at the rate of 4% per year. Virtually 100% of skin cancers are curable if they are diagnosed and excised early. Skin cancers occur more commonly in fair-skinned individuals who have been exposed to the sun, radiation, or ultraviolet light for prolonged periods of time. Chronic overexposure to sunlight is the cause of 95% of all basal cell carcinomas. Other risk factors for basal cell and squamous cell carcinomas include exposure to radiation, complications of burning or scarring, and contact with arsenic. Basal cell cancer is more common in older adults and affects men more frequently than women. Both basal cell and squamous cell cancers can occur in anyone with a history of prolonged sun exposure, and both are most likely to occur in sun-exposed areas. Factors placing individuals at increased risk for malignant melanoma include the presence of atypical moles and a personal or family history of skin cancer, especially malignant melanoma.

Recommendations of Major Authorities


American Academy of Dermatology and Skin Cancer Foundation --
Annual skin examinations are recommended for all patients.


Canadian Task Force on the Periodic Health Examination (CTFPHE), and US Preventive Services Task Force (USPSTF) --
There is insufficient evidence to recommend for or against routine screening for skin cancer by primary care clinicians with total skin examination. Clinicians should remain alert for skin lesions with malignant features when examining patients for other reasons, particularly in those with established risk factors. Risk factors include: melanocytic precursor or marker lesions (eg, atypical moles), large numbers of common moles, immunosuppression, a family or personal history of skin cancer, substantial cumulative lifetime sun exposure, intermittent intense sun exposure or severe sunburns in childhood, freckles, poor tanning ability, and light skin, hair, and eye color. The USPSTF states that clinicians should consider referring patients with melanocytic precursor or marker lesions to skin care specialists. The CTFPHE states that patients with family melanoma syndrome should receive total body skin examinations and be considered for referral to a specialist. Both the CTFPHE and the USPSTF state that there is insufficient evidence to recommend for or against routine counseling of patients to perform skin self-examination or to use sunscreens to prevent skin cancer. The CTFPHE states that use of sunscreen is recommended for patients with prior history of solar keratosis. The USPSTF states that use of sunscreen may be appropriate for such patients.


American Cancer Society --
Patients should undergo a cancer checkup that includes examination of the skin every 3 years for those 20 to 39 years of age, and yearly after age 40.


American College of Obstetricians and Gynecologists --
Skin examination should be performed for individuals with a family or personal history of skin cancer, increased occupational or recreational exposure to sunlight, or clinical evidence of precursor lesions (eg, dysplastic nevi and certain congenital nevi).
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Basics of Skin Examination

1. General Considerations: Perform the examination in a room that is comfortably warm; adjust lighting to produce optimal illumination. Basal cell or squamous cell carcinomas are likely to present in one of the following ways: as an open sore that bleeds, oozes, or crusts and is present for more than 3 weeks; as an irritated red patch that may itch or hurt; as a growth with a rolled border and central indentation; as a shiny bump or nodule; or as a scar-like area. Characteristics that may make a lesion suspicious for malignant melanoma may be remembered by following the ABCDs: A -- Asymmetry; B -- irregular Borders; C -- variation in Color from one area to another within the same lesion; and D -- a Diameter greater than 6 mm, about the size of a pencil eraser. Additional warning signs for malignant melanoma include sudden or continuous enlargement of a lesion; elevation of a previously macular pigmented lesion; surface changes, such as bleeding, crusting, erosion, oozing, scaliness, or ulceration; changes in the surrounding skin, such as redness, swelling, or satellite pigmentation; changes in sensation, such as itching, tenderness, or pain; changes in consistency, such as softening or friability; and the development of a new pigmented lesion, particularly in patients older than 40 years of age. Carefully evaluate all pigmented lesions.

2. With the Patient Seated: Examine the skin of the head, upper torso, and upper extremities while the patient is seated. Part the hair and inspect the scalp thoroughly and carefully. While examining the skin of the face and neck, take special note of the eyelids, forehead, ears, nose, and lips. Examine the upper extremities, shoulders, and back completely.

3. With the Patient Supine: Inspect the skin of the chest and abdomen with particular attention to the inguinal and genital areas. Elevate the scrotum to allow inspection of the perineal area. Carefully examine the feet, including the soles and the area between the toes.

4. With the Patient Lying on the Left Side: Examine the remaining skin of the back, legs, gluteal and perianal areas.

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Testicular Examination

Testicular cancer accounts for only about 1% of all cancers in men. However, it is the most common cancer in white men aged 20 to 34 years; 7200 new cases and 350 deaths are expected to occur in 1997. The prognosis for testicular cancer is very good, especially if it is treated early. The major risk factor is a history of cryptorchidism. Other risk factors include a previous history of testicular cancer, gonadal dysgenesis, Klinefelter's syndrome, and in utero exposure to diethylstilbestrol (DES). Testicular cancer is more common in white men than in African Americans; incidence rates are intermediate in Hispanics, American Indians, and Asians.

The two screening tests proposed for testicular cancer are health provider palpation of the testes and patient self-examination of the testes. No information is available on the sensitivity, specificity, or positive predictive value of testicular examination in asymptomatic men by either modality. Published evidence that self-examination can detect testicular cancer in asymptomatic men is limited to a small number of case reports.

Recommendations of Major Authorities


American Cancer Society --
Testicular examination should be a part of the cancer checkup received by men every 3 years from 20 to 39 years of age and annually beginning at age 40.


American Urological Association --
Yearly clinical examinations should begin at age 15.


Canadian Task Force on the Periodic Health Examination and US Preventive Services Task Force (USPSTF) --
There is insufficient evidence to recommend for or against routine screening of asymptomatic men for testicular cancer by physician examination or patient self-examination. The USPSTF has stated that recommendations against such screening can be made on other grounds, such as the current excellent prognosis of testicular cancer patients and the likelihood that a large number of false-positive results would result from screening. Patients with an increased risk of testicular cancer (those with a history of cryptorchidism or testicular atrophy) should be informed of their increased risk of testicular cancer and counseled about the options for screening (physician or self-examination). Adolescent and young adult males should be advised to seek prompt medical attention if they notice a testicular or intrascrotal abnormality.
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Basics of Testicular Examination

1. Inspection: With the patient standing, inspect the genital area for swelling, edema, and other visible abnormalities. Elevate the scrotum to permit inspection of the perineum.

2. Femoral Nodes: Palpate the horizontal chain of nodes inferior to the inguinal ligament and the vertical chain along the upper inner thigh. Nodes smaller than 1 cm in diameter may be normal if they are soft, discrete, and movable.

3. Palpation: With the patient standing, use both hands to examine each testicle individually. One hand holds the superior and inferior poles of the testicle while the other hand palpates the anterior, posterior, medial, and lateral surfaces. If any masses are noted, attempt to place a finger between the mass and the testicle. This will help differentiate between masses that originate from the testicle and those that arise from other structures within the scrotum. Next, attempt to transilluminate the mass. A tumor should not transilluminate. When a neoplasm is present, the testicle is usually enlarged, firm, and heavier than normal. If any abnormalities are noted, examine the patient while he is in the supine position to try to distinguish between solid masses (which will remain) and varicoceles (which may resolve).

4. Testicular Self-Examination: Authorities disagree about whether to encourage patients to examine their testes regularly. Clinicians wishing to do so may refer to pamphlets on self-examination listed in " Patient Resources " below.

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Thyroid Examination

Approximately 16,100 cases of thyroid cancer will be diagnosed in 1997 in the United States; approximately 1239 deaths will be attributable to the disease. Persons at increased risk include those who have undergone irradiation of the head and neck as children and persons with a family history of multiple endocrine neoplasia, type II. Thyroid malignancy occurs twice as frequently in women as in men.

Recommendations of Major Authorities


American Academy of Family Physicians --
Use of ultrasound screening in asymptomatic persons for detection of thyroid cancer is not recommended.


American Cancer Society --
A cancer checkup, including palpation of the thyroid, should be performed every 3 years on individuals 20 to 39 years of age and yearly for individuals aged 40 years and over.


American College of Obstetricians and Gynecologists --
Thyroid palpation should be part of the periodic health examination for all women over the age of 18 years.


Canadian Task Force on the Periodic Health Examination and US Preventive Services Task Force (USPSTF) --
There is insufficient evidence for or against the performance of thyroid palpation for screening for thyroid cancer. The USPSTF has stated that a recommendation for screening patients with a history of external upper-body (primarily head and neck) irradiation in infancy and childhood can be made on other grounds, such as patient preference or anxiety.
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Basics of Thyroid Examination

1. Inspection: The patient should be seated with the neck flexed slightly in order to relax the sternocleidomastoid muscles. To highlight any swelling, position a standing lamp so that it shines tangentially across the neck. Observe the neck as the patient takes a sip of water. Thyroid masses will move up and down with swallowing because of the thyroid's location within the fascial sheath of the trachea. A midline mass may also be a thyroglossal duct cyst.

2. Palpation: The patient should be sitting straight, with the neck flexed slightly forward and to the right. While standing behind the patient, use the fingertips of the left hand to push the trachea slightly to the right and the fingers of the right hand to retract the sternocleidomastoid muscle. While the patient takes a sip of water, palpate the medial and lateral margins of the thyroid with the fingertips of the right hand. Reverse the procedure on the left side. A malignancy may present as a discrete area of firmness or hardness. Thyroid gland tenderness may also be suggestive of malignancy.

3. Lymph Nodes: Examine the thyroid for the presence of lymphadenopathy. The uppermost pretracheal node that lies above or over the thyroid isthmus is called the Delphian node. An enlarged Delphian node may be the earliest sign of metastatic papillary cancer. Also examine the pre- and postauricular nodes, as well as the anterior and posterior cervical nodes. The anterior cervical nodes are clustered in a 7-shaped configuration, with the horizontal axis just below the body of the mandible and the vertical axis along the anterior border of the sternocleidomastoid muscle. The posterior cervical nodes are clustered in an L-shaped configuration, with the horizontal axis along the clavicle and the vertical axis along the anterior margin of the trapezius. Palpate the lymph nodes using a gentle circular motion of the finger pads. It is usually most efficient to palpate with both hands to permit comparison of the two. Normal nodes should feel movable, discrete, soft, and nontender.

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Patient Resources - Breast Cancer


Breast Cancer: Steps to Finding Breast Lumps Early. American Academy of Family Physicians, 8880 Ward Pkwy, Kansas City, MO 64114-2797; (800)944-0000. Internet address: http://www.aafp.org


How To Do Breast Self Examination; Breast Cancer - Questions and Answers; Cancer Facts for Women. American Cancer Society, 1599 Clifton Rd, NE, Atlanta, GA 30329-4251; 1-800-ACS-2345. Internet address: http://www.cancer.org


Mammography. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; (800)762-2264. Internet address: http://acog.com


Questions and Answers About Evaluating Breast Changes; Benign Breast Lumps and other Benign Breast Changes; What You Need To Know About Ovarian Cancer; The Pap Test: It Could Save Your Life (Spanish). Office of Cancer Communications, National Cancer Institute, Bldg 31, Room 10A16, Bethesda, MD 20892; 1-800-4-CANCER.


Chances are You Need a Mammogram; Are You Age 50 or Older? A Mammogram Could Save Your Life (English and Spanish). Office of Cancer Communications, National Cancer Institute, Bldg 31, Room 10A16, Bethesda, MD 20892; (800)4-CANCER. Internet address: http://cancernet.nci.nih.gov
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Provider Resources - Breast Cancer


Detecting and Treating Breast Problems. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024-2188; (202)638-5577. Internet address: http://www.acog.com


Nonmalignant Conditions of the Breast (ACOG Technical Bulletin 156; 1991). American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; 1-800-762-2264. Internet address: http://www.acog.com


Mammography Awareness Kit. Office of Cancer Communications, National Cancer Institute, Bldg 31, Room 10A16, Bethesda, MD 20892; (800)4-CANCER. Internet address: http://cancernet.nci.nih.gov
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Patient Resources - Cancers of the Oral Cavity


Head & Neck Cancer: Know What the Warning Signs Are. American Academy of Otolaryngology-Head and Neck Surgery, Order Department, 1 Prince St, Alexandria, VA 22314; (703)836-4444.


Facts on Oral Cancer; Self Oral Screen in Six Orderly Steps. American Cancer Society, 1599Clifton Rd, NE, Atlanta, GA 30329-4251; (800)ACS-2345. Internet address: http://www.cancer.org


What You Need to Know about Oral Cancer. Office of Cancer Communications, National Cancer Institute, Bldg 31, Room 10A16, Bethesda, MD 20892; (800)4-CANCER. Internet address: http://cancernet.nci.nih.gov
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Patient Resources - Cancer of Pelvic Organs


Preventing Cancer; Cancer of the Ovary. American College of Obstetricians and Gynecologists, 409 12th St SW, Washington, DC 20024; (800)762-2264. Internet address: http://www.acog.com


What You Need To Know About Ovarian Cancer; The Pap Test: It Could Save Your Life (Spanish). Office of Cancer Communications, National Cancer Institute, Bldg 31, Room 10A16, Bethesda, MD 20892; 1-800-4-CANCER.


Preventing Cancer; Cancer of the Ovary. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; (800)762-2264. Internet address: http://www.acog.com
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Provider Resources - Cancer of Pelvic Organs


Cervical Cytology: Evaluation and Management of Abnormalities. Technical Bulletin 183. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; 1-800-762-2264. Internet address: http://www.acog.com


The Pap Test. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington DC 20024; (800)762-2264. Internet address: http://www.acog.com
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Patient Resources - Prostate Cancer


For Men Only: Prostate Cancer; Cancer Facts for Men. American Cancer Society, 1599 Clifton Rd, NE, Atlanta, GA 30329-4251; 1-800-ACS-2345. Internet address: http://www.cancer.org


Prostate Disease: What Every Man Over 40 Should Know. Prostate Health Council, c/o American Foundation for Urologic Disease, Inc, 1128 N Charles St, Baltimore, MD 21201. Written requests only.


The prostate puzzle. Consumer Reports. 1993;58(7):459-465.
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Patient Resources - Colorectal Cancer


Colorectal Cancer, Questions & Answers. American Society of Colon and Rectal Surgeons, 800 E Northwest Hwy, Suite 1080, Palatine, IL 60067; (708)359-9184.


Colonoscopy: Questions and Answers; Polyps of the Colon and Rectum: Questions and Answers. American Society of Colon and Rectal Surgeons, 800 E Northwest Hwy, Suite1080, Palatine, IL 60067; (708)359-9184.


What You Need to Know about Cancer of the Colon and Rectum. Office of Cancer Communications, National Cancer Institute, Bethesda, MD 20892; (800)4-CANCER. Internet address: http://cancernet.nci.nih.gov
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Patient Resources - Skin Cancer


Skin Cancer: Saving Your Skin From Sun Damage. American Academy of Family Physicians, 8880 Ward Pkwy, Kansas City, MO 64114-2797; (800)944-0000. Internet address: http://www.aafp.org


The ABCDs of Moles & Melanomas; Dysplastic Nevi and Malignant Melanoma: A Patient's Guide; Skin Cancer: If You Can Spot It, You Can Stop It. The Skin Cancer Foundation, POBox 561, New York, NY 10156; (212)725-5176.


Facts on Skin Cancer. American Cancer Society, 1599 Clifton Rd, NE, Atlanta, GA 30329-4251. (800)ACS-2345. Internet address: http://www.cancer.org
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Provider Resource - Skin Cancer


Prevention and Early Detection of Malignant Melanoma. American Cancer Society, 1599 Clifton Rd, NE, Atlanta, GA 30329-4251. (800)ACS-2345. Internet address: http://www.cancer.org
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Patient Resource - Testicular Cancer


Testicular Cancer & Testicular Self-Examination. American Urological Association, Inc, 1120 N Charles St, Baltimore, MD 21201-5559; (410)727-1100.
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Provider Resource - General


PDQ: The Physician Data Query System for Cancer Information. PDQ is the National Cancer Institute's computerized database providing the most up-to-date cancer information available. Access to the system can be gained 24 hours a day, 7 days a week, using a personal computer and standard telephone line or through medical libraries. Ask a medical librarian for assistance or call (800)4-CANCER (line 3). In Hawaii, on Oahu, call 524-1234.


OncoLink - The University of Pennsylvania Cancer Center Resource. Internet address: http://cancer.med.upenn.edu
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American Cancer Society. . Cancer Facts & Figures-1997. Atlanta, Ga: American Cancer Society; 1997.

American Cancer Society. . Summary of American Cancer Society recommendations for the early detection of cancer in asymptomatic people. CA. 1993. 43: -.

American Cancer Society. . Cancer Information Database. Atlanta, Ga: American Cancer Society; June 1997.

American College of Obstetricians and Gynecologists. . Routine Cancer Screening. ACOG Committee Opinion #128. Washington, DC: American College of Obstetricians and Gynecologists; 1993.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Physicians. . Guidelines. In Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991:411-416.

American Society of Colon and Rectal Surgeons. . Practice Parameters for the Detection of Colorectal Neoplasms. Palatine, Ill: American Society of Colon and Rectal Surgeons; 1992.

American Urological Association. . Early Detection of Prostate Cancer. Baltimore, Md: American Urological Association; 1995.

Canadian Task Force on the Periodic Health Examination. . Prevention of skin cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 70.

Canadian Task Force on the Periodic Health Examination. . Screening for breast cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 65.

Canadian Task Force on the Periodic Health Examination. . Screening for colorectal cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 66.

Canadian Task Force on the Periodic Health Examination. . Screening for oral cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 69.

Canadian Task Force on the Periodic Health Examination. . Screening for ovarian cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 72.

Canadian Task Force on the Periodic Health Examination. . Screening for prostate cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 67.

Canadian Task Force on the Periodic Health Examination. . Screening for testicular cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 74.

Canadian Task Force on the Periodic Health Examination. . Screening for thyroid disorders and thyroid cancer in asymptomatic adults. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 51.

Canadian Task Force on the Periodic Health Examination. . The periodic health examination: 2. 1987 update: endometrial cancer. Can Med Assoc J. 1988;138:620-621.

DeGowin EL, DeGowin RL. . Bedside Diagnostic Examination. 5th ed. New York, NY: Macmillan Publishing Co; 1987.

Eddy DM, Gordon MA, Bredt A. . Screening for breast cancer. Ann Intern Med. In press.

Fink DJ, Mettlin CJ. . Cancer detection: the cancer-related checkup guidelines. In: Murphy GP, Lawrence W, Jr., Lenhard RE, Jr., eds. American Cancer Society Textbook of Clinical Oncology. 2nd ed. Atlanta, Ga: American Cancer Society; 1995: chap 10.

Friedman RJ, Rigel DS, Silverman MK, Kopf AW, Vossaert KA. . Malignant melanoma in the 1990s: the continued importance of early detection and the role of physician examination and self-examination of the skin. CA. 1991;41:201-227.

Gerber GS, Thompson IM, Thisted R, Chodak GW. . Disease-specific survival following routine prostate cancer screening by digital rectal examination. JAMA. 1993;269:61-64.

Jarvis C. . Physical Examination and Health Assessment. Philadelphia, Pa: WB Saunders Co; 1992.

MacLeod J, Munro J, eds. . Clinical Examination. 7th ed. New York, NY: Churchill Livingstone; 1986.

Mettlin C, Jones G, Averette H, et al. . Defining and updating the American Cancer Society guidelines for the cancer-related checkup: prostate and endometrial cancers. CA. 1993. 43: 42-46. (PubMed)

Moloy PJ. . How to (and how not to) manage the patient with a lump in the neck. In: Common Problems of the Head and Neck Region. Philadelphia, Pa: WB Saunders Co; 1992:129-150.

Parker SL, Tong T, Bolden S, Wingo PA. . Cancer statistics, 1997. CA. 1997. 47: 5-27. (PubMed) (Full Text in PMC)

Rhodes AR, Weinstock MA, Fitzpatrick TB, Mihm MC, Sober AJ. . Risk factors for cutaneous melanoma: a practical method of recognizing predisposed individuals. JAMA. 1987;258:3146-3153.

Garnick MB, Mayer RJ, Richie JP. . Testicular self-examination. N Engl J Med. 1980. 302: -.

Smart CR, Chu K, Conley V, Henson DE, Pommerenke F, Srivastova S. . Cancer screening and early detection. In: Holland JF, Frei EF III, Bast RC Sr. , Kufe DW, Morton DL, Weichselbaum RR, eds. Cancer Med. 3rd ed. Vol 1. Philadelphia, Pa: Lea and Febiger, 1993;408-431.

Swartz MH. . Textbook of Physical Diagnosis. Philadelphia, Pa: WB Saunders Co; 1989.

US Preventive Services Task Force. . Screening for breast cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 7.

US Preventive Services Task Force. . Screening for colorectal cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 8.

US Preventive Services Task Force. . Screening for oral cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 17.

US Preventive Services Task Force. . Screening for ovarian cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 14.

US Preventive Services Task Force. . Screening for prostate cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 10.

US Preventive Services Task Force. . Screening for skin cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 12.

US Preventive Services Task Force. . Screening for testicular cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 13.

US Preventive Services Task Force. . Screening for thyroid cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 18.

Wartofsky L. . Examination of the thyroid. In: Becker KL, ed. Principles and Practice of Endocrinology & Metabolism. New York, NY: JB Lippincott; 1990.

Wingo PA, Landis S, Ries LAG. . An adjustment to the 1997 estimate for new prostate cancer cases. CA. 1997. 47(4): 239-242. (PubMed)

Tables

Table 30.1. Leading Sites of Cancer Incidence and Death -- 1997 Estimates *

31. Cholesterol

High blood cholesterol is an important modifiable risk factor for coronary heart disease (CHD) -- the leading cause of death for both men and women in the United States. This year, as many as 1.5 million Americans will have a new or recurrent myocardial infarction, and about one third of these individuals will die. Large, population-based studies have demonstrated that total cholesterol levels are directly related to the incidence of CHD. The Multiple Risk Factor Intervention Trial (MRFIT) found that the 6-year risk of death from CHD in normotensive, nonsmoking, middle-aged men with blood cholesterol levels less than 182 mg/dL was one fourth that of men with blood cholesterol levels of 245 mg/dL or higher. An analysis of 22 epidemiologic studies has shown that elevated cholesterol is also a risk factor for CHD in women and in individuals > 65 years of age. Epidemiologic studies have also shown that cholesterol lipoprotein subfractions play an important role in CHD. LDL-cholesterol is directly, and HDL-cholesterol is inversely, associated with the incidence of CHD.

No long-term study has compared interventions to reduce cholesterol levels and CHD incidence based on routine cholesterol screening with interventions based on selective case-finding or with universal dietary advice. Because the recent increase in cholesterol screening had been accompanied by an improved knowledge and public awareness of dietary risk factors, isolating the contribution of screening from other factors that may account for improved outcomes may be difficult. The major evidence to support cholesterol screening is the ability of cholesterol-lowering interventions to reduce the risk of CHD in patients with high cholesterol.

A meta-analysis of cholesterol-lowering trials performed mainly in middle-aged men found that lowering blood cholesterol levels through dietary management or drug therapy significantly reduces the risk of CHD death and nonfatal myocardial infarction. The West of Scotland Coronary Prevention Study Group, a primary prevention trial, showed a reduction in cardiovascular mortality associated with drug treatment with no difference between treatment groups in the rate of death due to noncardiovascular causes. Similarly, the Scandinavian Simvastatin Survival Study, a secondary prevention trial, showed that in patients with a history of myocardial infarction, the reduction in CHD mortality associated with drug treatment was accompanied by a reduction in total mortality.

See chapter 4 for information on cholesterol screening for children and adolescents.

Recommendations of Major Authorities


American Academy of Family Physicians --
Males aged 35 to 65 years and females aged 45 to 65 years should be screened periodically for high cholesterol levels.


American College of Obstetricians and Gynecologists --
Adults (19 years of age and older) should have cholesterol measured every 5 years until 64 years of age, then every 3 to 5 years thereafter. (These are currently under review for a possible change to recommendations consistent with the US Preventive Services Task Force.)


American College of Physicians --
Screening for total cholesterol in the primary prevention of CHD is appropriate but not mandatory in men between 35 and 65 years of age and for women between 45 and 65 years of age. Screening for total cholesterol is not recommended for men younger than 35 years of age or women younger than 45 years of age unless the history or physical examination suggests a familial lipoprotein disorder, or at least two other characteristics place them at increased risk for developing CHD. There is insufficient evidence to recommend for or against screening in men and women between the ages of 65 and 75. Screening of individuals over 75 years of age is not recommended. In those individuals who are screened for the primary prevention of CHD, the total cholesterol level should be measured once. It should be repeated periodically if the measured value is near a treatment threshold. All patients with known CHD or whose history of other kinds of vascular disease places them at very high risk of CHD should have measurements of total cholesterol.


