ALLHAT. U.S. Department of Health and Human Services. National Institutes of Health. National Heart, Lung, and Blood Institute
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1 U.S. Department of Health and Human Services National Institutes of Health National Heart, Lung, and Blood Institute Review of Heart Failure Events in the Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial: ALLHAT Heart Failure Validation Study Paula Einhorn, Barry Davis, Henry Black, William Cushman, John Kostis, Daniel Levy, Barry Massie, Barbara deleon, Linda Piller, Lara Simpson, Chuke Nwachuku for The ALLHAT Collaborative Research Group Sponsored by the National Heart, Lung, and Blood Institute (NHLBI)
2 Heart Failure Validation Study Aimed to centrally review all hospitalized HF events in 42,418 ALLHAT participants.
3 42,418 High-risk hypertensive patients Randomized Design of ALLHAT BP Trial Consent / Randomize Amlodipine Chlorthalidone Doxazosin Lisinopril Follow until death or end of study (4-8 8 years, mean 4.9 years) JAMA. 2002;288:
4 Participants Hypertensive men and women Age 55 and older (mean 67) At least one additional CVD risk factor [old (>6 months) MI or stroke, LVH, h/o type 2 diabetes, current smoker, HDL<35, or documented other ASCVD] Excluded: h/o symptomatic HF and/or known LVEF <35%
5 ALLHAT provides a double-blind comparison of 4 drug classes in preventing transition from hypertension to overt heart failure
6 Hypertension and Heart Failure In Framingham Heart Study, hypertension was the most common risk factor for HF, antedating it in 91% of cases. (JAMA. 1996;275: ) In BP Lowering Treatment Trialists Collaboration, there were differences among drug classes in occurrence of HF. (Lancet 2003, 362: )
7 Hypertension Trial Randomized, double-blind Large, simple, practice-based trial No protocol-mandated central review of HF events Diagnoses assigned by clinic investigators guided by protocol-defined diagnostic criteria
8 ALLHAT HF Criteria Category A Must have one from each category: Category B Paroxysmal nocturnal dyspnea Orthopnea NYHA Classification III Dyspnea at rest Rales 2+ ankle edema Tachycardia >= 120/min Cardiomegaly by CXR CXR characteristic of CHF S 3 gallop ALLHAT Manual of Operations, JAMA.1997;278: Jugular venous distention
9 Origin of the HF Validation Study HF endpoint defined as treated in hospital or as outpatient, or fatal A component of combined CVD (CHD, stroke, HF, PAD) Systematic review of hospitalized HF events was initiated in 2001, on advice of the DSMB
10 HF Validation Study Objectives Evaluate ALLHAT investigator-assigned diagnoses Compare treatment effects to those previously reported (JAMA. 2002;288: )
11 HF Validation Study Relevant hospital records requested for 2952 hospitalizations in 2047 patients with a diagnosis of HF on admission or during hospital course Summary: face sheet, discharge /death summary, admitting H&P, ER notes Imaging reports: chest X-ray, cardiac catheterization, echocardiography, radionuclide imaging Other reports: pulmonary function tests, cardiology or pulmonary consultation, autopsy
12 HF Validation Study Definitions ALLHAT/SHEP Traditional Framingham Criteria Updated Framingham Criteria Reviewers global clinical judgment
13 HF Validation Study 2962 hospital records for 2045 patients received records of 1951 patients suitable for review. Abstracted by cardiology fellows blinded to treatment assignment. Each record independently reviewed by two reviewers. For algorithmic criteria (ALLHAT and Framingham), diagnoses were assigned by computer. Reviewers clinical judgment entered as yes, no, don t know.
