Evidence map›Paper›PMID 19433694›Full record

Trial reportArchives of internal medicine2009

ALLHAT findings revisited in the context of subsequent analyses, other trials, and meta-analyses.

Jackson T Wright, Jeffrey L Probstfield, William C Cushman, Sara L Pressel, Jeffrey A Cutler, Barry R Davis, Paula T Einhorn, Mahboob Rahman, Paul K Whelton, Charles E Ford and 6 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Archives of internal medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 2 pooled it
8.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 2 syntheses or guidelines pooled it, 116 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  15. Review
  16. Article
  17. Article
  18. [Austrian Consensus on High Blood Pressure 2019].Wiener klinische Wochenschrift · 2019
    Article
  19. Review
  20. Prevention and Control of Hypertension: JACC Health Promotion Series.Journal of the American College of Cardiology · 2018
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 1 institution in 1 country.

Jackson T WrightALLHAT Clinical Trials Center, University of Texas at Houston Health Science Center School of Public Health, 1200 Herman Pressler Street, Houston, TX 77030, USA.
Jeffrey L Probstfield
William C Cushman
Sara L Pressel
Jeffrey A Cutler
Barry R Davis
Paula T Einhorn
Mahboob Rahman
Paul K Whelton
Charles E Ford
L Julian Haywood
Karen L Margolis
Suzanne Oparil
Henry R Black
Michael H Alderman
ALLHAT Collaborative Research Group
The University of Texas Health Science Center at Houston · US

Funding

CLINICAL TRIALS CENTER FOR ALLHAT-N01HC35130-268035130N01HC035130 · HC · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · 1993 to 2005
$6.3M
ALLHATN01HC35130 · NHLBI · 2010 to 2010
$1.2M
NHLBI NIH HHS N01 HC035130NHLBI NIH HHS N01 HC 35130
6 · The paper itself

Abstract

The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) is reevaluated considering information from new clinical trials, meta-analyses, and recent subgroup and explanatory analyses from ALLHAT, especially those regarding heart failure (HF) and the association of drug treatment with new-onset diabetes mellitus (DM) and its cardiovascular disease (CVD) consequences. Chlorthalidone was superior to (1) doxazosin mesylate in preventing combined CVD (CCVD) (risk ratio [RR], 1.20; 95% confidence interval [CI], 1.13-1.27), especially HF (RR, 1.80; 95% CI, 1.40-2.22) and stroke (RR, 1.26; 95% CI, 1.10-1.46); (2) lisinopril in preventing CCVD (RR, 1.10; 95% CI, 1.05-1.16), including stroke (in black persons only) and HF (RR, 1.20; 95% CI, 1.09-1.34); and (3) amlodipine besylate in preventing HF, overall (by 28%) and in hospitalized or fatal cases (by 26%). Central independent blinded reassessment of HF hospitalizations confirmed each comparison. Results were consistent by age, sex, race (except for stroke and CCVD), DM status, metabolic syndrome status, and renal function level. Neither amlodipine nor lisinopril was superior to chlorthalidone in preventing end-stage renal disease overall, by DM status, or by renal function level. In the chlorthalidone arm, new-onset DM was not significantly associated with CCVD (RR, 0.96; 95% CI, 0.88-2.42). Evidence from subsequent analyses of ALLHAT and other clinical outcome trials confirm that neither alpha-blockers, angiotensin-converting enzyme inhibitors, nor calcium channel blockers surpass thiazide-type diuretics (at appropriate dosage) as initial therapy for reduction of cardiovascular or renal risk. Thiazides are superior in preventing HF, and new-onset DM associated with thiazides does not increase CVD outcomes.

Indexed as

AgedAngiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsCalcium Channel BlockersChlorthalidoneDiabetes MellitusDiureticsDouble-Blind MethodFemaleHeart FailureHumansHypolipidemic AgentsKidney Failure, ChronicMaleMiddle AgedMyocardial InfarctionAngiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsCalcium Channel BlockersChlorthalidoneDiureticsHypolipidemic Agents

Identifiers

PMID19433694
PMCPMC2803011
OpenAlexW2162713300

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.