Canadian Task Force on the Periodic Health Examination --
There is insufficient evidence for the inclusion or exclusion of universal screening for hypercholesterolemia in a periodic health examination. Nonetheless, case-finding through repeated measurements of the nonfasting total blood cholesterol level should be considered in men 30 to 59 years of age.


National Cholesterol Education Program (NCEP) of the National Heart, Lung, and Blood Institute --
Adults (20 years of age and older) should have a measurement of total blood cholesterol at least once every 5 years; HDL-cholesterol should be measured at the same time if accurate results are available. Lipoprotein analysis should be performed for all patients with CHD. In patients without CHD, lipoprotein analysis should be performed in any of the following circumstances: (1) if the total cholesterol is 240 mg/dL or above; (2) if the total cholesterol is 200 to 239 mg/dL and the patient also has two or more CHD risk factors; (3) if the patient has an HDL-cholesterol less than 35 mg/dL. See Tables 31.1 and 31.2 and Figures 31.1, 31.2, and 31.3 for NCEP recommendations on CHD risk factors and patient classification and identification.


US Preventive Services Task Force --
Periodic screening for high serum cholesterol is recommended for all men 35-65 years of age and women 45-65 years of age. There is insufficient evidence to recommend for or against screening asymptomatic persons after 65 year of age, but screening may be considered on a case-by-case basis. Older persons with major CHD risk factors (smoking, hypertension, diabetes) who are otherwise healthy may be more likely to benefit from screening, based on their high risk of CHD and the proven benefits of lowering cholesterol in older persons with symptomatic CHD. Cholesterol levels are not a reliable predictor of risk after age 75, however. There is also insufficient evidence to recommend for or against screening of young adults, although this may be recommended on other grounds to young adults at high risk, such as the greater absolute risk attributable to high cholesterol and potential long-term benefits of early lifestyle interventions. Risk factors include: family history of very high cholesterol, premature CHD in a first-degree relative (before age 50 in men or age 60 in women), diabetes, smoking, or hypertension. The appropriate interval for periodic screening is not known. Periodic screening is most important when cholesterol levels are increasing (eg, middle-aged men, perimenopausal women, and persons who have gained weight). An interval of five years has been recommended by experts, but longer intervals may be reasonable for low-risk subjects (including those with previously desirable cholesterol levels). There is insufficient evidence to recommend for or against routine measurement of HDL-cholesterol or triglycerides at initial screening.
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Basics of Cholesterol Screening

1. Do not screen patients who are acutely ill, losing weight, pregnant, or breast-feeding, because their cholesterol levels may not be representative of their usual levels. Cholesterol levels in patients who have had a myocardial infarction within the past 3 months are likely to be lower than usual. Therefore, recheck any results obtained during this period.

2. Inform patients that they need not vary their usual eating habits before undergoing screening for total blood cholesterol or HDL-cholesterol levels. Instruct patients undergoing lipoprotein analysis to fast for 12 hours before testing. Water and black coffee are acceptable, however.

3. If possible, perform cholesterol tests on venous blood samples, because cholesterol concentrations measured from finger-stick blood samples may be unreliable. The NCEP cut-off values for diagnostic and therapeutic actions refer to venous serum samples.

4. To prevent an effect of posture or stasis on the cholesterol value, perform venipuncture only after the patient has been in the sitting position for at least 5 minutes; apply the tourniquet for as brief a period as possible.

5. When interpreting results, be aware of the effects of medications on blood cholesterol levels. Anabolic steroids, progestins, bile salts, and chlorpromazine increase blood cholesterol levels. Be knowledgeable about conditions that may cause increased cholesterol levels, such as hypothyroidism, nephrotic syndrome, diabetes mellitus, and obstructive liver disease.

6. Cholesterol tests should be analyzed by an accredited laboratory that meets current standards for precision and accuracy. The Laboratory Standardization Panel of the National Cholesterol Education Program has set a goal that laboratories have systematic and precision errors of less than 3% each in processing total cholesterol samples. Inquire about a laboratory's performance history and its quality-control methods before using it for screening.

7. Cholesterol values in plasma samples tend to be lower than serum samples because of the effects of EDTA in plasma samples. NCEP has determined cholesterol level cut-off values based on serum samples and has designated that cholesterol levels obtained from plasma samples be multiplied by 1.03 to arrive at a serum equivalent.

8. Convert cholesterol values in mg/dL to mmol/L by multiplying by 0.02584. Convert triglyceride levels similarly by multiplying by 0.01129.

9. See Table 56.3 for information about NCEP's Step I and Step II Diet for treatment of patients with elevated cholesterol levels.

10. Provide dietary and weight-reduction counseling to all patients who are obese, regardless of their cholesterol levels (chapters 29 and 56). Provide advice about increasing physical activity to all patients who are physically inactive, regardless of their cholesterol levels (chapter 57).

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Patient Resources


Cholesterol: What You Can Do to Lower Your Level. American Academy of Family Physicians, 8880 Ward Parkway, Kansas City, MO 64114-2797; (800)944-0000; http://www.aafp.org


Cholesterol and Your Health. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024-2188; (800)762-2264. Internet address: http://www.acog.com


Cholesterol and Your Heart; Dietary Treatment of Hypercholesterolemia: A Manual for Patients; Eat Less Fat and High Cholesterol Foods; Heart Rx (a kit of materials for patients, providers, and staff). To order these and many other materials, contact the American Heart Association, 7320 Greenville Ave, Dallas, TX 75231. To receive the telephone number of your state office, call the main office at: (800)242-8721; materials vary by state. Internet address: http://www.amhrt.org


American Heart Association Low-Fat, Low-Cholesterol Cookbook. This publication is available at retail bookstores. Internet address: http://www.amhrt.org


Eat Right to Lower Your High Blood Cholesterol and Step by Step: Eating to Lower Your High Blood Cholesterol; So You Have High Blood Cholesterol. National Heart, Lung, and Blood Institute Information Center, PO Box 30105, Bethesda, MD 20824-0105; (301)251-1222. Internet address: http://www.nhlbi.nih.gov/nhlbi/nhlbi.htm. Information is available in both English and Spanish. The following materials are available in Spanish: Learn Your Cholesterol Number (Conozca su nivel de colesterol); Protect Your Health-Lower Your Blood Cholesterol (Proteja su corazon-baje su colesterol); and Heart-Healthy Latino Recipes (Platillos Latinos).
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Provider Resource


Summary of the Second Report of the National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II). Full report: National Cholesterol Education Program: Second Report of the Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II). National Heart, Lung, and Blood Institute Information Center, PO Box 30105, Bethesda, MD 20824-0105; (301)251-1222. Information is available in both English and Spanish. Internet address: http://www.nhlbi.nih.gov/nhlbi/nhlbi.htm
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Physicians, Clinical Efficacy Assessment Project. . Using serum cholesterol, high-density lipoprotein cholesterol, and triglycerides as screening tests for the prevention of coronary heart disease in adults. Ann Intern Med. In press.

American College of Physicians. . Guidelines. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991:402-403.

American Heart Association. . Heart and Stroke Facts: 1996 Statistical Supplement. Dallas, TX: American Heart Association; 1995.

Canadian Task Force on the Periodic Health Examination. . Lowering the total blood cholesterol level to prevent coronary heart disease. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 54.

Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. . Summary of the second report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II). JAMA. 1993. 269: 3015-3023. (PubMed)

Greenland P, Bowley NL, Meiklejohn B, Doane KL, Sparks CE. . Blood cholesterol concentration: fingerstick plasma vs venous serum sampling. Clin Chem. 1990. 36: 628-630. (PubMed)

National Cholesterol Education Program. . Second Report of the National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II). Bethesda, Md: National Heart, Lung, and Blood Institute. 1993. The full Adult Treatment Panel II report is also available in Circulation. 1994. 89: 1329-1445.

National Cholesterol Education Program. . Report of the Expert Panel on Population Strategies for Blood Cholesterol Reduction. Bethesda, Md: National Institutes of Health, National Heart, Lung, and Blood Institute; 1990. US Dept of Health and Human Services, PHS publication NIH 90-3046.

NIH Consensus Development Panel on Triglyceride, High-Density Lipoprotein, and Coronary Heart Disease. . Triglyceride, high-density lipoprotein, and coronary heart disease. JAMA. 1993. 269: 505-510. (PubMed)

Sempos CT, Cleeman JI, Carroll MD, et al. . Prevalence of high blood cholesterol among US adults: an update based on guidelines from the second report of the National Cholesterol Education Program Adult Treatment Panel. JAMA. 1993. 269: 3009-3014. (PubMed)

Shepherd J, Cobbe SM, Ford I, et al. . Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. N Engl J Med. 1995. 333: 1301-7. (PubMed)

US Preventive Services Task Force. . Screening for blood cholesterol. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 2.

Tables

Table 31.1. NCEP Coronary Heart Disease Risk Factors Other Than LDL-Cholesterol *

Table 31.2. Treatment Decisions Based on LDL-Cholesterol

[Figures]

Figure 31.1. Primary Prevention in Adults Without Evidence of CHD: Initial Classification Based on Total Cholesterol and HDL-Cholesterol

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Adapted from: National Cholesterol Education Program. Second Report of the National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II). Bethesda, Md: National Institutes of Health, National Heart, Lung, and Blood Institute; 1993. USDHHS Publication NIH 93-3095.top link

Figure 31.2. Primary Prevention in Adults Without Evidence of CHD: Subsequent Classification Based on LDL-Cholesterol

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*On the basis of the average of two determinations. If the first two LDL-cholesterol levels differ by more than 30 mg/dL, perform a third test within 1 to 8 weeks, and use the average value of the three tests.top link


Adapted from: National Cholesterol Education Program. Second Report of the National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II). Bethesda, Md: National Institutes of Health, National Heart, Lung, and Blood Institute; 1993. USDHHS Publication NIH 93-3095.top link

Figure 31.3. Secondary Prevention in Adults With Evidence of CHD: Classification Based on LDL-Cholesterol

**If the first two LDL-cholesterol levels differ by more than 30 mg/dL, perform a third test within 1 to 8 weeks, and use the average value of the three tests.

Adapted from: National Cholesterol Education Program. Second Report of the National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II). Bethesda, Md: National Institutes of Health, National Heart, Lung, and Blood Institute; 1993. USDHHS Publication NIH 93-3095.top link



*Perform lipoprotein analysis when the patient is not in the recovery phase from an acute coronary or other medical event that would lower the patient's usual LDL-cholesterol level.top link

32. Cognitive and Functional Impairment

Cognitive impairment includes deficits in memory, abstract thinking, judgement, speech, coordination, planning, or organization. A functional impairment is a deficit in an individual's ability to perform either the basic activities of daily living (ADLs), such as as dressing, bathing, and eating, or instrumental activities of daily living (IADLs) -- such as using transportation, shopping, or handling finances. A functional impairment can be the result of a cognitive, physical, social, or psychological disorder. Dementia is a syndrome of progressive decline in multiple cognitive abilities that eventually leads to functional impairment. The most common form of dementia is Alzheimer's disease.

It is estimated that between 5% and 10% of persons older than 65 years of age suffer from some form of cognitive impairment, and this increases dramatically with age. The most common causes of cognitive impairment, Alzheimer's disease and vascular infarctions, are largely untreatable. However, approximately 10% to 15% of cases of cognitive impairment in older adults are attributable to treatable causes, such as hypothyroidism and drug intoxications. In some instances, early intervention can result in the arrest or reversal of cognitive defects. Approximately 2% to 8% of community-dwelling elderly persons suffer from impairments of ADLs. As many as 25% of community-dwelling older adults may suffer from functional impairment in carrying out IADLs.

Cognitive and functional impairment are growing health concerns in the United States because of the aging population. In some instances, early identification of these impairments can lead to the reversal or slowing of the progression of the impairment. In other instances, early identification alerts affected persons and their families to potentially hazardous situations and is of value in terms of planning support services.

See chapter 58 on polypharmacy.

Recommendations of Major Authorities


The Alzheimer's Disease and Related Dementias Panel of the Agency of Health Care Policy and Research --
Health care providers should perform an initial assessment of dementia on clients with symptoms of increasing difficulties in the following areas: learning and retaining new information; handling complex tasks; reasoning ability; spatial ability and orientation; language or behavior.


American College of Obstetricians and Gynecologists --
Women over 65 years of age should be screened for changes in cognitive function as part of their routine preventive visits.


American College of Physicians --
Functional assessment screening by the clinician is useful for evaluating the health status of elderly patients and determining their needs for in-home assistance, home health services, or institutional placement. In the acute-care setting, functional assessment in selected patients facilitates discharge planning and is essential in patients over 75 years of age. Primary care providers should incorporate into the routine medical management of older adults procedures for measuring functional deficits and identifying dependency needs. Employing a comprehensive screening instrument followed by targeted screening instruments can be useful in systematically assessing functional deficits that otherwise might be overlooked by conventional examination methods.


Canadian Task Force on the Periodic Health Examination --
There is insufficient evidence to recommend for or against active screening for cognitive impairment in people over 65 years of age. However, prudent clinicians should be alert for symptoms suggestive of cognitive impairment and conduct appropriate assessments.


US Preventive Services Task Force --
There is insufficient evidence to recommend for or against routine screening for dementia in asymptomatic elderly persons. Clinicians should periodically ask patients about their functional status at home and at work, and they should remain alert to changes in performance with age. When possible, information about daily activities should be solicited from family members and other persons. Brief tests, such as the Mini-Mental State Exam, should be used to assess cognitive function in patients in whom the suspicion of dementia is raised by restrictions in daily activities, concerns of family members, or other evidence of worsening function (eg, trouble with finances, medications, transportation). Possible effects of education and cultural differences should be considered when interpreting abnormal results.
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Basics of Cognitive and Functional Impairment Screening

Cognitive Impairment

1. Effective screening for cognitive impairment requires assessment of multiple aspects of mental functioning, including orientation, short-term memory, receptive and expressive language ability, attention, and visual-spatial ability.

2. Orientation can be rapidly assessed by asking the patient to give the day of the week, the month, the year, and current location. Short-term memory can be rapidly assessed by asking the patient to repeat a seven-digit number or recall three objects. Language ability can be rapidly assessed by asking the patient to name simple objects, repeat a phrase, or write a sentence. Attention can be rapidly assessed by asking the patient to count backward from 100 to 65 by subtracting 7, or to name the months of the year in reverse order. Visual-spatial ability can be rapidly assessed by asking the patient to draw a complex figure, such as the face of a clock or a three-dimensional cube.

3. Use of a short, standardized screening instrument can accomplish this basic assessment and provide a baseline for assessing changes in cognitive function in the future. No single screening instrument best addresses all areas of cognition or is appropriate for all patients. The most widely used and studied brief screening instrument is the Mini-Mental State Examination (Table 32.1).

4. Any assessment of cognitive functioning must take into consideration the patient's level and clarity of consciousness (is the patient delirious?), affective state (is the patient depressed?), effects of medications and drugs (is the patient intoxicated?), level of education and baseline intelligence (would the patient have understood as a young person?), and native language (is the patient fluent in English?).

5. Patients with indications of cognitive impairment should be considered for referral to a specialist for more definitive evaluation before the diagnosis of dementia is made and treatment begun.

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Functional Impairment

1. Assessment of functional impairment can be performed by a variety of methods, including observation of the patient in the home; observation of the patient in the office; questioning of the patient, family, or both; and use of brief, structured questionnaires. Within the limits of time and resources, use a variety of methods of assessment.

2. Use structured questions to supplement, not replace, clinical observation and more extensive forms of assessment.

3. IADLs can be briefly evaluated by using the following five structured questions in Table 32.2.

4. ADLs can be briefly assessed using the six structured questions in Table 32.3

5. Investigate any identified impairments in function for etiology (physical, psychological, environmental) and possible means of treatment or amelioration (in-home support services, speech and language therapy, physical and occupational therapy).

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Patient Resources


Memory and Aging: Alzheimer's Disease and Related Disorders. To order this and many other materials, contact the Alzheimer's Association, 919 N Michigan Ave, Suite 1000, Chicago, IL 60611;(800)272-3900.


Memory Loss: What's Normal, What's Not. American Academy of Family Physicians, 8880 Ward Pkwy, Kansas City, MO 64114; (800)944-0000. Internet address: http://www.aafp.org


Where Did I Put My Keys? American Association of Retired Persons, Fulfillment Services, 601 E St, NW, Washington, DC 20049; (202)434-2534.


Age Page -- Senility: Myth or Madness; Age Page -- Confusion and Memory Loss in Old Age: It's Not What You Think. National Institute on Aging, Bldg 31, Room 5C27, Bethesda, MD 20892; (301)496-1752. Internet address: http://www.nih.gov/nia/health/pubpub/pubpub.htm


Early Alzheimer's Disease. AHCPR Publication no. 96-0704. Agency for Health Care Policy and Research, Publications Clearinghouse, P.O. Box 8547, Silver Spring MD 20907; (800)358-9295. Internet address: http://www.ahcpr.gov


Administration on Aging. 330 Independence Ave., SW, Washington, DC 20201, (202)619-1006. The national office can provide phone numbers and addresses for state and local agencies on aging. Internet address: http://www.aoa.dhhs.gov


The Elder Care Locator (800)667-1116 provides toll-free access to state agency networks.
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Provider Resources


Older Voices. To order this trainer's manual and resource materials for communication problems of older persons, contact the American Speech-Language-Hearing Association, 10801 Rockville Pike, Rockville, MD 20852; (301)897-5700.


Early Identification of Alzheimer's Disease and Related Dementias: Quick Reference Guide for Clinicians (Number 19). AHCPR Publication no. 97-0703. Agency for Health Care Policy and Research, Publications Clearinghouse, P.O. Box 8547, Silver Spring Md 20907; (800)358-9295. The full text of guideline documents for online retrieval is available on the AHCPR Home Page. Click on "Clinical Practice Guidelines Online." Internet address: http://www.ahcpr.gov/guide
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Selected References

American College of Physicians, Health and Public Policy Committee. . Comprehensive functional assessment for elderly patients. Ann Intern Med. 1988;109:70-72. View this and related citations using

Calkins DR, Rubenstein LV, Cleary PD, Davies AR, Jette AM, Fink A, Kosecoff J, et al. . Failure of physicians to recognize functional disability in ambulatory patients. Ann Intern Med. 1991. 114: 451-454. (PubMed)

Canadian Task Force on the Periodic Health Examination. . The periodic health examination. Can Med Assoc J. 1979. 121: 1193-1254. (PubMed) (Full Text in PMC)

Canadian Task Force on the Periodic Health Examination. . Periodic Health Examination Monograph. Hull, Quebec: Ministry of Supply and Services; 1980.

Canadian Task Force on the Periodic Health Examination. . Screening for cognitive impairment in the elderly. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 75.

Costa PT Jr, Williams TF, Somerfield M, et al. . Recognition and Initial Assessment of Alzheimer's Disease and Related Dementias. Clinical Practice Guideline No. 19. Rockville, Md: US Department of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, AHCPR Publication No. 97-0702. November 1996.

Fillenbaum GG. . Screening the elderly: a brief instrumental activities of daily living measure. J Amer Geriatr Soc. 1985. 33: 698-706.

Folstein MF, Folstein SE, McHugh P. . "Mini-mental state": a practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975. 12: 189-198. (PubMed)

Katz S, Ford AB, Moskowitz RW, Jackson BA, Jaffe MW, Cleveland MA. . The index of ADL: a standardized measure of biological and psychosocial function. JAMA. 1963. 185: 914-919. (PubMed)

National Institutes of Health, Consensus Development Panel. . Differential diagnosis of dementing diseases. JAMA. 1987. 258: 3411-3416. (PubMed)

Patterson CJ. . Detecting cognitive impairment in the elderly. In: Goldbloom RB, Lawrence RS. Preventing Disease: Beyond the Rhetoric. New York, NY: Springer-Verlag; 1990: chap 18.

Pfeiffer E. . A short portable mental status questionnaire for the assessment of organic brain deficit in elderly patients. J Amer Geriatr Soc. 1975. 23: 433-441.

Siu AL. . Screening for dementia and investigating its causes. Ann Intern Med. 1991. 115: 122-132. (PubMed)

Siu AL, Reuben DB, Hays RD. . Hierarchical measures of physical function in ambulatory geriatrics. J Amer Geriatr Soc. 1990. 38: 1113-1119. (PubMed)

Rubenstein LV, Calkins DR, Greenfield S, et al. . Health status assessment for elderly patients: report of the Task Force on Health Assessment, Society of General Internal Medicine. J Amer Geriatr Soc. 1989. 37: 562-569. (PubMed)

US Preventive Services Task Force. . Screening for dementia. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 48.

Weiner JM, Hanley RJ, Clark R, Van Nostrand JF. . Measuring the activities of daily living: comparisons across national surveys. Journal of Gerontology. 1990. 45(6): S229-237. (PubMed)

Tables

Table 32.1. Mini-Mental State Examination

Table 32.2. Questions for Evaluating Instrumental Activities of Daily Living (IADLs)

Table 32.3. Questions for Evaluating Activities of Daily Living (ADLs)

33. Depression

Major depressive episodes are common in adults, affecting more than 9 million Americans and costing between $33 million and $40 billion yearly. Depression affects persons of all ages, genders, and races. See Table 33.1 for a list of risk factors for major depression.

Between 5% and 10% of patients in primary care practices and 10% to 14% of medical inpatients meet the criteria for major depression, and many patients with depressive disorders are seen only by nonpsychiatric health-care providers. Research has shown that up to 50% of depressed persons seen in primary care settings are not recognized as having this disorder. Patients with major depressive disorders have a great deal of functional impairment, resulting in lost time on the job, decreased job performance, and decreased family and social functioning. Effective medical treatments are available for major depression.

Recommendations of Major Authorities


American College of Obstetricians and Gynecology --
All women should receive age-specific psychosocial evaluations to detect depression and other problems.


American College of Physicians --
Elderly patients should undergo functional assessment screening, including measures of emotional status.


Canadian Task Force on the Periodic Health Examination --
There is fair evidence to exclude the use of depression detection tests from the periodic health examination of asymptomatic people. However, physicians should be sensitive to the possibility of depression in their patients, particularly those at high risk.


US Preventive Services Task Force --
There is insufficient evidence to recommend for or against performance of routine screening tests for depression in asymptomatic primary care patients. Clinicians should, however, maintain an especially high index of suspicion for depressive symptoms in adolescents and young adults, persons with a family or personal history of depression, those with chronic illnesses, those who have or perceive they have experienced a recent loss, and those with sleep disorders, chronic pain, or multiple unexplained somatic complaints.
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Basics of Depression Screening

1. The diagnostic criteria for a major depressive episode, as defined in the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV), are given in Table 33.2. Because the essential feature is either depressed mood or loss of pleasure in usual activities for at least 2 weeks, these symptoms should be discussed first when taking a history.

2. Some features of depression in elderly persons may be confused with symptoms of dementia, resulting in what has been called pseudodementia due to depression. Keep in mind that disorientation, memory loss, and distractibility in the elderly may be signs of depression rather than dementia.

3. Basic steps for detecting depression in primary care patients include:
  • Maintaining a high index of suspicion, especially with patients who have risk factors
  • Using the clinical interview or a written questionnaire (see item 4 below)
  • Eliciting additional information by questioning family or caretakers (with patient consent)
  • Identifying (and treating, if present) other possible causes for mood disorders, such as medical illness, medication use, or substance abuse
  • Making the diagnosis of major depressive disorder and proceeding to treatment or referral if no other causes for the mood changes are found (or if the depression continues after treatment of other causes of mood changes)


4. Several short self-report questionnaires for depression have been evaluated and found to be useful in primary care settings (Coulehan et al, 1989). These include the Short Beck Depression Inventory (BDI), the Zung Self-Rating Depression Scale (SDS), and the Center for Epidemiologic Studies Depression Scale (CES-D). The CES-D is given in Table 33.3. Self-report questionnaires are helpful in finding patients with depressive symptoms, but they are not diagnostic instruments. Many patients with mild depression who do not meet diagnostic criteria for a major depressive episode will be identified with these questionnaires. If a patient scores above the cut-off point on a questionnaire, use the clinical interview to elicit the criterion symptoms of a major depressive episode. Because self-report questionnaires are very sensitive to depressive symptoms, they can also be used appropriately to exclude major depression in patients who score below the cut-off points.

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Patient Resources


Depression Is a Treatable Illness: A Patient's Guide. Agency for Health Care Policy and Research Publications Clearinghouse, PO Box 8547, Silver Spring, MD 20907; 1-800-358-9295.


Depression. ACOG Patient Education Pamphlet AP106. Washington, DC: American College of Obstetricians and Gynecologists, 1994. Internet address: http://www.acog.com


To obtain free brochures about clinical depression, including information on depression in women, depression in the workplace, and depression co-morbid with medical, psychiatric, and substance abuse disorders, contact the National Institute of Mental Health, 5600 Fishers Ln, Room 10-85, Rockville, MD 20857; (800)421-4211. Internet address: http://www.nimh.nih.gov


Many types of materials are available from the National Mental Health Association, 1021 Prince St, Alexandria, VA 22314; (800)969-6642.


