"The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure" provides a new guideline for hypertension prevention and management. The following are the key messages(1) In persons older than 50 years, systolic blood pressure (BP) of more than 140 mm Hg is a much more important cardiovascular disease (CVD) risk factor than diastolic BP; (2) The risk of CVD, beginning at 115/75 mm Hg, doubles with each increment of 20/10 mm Hg; individuals who are normotensive at 55 years of age have a 90% lifetime risk for developing hypertension; (3) Individuals with a systolic BP of 120 to 139 mm Hg or a diastolic BP of 80 to 89 mm Hg should be considered as prehypertensive and require health-promoting lifestyle modifications to prevent CVD; (4) Thiazide-type diuretics should be used in drug treatment for most patients with uncomplicated hypertension, either alone or combined with drugs from other classes. Certain high-risk conditions are compelling indications for the initial use of other antihypertensive drug classes (angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, β-blockers, calcium channel blockers); (5) Most patients with hypertension will require 2 or more antihypertensive medications to achieve goal BP (<140/90 mm Hg, or <130/80 mm Hg for patients with diabetes or chronic kidney disease); (6) If BP is more than 20/10 mm Hg above goal BP, consideration should be given to initiating therapy with 2 agents, 1 of which usually should be a thiazide-type diuretic; and (7) The most effective therapy prescribed by the most careful clinician will control hypertension only if patients are motivated. Motivation improves when patients have positive experiences with and trust in the clinician. Empathy builds trust and is a potent motivator. Finally, in presenting these guidelines, the committee recognizes that the responsible physician's judgment remains paramount.For more than 3 decades, the National Heart, Lung, and Blood Institute (NHLBI) has administered the National High Blood Pressure Education Program (NHBPEP) Coordinating Committee, a coalition of 39 major professional, public, and voluntary organizations and 7 federal agencies. One important function is to issue guidelines and advisories designed to increase awareness, prevention, treatment, and control of hypertension (high blood pressure [BP]). Since the publication of "The Sixth Report of the Joint National Committee on the Prevention, Detection, Evaluation, and Treatment of High Blood Pressure" (JNC VI) released in 1997,many large-scale clinical trials have been published.The decision to appoint a committee for "The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure" (JNC 7) was based on 4 factors: publication of many new hypertension observational studies and clinical trials; need for a new clear and concise guideline that would be useful for clinicians; need to simplify the classification of BP; and a clear recognition that the JNC reports were not being used to their maximum benefit. This JNC report is presented in 2 separate publications: this current succinct practical guide and a more comprehensive report to be published separately, which will provide a broader discussion and justification for the current recommendations. In presenting these guidelines, the committee recognizes that the responsible physician's judgment is paramount in managing his or her patients.METHODSSince publication of the JNC VI report, the NHBPEP Coordinating Committee, chaired by the director of the NHLBI, has regularly reviewed and discussed the hypertension clinical trials at their biannual meetings. In many instances, the principal investigator of the larger studies has presented the information directly to the Coordinating Committee. The Committee's presentations and reviews are summarized and posted on the NHLBI Web site.In agreeing to commission a new report, the director requested that the Coordinating Committee members provide in writing a detailed rationale explaining the necessity to update the guidelines and to describe the critical issues and concepts to be considered for a new report. The JNC 7 chair was selected in addition to a 9-member executive committee appointed entirely from the NHBPEP Coordinating Committee membership. The NHBPEP Coordinating Committee served as members of 5 writing teams, each of which were co-chaired by 2 executive committee members.The concepts identified by the NHBPEP Coordinating Committee membership were used to develop the report outline. A timeline was developed to complete and publish the work in 5 months. Based on the identified critical issues and concepts, the executive committee identified relevant Medical Subject Headings (MeSH) terms and keywords to further review the scientific literature. These MeSH terms were used to generate MEDLINE searches that focused on English-language, peer-reviewed scientific literature from January 1997 through April 2003. Various systems of grading the evidence were considered and the classification scheme used in JNC VI and other NHBPEP clinical guidelines was selected,which classifies studies in a process adapted from Last and Abramson.The executive committee met on 6 occasions, 2 of which included meetings with the entire Coordinating Committee. The writing teams also met by teleconference and used electronic communications to develop the report. Twenty-four drafts were created and reviewed in a reiterative fashion. At its meetings, the executive committee used a modified nominal group process to identify and resolve issues. The NHBPEP Coordinating Committee reviewed the penultimate draft and provided written comments to the executive committee. In addition, 33 national hypertension leaders reviewed and commented on the document. The NHBPEP Coordinating Committee approved the JNC 7 report.RESULTSClassification of BPTable 1provides a classification of BP for adults aged 18 years or older. The classification is based on the mean of 2 or more properly measured seated BP readings on each of 2 or more office visits. In contrast with the classification provided in the JNC VI report, a new category designated prehypertension has been added, and stages 2 and 3 hypertension have been combined. Patients with prehypertension are at increased risk for progression to hypertension; those in the 130/80 to 139/89 mm Hg BP range are at twice the risk to develop hypertension as those with lower values.Table 1.Classification and Management of Blood Pressure for Adults Aged 18 Years or OlderBP ClassificationSystolic BP, mm Hg*Diastolic BP, mm Hg*Management*Lifestyle ModificationInitial Drug TherapyWithout Compelling IndicationWith Compelling Indications†Normal<120and<80EncouragePrehypertension120-139or80-89YesNo antihypertensive drug indicatedDrug(s) for the compelling indications‡Stage 1 hypertension140-159or90-99YesThiazide-type diuretics for most; may consider ACE inhibitor, ARB, β-blocker, CCB, or combinationDrug(s) for the compelling indications Other antihypertensive drugs (diuretics, ACE inhibitor, ARB, β-blocker, CCB) as neededStage 2 hypertension≥160or≥100Yes2-Drug combination for most (usually thiazide-type diuretic and ACE inhibitor or ARB or β-blocker or CCB)§Drug(s) for the compelling indications Other antihypertensive drugs (diuretics, ACE inhibitor, ARB, β-blocker, CCB) as neededAbbreviations: ACE, angiotensin-converting enzyme; ARB, angiotensin-receptor blocker; BP, blood pressure; CCB, calcium channel blocker.