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Brief Summary

GUIDELINE TITLE

Hypertension diagnosis and treatment.

BIBLIOGRAPHIC SOURCE(S)

  • Institute for Clinical Systems Improvement (ICSI). Hypertension diagnosis and treatment. Bloomington (MN): Institute for Clinical Systems Improvement (ICSI); 2006 Oct. 53 p. [99 references]

GUIDELINE STATUS

Note: This guideline has been updated. The National Guideline Clearinghouse (NGC) is working to update this summary.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Note: This guideline has been updated. The National Guideline Clearinghouse (NGC) is working to update this summary. The recommendations that follow are based on the previous version of the guideline.

Note from the National Guideline Clearinghouse (NGC) and the Institute for Clinical Systems Improvement (ICSI): For a description of what has changed since the previous version of this guidance, refer to "Summary of Changes - October 2006.

The recommendations for the diagnosis and treatment of hypertension are presented in the form of an algorithm with 12 components, accompanied by detailed annotations. An algorithm is provided for Hypertension Diagnosis and Treatment. Clinical highlights and selected annotations (numbered to correspond with the algorithm) follow.

Class of evidence (A-D, M, R, X) ratings and key conclusion grades (I-III, Not Assignable) are defined at the end of the "Major Recommendations" field.

Clinical Highlights

  • Confirmation of hypertension is based on the initial visit, plus two follow-up visits with at least two blood pressure measures at each visit. (Annotation #2)
  • Standardized blood pressure measurement techniques (including out-of-office or home blood pressure measurements) should be employed when confirming an initially elevated blood pressure (BP) and for all subsequent measures during follow-up and treatment for hypertension. (Annotation #2, Appendix B - see original guideline document)
  • A thiazide-type diuretic should be considered as initial therapy in most patients with uncomplicated hypertension. (Annotation #6)
  • Physician reluctance to intensify treatment is a major obstacle to achieving treatment goals. (Annotation #8, 10)
  • Systolic blood pressure level should be the major factor for the detection, evaluation, and treatment of hypertension, especially in adults 50 years and older. (Annotation #7)
  • Fewer than 50% of patients with hypertension will be controlled with a single drug. (Annotation #8)

Hypertension Diagnosis and Treatment Algorithm Annotations

  1. Confirm Elevated Blood Pressure

    Key Points:

    • All elevated blood pressure readings should be confirmed.
    • A standardized blood pressure measurement process is important for correctly identifying hypertensive patients.

    If an elevated blood pressure reading has been obtained, the blood pressure level should be confirmed. Confirmation is based on the initial visit, plus two follow-up visits with at least two blood pressure readings at each visit. Explain the rationale; emphasize the reason for return and the need for confirmation of elevated blood pressure. Unconfirmed hypertension should be coded as indicated in the original guideline document. Confirmation and follow-up recommendations are noted in Tables 1 and 2 in the original guideline document.

    Standardized Blood Pressure Measurement

    Accurate, reproducible blood pressure (BP) measurement is important to allow comparisons between blood pressure values and to correctly classify blood pressure. Incorrectly labeling a hypertensive patient normotensive may increase risk for vascular events, since risk rises with increasing blood pressure. Labeling a patient with normal blood pressure as a hypertensive can affect insurability, employment, morbidity from medications, loss of time from work, and unnecessary lab and physician visits.

    Standardized blood pressure technique should be employed when confirming an elevated reading and for all subsequent readings during follow-up and treatment for hypertension. See Appendix B, "Standards for Blood Pressure Measurement," in the original guideline document.

    Confirmed elevated blood pressure should be classified as to the appropriate hypertension stage.

    Ambulatory blood pressure monitoring (ABPM) provides information about BP during daily activities and sleep. It is particularly helpful in the assessment of white coat or office effect (i.e., patients with elevated office BP who lack evidence of hypertensive target organ damage and who have normal out-of-office BP readings). This phenomenon may be present in 20 to 35% of patients diagnosed with hypertension. In general, however, this diagnosis can be reliably established without ABPM in patients with elevated office readings who lack target organ damage, and who have accurately measured out-of-office BP readings that are consistently less than 135/85 mm Hg. Other clinical situations in which ABPM may be helpful include the assessment of drug resistance, hypotensive symptoms, episodic hypertension, and suspected autonomic dysfunction. ABPM also appears to predict subsequent cardiovascular events more reliably than office blood pressure measurements. ABPM may be inaccurate with atrial fibrillation.

    Out-of-office or home blood pressure measurements also provide important information regarding the diagnosis and treatment of hypertension and they are less expensive than ABPM. Home blood pressure readings are a stronger predictor of subsequent cardiovascular events than are office readings. In addition, the use of home blood pressure measurements might reveal the patient with "masked hypertension" (i.e., normal office and elevated home readings). Fully automated devices using an appropriately sized upper arm cuff are preferred over aneroid devices or automated devices that measure blood pressure at the wrist or on the finger. Accuracy of the patient's automated device should be confirmed periodically (e.g., annually) by the patient's health care professional.

    The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC7) reflects the creation of a new classification, termed as "prehypertension," that is intended to identify individuals in whom early intervention of healthy lifestyle changes could reduce BP, decrease the rate of the progression of BP to hypertensive levels with age, or prevent hypertension entirely.

