从临床试验到JNC7-课件.ppt
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1、10095908085Achieved DBP(mm Hg)Optimal DBP reductionHansson L et al.Lancet.1998;351:1755-1762Percentriskreduction in major CV events*Fatal and nonfatal MI,stroke,all other CV deaths.170160150130140Achieved SBP(mm Hg)Hansson L et al.Lancet.1998;351:1755-1762*Fatal and nonfatal MI,stroke,all other CV d
2、eaths.Percentriskreductionin majorCV events*Optimal SBP reductionHansson et al.,Lancet 1998:351:1755Hansson et al.,Lancet 1998:351:1755AASK Study Group,JAMA.2002;288:2421-2431Follow-up BP by Drug GroupFollow-up BP by Drug Group(Mean(Mean Summaries include visits after three months and exclude GFR vi
3、sits*Significant difference between amlodipine and metoprolol groups(p 0.05)AASK Study Group,JAMA.2002;288:2421-2431Main Clinical Composite OutcomeMain Clinical Composite OutcomeDeclining GFR Event,ESRD,or DeathDeclining GFR Event,ESRD,or Death%wi th EventsMetoprolol vs.Amlodipine:RR=20%,p=0.17 Rami
4、pril vs.Amlodipine:RR=38%,p=0.004 MetoprololRamiprilAmlodipine0510152025303540Follow-up Month06121824303642485460Ramipril vs.MetoprololRR=22%,p=0.042RR=Risk Reduction,Adjusting for Baseline CovariatesAASK Study Group,JAMA.2002;288:2421-2431Hard Clinical Endpoint Composite Hard Clinical Endpoint Comp
5、osite Of ESRD or DeathOf ESRD or Death Follow-up MonthMetoprolol vs.Amlodipine:RR=42%,p=0.003 Ramipril vs.Amlodipine:RR=49%,p 300 mg/24 hrs%of Patients Reached Urine Protein 300 mg/24 hrsDuring Follow-up by Drug GroupDuring Follow-up by Drug GroupRamipril vs.Metoprolol:p=0.014Amlodipine vs.Metoprolo
6、l:p=0.009Ramipril vs.Amlodipine:p0.001%wi th Events0102030405060Follow-up Month06121824303642485460Analysis of patients with UP/Cr 0.22 at baselineMetoprololRamiprilAmlodipineAASK Study Group,JAMA.2002;288:2421-2431%Controlled 140/90 mm HgRelative Risk(95%CI)AmlodipineLisinoprilFavors LisinoprilU.S.
7、Department of Health and Human ServicesNational Institutes of HealthNational Heart,Lung,and Blood InstituteThe Seventh Report of the Joint National Committee onPrevention,Detection,Evaluation,and Treatment of High Blood Pressure(JNC 7)For persons over age 50,SBP is a more important than DBP as CVD r
8、isk factor.Starting at 115/75 mmHg,CVD risk doubles with each increment of 20/10 mmHg throughout the BP range.Persons who are normotensive at age 55 have a 90%lifetime risk for developing HTN.Those with SBP 120139 mmHg or DBP 8089 mmHg should be considered prehypertensive who require health-promotin
9、g lifestyle modifications to prevent CVD.New Features and Key MessagesRisk of hypertension(%)Residual risk of developing hypertension among people with blood pressure 20/10 mmHg above goal,initiate therapy with two agents,one usually should be a thiazide-type diuretic.The most effective therapy pres
10、cribed by the careful clinician will control HTN 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.The responsible physicians judgment remains paramount.Classification of BP CVD Ri
11、sk Benefits of Lowering BP BP Control Rates BP Measurement Techniques In-office Ambulatory BP Monitoring Self-measurement Patient Evaluation Laboratory Tests and Other Diagnostic ProceduresSystolicDiastolicNormal129139 120-130-80-8485-89High NormalOptimal135/85 mmHg and during sleep 120/75 mmHg.BP d
12、rops by 10 to 20%during the night;if not,signals possible increased risk for cardiovascular events.Staessen et al.,JAMA 1997;278:1065Verdecchia P et al.Hypertension 24:793-801,1994 N=1187,mean age 4515 yearsNml.Daytime BP=136/87 for men 135/85 mmHg is generally considered to be hypertensive.Home mea
13、surement devices should be checked regularly.Evaluation of patients with documented HTN has three objectives:1.Assess lifestyle and identify other CV risk factors or concomitant disorders that affect prognosis and guide treatment.2.Reveal identifiable causes of high BP.3.Assess the presence or absen
14、ce of target organ damage and CVD.*Start with H&P:complete but CV-focused(fundi,pulses,bruits,etc)Sleep apnea Drug-induced or related causes Chronic kidney disease Primary aldosteronism Renovascular disease Chronic steroid therapy and Cushings syndrome Pheochromocytoma Coarctation of the aorta Thyro
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