*Treatment determined by highest BP category.†See Table 6.‡Treat patients with chronic kidney disease or diabetes to BP goal of less than 130/80 mm Hg. §Initial combined therapy should be used cautiously in those at risk for orthostatic hypotension.Cardiovascular Disease RiskHypertension affects approximately 50 million individuals in the United States and approximately 1 billion individuals worldwide. As the population ages, the prevalence of hypertension will increase even further unless broad and effective preventive measures are implemented. Recent data from the Framingham Heart Studysuggest that individuals who are normotensive at 55 years of age have a 90% lifetime risk for developing hypertension.The relationship between BP and risk of cardiovascular disease (CVD) events is continuous, consistent, and independent of other risk factors. The higher the BP, the greater the chance of myocardial infarction, heart failure (HF), stroke, and kidney disease. For individuals aged 40 to 70 years, each increment of 20 mm Hg in systolic BP or 10 mm Hg in diastolic BP doubles the risk of CVD across the entire BP range from 115/75 to 185/115 mm Hg.The classification prehypertension, introduced in this report (Table 1), recognizes this relationship and signals the need for increased education of health care professionals and the public to decrease BP levels and prevent the development of hypertension in the general population.Hypertension prevention strategies are available to achieve this goal (see "Lifestyle Modifications" section).Benefits of Lowering BPIn clinical trials, antihypertensive therapy has been associated with 35% to 40% mean reductions in stroke incidence; 20% to 25% in myocardial infarction; and more than 50% in HF.It is estimated that in patients with stage 1 hypertension (systolic BP, 140-159 mm Hg and/or diastolic BP, 90-99 mm Hg) and additional cardiovascular risk factors, achieving a sustained 12-mm Hg decrease in systolic BP for 10 years will prevent 1 death for every 11 patients treated. In the presence of CVD or target-organ damage, only 9 patients would require this BP reduction to prevent a death.BP Control RatesHypertension is the most common primary diagnosis in the United States with 35 million office visits as the primary diagnosis.Current control rates (systolic BP <140 mm Hg and diastolic BP <90 mm Hg), although improved, are still far below the Healthy People 2010 goal of 50%; 30% are still unaware they have hypertension (Table 2). In the majority of patients, controlling systolic hypertension, which is a more important CVD risk factor than diastolic BP except in patients younger than 50 yearsand occurs much more commonly in older persons, has been considerably more difficult than controlling diastolic hypertension. Recent clinical trials have demonstrated that effective BP control can be achieved in most patients with hypertension, but the majority will require 2 or more antihypertensive drugs.When physicians fail to prescribe lifestyle modifications, adequate antihypertensive drug doses, or appropriate drug combinations, inadequate BP control may result.Table 2.Trends in Awareness, Treatment, and Control of High Blood Pressure in Adults With Hypertension Aged 18 to 74 Years*National Health and Nutrition Examination Surveys, Weighted %II (1976-1980)III (Phase 1, 1988-1991)III (Phase 2, 1991-1994)1999-2000Awareness51736870Treatment31555459Control†10292734*Data for 1999-2000 were computed (M. Wolz, unpublished data, 2003) from the National Heart, Lung, and Blood Institute and data for National Health and Nutrition Examination Surveys II and III (phases 1 and 2) are from "The Sixth Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure."High blood pressure is systolic blood pressure of at least 140 mm Hg or diastolic blood pressure of at least 90 mm Hg or taking antihypertensive medication.†Systolic blood pressure of less than 140 mm Hg and diastolic blood pressure of less than 90 mm Hg.Accurate BP Measurement in the OfficeThe auscultatory method of BP measurement with a properly calibrated and validated instrument should be used.Patients should be seated quietly for at least 5 minutes in a chair rather than on an examination table, with feet on the floor and arm supported at heart level. Measurement of BP in the standing position is indicated periodically, especially in those at risk for postural hypotension. An appropriate-sized cuff (cuff bladder encircling at least 80% of the arm) should be used to ensure accuracy. At least 2 measurements should be made. Systolic BP is the point at which the first of 2 or more sounds is heard (phase 1) and diastolic BP is the point before the disappearance of sounds (phase 5). Physicians should provide to patients, verbally and in writing, their specific BP numbers and BP goals.Ambulatory BP MonitoringAmbulatory BP monitoringprovides information about BP during daily activities and sleep. Ambulatory BP monitoring is warranted for evaluation of (white-coat) hypertension in the absence of target-organ injury. It is also helpful to assess patients with apparent drug resistance, hypotensive symptoms with antihypertensive medications, episodic hypertension, and autonomic dysfunction. The ambulatory BP values are usually lower than clinic readings. Awake hypertensive individuals have a mean BP of more than 135/85 mm Hg and during sleep, more than 120/75 mm Hg. The level of BP using ambulatory BP monitoring correlates better than office measurements with target-organ injury.Ambulatory BP monitoring also provides a measure of the percentage of BP readings that are elevated, the overall BP load, and the extent of BP reduction during sleep. In most individuals, BP decreases by 10% to 20% during the night; those in whom such decreases are not present are at increased risk for cardiovascular events.Self-measurement of BPBlood pressure self-measurements may benefit patients by providing information on response to antihypertensive medication, improving patient adherence with therapy,and in evaluating white-coat hypertension. Individuals with a mean BP of more than 135/85 mm Hg measured at home are generally considered to be hypertensive. Home measurement devices should be checked regularly for accuracy.Patient EvaluationEvaluation of patients with documented hypertension has 3 objectives: (1) to assess lifestyle and identify other cardiovascular risk factors or concomitant disorders that may affect prognosis and guide treatment (Box 1); (2) to reveal identifiable causes of high BP (Box 2); and (3) to assess the presence or absence of target-organ damage and CVD. The data needed are acquired through medical history, physical examination, routine laboratory tests, and other diagnostic procedures.Box 1. Cardiovascular Risk Factors*Major Risk FactorsHypertension†Cigarette smokingObesity (BMI ≥30)†Physical inactivityDyslipidemia†Diabetes mellitus†Microalbuminuria or estimated GFR <60 mL/minAge (>55 years for men, >65 years for women)Family history of premature cardiovascular disease (men <55 years or women 65 years)Target-Organ DamageHeart Left ventricular hypertrophy Angina or prior myocardial infarction Prior coronary revascularization Heart failureBrain Stroke or transient ischemic attackChronic kidney diseasePeripheral arterial diseaseRetinopathy*BMI indicates body mass index calculated as weight in kilograms divided by the square of height in meters; GFR, glomerular filtration rate.