    JNC 7 has also combined stage 2 and stage 3 hypertension into a single stage 2 category. This change was made primarily because the management of the two former groups is similar.

    Blood Pressure Screening Clarification

    Because all stages of hypertension are associated with increased vascular events, the previous classifications of mild and moderate hypertension were discarded in favor of stages that emphasize these risks. The current classification emphasizes systolic as well as diastolic standards, as systolic hypertension has been associated with increased fatal and nonfatal cardiovascular events, and treatment has been shown to reduce cardiovascular morbidity and mortality.

    A proposed follow-up schedule based on the initial blood pressure level as well as prior diagnosis and treatment of cardiovascular disease and risk factors – is noted in JNC VI Table 3.

    Refer to the original guideline document for the International Classification of Diseases, Ninth Revision (ICD-9) code to be used for the initial encounter ("Elevated blood pressure reading without diagnosis of hypertension." Note: this category is to be used to record an episode of elevated blood pressure in a patient in whom no formal diagnosis of hypertension has been made, or as an incidental finding.)

    This guideline encourages increased use of this ICD-9 code because elevated BP without hypertension is currently believed to be underreported.

    Evidence supporting this recommendation is of classes: A, B, C, D, R

  1. Complete Initial Assessment: Evaluate, Accurately Stage, and Complete Risk Assessment

    Key Points:

    • It is important to assess and accurately stage newly confirmed hypertension.
    • A complete review of all medications (prescription and over-the-counter) and herbal supplements is very important.

    The goal of the clinical evaluation in newly confirmed hypertension is to determine whether the patient has primary or secondary hypertension, target organ disease, and other cardiovascular risk factors (risk assessment).

    1. Accurately Stage

      This treatment guideline is designed to be used in new or previously diagnosed hypertensive patients in conjunction with the National Guideline Clearinghouse (NGC) summary of the Institute for Clinical Systems Improvement (ICSI) Preventive Services for Adults guideline. See Appendix B, "Standards for Blood Pressure Measurement," in the original guideline document.

      Hypertension Stages Systolic   Diastolic
      Prehypertension 120-139 or 80-89
      Stage 1 hypertension 140-159 or 90-99
      Stage 2 hypertension >160 or >100

      When systolic and diastolic pressures fall into different categories, the higher category should be selected in classifying the individual's blood pressure status.

    1. Risk Assessment

      The risk for cardiovascular disease in patients with hypertension is determined not only by the level of blood pressure but also by the presence or absence of target organ damage or other risk factors such as smoking, dyslipidemia and diabetes, as shown in JNC 7. These factors independently modify the risk for subsequent cardiovascular disease, and their presence or absence is determined during the routine evaluation of patients with hypertension (i.e., history, physical examination, laboratory tests).

    1. Medical History

      The history should focus on modifiable lifestyle factors including weight change, dietary intake of sodium and cholesterol, level of exercise, psychosocial stressors, and patterns of alcohol and tobacco use.

      Determine all medications being used--including herbal supplements, over-the-counter, prescription, and illicit drugs--as many agents may temporarily elevate blood pressure and/or adversely affect blood pressure control. See Appendix E, "Recommended Education Messages" in the original guideline document.

      A family history of hypertension, cardiovascular disease, cerebrovascular disease, diabetes mellitus, and dyslipidemia should be documented.

      Assess for symptoms and signs of target organ disease and secondary hypertension via a directed history.

    1. Physical Examination

      The initial physical examination should include the following:

      • Two or more blood pressure measurements separated by two minutes with the patient seated and after standing for at least two minutes in accordance with the recommended techniques as stated in Appendix B, "Standards for Blood Pressure Measurement" in the original guideline document
      • Verification in the contralateral arm (if values are different, the higher value should be used)
      • Measurement of height, weight, and waist circumference
      • Funduscopic examination for hypertensive retinopathy (i.e., arteriolar narrowing, focal arteriolar constrictions, arteriovenous crossing changes, hemorrhages and exudates, disc edema)
      • Examination of the neck for carotid bruits, distended veins, or an enlarged thyroid gland
      • Examination of the heart for abnormalities in rate and rhythm, increased size, precordial heave, clicks, murmurs, and third and fourth heart sounds
      • Examination of the lungs for rales and evidence for bronchospasm
      • Examination of the abdomen for bruits, enlarged kidneys, masses, and abnormal aortic pulsation
      • Examination of the extremities for diminished or absent peripheral arterial pulsations, bruits, and edema
      • Neurological assessment
    1. Initial Laboratory Studies

      Initial lab screen should include 12-lead electrocardiogram (ECG), urinalysis, fasting blood glucose, hematocrit, serum sodium, potassium, creatinine (or estimated or measured glomerular filtration rate [GFR]), calcium, and lipid profile (total cholesterol, high density lipoprotein [HDL]-cholesterol, low density lipoprotein [LDL]-cholesterol and triglycerides). Additional laboratory and diagnostic studies may be required in individuals with suspected secondary hypertension and/or evidence of target-organ disease.

      Some of these tests are needed for determining presence of target organ disease and possible causes of hypertension. Others relate to cardiovascular risk factors or provide baseline values for judging biochemical effects of therapy.

