Evidence map›Paper›PMID 37555345›Full record

Trial reportCirculation2023

Arrhythmia and Death Following Percutaneous Revascularization in Ischemic Left Ventricular Dysfunction: Prespecified Analyses From the REVIVED-BCIS2 Trial.

Divaka Perera, Holly P Morgan, Matthew Ryan, Matthew Dodd, Tim Clayton, Peter D O'Kane, John P Greenwood, Simon J Walsh, Roshan Weerackody, Adam McDiarmid and 15 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Circulation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01920048 (REVascularisation for Ischaemic VEntricular Dysfunction), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
7.5field-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.

NCT01920048 nacompletednot on this map

REVascularisation for Ischaemic VEntricular Dysfunction (REVIVED): a Randomized Comparison of Percutaneous Coronary Intervention (With Optimal Medical Therapy) Versus Optimal Medical Therapy Alone for Treatment of Heart Failure Secondary to Coronary Disease

TypeinterventionalSponsorKing's College LondonRan2013 to 2022Enrolled700ConditionsIschemic CardiomyopathyArmsPercutaneous Coronary Intervention, Drug Therapy for Heart Failure, Device Therapy for Heart Failure
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Surgical Risk and Long-Term Mortality With PCI and CABG in Ischemic Left Ventricular Systolic Dysfunction.Journal of the Society for Cardiovascular Angiography & Interventions · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Incidence and risk factors for first and recurrent ICD shock therapy in patients with an implantable cardioverter defibrillator.Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Stem Cell Therapy against Ischemic Heart Disease.International journal of molecular sciences · 2024
    Review
  12. Article
  13. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 20 institutions in 1 country.

Divaka PereraNational Institute for Health Research Biomedical Research Center and British Heart Foundation Center of Research Excellence at the School of Cardiovascular Medicine and Sciences, King's College London, United Kingdom (D.P., H.P.M., M.R.).ORCID 0000-0001-6362-1291
Holly P MorganNational Institute for Health Research Biomedical Research Center and British Heart Foundation Center of Research Excellence at the School of Cardiovascular Medicine and Sciences, King's College London, United Kingdom (D.P., H.P.M., M.R.).ORCID 0000-0002-6636-6174
Matthew RyanNational Institute for Health Research Biomedical Research Center and British Heart Foundation Center of Research Excellence at the School of Cardiovascular Medicine and Sciences, King's College London, United Kingdom (D.P., H.P.M., M.R.).
Matthew DoddLondon School of Hygiene & Tropical Medicine, United Kingdom (M.D., T.C., R.E.).ORCID 0000-0002-6207-6604
Tim ClaytonLondon School of Hygiene & Tropical Medicine, United Kingdom (M.D., T.C., R.E.).ORCID 0000-0002-1266-3288
Peter D O'KaneRoyal Bournemouth and Christchurch Hospital, Bournemouth, United Kingdom (P.D.O.).ORCID 0000-0001-5245-4547
John P GreenwoodLeeds Teaching Hospitals NHS Trust and University of Leeds, United Kingdom (J.P.G., M.A.).ORCID 0000-0002-2861-0914
Simon J WalshBelfast Health and Social Care NHS Trust, United Kingdom (S.J.W.).
Roshan WeerackodyBarts Health NHS Trust, London, United Kingdom (R.W.).
Adam McDiarmidNewcastle Hospitals NHS Foundation Trust, United Kingdom (A.M.).
George Amin-YoussefKing's College Hospital NHS Foundation Trust, London, United Kingdom (G.A.-Y.).
Julian StrangeUniversity Hospitals Bristol NHS Foundation Trust, United Kingdom (J.S.).ORCID 0000-0003-0476-0886
Bhavik ModiUniversity Hospitals of Leicester NHS Trust, United Kingdom (B.M.).
Timothy LockieRoyal Free Hospital, London, United Kingdom (T.L.).
Kai HogrefeKettering General Hospital, Northampton, United Kingdom (K.H.).
Fozia Z AhmedManchester Royal Infirmary, University NHS Foundation Trust, United Kingdom (F.Z.A.).ORCID 0000-0001-9769-0180
Miles BehanEdinburgh Royal Infirmary, United Kingdom (M.B.).
Nicholas JenkinsSunderland Royal Hospital, United Kingdom (N.J.).
Eltigani AbdelaalWythenshawe Hospital, Manchester, United Kingdom (E.A.).
Michelle AndersonLeeds Teaching Hospitals NHS Trust and University of Leeds, United Kingdom (J.P.G., M.A.).ORCID 0000-0002-9400-7195
Stuart WatkinsInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom (S.W., M.C.P.).ORCID 0000-0003-1579-6294
Richard EvansLondon School of Hygiene & Tropical Medicine, United Kingdom (M.D., T.C., R.E.).
Christopher A RinaldiGuy's and St Thomas' NHS Foundation Trust, London, United Kingdom (D.P., C.A.R.).
Mark C PetrieInstitute of Cardiovascular and Medical Sciences, University of Glasgow, United Kingdom (S.W., M.C.P.).ORCID 0000-0002-6333-9496
REVIVED-BCIS2 Investigators
Leeds Teaching Hospitals NHS Trust · GBThe Royal Free Hospital · GBUniversity of London · GBBelfast Health and Social Care Trust · GBGuy's and St Thomas' NHS Foundation Trust · GBSt Mark's Hospital · GBSunderland Royal Hospital · GBUniversity Hospitals Bristol NHS Foundation Trust · GBBarts Health NHS Trust · GBBritish Heart Foundation · GBEdinburgh Royal Infirmary · GBKettering General Hospital · GBKing's College Hospital NHS Foundation Trust · GBManchester Royal Infirmary · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBRoyal Bournemouth Hospital · GBSt Thomas' Hospital · GBUniversity Hospitals of Leicester NHS Trust · GBUniversity of Glasgow · GBWythenshawe Hospital · GB

Funding

British Heart Foundation FS/CRTF/21/24190British Heart Foundation RE/18/2/34213Department of Health 10/57/67
6 · The paper itself

Abstract

backgroundVentricular arrhythmia is an important cause of mortality in patients with ischemic left ventricular dysfunction. Revascularization with coronary artery bypass graft or percutaneous coronary intervention is often recommended for these patients before implantation of a cardiac defibrillator because it is assumed that this may reduce the incidence of fatal and potentially fatal ventricular arrhythmias, although this premise has not been evaluated in a randomized trial to date.

methodsPatients with severe left ventricular dysfunction, extensive coronary disease, and viable myocardium were randomly assigned to receive either percutaneous coronary intervention (PCI) plus optimal medical and device therapy (OMT) or OMT alone. The composite primary outcome was all-cause death or aborted sudden death (defined as an appropriate implantable cardioverter defibrillator therapy or a resuscitated cardiac arrest) at a minimum of 24 months, analyzed as time to first event on an intention-to-treat basis. Secondary outcomes included cardiovascular death or aborted sudden death, appropriate implantable cardioverter defibrillator (ICD) therapy or sustained ventricular arrhythmia, and number of appropriate ICD therapies.

resultsBetween August 28, 2013, and March 19, 2020, 700 patients were enrolled across 40 centers in the United Kingdom. A total of 347 patients were assigned to the PCI+OMT group and 353 to the OMT alone group. The mean age of participants was 69 years; 88% were male; 56% had hypertension; 41% had diabetes; and 53% had a clinical history of myocardial infarction. The median left ventricular ejection fraction was 28%; 53.1% had an implantable defibrillator inserted before randomization or during follow-up. All-cause death or aborted sudden death occurred in 144 patients (41.6%) in the PCI group and 142 patients (40.2%) in the OMT group (hazard ratio, 1.03 [95% CI, 0.82-1.30];

conclusionsPCI was not associated with a reduction in all-cause mortality or aborted sudden death. In patients with ischemic cardiomyopathy, PCI is not beneficial solely for the purpose of reducing potentially fatal ventricular arrhythmias. REGISTRATION: URL: https://www. CLINICALTRIALS: gov; Unique identifier: NCT01920048.

Indexed as

Defibrillators, ImplantableVentricular Dysfunction, LeftAgedArrhythmias, CardiacDeath, Sudden, CardiacFemaleHumansMaleStroke VolumeTreatment OutcomeVentricular Function, Leftarrhythmias, cardiaccardiomyopathiesdeath, sudden, cardiacdefibrillators, implantableheart failuremyocardial revascularizationpercutaneous coronary intervention

Identifiers

PMID37555345
PMCPMC10487377
OpenAlexW4385683767

What OpenQuestion holds

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LicenceCC BY
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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.