†Components of the metabolic syndrome.Box 2. Identifiable Causes of HypertensionSleep apneaDrug-induced or drug-related (see Box 3)Chronic kidney diseasePrimary aldosteronismRenovascular diseaseChronic steroid therapy and Cushing syndromePheochromocytomaCoarctation of the aortaThyroid or parathyroid diseaseThe physical examination should include an appropriate measurement of BP, with verification in the contralateral arm; examination of the optic fundi; body mass index calculated as weight in kilograms divided by the square of height in meters (measurement of waist circumference also may be useful); auscultation for carotid, abdominal, and femoral bruits; palpation of the thyroid gland; thorough examination of the heart and lungs; examination of the abdomen for enlarged kidneys, masses, and abnormal aortic pulsation; palpation of the lower extremities for edema and pulses; and neurological assessment.Laboratory Tests and Other Diagnostic ProceduresRoutine laboratory tests recommended before initiating therapy include an electrocardiogram; urinalysis; blood glucose and hematocrit; serum potassium, creatinine (or the corresponding estimated glomerular filtration rate), and calcium; and a lipid profile (after a 9- to 12-hour fast) that includes high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, and triglycerides. Optional tests include measurement of urinary albumin excretion or albumin/creatinine ratio. More extensive testing for identifiable causes is not indicated generally unless BP control is not achieved.TreatmentGoals of Therapy.The ultimate public health goal of antihypertensive therapy is the reduction of cardiovascular and renal morbidity and mortality. Because most patients with hypertension, especially those aged at least 50 years, will reach the diastolic BP goal once systolic BP is at goal, the primary focus should be on achieving the systolic BP goal (Figure 1). Treating systolic BP and diastolic BP to targets that are less than 140/90 mm Hg is associated with a decrease in CVD complications. In patients with hypertension with diabetes or renal disease, the BP goal is less than 130/80 mm Hg.Figure.Algorithm for Treatment of HypertensionBP indicates blood pressure; ACE, angiotensin-converting enzyme; ARB, angiotensin-receptor blocker; and CCB, calcium channel blocker.Lifestyle Modifications.Adoption of healthy lifestyles by all individuals is critical for the prevention of high BP and an indispensable part of the management of those with hypertension. Major lifestyle modifications shown to lower BP include weight reduction in those individuals who are overweight or obese; adoption of Dietary Approaches to Stop Hypertension eating plan,which is rich in potassium and calcium; dietary sodium reduction; physical activity; and moderation of alcohol consumption (Table 3).Lifestyle modifications decrease BP, enhance antihypertensive drug efficacy, and decrease cardiovascular risk. For example, a 1600-mg sodium Dietary Approaches to Stop Hypertension eating plan has effects similar to single drug therapy.Combinations of 2 or more lifestyle modifications can achieve even better results.Table 3.Lifestyle Modifications to Manage Hypertension*ModificationRecommendationApproximate Systolic BP Reduction, RangeWeight reductionMaintain normal body weight (BMI, 18.5-24.9)5-20 mm Hg/10-kg weight lossAdopt DASH eating planConsume a diet rich in fruits, vegetables, and low-fat dairy products with a reduced content of saturated and total fat8-14 mm HgDietary sodium reductionReduce dietary sodium intake to no more than 100 mEq/L (2.4 g sodium or 6 g sodium chloride)2-8 mm HgPhysical activityEngage in regular aerobic physical activity such as brisk walking (at least 30 minutes per day, most days of the week)4-9 mm HgModeration of alcohol consumptionLimit consumption to no more than 2 drinks per day (1 oz or 30 mL ethanol [eg, 24 oz beer, 10 oz wine, or 3 oz 80-proof whiskey]) in most men and no more than 1 drink per day in women and lighter-weight persons2-4 mm HgAbbreviations: BMI, body mass index calculated as weight in kilograms divided by the square of height in meters; BP, blood pressure; DASH, Dietary Approaches to Stop Hypertension.*For overall cardiovascular risk reduction, stop smoking. The effects of implementing these modifications are dose and time dependent and could be higher for some individuals.Pharmacologic Treatment.Excellent clinical trial outcome data prove that lowering BP with several classes of drugs, including angiotensin-converting enzyme (ACE) inhibitors, angiotensin-receptor blockers (ARBs), β-blockers, calcium channel blockers (CCBs), and thiazide-type diuretics, will all reduce the complications of hypertension.Table 4and Table 5provide a list of commonly used antihypertensive agents.Table 4.Oral Antihypertensive Drugs* Table 4.Oral Antihypertensive Drugs (cont)*ClassDrug (Trade Name)Usual Dose, Range, mg/dDaily FrequencyThiazide diureticsChlorothiazide (Diuril)125-5001Chlorthalidone (generic)12.5-251Hydrochlorothiazide (Microzide, HydroDIURIL)†12.5-501Polythiazide (Renese)2-41Indapamide (Lozol)†1.25-2.51Metolazone (Mykrox)0.5-1.01Metolazone (Zaroxolyn)2.5-51Loop diureticsBumetanide (Bumex)†0.5-22Furosemide (Lasix)†20-802Torsemide (Demadex)†2.5-101Potassium-sparing diureticsAmiloride (Midamor)†5-101-2Triamterene (Dyrenium)50-1001-2Aldosterone-receptor blockersEplerenone (Inspra)50-1001-2Spironolactone (Aldactone)†25-501-2β-BlockersAtenolol (Tenormin)†25-1001Betaxolol (Kerlone)†5-201Bisoprolol (Zebeta)†2.5-101Metoprolol (Lopressor)†50-1001-2Metoprolol extended release (Toprol XL)50-1001Nadolol (Corgard)†40-1201Propranolol (Inderal)†40-1602Propranolol long-acting (Inderal LA)†60-1801Timolol (Blocadren)†20-402β-Blockers with intrinsicAcebutolol (Sectral)†200-8002sympathomimetic activityPenbutolol (Levatol)10-401Pindolol (generic)10-402Combined α- and β-blockersCarvedilol (Coreg)12.5-502Labetalol (Normodyne, Trandate)†200-8002ACE inhibitorsBenazepril (Lotensin)†10-401-2Captopril (Capoten)†25-1002Enalapril (Vasotec)†2.5-401-2Fosinopril (Monopril)10-401Lisinopril (Prinivil, Zestril)†10-401Moexipril (Univasc)7.5-301Perindopril (Aceon)4-81-2Quinapril (Accupril)10-401Ramipril (Altace)2.5-201Trandolapril (Mavik)1-41ClassDrug (Trade Name)Usual Dose, Range, mg/dDaily FrequencyAngiotensin II antagonistsCandesartan (Atacand)8-321Eprosartan (Tevetan)400-8001-2Irbesartan (Avapro)150-3001Losartan (Cozaar)25-1001-2Olmesartan (Benicar)20-401Telmisartan (Micardis)20-801Valsartan (Diovan)80-3201Calcium channel blockers−non-dihydropyridinesDiltiazem extended release (Cardizem CD, Dilacor XR, Tiazac)†180-4201Diltiazem extended release (Cardizem LA)120-5401Verapamil immediate release (Calan, Isoptin)†80-3202Verapamil long-acting (Calan SR, Isoptin SR)†120-3601-2Verapamil-coer (Covera HS, Verelan PM)120-3601Calcium channelAmlodipine (Norvasc)2.5-101blockers−dihydropyridinesFelodipine (Plendil)2.5-201Isradipine (Dynacirc CR)2.5-102Nicardipine sustained release (Cardene SR)60-1202Nifedipine long-acting (Adalat CC, Procardia