      Additional tests may be ordered at the discretion of the provider based on clinical findings. These may include but are not limited to complete blood count (CBC), chest x-ray, uric acid, and urine microalbumin.

      See Appendix A, "Clinical Evaluation of Confirmed Hypertension" in the original guideline document.

    JNC 7 Cardiovascular Risk Factors/Target Organ Damage

    Major Risk Factors

    • Hypertension
    • Age (older than 55 for men, 65 for women)*
    • Diabetes mellitus**
    • Elevated LDL cholesterol
    • Low HDL cholesterol**
    • Estimated glomerular filtration rate (GFR) less than 60 mL/min
    • Microalbuminuria
    • Family history of premature cardiovascular disease (men younger than 55 or women younger than 65)
    • Obesity** (body mass index greater than or equal to 30 kg/m2, waist circumference greater than 40 inches for men and greater than 35 inches in women)
    • Physical inactivity
    • Tobacco usage, particularly cigarettes

    Target Organ Damage

    • Heart
      • Left ventricular hypertrophy
      • Angina/prior myocardial infarction
      • Prior coronary revascularization
      • Heart failure
    • Brain
      • Stroke or transient ischemic attack
      • Dementia
    • Chronic kidney disease
    • Peripheral arterial disease
    • Retinopathy

    * Increased risk begins at approximately 55 and 65 for men and women, respectively. Adult Treatment Panel III used earlier age cutpoints to suggest the need for earlier action.

    ** Components of the metabolic syndrome. Reduced HDL and elevated triglycerides are components of the metabolic syndrome. Abdominal obesity is also a component of metabolic syndrome.

    A point scale approach for estimating 10-year coronary heart disease risk can also be used. Refer to Appendix D, "10-year CVD Risk Calculator (Risk Assessment)" in the original guideline document.

    Evidence supporting this recommendation is of classes: B, R

  1. Is Secondary Cause Suspected?

    The term "secondary hypertension" implies that a patient's blood pressure elevation is the result of an underlying discoverable disease process. Secondary causes account for only a small percentage of all documented cases of hypertension, but their detection is important as appropriate intervention may be curative and lead to reversal of hypertension.

    Evaluate for features suggestive of secondary hypertension. Suspect a diagnosis of secondary hypertension in patients with an abrupt onset of symptomatic hypertension, with Stage 2 hypertension, hypertensive crisis, sudden loss of blood pressure control after many years of stability on drug therapy, drug resistant hypertension, and in those individuals with no family history of hypertension. Differential diagnosis of secondary hypertension includes:

    • Chronic kidney disease/obstructive uropathy
    • Thyroid and parathyroid disease
    • Drugs (prescription, over-the-counter, herbal supplement, illicit drugs)
    • Excessive alcohol use
    • Obstructive sleep apnea
    • Primary aldosteronism
    • Renal artery stenosis
    • Pheochromocytoma
    • Cushing's syndrome
    • Aortic coarctation
    • Obesity

    See Appendix C, "Suspicion of Secondary Hypertension," in the original guideline document.

    Note recommendations for additional diagnostic procedures. Be sure advanced testing is correctly chosen and done properly to avert the need for repeat studies. This may require discussion with or referral to a specialist.

  1. Order Additional Work-Up/Consider Referral

    Consider appropriate referral or additional workup if secondary hypertension is identified, or suspected.

    If you suspect a diagnosis of secondary hypertension, it is recommended that you perform a phone consultation and/or refer the patient to a specialist early in order to confirm the most efficient and cost-effective approach to patient evaluation and management.

    Evidence supporting this recommendation is of class: R

  1. Lifestyle Modifications +/- Drug Therapy

    Key Points:

    • Lifestyle modifications should be the cornerstone of the initial therapy for hypertension.

    Clinical studies show that the blood pressure-lowering effects of lifestyle modifications can be equivalent to drug monotherapy. Lifestyle modification is best initiated and sustained through an educational partnership between the patient and a multidisciplinary health care team. While team members may vary by clinical setting, behavior change strategies should include nutrition, exercise, and smoking cessation services. Lifestyle modifications should be reviewed and re-emphasized at least annually.

    Some patient education should occur and be documented at every visit. For recommended education messages, see Appendix E, "Recommended Education Messages," in the original guideline document.

    Table. Lifestyle Modifications to Prevent and Manage Hypertension*

    Modification Recommendation Approximate Systolic Blood Pressure (SBP) Reduction (Range)**
    Weight reduction Maintain normal body weight (body mass index 18.5 to 24.9 kg/m2) 5 to 20 mm Hg/10 kg
    Adopt Dietary Approaches to Stop Hypertension (DASH) eating plan Consume a diet rich in fruits, vegetables, and low-fat dairy products with a reduced content of saturated and total fat. 8 to 14 mm Hg
    Dietary sodium reduction Reduce dietary sodium intake to no more than 100 mmol per day (2.4 g sodium or 6 g sodium chloride). 2 to 8 mm Hg
    Physical activity Engage in regular aerobic physical activity such as brisk walking (at least 30-45 minutes per day, most days of the week) 4 to 9 mm Hg
    Moderation of alcohol consumption Limit consumption to no more than 2 drinks (e.g., 24 oz. beer, 10 oz. wine, or 3 oz. 80 proof whiskey) per day in most men and to no more than one drink per day in women and lighter-weight persons. 2 to 4 mm Hg

    *For overall cardiovascular risk reduction, stop smoking
    **The effects of implementing these modifications are dose- and time-dependent and could be greater for some individuals.