The National Depressive and Manic Depressive Association, 730 North Franklin Street, Suite 501, Chicago, IL 60610. (800)826-3632.


The National Mental Health Services Knowledge Exchange Network (KEN), P.O. Box 42490, Washington, DC 20015. KEN is a national, one-stop resource for mental health information and referrals that is accessible through a toll-free telephone number, (800)789-CMHS (2647); a toll-free electronic bulletin board system (BBS), (800)790-CMHS (2647). Internet address: http://www.mentalhealth.org/
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Provider Resources


Depression in Primary Care: Detection and Diagnosis (vol 1; AHCPR publication 93-0550); Treatment of Major Depression (vol 2; AHCPR publication 93-0551). These publications are available through the US Government Printing Office; call (202)510-1800.


Diagnosis and Treatment (Quick Reference Guide for Clinicians; AHCPR publication 93-0552). Agency for Health Care Policy and Research Publications Clearinghouse, PO Box 8547, Silver Spring, MD 20907; (800)358-9295.


Depression in Women. American College of Obstetricians and Gynecologists Technical Bulletin #182, 1992. ACOG Resource Center, 409 12th St., SW, Washington, DC 20024-2188; 1-800-762-2264. Internet address: http://www.acog.com


Diagnosis and Treatment of Depression in Late Life (NIH Consensus Development Conference, November 4-6, 1991; NIH Consensus Statements vol 9, no 3). NIH Consensus Clearing House, PO Box 2577, Kensington, MD 20891, 1-888-644-2667.
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Selected References

Agency for Health Care Policy and Research, Depression Guideline Panel. . Depression in primary care: detection, diagnosis, and treatment quick reference guide for clinicians 5. Rockville, Md: US Department of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, AHCPR Publication 93-0552; April 1993.

American College of Obstetricians and Gynecologists. . Depression in Women. Washington, DC: American College of Obstetricians and Gynecologists; 1993.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Physicians, Health and Public Policy Committee. . Comprehensive functional assessment for elderly patients. Ann Intern Med. 1988. 109: 70-72. (PubMed)

American Psychiatric Association. . Diagnostic and Statistical Manual of Mental Disorders. 3rd ed, rev. Washington, DC: American Psychiatric Association; 1987.

Beck AT, Rial WY, Rickels K. . Short form of depression inventory: cross validation. Psychological Reports. 1974. 34: 1184-1186. (PubMed)

Canadian Task Force on the Periodic Health Examination. . Early detection of depression. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 39.

Coulehan JL, Schulberg HC, Block MR. . The efficiency of depression questionnaires for case-finding in primary medical care. J Gen Intern Med. 1989. 4: 542-547.

Kamerow DB, Pincus HA, Macdonald DI. . Alcohol abuse, other drug abuse, and mental disorders in medical practice: prevalence, costs, recognition, and treatment. JAMA. 1986. 255: 2054-2057. (PubMed)

Radloff LS. . The CES-D Scale: a self-report depression scale for research in the general population. Appl Psychol Meas. 1977. 1: 385-401.

US Preventive Services Task Force. . Screening for depression. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 49.

Wells KB, Stewart A, Hays RD, et al. . The functioning and well-being of depressed patients: results from the Medical Outcomes Study. JAMA. 1989. 4: 7-13.

Zung WWK. . A self-rating depression scale. Arch Gen Psychiatry. 1965. 12: 63-70. (PubMed)

Tables

Table 33.1. Risk Factors for Depression

Table 33.2. Criteria for Major Depressive Disorder

Table 33.3. Center for Epidemiologic Studies Depression Scale *

34. Fecal Occult Blood

In 1997, approximately 131,200 new cases of colorectal cancer will occur, resulting in 54,900 deaths. Principal risk factors for colorectal cancer include a history of one of the familial polyposis syndromes, familial cancer syndromes, colorectal cancer in first-degree relatives, or a personal history of ulcerative colitis, adenomatous polyps, or endometrial, ovarian, or breast cancer. Colorectal cancer detected at an early stage can be successfully treated with surgery.

Malignancies and, to a lesser extent, polyps, bleed intermittently. Fecal occult blood tests (FOBT) can detect this bleeding by identifying occult blood or breakdown products of blood in fecal material. The reported sensitivity of FOBT for detecting colorectal cancer in asymptomatic individuals ranges from 26% to 92% but with most data suggesting a sensitivity of less than 40%. The specificity ranges form 90% to 99%. Measures of sensitivity and specificity are usually based on two samples from three consecutive and easily passed stools.

Until recently, no studies had shown that fecal occult blood testing resulted in decreased mortality. In 1993, however, Mandel et al found that yearly fecal occult blood testing using rehydrated stool specimens decreased mortality from colorectal cancer by about one third. In that study, guaiac-impregnated paper slides were used to test for fecal blood.

Rehydration of dried samples before testing can increase sensitivity but also produces more false-positive results. The predictive value of a positive fecal occult blood test for colorectal cancer in general populations is only 5% to 10%. Thus, up to 75% of cancers will be missed, and for every case of colorectal cancer that is detected by fecal occult blood testing, up to 20 patients will undergo workups that will be negative.

See chapters 30 and 41 for information about other methods of screening for colorectal cancer.

Recommendations of Major Authorities


American Academy of Family Physicians --
Adults aged 40 years and older with a family history of early colorectal cancer and all adults aged 50 years and older should be screened for colorectal cancer with fecal occult blood testing (annually), sigmoidoscopy, colonoscopy, or barium enema.


American Cancer Society --
Annual fecal occult blood testing is recommended in combination with flexible sigmoidoscopy every 5 years in normal risk individuals beginning at 50 years of age. The American Cancer Society further recommends that digital rectal examination be performed along with sigmoidoscopy. (See chapter 41 for details.)


American College of Obstetrics and Gynecology --
Fecal occult blood testing should be done for all women 50 years of age and older as part of their periodic health examination.


American College of Physicians --
Persons who decline screening colonoscopies and barium enemas, and especially people who decline screening flexible sigmoidoscopies, should be offered annual fecal occult blood testing from 50 to 70 or 80 years of age. No recommendation is made about the optimal frequency for screening with FOBT. In general, persons who have positive results on a fecal occult blood test should have a full colonic examination. More research is needed to understand and improve the sensitivity and specificity of the fecal occult blood test.


Canadian Task Force on the Periodic Health Examination(CTFPHE) --
There is insufficient evidence to recommend including or excluding fecal occult blood testing in the periodic health examination of individuals over 40 years of age. There is also insufficient evidence to provide fecal occult blood testing to adults at risk because of family history. Patients with true cancer family syndrome should be screened with colonoscopy, not fecal occult blood testing.


US Preventive Services Task Force --
Screening for colorectal cancer is recommended for all persons 50 years of age or older. This can be accomplished with annual fecal occult blood testing or sigmoidoscopy (frequency unspecified). There is insufficient evidence to determine which method is preferable or whether combining both methods produces results superior to either method alone.
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Basics of Fecal Occult Blood Screening

1. Three types of tests are available for detecting fecal occult blood: guaiac-impregnated cards and other carriers that detect the peroxidase-like activity of hemoglobin (Hemoccult[reg]); quantitative tests based on the conversion of heme to fluorescent porphyrins (HemoQuant[reg]); and immunoassay tests for human hemoglobin. Currently only the first two types are routinely used in practice. Guaiac-based tests have the disadvantage of giving false-negative and false-positive results because of dietary factors, and thus are more accurate if patients restrict their diets (see Table 34.1). Guaiac-based tests have the advantages of being relatively easy for patients and clinicians to use and relatively specific for lower gastrointestinal tract bleeding. The quantitative porphyrin tests are not affected by dietary factors and are potentially more sensitive than the other tests, depending on the cut point designated for a positive result. Recent evidence indicates, however, that at matched levels of specificity, the quantitative porphyrin tests are not significantly more sensitive than guaiac-based tests. Quantitative porphyrin tests have the potential disadvantages of not being specific for lower gastrointestinal tract bleeding and of requiring interpretation by a laboratory.

2. Do not collect a stool sample from patients with hematuria or obvious rectal bleeding (eg, from hemorrhoids). Instruct women to avoid collecting stool samples during or just after a menstrual period.

3. If possible, patients should avoid using medications that cause gastric irritation and bleeding for at least 48 hours before and during the testing period. Such medications include aspirin, nonsteroidal antiinflammatory drugs (NSAIDs), corticosteroids, anticoagulants, reserpine, antimetabolites, and chemotherapeutic agents. Consumption of excess amounts of alcohol should be avoided. The manufacturer of Hemoccult[reg] recommends avoidance of aspirin and NSAIDs for 7 days before the test. When guaiac-based tests are used, patient adherence to the dietary guidelines in Table 34.1 for at least 48 hours before and during the testing period can help avoid false-positive and false-negative results. Despite previous reports, dietary iron does not cause false-positive test results. To prevent false-positive test results, avoid applying antiseptic preparations containing iodine to the anal area immediately before and during the testing period.

4. When guaiac-impregnated cards are used, collect two separate samples from different sections of three consecutive bowel movements; use the supplied applicator and apply thin smears of the samples to the cards. Instruct patients to return samples as soon as possible for processing. Optimally, processing of the cards should occur within 6 days of collection but definitely not after 14 days. Rehydration of the samples with a drop of water before application of the developer increases sensitivity by approximately 30% to 40%, but it also decreases specificity by 2% to 3%, leading to significantly more false-positive results. For this reason, authorities disagree about the use of rehydration. A positive result on even one sample qualifies the entire test as positive. Store both cards and developer at room temperature, protected from heat and light.

5. Patients who return samples through the mail should use special US Postal Service-approved envelopes. These may be obtained by contacting the manufacturers of the fecal occult blood test system.

6. Because of the intermittent nature of bleeding in patients with colorectal cancer, malignancy cannot be conclusively ruled out by repeat fecal occult blood testing.

7. Follow-up of a positive fecal occult blood test requires diagnostic procedures such as sigmoidoscopy, colonoscopy, or barium enema.

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Patient Resources


Colonoscopy: Questions and Answers; Colorectal Cancer: Questions & Answers; Polyps of the Colon and Rectum: Questions and Answers. American Society of Colon and Rectal Surgeons, 800 E Northwest Hwy, Suite 1080, Palatine, IL 60067; (708)359-9184.


What You Need to Know about Cancer of the Colon and Rectum. Office of Cancer Communications, National Cancer Institute, Bethesda, MD 20892; (800)4-CANCER; Internet address: http://cancernet.nci.nih.gov
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Selected References

Ahlquist DA, Wieand HS, Moertal CG, et al. . Accuracy of fecal occult blood screening for colorectal neoplasia. JAMA. 1993. 269: 1262-1267. (PubMed)

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American Cancer Society. . Cancer Information Database. Atlanta, Ga: American Cancer Society; June 1997.

American Cancer Society. . Cancer Facts & Figures-1997. Atlanta, Ga: American Cancer Society; 1997.

American Cancer Society. . Summary of American Cancer Society recommendations for the early detection of cancer in asymptomatic people. CA. 1993. 43: -.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Obstetricians and Gynecologists. . Routine Cancer Screening. ACOG Committee Opinion. Washington, DC: American College of Obstetricians and Gynecologists; In press.

American College of Physicians. . Guidelines. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991:415-416.

American College of Physicians. . Suggested technique for fecal occult blood testing and interpretation in colorectal cancer screening. Ann Intern Med. 1997. 126: 808-810. (PubMed)

American College of Physicians. . Screening for colorectal cancer with the fecal occult blood test: a background paper. Ann Intern Med. 1997. 126: 811-822. (PubMed)

Canadian Task Force on the Periodic Health Examination. . Screening for colorectal cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 66.

Eddy DM. . Screening for colorectal cancer. Ann Intern Med. 1990. 113: 373-384. (PubMed)

Eddy DM, Ferioli C, Anderson DS. . Screening for colorectal cancer. Ann Intern Med. In press.

Fleischer DE, Goldberg SB, Browing TH, et al. . Detection and surveillance of colorectal cancer. JAMA. 1989. 261: 580-585. (PubMed)

Gnauck R, Macrae FA, Fleisher M. . How to perform the fecal occult blood test. CA. 1984. 34: 134-137. (PubMed)

Kewenter J, Bjork S, Haglind E, Smith L, Svanvik J, Ahren C. . Screening and rescreening for colorectal cancer: a controlled trial of fecal occult blood testing in 27,700 subjects. Cancer. 1988. 62: 645-651. (PubMed)

Knight KK, Fielding JE, Battista RN. . Occult blood screening for colorectal cancer. JAMA. 1989. 261: 587-593. (PubMed) (Full Text in PMC)

Levin B, Murphy GP. . Revision in American Cancer Society recommendations for the early detection of colorectal cancer. CA. 1992. 42: 296-299. (PubMed)

Mandel JS, Bond JH, Church TR, et al. . Reducing mortality from colorectal cancer by screening for fecal occult blood. N Engl J Med. 1993. 328: 1365-1371. (PubMed)

Macrae FA, St John JB, Caligiore P, Taylor LS, Legge JW. . Optimal dietary conditions for Hemoccult[reg] testing. Gastroenterology. 1982. 82: 899-903. (PubMed)

Parker SL, Tong T, Bolden S, Wingo PA. . Cancer statistics, 1997. CA. 1997. 47: 5-27. (PubMed) (Full Text in PMC)

Pye G, Thomas WM, Hardcastle JD. . Comparison of coloscreen self-test and Haemoccult faecal occult blood tests in the detection of colorectal cancer in symptomatic patients. Br J Surg. 1990. 77: 630-631. (PubMed)

Ransohoff DF, Lang CA. . Screening for Colorectal Cancer. N Engl J Med. 1991. 325: 37-41. (PubMed)

Selby JV, Friedman GD, Quesenberry CP, Weiss NS. . Effect of fecal occult blood testing on mortality from colorectal cancer: a case-control study. Ann Intern Med. 1993. 118: 1-6. (PubMed)

Selby JV. . How should we screen for colorectal cancer? JAMA. 1993. 269: 1294-1296. (PubMed)

SmithKline Diagnostics. . Product Instructions for Hemoccult[reg]. San Jose, Calif: SmithKline Diagnostics, Inc; 1994.

US Preventive Services Task Force. . Screening for colorectal cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 8.

Walter SD, Frommer DJ, Cook RJ. . The estimation of sensitivity and specificity in colorectal cancer screening methods. Cancer Detect Prev. 1991. 15: 465-469. (PubMed)

Winawer SJ, Fletcher RH, Miller L, et al. . Colorectal cancer screening: clinical guidelines and rationale. Gastroenterology. 1997. 112: 594-642. (PubMed)

Winawer SJ, Schottenfeld D, Flehinger BJ. . Colorectal cancer screening. J Natl Cancer Inst. 1991. 83: 243-253. (PubMed)

Tables

Table 34.1. Additional Instructions for Patients Using Guaiac-Based Tests

35. Hearing

The prevalence of hearing loss increases with advancing age and is very common in older adults. Approximately one fourth of adults aged 65 to 74 years and half of adults aged 85 years and older report some degree of hearing loss. Hearing loss, particularly when it develops late in life and is progressive in nature, can compromise an individual's ability to perform many important activities, such as using the telephone, driving, and shopping. Hearing loss also may lead to social withdrawal, depression, and exacerbation of coexisting psychiatric problems. Some older people with hearing loss also have cognitive impairment, and evidence suggests that improvement of hearing may contribute to improvement in cognitive ability. Many types of hearing loss can be improved with the use of hearing aids; however, only 10% to 15% of patients who could benefit from a hearing aid actually use one.

See chapter 6 for information about hearing screening for children and adolescents.

Recommendations of Major Authorities


American Academy of Family Physicians --
Clinicians should question elderly adults about hearing impairment and counsel about the availability of treatment when appropriate.


American College of Obstetricians and Gynecologists --
Women 65 years and older should be evaluated for hearing loss.


American Speech-Language-Hearing Association --
Considerable debate concerning the efficacy of selected screening protocols for older adults has taken place in recent years. Whether the choice of protocol actually influences compliance with the follow-up recommendations remains unclear. The clinician may choose to use a hearing handicap questionnaire, pure-tone audiometry, or both. The rationale for using a questionnaire and pure-tone audiometry in combination is that compliance with audiologic recommendations is often greater when individuals perceive their hearing loss to be a handicap. Selection of the protocol should take into consideration cost, compliance data for the particular population, and the specificity, sensitivity, and predictive values of screening. Equipment used should be appropriately calibrated, and self-assessment scales must be reliable. Compliance-improving strategies (eg, educational materials) should be an integral part of any screening program and appropriate follow-up services should be available.


Canadian Task Force on the Periodic Health Examination --
There is fair justification for looking for hearing loss in adults seen for other reasons. Further study is warranted if adults report being hard of hearing or fail to respond to the normal spoken voice; have a medical or family history placing them at high risk for hearing loss (eg, family history of hearing loss, occupational history of exposure to noise, pursuit of noisy leisure activities, or history of recurring ear problems). Screening for hearing impairment using an audioscope, a single question about hearing difficulty, or whispered voice out of the patient's field of vision is recommended as part of the periodic health examination for persons 65 years of age and older.


US Preventive Services Task Force --
Screen older patients for hearing impairment by periodically questioning them about their hearing. Counseling should be provided about the availability of hearing aid devices and referrals made for abnormalities as appropriate. The optimal frequency of such screening is left to clinical discretion. An otoscopic examination and audiometric testing should be performed on all persons with evidence of impaired hearing by patient inquiry. There is insufficient evidence to recommend routinely screening adults with audiometric testing. Screening of workers for noise-induced hearing loss should be performed in the context of existing worksite programs and occupational medicine guidelines.
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Basics of Hearing Screening

1. Question all older adult patients about signs of hearing loss. Because patients may not be fully aware of impairment, also question their family members, if possible.

2. A screening questionnaire may be used to screen for communication problems and social and emotional handicaps stemming from hearing loss. Questionnaires may be filled out by the patient or administered by staff. One type of standardized questionnaire for this purpose is presented in Table 35.1. This instrument has been shown to have sensitivity and specificity values in the range of 60% to 80%; these values are almost as high as those attained by pure-tone audiometry screening. Some authorities recommend audiologic referral for patients who score 10 or higher on this questionnaire. Screening questionnaires have the advantage of identifying patients who perceive hearing loss to be a problem and who may be particularly motivated to use a hearing aid. Some authorities recommend using both a questionnaire and pure-tone testing for screening. This approach may modestly improve sensitivity and specificity.

3. Pure-tone screening can be administered using either a standard pure-tone audiometer or a hand-held audioscope (an otoscope that emits tones of calibrated frequencies and intensities). When using either method, keep the environment in which screening is administered as quiet as possible. Use frequencies that are within the speech range. Disagreement exists about the sound intensity that should be used for screening. Following are two examples of suggested screening protocols:
  • Present pure tones at 25 dB at 1000 Hz, 2000 Hz, and 4000 Hz. Failure to respond to any one frequency in either ear at 25 dB constitutes a "fail." For adults younger than age 65 years, this may be the preferred protocol, but the majority of persons aged 65 years and older who are screened with this protocol may fail. Because of this difference, some authorities recommend using a 40-dB tone at 4000 Hz.
  • Present pure tones at 25 dB at 1000 Hz, 2000 Hz and 4000 Hz (optional). Failure to respond to the 40-dB tone at any one frequency in either ear constitutes a "fail". Inability to hear any one frequency 25 dB places an individual "at risk" for hearing loss. A referral for audiologic assessment may be appropriate if the person reports being handicapped by hearing loss. Persons who fail the screening should be monitored annually to determine whether their hearing loss is progressive.


4. Simple physical examination procedures for hearing screening, such as the whispered voice and finger-rub tests, are not recommended by major authorities. Although these crude hearing tests are fairly accurate, they are insensitive to disorders of central auditory processing and the understanding of speech.

5. Patients with evidence of hearing loss should be considered for referral to a specialist for comprehensive audiologic evaluation, especially if they feel handicapped by hearing loss. Because approximately 10% of individuals with hearing loss are amenable to medical or surgical treatment, and some patients are incorrectly identified as having hearing loss by screening, do not refer patients directly to a hearing aid dealer.

6. Provide appropriate follow-up management for all patients who are referred for audiologic evaluation. Patients may need considerable support and training to use their hearing aids effectively.

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Patient Resources


Answers to Questions About Noise and Hearing Loss; How to Buy a Hearing Aid. American Speech-Language-Hearing Association, 10801 Rockville Pike, Rockville, MD 20852; (800)638-TALK (voice or TTY); (301)897-8682 (in Maryland). To order, call (301)897-5700, ext. 218. Internet address: http://www.asha.org


Age Page: Hearing and the Elderly. National Institute on Aging. Bldg 31, Room 5C27, 31 Center Drive, MSC 2922 Bethesda, MD 20892-2922; (301)496-1752. Internet address: http://www.nih.gov/nia/health/pubpub/pubpub.htm
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Provider Resources


Older Voices. To order this trainer's manual and resource materials for communication problems of older persons, contact the American Speech-Language-Hearing Association, 10801 Rockville Pike, Rockville, MD 20852; (301)897-5700, ext 218. For general information, call (800)638-8255; http://www2.asha.org
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American Speech-Language-Hearing Association, Ad Hoc Committee on Hearing Screening in Adults. . Considerations in screening adults/older persons for handicapping hearing impairments. ASHA. 1992. 34: 81-85. (PubMed)

Bess FH, Lichtenstein MJ, Logan SA, et al. . Hearing impairment as a determinant of function in the elderly. J Am Geriatr Soc. 1989. 37: 123-128. (PubMed)

Canadian Task Force on the Periodic Health Examination. . The periodic health examination: 2. 1984 update. Can Med Assoc J. 1984. 130: 1278-1285.

Canadian Task Force on the Periodic Health Examination. . Prevention of hearing impairment and disability in the elderly. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 80.

Gennis V, Garry PJ, Haaland KY, Yeo RA, Goodwin JS. . Hearing and cognition in the elderly; new findings and a review of the literature. Arch Intern Med. 1991; 151: 2259-2264.

Havlik RJ. . Aging in the eighties: impaired senses for sound and light in persons aged 65 years and over: preliminary data from the Supplement on Aging to the National Health Interview Survey: United States; January-June 1984. Vital and Health Statistics. Hyattsville, Md: National Center for Health Statistics; 1986;125. US Department of Health and Human Services publication PHS 86-1250.

Lichtenstein ME, Bess FH, Logan SA. . Screening for impaired hearing in the elderly. JAMA. 1988. 260: 3589-3590. (PubMed)

Macphee GJ, Crowther JA, McAlpine CH. . A simple screening test for hearing impairment in elderly patients. Age Aging. 1988. 17: 347-351.

Mulrow CD, Lichtenstien MJ. . Screening for hearing impairment in the elderly: rationale and strategy. J Gen Intern Med. 1991;6:249-258.

Pappas JJ, Graham SS. . Hearing Aid Dispensing Within a Medical Setting. Alexandria, Va: American Academy of Otolaryngology  --- Head and Neck Surgery Foundation; 1990.

Schow R, Nerbonne M. . Communication screening profile uses with elderly clients. Ear Hearing. 1982. 3: 133-147.

Uhlmann RF, Larson EB, Rees TS, Koepsel TD, Duckert LG. . Relationship of hearing impairment to dementia and cognitive dysfunction in older adults. JAMA. 1989. 262: 1916-1919. (PubMed)

Uhlmann RF, Rees TS, Psaty BM, Duckert LG. . Validity and reliability of auditory screening tests in demented and non-demented older adults. J Gen Intern Med. 1989. 4: 90-96. (PubMed)

US Preventive Services Task Force. . Screening for hearing impairment. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 35.

Ventry I, Weinstein B. . Identification of elderly people with hearing problems. ASHA. 1983. 25: 37-42.

Tables

Table 35.1. Hearing Handicap Inventory in the Elderly  --- Screening Questionnaire

36. Mammography

Breast cancer is the most common type of cancer in women and the second leading cause of cancer death in American women after lung cancer. The American Cancer Society predicts that there will be an estimated 180,200 new cases of breast cancer in women and 43,900 related deaths in 1997. In the United States, a woman's average lifetime risk for developing breast cancer is approximately one in eight. Breast cancer mortality increases with age. Mortality from breast cancer does not plateau, even in extreme old age. After age, the next strongest risk factor is a family history of breast cancer in a first-degree relative (sister or mother). Very modest increases in risk are also associated with nulliparity, first pregnancy after 30 years of age, menarche before 12 years of age, menopause after 50 years of age, postmenopausal obesity, some types of benign breast disease, high socioeconomic status, and a personal history of ovarian or endometrial cancer.

