Evidence map›Paper›PMID 18753639›Full record

Trial reportThe New England journal of medicine2008

Telmisartan to prevent recurrent stroke and cardiovascular events.

Salim Yusuf, Hans-Christoph Diener, Ralph L Sacco, Daniel Cotton, Stephanie Ounpuu, William A Lawton, Yuko Palesch, Reneé H Martin, Gregory W Albers, Philip Bath and 25 more

2 registry-linked trialsOpen access · bronzeAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The New England journal of medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 241 papers, 32 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
241citing papers in PubMed, 32 pooled it
52.8field-weighted citation impact, top 1% 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.

NCT00153062 phase4completednot on this map

PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes: A Double-blind, Active and Placebo Controlled Study of Aggrenox vs. Clopidogrel, With and Without Micardis

TypeinterventionalSponsorBoehringer IngelheimRan2003Enrolled20,332ConditionsStrokeArmsAggrenox, Clopidogrel placebo, Micardis, Aggrenox placebo, Clopidogrel
NCT00991029 phase3terminatednot on this mapstarted 2010, after this paper: background citation

Platelet-Oriented Inhibition in New TIA and Minor Ischemic Stroke (POINT) Trial

TypeinterventionalSponsorUniversity of California, San FranciscoRan2010 to 2018Enrolled4,881ConditionsIschemic Attack, TransientArmsClopidogrel, placebo
3 · Its place in the literature

Who cites it

241 citing papers in PubMed, 32 syntheses or guidelines pooled it, 778 citations in OpenAlex.

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  11. Pharmacotherapy for hypertension-induced left ventricular hypertrophy.The Cochrane database of systematic reviews · 2021
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  15. Pharmacotherapy for hypertension in adults 60 years or older.The Cochrane database of systematic reviews · 2019
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  17. First-line drugs for hypertension.The Cochrane database of systematic reviews · 2018
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181 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

35 authors at 20 institutions in 16 countries.

Salim YusufPopulation Health Research Institute, McMaster University, Hamilton, ON, Canada.
Hans-Christoph Diener
Ralph L Sacco
Daniel Cotton
Stephanie Ounpuu
William A Lawton
Yuko Palesch
Reneé H Martin
Gregory W Albers
Philip Bath
Natan Bornstein
Bernard P L Chan
Sien-Tsong Chen
Luis Cunha
Björn Dahlöf
Jacques De Keyser
Geoffrey A Donnan
Conrado Estol
Philip Gorelick
Vivian Gu
Karin Hermansson
Lutz Hilbrich
Markku Kaste
Chuanzhen Lu
Thomas Machnig
Prem Pais
Robin Roberts
Veronika Skvortsova
Philip Teal
Danilo Toni
Cam VanderMaelen
Thor Voigt
Michael Weber
Byung-Woo Yoon
PRoFESS Study Group
Boehringer Ingelheim (United States) · USMedical University of South Carolina · USBoehringer Ingelheim (Canada) · CAChang Gung Memorial Hospital · TWHelsinki University Hospital · FIHospitais da Universidade de Coimbra · PTHuashan Hospital · CNMcMaster University · CANational University Hospital · SGPirogov Russian National Research Medical University · RUPopulation Health Research Institute · CASahlgrenska University Hospital · SESapienza University of Rome · ITSeoul National University Hospital · KRStanford Medicine · USSt.John's Medical College Hospital · INSUNY Downstate Health Sciences University · USThe University of Melbourne · AUUniversity Medical Center Groningen · NLUniversity of British Columbia · CA

Funding

Collateral Circulation in Acute Ischemic StrokeK23NS054084 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LIEBESKIND, DAVID SIGMUND · 2006 to 2010
$764k
NINDS NIH HHS K23 NS054084
6 · The paper itself

Abstract

backgroundProlonged lowering of blood pressure after a stroke reduces the risk of recurrent stroke. In addition, inhibition of the renin-angiotensin system in high-risk patients reduces the rate of subsequent cardiovascular events, including stroke. However, the effect of lowering of blood pressure with a renin-angiotensin system inhibitor soon after a stroke has not been clearly established. We evaluated the effects of therapy with an angiotensin-receptor blocker, telmisartan, initiated early after a stroke.

methodsIn a multicenter trial involving 20,332 patients who recently had an ischemic stroke, we randomly assigned 10,146 to receive telmisartan (80 mg daily) and 10,186 to receive placebo. The primary outcome was recurrent stroke. Secondary outcomes were major cardiovascular events (death from cardiovascular causes, recurrent stroke, myocardial infarction, or new or worsening heart failure) and new-onset diabetes.

resultsThe median interval from stroke to randomization was 15 days. During a mean follow-up of 2.5 years, the mean blood pressure was 3.8/2.0 mm Hg lower in the telmisartan group than in the placebo group. A total of 880 patients (8.7%) in the telmisartan group and 934 patients (9.2%) in the placebo group had a subsequent stroke (hazard ratio in the telmisartan group, 0.95; 95% confidence interval [CI], 0.86 to 1.04; P=0.23). Major cardiovascular events occurred in 1367 patients (13.5%) in the telmisartan group and 1463 patients (14.4%) in the placebo group (hazard ratio, 0.94; 95% CI, 0.87 to 1.01; P=0.11). New-onset diabetes occurred in 1.7% of the telmisartan group and 2.1% of the placebo group (hazard ratio, 0.82; 95% CI, 0.65 to 1.04; P=0.10).

conclusionsTherapy with telmisartan initiated soon after an ischemic stroke and continued for 2.5 years did not significantly lower the rate of recurrent stroke, major cardiovascular events, or diabetes. (ClinicalTrials.gov number, NCT00153062.)

Indexed as

AgedAngiotensin-Converting Enzyme InhibitorsBenzimidazolesBenzoatesBlood PressureCardiovascular DiseasesCreatinineDiabetes MellitusFemaleFollow-Up StudiesHeart FailureHumansKaplan-Meier EstimateMaleMiddle AgedMyocardial InfarctionAngiotensin-Converting Enzyme InhibitorsBenzimidazolesBenzoatesCreatininePotassiumTelmisartan

Identifiers

PMID18753639
PMCPMC2714258
OpenAlexW2111421663

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.