    Weight Reduction and Maintenance

    Hypertension is closely correlated with excess body weight. The prevalence of hypertension is 50% higher among overweight individuals, and 20 to 30% of hypertensive patients are overweight.

    Research studies have documented the positive effects of weight reduction as a strategy for blood pressure control. Whenever indicated, weight reduction should be recommended either as an initial non-pharmacologic therapy or as an adjunct to pharmacologic therapy. The decrease in blood pressure is related to the amount of weight loss. However, even an initial loss of as little as 10 pounds can have a positive effect on blood pressure. Weight loss can also improve the efficacy of antihypertensive medications and the cardiovascular risk profile.

    Initial weight loss and long-term weight control are both enhanced by a regular exercise program.

    Patient education and/or nutritional counseling should be provided.

    Moderation of Dietary Sodium

    A relationship between dietary sodium intake and blood pressure has been demonstrated in multiple clinical and epidemiological studies. Modest sodium restriction may also reduce the amount of antihypertensive medications required.

    However, individuals vary in response to a reduced sodium intake. Among hypertensives, African Americans, older patients, and patients with renal disease seem to be more sodium sensitive.

    Moderation of Alcohol Intake

    Several epidemiological studies have demonstrated an association between alcohol consumption and blood pressure. Alcohol affects both systolic and diastolic pressures, but its effects appear to be greater on systolic pressure. Significant elevations in blood pressure have been shown in individuals who consumed an average of at least three standard drinks per day compared with non-drinkers. Alcoholism may cause hypertension, and the alcoholic is less likely to respond to any hypertension treatment recommendations. Some persons may develop transitory hypertension during the first days of detoxification. Alcohol is also a concentrated calorie source that does not provide any nutrients. Reducing alcohol intake can help with weight reduction and may decrease triglyceride levels. The recommendation is to not exceed a daily alcohol intake of 1 ounce of ethanol. One ounce (30 mL) of ethanol is equivalent to two drinks per day. It is recommended that men have no more than one ounce of ethanol per day (two drinks) and women have no more than 0.5 ounce of ethanol per day (one drink). One drink is 12 ounces of beer, 5 ounces of wine or 1.5 ounces of 80 proof liquor.

    Adequate Physical Activity

    Epidemiological studies suggest that regular aerobic physical activity may be beneficial for both prevention and treatment of hypertension, to enable weight loss, for functional health status, and to diminish all-cause mortality and risk of cardiovascular disease. 30 to 45 minutes of brisk walking most days of the week at target heart rate ([220-age] x 75% = target heart rate) is adequate, inexpensive, and effective. Other aerobic activities (biking, swimming, jogging, etc.) may be more enjoyable. Resistive isotonic activities, when done as the only form of exercise training, are not recommended to lower blood pressure in hypertensive patients.

    Potassium

    There is no direct evidence that potassium supplementation lowers blood pressure chronically.

    Tobacco Avoidance

    Recent data using ambulatory blood pressure monitoring suggests that nicotine may indeed increase blood pressure and could account for some degree of blood pressure lability. In addition, it is a major risk factor for atherosclerotic cardiovascular disease. At each visit, establish tobacco use status and follow the NGC summary of the ICSI Tobacco Use Prevention and Cessation for Adults and Mature Adolescents guideline.

    Relaxation and Stress Management

    Although studies have not demonstrated a significant long-term effect of relaxation methods on blood pressure reduction, relaxation therapy may enhance an individual's quality of life and may have independent effects on lowering coronary heart disease risk.

    Drug Therapy

    A thiazide-type diuretic should be considered as initial therapy in most patients with uncomplicated hypertension. Diuretics have been shown to be as good as or superior to other classes of drug therapy in preventing cardiovascular disease (CVD) morbidity and mortality and they are inexpensive. Thiazide-type diuretics are especially useful for patients age 55 years or older with hypertension and additional risk factors for cardiovascular disease and for patients age 60 years or older with isolated systolic hypertension. In patients for whom diuretics are contraindicated or poorly tolerated, use of a beta-blocker, angiotensin-converting enzyme (ACE) inhibitor, angiotensin receptor blocker, or calcium antagonist is appropriate. Long-acting dihydropyridine calcium antagonists have been shown to be effective for patients age 60 years or older with isolated systolic hypertension. Co-existing medical conditions may also justify the use of one of these classes of drugs. An example is the use of an angiotensin-converting enzyme inhibitor in a patient with heart failure or diabetic nephropathy. Please see the NGC summary of the ICSI guideline Management of Type 2 Diabetes Mellitus for further information. Based on meta-analyses of previous studies, beta-blockers may be less efficacious than other first-line alternatives in patients who are 60 years and older, especially for stroke prevention. Thus, use of these drugs as initial therapy in older patients probably should be restricted to situations where there is another indication for their use (e.g., heart failure, previous myocardial infarction [MI], angina.) They still should be considered alternative first-line agents in younger patients, where they appear to lessen cardiovascular morbidity as well as other recommended drugs. Other classes of drugs should be reserved for special situations or as additive therapy (see Appendix F, "Therapies," in the original guideline document.)