XL)30-601Nisoldipine (Sular)10-401α1-BlockersDoxazosin (Cardura)1-161Prazosin (Minipress)†2-202-3Terazosin (Hytrin)1-201-2Central α2-agonists and otherClonidine (Catapres)†0.1-0.82centrally acting drugsClonidine patch (Catapres TTS)0.1-0.31 weeklyMethyldopa (Aldomet)†250-10002Reserpine (generic)0.05-0.251‡Guanfacine (generic)0.5-21Direct vasodilatorsHydralazine (Apresoline)†25-1002Minoxidil (Loniten)†2.5-801-2(continued)Table 5.Combination Drugs for HypertensionCombination TypeFixed-Dose Combination, mg*Trade NameACE inhibitors and CCBsAmlodipine/benazepril hydrochloride (2.5/10, 5/10, 5/20, 10/20)LotrelEnalapril maleate/felodipine (5/5)LexxelTrandolapril/verapamil (2/180, 1/240, 2/240, 4/240)TarkaACE inhibitors and diureticsBenazepril/hydrochlorothiazide (5/6.25, 10/12.5, 20/12.5, 20/25)Lotensin HCTCaptopril/hydrochlorothiazide (25/15, 25/25, 50/15, 50/25)CapozideEnalapril maleate/hydrochlorothiazide (5/12.5, 10/25)VasereticLisinopril/hydrochlorothiazide (10/12.5, 20/12.5, 20/25)PrinzideMoexipril HCl/hydrochlorothiazide (7.5/12.5, 15/25)UnireticQuinapril HCl/hydrochlorothiazide (10/12.5, 20/12.5, 20/25)AccureticARBs and diureticsCandesartan cilexetil/hydrochlorothiazide (16/12.5, 32/12.5)Atacand HCTEprosartan mesylate/hydrochlorothiazide (600/12.5, 600/25)Teveten HCTIrbesartan/hydrochlorothiazide (75/12.5, 150/12.5, 300/12.5)AvalideLosartan potassium/hydrochlorothiazide (50/12.5, 100/25)HyzaarTelmisartan/hydrochlorothiazide (40/12.5, 80/12.5)Micardis HCTValsartan/hydrochlorothiazide (80/12.5, 160/12.5)Diovan HCTβ-Blockers and diureticsAtenolol/chlorthalidone (50/25, 100/25)TenoreticBisoprolol fumarate/hydrochlorothiazide (2.5/6.25, 5/6.25, 10/6.25)ZiacPropranolol LA/hydrochlorothiazide (40/25, 80/25)InderideMetoprolol tartrate/hydrochlorothiazide (50/25, 100/25)Lopressor HCTNadolol/bendroflumethiazide (40/5, 80/5)CorzideTimolol maleate/hydrochlorothiazide (10/25)TimolideCentrally acting drug and diureticMethyldopa/hydrochlorothiazide (250/15, 250/25, 500/30, 500/50)AldorilReserpine/chlorothiazide (0.125/250, 0.25/500)DiupresReserpine/hydrochlorothiazide (0.125/25, 0.125/50)HydropresDiuretic and diureticAmiloride HCl/hydrochlorothiazide (5/50)ModureticSpironolactone/hydrochlorothiazide (25/25, 50/50)AldactoneTriamterene/hydrochlorothiazide (37.5/25, 50/25, 75/50)Dyazide, MaxzideAbbreviations: ACE, angiotensin-converting enzyme; ARB, angiotensin-receptor blocker; CCB, calcium channel blocker; HCl, hydrochloride; HCT, hydrochlorothiazide; LA, long-acting.*Some drug combinations are available in multiple fixed doses. Each drug dose is reported in milligrams.Thiazide-type diuretics have been the basis of antihypertensive therapy in most outcome trials.In these trials, including the recently published Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial,diuretics have been virtually unsurpassed in preventing the cardiovascular complications of hypertension. The exception is the Second Australian National Blood Pressure trialthat reported slightly better outcomes in white men with a regimen that began with an ACE inhibitor compared with one starting with a diuretic. Diuretics enhance the antihypertensive efficacy of multidrug regimens, can be useful in achieving BP control, and are more affordable than other antihypertensive agents. Despite these findings, diuretics remain underused.Thiazide-type diuretics should be used as initial therapy for most patients with hypertension, either alone or in combination with 1 of the other classes (ACE inhibitors, ARBs, β-blockers, CCBs) demonstrated to be beneficial in randomized controlled outcome trials. The list of compelling indications requiring the use of other antihypertensive drugs as initial therapy are listed in Table 6. If a drug is not tolerated or is contraindicated, then 1 of the other classes proven to reduce cardiovascular events should be used instead.Table 6.Clinical Trial and Guideline Basis for Compelling Indications for Individual Drug ClassesHigh-Risk Conditions With Compelling Indication*Recommended DrugsClinical Trial Basis†Diureticβ-BlockerACE InhibitorARBCCBAldosterone AntagonistHeart failure•••••ACC/AHA Heart Failure Guideline,MERIT-HF,COPERNICUS,CIBIS,SOLVD,AIRE,TRACE,ValHEFT,RALESPost–myocardial infarction•••ACC/AHA Post-MI Guideline,BHAT,SAVE,Capricorn,EPHESUSHigh coronary disease risk••<•>•ALLHAT,HOPE,ANBP2,LIFE,CONVINCEDiabetes•••••NKF-ADA Guideline,UKPDS,ALLHATChronic kidney disease••NKF Guideline,Captopril Trial,RENAAL,IDNT,REIN,AASKRecurrent stroke prevention••PROGRESSAbbreviations: AASK, African American Study of Kidney Disease and Hypertension; ACC/AHA, American College of Cardiology/American Heart Association; ACE, angiotensin-converting enzyme; AIRE, Acute Infarction Ramipril Efficacy; ALLHAT, Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial; ANBP2, Second Australian National Blood Pressure Study; ARB, angiotensin-receptor blocker; BHAT, β-Blocker Heart Attack Trial; CCB, calcium channel blocker; CIBIS, Cardiac Insufficiency Bisoprolol Study; CONVINCE, Controlled Onset Verapamil Investigation of Cardiovascular End Points; COPERNICUS, Carvedilol Prospective Randomized Cumulative Survival Study; EPHESUS, Eplerenone Post-Acute Myocardial Infarction Heart Failure Efficacy and Survival Study; HOPE, Heart Outcomes Prevention Evaluation Study; IDNT, Inbesartan Diabetic Nephropathy Trial; LIFE, Losartan Intervention For Endpoint Reduction in Hypertension Study; MERIT-HF, Metoprolol CR/XL Randomized Intervention Trial in Congestive Heart Failure; NKF-ADA, National Kidney Foundation–American Diabetes Association; PROGRESS, Perindopril Protection Against Recurrent Stroke Study; RALES, Randomized Aldactone Evaluation Study; REIN, Ramipril Efficacy in Nephropathy Study; RENAAL, Reduction of Endpoints in Non–Insulin-Dependent Diabetes Mellitus with the Angiotensin II Antagonist Losartan Study; SAVE, Survival and Ventricular Enlargement Study; SOLVD, Studies of Left Ventricular Dysfunction; TRACE, Trandolapril Cardiac Evaluation Study; UKPDS, United Kingdom Prospective Diabetes Study; ValHEFT, Valsartan Heart Failure Trial.*Compelling indications for antihypertensive drugs are based on benefits from outcome studies or existing clinical guidelines; the compelling indication is managed in parallel with the blood pressure.