1 The JNC 7 recommendations for initial or combination drug therapy are based on sound scientific evidence.

Slides:



Advertisements
Similar presentations
The Seventh Report of the Joint National Committee on the Prevention, Detection, Evaluation, and Treatment of High Blood Pressure Internal Medicine/Pediatrics.
Advertisements

JNC 8 Guidelines….
11/2/ Implications of ASCOT Results for ALLHAT Conclusions ALLHAT.
1 SECOND AUSTRALIAN NATIONAL BLOOD PRESSURE STUDY (ANBP-2) Enalapril/ACEI vs. HCTZ, n = 6,083 Randomized, open-label (blinded endpoint review) All CV events.
BLOOD PRESSURE LOWERING. UKPDS design Aim To determine whether intensified blood glucose control, with either sulphonylurea or insulin, reduces the risk.
Valsartan Antihypertensive Long-Term Use Evaluation Results
ASCOT TRIAL Abbas Zaidi 20/09/05. Hypertension is one of the most prevalent risk factors for cardiovascular disease, affecting as many as 800 million.
Benefits of intensive multiple risk factor intervention.
Hypertension Diagnosis and Treatment  Based on JNC 7 – published in 2003  Goal: BP
Canadian Diabetes Association Clinical Practice Guidelines Treatment of Hypertension Chapter 25 Richard E. Gilbert, Doreen Rabi, Pierre LaRochelle, Lawrence.
Hypertension and The Older Patient
Hypertension in the Elderly
WHEN SHOULD ONE INITIATE SUCCESSIVE ANTIHYPERTENSIVE DRUGS? Henry R. Black M.D. RUSH University Medical Center Chicago, IL June 15, 2005.
CHARM-Preserved: Candesartan in Heart failure: Assessment of Reduction in Mortality and morbidity - Preserved Purpose To determine whether the angiotensin.
Results of Monotherapy in ALLHAT: On-treatment Analyses ALLHAT Outcomes for participants who received no step-up drugs.
Improving the Care of the Hypertensive Patient: US Perspective William Cushman, MD Professor, Preventive Medicine and Medicine University of Tennessee.
1 Presenter Disclosure Information FINANCIAL DISCLOSURE: DSMB’s: Merck, Takeda Barry R. Davis, MD, PhD Clinical Outcomes in Participants with Dysmetabolic.
6 / 5 / RENAL DISEASE OUTCOMES IN HYPERTENSIVE PATIENTS STRATIFIED INTO 3 GROUPS BY BASELINE GLOMERULAR FILTRATION RATE (GFR) ALLHAT.
The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial ALLHAT study overview Double-blind, randomized trial to determine whether.
Randomized, double-blind, multicenter, controlled trial.
Blood Pressure Control By Randomized Drug Group In ALLHAT William C. Cushman, Charles E. Ford, Paula T. Einhorn, Jackson T. Wright, Jr., Richard A. Preston,
DR. IDOWU AKOLADE EDM DIVISION LUTH
ACUTE STROKE — Hypertension is a common problem in patients with both type 1 and type 2 diabetes but the time course in relation to the duration.
Success and Predictors of Blood Pressure Control in Diverse North American Settings: The Antihypertensive and Lipid- lowering Treatment to Prevent Heart.
Daily Dilemmas in Hypertension Management. Objectives Review the impact of hypertension on society Review the impact of hypertension on society Review.
Is It the Achieved Blood Pressure or Specific Medications that Make a Difference in Outcome, or Is the Question Moot? William C. Cushman, MD Professor,
Hypertension In elderly population. JNC VII BP Classification SBP mmHgDBP mmHg Normal
Systolic hypertension not an isolated problem Michael Weber, MD Professor of Medicine Associate Dean Downstate College of Medicine State University of.
1 ATRIAL FIBRILLATION AT BASELINE AND DURING FOLLOW-UP in The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial November 9, 2003.
1 U.S. Department of Health and Human Services National Institutes of Health National Heart, Lung, and Blood Institute Major Outcomes in High Risk Hypertensive.
1 Role of Diuretics in the Prevention of Heart Failure - The Antihypertensive and Lipid- Lowering Treatment to Prevent Heart Attack Trial ALLHAT Davis.