    Many patients will require more than one drug for blood pressure control. Combination therapies that include a diuretic are often effective, lessen the risk for side effects (by use of low doses of each component drug), and enhance adherence by simplification of the treatment program. For patients with chronic kidney disease three or more drugs may be needed to achieve goal.

    Other considerations when selecting initial drug therapy include age, race, cost, drug interactions, side effects, and quality of life issues. In general, diuretics and calcium channel blockers appear to be more effective as an initial treatment of hypertension in African Americans.

    The lowest recommended dose of the chosen drug should be used initially. If tolerated, the dose can be increased or additional medications added to achieve goal blood pressure.

    Because thiazide-type diuretics have been shown to be as good as or superior to other drug classes in preventing CVD morbidity and mortality, they should be considered preferred initial therapy in most patients. However, studies support the use of specific alternative drugs as initial therapy in the presence of specific co-existing diseases. ACE-inhibitors (ACEI) and angiotensin receptor blockers have been shown to be beneficial for patients with proteinuric renal disease (both diabetic and non-diabetic) by reducing proteinuria and slowing the rate of decline in renal function. ACEI have also been shown to provide symptomatic relief and prolong life for patients with heart failure (HF) and are the initial drug of choice for this condition. Beta-blockers reduce the risk of sudden death and recurrent myocardial infarction for patients with an initial MI. ACEI also reduce the risk of subsequent MI and progression to HF for patients who experience a large MI associated with impairment of left ventricular function. They also may reduce risk for patients with (or at high risk for) cardiovascular disease. Initial monotherapy with one of these agents is appropriate in these patient populations. A diuretic should be added if blood pressure response is not satisfactory.

    Evidence from a recent large study refutes concerns about increased risk of myocardial infarction, cancer, or gastrointestinal bleeding from use of long-acting calcium antagonists. However, data does suggest that this class of drugs may be less effective in preventing HF. The guideline developers suggest these drugs be limited to those conditions listed in Appendix F, "Therapies," in the original guideline document. Data supporting potential dangers of calcium antagonists are limited to short-acting preparations (especially nifedipine) that are not approved for the treatment of hypertension.

    Evidence from a recent large trial suggests that ACEI may be less effective in African Americans than thiazide-type diuretics in controlling blood pressure and in preventing stroke and cardiovascular disease.

    Evidence supporting this recommendation is of classes: A, B, C, D, M, R

  1. Blood Pressure (BP) at Goal?

    Key Points:

    • Systolic hypertension in patients aged 60 and older is an important modifiable cardiovascular risk factor.
    • Accurate home monitoring systems are an important tool for assessing blood pressure control.
    • Review drugs, over-the-counter medications, and herbal therapies that may interfere with BP goal.

    Goal office blood pressures should be less than 140 mmHg systolic and less than 90 mmHg diastolic for all adults. Goal blood pressures measured out of the office setting should be less than 135 mm Hg systolic and less than 85 mmHg diastolic.

    For patients with a history of heart failure, goal office blood pressures are less than 130 mmHg systolic and less than 80 mmHg diastolic.

    For patients with chronic kidney disease, goal office blood pressures are less than 130 mmHg systolic and less than 80 mmHg diastolic.

    For patients with diabetes mellitus, goal office blood pressures are less than 130 mmHg systolic and less than 80 mmHg diastolic. Progressive reduction of systolic blood pressure to as low as 110 mmHg has been shown to be associated with lower risk of microvascular and macrovascular complications.

    For patients 60 years or older with isolated systolic hypertension who have markedly increased systolic blood pressure levels prior to treatment, it may not be possible to lower systolic blood pressure to less than 140 mmHg. An interim goal of 160 mmHg or what can be achieved by optimal doses of three antihypertensive drugs would be reasonable.

    Systolic hypertension in patients age 60 and older is an important modifiable cardiovascular risk factor. [Conclusion Grade I: See Conclusion Grading Worksheet A - Annotation #7 (Isolated Systolic Hypertension) in the original guideline document.]

    Drug treatment for Stage 1 (systolic blood pressure [SBP] 140 to 159 mmHg) systolic hypertension in patients age 60 and older is effective in reducing cardiovascular disease morbidity and mortality. [Conclusion Grade III: See Conclusion Grading Worksheet A - Annotation #7 (Isolated Systolic Hypertension) in the original guideline document.]

    Drug treatment for Stage 2 (SBP greater than or equal to 160 to 180 mmHg) systolic hypertension in patients age 60 and older is effective in reducing cardiovascular disease morbidity and mortality. [Conclusion Grade I: See Conclusion Grading Worksheet A - Annotation #7 (Isolated Systolic Hypertension) in the original guideline document]

    Concerns have been raised that excessive lowering of diastolic blood pressure increases the risk of coronary events in patients with established coronary artery disease or left ventricular hypertrophy by lowering diastolic perfusion pressure in the coronary circulation. This is known as the J-curve hypothesis. Recent studies have also raised concerns about a J-curve relationship between diastolic blood pressure level and risk for stroke in elderly patients treated for isolated systolic hypertension. No such J-shaped relationship has been observed between adverse event rates and systolic blood pressure level. Although not resolved, caution should be applied in lowering diastolic blood pressure below 75 mmHg in patients with coronary artery disease or left ventricular hypertrophy or below 65 mmHg in all elderly patients with isolated systolic hypertension. In the latter situation, this may require compromise of the goal level of systolic blood pressure achieved.