†Conditions for which clinical trials demonstrate benefit of specific classes of antihypertensive drugs.Achieving BP Control in Individual Patients.Most patients with hypertension will require 2 or more antihypertensive medications to achieve their BP goals.Addition of a second drug from a different class should be initiated when use of a single drug in adequate doses fails to achieve the BP goal. When BP is more than 20/10 mm Hg above goal, consideration should be given to initiating therapy with 2 drugs, either as separate prescriptions or in fixed-dose combinations (Figure 1). The initiation of drug therapy with more than 1 agent may increase the likelihood of achieving the BP goal in a more timely fashion, but particular caution is advised in those at risk for orthostatic hypotension, such as patients with diabetes, autonomic dysfunction, and some older persons. Use of generic drugs or combination drugs should be considered to reduce prescription costs.Follow-up and Monitoring.Once antihypertensive drug therapy is initiated, most patients should return for follow-up and adjustment of medications at approximately monthly intervals until the BP goal is reached. More frequent visits will be necessary for patients with stage 2 hypertension or with complicating comorbid conditions. Serum potassium and creatinine should be monitored at least 1 to 2 times per year.After BP is at goal and stable, follow-up visits can usually be at 3- to 6-month intervals. Comorbidities, such as HF, associated diseases, such as diabetes, and the need for laboratory tests influence the frequency of visits. Other cardiovascular risk factors should be treated to their respective goals, and tobacco avoidance should be promoted vigorously. Low-dose aspirin therapy should be considered only when BP is controlled, because the risk of hemorrhagic stroke is increased in patients with uncontrolled hypertension.Special ConsiderationsThe patient with hypertension and certain comorbidities requires special attention and follow-up by the clinician.Compelling Indications.Table 6describes compelling indications that require certain antihypertensive drug classes for high-risk conditions. The drug selections for these compelling indications are based on favorable outcome data from clinical trials. Combination of agents may be required. Other management considerations include medications already in use, tolerability, and desired BP targets. In many cases, specialist consultation may be indicated.Ischemic Heart Disease.Ischemic heart disease is the most common form of target-organ damage associated with hypertension. In patients with hypertension and stable angina pectoris, the first drug of choice is usually a β-blocker; alternatively, long-acting CCBs can be used.In patients with acute coronary syndromes (unstable angina or myocardial infarction), hypertension should be treated initially with β-blockers and ACE inhibitors,with addition of other drugs as needed for BP control. In patients with postmyocardial infarction, ACE inhibitors, β-blockers, and aldosterone antagonists have proven to be most beneficial.Intensive lipid management and aspirin therapy are also indicated.Heart Failure.Heart failure, in the form of systolic or diastolic ventricular dysfunction, results primarily from systolic hypertension and ischemic heart disease. Fastidious BP and cholesterol control are the primary preventive measures for those at high risk for HF.In asymptomatic individuals with demonstrable ventricular dysfunction, ACE inhibitors and β-blockers are recommended.For those with symptomatic ventricular dysfunction or end-stage heart disease, ACE inhibitors, β-blockers, ARBs, and aldosterone blockers are recommended along with loop diuretics.Diabetic Hypertension.Combinations of 2 or more drugs are usually needed to achieve the target BP goal of less than 130/80 mm Hg.Thiazide diuretics, β-blockers, ACE inhibitors, ARBs, and CCBs are beneficial in reducing CVD and stroke incidence in patients with diabetes.The ACE inhibitor– or ARB-based treatments favorably affect the progression of diabetic nephropathy and reduce albuminuria,and ARBs have been shown to reduce progression to macroalbuminuria.Chronic Kidney Disease.In patients with chronic kidney disease, defined by either (1) reduced excretory function with an estimated glomerular filtration rate of less than 60 mL/min per 1.73 m2(corresponding approximately to a creatinine of >1.5 mg/dL [>132.6 µmol/L] in men or >1.3 mg/dL [>114.9 µmol/L] in women)or (2) the presence of albuminuria (>300 mg/d or 200 mg albumin per gram of creatinine), therapeutic goals are to slow deterioration of renal function and prevent CVD. Hypertension appears in the majority of these patients and they should receive aggressive BP management, often with 3 or more drugs to reach target BP values of less than 130/80 mm Hg.The ACE inhibitors and ARBs have demonstrated favorable effects on the progression of diabetic and nondiabetic renal disease.A limited increase in serum creatinine of as much as 35% above baseline with ACE inhibitors or ARBs is acceptable and not a reason to withhold treatment unless hyperkalemia develops.With advanced renal disease (estimated glomerular filtration rate <30 mL/min per 1.73 m2, corresponding to a serum creatinine of 2.5-3.0 mg/dL [221-265 µmol/L]), increasing doses of loop diuretics are usually needed in combination with other drug classes.Cerebrovascular Disease.The risks and benefits of acute lowering of BP during an acute stroke are still unclear; control of BP at intermediate levels (approximately 160/100 mm Hg) is appropriate until the condition has stabilized or improved. Recurrent stroke rates are lowered by the combination of an ACE inhibitor and thiazide-type diuretic.Other Special Situations. Minority Populations.Blood pressure control rates vary in minority populations and are lowest in Mexican Americans and Native Americans.In general, the treatment of hypertension is similar for all demographic groups, but socioeconomic factors and lifestyle may be important barriers to BP control in some minority patients. The prevalence, severity, and impact of hypertension are increased in blacks, who also demonstrate somewhat reduced BP responses to monotherapy with β-blockers, ACE inhibitors, or ARBs compared with diuretics or CCBs. These differential responses are largely eliminated by drug combinations that include adequate doses of a diuretic. Angiotensin-converting enzyme inhibitor–induced angioedema occurs 2 to 4 times more frequently in black patients with hypertension than in other groups.Obesity and the Metabolic Syndrome.Obesity (body mass index ≥30) is an increasingly prevalent risk factor for the development of hypertension and CVD. The Adult Treatment Panel III guideline for cholesterol management defines the metabolic syndrome as the presence of 3 or more of the following conditions: abdominal obesity (waist circumference >102 cm [>40 in] in men or >89 cm [>35 in] in women), glucose intolerance (fasting glucose ≥110 mg/dL [≥6.1 mmol/L]), BP of at least 130/85 mm Hg, high triglycerides (≥150 mg/dL [≥1.70 mmol/L]), or low high-density lipoprotein cholesterol (<40 mg/dL [<1.04 mmol/L] in men or <50 mg/dL [<1.30 mmol/L] in women).Intensive lifestyle modification should be pursued in all individuals with the metabolic syndrome, and appropriate drug therapy should be instituted for each of its components as indicated.Left Ventricular Hypertrophy.Left ventricular hypertrophy is an independent risk factor that increases the risk of subsequent CVD. Regression of left ventricular hypertrophy occurs with aggressive BP management, including weight loss, sodium restriction, and treatment with all classes of antihypertensive agents except the direct vasodilators, hydralazine and minoxidil.Peripheral Arterial Disease.Peripheral arterial disease is equivalent in risk to ischemic heart disease. Any class of antihypertensive drugs can be used in most patients with peripheral arterial disease. Other risk factors should be managed aggressively and aspirin should be used.Hypertension in Older Individuals.Hypertension occurs in more than two thirds of individuals after age 65 years.This is also the population with the lowest rates of BP control.Treatment recommendations for older individuals with hypertension, including