14 Framingham HF Criteria Two major or one major plus two minor criteria: Major Paroxysmal nocturnal dyspnea Jugular venous distention Rales Cardiomegaly on CXR Acute pulmonary edema S 3 gallop Central venous pressure Circ. time >25 seconds Hepatojugular reflux Autopsy findings: pulmonary edema, congestion, or cardiomegaly Minor Bilateral ankle edema Nocturnal cough Dyspnea on exertion Hepatomegaly Pleural effusion Vital capacity 1/3 from max. Tachycardia > 120/min. Major or minor Weight loss > 4.5 kg in 5 days in response to treatment of HF KKL Ho et al, Circulation 88:107, 1993
15 Major PND or orthopnea Jugular Venous Distention Pulmonary rales S 3 gallop Hepatojugular reflux Diuresis of 10 lbs or 5 kg in response to diuretic treatment with clinical improvement in congestive symptoms Updated Framingham Criteria Require 2 major or 1 major plus 2 minor criteria; one has to be diagnostic and one clinical Part 1: Clinical Findings Minor Bilateral ankle edema Nocturnal cough Dyspnea on exertion Hepatomegaly
16 Major Acute pulmonary edema on CXR PCWP>= 20 mm Hg LVEF =< 35% Cardiac Index < 2.0 Evidence of severe valvular disease Pulmonary edema, congestion, or cardiomegaly on autopsy Updated Framingham Criteria Require 2 major or 1 major plus 2 minor criteria; one has to be diagnostic and one clinical Part 2: Diagnostic Findings Minor Pleural effusion or vascular engorgement or redistribution on CXR PCWP mm Hg LVEF 36 44% Cardiac Index Evidence of moderate valvular disease
17 Percent agreement with investigator-assigned diagnosis % agreement ALLHAT Framingham1 Framingham 2 Reviewers Data refer to percentage of participants with at least one event of hospitalized or fatal heart failure that meet the criteria by at least one of the reviewers.
18 Percent Agreement with investigator-assigned diagnosis Chlor Amlod Lisin TOTAL N (patients with event reviewed) ALLHAT 1 69% 73% 72% 71% ALLHAT 2 69% 72% 71% 70% ALLHAT 3 66% 69% 70% 68% ALLHAT 4 56% 58% 56% 57% Framingham 1 79% 81% 79% 80% Framingham2 72% 73% 71% 72% Reviewers agree HF 82% 86% 84% 84%
19 Percent Agreement with investigator-assigned diagnosis Chlor Dox TOTAL N (patients with event reviewed) ALLHAT 1 67% 69% 68% ALLHAT 2 66% 68% 67% ALLHAT 3 64% 67% 65% ALLHAT 4 53% 53% 53% Framingham 1 77% 76% 77% Framingham2 69% 69% 69% Reviewers agree HF 80% 83% 82%
20 HF Validation Study Verification of Treatment Effects For the various Validation Study definitions of HF, relative risks and 95% CIs were calculated using first events confirmed by a given definition.
21 Validation Study ACEI versus diuretic Definition, Relative Risk and 95% Confidence Intervals HF* 1.19 ( ) Hosp/fatal HF 1.10 ( ) ALLHAT ( ) ALLHAT ( ) ALLHAT ( ) ALLHAT ( ) Framingham ( ) Framingham ( ) Reviewer agree 1.15 ( ) Favors Lisinopril Favors Chlorthalidone RR estimates calculated from 2-by-2 table Pre-specified endpoint of treated in hospital or as outpatient or fatal
22 Validation Study CCB versus diuretic Definition, Relative Risk and 95% Confidence Intervals HF* 1.37 ( ) Hosp/fatal HF 1.35 ( ) ALLHAT ( ) ALLHAT ( ) ALLHAT ( ) ALLHAT ( ) Framingham ( ) Framingham ( ) Reviewer agree 1.45 ( ) Favors Amlodipine Favors Chlorthalidone Pre-specified endpoint of treated in hospital or as outpatient or fatal RR estimates calculated from 2-by-2 table
23 Validation Study α-blocker versus diuretic Definition, Relative Risk and 95% Confidence Intervals HF* 1.77 ( ) Hosp/fatal HF 1.60 ( ) ALLHAT ( ) ALLHAT ( ) ALLHAT ( ) ALLHAT ( ) Framingham ( ) Framingham ( ) Reviewer agree 1.72 ( ) Favors Doxazosin Favors Chlorthalidone Pre-specified endpoint of treated in hospital or as outpatient or fatal RR estimates calculated from 2-by-2 table
24 Summary An independent review of hospital records showed a high degree of agreement with the diagnoses assigned by ALLHAT investigators (71 84% agreement) Relative risks calculated for several stringent definitions of HF confirm superiority of a thiazide-type diuretic over a CCB, an ACE-I and an alpha-blocker in preventing the onset of symptomatic HF in hypertensive patients with at least one additional risk factor.
25 Implications HF is a costly and deadly complication of hypertension Thiazide-type diuretics have greater efficacy for HF prevention and should be considered first-step therapy for prevention of HF in high risk patients with hypertension
26
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