    Evidence supporting this recommendation is of classes: A, B, C, M, R

  1. Change Treatment

    Once a hypertensive drug therapy is initiated, most patients should return for follow-up and medication adjustments at least at monthly intervals until BP goal is reached.

    Fewer than 50% of patients with hypertension will be controlled with a single drug.

    If blood pressure goals are not met, the clinician has three options for subsequent therapy:

    • Increase the dose of the initial drug toward maximal levels.
    • Substitute an agent from another class.
    • Add a second drug from another class.

    Individualized drug selection is based on several principles:

    • If the initial response to one drug is adequate, continue the same drug.
    • If the response is partial on one agent, increase the dose or add a second drug of a different class.
    • If there is little response, substitute another single drug from a different class.
    • Consider low-dose diuretic use early or as a first addition.
    • Consider loop diuretic agents instead of thiazide or thiazide-like diuretics when creatinine is greater than 2.0 mg/dL or estimated GFR less than 30 mL/min per 1.73 m2.
    • Do not combine two drugs of the same class.
    • The use of combination agents can be effective.

    For many patients, two or more drugs in combination may be needed to reach hypertension goals. This is especially true for patients with hypertension goals focused on the low end or patients with chronic renal failure.

    Evidence supporting this recommendation is of classes: A, R

  1. BP at Goal?

    Key Points:

    • Carefully review potential barriers to long-term adherence to therapy, including the possible secondary diagnosis of depression.
    • Systolic hypertension in patients aged 60 and older is an important modifiable cardiovascular risk factor.
    • Accurate home monitoring systems are an important tool for assessing blood pressure control.
    • Review drugs (prescription and over-the-counter) and herbal therapies that may interfere with BP goal.

    If at this point acceptable response has not been achieved, several issues should be addressed or revisited. These include adherence to appropriate lifestyle modifications, consistent use of prescribed drugs, and tolerance of treatment modalities. Non-adherence rates to prescribed medications are estimated at 50% and are slightly higher for elderly and adolescent patients. Since there is not a simple test to accurately measure adherence, there are some practical methods that can be used for all patients: asking the patient about missed doses, watching treatment response, tracking missed appointments, tracking prescription refills, asking about issues of cost, and monitoring side effects. Although patients will generally overestimate their adherence, simply asking the question will help identify up to 50% of low-adherence patients. Standardized instruction in self-blood pressure measurement will allow assessment of "white coat" syndrome. Interfering substances which can adversely affect treatment include non-steroidal anti-inflammatory drugs, oral contraceptives, sympathomimetics, antidepressants, glucocorticoids, nasal decongestants, licorice-containing substances (e.g., chewing tobacco), cocaine, cyclosporine, and erythropoietin. Intermittent use of alcohol, particularly in alcoholics who are binge drinkers, may cause difficulties with widely fluctuating blood pressures.

    Non-specific symptoms such as fatigue, lightheadedness, or vaguely impaired cognition may be due to an acute decline in blood pressure level and may resolve within four to six weeks while continuing the drug. Other minor drug-related symptoms unrelated to blood pressure change may also resolve in time without discontinuing the drug. Non-office standardized blood pressure measurement is desirable to monitor blood pressure control.

    The factors that lead to non-adherence are multifactorial: misunderstanding of the treatment and the reason for it, adverse reactions (or fear of them), depression, complex dosing regimens, financial constraints, or simple forgetfulness. Asking open-ended/non-judgmental questions about treatment regimens can lead to a good discussion between the provider and patient about why the patient may have difficulty adhering. There are a number of recommendations that in various combinations may lead to better patient adherence. These suggestions are based on available evidence from randomized clinical trials that evaluated the usefulness of adherence interventions. To increase adherence on a long-term basis: provide education about the medication and how it fits with the treatment plan, simplify the regimen (e.g., less frequent dosing, combination medications, controlled release dosage forms), use patient adherence aids (e.g., pill boxes, alarms), offer support group sessions, send reminders for medication refills and appointments, cue medications to daily events (e.g., breakfast, bedtime), offer positive reinforcement (acknowledge the patient's efforts to adhere), monitor with regular physician follow-up, and actively involve family members and significant others. When choosing antihypertensive drugs, preference should be given to long-acting drugs that can be dosed once daily to enhance long-term compliance.

    Evidence supporting this recommendation is of classes: M, R

  1. Resistant Hypertension?

    A patient has resistant hypertension when blood pressure goals are not met despite compliance with a triple drug regimen that includes a diuretic. Numerous reasons may exist for an inadequate or poor response to two, three, or more drugs, with volume overload due to excessive sodium intake or inadequate diuretic use being the more likely reasons. Other causes include nonadherence to therapy due to patient or health care provider issues, drug related causes (using a nonantihypertensive drug that can raise blood pressure), unrecognized secondary hypertension, pseudohypertension, or associated conditions including obesity and ethanol abuse.