those who have isolated systolic hypertension, should follow the same principles outlined for the general care of hypertension. In many individuals, lower initial drug doses may be indicated to avoid symptoms; however, standard doses and multiple drugs are needed in the majority of older individuals to reach appropriate BP targets.Postural Hypotension.A decrease in standing systolic BP of more than 10 mm Hg, when associated with dizziness or fainting, is more frequent in older patients with systolic hypertension, diabetes, and those taking diuretics, venodilators (eg, nitrates, α-blockers, and sildenafil-like drugs), and some psychotropic drugs. Blood pressure in these individuals should also be monitored in the upright position. Caution should be used to avoid volume depletion and excessively rapid dose titration of antihypertensive drugs.Dementia.Dementia and cognitive impairment occur more commonly in patients with hypertension. Reduced progression of cognitive impairment may occur with effective antihypertensive therapy.Hypertension in Women.Oral contraceptives may increase BP and the risk of hypertension increases with duration of use. Women taking oral contraceptives should have their BP checked regularly. Development of hypertension is a reason to consider other forms of contraception. In contrast, hormone replacement therapy does not raise BP.Women with hypertension who become pregnant should be followed carefully because of increased risks to mother and fetus. Methyldopa, β-blockers, and vasodilators are preferred medications for the safety of the fetus.Angiotensin-converting enzyme inhibitors and ARBs should not be used during pregnancy because of the potential for fetal defects and should be avoided in women who are likely to become pregnant. Preeclampsia, which occurs after the 20th gestation week of pregnancy, is characterized by new-onset or worsening hypertension, albuminuria, and hyperuricemia, sometimes with coagulation abnormalities. In some patients, preeclampsia may develop into a hypertensive urgency or emergency and may require hospitalization, intensive monitoring, early fetal delivery, and parenteral antihypertensive and anticonvulsant therapy.Children and Adolescents.In children and adolescents, hypertension is defined as BP that is, on repeated measurement, at the 95th percentile or greater adjusted for age, height, and sex.The fifth Korotkoff sound is used to define diastolic BP. Clinicians should be alert to the possibility of identifiable causes of hypertension in younger children (ie, kidney disease, coarctation of the aorta). Lifestyle interventions are strongly recommended, with pharmacologic therapy instituted for higher levels of BP, or if there is insufficient response to lifestyle modifications.Choices of antihypertensive drugs are similar in children and adults, but effective doses for children are often smaller and should be adjusted carefully. Angiotensin-converting enzyme inhibitors and ARBs should not be used in pregnant or sexually active girls. Uncomplicated hypertension should not be a reason to restrict children from participating in physical activities, particularly because long-term exercise may lower BP. Use of anabolic steroids should be strongly discouraged. Vigorous interventions also should be conducted for other existing modifiable risk factors (eg, smoking).Hypertensive Urgencies and Emergencies.Patients with marked BP elevations and acute target-organ damage (eg, encephalopathy, myocardial infarction, unstable angina, pulmonary edema, eclampsia, stroke, head trauma, life-threatening arterial bleeding, or aortic dissection) require hospitalization and parenteral drug therapy.Patients with markedly elevated BP but without acute target-organ damage usually do not require hospitalization, but they should receive immediate combination oral antihypertensive therapy. They should be carefully evaluated and monitored for hypertension-induced heart and kidney damage and for identifiable causes of hypertension (Box 2).Additional Considerations in Antihypertensive Drug Choices.Antihypertensive drugs can have favorable or unfavorable effects on other comorbidities.Potential Favorable Effects.Thiazide-type diuretics are useful in slowing demineralization in osteoporosis. β-Blockers can be useful in the treatment of atrial tachyarrhythmias/fibrillation, migraine, thyrotoxicosis (short-term), essential tremor, or perioperative hypertension. Calcium channel blockers may be useful in Raynaud syndrome and certain arrhythmias, and α-blockers may be useful in prostatism.Potential Unfavorable Effects.Thiazide diuretics should be used cautiously in patients who have gout or who have a history of significant hyponatremia. β-Blockers should generally be avoided in individuals who have asthma, reactive airways disease, or second- or third-degree heart block. Angiotensin-converting enzyme inhibitors and ARBs should not be given to women likely to become pregnant and are contraindicated in those who are; ACE inhibitors should not be used in individuals with a history of angioedema. Aldosterone antagonists and potassium-sparing diuretics can cause hyperkalemia and should generally be avoided in patients who have serum potassium values of more than 5.0 mEq/L while not taking medications.Improving Hypertension ControlAdherence to Regimens.Behavioral models suggest that the most effective therapy prescribed by the most careful clinician will control hypertension only if the patient is motivated to take the prescribed medication and to establish and maintain a health-promoting lifestyle. Motivation improves when patients have positive experiences with and trust in their clinicians. Empathy builds trust and is a potent motivator.Patient attitudes are greatly influenced by cultural differences, beliefs, and previous experiences with the health care system.These attitudes must be understood if the clinician is to build trust and increase communication with patients and families.Failure to titrate or combine medications, despite knowing the patient is not at goal BP, represents clinical inertia and must be overcome.Decision support systems (ie, electronic and paper), flow sheets, feedback reminders, and involvement of nurse clinicians and pharmacists can be helpful.The patient and clinician must agree on BP goals. A patient-centered strategy to achieve the goal and an estimation of the time needed to reach the goal are important.When BP is above goal, alterations in the plan should be documented. Blood pressure self-monitoring can also be useful. Patients' nonadherence to therapy is increased by misunderstanding of the condition or treatment, denial of illness because of lack of symptoms or perception of drugs as symbols of ill health, lack of patient involvement in the care plan, or unexpected adverse effects of medications. The patient should be made to feel comfortable in telling the clinician all concerns and fears of unexpected or disturbing drug reactions.The cost of medications and the complexity of care (ie, transportation, patient difficulty with polypharmacy, difficulty in scheduling appointments, and life's competing demands) are additional barriers that must be overcome to achieve goal BP. All members of the health care team (eg, physicians, nurse case