Evidence map›Paper›PMID 41211954›Full record

SynthesisThe New England journal of medicine2026

Beta-Blockers after Myocardial Infarction with Normal Ejection Fraction.

Anna Meta Dyrvig Kristensen, Xavier Rossello, Dan Atar, Troels Yndigegn, Takeshi Kimura, Roberto Latini, Bertil Lindahl, Sigrun Halvorsen, Michael Hecht Olsen, Valentin Fuster and 21 more

Abstract readMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in The New England journal of medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

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

32 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Hypertension: a missing piece in HFpEF?Hypertension research : official journal of the Japanese Society of Hypertension · 2026
    Review
  4. Article
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  12. Observational
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  15. Review
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  18. Cardiovascular pharmacotherapy in 2025.European heart journal. Cardiovascular pharmacotherapy · 2026
    Review
  19. Article
  20. Predicting atrial fibrillation after an acute coronary syndrome: insights from the BACS & BAMI study.Clinical research in cardiology : official journal of the German Cardiac Society · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors.

Anna Meta Dyrvig KristensenDepartment of Cardiology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Copenhagen.
Xavier RosselloCentro Nacional de Investigaciones Cardiovasculares Carlos III, Madrid.
Dan AtarDepartment of Cardiology, Oslo University Hospital, Ullevål, Oslo.
Troels YndigegnDepartment of Cardiology, Clinical Sciences, Lund University, Lund, Sweden.
Takeshi KimuraDepartment of Cardiology, Hirakata Kohsai Hospital, Osaka, Japan.
Roberto LatiniDepartment of Acute Brain and Cardiovascular Injury, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan.
Bertil LindahlDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.
Sigrun HalvorsenDepartment of Cardiology, Oslo University Hospital, Ullevål, Oslo.
Michael Hecht OlsenDepartment of Clinical Medicine, University of Copenhagen, Copenhagen.
Valentin FusterCentro Nacional de Investigaciones Cardiovasculares Carlos III, Madrid.
Robin HofmannDepartment of Clinical Science and Education, Division of Cardiology, Södersjukhuset, Stockholm.
Kjell VikenesDepartment of Heart Disease, Haukeland University Hospital, Bergen, Norway.
Michael MaengDepartment of Cardiology, Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0002-4310-6433
David ErlingeDepartment of Cardiology, Clinical Sciences, Lund University, Lund, Sweden.
Stuart PocockCentro Nacional de Investigaciones Cardiovasculares Carlos III, Madrid.
Patric KarlströmDepartment of Internal Medicine, Ryhov County Hospital, Jönköping, Sweden.
Arnhild BakkenDepartment of Cardiology, Oslo University Hospital, Ullevål, Oslo.
Theis LangeSection of Biostatistics, Department of Public Health, University of Copenhagen, Copenhagen.
Jose A BarrabésCentro de Investigación Biomédica en Red en Enfermedades Cardiovasculares, Madrid.
Jocelyne BenatarDepartment of Cardiology, Auckland City Hospital, Auckland, New Zealand.
Sergio Raposeiras-RoubinCentro Nacional de Investigaciones Cardiovasculares Carlos III, Madrid.
Claes HeldDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.
Massimo PiepoliUniversity Cardiology, IRCCS Policlinico San Donato Milanese, Milan.
Morten Wang FagerlandOslo Center for Biostatistics and Epidemiology, Research Support Services, Oslo University Hospital, Oslo.
Therese HolmagerDepartment of Cardiology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Copenhagen.
Neiko OzasaDepartment of Cardiology, Kansai Heart Center, Takanohara Central Hospital, Nara, Japan.
Eva Irene Bossano PrescottDepartment of Cardiology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Copenhagen.
John MunkhaugenDepartment of Medicine, Drammen Hospital, Vestre Viken Trust, Drammen, Norway.
Tomas JernbergDepartment of Clinical Sciences, Danderyd Hospital, Karolinska Institutet, Stockholm.
Borja IbanezCentro Nacional de Investigaciones Cardiovasculares Carlos III, Madrid.
Beta-Blocker Trialists’ Collaboration Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe benefit of beta-blockers after myocardial infarction in patients with a preserved left ventricular ejection fraction (LVEF) is unclear.

methodsWe conducted a meta-analysis at the individual-patient level using data from five open-label trials that randomly assigned patients with recent myocardial infarction, no other indications for beta-blocker therapy, and an LVEF of at least 50% to receive beta-blocker therapy or no beta-blocker therapy. The primary end point was a composite of death from any cause, myocardial infarction, or heart failure. Event rates were analyzed with a one-stage fixed-effects Cox proportional-hazards model.

resultsA total of 17,801 patients were included from the REBOOT (7459 patients), REDUCE-AMI (4967 patients), BETAMI (2441 patients), DANBLOCK (2277 patients), and CAPITAL-RCT (657 patients) trials. Of these 17,801 patients, 8831 (49.6%) were assigned to receive a beta-blocker and 8970 (50.4%) were assigned to receive no beta-blocker. During a median follow-up of 3.6 years (interquartile range, 2.3 to 4.6), a primary-end-point event occurred in 717 patients (8.1%) in the beta-blocker group and 748 patients (8.3%) in the no-beta-blocker group (hazard ratio, 0.97; 95% confidence interval [CI], 0.87 to 1.07; P = 0.54). Death from any cause occurred in 335 patients in the beta-blocker group and 326 patients in the no-beta-blocker group (hazard ratio, 1.04; 95% CI, 0.89 to 1.21); myocardial infarction occurred in 360 and 407 patients, respectively (hazard ratio, 0.89; 95% CI, 0.77 to 1.03); and heart failure occurred in 75 and 87 patients (hazard ratio, 0.87; 95% CI, 0.64 to 1.19).

conclusionsIn this meta-analysis including individual-patient data from five randomized trials, beta-blocker therapy did not reduce the incidence of death from any cause, myocardial infarction, or heart failure in patients with an LVEF of at least 50% after myocardial infarction without other indications for beta-blockers. (Funded by Centro Nacional de Investigaciones Cardiovasculares Carlos III and others; PROSPERO database number, CRD420251119176.).

Indexed as

Adrenergic beta-AntagonistsHeart FailureMyocardial InfarctionStroke VolumeAgedFemaleFollow-Up StudiesHumansIncidenceMaleMiddle AgedProportional Hazards ModelsRandomized Controlled Trials as TopicRecurrenceTreatment OutcomeVentricular Function, LeftAdrenergic beta-Antagonists

Identifiers

PMID41211954

What Socratic holds

Textmetadata
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 Socratic graph.