Mortality from breast cancer is strongly influenced by stage at detection. The 5-year survival rate for women in whom local disease is found is 96%. In contrast, the 5-year survival rate for women with distant metastasis is only 20%. Survival rates at every stage of diagnosis are lower among African-American women compared with Caucasian women.

Mammography is the most effective approach to early detection of breast cancer and is associated with sensitivity of 70% to 90% and specificity of 90% to 95%. Although mammography can detect small tumors in younger women, controversy exists regarding whether mammography screening reduces mortality in women younger than age 50 years.

Well-maintained, modern mammography equipment is very safe, requiring very low levels of radiation. Screening does, however, carry the added risk of morbidity attributable to any unnecessary biopsies that are performed following false-positive mammography results.

See chapter 30 for information about clinical breast examination to detect breast cancer.

Recommendations of Major Authorities

Women Aged 50 Years and Older


American Academy of Family Physicians (AAFP), American Cancer Society (ACS), American College of Obstetricians and Gynecologists (ACOG), American College of Physicians (ACP), American College of Preventive Medicine (ACPM), American Medical Association, Canadian Task Force on the Periodic Health Examination (CTFPHE), National Cancer Institute (NCI) and the US Preventive Services Task Force (USPSTF) --
Routine mammography screening is recommended. Yearly screening is recommended by ACS, ACOG and CTFPHE. AAFP, ACP, ACPM, NCI, and USPSTE recommend a frequency of 1 to 2 years. The CTFPHE, AAFP and USPSTF recommend screening until 70 years of age. The AAFP and USPSTF indicate that there is insufficient evidence to recommend for or against screening of women 70 years of age or older, although recommendations for this can be made on other grounds for women in this age category with a reasonable life expectancy. ACPM advises that women aged 70 or older should continue undergoing mammography screening provided their health status permits breast cancer treatment. ACP states that the use of mammography above 75 years of age should be discouraged. The American Geriatrics Society recommends that women over 65 years of age receive mammograms at least every 2 or 3 years until at least 85 years of age.
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Women Under 50 Years of Age


American Academy of Family Physicians --
Recommends counseling about potential risks and benefits of mammography and clinical breast exam for women ages 40 to 49 years.


American Cancer Society (ACS), American College of Obstetricians and Gynecologists (ACOG), American Medical Association (AMA), and National Cancer Institute (NCI) --
The ACS recommends that women begin annual mammography at age 40. ACOG, NCI, and the AMA recommend screening mammograms every 1 to 2 years for women 40 to 49 years of age.


American College of Physicians and Canadian Task Force on the Periodic Health Examination --
Women under 50 should not be screened.


American College of Preventive Medicine and US Preventive Services Task Force --
There is insufficient evidence to recommend for or against routine screening in this age group, but screening high risk younger women may be appropriate despite the lack of direct evidence of benefit.


National Institutes of Health Consensus Development Panel on Breast Cancer Screening for Women Ages 40 to 49 (an independent panel) --
Currently available data does not warrant a universal recommendation for mammography for all women in their forties. Each woman should decide whether to undergo mammography.
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High-Risk Women


American College of Obstetricians and Gynecologists --
Women with a family history of premenopausally diagnosed breast cancer in a first-degree relative should have mammography regularly beginning at 35 years of age.


American College of Physicians --
High-risk women should receive the same recommendations as average-risk women, unless a woman expresses great anxiety about breast cancer and insists on more intensive screening.


American College of Preventive Medicine and US Preventive Services Task Force --
Although there is no direct evidence evaluating mammography in high-risk women under 50 years of age, recommendations for screening such women can be made on other grounds. Women at high risk include those with a family history of premenopausal breast cancer in a first-degree relative or those with a history of breast and/or gynecologic cancer.


Canadian Task Force on the Periodic Health Examination --
Physicians may elect to recommend mammography starting at age 35 for women at high risk, especially those whose first-degree relatives have had breast cancer diagnosed before menopause.
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Basics of Mammography Screening

1. Emphasize the importance of mammography. A major reason reported by patients for not undergoing mammography is that they did not know they needed a mammogram. Counsel women on the need for regular mammography, not just one mammogram.

2. Use pamphlets, videotapes, and other media to educate and motivate patients to receive mammographic screening.

3. Because cost can be a significant barrier to patients obtaining mammography, the clinician should be knowledgeable about low-cost, high-quality mammography facilities available in the community and should make referrals to these facilities as needed. For information on the availability of low cost mammography at accredited facilities, contact your local office of the American Cancer Society or call the national toll-free number: (800)ACS-2345.

4. Instruct the patient to wear pants or a skirt, because she will have to undress from the waist up. Instruct her to avoid use of deodorants, powders, or other topical agents on the breasts or in underarm areas, because these may cause artifacts on the mammogram.

5. Because of potential perimenstrual breast tenderness, scheduling mammography at other times in the patient's menstrual cycle is preferred.

6. Patients commonly experience mild discomfort during mammography. Instruct patients to tell the technician if the level of discomfort becomes unacceptable.

7. Verify that mammography facilities use only dedicated mammography equipment that meets minimum safety and image-quality standards. Facilities that receive Medicare reimbursement must use equipment that complies with minimum standards for patient safety. The American College of Radiology provides certification for compliance with minimum standards for image quality. As of October 1, 1994, all US mammography facilities must be certified by the Food and Drug Administration (FDA) as providing quality mammography. Certification requirements cover personnel, equipment, radiation exposure, quality assurance programs, and record-keeping and reporting. Further information on this program is available from the FDA Center for Devices and Radiological Health, Office of Training and Assistance, Division of Mammography Quality and Radiation Programs, HFZ-240, 5600 Fishers Ln, Rockville, MD 20857.

8. Establish a tracking system to ensure that mammograms that are ordered are actually performed, that results return in a timely fashion, and that patients who are not seen frequently can be called or contacted by letter about the importance of getting mammograms and other needed preventive care. Encourage patients to keep track of and prompt their own mammography through use of a patient-held record form or card.

9. Any palpable breast lump, even with a normal mammogram, requires careful evaluation, including possible biopsy.

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Patient Resources


Breast Cancer: Steps to Finding Breast Lumps Early. American Academy of Family Physicians, 8880 Ward Pkwy, Kansas City, MO 64114-2797; (800)944-0000. Internet address: http://www.aafp.org


Mammography. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; (800)762-2264. Internet address: http://www.acog.com


What You Need To Know About Breast Cancer; A Mammogram Once a Year for Life; Smart Advice for Women 40 and Over: Have a Mammogram. Office of Cancer Communications, National Cancer Institute, Bldg 31, Room 10A24, Bethesda, MD 20892; (800)4-CANCER.


Chances are You Need a Mammogram; Are you age 50 or Older? A Mammogram Could Save Your Life. Available in both English and Spanish. Office of Cancer Communications, National Cancer Institute, Bldg 31, Room 10A16, Bethesda, MD 20892; (800)4-CANCER. Internet address: http://cancernet.nci.nih.gov
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Provider Resources


Mammography. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; (800)762-2264. Internet address: http://www.acog.com


Educating Older Women About Mammography: A Guide For Program Planners and Volunteer Leaders. American Association of Retired Persons, 1909 K Street, NW, Washington, DC 20049; (202)434-2277.


Detecting and Treating Breast Problems. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024-2188; (202)638-5577. Internet address: http://www.acog.com


Mammography Awareness Kit. Office of Cancer Communications, National Cancer Institute, Bldg 31, Room 10A16, Bethesda, MD 20892; (800)4-CANCER. Internet address: http://cancernet.nci.nih.gov


OncoLink  --- The University of Pennsylvania Cancer Resource. Internet address: http://cancer.med.upenn.edu


PDQ: The Physician Data Query System for Cancer Information. PDQ is the National Cancer Institute's computerized database providing the most up-to-date cancer information available. Access to the system can be gained 24 hours a day, 7 days a week, using a personal computer and standard telephone line, or through medical libraries. Ask a medical librarian for assistance or call (800)4-CANCER (line 3). In Hawaii, on Oahu, call 524-1234.
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American Cancer Society. . Cancer Facts & Figures-1997. Atlanta, Ga: American Cancer Society; 1997.

American Cancer Society. . Summary of American Cancer Society recommendations for the early detection of cancer in asymptomatic people. CA. 1993. 43: -.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Physicians. . Guidelines. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991:411-412.

American Geriatrics Society, Clinical Practice Committee. . Screening for breast cancer in elderly women. J Amer Geriatr Soc. 1989. 37: 883-884.

American Medical Association, Council on Scientific Affairs. . Mammographic screening in asymptomatic women aged 40 years and older. JAMA. 1989. 261: 2535-2542. (PubMed)

Breast Cancer Screening for Women Ages 40-49. . NIH Consensus Statement. 1997; Jan 21-23; 15(1):1-35.

Canadian Task Force on the Periodic Health Examination. . Screening for breast cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 65.

Eddy DM. . Screening for breast cancer. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991: chap 9.

Eddy DM, Gordon MA, Bredt A. . Screening for breast cancer. Ann Intern Med. In press.

Ferrini R, Mannino E, Ramsdell E, et al. . Screening mammography for breast cancer: American College of Preventive Medicine. Am J Prev Med. 1996. 12(5): 340-341. (PubMed)

National Cancer Institute. . Cancer Facts: Questions and Answers About Mammography Screening. Bethesda, Md: National Institutes of Health; 1997.

US Preventive Services Task Force. . Screening for breast cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 7.

37. Papanicolaou Smear

In 1997 approximately 14,500 cases of invasive cervical cancer are expected to be diagnosed in the United States and 4800 women are expected to die of the disease. The major risk factor for cervical cancer is sexually transmitted infection with human papillomavirus (HPV). Other risk factors include early age at first intercourse, having multiple sexual partners, long-term use ( > 5 years) of oral contraceptives, low socioeconomic status, and cigarette smoking. Rates for carcinoma in situ reach a peak in both African-American and white women between the ages of 20 and 30 years. After age 25 years, the incidence of invasive cancer in African-American women increases dramatically with advancing age. In Caucasian women, the incidence rises more slowly. Over 25% of invasive cervical cancers occur in women older than age 65 years, and 40% to 50% of all women who die of cervical cancer are older than age 65 years.

The effectiveness of early detection through Papanicolaou (Pap) smear testing and early treatment has been impressive, resulting in a marked decrease in mortality from cervical cancer. The incidence of invasive cervical cancer has decreased an estimated 70% because of screening. Nonetheless, a large proportion of women, particularly elderly African-American women and middle-aged women of lower socio-economic status, do not have regular Pap smears. In some geographic areas, as many as 75% of women over age 65 years report not having a Pap smear within the previous 5 years.

Depending on the technique used, Pap testing has a sensitivity of 50% to 90% and a specificity of 90% to 99%. A large proportion of false-negative Pap smear results are thought to be attributable to inadequate collection technique (up to 50% of all false-negative results) and inadequate laboratory interpretation. Because of the long lead time from development of precancerous changes until development of invasive carcinoma (8 to 9 years by some estimates), almost all precancerous or early-stage malignancies initially missed can be detected by repeat testing.

Recommendations of Major Authorities


American Academy of Family Physicians --
All women who are or have been sexually active and who have a cervix should be offered a Pap smear at least every 3 years. Use of Pap smears is not recommended in women who have had hysterectomies for reasons other than cancer.


American Cancer Society and American College of Obstetricians and Gynecologists, and National Cancer Institute --
All women should begin having annual Pap tests at the onset of sexual activity or at 18 years of age, whichever occurs first. After a woman has had three or more consecutive satisfactory normal annual examinations, the Pap test may be performed less frequently in low-risk women at the discretion of the patient and clinician.


American College of Physicians --
Sexually active women between 20 and 65 years of age should be screened with a Pap smear every 3 years. Women 66 to 75 years of age who have not been screened within the 10 years prior to age 66 should be screened every 3 years. Women at increased risk for cervical cancer should be screened every 2 years. Initial screening tests may be done as frequently as annually for two or three examinations to ensure diagnostic accuracy.


American College of Preventive Medicine --
Screening for cervical cancer by regular Pap tests should be performed in all women who are or have been sexually active, and should be instituted after a woman first engages in sexual intercourse. If the sexual history is unknown or considered unreliable, screening should begin at age 18. At least two initial screening tests should be performed one year apart. For women who have had at least two normal annual smears, the screening interval may be lengthened at the discretion of the patient and physician but should not exceed three years. Screening may be discontinued at age 65 if the following criteria are met: the women has been regularly screened, has had two satisfactory smears, and has had no abnormal smears within the previous nine years. For all women over age 65 who have not been previously screened, three normal annual smears should be documented prior to discontinuation of screening.


Canadian Task Force on the Periodic Health Examination --
Pap smears to screen for cervical cancer are recommended for women who have been sexually active. The optimum frequency of screening is not known, but it is suggested that women in the general population be screened annually until two normal smears are reported and then every 3 years to age 69 years. More frequent screening should be considered for women with risk factors: age of first sexual intercourse less than 18 years, many sexual partners or a consort with many partners, smoking, or low socioeconomic status.


US Preventive Services Task Force --
All women who are or have been sexually active should have regular Pap tests. Testing should begin at the age when the woman first engages in sexual intercourse. Adolescents whose sexual history is thought to be unreliable should be presumed to be sexually active at age 18. There is little evidence that annual screening achieves better outcomes than screening every 3 years. Pap tests should be performed at least every 3 years. The interval for each patient should be recommended by the physician based on risk factors (eg, early onset of sexual intercourse, history of multiple sexual partners, low socioeconomic status). Women infected with human immunodeficiency virus require more frequent screening according to established guidelines. There is insufficient evidence to recommend for or against an upper age limit for Pap testing, but recommendations can be made on other grounds to discontinue regular testing after 65 years of age in women who have had regular previous screening with consistently normal results. Women who have undergone a hysterectomy in which the cervix was removed do not require Pap testing, unless the hysterectomy was performed because of cervical cancer or its precursors.
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Basics of Pap Smear Screening

1. Attempt to ensure that performance of a Pap smear is not an unpleasant or painful experience for the patient. Be sure to clearly explain the importance of the procedure and the steps used to carry it out.

2. Instruct patients not to douche on the day of the examination. Do not perform a Pap smear if the patient has significant menstrual flow or obvious inflammation.

3. Perform the Pap smear before performing the bimanual examination and before obtaining culture specimens. In general, do not lubricate the speculum with anything except water, because contamination of Pap smear specimens with lubrication jelly tends to obscure cellular detail. Use of a small amount of lubricating jelly may be necessary for speculum insertion in some older patients.

4. Visualize the cervix and vagina completely before collecting the specimen. Gently remove any excess cervical mucus with a swab.

5. The traditional gold standard for the adequacy of a Pap smear has been the presence of endocervical cells in the sample: 90% of cervical cancers develop at the junction of the squamous epithelium of the ectocervix and the columnar epithelium of the endocervix (located at the external os in young women and inside the endocervical canal in older women). Studies differ regarding whether the presence of endocervical cells actually improves detection rates of abnormalities, but the presence of endocervical cells and/or squamous metaplastic cells remain widely accepted as a standard of adequacy for Pap smears.

6. A variety of implements have been used to obtain Pap smear samples, including simple cotton swabs, wooden and plastic spatulas, and endocervical and combined endocervical-exocervical brushes. The best sensitivity (defined as presence of endocervical cells) is achieved by using both a spatula (preferably Ayer's type) and an endocervical brush. Use the spatula first, because bleeding is commonly caused by the endocervical brush, and endocervical cells are susceptible to drying effects.

7. Gently yet firmly rotate the spatula around the os at least one complete turn to obtain a 360 ° sample. Promptly transfer the specimen to a glass slide (or to a preservative vial if your laboratory is using a thin layer technique). Patients who have been exposed to DES should also have smears taken circumferentially with a spatula from the upper two thirds of the vagina. To obtain the endocervical sample, insert the brush into the os no deeper than the length of the bristled section. Rotate the brush 360 ° (avoiding excessive rotation), then transfer the specimen by rolling the brush on a glass slide or by placing the material in a preservative vial as instructed by your laboratory for the thin layer technique.

8. Apply specimens to the slides uniformly and without clumping. Perform fixation promptly, and take care to minimize air drying of the specimens. If one slide is used for both specimens, collect, transfer, and fix the endocervical sample as quickly as possible. Use of two separate slides can help avoid prolonged air exposure of the spatula specimen while the endocervical specimen is being collected. Use of two slides does, however, double the amount of work for the cytotechnologist. Use of a combined endocervical-exocervical brush requires collection and fixation of only a single specimen (thus decreasing the risk of air drying), but such use has been shown to be somewhat less sensitive than use of a spatula and an endocervical brush.

9. Inquire about the quality control procedures of the laboratories to which specimens are sent. Laboratories should be certified by the American Society of Cytopathology, the College of American Pathologists, the Health Care Financing Administration, the Joint Commission on the Accreditation of Health Care Organizations, or the New York State Department of Health.

10. Many authorities recommend that laboratories use the new Bethesda System developed by a National Cancer Institute consensus conference for reporting results (Table 37.1). The Bethesda System attempts to standardize classification categories and provides for reporting on aspects of the sample not addressed in traditional Pap smear reports, such as adequacy of the sample submitted. In the Bethesda System, HPV infection is classified as a low-grade squamous intraepithelial lesion. Both moderate and severe dysplasia are classified as high-grade squamous intraepithelial lesions. Some concern exists, although unsubstantiated by research, that these classifications may lead to excessive use of colposcopic examination for patients with HPV infection or moderate dysplasia. The American College of Obstetricians and Gynecologists has issued guidelines for Pap smear reporting and follow-up in their publication Cervical Cytology: Evaluation and Management of Abnormalities (Selected References).

11. General recommendations for initial follow-up of abnormal PAP smears according to the American College of Obstetricians and Gynecologists include:

ASCUS (Atypical Squamous Cells of Undetermined Significance): The prognosis of women with ASCUS varies depending on the cytopathologist or laboratory. Clinicians are encouraged to communicate with the cytopathologist or to monitor a number of patients with an ASCUS report to help determine the appropriate follow-up and the need for colposcopy.

LSIL (Low-grade Squamous Intraepithelial Lesions): Repeat Pap test at intervals of 4 to 6 months and colposcopy if abnormalities persist.

High-grade Squamous Intraepithelial Lesions: Colposcopy and directed biopsy.

12. Only about 60% of women with abnormal Pap smear results return for follow-up. Establish a tracking system to make sure that Pap smears are performed regularly, that results return in a timely fashion, that patients with abnormal results are contacted, and that women who are not seen frequently are called or contacted by letter about the importance of getting Pap smears and other needed preventive care. Encourage patients to keep track of the results and prompt their own Pap smears through use of a patient-held record form or card.top link

Patient Resources


The Pap Test. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington DC 20024; (800)762-2264. Internet address: http://www.acog.com


The Pap Test: It Could Save Your Life. To order this information (in Spanish), contact the Office of Cancer Communications, National Cancer Institute, Bldg 31, Room 10A16, Bethesda, MD 20892; 1-800-4-CANCER.
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Provider Resources


Cervical Cytology: Evaluation and Management of Abnormalities. Technical Bulletin 183. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; 1-800-762-2264. Internet address: http://www.acog.com


Recommended Actions to Assure Quality Pap Tests (Pap Smears). The American Society of Clinical Pathologists. American Society of Clinical Pathologists, 1225 New York Ave, NW, Suite 250, Washington, DC 20005; 202-347-4450. Internet address: http://www.ascp.org


PDQ: The Physician Data Query System for Cancer Information. PDQ is the National Cancer Institute's computerized database providing the most up-to-date cancer information available. Access to the system can be gained 24 hours a day, 7 days a week, using a personal computer and a standard telephone line or through medical libraries. Ask a medical librarian for assistance or call (800)4-CANCER (line 3). In Hawaii, on Oahu, call 524-1234.
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American Cancer Society. . Cancer Facts and Figures  --- 1997. Atlanta, Ga: American Cancer Society; 1997.

American Cancer Society. . Summary of American Cancer Society recommendations for the early detection of cancer in asymptomatic people. CA. 1993. 43: -.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Physicians. . Guidelines. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991:413-414.

Appleby J. . Management of the abnormal Papanicolaou smear. Med Clin North Am. 1995. 79: 345-360. (PubMed)

Boon ME, de Graaff Guilloud JC, Rietveld WJ. . Analysis of five sampling methods for the preparation of cervical smears. Acta Cytol. 1989. 33: 843-848. (PubMed)

Canadian Task Force on the Periodic Health Examination. . Screening for cervical cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 73.

Crouse BS, Elliott BA, Nesin N. . Clinical follow-up of cervical sampling with the Ayre spatula and Zelsmyr cytobrush. Arch Fam Med. 1993;2:145-148.

Eddy DM. . Screening for cervical cancer. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991: chap 10.

Hawkes AP, Kronenberger CB, MacKenzie TD, et al. . Cervical cancer screening: American College of Preventive Medicine practice policy statement. Am J Prev Med. 1996. 12(5): 342-344. (PubMed)

Herbst AL. . The Bethesda System for cervical/vaginal cytologic diagnoses: a note of caution. Obstet Gynecol. 1990;449-450.

Kruman RJ, Solomon D. . The Bethesda System for Reporting Cervical/Vaginal Cytologic Diagnoses. Definitions, Criteria, and Explanatory Notes for Terminology and Specimen Adequacy. New York, NY: Springer-Verlag; 1994.

Lai-Goldman M, Nieberg RK, Mulcahy D, Wiesmeier. . The cytobrush for evaluating routine cervicovaginal-endocervical smears. J Repro Med. 1990. 35: 959-963.

McCord ML, Stovall TG, Meric JL, Summitt RL, Coleman SA. . Cervical cytology: a randomized comparison of four sampling methods. Am J Obstet Gynecol. 1992. 166: 1772-1779. (PubMed)

Mandelblatt J, Gopaul I, Wistreich M. . Gynecological care of elderly women: another look at Papanicolaou testing. JAMA. 1986. 256: 367-371. (PubMed)

Miller AB, Anderson G, Brisson J, et al. . Report of a national workshop on screening for cancer of the cervix. Can Med Assoc J. 1991. 145: 1301-1325.

National Cancer Institute Workshop. . The 1988 Bethesda System for reporting cervical/vaginal cytologic diagnoses. JAMA. 1989. 262: 931-934. (PubMed) (Full Text in PMC)

National Cancer Institute Workshop. . The revised Bethesda System for reporting cervical/vaginal cytologic diagnoses: report of the 1991 Bethesda workshop. Acta Cytol. 1992. 36: 273-275. (PubMed) (Full Text in PMC)

Neinstein JS, Church J, Akiyoshi T. . Comparison of cytobrush with cervix-brush for endocervical cytologic sampling. J Adoles Health. 1992. 13: 520-523.

Ruffin MT, Van Noord GR. . Improving the yield of endocervical elements in a Pap smear with the use of the cytology brush. Fam Med. 1991. 23: 365-369. (PubMed)

Schumann JL, O'Connor DM, Covell JL, Greening SE. . Pap smear collection devices: technical, clinical, diagnostic, and legal considerations associated with their use. Diagn Cytopathol. 1992;8:492-502.

US Preventive Services Task Force. . Screening for cervical cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 9.

Tables

Table 37.1.The Revised Bethesda System for Reporting Cervical and/or Vaginal Cytologic Diagnoses

38. Plasma Glucose

An estimated 16 million Americans suffer from diabetes mellitus (DM), and approximately half of these cases are undiagnosed. Diabetes mellitus is the seventh leading cause of death in the United States. Approximately 5% of all persons with diabetes have type 1 DM, an absolute insulin deficiency, and require insulin for survival. Onset of type 1 DM is bi-modal, with the largest peak in the number of new cases occurring during childhood and a smaller peak occurring in early adulthood. Type 1 DM can occur as late as the eighth or ninth decade. Persons with type 1 DM tend to present with symptoms, and the disease is usually diagnosed soon after its clinical onset. The remaining 95% of individuals with diabetes have type 2 DM, a relative insulin deficiency and insulin resistance. As such, onset of their disease is insidious. They can be relatively symptom-free for years before diagnosis. Risk factors for type 2 DM include advancing age (older than age 45 years), obesity, family history, and a history of gestational DM.

Although DM affects approximately 6.2% of the US population, the prevalence of DM is significantly higher among certain ethnic groups, including Hispanics, African Americans, and American Indians. Diabetic complications are varied and serious. DM accounts for 30% of all cases of end-stage renal disease, and it is the leading cause of blindness and non-traumatic lower extremity amputations in adults. Other complications include neuropathy, cardiovascular disease, and peripheral vascular disease.

Screening can identify occult cases of type 2 DM. The most accurate method of screening is measurement of a fasting plasma glucose. Measurement of urine glucose has been used in the past but is much less accurate and is no longer recommended. Evidence indicates that early treatment of patients with established type 1 DM decreases the number of long-term, microvascular complications. This is also probably true of type 2 DM. Evidence also suggests that weight reduction, exercise, and diet change are beneficial for secondary prevention in type 2 DM. Primary prevention trials for both type 1 and 2 DM are presently underway. Most authorities recommend screening only those persons who are at increased risk for developing DM.