managers, other nurses, physician assistants, pharmacists, dentists, registered dietitians, optometrists, and podiatrists) must work together to influence and reinforce instructions to improve patients' lifestyles and BP control.Resistant Hypertension.Resistant hypertension is the failure to reach goal BP in patients who are adhering to full doses of an appropriate 3-drug regimen that includes a diuretic. After excluding potential identifiable hypertension (Box 2), clinicians should carefully explore reasons why the patient is not at goal BP (Box 3). Particular attention should be paid to diuretic type and dose in relation to renal function (see "Chronic Kidney Disease" section). Consultation with a hypertension specialist should be considered if goal BP cannot be achieved.Box 3. Causes of Resistant HypertensionImproper blood pressure measurementVolume overload and pseudotoleranceExcess sodium intakeVolume retention from kidney diseaseInadequate diuretic therapyDrug-induced or other causesNonadherenceInadequate dosesInappropriate combinationsNonsteroidal anti-inflammatory drugs; cyclooxygenase 2 inhibitorsCocaine, amphetamines, other illicit drugsSympathomimetics (decongestants, anorectics)Oral contraceptivesAdrenal steroidsCyclosporine and tacrolimusErythropoietinLicorice (including some chewing tobacco)Selected over-the-counter dietary supplements and medicines (eg, ephedra, ma haung, bitter orange)Associated conditionsObesityExcess alcohol intakeIdentifiable causes of hypertension (see Box 2)Public Health Challenges and Community ProgramsPublic health approaches, such as reducing calories, saturated fat, and salt in processed foods and increasing community and school opportunities for physical activity, can achieve a downward shift in the distribution of a population's BP, thus potentially reducing morbidity, mortality, and the lifetime risk of an individual becoming hypertensive. This becomes especially critical as the body mass index of individuals in the United States has increased to epidemic levels. Currently, 122 million adults are overweight or obese, which contributes to the rise in BP and related conditions.The JNC 7 endorses the American Public Health Association resolution that the food manufacturers and restaurants reduce sodium in the food supply by 50% during the next decade. When public health intervention strategies address the diversity of racial, ethnic, cultural, linguistic, religious, and social factors in the delivery of their services, the likelihood of their acceptance by the community increases. These public health approaches can provide an attractive opportunity to interrupt and prevent the continuing costly cycle of managing hypertension and its complications.Scheme Used for Classification of the EvidenceMMeta-analysis; use of statistical methods to combine the results from clinical trialsRaRandomized controlled trials; also known as experimental studiesReRetrospective analyses; also known as case-control studiesFProspective study; also known as cohort studies, including historical or prospective follow-up studiesXCross-sectional survey; also known as prevalence studiesPrPrevious review or position statementsCClinical interventions (nonrandomized)These symbols are appended to the citations in the reference list. The studies that provided evidence supporting the recommendations of this report were classified and reviewed by the staff and the executive committee. 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Roccella, PhD, MPH, National Heart, Lung, and Blood Institute, National Institutes of Health, 31 Center Dr, MSC 2480, Bethesda, MD 20892 (e-mail: email@example.com).Additional Authors/National High Blood Pressure Education Program Coordinating Committee Participants:Claude Lenfant, MD, chair(National Heart, Lung, and Blood Institute, Bethesda, Md); George L. Bakris, MD, Henry R. Black, MD (Rush Presbyterian-St Luke's Medical Center, Chicago, Ill); Barry L. Carter, PharmD (University of Iowa, Iowa City); Jerome D. Cohen, MD (St Louis University School of Medicine, St Louis, Mo); Pamela J. Colman, DPM (American Podiatric Medical Association, Bethesda, Md); William C. Cushman, MD (Veterans Affairs Medical Center, Memphis, Tenn); Mark J. Cziraky, PharmD (Health Core, Inc, Newark, Del); John J. Davis, PA-C (American Academy of Physician Assistants, Memphis, Tenn); Keith Copelin Ferdinand, MD (Heartbeats Life Center, New Orleans, La); Ray W. Gifford, Jr, MD (Cleveland Clinic Foundation, Fountain Hills, Ariz); Michael Glick, DMD (UMDNJ, New Jersey Dental School, Newark); Lee A. Green, MD, MPH (University of Michigan, Ann Arbor); Stephen Havas, MD, MPH, MS (University of Maryland School of Medicine, Baltimore); Thomas H. Hostetter, MD (National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Md); Joseph L. Izzo, Jr, MD (State University of New York at Buffalo School of Medicine, Buffalo); Daniel W. Jones, MD (University of Mississippi Medical Center, Jackson); Lynn Kirby, RN, NP, COHNS (Sanofi-Synthelabo Research, Malvern, Pa); Kathryn M. Kolasa, PhD, RD, LDN (Brody School of Medicine at East Carolina University, Greenville, NC); Stuart Linas, MD (University of Colorado Health Sciences Center, Denver); William M. Manger, MD, PhD (New York University Medical Center, New York); Edwin C. Marshall, OD, MS, MPH (Indiana University School of Optometry, Bloomington); Barry J. Materson, MD, MBA (University of Miami, Miami, Fla); Jay Merchant, MHA (Centers for Medicare and Medicaid Services, Washington, DC); Nancy Houston Miller, RN, BSN (Stanford University School of Medicine, Palo Alto, Calif); Marvin Moser, MD (Yale University School of Medicine, Scarsdale, NY); William A. Nickey, DO (Philadelphia College of Osteopathic Medicine, Philadelphia, Pa); Suzanne Oparil, MD (University of Alabama at Birmingham); Otelio S. Randall, MD (Howard University Hospital, Washington, DC); James W. Reed, MD (Morehouse School of Medicine, Atlanta, Ga); Edward J. Roccella, PhD, MPH (National Heart, Lung, and Blood Institute, Bethesda, Md); Lee Shaughnessy (National Stroke Association, Englewood, Colo); Sheldon G. Sheps, MD (Mayo Clinic, Rochester, Minn); David B. Snyder, RPh, DDS (Health Resources and Services Administration, Rockville, Md); James R. Sowers, MD (SUNY Health Science Center at Brooklyn, Brooklyn, NY); Leonard M. Steiner, MS, OD (Eye Group, Oakhurst, NJ); Ronald Stout, MD, MPH (Procter and Gamble, Mason, Ohio); Rita D. Strickland, EdD, RN (New York Institute of Technology, Springfield Gardens, NY); Carlos Vallbona, MD (Baylor College of Medicine, Houston, Tex); Howard S. Weiss, MD, MPH (Georgetown University Medical Center, Washington Hospital Center, Walter Reed Army Medical Center, Washington, DC); Jack P. Whisnant, MD (Mayo Clinic and Mayo Medical School, Rochester, Minn); Gerald J. Wilson, MA, MBA (Citizens for Public Action on High Blood Pressure and Cholesterol, Inc, Potomac, Md); Mary Winston, EdD, RD (American Heart Association, Dallas, Tex); Jackson T. Wright, Jr, MD, PhD (Case Western Reserve University, Cleveland, Ohio); Staff: Joanne Karimbakas, MS, RD (American Institutes for Research Health Program, Silver Spring, Md).Financial Disclosures:The following authors have received honoraria for serving as a speaker: Dr Chobanian (Monarch, Wyeth, Astra-Zeneca, Solvay, Bristol-Myers