Evidence map›Paper›PMID 30153268›Full record

Trial reportPloS one2018

Long-term use of carvedilol in patients with ST-segment elevation myocardial infarction treated with primary percutaneous coronary intervention.

Hiroki Watanabe, Neiko Ozasa, Takeshi Morimoto, Hiroki Shiomi, Bao Bingyuan, Satoru Suwa, Yoshihisa Nakagawa, Chisato Izumi, Kazushige Kadota, Shigeru Ikeguchi and 18 more

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 10 pooled it
3.8field-weighted citation impact, top 6% 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

47 citing papers in PubMed, 10 syntheses or guidelines pooled it, 113 citations in OpenAlex.

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  9. Beta-blockers in patients without heart failure after myocardial infarction.The Cochrane database of systematic reviews · 2021
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  10. Beta-blockers for suspected or diagnosed acute myocardial infarction.The Cochrane database of systematic reviews · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors at 20 institutions in 1 country.

Hiroki WatanabeDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Neiko OzasaDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takeshi MorimotoDepartment of Clinical Epidemiology, Hyogo College of Medicine, Hyogo, Japan.ORCID 0000-0002-6844-739X
Hiroki ShiomiDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Bao BingyuanDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Satoru SuwaDivision of Cardiology, Juntendo University Shizuoka Hospital, Izunokuni, Japan.
Yoshihisa NakagawaDivision of Cardiology, Tenri Hospital, Nara, Japan.
Chisato IzumiDivision of Cardiology, Tenri Hospital, Nara, Japan.
Kazushige KadotaDivision of Cardiology, Kurashiki Central Hospital, Kurashiki, Japan.
Shigeru IkeguchiDivision of cardiology, Shiga General Hospital, Moriyama, Japan.
Kiyoshi HibiDivision of Cardiology, Yokohama City University Medical Center, Yokohama, Japan.
Yutaka FurukawaDivision of Cardiology, Kobe City Medical Center General Hospital, Kobe, Japan.
Shuichiro KajiDivision of Cardiology, Kobe City Medical Center General Hospital, Kobe, Japan.
Takahiko SuzukiDivision of Cardiology, Toyohashi Heart Center, Toyohashi, Japan.
Masaharu AkaoDepartment of Cardiology, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.
Tsukasa InadaCardiovascular Center, Osaka Red Cross Hospital, Osaka, Japan.
Yasuhiko HayashiDivision of Cardiology, Tsuchiya General Hospital, Hiroshima, Japan.
Mamoru NanasatoCardiovascular Center, Nagoya Daini Red Cross Hospital, Nagoya, Japan.
Masaaki OkutsuDivision of Cardiology, Nozaki Tokushukai Hospital, Osaka, Japan.ORCID 0000-0002-1215-1186
Ryosuke KametaniDivision of Cardiology, Nagoya Tokushukai General Hospital, Kasugai, Japan.
Takahito SoneDivision of Cardiology, Ogaki Municipal Hospital, Ogaki, Japan.
Yoichi SugimuraDivision of Cardiology, Kawakita General Hospital, Tokyo, Japan.
Kazuya KawaiDivision of Cardiology, Chikamori Hospital, Kochi, Japan.
Mitsunori AbeDivision of Cardiology, Yotsuba Circulation Clinic, Matsuyama, Japan.
Hironori KanekoDivision of Cardiology, Hoshi General Hospital, Koriyama, Japan.
Sunao NakamuraDivision of Cardiology, New Tokyo Hospital, Chiba, Japan.
Takeshi KimuraDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID 0000-0002-5256-8322
CAPITAL-RCT investigators
Kyoto University · JPKobe City Medical Center General Hospital · JPTenri Hospital · JPChikamori Hospital · JPFukuoka Tokushukai Hospital · JPHiroshima General Hospital · JPHyogo Medical University · JPJapanese Red Cross Nagoya Daini Hospital · JPJuntendo University Shizuoka Hospital · JPKurashiki Central Hospital · JPKyoto Medical Center · JPNew Tokyo Hospital · JPOgaki Municipal Hospital · JPOsaka Red Cross Hospital · JPShiga Medical Center · JPShowa General Hospital · JPStar General Hospital · JPToyohashi Heart Center · JPYao Tokushukai General Hospital · JPYokohama City University Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite its recommendation by the current guidelines, the role of long-term oral beta-blocker therapy has never been evaluated by randomized trials in uncomplicated ST-segment elevation myocardial infarction (STEMI) patients without heart failure, left ventricular dysfunction or ventricular arrhythmia who underwent primary percutaneous coronary intervention (PCI). METHODS AND

resultsIn a multi-center, open-label, randomized controlled trial, STEMI patients with successful primary PCI within 24 hours from the onset and with left ventricular ejection fraction (LVEF) ≥40% were randomly assigned in a 1-to-1 fashion either to the carvedilol group or to the no beta-blocker group within 7 days after primary PCI. The primary endpoint is a composite of all-cause death, myocardial infarction, hospitalization for heart failure, and hospitalization for acute coronary syndrome. Between August 2010 and May 2014, 801 patients were randomly assigned to the carvedilol group (N = 399) or the no beta-blocker group (N = 402) at 67 centers in Japan. The carvedilol dose was up-titrated from 3.4±2.1 mg at baseline to 6.3±4.3 mg at 1-year. During median follow-up of 3.9 years with 96.4% follow-up, the cumulative 3-year incidences of both the primary endpoint and any coronary revascularization were not significantly different between the carvedilol and no beta-blocker groups (6.8% and 7.9%, P = 0.20, and 20.3% and 17.7%, P = 0.65, respectively). There also was no significant difference in LVEF at 1-year between the 2 groups (60.9±8.4% and 59.6±8.8%, P = 0.06).

conclusionLong-term carvedilol therapy added on the contemporary evidence-based medications did not seem beneficial in selected STEMI patients treated with primary PCI.

trial registrationCAPITAL-RCT (Carvedilol Post-Intervention Long-Term Administration in Large-scale Randomized Controlled Trial) ClinicalTrials.gov.number, NCT 01155635.

Indexed as

Percutaneous Coronary InterventionAgedCarvedilolCombined Modality TherapyFemaleHumansMaleMiddle AgedST Elevation Myocardial InfarctionTime FactorsTreatment OutcomeCarvedilol

Identifiers

PMID30153268
PMCPMC6112626
OpenAlexW2889501145

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.