Screening for gestational DM, often performed as an aspect of prenatal care, is beyond the scope of this book.

Recommendations of Major Authorities


American College of Obstetricians and Gynecologists --
Patients with one or more of the following risk factors should be screened for diabetes: family history in parents or siblings; obesity (body weight greater than 120% of ideal); high-risk ethnicity (American Indian, Hispanic, African American); history of glucose intolerance; hypertension or hyperlipidemia; history of gestational diabetes or macrosomia.


American College of Physicians --
Screening for DM in healthy asymptomatic individuals is not recommended. Screening is reasonable in obese adults over the age of 40 years if a diagnosis of DM would motivate weight loss. Screening may also be indicated for women planning to become pregnant who are at increased risk of DM and in other people with one or more of the following risk factors: history of DM in a first-degree relative, age over 50 years, weight more than 25% over ideal body weight, personal history of gestational DM, and membership in an ethnic group with a high prevalence of DM.


American Diabetes Association --
Screening for DM every 3 years should be considered for all adults age 45 and above. Testing should be considered at a younger age or more frequently in people with the following risk factors: history of DM in a first-degree relative; more than 20% over ideal body weight; American Indian, Hispanic, or African American heritage; on previous testing had impaired fasting glucose or impaired glucose tolerance; hypertension, HDL cholesterol at or below 35 mg/dL and/or a triglyceride level at or above 250 mg/dL; personal history of gestational DM or of one or more infants weighing more than 9 lb at birth.


Canadian Task Force on the Periodic Health Examination --
Screening for diabetes mellitus in asymptomatic nonpregnant adults is not recommended. Selective case-finding (screening patients seen for other reasons) may be considered for adults with the following risk factors: obesity, older age, family history of diabetes, belonging to a high-risk ethnic group.


US Preventive Services Task Force --
There is insufficient evidence to recommend for or against universal screening for type 2 diabetes in nonpregnant adults. Although evidence of a benefit of early detection is not available for any group, clinicians may decide to screen selected persons at high risk of type 2 DM on other grounds, including the increased predictive value of a positive test in individuals with risk factors and the potential (although unproven) benefits of reducing asymptomatic hyperglycemia through diet and exercise. Individuals at high risk of diabetes include obese men and women over 40, patients with a strong family history of diabetes, and members of certain ethnic groups (American Indians, Hispanics, African Americans).
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Basics of Plasma Glucose Screening

1. Measurement of fasting plasma glucose is the principal method of screening in nonpregnant, asymptomatic adults.

2. Instruct patients not to ingest food or beverages (other than water) for at least 8 hours before the blood sample is collected. Performing the procedure in the morning is most convenient as patients will have fasted overnight. A venous blood sample is more accurate, but capillary samples may be more practical for office-based screening purposes.

3. A fasting plasma glucose level lower than 110 mg/dL is considered normal. According to the new guidelines from the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus (Table 38.1), fasting blood glucose level greater than 126 mg/dL is considered elevated and fulfills the provisional diagnosis for diabetes. Fasting plasma glucose levels greater than 110 mg/dL and less than 126 mg/dL meet criteria for impaired fasting glucose (IFG) and require further monitoring according to these recent guidelines.

4. If a fasting sample is not available, random blood glucose levels can also be used in screening for DM. A random blood glucose level in excess of 200 mg/dL is considered elevated and an indicator for further assessment.

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Patient Resources


Diagnosis Diabetes. To order this and other materials, contact the American Diabetes Association, 1660 Duke St, Alexandria, VA 22314; (800)232-3472.
The National Diabetes Information Clearinghouse has the following fact sheets and booklets available: Diabetes in African Americans; Diabetes in Hispanics; Diabetes Research and Training Centers; Diabetic Neuropathy: The Nerve Damage of Diabetes; Diabetes Overview; Diabetes Control and Complications Trial; Diabetes Statistics; Hypoglycemia; Kidney Disease of Diabetes; Insulin-Dependent Diabetes; Noninsulin-Dependent Diabetes; The Diabetes Dictionary (available in Spanish); End-Stage Renal Disease: Choosing a Treatment That's Right for You; Directory of Diabetes Resources (available in Spanish). 1 Information Way, Bethesda, MD 20892-3560, phone 301-654-3327.
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Selected References

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996:84-85.

American College of Physicians. . Guidelines. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991:404-405.

Canadian Task Force on the Periodic Health Examination. . Screening for diabetes mellitus in the non-pregnant adult. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 50.

Engelgau MM, Aubert RE, Thompson TH, Herman WH. . Screening for NIDDM in nonpregnant adults. Diabetes Care. 1995. 18: 1606-1618. (PubMed)

Eriksson KF, Lindgarde F. . Prevention of type 2 (noninsulin-dependent) diabetes mellitus by diet and physical exercise. Diabetologia. 1991. 34: 891-898. (PubMed)

Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. . Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care. 1997. 20(7): 1183-1197. (PubMed)

Gerken KM, Van Lente E. . Effectiveness of screening for diabetes. Arch Pathol Lab Med. 1990. 114: 201-203. (PubMed)

Harris, MI, Eastman, RC. . Early detection of undiagnosed non-insulin-dependent diabetes mellitus. JAMA. 1996; 276:1261-2.

Howard BV, Abbott WGH, Swinburn BA. . Evaluation of metabolic effects of substitution of complex carbohydrates for saturated fat in individuals with obesity and NIDDM. Diabetes Care. 1991. 14: 786-795. (PubMed)

Manson JE, Nathan DM, Krolewski AS, Stampfer MJ, Willett WC, Hennekens CH. . A prospective study of exercise and incidence of diabetes among US male physicians. JAMA. 1992. 268: 63-67. (PubMed)

Manson JE, Rimm EB, Stampfer MJ, et al. . Physical activity and incidence of non-insulin-dependent diabetes mellitus in women. Lancet. 1991. 338: 774-778. (PubMed)

Marshall JA, Hamman RF, Baxter J. . High-fat, low-carbohydrate diet and the etiology of noninsulin-dependent diabetes mellitus: The San Luis Valley diabetes study. Am J Epidemiol. 1991. 134: 590-603. (PubMed)

Schwartz MK. . The role of the laboratory in the prevention and detection of chronic disease. Clin Chem. 1992. 38: 1539-1546. (PubMed)

Singer DE, Samet JH, Coley CM, Nathan DM. . Screening for diabetes mellitus. Ann Intern Med. 1988. 109: 639-649. (PubMed)

US Preventive Services Task Force. . Screening for diabetes mellitus. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 19.

World Health Organization Expert Committee on Diabetes Mellitus. . Third Report on Diabetes Mellitus. Geneva, Switzerland: World Health Organization; 1985. WHO Technical ReportSeries 727.

Tables

Table 38.1. Criteria for Diagnosing Diabetes in Nonpregnant Adults

39. Prostate-Specific Antigen

Prostate cancer is the most frequently diagnosed cancer in men in the United States, with 209,900 new cases estimated for 1997 and 41,800 deaths. Prostate cancer is the second leading cause of cancer death in men. Risk factors for prostate cancer include increasing age (80% of prostate cancers are diagnosed in men over 65), African American race, family history, and (perhaps) increased dietary fat intake. Although prostate cancer is common, its course is extremely variable. Some prostate cancers grow rapidly, metastasize, and quickly lead to death. Many other prostate cancers, however, are clinically silent and found only incidentally at autopsy. Autopsy studies indicate that approximately 30% of men over age 50 have histologic evidence of prostate cancer, yet carry only a 3% lifetime risk for death from this disease.

The principal screening tests for prostate cancer are the digital rectal examination (DRE) (chapter 30) and elevated levels of certain tumor markers (eg, prostate-specific antigen (PSA) and prostatic acid phosphatase). PSA is a glycoprotein that is specific to the prostate but not to prostate cancer. Thus, it is produced by all types of prostate tissue, whether normal, hyperplastic, or malignant. Incomplete information regarding true- and false-negative results makes accurate calculations of the sensitivity and specificity of PSA screening impossible. The positive predictive value of a positive PSA test (values greater than 4 ng/dL) are reported in the range of 20% to 30%. Many men with benign prostatic hyperplasia will have an elevated PSA level, and some men with prostate cancer will have PSA tests in the normal range. Prostatic acid phosphatase has a much lower sensitivity and positive predictive value than PSA; thus, PSA has largely replaced it in screening.

Whether to screen asymptomatic men for prostate cancer with PSA testing is controversial. Unlike the use of Pap smears and mammograms, there are no data indicating that PSA screening decreases mortality from prostate cancer. Definitive evidence is lacking that treatments such as radical prostatectomy are superior to "watchful waiting" for localized prostate cancer.

See chapter 30 for information about digital rectal examination to detect prostate cancer.

Recommendations of Major Authorities


American Academy of Family Physicians --
Clinicians should counsel men ages 50 to 65 years about the known risks and uncertain benefits of screening for prostate cancer.


American Cancer Society --
Annual PSA testing in combination with annual digital rectal exam should be offered annually beginning at age 50 to all men who have a life expectancy of at least 10 years, or earlier to men at high risk for prostate cancer.


American College of Physicians --
Rather than screening all men for prostate cancer as a matter of routine, physicians should describe the potential benefits and known harms of screening, diagnosis, and treatment; listen to the patient's concerns; and then individualize the decision to screen. The College strongly recommends that physicians help enroll eligible men in ongoing clinical studies.


American College of Radiology --
Annual PSA testing is recommended for all men aged 50 years and older. Annual PSA testing beginning at age 40 is recommended for African American men and men with a family history of prostate cancer.


American Urological Association --
Annual PSA testing in combination with annual digital rectal examination should be offered to all men aged 50 years and older with a life expectancy of ten years or more. Annual screening should be offered at age 40 to men at high risk for prostate cancer.


Canadian Task Force on the Periodic Health Examination --
Routine use of PSA testing as part of the periodic health examination is not recommended.


US Preventive Services Task Force --
Routine screening for prostate cancer with serum tumor markers (eg, PSA), digital rectal examination, or transrectal ultrasound is not recommended.
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Basics of Prostate-Specific Antigen Screening

1. Many experts recommend that men 50 years of age and over receive individualized counseling about the known risks and possible benefits of PSA testing. Patients should be informed that:
  • Prostate cancer is an important health problem.
  • The benefits of one-time or repeated screening and aggressive treatment of prostate cancer have not yet been proven. The potential benefit of PSA screening is decreased mortality from prostate cancer that is discovered early, but there are no data to show that PSA testing decreases mortality from prostate cancer.
  • DRE and PSA can both have false-positive and false-negative results.
  • The probability that further invasive evaluation will be required as a result of testing is relatively high. Aggressive therapy is necessary to realize any benefit from the discovery of a tumor. Prostate cancer treatments have serious side effects that can include impotence, incontinence, and surgical mortality ranging from 15% to 2%. Radical prostatectomy, radiation therapy, or both in combination have not been proven to be superior to watchful waiting for localized disease.
  • Early detection may save lives and may avert future cancer-related
    illness.


2. Concerns had been raised that PSA results, like prostatic acid phosphatase levels, would be falsely elevated by the compression of the prostate occurring during a DRE. A recent study by Crawford, et al, reported that the variations in PSA levels due to digital rectal examinations had little clinical significance (Selected References).

3. Although there is debate about the upper limits of normal for PSA testing, manufacturers recommend using 4.0 ng/mL for monoclonal PSA tests and 2.5 ng/mL for polyclonal PSA tests. Some authorities recommend varying the strategy for follow-up of a positive PSA depending on the degree of elevation. Thus, patients with levels of 10 ng/mL or more may all get a biopsy to determine if cancer is present, but those with levels greater than 4 and less than 10 ng/mL may first receive a rectal examination, a transrectal ultrasound of the prostate, or both to help determine whether a biopsy is needed.

4. Four methods have been proposed to improve the accuracy of PSA testing. PSA density (PSA concentration divided by the gland volume as measured by transrectal ultrasound) has been proposed as a more accurate marker for cancer because malignant tissue results in a higher level of PSA per unit weight than does normal or hypertrophied prostate tissue. PSA velocity is the annual calculation of the rate of change of PSA. Age-adjusted PSA cutoffs have also been advanced to address mean PSA increases with age. Percent free PSA is the proportion of free PSA, a particular molecular form of PSA, to the total PSA. Prostate cancer has been associated with a lower percent free PSA. These references are reviewed in Vashi (Selected References). Most authorities recommending the test advocate combining it with other modalities, such as digital rectal examination or transrectal ultrasound, to increase the positive predictive value.

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Patient Resources


Prostate Disease: What Every Man Over 40 Should Know, and other patient materials on prostate cancer and PSA testing. Prostate Health Council. American Foundation for Urologic Disease, 1128 N. Charles Street, Baltimore, MD 21201.
The Prostate Puzzle. Consumer Report. 1993; 58(7):459-465.
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Provider Resource


PDQ: The Physician Data Query System for Cancer Information. PDQ is the National Cancer Institute's computerized database providing the most up-to-date cancer information available. Access to the system can be gained 24 hours a day, 7 days a week, using a personal computer and standard telephone line, or through medical libraries. Ask a medical librarian or call 1-800 4-CANCER (option 3). In Hawaii, on Oahu, call 524-1234.
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American Cancer Society. . Cancer Facts and Figures-1997. Atlanta, Ga: American Cancer Society; 1997.

American Cancer Society. . Summary of American Cancer Society Recommendations for the Early Detection of Cancer in Asymptomatic People. Atlanta, Ga: American Cancer Society; 1992.

American Cancer Society. . Cancer Information Database. Atlanta, Ga: American Cancer Society; June 1997.

American College of Physicians. . Screening for prostate cancer. Ann Intern Med. 1997. 126: 480-484. (PubMed)

American Urological Association. . Early Detection of Prostate Cancer. Baltimore, Md: American Urological Association; 1995.

Benson MC, Whang IS, Olsson CA, et al. . The use of prostate-specific antigen density to enhance the predictive value of intermediate levels of serum prostate-specific antigen. J Urol. 1992. 147: 817-21. (PubMed)

Canadian Task Force on the Periodic Health Examination. . Screening for prostate cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 67.

Carter HB, Pearson JD, Metter EJ, et al. . Longitudinal evaluation of prostate-specific antigen levels in men with and without prostate disease. JAMA. 1992. 267: 2215-20. (PubMed)

Catalona WJ, Smith DS, Ratliff TL. . Measurement of prostate-specific antigen in serum as a screening test for prostate cancer. N Engl J Med. 1991. 324: 1156-61. (PubMed)

Crawford ED, Schutz MJ, Clejan S. . The effect of digital rectal examination on prostate-specific antigen levels. JAMA. 1992. 267: 2227-2228. (PubMed)

Coley CM, Barry MJ, Fleming C and Mulley AG. . Early detection of prostate cancer  --- part I: prior probability and effectiveness of tests. Ann Intern Med. 1997. 126: 394-406. (PubMed)

Coley CM, Barry MH, Fleming C et al. . Early detection of prostate cancer  --- part II: estimating the risks, benefits, and costs. Ann Intern Med. 1997; 126:468-479. View this and related citations using

Fleming C, Wasson JH, Albertsen PC, Barry MJ, Wennberg JE. . A decision analysis of alternative treatment strategies for clinically localized prostate cancer. JAMA. 1993. 269: 2650-2658. (PubMed)

Kramer BS, Brown ML, Prorok PC, Potosky AL, Hohagan JK. . Prostate cancer screening: what we know and what we need to know. Ann Intern Med. 1993: 119:914-923. View this and related citations using

Littrup PJ, Lee F, Mettlin C. . Prostate cancer screening: current trends and future implications. CA. 1992. 42: 198-212. (PubMed)

Lu-Yao GL, McLerran D, Wasson J, Wennberg JE. . An assessment of radical prostatectomy: time trends, geographic variation, and outcomes. JAMA. 1993. 269: 2633-2636. (PubMed)

Mettlin C, Jones G, Averette H, et al. . Defining and updating the American Cancer Society guidelines for the cancer-related checkup: prostate and endometrial cancers. CA. 1993. 43: 42-46. (PubMed)

Stuart ME, Handley MA, Thompson RS, Conger M, Timlin D. . Clinical practice and new technology: prostate-specific antigen (PSA). HMO Practice. 1993. 6(4): 5-11.

US Preventive Services Task Force. . Screening for prostate cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 10.

Vashi AR, Oesterling JE. . Percent free prostate-specific antigen: entering a new era in the detection of prostate cancer. Mayo Clinic Proceedings. 1997. 72: 337-344. (PubMed)

Wingo PA, Landis S, Ries LAG. . An adjustment to the 1997 estimate for new prostate cancer cases. CA. 1997;239-242.

40. Sexually Transmitted Diseases and HIV Infection

Sexually transmitted diseases (STDs) are common and damaging communicable diseases. Chlamydial infection, gonorrhea, and syphilis are easily treated when diagnosed early. If these conditions are not detected and treated, serious complications can result. Although no cure for HIV infection currently exists, early diagnosis and treatment can delay onset of acquired immunodeficiency syndrome (AIDS) and permit persons who are infected to avoid transmitting the virus. Groups at particularly high risk for STDs and HIV infection include sexually active persons younger than age 25 years, those who have multiple sexual partners, persons with a prior history of an STD, persons who practice anal intercourse, prostitutes and their sex partners, users of illicit drugs, and inmates of detention centers.

Prevention and control of STDs and HIV infection depend on four major activities: (1) educating persons who are at risk about means of reducing transmission; (2) detecting untreated cases, both symptomatic and asymptomatic; (3) effectively diagnosing and treating infection and counseling infected individuals; and (4) evaluating, counseling, and treating the sex partners of infected persons. Screening -- along with early diagnosis, counseling, and treatment -- plays an essential role in preventing STDs and HIV infection.

Many sexually transmitted diseases (AIDS; chancroid; Chlamydia trachomatis [genital infections only]; gonorrhea; hepatitis B; hepatitis C/non-A, non-B; HIV infection [pediatric cases only]; and syphilis) are currently designated as infectious diseases notifiable at the national level. Refer to Appendix C for further information on nationally notifiable diseases.

See chapters 23 and 59 for information on STD and HIV prevention counseling in adolescents and adults, respectively; chapters 14 and 48 for information on hepatitis B immunization and prophylaxis in children/adolescents and adults, respectively; chapters 25 and 61 for information about counseling on preventing unintended pregnancy in adolescents and adults, respectively. Screening for and treatment of STDs during pregnancy is an important component of prenatal care, but this topic is beyond the scope of this book.

Syphilis

The reported incidence of syphilis (all stages) increased dramatically between 1985 and 1990, from 28.5 to 54.3 cases per 100,000 population. The incidence decreased to 32.0 cases per 100,000 population in 1994. The incidence of congenital syphilis increased from 7 cases per 100,000 live births in 1985 to 107.2 cases per 100,000 live births in 1991, and decreased to 94.3 cases per 100,000 live births in 1992. More than 30,000 new cases of primary and secondary syphilis occur annually, and the prevalence of HIV infection among syphilis-infected persons is increasing.

The usual presentation of primary syphilis is a single painless ulcer or chancre on the genitalia. The ulcer usually heals spontaneously in 4 to 6 weeks without antibiotic therapy. Primary syphilis may not manifest at all, however, and may go unrecognized. Most untreated cases of primary syphilis progress to secondary syphilis. Clinical manifestations of secondary syphilis, which include skin lesions and generalized nontender lymphadenopathy, appear approximately 6 weeks after the healing of the chancre. These lesions subside in 2 to 6 weeks, and untreated patients enter the latent stage of the disease. About one third of untreated cases of latent syphilis eventually manifest as neurosyphilis or other late complications, such as gummatous lesions of bone, tissue, and skin, as well as cardiovascular problems (aortic valve lesions and aneurysms). Neurosyphilis can occur at any point in the course of untreated syphilis and may consist of meningitis, meningovascular lesions, psychiatric illnesses, and tabes dorsalis. Early diagnosis and treatment can prevent these grave complications.

Recommendations of Major Authorities


All major authorities, including the American Academy of Family Physicians (AAFP), American Academy of Pediatrics (AAP), American College of Obstetricians and Gynecologists, American College of Physicians (ACP), American Medical Association (AMA), Canadian Task Force on the Periodic Health Examination, Centers for Disease Control and Prevention, and US Preventive Services Task Force (USPSTF) --
Syphilis screening should be performed on individuals at high risk of developing syphilis, sexual partners of known syphilis cases, and individuals with multiple sexual partners -- especially in areas where syphilis prevalence is high. AAP, AMA, and ACP also recommend that males who engage in sex with other males be routinely screened; AAFP, AAP, AMA, and USPSTF also suggest screening prostitutes and persons who trade sex for drugs. AAFP also recommends syphilis screening for individuals seeking treatment for other sexually transmitted diseases.

American Academy of Family Physicians --
Syphilis screening should be performed on sexual contacts of syphilis cases and prostitutes and on individuals seeking treatment for other sexually transmitted diseases.
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Basics of Syphilis Screening

1. Because the causative agent of syphilis cannot be cultured, screening relies on serology. A nontreponemal test -- usually either the Venereal Disease Research Laboratory (VDRL) test or the Rapid Plasma Reagin (RPR) test -- is recommended for initial screening.

2. Occasionally, uninfected individuals may have reactive tests. If a sample is RPR- or VDRL-reactive, a treponemal test, such as the fluorescent treponemal antibody absorption (FTA-ABS) test, should be obtained to confirm the diagnosis. It is very uncommon for an individual to test falsely reactive to both treponemal and nontreponemal tests. Some causes of falsely reactive syphilis serologies are listed in Table 40.1.

3. Early in the course of syphilis, serology may be nonreactive. As many as 25% of all patients with primary syphilis may have nonreactive RPR and VDRL tests. Patients who have had recent contact with an individual who has documented syphilis (or is suspected of having primary syphilis) should be treated, even if serologic tests are nonreactive.

4. RPR and VDRL test titers correlate with disease activity, usually becoming nonreactive after therapy; however, even in untreated patients, tests can revert to nonreactive after many years. FTA-ABS tests usually remain reactive for life. A reactive FTA-ABS test may not necessarily indicate the need for therapy if the patient was adequately treated for syphilis previously. If a patient's test is reactive, an accurate history and thorough search for previous syphilis tests or treatment are essential to determine the duration of infection and to plan appropriate therapy.

5. Screen patients with known exposure to syphilis and those with proven or suspected infection for other STDs; counsel patients to practice safe sex, including the use of latex condoms; and advise patients to seek HIV and hepatitis B counseling and testing.

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Chlamydia And Gonorrhea

Chlamydial infection is the most common sexually transmitted disease in the United States, causing more than 4 million infections each year since 1992. Gonorrhea is the second most common sexually transmitted disease, with an estimated 1.1 million infections reported in 1992. These two infections usually cause urethritis in men and cervicitis in women. The clinical presentation of gonococcal infection is usually swifter and more dramatic than that of chlamydial infection, but the two conditions cannot be distinguished solely by history and physical findings. Often the two causative organisms are transmitted together; thus, the infections must be treated simultaneously. Usual symptoms in men include penile discharge and dysuria. Occasionally these infections can lead to epididymitis. Women may experience vaginal discharge and symptoms of pelvic inflammatory disease (PID). PID can result in infertility. Unlike chlamydial infection, gonorrhea may also cause pharyngitis, proctitis, and a disseminated infection involving dermatitis, tenosynovitis, and arthritis; rarely, it may cause meningitis and endocarditis. Both chlamydial infection and gonorrhea may cause only subtle symptoms, or infection may occur entirely without symptoms, particularly in females. Therefore, screening to detect asymptomatic carriers is important for preventing complicated infections and for controlling the spread of infection in the community.

Recommendations of Major Authorities


American Academy of Family Physicians --
High-risk women, including those who exchange sex for money or drugs, have multiple or new sexual partners, have a history of sexually transmitted disease, and/or nonuse or inconsistent use of barrier contraceptives should be screened for gonorrhea and chlamydia.


American Academy of Pediatrics and American Medical Association --
All sexually active adolescents should be screened annually for chlamydia and gonorrhea. Screening for boys can be performed with the use of a dipstick urinalysis test for leukocyte esterase.


American College of Obstetricians and Gynecologists, Centers for Disease Control and Prevention, andUS Preventive Services Task Force --
Asymptomatic individuals attending STD, family planning, or adolescent health clinics should be screened for chlamydia and gonorrhea. Those who have multiple sexual partners and sexually active individuals less than 20 years of age should also be screened. Prostitutes and individuals with a history of STDs should also be screened. Recent sexual partners of individuals with a documented gonococcal or chlamydial infection should be tested and treated.