Squibb); Dr Bakris (Astra-Zeneca, Abbott, Alteon, Biovail, Boerhinger-Ingelheim, Bristol-Myers Squibb, Forest, GlaxoSmithKline, Merck, Novartis, Sanofi, Sankyo, Solvay); Dr Black (Astra-Zeneca, Bristol-Myers Squibb, Novartis, Pfizer, Pharmacia, Wyeth-Ayerst); Dr Izzo (Boehringer-Ingelheim, Merck, Pfizer, Astra-Zeneca, Solvay, Novartis, Forest, Sankyo); Dr Sowers (Med Com Vascular Biology Working Group, Joslin Clinic Foundation); Dr Wright (Astra, Aventis, Bayer, Bristol-Myers Squibb, Forest, Merck, Norvartis, Pfizer, Phoenix Pharmaceuticals, GlaxoSmithKline, Solvay/Unimed).The following authors have received funding/grant support for research projects: Dr Bakris (National Institutes of Health, Astra-Zeneca, Abbott, Alteon, Boerhinger-Ingelheim, Forest, GlaxoSmithKline, Merck, Novartis, Sankyo, Solvay); Dr Black (Bristol-Myers Squibb, Boehringer-Ingelheim, Merck, Pfizer, Pharmacia); Dr Cushman (Astra-Zeneca, Merck, Pfizer, Kos, Aventis Pharma, King Pharmaceuticals, GlaxoSmithKline, Boehringer-Ingelheim); Dr Izzo (Boehringer-Ingelheim, Merck, Astra-Zeneca, Novartis, GlaxoSmithKline, Biovail); Dr Oparil (Abbott Laboratories, Astra-Zeneca, Aventis, Boehringer-Ingelheim, Bristol-Myers Squibb, Eli Lilly, Forest, GlaxoSmithKline, Monarch, Novartis [Ciba], Merck, Pfizer, Sanofi/BioClin, Schering Plough, Schwarz Pharma, Scios Inc, GD Searle, Wyeth-Ayerst, Sankyo, Solvay, Texas Biotechnology Corporation); Dr Sowers (Novartis, Astra-Zeneca); Dr Wright (Astra, Aventis, Bayer, Biovail, Bristol-Myers Squibb, Forest, Merck, Norvartis, Pfizer, Phoenix Pharmaceuticals, GlaxoSmithKline, Solvay/Unimed).The following authors have served as a consultant/advisor: Dr Bakris (Astra-Zeneca, Abbott, Alteon, Biovail, Boerhinger-Ingelheim, Bristol-Myers Squibb, Forest, GlaxoSmithKline, Merck, Novartis, Sanofi, Sankyo, Solvay); Dr Black (Abbott, Astra-Zeneca, Biovail, Bristol-Myers Squibb, GlaxoSmithKline, Merck, Pfizer, Pharmacia); Dr Carter (Bristol-Myers Squibb); Dr Cushman (Bristol-Myers Squibb, Sanofi, GlaxoSmithKline, Novartis, Pfizer, Solvay, Pharmacia, Takeda, Sankyo, Forest, Biovail); Dr Izzo (Merck, Astra-Zeneca, Novartis, Intercure, Sankyo, Nexcura); Dr Jones (Pfizer, Bristol-Myers Squibb, Merck, Forest, Novartis); Dr Manger (NHBPEP Coordinating Committee); Dr Materson (Unimed, Merck, GlaxoSmithKline, Novartis, Reliant, Tanabe, Bristol-Myers Squibb, Pfizer, Pharmacia, Noven, Boehringer-Ingelheim, Solvay); Dr Oparil (Bristol-Myers Squibb, Merck, Pfizer, Sanofi, Novartis, The Salt Institute, Wyeth-Ayerst).The following author has stock holdings: Dr Izzo (Intercure, Nexcura).Dr Oparil is also on the Board of Directors for the Texas Biotechnology Corporation.The NHBPEP Coordinating Committee Thanks the Following Reviewers:William B. Applegate, MD, MPH (Wake Forest University School of Medicine, Winston Salem, NC); Jan N. Basile, MD (Veterans Administration Hospital, Charleston, SC); Robert Carey, MD (University of Virginia Health System, Charlottesville, Va); Victor Dzau, MD (Brigham and Women's Hospital, Boston, Mass); Brent M. Egan, MD (Medical University of South Carolina, Charleston, SC); Bonita Falkner, MD (Jefferson Medical College, Philadelphia, Pa); John M. Flack, MD, MPH (Wayne State University School of Medicine, Detroit, Mich); Edward D. Frohlich, MD (Ochsner Clinic Foundation, New Orleans, La); Haralambos Gavras, MD (Boston University School of Medicine, Boston, Mass); Martin Grais, MD (Feinberg School of Medicine, Northwestern University, Chicago, Ill); Willa A. Hsueh, MD (David Geffen School of Medicine, University of California at Los Angeles); Kenneth A. Jamerson, MD (University of Michigan Medical Center, Ann Arbor); Norman M. Kaplan, MD (University of Texas Southwestern Medical Center, Dallas); Theodore A. Kotchen, MD (Medical College of Wisconsin, Milwaukee); Daniel Levy, MD (National Heart, Lung, and Blood Institute, Framingham, Mass); Michael A. Moore, MD (Wake Forest University School of Medicine and Dan River Region Cardiovascular Health Initiative Program, Danville, Va); Thomas J. Moore, MD (Boston University Medical Center, Boston, Mass); Vasilios Papademetriou, MD (Veterans Administration Medical Center, Washington, DC); Carl J. Pepine, MD (University of Florida, College of Medicine, Gainesville, Fla); Robert A. Phillips, MD, PhD (New York University, Lenox Hill Hospital, New York); Thomas G. Pickering, MD, DPhil (Mount Sinai Medical Center, New York, NY); L. Michael Prisant, MD (Medical College of Georgia, Augusta); C. Venkata S. Ram, MD (University of Texas Southwestern Medical Center and Texas Blood Pressure Institute, Dallas); Elijah Saunders, MD (University of Maryland School of Medicine, Baltimore); Stephen C. Textor, MD (Mayo Clinic, Rochester, Minn); Donald G. Vidt, MD (Cleveland Clinic Foundation, Cleveland, Ohio); Myron H. Weinberger, MD (Indiana University School of Medicine, Indianapolis); Paul K. Whelton, MD, MSc (Tulane University Health Sciences Center, New Orleans, La).Funding/Support:This work was supported entirely by the National Heart, Lung, and Blood Institute. The executive committee, writing teams, and reviewers served as volunteers without remuneration.The NHBPEP Coordinating Committee Includes Representatives From the Following Member Organizations:American Academy of Family Physicians; American Academy of Neurology; American Academy of Ophthalmology; American Academy of Physician Assistants; American Association of Occupational Health Nurses; American College of Cardiology; American College of Chest Physicians; American College of Occupational and Environmental Medicine; American College of Physicians-American Society of Internal Medicine; American College of Preventive Medicine; American Dental Association; American Diabetes Association; American Dietetic Association; American Heart Association; American Hospital Association; American Medical Association; American Nurses Association; American Optometric Association; American Osteopathic Association; American Pharmaceutical Association; American Podiatric Medical Association; American Public Health Association; American Red Cross; American Society of Health-System Pharmacists; American Society of Hypertension; American Society of Nephrology; Association of Black Cardiologists; Citizens for Public Action on High Blood Pressure and Cholesterol, Inc; Hypertension Education Foundation, Inc; International Society on Hypertension in Blacks; National Black Nurses Association, Inc; National Hypertension Association, Inc; National Kidney Foundation, Inc; National Medical Association; National Optometric Association; National Stroke Association; NHLBI Ad Hoc Committee on Minority Populations; Society for Nutrition Education; The Society of Geriatric Cardiology. Federal Agencies:Agency for Healthcare Research and Quality; Centers for Medicare and Medicaid Services; Department of Veterans Affairs; Health Resources and Services Administration; National Center for Health Statistics; National Heart, Lung, and Blood Institute; National Institute of Diabetes and Digestive and Kidney Diseases.Acknowledgment:We appreciate the assistance of Carol Creech, MILS, and Gabrielle Gessner, BS, from American Institutes for Research Health Program, Silver Spring, Md.
JAMA – American Medical Association
Published: May 21, 2003