Morbidity and Mortality in Contemporary CAD Patients With Hypertension Treated With Either a Verapamil/Trandolapril or Beta-Blocker/Diuretic Strategy (INVEST):
1 Can One Evaluate An Outcomes Claim Based On An Active Controlled Study? Pfizer Response Cardiovascular and Renal Drugs Advisory Committee Rockville,
Hypertension: New Trials – Best Treatments Karen Moncher, MD Assistant Professor University of Wisconsin School of Medicine and Public Health.
Avoiding Cardiovascular Events through COMbination Therapy in Patients LIving with Systolic Hypertension The First Outcomes Trial of Initial Therapy With.
1 Current & New treatment strategies to address CV Risk.
Aim To determine the effects of a Coversyl- based blood pressure lowering regimen on the risk of recurrent stroke among patients with a history of stroke.
SPARCL Stroke Prevention by Aggressive Reduction in Cholesterol Levels trial.
HvC Comparative Effectiveness Project Groups 5 and 6
ALLHAT Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial JAMA 2002;288:
7/27/2006 Outcomes in Hypertensive Black and Nonblack Patients Treated with Chlorthalidone, Amlodipine, and Lisinopril* * Wright JT, Dunn JK, Cutler JA.
Hypertension Family Medicine Specialist CME October 15-17, 2012 Pakse.
ASCOT and Steno-2: Aggressive risk reduction benefits two different patient populations *Composite of CV death, nonfatal MI or stroke, revascularization,
UKHDS (UKPDS): UK Hypertension in Diabetes Study Purpose To determine whether tight control of blood pressure (aiming for BP
HYPERTENSION RECOMMENDATIONS FOR FOLLOW UP BASED ON INITIAL BP READING
Is there evidence to justify different claims for different drug classes? Presentation to: Cardiovascular & Renal Drugs Advisory Committee Food & Drug.
Objective: To asses the efficacy of hydrochlorothiazide on 24-h blood pressure (BP) control.Methods: Review of all the randomized trials that assessed.
ALLHAT 6/5/ CARDIOVASCULAR DISEASE OUTCOMES IN HYPERTENSIVE PATIENTS STRATIFIED BY BASELINE GLOMERULAR FILTRATION RATE (3 GROUPS by GFR)
Pre-ALLHAT Drug Use IMS Health NDTI, Year % of Treated Patients on Medication CCBs Beta Blockers Diuretics ACE Inhibitors.
VBWG Growth in heart disease, 2000–2050 Deaths Population Foot DK et al. J Am Coll Cardiol. 2000;35:
1 ALLHAT Antihypertensive Trial Results by Baseline Diabetic Status January 28, 2004.
6/5/ CARDIOVASCULAR DISEASE OUTCOMES IN HYPERTENSIVE PATIENTS STRATIFIED BY BASELINE GLOMERULAR FILTRATION RATE (4 GROUPS by GFR) ALLHAT.
MACROVASCULAR COMPLICATIONS, DYSLIPIDEMIA and HYPERTENSION 2003 Clinical Practice Guidelines for the Prevention and Management of Diabetes in Canada.
Therapeutics Conference. Fluid Resuscitation Early correction of fluid deficit is essential in hypovolemic shock to prevent decline in tissue perfusion.
Results from ASCOT-BPLA: Anglo-Scandinavian Cardiac Outcomes Trial–Blood Pressure Lowering Arm VBWG.
Antonio Coca, MD, PhD, FRCP, FESC
Hypertension JNC VIII Guidelines.
Blood Pressure and Age in Controlling Hypertension
Health and Human Services National Heart, Lung, and Blood Institute
ALLHAT ALLHAT Antihypertensive Trial Results by Baseline Diabetic & Fasting Glucose Status.
The Anglo Scandinavian Cardiac Outcomes Trial
The following slides highlight a presentation at the Hotline Session of the European Society of Cardiology Annual Congress, September 3-7, 2005 in Stockholm,
Progress and Promise in RAAS Blockade
ALLHAT: What Outcomes Would Have Been Expected?
The Hypertension in the Very Elderly Trial (HYVET)
Insights from the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT)
Health and Human Services National Heart, Lung, and Blood Institute
Table of Contents Why Do We Treat Hypertension? Recommendation 5
The following slides highlight a report by Dr
Managing Blood Pressure
Presentation transcript:

1 The JNC 7 recommendations for initial or combination drug therapy are based on sound scientific evidence.

2 7 th Joint National Committee Report on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure

3 Algorithm for Drug Treatment of Hypertension Initial Drug Choices Without Specific or Compelling Indications Stage 1 Hypertension (SBP 140–159 or DBP 90–99 mmHg) Thiazide-type diuretics for most. May consider ACEI, ARB, BB, CCB, or combination. Stage 2 Hypertension* (SBP >160 or DBP >100 mmHg) 2-drug combination for most (usually thiazide-type diuretic and ACEI, or ARB, or BB, or CCB) * Combination therapy may also be appropriate initial therapy in patients with diabetes or renal disease

4 Most of the trials upon which the JNC 7 recommendations were based were multiple drug trials. Specific recommendations for monotherapy for specific patient groups may be difficult to justify.

5 What were the results of the diuretic/ B-blocker controlled long-term hypertension treatment trials?

6 Results of Therapy Effect of Antihypertensive Drug Treatment on Cardiovascular Events *Combined results from 17 randomized placebo controlled treatment trials ( subjects) Diuretic or Beta-blocker based **All differences are statistically significant J Am Coll Cardiol. 1996;27: ; Arch Intern Med 1993;S76-S71 % Reduction in Events ** CHFStrokesLVHCVDCHD events Fatal/Non-fatalDeathsFatal/Non-fatal

7 A diuretic or diuretic-based treatment regimen has lowered blood pressure reduced cerebro and cardiovascular events been as well tolerated as any treatment program based on other antihypertensive regimens

8 Specific or Compelling Indications for Different Medications Initial TherapyIndication Thiazide diuretic, ACEI ACEI, ARB Thiazide diuretic, BB, ACEI, ARB, CCB Recurrent stroke prevention Chronic kidney disease Diabetes

9 Specific or Compelling Indications for Different Medications Initial TherapyIndication Thiazide diuretic, BB, ACEI, CCB BB, ACEI, aldosterone antagonist Thiazide diuretic, BB, ACEI, ARB, aldosterone antagonist High CAD risk Post-myocardial infarction Heart failure

10 JNC 7 Key Messages  Thiazide-type diuretics should be initial drug therapy for most hypertensive patients, alone or combined with other medications  If BP is >160/100 mmHg, therapy should probably started with two medications, one of which should be a thiazide-type diuretic

11 Antihypertensive Trial Design Randomized, double-blind, multi-center clinical trial Determine whether occurrence of fatal CHD or nonfatal MI is lower for high-risk hypertensive patients treated with newer agents (CCB, ACEI, alpha-blocker) compared with a diuretic 42,418 high-risk hypertensive patients ALLHAT

12 Step 1 Treatment Protocol 8421Doxazosin * mg/day Lisinopril Amlodipine Chlorthalidone Dose 3*Dose 2*Dose 1*Initial Dose*Step 1 Agent ALLHAT

13 Percent of Patients Who Received a Step -2 or Step-3 Medication in the ALLHAT Study Percent *JAMA 2000;283(15):

14 ALLHAT Trial Results indicate that in hypertensive patients (mean age of 67 years) >90% can be controlled with a DBP 60% with a SBP <140 mm Hg and >60% with BPs <140/90 mm Hg – with a less than ideal regimen.

15 Blood Pressure Differences in the ALLHAT Trial: Diuretic compared to ACE-I SBP 4 mm Hg less in Blacks 3 mm Hg less in >65

16 Years to CHD Event Cumulative CHD Event Rate Cumulative Event Rates for the Primary Outcome (Fatal CHD or Nonfatal MI) by ALLHAT Treatment Group ( )L/CL/C ( )A/CA/C p valueRR (95% CI) Chlorthalidone Amlodipine Lisinopril

17 Cumulative CHF Rate Years to HF Cumulative Event Rates for Heart Failure by ALLHAT Treatment Group < ( )L/C < ( )A/C p valueHR (95% CI) Chlorthalidone Amlodipine Lisinopril

18 Significant Differences in Outcomes in the Clinical Trials Heart Failure: Other Rx Compared to Diuretics/B-Blockers LA Nifedipine 2xINSIGHT Amlodipine 1.4xALLHAT Verapamil (high risk) 1.3xCONVINCE

19 Antihypertensive monotherapy is effective in only about 40-60% of hypertensive patients, irrespective of the category of the agent that is used. Therefore, there is frequently a need for the use of two medications with different mechanisms of action. Monotherapy

20 BP Control Rates with Low-dose Beta-blocker /Diuretic Combination Compared to Monotherapy with Other Agents PlaceboBisoprolol/AmlodipineEnalapril N=78 HCTZ N=82N=84 N=77 † P=.0001 vs Placebo‡ P=.075 vs Amlodipine*P=.0001 vs Enalapril Cardiovascular Rev Rep. 1996;17:1-9. Patients with DBP <90 mmHg (%)

21 ACE Inhibitor/Diuretic Combination Therapy: Racial Differences in Response  mm Hg Vidt. J Hypertens. 1984;2(suppl 2):81-88 EnalaprilHCTZEnalapril/HCTZ 10mg BID25 mg BID10/25 mg BID (n=66)(n=110)(n=97)(n=92)(n=41)(n=49) Black Nonblack