Canadian Task Force on the Periodic Health Examination --
Persons at high risk should be screened for gonorrhea and chlamydia. For gonorrhea, those at high risk are: males or females under 30 years of age who have had at least two sexual partners in the previous year, had first intercourse at less than 16 years of age, prostitutes, and sexual contacts of individuals known to have a sexually transmitted disease. There is fair evidence to support screening and treatment of pregnant women for chlamydia during the first trimester as well as annual screening and treatment of high-risk groups (sexually active females less than 25 years of age, men and women with a new partner or mulitple sexual partners in the preceding year, women who use nonbarrier contraceptive methods, women with symptoms of chlamydial infection: cervical friability, mucopurulent discharge, or intermenstrual bleeding). There is fair evidence to exclude routine screening for chlamydia in the general population.


US Preventive Services Task Force --
Females at risk should be routinely screened for chlamydia and gonorrhea. For chlamydia, all sexually active adolescents should be screened and other women at risk due to: a history of prior STDs, a new partner or multiple sex partners, age under 25 years, inconsistent barrier contraceptive use, cervical ectopy, or being unmarried. In areas of high prevalence, screening of all women for chlamydia is justified. For gonorrhea, women at risk are: commercial sex workers, those with repeated episodes of gonorrhea, and women under 25 years of age with two or more sex partners in last year. In settings where prevalence is high, broader screening for gonorrhea may be justified. There is insufficient evidence to recommend for or against screening asymptomatic men for chlamydia and gonorrhea. In settings where prevalence is high, such as urban adolescent clinics, screening of males for chlamydia and gonorrhea may be justified on other grounds, including the potential benefits of early treatment for preventing transmission to uninfected sex partners. Screening of males with a dipstick urinalysis for leukocyte esterase is convenient and inexpensive, but is less sensitive and specific for asymptomatic chlamydial infections than more expensive urine assays and also requires confirmation of positive results.
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Basics of Chlamydia and Gonorrhea Screening

1. Because chlamydial infection and gonorrhea cause similar symptoms and often occur simultaneously, diagnostic and screening tests for the two infections are usually performed together.

2. Collect specimens from the urethra in males and from the endocervix in females. In women who have had a hysterectomy, obtain urethral specimens. If spontaneous discharge from the urethra or cervix is apparent, perform diagnostic studies, including a Gram stain.

3. Gonorrhea: Gonorrhea culture remains the gold standard for screening and diagnosis of gonococcal infections. For routine screening and diagnosis of males, however, Gram staining is nearly as specific and sensitive as the culture. Performing a Gram stain in addition to a culture may be preferable because results can be obtained immediately. Perform specimen collection, Gram stain, and inoculation for gonorrhea culture as follows:
  • For male patients: Instruct patients to refrain from urinating for at least 2 hours before testing to minimize the possibility of a false-negative test result. An adequate sample can often be obtained by milking the penis from the base of the shaft to the glans, expressing exudate, and collecting it with a swab. If no exudate is apparent, insert a small calcium alginate or dacron swab into the urethral meatus, advance it into the canal 2 to 3 cm, and gently rotate it.
  • For female patients: Unless the need for urethral samples is anticipated, instruct the patient to void before the examination. Obtain the specimen by gently inserting a calcium alginate or dacron swab into the endocervical canal and rotating it. Also perform a bimanual and rectal examination, with careful attention to signs of PID: cervical motion tenderness, fundal or adnexal tenderness, or masses. Sample any endocervical discharge for microscopic examination.
  • Gram staining:
    1. Apply a thin film of exudate or discharge from the swab to a clean glass slide.

    2. Air-dry and fix the slide by passing it several times through a flame.

    3. Flood slide with crystal or gentian violet for 10 seconds, then rinse with running water.

    4. Flood with Gram's iodine for 10 seconds, then rinse with running water.

    5. Decolorize with 95% ethanol until thin areas of the smear are colorless. Rinse with running water.

    6. Flood with safranin for 10 seconds, then rinse with water. Air- or blot-dry.

  • Cultures: Z-streak the swab onto a Thayer-Martin (chocolate agar) or Martin-Lewis plate that has been brought to room temperature, and transport inoculated culture plates to the laboratory in a candle jar or other CO2-enriched environment.


4. Chlamydia: Culture and nonculture methods (such as enzyme immunoassay [EIA], direct fluorescent antibody, DNA probe, polymerase chain reaction, or solid-phase colorimetric assays) are available to detect chlamydial infection, but all available methods frequently give false-negative results. Although nonculture antigen detection methods are somewhat less sensitive and specific than culture, they have the advantages of being more economical and less technically demanding. Therefore, nonculture tests are more appropriate for screening purposes.

The objective of good specimen collection to detect chlamydial infection is to obtain columnar epithelial cells from the endocervix or the urethra. Collect specimens as follows:
  • Endocervical specimens: Obtain specimens for chlamydial testing after collecting any specimens for Gram's staining, gonorrhea culture, and Papanicolaou smear. Before taking a specimen for a chlamydial test, remove all secretions and discharge from the cervical os with a sponge or a proctology or other large swab. Insert the appropriate swab or endocervical brush 1 to 2 cm into the endocervical canal (past the squamocolumnar junction). Rotate the swab against the wall of the endocervical canal several times during a 10- to 30-second period, then withdraw it without touching any vaginal surfaces, and place it in the appropriate transport medium (if it will be used for culture, EIA, or DNA probe testing), or use it to prepare a slide for direct fluorescent antibody (DFA) testing.
  • Urethral specimens: If possible, delay taking specimens until at least 2 hours after the patient has voided. Obtain specimens for chlamydial tests after obtaining any specimens for Gram's staining or gonorrhea culture. Gently insert the appropriate urogenital swab into the urethra (1 to 2 cm in females, 2 to 4 cm in males). Rotate the swab in one direction for at least one revolution for approximately 5 seconds, then withdraw it, and place it in the appropriate transport medium (if it will be used for culture, EIA, or DNA probe testing), or use it to prepare a slide for DFA testing.
  • Swabs to use for chlamydia screening: For nonculture chlamydia tests, use the swab and transport media supplied or specified by the manufacturer of the test.

    For culture specimens, swabs with plastic or wire shafts are usually satisfactory. Swab tips can be made of cotton, rayon, dacron, or calcium alginate, although certain manufacturers' lots of calcium alginate swabs have been shown to be toxic for chlamydia. Do not use swabs with wooden shafts, because the wood may contain substances that are toxic to chlamydia. As part of routine quality control, labs offering chlamydia culture services should provide clinicians with prescreened swabs.
  • Specimen transport: Insert the specimen into chlamydia transport medium, and break off the tip to leave it immersed in the medium. The container should be sealed and transported to the laboratory. If specimens cannot be processed within 24 hours, they should be frozen at -70 ° C. For nonculture tests, follow the manufacturers' instructions.


5. Negative culture or nonculture screening test results do not completely rule out infection. Patients who have had sexual contact with a person having a documented gonorrheal or chlamydial infection should be treated immediately after cultures are taken, before the results are reported back.

6. Positive nonculture screening tests in patients from communities with a low prevalence of infection may be false-positives, and a second confirmatory test should be considered.

7. Some authorities have recently recommended using dipstick urinalysis to screen young males for chlamydial and gonorrheal infection. See chapter 10 for further information.

8. In areas with a high prevalence of syphilis, all patients with gonorrhea or chlamydial infection should have a serologic test for syphilis and should be offered confidential counseling and testing for HIV and hepatitis B infection.

9. Test and treat all recent sexual contacts of patients with gonorrhea or chlamydial infection.

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HIV Infection

From 1981 through 1996, a total of 573,800 cases of AIDS in persons aged 13 years or older were reported to the Centers for Disease Control and Prevention. In 1995, approximately 50,000 deaths were attributed to AIDS. Although the number of deaths due to AIDS during the first 6 months of 1996 decreased for the first time since monitoring began, HIV infection remained the leading cause of death among persons aged 25 to 44 years in 1995. Seroprevalence studies show that HIV infection is present in 0.2% to 8.9% of patients visiting emergency departments and in 0.1% to 7.8% of patients admitted to acute-care hospitals. Groups at high risk of contracting HIV are identified in Recommendations of Major Authorities.

Many HIV-infected individuals are unaware of their status, since the characteristic symptoms of AIDS usually do not develop until years after infection. Early knowledge of HIV infection allows infected individuals to seek early treatment, which has been shown to delay the onset of AIDS, and to change high-risk behavior. Counseling and screening are, therefore, essential strategies for preventing the spread of HIV infection and the progression of symptoms. Screening high-risk individuals may be useful even when their test results are negative. The related counseling may change their behavior and thus may keep them free of disease.

Recommendations of Major Authorities

All major authorities including American College of Obstetricians and Gynecologists, American Medical Association (AMA), Canadian Task Force on the Periodic Health Examination (CTFPHE), Centers for Disease Control and Prevention (CDC), and US Preventive Services Task Force (USPSTF) -- HIV screening should be offered to patients with another STD; homosexual and bisexual men; past or present injection drug users; individuals with a history of prostitution or multiple sexual partners; individuals whose past (or present) sexual partners are HIV-infected or injection drug users; patients with a history of blood transfusion between 1978 and 1985; and individuals born in or with long-term residence in a community where HIV is prevalent. AMA also recommends offering testing and counseling to high-risk individuals receiving family planning services or undergoing surgery. CDC recommends that health facilities with an HIV seroprevalence rate of at least 1% or an AIDS diagnosis rate of one or more per 1000 discharges should consider a policy of routine counseling and voluntary HIV testing for patients aged 15 to 54 years. The CDC recommends informing all new mothers who have not been screened for HIV of the potential benefits of screening for their infants. The CTFPHE recommends HIV antibody screening for neonates of HIV-positive women. The USPSTF recommends screening of infants born to high-risk mothers whose antibody status is not known.


American Academy of Family Physicians --
HIV screening should be offered to the following individuals: men who had sex with men after 1975; past or present injection drug users; persons who exchange sex for money or drugs and their sex partners; those with current or past sex partners who were injection drug users, bisexual, or HIV-positive; persons seeking treatment for STDs; and infants born to high-risk mothers (as described above) whose HIV status is unknown.
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Types of HIV Tests: Blood Screening

Serologic studies for the presence of antibodies to HIV-1 are the standard method of screening for HIV infection. Enzyme immunoassay (EIA) is the most widely used screening test for HIV-1 infection. Because any screening test can result in a false-positive reaction, positive results are validated with confirmatory testing, usually a Western blot test. HIV culture and polymerase chain reaction (PCR) testing are currently not used for screening.

Basics of HIV Blood Screening

1. A single serum or plasma specimen is tested first by EIA. If the test result is positive (reactive), multiple samples from the initial specimen are retested. If at least two of three retests are reactive, the specimen is considered repeatedly reactive, and the result must be verified with a supplemental test such as the Western blot.

2. The percentage of repeatedly reactive samples found positive with additional, more specific, tests varies according to the true antibody prevalence in the tested population. It has been estimated that when an EIA is properly performed, the average specificity is greater than 99.8%. In populations with a low prevalence of HIV-1 infection, the positive predictive value remains low (8-10%) despite this high level of specificity. The problem of low positive predictive value is addressed by further testing of repeatedly reactive EIAs with supplemental tests such as the Western blot, yielding positive predictive values approaching 100% for the complete testing algorithm.

3. Western blot tests may be interpreted as positive, negative, or indeterminate. In low-risk populations, it is estimated that the false-positive rate of combined EIA and Western blot testing is less than one in 100,000. Indeterminate Western blot patterns, which can occur in up to 15% of samples tested, require careful interpretation. Current experience suggests that indeterminate Western blot patterns that are persistent for 6 months or more indicate a lack of HIV infection. Persons presenting with indeterminate Western blots should be counseled that they should continue to be monitored for their band pattern by Western blot for at least 6 months. If no additional bands develop by that time and the patient has not engaged in any high-risk behavior, he or she can be considered negative for HIV-1 infection and so advised.

4. A time interval exists between infection with HIV and the development of detectable antibodies to HIV (seroconversion). The interval between infection and seroconversion is called the "window" period. At least 95% of infected persons seroconvert within 6 months. Individuals who test negative should be reminded that their test may have been taken during the "window period," and that they may be infected despite the initial negative test. Counsel all persons to stop engaging in high-risk behaviors and to return for retesting in 6 months or earlier, to make sure they have not converted to a positive test result. Patients who continue practicing high-risk behavior should be counseled and retested periodically.

5. HIV screening must always include pre- and post-test counseling. Individualized patient-centered counseling is recommended. Specially trained clinicians or counselors should provide patients with accurate, clear, understandable information regarding HIV testing at both pre- and post-test counseling sessions. Table 40.2 includes guidelines for information that should be provided in pre- and post-test counseling sessions. Also see chapter 59 for information about HIV counseling.

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Types of HIV Tests: Oral Fluid Test

On December 23, 1994, the FDA approved the first HIV oral test system in the United States, intended for use in subjects 13 years of age or older. This test is not as accurate as the approved HIV-antibody tests used on blood. Studies show that for every 100 persons infected with HIV, the oral-fluid-based test will miss one or two, and for every 100 persons who are not infected, test results will be incorrectly positive in approximately two. The test system includes a specially treated cotton pad on a stick and a preservative solution in a plastic container. A trained collector instructs the subject to place the pad between the lower gum and cheek to obtain a sample of oral fluid. The pad is then stored in the preservative until the sample is processed and analyzed by a qualified laboratory using an enzyme-linked immunosorbent assay (ELISA) specifically licensed for testing oral fluid samples. FDA approved this HIV test system with the following restrictions:

  • The test system is available for purchase and distribution only through physicians.
  • The test system may be administered only by individuals properly trained in its use.
  • The test must not be provided to subjects for home use.
  • Testing of the oral fluid samples for HIV antibodies may be carried out only with the Oral Fluid Vironostika HIV-1 Microelisa[reg] System, manufactured by Organon Teknika Corporation of Durham, NC.
  • The test may be used for diagnosis only and must not be used to screen blood donors.
  • Before the oral fluid specimen is collected, subjects must be given information on HIV prevention and transmission, as well as technical information regarding the oral test. Because there are no confirmatory tests that use oral fluid samples, subjects must be informed that in the event of a positive oral fluid sample, they should have blood samples drawn and tested to verify their HIV status.
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Types of HIV Tests: Urine-Based HIV Test

On August 6, 1996, the FDA approved the first HIV test that uses urine samples to detect the presence of antibodies to HIV-1 using an enzyme-linked immunosorbent assay (ELISA) method. This test will be available under two brand names: Calypte HIV-1 Urine EIATM and Seradyn SentinelTM HIV-1 Urine EIA. The test can be ordered only by a physician, and samples will be analyzed in certified medical laboratories. Any initially reactive sample will be retested twice. If either of the second tests is reactive, the screening test will be considered positive. A positive screening test must be followed by a blood test to confirm the results.

A patient information sheet provided with the new test will outline the limitations of urine HIV-1 testing in addition to HIV/AIDS information. After reading the information sheet, the person being tested will initial a statement confirming the receipt of the pretest counseling, peel off the sample label, and apply it to the urine collection cup.

The urine-based ELISA test is not approved to screen blood donors. In clinical studies, urine and blood samples were taken from 298 patients diagnosed with AIDS and tested with both the Calypte HIV-1 Urine EIA and a licensed ELISA test using a blood specimen. The urine test was positive as an initial screening test 99.3% of the time in persons known to have AIDS. In asymptomatic HIV-1-infected patients, the test would be expected to miss one or two persons out of every 100. Other studies showed that the urine-based test would give a falsely positive result in one or two persons of 100 without HIV-1 antibodies in their blood, compared to one in 1000 with a blood-based ELISA test.top link

Patient Resources


How to Prevent Sexually Transmitted Diseases; Genital Herpes, Gonorrhea and Chlamydia Infections, Pelvic Inflammatory Disease. American College of Obstetricians and Gynecologists, 409 12th St SW, Washington, DC 20024; (800)762-2264. Internet address: http://www.acog.com


National STD Hotline. (800)227-8922.


AIDS: How To Reduce Your Risk of Catching It. American Academy of Family Physicians, 8880 Ward Pkwy, Kansas City, MO 64114-2797; (800)944-0000. Internet address: http://www.aafp.org


Surgeon General's Report to the American Public on HIV Infection and AIDS; Condoms and Sexually Transmitted Diseases... Especially AIDS. CDC National AIDS Information Hot Line; 1-800-342-AIDS (English speaking); 1-800-344-SIDA (Spanish speaking); 1-800- AIDS-TTY (hearing impaired). All phone calls are confidential.


HIV in America: A Profile of the Challenges Facing Americans Living With HIV. National Association of People Living with AIDS, 1413 K St, NW, Washington, DC 20005; (202)898-0435.
Hemophilia and AIDS Network for the Dissemination of Information, 110 Green St, New York, NY 10012; (800)424-2634.
National AIDS Information Clearinghouse, PO Box 6003, Rockville, MD 20850; (800)458-5231 (English and Spanish).
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Provider Resources


Gonorrhea and Chlamydial Infections (technical bulletin #190), 1994. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; (800)762-2264. Internet address: http://www.acog.com


Gynecologic Herpes Simplex Virus Infection (technical bulletin #119). American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; (800)762-2264. Internet address: http://www.acog.com


HIV Infection and Physician Emotions (videotape and discussion guide). American Academy of Family Physicians, 8880 Ward Pkwy, Kansas City, MO 64114-2797; (800)944-0000. Internet address: http://www.aafp.org
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American Academy of Pediatrics, Committee on Infectious Diseases. . 1994 Red Book: Report of the Committee on Infectious Diseases. Elk Grove Village, Ill: American Academy of Pediatrics; 1994.

American Academy of Pediatrics, Committee on Practice and Ambulatory Medicine. . Recommendations for pediatric preventive health care. Pediatrics. 1995. 96: 373-374. (PubMed)

American Medical Association. . Rationale and recommendations: infectious diseases. In: AMA Guidelines for Adolescent Preventive Services (GAPS): Recommendations and Rationale. Chicago, Ill: American Medical Association; 1994: chap 15.

Canadian Task Force on the Periodic Health Examination. . Prevention of gonorrhea. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 59.

Canadian Task Force on the Periodic Health Examination. . Screening for HIV antibody. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 58.

Center for Health Statistics. . Health, United States, 1995. Hyattsville, Md: Public Health Service; 1996

Centers for Disease Control and Prevention. . [Update:] Trends in AIDS incidence, deaths, and prevalence  --- United States, 1996. MMWR. 1997. 46(8): 165-173.

Centers for Disease Control. . Estimates of HIV prevalence and projected AIDS cases: summary of a workshop, October 31-November 1, 1989. MMWR. 1990. 39: 110-112,117-119.

Centers for Disease Control. . Public health service guidelines for counseling and antibody testing to prevent HIV infection and AIDS. MMWR. 1987. 36: 509-515.

Centers for Disease Control and Prevention. . Sexually transmitted diseases treatment guidelines. MMWR. 1993;42 (No. RR-14).

Centers for Disease Control. . Primary and secondary syphilis  --- United States, 1981-1990. MMWR. 1991. 40: 314-323. (PubMed)

Centers for Disease Control and Prevention. . Recommendations for HIV testing services for inpatients and outpatients in acute-care hospital settings and technical guidance on HIV counseling. MMWR. 1993. 42: 1-17.

Centers for Disease Control and Prevention. . Recommendations for the prevention and management of Chlamydia trachomatis infections. MMWR. 1993. 42(No. RR-12): 1-39.

Centers for Disease Control and Prevention. . US Public Health Service recommendations for human immunodeficiency virus counseling and voluntary testing for pregnant women. MMWR. 1995. 44(No. RR-7): 1-15.

Davies HD, Wang EL. . Periodic Health Examination, 1996 Update: 2. Screening for chlamydial infections. Can Med Assoc J. 1996. 154(11): 1631-1777.

Food and Drug Administration. . FDA approves first urine-based HIV test. FDA Talk Paper. 1996; T96-55; http://www.fda.gov/bbs/topics/ANSWERS/ANS00752.html

Hardy AM. . AIDS knowledge and attitudes for January-March 1991: provisional data from the National Health Interview Survey. Advance Data. August 21, 1992:216.

Hashimoto T. . Gram Stain Technique. Gram Stain. Updated April 30, 1996.

Higgins DL, Galavotti C, O'Reilly KR, et al. . Evidence for the effects of HIV antibody counseling and testing on risk behaviors. JAMA. 1991. 266: 2419-2429. (PubMed)

Hook EW, Marra CM. . Acquired syphilis in adults. N Engl J Med. 1992. 326: 1060-1069. (PubMed)

Larson SA. . Syphilis. Clin Lab Med. 1989. 9: 545-557. (PubMed)

Sellors JW, Pickard L, Gafini A, et al. . Effectiveness and efficiency of selective vs. universal screening for chlamydia infection in sexually active young women. Arch Intern Med. 1992. 152(9): 1837-1844. (PubMed)

Swango PA, Kleinman DV, Konzelman JL. . HIV and periodontal health. J Am Dent Assoc. 1991. 122: 49-54.

US Preventive Services Task Force. . Screening for chlamydial infection (including ocular prophylaxis in newborns). In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 29.

US Preventive Services Task Force. . Screening for infection with human immunodeficiency virus. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 28.

US Preventive Services Task Force. . Screening for gonorrhea (including ocular prophylaxis in newborns). In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 27.

US Preventive Services Task Force. . Screening for syphilis. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 26.

Tables

Table 40.1. Conditions That May Cause Falsely Reactive Syphilis Tests

Table 40.2. Pre- and Post-test Information for HIV Testing

41. Sigmoidoscopy

Colorectal cancer is the third leading cause of death from cancer in the United States. The disease most often afflicts persons older than age 40 years. Of the three widely used methods of screening for colorectal cancer (digital rectal examination, sigmoidoscopy, and fecal occult blood testing), examination using a sigmoidoscope is the most specific and sensitive. The specificity of sigmoidoscopy approaches 100%, because this procedure enables the examiner to perform a biopsy during the procedure. The sensitivity of sigmoidoscopy is largely determined by the skill of the examiner and the length of the instrument. Approximately 30% of colorectal cancers are within reach of the 25-cm rigid sigmoidoscope. The 35-cm flexible sigmoidoscope can reach 45% to 50% of cancers, and the 60-cm flexible sigmoidoscope can reach 50% to 60% of cancers.

Screening with sigmoidoscopy has been limited by costs, patient and provider compliance, and earlier controversies about the effectiveness of this approach. Patient compliance problems have been somewhat diminished by development of the more comfortable flexible instruments. The 35-cm sigmoidoscope is particularly well accepted by patients, and the 60-cm sigmoidoscope is relatively well accepted. The controversy about effectiveness had stemmed from a lack of evidence that screening with sigmoidoscopy decreases mortality from colorectal cancer. Two recent case-control studies (Selby et al, 1992; Newcomb et al, 1992) demonstrated significant decreases (59% and 79%, respectively) in the risk of death from colorectal cancer among screened patients. In the Selby study, a significant benefit of rigid sigmoidoscopy was suggested even if screening was performed as infrequently as every 10 years.

See chapters 30 and 34 for information about colorectal cancer and other methods of screening for it.

Recommendations of Major Authorities

Normal Risk


American Academy of Family Physicians --
Individuals aged 50 years and older and those aged 40 years and older with a family history of early colorectal cancer should be screened for colorectal cancer with fecal occult blood tests, sigmoidoscopy, colonoscopy, or barium enema.


American Cancer Society (ACS) and American Gastroenterological Association --
Patients at normal risk should be screened with sigmoidoscopy every 5 years in combination with yearly fecal occult blood testing beginning at 50 years of age. Other recommended screening options beginning at age 50 include: colonoscopy every 10 years or double contrast barium enema every 5 to 10 years. The ACS further advises that digital rectal examination be performed along with the endoscopic or radiological procedure.


American College of Obstetricians and Gynecologists --
Patients at normal risk should be screened with sigmoidoscopy every 3 to 5 years beginning at 50 years of age.


American College of Physicians --
Men and women should be offered flexible sigmoidoscopies every 10 years from 50 to 70 years of age. In most settings and for most people, this strategy will provide the best balance of benefits and harms, logistic feasibility, and costs. In settings where it is logistically feasible and cost is reasonable, persons who want to achieve the maximum protection against colorectal cancer should be offered colonoscopy every 10 years from 50 to 70 years of age. In some settings, air-contrast barium enemas every 10 years from 50 to 70 years of age might be logistically preferable to colonoscopies, and some patients might prefer that procedure. For persons who decline these options, annual fecal occult blood testing should be offered.


Canadian Task Force on the Periodic Health Examination --
There is insufficient evidence to support the inclusion or exclusion of sigmoidoscopic or colonoscopic screening of asymptomatic individuals over 40 years of age in the periodic health examination.


US Preventive Services Task Force --
Screening for colorectal cancer is recommended for all persons 50 years of age or over. Sigmoidoscopy and fecal occult blood testing are effective methods of screening. There is insufficient evidence to determine which of these methods is preferable or whether the combination of both methods produces greater benefit than either method alone. There is insufficient evidence to recommend a periodicity for sigmoidoscopy screening.
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Increased Risk


All major authorities --
Patients at increased risk of colorectal cancer should consider more intensive screening. What constitutes increased risk and the nature and frequency of recommended screening differs slightly among the authorities.


American Cancer Society --
For patients having a first-degree relative with a history of colorectal cancer at 55 years of age or younger, the entire colon and rectum should be examined with colonoscopy or air-contrast barium enema every 5 years beginning at 35 to 40 years of age. Members of families with a history of familial adenomatous polyposis should receive earlier screening utilizing flexible sigmoidoscopy. Members of families with a history of hereditary nonpolyposis colorectal cancer require earlier and more intense surveillance utilizing colonoscopy. Individuals with inflammatory bowel disease are at exceptionally high risk and require individualized treatment. Patients under age 55 years with a first-degree family member with a history of colorectal cancer are at increased risk and may need earlier and more frequent examinations. People with a history of breast, ovarian, or endometrial cancer are at some increased risk but should follow screening recommendations for normal-risk patients.


American College of Obstetricians and Gynecologists --
Colonoscopy should be a part of primary preventive care for individuals with a personal history of inflammatory bowel disease or colonic polyps, or a family history of familial polyposis coli, colorectal cancer, or cancer family syndrome.


American College of Physicians --
Individuals who have one or more first-degree relatives with colorectal cancer should be offered colonoscopy at 40 years of age and at least every 10 years thereafter.


American Gastroenterological Association --
Individuals with a first-degree relative who has had colorectal cancer or an adenomatous polyp should be screened beginning at age 40 years. Gene carriers for familial adenomatous polyposis (FAP) or people with a family history of FAP whose gene carrier status is indeterminate should be offered yearly flexible sigmoidoscopy beginning at puberty to see if they are expressing the gene. If polyposis is present, they should begin to consider when they should have colectomy. People with a family history of hereditary nonpolyposis colorectal cancer should be offered an examination of the entire colon (via colonoscopy or double contrast barium enema, preferably with sigmoidoscopy) every 1 to 2 years starting between the ages 20 and 30 years and every year after age 40 years. In patients with long-standing, extensive inflammatory bowel disease, surveillance colonoscopy should be considered, along with the extent and duration of the disease, as a guide to when or if colectomy should be considered. A common practice is to perform surveillance colonoscopy every 1 to 2 years beginning after 8 years of disease in patients with pancolitis or after 15 years in those with colitis involving only the left colon.


Canadian Task Force on the Periodic Health Examination --
There is insufficient evidence to recommend for or against the inclusion or exclusion of sigmoidoscopy in the periodic health examination of asymptomatic individuals over 40 years old (including those with a family history of one or two relatives with colorectal cancer). There is fair evidence to exclude sigmoidoscopy from the periodic health examination of individuals with true cancer family syndrome; however, there is fair evidence for the inclusion of colonoscopy in the periodic health examination of individuals with true cancer family syndrome.


US Preventive Services Task Force --
In high-risk groups, there is insufficient evidence to recommend for or against early or frequent screening or the use of colonoscopy rather than sigmoidoscopy. However, early and frequent colonoscopy screening of patients with a family history of familial polyposis coli or cancer family syndrome or with personal histories of previous adenomatous polyps or colorectal cancer may be recommended on other grounds, including the increased risk of colorectal cancer and of lesions in the proximal colon.
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Basics of Sigmoidoscopy Screening

Performing sigmoidoscopies requires technical training and practice. It is beyond the scope of this book to explain the performance of this procedure; only very basic aspects will be addressed.

1. Training:

Sigmoidoscopy should be performed only by or under the supervision of a trained examiner. Training should be obtained from an experienced endoscopist. Training may consist of diagnostic instruction with audiovisual materials, endoscopic models, and photo atlases, followed by patient demonstrations and successful completion of a number of supervised examinations.top link

2. Sigmoidoscope type:

Most authorities recommend use of a flexible sigmoidoscope (preferably 60 cm in length) rather than a rigid sigmoidoscope because of better patient acceptance and the ability to visualize lesions higher in the sigmoid colon.top link

3. Patient preparation:

Proper bowel preparation is essential for performance of an adequate screening examination. Recommendations for bowel preparation differ somewhat. The minimum preparation consists of administration of two enemas a few hours before examination.top link

4. Follow-up of abnormal results:

All authorities agree that patients found to have adenomatous polyps of 1 cm or larger need colonoscopic examination of the entire colon. Approximately 10% of individuals screened will have small tubular adenomas less than 1 cm in diameter. Controversy exists about whether patients with these lesions need colonoscopic follow-up in view of their low potential for malignancy.top link

5. Maintenance of competence:

Clinicians need to perform sigmoidoscopy routinely to maintain competence. Performing procedures only occasionally may lead to missed or inappropriate diagnoses and a high rate of complications.top link

Patient Resources


Colorectal Cancer: Questions & Answers; Colonoscopy: Questions and Answers; Polyps of the Colon and Rectum: Questions and Answers. American Society of Colon and Rectal Surgeons, 800 E Northwest Hwy, Suite 1080, Palatine, IL 60067; (708)359-9184.


What You Need to Know about Cancer of the Colon and Rectum. Office of Cancer Communications, National Cancer Institute, Bethesda, MD 20892; (800)4-CANCER.
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Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American Cancer Society. . Cancer Facts & Figures-1997. Atlanta, Ga: American Cancer Society; 1997.

American Cancer Society. . Cancer Information Database. Atlanta, Ga: American Cancer Society; June 1997.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Physicians, Health and Public Policy Committee. . Clinical competence in the use of flexible sigmoidoscopy for screening purposes. Ann Intern Med. 1987. 107: 589-591. (PubMed)

American College of Physicians. . Guidelines. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991:415-416.

Canadian Task Force on the Periodic Health Examination. . Screening for colorectal cancer. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 66.

Eddy DM. . Screening for colorectal cancer. Ann Intern Med. 1990. 113: 373-384. (PubMed)

Eddy DM, Ferioli C, Anderson DS. . Screening for colorectal cancer. Ann Intern Med. In press.

Fleischer DE, Goldberg SB, Browning TH, et al. . Detection and surveillance of colorectal cancer. JAMA. 1989. 261: 580-585. (PubMed)

Gorse GJ, Messner RL. . Infection control practices in gastrointestinal endoscopy in the United States: a national survey. Infect Control Hosp Epidemiol. 1991. 12: 289-296. (PubMed)

Newcomb PA, Norfleet RG, Storer B, Surawicz, Marcus PM. . Screening sigmoidoscopy and colorectal cancer mortality. J Natl Cancer Inst. 1992. 84: 1572-1575. (PubMed)

Ransohoff DF, Lang CA. . Sigmoidoscopic screening in the 1990s. JAMA. 1993. 269: 1278-1281. (PubMed)

Selby JV, Friedman GD. . Sigmoidoscopy in the periodic examination of asymptomatic adults. JAMA. 1989. 261: 595-601. (PubMed) (Full Text in PMC)

Selby JV, Friedman GD, Quesenberry CP, Weiss NS. . A case-control study of screening sigmoidoscopy and mortality from colorectal cancer. N Engl J Med. 1992. 326: 653-657. (PubMed)

US Preventive Services Task Force. . Screening for colorectal cancer. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 8.

Wigton RS, Blank LL, Monsour H, Nicolas JA. . Procedural skills of practicing gastroenterologists. [A national survey of 700 members of the American College of Physicians.] Ann Intern Med. 1990. 113: 540-546. (PubMed)

Winawer SJ, Fletcher RH, Miller L, et al. . Colorectal cancer screening: clinical guidelines and rationale. Gastroenterology. 1997. 112: 594-642. (PubMed)

42. Thyroid Function

Thyroid dysfunction affects 1% to 4% of adults in the United States. The annual incidence of hypothyroidism is 0.08%. The estimated annual incidence of hyperthyroidism is 0.05%. Both forms of thyroid dysfunction are more common in women, older adults, and persons with a family history of thyroid disease. Laboratory evidence of hypothyroidism is found in up to 10% of women and 2% of men aged 60 years and older. Other risk factors for thyroid hypofunction include prior autoimmune conditions, history of head or neck surgery or radiation exposure, Down's syndrome, and the postpartum state. In most affected persons, symptoms typically develop shortly after the onset of thyroid dysfunction. Lethargy, weight gain, confusion, cold intolerance, constipation, alopecia, dyspnea, myalgias, and paresthesias are common features of hypothyroidism. Restlessness, emotional lability, insomnia, heat intolerance, dyspnea, palpitations, ophthalmopathy, diarrhea, muscle atrophy, weakness, tremors, and tachycardia are symptoms of hyperthyroidism.

Some individuals, particularly older adults, can experience an insidious onset of thyroid disease. Apathetic hyperthyroidism occurs without the usual goiter, ophthalmopathy, and signs of sympathetic nervous system hyperactivity. Symptoms of hypothyroidism, such as fatigue, constipation, dry skin, and poor concentration may be attributed to the aging process or may be less frequent in older populations. Because hypothyroidism can cause secondary dyslipidemia, patients with subclinical hypothyroidism may first present with high cholesterol levels. Studies suggest that some patients with subclinical disease or mild alterations in thyroid function tests may benefit from early treatment if they are identified through screening. For this reason, some authorities recommend screening of certain high-risk populations for thyroid dysfunction.

See chapters 8 and 30 for information about screening for congenital hypothyroidism and thyroid cancer, respectively.

Recommendations of Major Authorities

High-risk Populations


American College of Obstetricians and Gynecologists --
Thyroid-stimulating hormone (TSH) levels should be obtained every 3 to 5 years from all women aged 65 years and older and from younger women with an autoimmune condition or strong family history of thyroid disease.


American College of Physicians --
Routine screening for thyroid disease is not indicated in asymptomatic individuals nor in patients admitted to the hospital for acute medical or psychiatric illnesses; testing may be indicated to identify unsuspected disease in women over 50 years of age who have general symptoms that could be caused by thyroid disease.


American Thyroid Association --
Tests of thyroid function should not be a part of multiphasic screening for patients who are not suspected of having thyroid disease except in certain high-risk populations. Suspect populations include individuals with a strong family history of thyroid disease, elderly patients, postpartum women 4 to 8 weeks after delivery, and patients with autoimmune diseases.


Canadian Task Force on the Periodic Health Examination --
There is insufficient evidence to support screening for hyperthyroidism and hypothyroidism among asymptomatic adults. The high prevalence of hypothyroidism among perimenopausal and postmenopausal women warrants a high index of suspicion and liberal use of the sensitive thyroid stimulating hormone (TSH) assay in the presence of even vague and subtle complaints.


Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults --
Because hypothyroid states can raise LDL-cholesterol levels, any patient with LDL-cholesterol exceeding 190 mg/dL should be tested for hypothyroidism.


US Preventive Services Task Force --
Routine screening for thyroid disorders is not warranted in asymptomatic adults. There is insufficient evidence to recommend for or against screening for thyroid disease with thyroid function tests in high-risk patients, including the elderly, postpartum women, and persons with Down's syndrome, but recommendations for such screening may be made on other grounds, such as the high prevalence of disease and the increased likelihood that symptoms of thyroid disease will be overlooked in these patients. Clinicians should remain alert for subtle or nonspecific symptoms of thyroid dysfunction when examining such patients, and maintain a low threshold for diagnostic evaluation of thyroid function.
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Basics of Thyroid Function Screening

1. Many authorities now recommend performing a TSH level using a "sensitive" TSH assay as the initial screen and obtaining a free thyroxine (FT4) or free thyroxine index (FT4I) level only if the TSH level is abnormal. In unselected populations, these TSH assays have sensitivities of 85% to 95% and specificities of 90% to 96% for thyroid dysfunction. Determination of total thyroxine (TT4) and FT4I levels, while less expensive, is less sensitive and less specific compared with use of the "sensitive" TSH assays.

2. An elevated TSH value (>7 mU/L) and a suppressed FT4 level (<0.8 ng/dL) suggest primary thyroid failure necessitating therapy. (Normal values may vary with each laboratory.) Whether asymptomatic patients with an elevated TSH level but a normal FT4 or FT4I level will benefit from treatment is unclear. Some evidence suggests that thyroid replacement may diminish the potential for developing long-term complications of subclinical thyroid hypofunction. Because overt disease develops in only a small number of these individuals, some authorities recommend serial testing of these patients rather than immediate use of replacement therapy.

3. A depressed TSH level (<0.4 mU/L) usually, but not always, indicates the presence of an elevated serum thyroxine (T4) level. If clinical findings of hyperthyroidism are present, and the T4 level is normal, measure serum total triiodothyronine (TT3), because the patient may have T3 thyrotoxicosis. In the absence of clinical findings, many authorities recommend following the patient closely and deferring treatment until symptoms develop.

4. Medications and clinical conditions can affect the interpretation of thyroid screening tests. TSH levels may be depressed in euthyroid patients who are taking large doses of glucocorticoids or dopamine. Also, the TSH level may be misleading in the presence of pituitary or hypothalamic hypothyroidism and during changes in thyroid status that occur in cases of subacute thyroiditis or after treatment of hyperthyroidism. In such cases, measurement of the FT4 level is preferred. Phenytoin, carbamazepine, and rifampin can depress TT4 levels. The effect of drugs on reported FT4 levels varies with the laboratory method used. Increased levels of thyroid-binding globulin (TBG), resulting in elevated TT4 levels, may occur with pregnancy, oral contraceptive or estrogen use, acute or chronic active hepatitis, acute intermittent porphyria, and certain inherited traits. Patients with cirrhosis, nephrotic syndrome, severe illness, and those using testosterone or corticosteroids may have slightly reduced TT4 levels because of diminished TBG. Severe illnesses, such as those requiring treatment in an intensive-care unit, can also affect the production, secretion, distribution, and metabolism of thyroid hormone.

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Patient Resources


Your Thyroid Gland: A Guide for the Patient. American Academy of Otolaryngology-Head and Neck Surgery, Order Department, 1 Prince St, Alexandria, VA 22314; (703)836-4444.
top link

Provider Resources


Directory of Organizations for Endocrine and Metabolic Diseases; Thyroid Hormone Action and Nuclear Receptors; Attention Deficit Hyperactivity Disorder and Generalized Resistance to Thyroid Hormone. National Institute Diabetes and Digestive and Kidney Diseases, Bldg 31, Rm 9A04, Bethesda, MD 20892; (301)496-3583. Internet address: http://www.niddk.nih.gov/health/endo/endo.htm
top link

Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American College of Physicians. . Guidelines. In: Eddy DM, ed. Common Screening Tests. Philadelphia, Pa: American College of Physicians; 1991:406-408.

Becker DV, Bigos ST, Gaitan E, et al. . Optimal use of blood tests for assessment of thyroid function. JAMA. 1993. 269: 2736-2737. (PubMed)

Canadian Task Force on the Periodic Health Examination. . Screening for thyroid disorders and thyroid cancer in asymptomatic adults. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 51.

de los Santos ET, Starich GH, Mazzaferri EL. . Sensitivity, specificity, and cost-effectiveness of the sensitive thyrotropin assay in the diagnosis of thyroid disease in ambulatory patients. Arch Intern Med. 1989. 149: 526-532. (PubMed)

Hay ID, Bayer MF, Kaplan MM, Klee GG, Larsen PR, Spencer CA. . American Thyroid Association assessment of free thyroid hormone and thyrotropin measurements and guidelines for future clinical assays. Clin Chem. 1991. 37: 2002-2008. (PubMed)

Helfand M, Crapo LM. . Screening for thyroid disease. Ann Intern Med. 1990. 112: 840-849. (PubMed)

National Cholesterol Education Program. . Second Report of the Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II). Bethesda, Md: National Heart, Lung and Blood Institutes, National Institutes of Health, 1994. (NIH Publication no. 93-3095.)

Sawin CT, Geller A, Kaplan MM, Bacharach P, Wilson PWF, Hershman JM. . Low serum thyrotropin (thyroid-stimulating hormone) in older persons without hyperthyroidism. Arch Intern Med. 1991. 151: 165-168. (PubMed)

Sawin CT. . Thyroid dysfunction in older persons. Advances Intern Med. 1992. 37: 223-248.

Staub JJ, Althaus BU, Engler H, et al. . Spectrum of subclinical and overt hypothyroidism: effect on thyrotropin, prolactin, and thyroid reserve, and metabolic impact on peripheral target tissues. Am J Med. 1992. 92: 631-642. (PubMed)

Surks MI, Chopra IJ, Mariash CN, Nicoloff JT, Solomon DH. . American Thyroid Association guidelines for use of laboratory tests in thyroid disorders. JAMA. 1990. 263: 1529-1532. (PubMed)

US Preventive Services Task Force. . Screening for thyroid disease. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 20.

43. Tuberculosis (Including Prophylaxis and BCG Vaccination)

In 1995, a total of 22,860 new cases of active tuberculosis (TB) were reported in the United States. This marked the third consecutive year that the number of reported cases decreased and reflected the lowest rate of reported TB cases since national surveillance began in 1953. During the 1980s and early 1990s, the number of TB cases increased significantly. Factors that contributed to the increase included adverse social and economic conditions, the human immunodeficiency virus (HIV) epidemic, immigration of individuals with Mycobacterium tuberculosis infection, and clinician and patient noncompliance with recommended screening and treatment regimens. Efforts to control the spread of TB were also complicated by the emergence of strains of M. tuberculosis resistant to multiple drugs.

The more recent decline in the number of TB cases probably reflects a number of factors, according to the Centers for Disease Control and Prevention, including (1) improved laboratory methods to allow prompt identification of M. tuberculosis; (2) broader use of drug-susceptibility testing; (3) expanded use of preventive therapy in high-risk groups; (4) decreased transmission of M. tuberculosis in congregate settings (eg, hospital and correctional facilities) because of implementation of infection-control guidelines; and (5) improved follow-up of persons with TB.

In the United States, control of tuberculosis depends on screening high-risk populations and providing preventive therapy to persons in whom active disease is most likely to develop. Groups at high risk for TB infection include: (1) close contacts of persons known or suspected to have TB; (2) persons infected with HIV; (3) persons who inject illicit drugs or other locally identified high-risk substance abusers (eg, crack cocaine users); (4) persons who have medical risk factors known to increase the risk for TB disease if infection occurs; (5) residents and employees of high-risk congregate settings (eg, correctional institutions, nursing homes, mental institutions, other long-term residential facilities, and shelters for the homeless); (6) health care workers who serve high-risk clients; (7) foreign-born persons, including children, who have arrived within 5 years from countries with a high incidence or prevalence of TB; and (8) some medically underserved, low-income populations. Conditions and chronic diseases that predispose patients to development of TB disease include HIV infection, diabetes mellitus, end-stage renal disease, and hematologic and reticuloendothelial diseases; history of intestinal bypass or gastrectomy, chronic malabsorption syndromes, silicosis, cancers of the upper
gastrointestinal tract or oropharynx, prolonged steroid use and immunosuppressive therapy; and being 10% or more below desirable body weight.

Prophylaxis with isoniazid is very effective in preventing the onset of clinical tuberculous disease. Use of isoniazid for 12 months in an at-risk population has been shown to reduce the occurrence of TB disease by 54% to 88%. Its efficacy is directly related to the length of prophylaxis, the extent of patient compliance with the prophylactic regimen, and the susceptibility of the infecting organism to isoniazid. The effectiveness of bacillus of Calmette and Guérin (BCG) vaccination is considerably less certain; effectiveness rates varied from 0% to 76% in major trials.

See chapter 9 for information on TB screening, preventive therapy, and BCG immunization in children and adolescents.

Tuberculosis is currently designated as an infectious disease notifiable at the national level. Refer to Appendix C for further information on nationally notifiable diseases.

Recommendations of Major Authorities

Screening


All major authorities, including American Academy of Family Physicians, American College of Obstetricians and Gynecologists, American Thoracic Society, Canadian Task Force on the Periodic Health Examination, Centers for Disease Control and Prevention, and US Preventive Services Task Force --
Tuberculin skin testing should be performed on all individuals at high risk. The need for repeat skin testing should be determined by the likelihood of continuing exposure to infectious TB.
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Prophylaxis


American Thoracic Society (ATS), Canadian Task Force on the Periodic Health Examination, Centers for Disease Control and Prevention (CDC), and US Preventive Services Task Force --
Adults with a reactive skin test and no evidence of active disease should be considered for preventive therapy with isoniazid based on age and risk factors. ATS and CDC also recommend that anergic patients recently exposed to an active TB case or from populations where the prevalence of TB is greater than 10% (injection drug users, homeless individuals, migrant laborers, and first-generation immigrants from Asia, Africa, or Latin America) should be considered for isoniazid prophylaxis even when their skin test is negative.
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BCG Vaccination


American Thoracic Society, Centers for Disease Control and Prevention (CDC), and US Preventive Services Task Force --
Vaccination with BCG is not recommended for adults in the United States. However, CDC recommends that BCG vaccination should be considered for health care workers who work in settings in which (a) a high percentage of TB patients are infected with M. tuberculosis resistant to both isoniazid and rifampin, (b) transmission of such drug-resistant M. tuberculosis strains is likely, and (c) comprehensive infection control precautions have been implemented and have not been successful.


Canadian Task Force on the Periodic Health Examination --
recommends BCG vaccination for tuberculin-negative contacts of persons with active TB in Canadian communities in which the infection rate is high.
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Basics of Tuberculosis Screening

1. Use the Mantoux test exclusively in high-risk populations. The Mantoux test is the standard methods of testing. Multiple-puncture tests should not be used to determine whether a person is infected.

2. For the Mantoux test, administer 0.1 mL of purified protein derivative (PPD) containing 5 tuberculin units (TU) on the volar or ventral surface of the forearm. Administer the injection intradermally using a disposable tuberculin syringe with the bevel of the needle facing upward. The injection should produce a pale, discrete 6-mm to 10-mm weal on the skin.

3. Read the test results 48 to 72 hours after administration by palpating the margin of induration and measuring the diameter transverse to the long axis of the forearm. It may be helpful to outline the margin of induration with a ballpoint pen. Always record the actual millimeters of induration, not the erythema surrounding the induration. Simply recording "positive" or "negative" is not precise enough and may lead to improper treatment.

4. Absence of a tuberculin reaction does not exclude a diagnosis of TB infection, especially when symptoms suggest the presence of active disease. Induration of less than 5 mm may occur early in the course of TB infection or in individuals with altered immune function. Anergy testing with at least two other delayed-type hypersensitivity skin tests (eg, Candida, mumps, or tetanus toxoid) may be conducted in conjunction with PPD testing in adults at risk for decreased cell-mediated immune function (including persons with HIV infection). The scientific basis for anergy testing is tenuous, however, and no standardization exists for most skin-test antigens used for anergy testing. Therefore, anergy testing is not part of routine screening for TB infection.

5. Reactions to PPD may wane with age but can be restored by repeat testing. Because of this "booster effect," patients (particularly those over age 55 years) who undergo repeat testing may be falsely classified as new converters and unnecessarily treated with isoniazid. Some authorities recommend initially screening adults in institutional and hospital settings using a two-step PPD testing procedure. If the first Mantoux test result is negative, perform a second test 1 to 2 weeks later. Reaction to the "booster" test usually indicates old -- not new -- TB infection. CDC recommends this two-step procedure for the initial screening of residents and employees of long-term care facilities, such as nursing homes, adult foster-care homes, and board and care homes.

6. A small percentage of tuberculin reactions may be caused by errors in administering the test or reading the result, cross-reaction with antigens shared between mycobacteria, and vaccination with BCG. The probability that a positive skin test results from infection with M. tuberculosis rather than from BCG vaccination increases: (1) as the size of the reaction increases; (2) when the patient is a contact of a person who has TB; (3) when the patient has a family history of TB or the incidence/prevalence of TB in their country of origin is high; and (4) as the interval between vaccination and tuberculin testing increases (vaccination-induced reactivity is unlikely to occur for 10 years after vaccination).

7. Live vaccines, such as measles-mumps-rubella (MMR) and oral polio vaccine (OPV), may interfere with the response to the Mantoux test. To avoid confusion, administer live vaccines and the TB test concurrently, or delay the TB test for 4 to 6 weeks.