    The drug regimen should include a diuretic plus near maximal doses of two of the following classes of drugs:

    • Beta-adrenergic-blocker or other anti-adrenergic agent
    • Direct vasodilator
    • Calcium channel-blocker
    • ACE inhibitor
    • Angiotensin receptor blocker

    Several causes of resistant hypertension may be present:

    • Improper BP measurement (over inflation of the cuff or using a cuff that is too small for the arm) can lead to inaccurately high readings.
    • Brachial arteries may be heavily calcified or arteriosclerotic and cannot be fully compressed (pseudohypertension).
    • Clinic or white coat hypertension
    • Failure to receive adequate doses of medication (may be reluctance by patient or practitioner)
    • Inadequate diuretic therapy
    • Drug interactions

    Evidence supporting this recommendation is of classes: A, D

  1. Hypertension Consult

    Consider hypertension consultation if a patient's blood pressure is not controlled on two medications or if secondary hypertension is suspected. All patients with BP that is not controlled on three medications should be referred for consultation.

  1. Hypertension Continuing Care

    Key Points:

    • On follow-up visits, history and physical examination should be directed toward detection of hypertensive target organ damage.
    • In patients with office BP at goal who demonstrate progressive target organ disease, home monitoring may be beneficial.

    Once blood pressure is at goal and stable, the patient should be seen usually at three- to six-month intervals by the provider to assess patient adherence, patient satisfaction, and any changes in target organ status. Patients' comorbidities such as heart failure, associated diseases such as diabetes, and need for laboratory tests influence the frequency of visits. Lifestyle modifications should be reviewed, re-emphasized, and documented annually. Patients should monitor blood pressure more frequently by home monitoring or by other allied health professionals.

    Ongoing care can be facilitated by physicians or specially trained allied health care professionals who provide education, reinforcement, realistic short- and long-term goal setting, and adjustment of medications according to the individual clinical situation. Intervention strategies that seek to involve the patient in decision-making can improve long-term adherence to therapy and thus better blood pressure control. Additionally, such an ongoing relationship might better identify those patients who are suitable candidates for a reduction or withdrawal of antihypertensive drug therapy following a prolonged interval of excellent blood pressure control.

    On follow-up visits, history and physical examination should be directed toward detection of hypertensive target organ damage.

    One may consider decreasing the dosage or number of antihypertensive drugs while maintaining lifestyle modification if:

    • Patient has uncomplicated hypertension that is well controlled.
    • Blood pressure has been maintained and documented for at least 1 year.

    Evidence supporting this recommendation is of classes: M, R

Definitions:

Classes of Research Reports:

  1. Primary Reports of New Data Collection:

    Class A:

    • Randomized, controlled trial

    Class B:

    • Cohort study

    Class C:

    • Non-randomized trial with concurrent or historical controls
    • Case-control study
    • Study of sensitivity and specificity of a diagnostic test
    • Population-based descriptive study

    Class D:

    • Cross-sectional study
    • Case series
    • Case report
  2. Reports that Synthesize or Reflect upon Collections of Primary Reports:

    Class M:

    • Meta-analysis
    • Systematic review
    • Decision analysis
    • Cost-effectiveness analysis

    Class R:

    • Consensus statement
    • Consensus report
    • Narrative review

    Class X:

    • Medical opinion

Conclusion Grades:

Grade I: The evidence consists of results from studies of strong design for answering the question addressed. The results are both clinically important and consistent with minor exceptions at most. The results are free of any significant doubts about generalizability, bias, and flaws in research design. Studies with negative results have sufficiently large samples to have adequate statistical power.

Grade II: The evidence consists of results from studies of strong design for answering the question addressed, but there is some uncertainty attached to the conclusion because of inconsistencies among the results from the studies or because of minor doubts about generalizability, bias, research design flaws, or adequacy of sample size. Alternatively, the evidence consists solely of results from weaker designs for the question addressed, but the results have been confirmed in separate studies and are consistent with minor exceptions at most.

Grade III: The evidence consists of results from studies of strong design for answering the question addressed, but there is substantial uncertainty attached to the conclusion because of inconsistencies among the results of different studies or because of serious doubts about generalizability, bias, research design flaws, or adequacy of sample size. Alternatively, the evidence consists solely of results from a limited number of studies of weak design for answering the question addressed.

Grade Not Assignable: There is no evidence available that directly supports or refutes the conclusion.

CLINICAL ALGORITHM(S)

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and classified for selected recommendations (see "Major Recommendations").

In addition, key conclusions contained in the Work Group's algorithm are supported by a grading worksheet that summarizes the important studies pertaining to the conclusion. The type and quality of the evidence supporting these key recommendations (i.e., choice among alternative therapeutic approaches) is graded for each study.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Institute for Clinical Systems Improvement (ICSI). Hypertension diagnosis and treatment. Bloomington (MN): Institute for Clinical Systems Improvement (ICSI); 2006 Oct. 53 p. [99 references]

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

1995 Jun (revised 2006 Oct)

GUIDELINE DEVELOPER(S)