22 Percentage Response (SBP <140 mm Hg; DBP <90 mm Hg) on Combination Therapy with 2 Drugs that Either Do or Do Not Include Hydrochlorothiazide* /3929/6327/3932/63 Systolic BPDiastolic BP * Example, captopril + diltiazem, or captopril +diuretic From Materson, et al. J Human Hypertension 1995;9: Percent Response With HCTZ Without HCTZ

23 Stroke Risk Reduction ACE/diuretic Treated Patients Compared to Patients on Other Medications Lancet 2001:358: – PROGRESS Study (Years) Proportion with Event

24 In several trials in high-risk patients (HOPE, IRMA, IDNT, RENAAL, and LIFE), the use of an ACE-I (or an ARB) usually with a diuretic) reduced CV events more than a regimen that did not include these medications.

25 Conclusions Among non diabetics, incidence of fasting glucose  126 mg/dL at 4 years was 1.8% higher in chlorthalidone vs amlodipine, and 3.5% higher in chlorthalidone vs lisinopril. Overall, metabolic differences did not translate into more adverse cardiovascular events, or into higher all-cause mortality, with chlorthalidone. ALLHAT

26 Are JNC goal levels based on good data?

27 Cardiovascular Events in Diabetics in the Hypertension Optimal Treatment Study CV Events/1000 Patient-Years Major CV Events Myocardial Infarctions CV Mortality CV events were reduced to a greater degree in diabetics who achieved the lowest levels of diastolic blood pressure Hansson L, et al. Lancet 1998;351:

28 Cardiovascular Event Free Survival Adjusted for age ANBP2 Female Male ACEI DIURETIC || Years Since Randomization

29 Oftentimes, all of the i s cannot be dotted or the T s crossed in finalizing recommendations. These are based on judgement and interpretation of outcome data.

30

31

32 Results of Different Levels of Blood Pressure Control in Hypertensive Patients with Type 2 Diabetes: B-Blocker compared with ACE Inhibitor-Based Treatment Program Better control of blood pressure compared with less aggressive treatment in 8.4-year follow-up of 1148 subjects (achieved blood pressure of 144/82 mm Hg compared with 154/87 mm Hg) Reduced risk of: –Stroke (44%) –Fatal strokes (58%) –Death related to diabetes (32%) –Heart failure (56%) –Fatal and nonfatal coronary heart disease events (21%) (trend but not significant) No difference in outcome between a captopril-based and an atenolol- based treatment program UKPDS. BMJ 1998;317:

33 Suggested Approaches for Initiation of Pharmacologic Therapy *Risk factors include: male >55, female >65, diabetes, smoking history, hyperlipidemia, target organ involvement, or obesity Low Risk Male <55 years of age Female <65 years of age Stage 1 hypertension ( /90-99 mm Hg) with no other risk factors* Lifestyle modifications for 3 to 4 months If BP >140/90 mm Hg, begin medicaton

34 Suggested Approaches for Initiation of Pharmacologic Therapy Medium Risk Stage 1 hypertension with one other risk factor* Lifestyle modifications for 2 to 3 months If BP >140/90 mm Hg, begin medication *Risk factors include: male >55, female >65, diabetes, smoking history, hyperlipidemia, target organ involvement, or obesity

35 High Risk BP >140/90 mm Hg with evidence of CVdisease and/or diabetes, with/without other risk factors* Stage 2 hypertension Stage 1 or 2 hypertension with at least three other risk factors* Lifestyle modifications and medication Suggested Approaches for Initiation of Pharmacologic Therapy * Risk factors include: male >55, female >65, diabetes, smoking history, hyperlipidemia, target organ involvement, or obesity

The Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial (ALLHAT)

37 Cumulative 5-Year Rates (1000 Patient Years) of Cardiovascular Events in the Systolic Hypertension in the Elderly program Active Therapy Placebo Therapy Placebo Major CHD events Nonfatal MI or fatal CHD Nonfatal and fatal strokes Major cerebrovascular disease events Placebo-treated diabetic patients had about 2-3 times the risk of a cardiovascular event as placebo-treated nondiabetics DiabeticNon Diabetic

38 Nonfatal MI + CHD Death0.97 ( ) All-Cause Mortality0.96 ( ) Combined CHD1.04 ( ) Combined CVD1.05 ( ) Stroke0.93 ( ) Heart Failure1.33 ( ) End Stage Renal Disease1.12 ( ) AHT Age 65+ Amlodipine/Chlorthalidone Relative Risk and 95% Confidence Intervals Favors Amlodipine Favors Chlorthalidone ALLHAT 05/15/03

