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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 AdultsScreening 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 AuthoritiesScreening for Anemia
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.
Hemoglobinopathies
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.
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.
Patient Resource
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.
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
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
1.
Instruct patients not to use tobacco or caffeine for 30 minutes before the measurement is performed.
Patient Resources
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.
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
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
Weight(kg)
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
[Figures] Figure 29.1. Weight Chart for Adult Men and Women*
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 ExaminationCancer 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 AuthoritiesWomen Under 40 Years of Age
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.
Oral Cavity Examination
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. 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
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.
Pelvic Examination And Ovarian Cancer
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. 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
1.
General Considerations: Use good lighting and proper examination procedure. Instruct the patient to empty her bladder and rectum before examination.
Digital Rectal Examination For Colorectal And Prostate Cancer
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. 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
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.
Skin 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. 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
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.
Testicular Examination
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. 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
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.
Thyroid Examination
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. 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
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.
Patient Resources - Breast Cancer
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.
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 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
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.
Patient Resources
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).
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
[Figures] Figure 31.1. Primary Prevention in Adults Without Evidence of CHD: Initial Classification Based on Total Cholesterol and HDL-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.
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
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.
Functional Impairment
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.
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.
Patient Resources
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).
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
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
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.
Patient Resources
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:
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.
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 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
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);
quantitative tests based on the conversion of heme to fluorescent porphyrins (HemoQuant);
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.
Patient Resources
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 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.
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 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. 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 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
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.
Patient Resources
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:
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.
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 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 AuthoritiesWomen Aged 50 Years and Older
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.
Patient Resources2. 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.
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
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. Patient Resources
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 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
1.
Measurement of fasting plasma glucose is the principal method of screening in nonpregnant, asymptomatic adults.
Patient Resources
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.
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 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
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:
Patient Resources
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.
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. SyphilisThe 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
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.
Chlamydia And Gonorrhea
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. 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
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:
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:
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.
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 AuthoritiesAll 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.
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.
Types of HIV Tests: Oral Fluid Test
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. 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:
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. Patient Resources
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
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 AuthoritiesNormal Risk
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. 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. 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. 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. 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. Patient Resources
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 AuthoritiesHigh-risk Populations
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.
Patient Resources
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.
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
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 AuthoritiesScreening
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.
Basics of Tuberculosis Prophylaxis
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. 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). 2. Dose and AdministrationInitiate 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). 3. Contraindications/PrecautionsContraindications 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. 4. Adverse ReactionsWhile 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. Basics of BCG Vaccination1. Indications Routine BCG vaccination is not recommended for adults in the United States. 2. Dose and AdministrationThe Tice 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). 3. PrecautionsDo not administer BCG vaccine to individuals who may be immunocompromised or immunosuppressed, including those with known or suspected HIV infection. 4. Adverse ReactionsSide effects occur in 1% to 10% of vaccinated individuals and may include severe or prolonged ulceration at the vaccination site, lymphadenitis, and lupus vulgaris. Patient Resources
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 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 BacteriuriaUrinalysis 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. Occult HematuriaScreening 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. ProteinuriaScreening 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. Recommendations of Major Authorities
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.
Patient Resources 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).
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 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
1.
Refer older adults and individuals at high risk to eye-care professionals for periodic examinations. See Recommendations of Major Authorities.
Patient Resources
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).
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 |