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Basics of Tuberculosis Prophylaxis

1. Indications

CDC has issued recommendations for preventive therapy in previously untreated adults without evidence of active TB (Table 43.1). Certain anergic patients should be considered for preventive therapy regardless of their skin test reaction. Other groups for whom prophylaxis is indicated include adults who have had close contact with a person with infectious TB in the past 3 months and individuals who are members of populations in which the prevalence of TB is greater than 10% (eg, injection drug users, homeless persons, migrant laborers, and persons born in Asia, Africa, or Latin America).top link

2. Dose and Administration

Initiate preventive therapy with isoniazid (INH). The correct daily dose of isoniazid for adults is 5 mg/kg (maximum, 300 mg) taken orally. For noncompliant adult patients, isoniazid may be administered by a health professional on a twice-weekly schedule of 15 mg/kg per dose (maximum, 900 mg). In general, continue isoniazid prophylaxis for at least 6 months, up to a maximum of 12 months. Patients who are HIV-positive or have evidence of prior untreated TB on chest X-ray should receive isoniazid prophylaxis for 12 months. If a patient has had contact with a person known to have infectious TB that is resistant to isoniazid, consider administering preventive therapy with rifampin (600 mg by mouth daily for 1 year).top link

3. Contraindications/Precautions

Contraindications to isoniazid prophylaxis include acute or active liver disease of any etiology or previous adverse reaction to isoniazid. Among adults over 35 years of age, the incidence of mild isoniazid-induced liver function test abnormalities is 10% to 20%. During the course of therapy, adults over age 35 years should undergo baseline and periodic (monthly) testing for transaminase (ALT or AST) levels. If the transaminase level is three to five times higher than the upper limit of the laboratory normal range, consider discontinuing isoniazid. Closely monitor individuals who use alcohol daily or in whom chronic liver disease is suspected for isoniazid-induced hepatitis. Supplementation with pyridoxine (vitamin B6, 50 mg by mouth daily) may be helpful in preventing neuropathy in certain patients on isoniazid, such as those with diabetes, uremia, alcoholism, or malnutrition. Delay therapy for pregnant women who are candidates for preventive treatment until after delivery. If it is likely that the woman has been recently infected, therapy may be instituted after completion of the first trimester of pregnancy.top link

4. Adverse Reactions

While patients are taking isoniazid, monitor them monthly for signs and symptoms of adverse reactions. These include drug fever or rash, hypersensitivity reactions, peripheral neuritis, and hepatitis. Signs and symptoms of hepatitis include loss of appetite, nausea, vomiting, persistent dark urine, jaundice, fever, and abdominal tenderness  --- especially in the right upper quadrant. Patients who are taking other medications concurrently with isoniazid should be monitored for potential drug interactions.top link

Basics of BCG Vaccination

1. Indications

Routine BCG vaccination is not recommended for adults in the United States.top link

2. Dose and Administration

The Tice [reg] strain is the only BCG preparation currently available in the United States. The dose and administration is the same for both adults and children ( see chapter 9 for details).top link

3. Precautions

Do not administer BCG vaccine to individuals who may be immunocompromised or immunosuppressed, including those with known or suspected HIV infection.top link

4. Adverse Reactions

Side effects occur in 1% to 10% of vaccinated individuals and may include severe or prolonged ulceration at the vaccination site, lymphadenitis, and lupus vulgaris.top link

Patient Resources


Tuberculosis: Get the Facts; Tuberculosis: Connection between TB and HIV; Questions and Answers about TB. Centers for Disease Control and Prevention, Attn: Information, Technology and Services Office, NCHSTP, CDC, 1600 Clifton Rd NE, M/S E-06, Atlanta, GA 30333; or National Center for HIV, STD, and TB Prevention Voice Information System: (404)639-1819.


Facts About the TB Skin Test; Facts About Tuberculosis. American Lung Association, 1740 Broadway, New York, NY 10019-4374; (212)315-8700.
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Provider Resources


Multidrug Resistant Tuberculosis; TB Care Guide; Core Curriculum on Tuberculosis; TB Treatment: A Clinical Care Guide; Improving Patient Adherence to Tuberculosis Treatment; Reported TB in the United States; Tuberculosis Control Laws-United States. To order these and other documents, contact the Centers for Disease Control and Prevention, Attn: Information, Technology and Services Office, NCHSTP, CDC, 1600 Clifton Rd, NE, M/S E-06, Atlanta, GA 30333; or the National Center for HIV, STD, and TB Prevention Voice Information System: (404)639-1819.
top link

Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

American Thoracic Society. . Control of tuberculosis in the United States. Am Rev Respir Dis. 1992. 146: 1623-1633. (PubMed)

American Thoracic Society. . Treatment of tuberculosis and tuberculosis infection in adults and children. Am J Respir Crit Care Med. 1994. 149: 1359-1374. (PubMed)

American Thoracic Society/Centers for Disease Control. . Diagnostic standards and classification of tuberculosis. Am Rev Respir Dis. 1990. 142: 725-735. (PubMed)

Canadian Task Force on the Periodic Health Examination. . Screening and isoniazid prophylactic therapy for tuberculosis. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 62.

Centers for Disease Control and Prevention. . Prevention and control of tuberculosis in correctional facilities: recommendations of the Advisory Council for the Elimination of Tuberculosis. MMWR. 1996. 45(No. RR-8): 1-27.

Centers for Disease Control and Prevention. . Guidelines for preventing the transmission of Mycobacterium tuberculosis in health-care facilities, 1994. MMWR. 1994. 43(No. RR-13): 1-132.

Centers for Disease Control. . Prevention and control of tuberculosis in facilities providing long-term care to the elderly: recommendations of the Advisory Committee for Elimination of Tuberculosis. MMWR. 1990. 39(No. RR-10): 7-20. (PubMed)

Centers for Disease Control. . Prevention and control of tuberculosis in U.S. communities with at-risk minority populations and prevention and control of tuberculosis among homeless persons: recommendations of the Advisory Council for Elimination of Tuberculosis. MMWR. 1992. 41(No. RR-5): 1-23. (PubMed)

Centers for Disease Control. . Purified protein derivative (PPD) tuberculin anergy and HIV infection: guidelines for anergy testing and management of anergic persons at risk of tuberculosis. MMWR. 1991. 40(No. RR-5): 27-33. (PubMed)

Centers for Disease Control and Prevention. . Screening for tuberculosis and tuberculosis infection in high-risk populations: recommendations of the Advisory Committee for the Elimination of Tuberculosis. MMWR. 1995. 44(No. RR-11): 19-34. (PubMed)

Centers for Disease Control and Prevention. . Tuberculosis morbidity, United States, 1995. MMWR. 1996. 45: 365-370.

Centers for Disease Control and Prevention. . The role of BCG vaccine in the prevention of tuberculosis in the United States: a joint statement by the Advisory Committee for Immunization Practices and the Advisory Committee for Elimination of Tuberculosis. MMWR. 1996. 45(No. RR-4): 1-18. (PubMed)

Centers for Disease Control. . The use of preventive therapy for tuberculous infection in the United States: recommendations of the Advisory Committee for the Elimination of Tuberculosis. MMWR. 1990. 39(No. RR-8): 9-12.

Frieden TR, Sterling T, Pablos-Mendez A. . The emergence of drug-resistant tuberculosis in New York City. N Engl J Med. 1993. 328: 523-526. (PubMed)

Iseman MD, Cohn DL, Sbarbaro JA. . Directly observed treatment of tuberculosis: we can't afford not to try it. N Engl J Med. 1993. 328: 576-578. (PubMed)

Physician's Desk Reference. . Oradell, NJ: Medical Economics Company; 1993:898-899, 1689-1692.

Pust RE. . Tuberculosis in the 1990's: resurgence, regimens, and resources. South Med J. 1992. 85: 584-593. (PubMed)

US Preventive Services Task Force. . Screening for tuberculosis infection (including BCG immunization). In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 25.

Tables

Table 43.1. Criteria for Determining Need for Preventive Therapy by Category and Age Group

44. Urinalysis

Examination of urine for signs of occult disease has a long tradition in medical care. The development of modern "dipsticks" that can perform multiple tests in a matter of minutes has made urinalysis inexpensive and quick. Most of the abnormalities detected by screening adults with urinalysis are indicative of benign disorders, such as idiopathic proteinuria, or of conditions for which the value of treatment is unclear, such as occult bacteriuria. For this reason, most authorities recommend use of screening urinalysis only for certain conditions in specific high-risk populations.

Occult Bacteriuria

Urinalysis is most often recommended to screen for occult bacteriuria. Urinary tract infections are a significant source of disease and morbidity in diabetic women, pregnant women, and older persons (particularly women). Table 44.1 shows the prevalence of asymptomatic bacteriuria in selected adult populations and the positive predictive value of nitrite and leukocyte esterase (LE) dipstick tests for detecting asymptomatic bacteriuria in these populations. The positive predictive value of urinalysis in these groups is relatively low, except in institutionalized older adults and women with diabetes.

Treatment of asymptomatic bacteriuria in institutionalized older adults has not been shown to decrease morbidity or mortality or even to lead to sustained periods without bacteriuria. Some evidence suggests that treating elderly women in the community leads to fewer symptomatic infections, but the significance of such an approach for long-term health is unknown. The theory that treatment of women with diabetes leads to fewer symptomatic urinary tract infections and decreased long-term morbidity is plausible but not proven. Treating asymptomatic bacteriuria in pregnant women is of definite proven benefit. For this reason, pregnant women are routinely screened with urine culture, which is more sensitive and specific than dipstick testing.top link

Occult Hematuria

Screening has also been advocated to detect occult hematuria, which can be indicative of urinary tract malignancies. The incidence of these malignancies increases significantly after age 40 years, and they occur twice as frequently in men as in women. Dipsticks are reasonably accurate for detecting hematuria, but microscopic hematuria is not specific for bladder cancer or other urologic cancers. The positive predictive value of a positive heme dipstick test for malignancy in older men has been found to be between 6% and 8%. Unnecessary evaluations for a potential urinary tract malignancy can be harmful. Intravenous pyelograms, for example, can lead to diminished renal function and, rarely, death.top link

Proteinuria

Screening for proteinuria in the general population is of little value, because most causes are either benign or untreatable. Screening for diabetes with urinalysis is very inaccurate and is better accomplished with plasma glucose measurements (chapter 38). See chapter 10 for a discussion of the use of screening urinalysis in children.top link

Recommendations of Major Authorities


All major authorities --
Screening urinalysis is recommended in prenatal care for pregnant women.


American Academy of Family Physicians and US Preventive Services Task Force (USPSTF) --
Routine screening of males and most females for asymptomatic bacteriuria is not recommended. In diabetic or elderly ambulatory women evidence is insufficient to recommend for or against screening for asymptomatic bacteriuria, but recommendations against such screening may be made on other grounds, including the high likelihood of recurrence and the potential adverse effects of antibiotic therapy. The USPSTF recommends screening for asymptomatic bacteriuria by urine culture in all pregnant women.


American College of Obstetricians and Gynecologists --
Urinalysis for asymptomatic bacteriuria is recommended for women over 65 years of age or with diabetes mellitus as part of periodic evaluation visits, which should occur yearly or as appropriate.


American College of Physicians --
Urinalysis and urine culture should not be routinely used to screen for asymptomatic bacteriuria.


Canadian Task Force on the Periodic Health Examination --
Dipstick urinalysis for protein to prevent progressive renal disease is recommended for patients with insulin-dependent diabetes mellitus. Urinalysis to detect asymptomatic bacteriuria in the elderly is not recommended. However, for ambulatory elderly women the evidence is insufficient to recommend for or against screening for asymptomatic bacteriuria.
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Basics of Urinalysis Screening

1. Urine collected early in the morning, at least 6 hours after previous voiding and after 8 hours of fasting, is most concentrated and most likely to reveal abnormalities. Do not perform routine screening urinalysis on menstruating women.

2. Obtain a specimen using the "clean catch" technique, which permits a follow-up culture if indicated. Instruct women to clean the vulvar region with lukewarm water, spreading the labia and washing the urethral meatus with a moistened cotton wad or pad several times from front to back. Use each wad or pad only once. Avoid use of soap or disinfectants because of possible effects on the sample. Instruct men to clean the glans and urethral meatus several times with a cotton wad or pad, using each only once. Instruct uncircumcised men to draw back their foreskins.

3. Provide patients with a clean container to collect a midstream "clean catch" sample of urine. Instruct uncircumcised men to retract the foreskin to avoid impingement of the urine flow. Instruct women to hold their labia open to avoid impingement of the urine flow. Patients should start to urinate in the toilet and switch to the specimen container. Fill the container half full and finish urinating in the toilet.

4. Perform urinalysis as soon as possible after collection, using any one of the many available types of urine dipsticks. No major authority recommends using urine cultures for routine screening of nonpregnant adults. Immediately refrigerate specimens that cannot be examined immediately.

5. When interpreting the test, keep in mind the possible causes of false-positive and false-negative results (Tables 44.2 and 44.3).

top link

Patient Resources


Urinary Tract Infections. American College of Obstetricians and Gynecologists. ACOG Patient Education Pamphlet AP050. American College of Obstetricians and Gynecologists, 409 12th St, SW, Washington, DC 20024; (800)762-2264. Internet address: http://www.acog.org


Urinary Tract Infection: A Common Problem for Some Women. American Academy of Family Physicians, 8880 Ward Parkway, Kansas City, MO 64114-2797; (800)944-0000. Internet address: http://www.aafp.org


Urinary Tract Infection in Adults. National Institute of Diabetes and Digestive and Kidney Diseases' National Kidney and Urologic Diseases Information Clearinghouse, 3 Information Way, Bethesda, MD 20892-3580; (301)654-4415. Internet address: http://www.niddk.nih.gov/health/endo/endo.htm
top link

Selected References

American Academy of Family Physicians. . Summary of Policy Recommendations for Periodic Health Examination. Kansas City, Mo: American Academy of Family Physicians; 1997.

American College of Obstetricians and Gynecologists. . Guidelines for Women's Health Care. Washington, DC: American College of Obstetricians and Gynecologists; 1996.

Boscia JA, Kobasa WD, Knight RA, et al. . Therapy vs no therapy for bacteriuria in elderly ambulatory nonhospitalized women. JAMA. 1987. 257: 1067-1071. (PubMed)

Canadian Task Force on the Periodic Health Examination. . Dipstick proteinuria screening of asymptomatic adults to prevent progressive renal disease. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 38.

Canadian Task Force on the Periodic Health Examination. . Screening for Asymptomatic bacteriuria in the elderly. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 81.

Canadian Task Force on the Periodic Health Examination. . Periodic Health Examination Monograph. Hull, Quebec: Minister of Supply and Services; 1980.

Komaroff AL. . Urinalysis and urine culture in women with dysuria. In: Sox HC Jr, ed. Common Diagnostic Tests: Use and Interpretation. 2nd ed. Philadelphia, Pa: American College of Physicians; 1990:286-301.

Pels RJ, Bor DH, Woolhandler S, Himmelstein DU, Lawrence RS. . Bacteriuria. In: Goldbloom RB, Lawrence RS, eds. Preventing Disease: Beyond the Rhetoric. New York, NY: Springer-Verlag; 1990: chap 8.

US Preventive Services Task Force. . Screening for asymptomatic bacteriuria. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 31.

Woolhandler S, Pels RJ, Bor DH, Himmelstein DU, Lawrence RS. . Hematuria and proteinuria. In: Goldbloom RB, Lawrence RS, eds. Preventing Disease: Beyond the Rhetoric. New York, NY: Springer-Verlag; 1990: chap 37.

Tables

Table 44.1. Prevalence of Asymptomatic Bacteriuria in Adults and Estimated Positive Predictive Values of Nitrite and Leukocyte Esterase Dipstick Tests

Table 44.2. Causes of Inaccurate Nitrite Dipstick Tests

Table 44.3. Causes of Inaccurate Leukocyte Esterase (LE) Dipstick Tests

45. Vision

Vision loss is common in adults, and the prevalence of vision loss increases with advancing age. Approximately 13% of persons aged 65 years and older and 28% of those aged 85 years and older report some degree of visual impairment. More than 90% of older adults need corrective lenses at some time. Common visual disorders affecting adults include cataracts, macular degeneration, glaucoma, and diabetic retinopathy. Such disorders frequently contribute to trauma from falls, automobile crashes, and other types of accidental injuries. According to one study, 18% of hip fractures are attributable to impaired vision. Many older adults are unaware of decreases in their visual acuity, and up to 25% of such persons may have the wrong corrective lens prescription.

Surgical treatment of cataracts can lead to improved vision and quality of life. Medical and surgical treatment of glaucoma may help prevent visual loss. Early laser surgical treatment can help prevent visual loss attributable to diabetic retinopathy and (in some cases) macular degeneration. Visual acuity testing can be performed easily and accurately by primary care clinicians. Glaucoma screening, however, as usually practiced by primary care clinicians using a Schiotz tonometer, is relatively insensitive and nonspecific. The predictive value of a positive Schiotz test is only about 5%.

Recommendations of Major Authorities


American Academy of Family Physicians --
Vision screening with Snellen acuity testing is recommended for the elderly.


American Academy of Ophthalmology --
A comprehensive eye examination, including screening for visual acuity and glaucoma by an ophthalmologist, should be performed every 3 to 5 years in African Americans aged 20 to 39 years, and, regardless of race, every 2 to 4 years in individuals aged 40 to 64 years, and every 1 to 2 years beginning at age 65 years. Diabetic patients, at any age, should have exams at least yearly.


American College of Obstetricians and Gynecologists --
Women 65 years of age and older should be evaluated for visual acuity yearly or as appropriate.


American Optometric Association --
Comprehensive eye and vision examinations are recommended for normal-risk adults as follows: 19 to 40 years of age, every 2 to 3 years; 41 to 60 years of age, every 2 years; 61 years of age and older, yearly. Adults 19 to 60 years of age at increased risk for eye disease (eg, with diabetes, hypertension, family history of glaucoma, work in highly visually demanding or eye hazardous occupations, taking certain systemic medications with ocular side effects) should have examinations every 1 to 2 years or as recommended.


Canadian Task Force on the Periodic Health Examination --
There is fair evidence to include in the periodic health examination visual acuity testing with a Snellen sight chart for adults aged 65 years or older. In addition, funduscopy or retinal photography is recommended for elderly patients (> 65 years) with diabetes of at least 5 years' duration. The place of funduscopy in the detection of age-related macular degeneration and glaucomatous changes is controversial. For patients at high risk for glaucoma (eg, positive family history, African American race, severe myopia, diabetes), a prudent recommendation would be to include periodic assessment by an ophthalmologist.


National Eye Institute --
A comprehensive eye examination, including screening for visual acuity and glaucoma, should be performed by an eye care professional every 2 years beginning at age 40 years in African Americans and at age 60 years in all other individuals. Diabetic patients, at any age, should have yearly exams.


US Preventive Services Task Force --
Routine vision screening with Snellen acuity testing is recommended among the elderly. The frequency is left to clinical discretion. Selected questions about vision may be helpful in detecting vision problems in the elderly, but do not appear to be as sensitive or specific as direct assessment of acuity. There is insufficient evidence to recommend for or against routine screening for diminished visual acuity among non-elderly adults. There is also insufficient evidence to recommend for or against routine screening by primary care clinicians for elevated intraocular pressure or early glaucoma. Effective screening for glaucoma is best performed by eye specialists who have access to specialized equipment to evaluate the optic disc and measure visual fields. Recommendations may be made on other grounds to refer patients at high risk for glaucoma for evaluation by eye specialists including: the substantial prevalence of unrecognized glaucoma in these populations, the progressive nature of untreated disease, and expert consensus that reducing intraocular pressure may slow the rate of visual loss with early glaucoma or severe intraocular hypertension. Patients at high risk for glaucoma include: African Americans over 40 years of age; Caucasians over 65 years of age; patients with diabetes, severe myopia, or a family history of glaucoma. The optimal frequency for glaucoma screening has not been determined.
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Basics of Vision Screening

1. Refer older adults and individuals at high risk to eye-care professionals for periodic examinations. See Recommendations of Major Authorities.

2. Perform visual acuity screening using a standard Snellen wall chart at a distance of 20 feet. A tumbling "E" chart may be used for patients who are not familiar with the Western alphabet. Give a passing score for each line for which the patient gives a majority of correct responses. Test each eye separately. The patients should wear any corrective lenses during screening. If a patient is found to have significant changes in visual acuity or visual acuity of 20/40 or less when using corrective lenses, refer him or her to an eye-care specialist for further examination.

3. Risk factors for glaucoma include increasing age, family history of glaucoma, African American race, diabetes mellitus, and myopia. Evaluate each patient's risk factors for glaucoma and other ocular problems, and refer appropriate patients to eye-care professionals for screening.

4. Loss of vision can begin slowly and may go unnoticed for some time, particularly in older adults. Encourage patients to seek evaluation at the first sign of vision problems. Use of a standardized, self-administered questionnaire (Table 45.1) can help identify individuals needing evaluation of their vision. More extensive questionnaires have been developed (Mangione et al, 1992).

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Patient Resources


Your Vision, the Second Fifty Years; Do Adult Vision Problems Cause Reading Problems? and other publications. American Optometric Association, 243 N Lindbergh Blvd, St. Louis, MO 63141; (314)991-4100. Internet address: http://www.aoanet.org/


Age-Related Macular Degeneration; Cataracts; Diabetic Retinopathy; Don't Lose Sight of Diabetic Eye Disease; Don't Lose Sight of Glaucoma; Glaucoma. National Eye Health Education Program, National Institutes of Health, 2020 Vision Pl, Bethesda, MD 20892; (301)496-5248. Internet address: http://www.nei.nih.gov


Age Page  --- Aging and Your Eyes. National Institute on Aging, Bldg 31, Room 5C27, 31 Center Dr MSC 2922 Bethesda, MD 20892-2922; (301)496-1752. Internet address: http://www.nih.gov/nia
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Provider Resources


Glaucoma; Cataracts; Strabismus in Adults; Cataract Surgery; Diabetic Retinopathy. American Academy of Ophthalmology, PO Box 7424, San Francisco, CA 94120. Send a business-size, self-addressed, stamped envelope with your request. Internet address: http://www.eyenet.org


Policy Statement: Frequency of Ocular Examinations; National Eyecare Project (for those who do not have an eye doctor); Glaucoma 2001 Project (for people at risk for glaucoma). American Academy of Ophthalmology, PO Box 7424, San Francisco, CA 94120. Send a business-size, self-addressed, stamped envelope with your request. Internet address: http://www.eyenet.org


Comprehensive Adult Eye and Vision Examination and other clinical practice guidelines. American Optometric Association, 243 N Lindbergh Blvd, St. Louis, MO 63141; (314)991-4100. Internet address: http://www.aoanet.org/


National Eye Institute Statement on Detection of Glaucoma; National Eye Institute Statement on Vision Screening in Adults. National Eye Health Education Program, National Institutes of Health, 2020 Vision Pl, Bethesda, MD 20892; (301)496-5248. Internet address: http://www.nei.nih.gov
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Selected References

American Academy of Family Physicians, Summary of Policy Recommendations for Periodic Health Examination. . Kansas City, Mo: American Academy of Family Physicians; 1997.

American Academy of Ophthalmology, Quality of Care Committee. . Comprehensive Adult Eye Examination. San Francisco, Ca: American Academy of Ophthalmology; 1992.

American Academy of Ophthalmology. . Detection and Control of Diabetic Retinopathy. San Francisco, Ca: American Academy of Ophthalmology; 1992.

American Optometric Association. . Comprehensive Adult Eye and Vision Examination. St. Louis, Mo: American Optometric Association; 1994.

Canadian Task Force on the Periodic Health Examination. . Screening for visual impairment in the elderly. In: The Canadian Guide to Clinical Preventive Health Care. Ottawa, Canada: Minister of Supply and Services; 1994: chap 78.

Leske MC. . The epidemiology of open-angle glaucoma: a review. Am J Epidemiol. 1983. 118: 166-169. (PubMed)

Mangione CM, Phillips RS, Seddon JM, et al. . Development of the activities of daily vision scale: a measure of visual functional status. Med Care. 1992. 30: 1111-1126. (PubMed) (Full Text in PMC)

Nelson KA. . Visual impairment among elderly Americans: statistics in transition. J Vis Impair Blind. 1987. 81: 331-334.

Podgor MJ, Leske MC, Ederer F. . Incidence estimates for lens changes, macular changes, open angle glaucoma and diabetic retinopathy. Am J Epidemiology. 1983. 118: -.

Reuben DB. . Visual impairment. In: Beck JC, ed. Geriatrics Review Syllabus: A Core Curriculum in Geriatric Medicine. New York, NY: American Geriatrics Society; 1991.

Rubenstein LZ, Lohr KN. . Conceptualization and Measurement of Physiologic Health for Adults. vol 12: Visual Impairments. Santa Monica, Ca: Rand Corporation; 1982. Publication R-2262/12-HHS.

US Preventive Services Task Force. . Screening for glaucoma. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 34.

US Preventive Services Task Force. . Screening for visual impairment. In: Guide to Clinical Preventive Services. 2nd ed. Washington, DC: US Department of Health and Human Services; 1996: chap 33.

Winograd CH, Gerety MB. . Geriatric assessment and concepts: visual and hearing assessment. New York, NY: American Geriatrics Society; 1989. Abstract.

Tables

Table 45.1. Visual Impairment Questionnaire


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