Institute for Clinical Systems Improvement - Private Nonprofit Organization

GUIDELINE DEVELOPER COMMENT

Organizations participating in the Institute for Clinical Systems Improvement (ICSI): Affiliated Community Medical Centers, Allina Medical Clinic, Altru Health System, Aspen Medical Group, Avera Health, CentraCare, Columbia Park Medical Group, Community-University Health Care Center, Dakota Clinic, ENT Specialty Care, Fairview Health Services, Family HealthServices Minnesota, Family Practice Medical Center, Gateway Family Health Clinic, Gillette Children's Specialty Healthcare, Grand Itasca Clinic and Hospital, HealthEast Care System, HealthPartners Central Minnesota Clinics, HealthPartners Medical Group and Clinics, Hutchinson Area Health Care, Hutchinson Medical Center, Lakeview Clinic, Mayo Clinic, Mercy Hospital and Health Care Center, MeritCare, Mille Lacs Health System, Minnesota Gastroenterology, Montevideo Clinic, North Clinic, North Memorial Care System, North Suburban Family Physicians, Northwest Family Physicians, Olmsted Medical Center, Park Nicollet Health Services, Pilot City Health Center, Quello Clinic, Ridgeview Medical Center, River Falls Medical Clinic, Saint Mary's/Duluth Clinic Health System, St. Paul Heart Clinic, Sioux Valley Hospitals and Health System, Southside Community Health Services, Stillwater Medical Group, SuperiorHealth Medical Group, University of Minnesota Physicians, Winona Clinic, Ltd., Winona Health

ICSI, 8009 34th Avenue South, Suite 1200, Bloomington, MN 55425; telephone, (952) 814-7060; fax, (952) 858-9675; e-mail: icsi.info@icsi.org; Web site: www.icsi.org.

SOURCE(S) OF FUNDING

The following Minnesota health plans provide direct financial support: Blue Cross and Blue Shield of Minnesota, HealthPartners, Medica, Metropolitan Health Plan, PreferredOne and UCare Minnesota. In-kind support is provided by the Institute for Clinical Systems Improvement's (ICSI) members.

GUIDELINE COMMITTEE

Cardiovascular Steering Committee

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Work Group Members: Gary Schwartz, MD (Work Group Leader) (Mayo Clinic) (Hypertension); Vincent Canzanello, MD (Mayo Clinic) (Hypertension); Anthony Woolley, MD (Park Nicollet Health Services) (Internal Medicine/Hypertension); Troy Miller, DO (Sioux Valley Hospitals and Health System) (Family Practice); Patrick O'Connor, MD (HealthPartners Research Foundation) (Family Practice); Deborah Klein, PharmD (Allina Medical Clinic) (Pharmacy); Nancy Jaeckels (Institute for Clinical Systems Improvement) (Measurement Advisor); Ann-Marie Evenson, BS, RHIT (Institute for Clinical Systems Improvement) (Facilitator)

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

GUIDELINE STATUS

Note: This guideline has been updated. The National Guideline Clearinghouse (NGC) is working to update this summary.

GUIDELINE AVAILABILITY

Electronic copies of the updated guideline: Available from the Institute for Clinical Systems Improvement (ICSI) Web site.

Print copies: Available from ICSI, 8009 34th Avenue South, Suite 1200, Bloomington, MN 55425; telephone, (952) 814-7060; fax, (952) 858-9675; Web site: www.icsi.org; e-mail: icsi.info@icsi.org.

AVAILABILITY OF COMPANION DOCUMENTS

The following is available:

Print copies: Available from ICSI, 8009 34th Avenue South, Suite 1200, Bloomington, MN 55425; telephone, (952) 814-7060; fax, (952) 858-9675; Web site: www.icsi.org; e-mail: icsi.info@icsi.org.

PATIENT RESOURCES

The following is available:

  • Health care guideline for patients and families: Diagnosing and treating hypertension (high blood pressure). Bloomington (MN): Institute for Clinical Systems Improvement, 2006 Nov. 16 p.

Electronic copies: Available in Portable Document Format (PDF) from the Institute for Clinical Systems Improvement (ICSI) Web site.

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This summary was completed by ECRI on May 5, 1999. The information was verified by the guideline developer on July 6, 1999. This summary was updated by ECRI on April 19, 2001. The updated information was verified by the guideline developer as of June 28, 2001. This summary was updated again on June 18, 2002 and verified by the guideline developer on August 8, 2002. This summary was updated again by ECRI on January 28, 2004, July 28, 2004, December 15, 2005, and most recently on January 31, 2007.

COPYRIGHT STATEMENT

This NGC summary (abstracted Institute for Clinical Systems Improvement [ICSI] Guideline) is based on the original guideline, which is subject to the guideline developer's copyright restrictions.

The abstracted ICSI Guidelines contained in this Web site may be downloaded by any individual or organization. If the abstracted ICSI Guidelines are downloaded by an individual, the individual may not distribute copies to third parties.

If the abstracted ICSI Guidelines are downloaded by an organization, copies may be distributed to the organization's employees but may not be distributed outside of the organization without the prior written consent of the Institute for Clinical Systems Improvement, Inc.

All other copyright rights in the abstracted ICSI Guidelines are reserved by the Institute for Clinical Systems Improvement, Inc. The Institute for Clinical Systems Improvement, Inc. assumes no liability for any adaptations or revisions or modifications made to the abstracts of the ICSI Guidelines.

DISCLAIMER

NGC DISCLAIMER

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Guidelines represented on the NGC Web site are submitted by guideline developers, and are screened solely to determine that they meet the NGC Inclusion Criteria which may be found at http://www.guideline.gov/about/inclusion.aspx .

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Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
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