39 Nonfatal MI + CHD Death1.01 ( ) All-Cause Mortality1.03 ( ) Combined CHD1.11 ( ) Combined CVD1.13 ( ) Stroke1.13 ( ) Heart Failure1.20 ( ) End Stage Renal Disease1.01 ( ) AHT Age 65+ Lisinopril/Chlorthalidone Relative Risk and 95% Confidence Intervals Favors Lisinopril Favors Chlorthalidone ALLHAT 05/15/03

40 05/11/03 ALLHAT Nonfatal MI + CHD Death1.06 ( ) All-Cause Mortality1.00 ( ) Combined Coronary Heart Disease1.06 ( ) Combined Cardiovascular Disease1.12 ( ) Stroke1.10 ( ) Heart Failure1.20 ( ) End Stage Renal Disease1.39 ( ) Favors Lisinopril Favors Chlorthalidone Relative Risk and 95% Confidence Intervals Lisinopril/Chlorthalidone AHT Age 75+

41 Nonfatal MI + CHD Death0.95 ( ) All-Cause Mortality0.91 ( ) Combined Coronary Heart Disease1.02 ( ) Combined Cardiovascular Disease1.03 ( ) Stroke0.86 ( ) Heart Failure1.22 ( ) End Stage Renal Disease0.98 ( ) /11/03 ALLHAT Favors Amlodipine Favors Chlorthalidone Relative Risk and 95% Confidence Intervals Amlodipine/Chlorthalidone AHT Age 75+

Year Studies Directly Comparing a Diuretic-Based Treatment Regimen to other Therapies Diuretic vs B-blocker MRC Elderly Diuretic vs ACE inhibitor ALLHAT Double blind ANBP-2Open STOP-2Open CAPPP (B-blocker or diuretic) Open

43 Systolic and Diastolic Blood Pressure after Randomization N Engl J Med. 2003;348(7): Diastolic Systolic ACEI Diuretic

Second Australian National Blood Pressure Study (ANBP 2) To determine in hypertensive patients aged years whether there is any difference in total cardiovascular events (fatal and non- fatal) over a 5 year treatment period between treatment with either a diuretic-based regimen or an ACE inhibitor-based regimen ANBP2

45 ANBP 2 Conclusion Initiation of antihypertensive treatment in older patients with an ACE inhibitor in males has an advantage over a diuretic.

46 Primary Result ANBP2 Hazard Ratio (95% CI) p ACEI betterDiuretic better All CV Events or Any Death 0.89 (0.79,1.00) 0.05 First CV Event or Any Death 0.89 (0.79,1.01) 0.06 Any Death 0.90 (0.75,1.09) 0.27

47 JNC 7 Key Messages For persons over age 50, SBP is more important than DBP as CVD risk factor Normotensive individuals at age 55 have a 90% lifetime risk for developing hypertension Those with SBP mm Hg or DBP mm Hg should be considered prehypertensive; they may require lifestyle modifications to prevent CVD

48 “Intensive control of blood pressure reduces cardiovascular morbidity and mortality in diabetic patients regardless of whether low- dose diuretics, B-blockers, angiotensin- converting enzyme inhibitors, or calcium antagonists are used as first-line treatment.” Grossman, Messerli…Arch Intern Med 2000;?60;

49 Primary Result - Females ANBP2 All events Hazard Ratio (95% CI) p ACEI betterDiuretic better All CV Events or Any Death1.00 (0.83,1.21) 0.98 First CV Event or Any Death1.00 (0.83,1.20) 0.98 Any Death1.01 (0.76,1.35) 0.94

50 Cumulative 5-Year Rates (1000 Patient Years) of Cardiovascular Events in the Systolic Hypertension in the Elderly program Active Therapy Placebo Therapy Placebo Major CHD events Nonfatal MI or fatal CHD Nonfatal and fatal strokes Major cerebrovascular disease events Placebo-treated diabetic patients had about 2-3 times the risk of a cardiovascular event as placebo-treated nondiabetics DiabeticNon Diabetic

Year Studies Directly Comparing a Diuretic-Based Treatment Regimen to other Therapies Diuretic vs CCBINSIGHT Double-blind NORDIL (BB or D)Open SHELL Open STOP-2 Open VHAS Open

52 Results of Tight Blood Pressure Control Compared with Less-Tight BP Control in the UKPDS Study Risk Reduction (%) Any diabetes related end- point Diabetes related death StrokeMicro vascular endpoints Retinopathy progression Deterior- ation of vision Heart failure BMJ 1998;317: