Evidence map›Paper›PMID 26700834›Full record

Trial reportJournal of the American College of Cardiology2015

Complete Versus Lesion-Only Primary PCI: The Randomized Cardiovascular MR CvLPRIT Substudy.

Gerry P McCann, Jamal N Khan, John P Greenwood, Sheraz Nazir, Miles Dalby, Nick Curzen, Simon Hetherington, Damian J Kelly, Daniel J Blackman, Arne Ring and 6 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American College of Cardiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 5 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

26 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Completeness, timing, and guidance of percutaneous coronary intervention for myocardial infarction and multivessel disease: a systematic review and network meta-analysis.EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology · 2025
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  6. Impact of complete revascularisation in relation to left ventricular function in patients with ST-segment elevation myocardial infarction and multivessel disease: a post hoc analysis of the COMPLETE randomised trial.EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology · 2025
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  14. Complete Revascularisation Following Acute MI: A Contemporary Review.Interventional cardiology (London, England) · 2025
    Review
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  18. Acute coronary syndromes.Lancet (London, England) · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Gerry P McCannDepartment of Cardiovascular Sciences, University of Leicester and the National Institute of Health Research (NIHR) Leicester Cardiovascular Biomedical Research Unit, University Hospitals of Leicester National Health Service (NHS) Trust, Glenfield Hospital, Leicester, United Kingdom. Electronic address: gpm12@le.ac.uk.
Jamal N KhanDepartment of Cardiovascular Sciences, University of Leicester and the National Institute of Health Research (NIHR) Leicester Cardiovascular Biomedical Research Unit, University Hospitals of Leicester National Health Service (NHS) Trust, Glenfield Hospital, Leicester, United Kingdom.
John P GreenwoodMultidisciplinary Cardiovascular Research Centre & Division of Cardiovascular and Diabetes Research, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM), University of Leeds, Leeds, United Kingdom.
Sheraz NazirDepartment of Cardiovascular Sciences, University of Leicester and the National Institute of Health Research (NIHR) Leicester Cardiovascular Biomedical Research Unit, University Hospitals of Leicester National Health Service (NHS) Trust, Glenfield Hospital, Leicester, United Kingdom.
Miles DalbyDepartment of Cardiology, Royal Brompton and Harefield Foundation Trust, Harefield Hospital, Middlesex, United Kingdom, and the Cardiovascular Biomedical Research Unit of Royal Brompton and Harefield NHS Foundation Trust and Imperial College London, London, United Kingdom.
Nick CurzenDepartment of Cardiology and Radiology, University Hospital Southampton NHS Foundation Trust and University of Southampton, Southampton, United Kingdom.
Simon HetheringtonDepartment of Cardiology, Kettering General Hospital, Kettering, United Kingdom.
Damian J KellyDepartment of Cardiology, Royal Derby Hospital, Derby, United Kingdom.
Daniel J BlackmanMultidisciplinary Cardiovascular Research Centre & Division of Cardiovascular and Diabetes Research, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM), University of Leeds, Leeds, United Kingdom.
Arne RingLeicester Clinical Trials Unit, University of Leicester, Leicester, United Kingdom; Department of Mathematical Statistics and Actuarial Science, University of the Free State, Bloemfontein, South Africa.
Charles PeeblesDepartment of Cardiology and Radiology, University Hospital Southampton NHS Foundation Trust and University of Southampton, Southampton, United Kingdom.
Joyce WongDepartment of Cardiology, Royal Brompton and Harefield Foundation Trust, Harefield Hospital, Middlesex, United Kingdom, and the Cardiovascular Biomedical Research Unit of Royal Brompton and Harefield NHS Foundation Trust and Imperial College London, London, United Kingdom.
Thiagarajah SasikaranClinical Trials & Evaluation Unit, Royal Brompton & Harefield NHS Foundation Trust and Imperial Clinical Trials Unit, Imperial College London, London, United Kingdom.
Marcus FlatherClinical Trials Unit, Norfolk and Norwich University Hospitals NHS Foundation Trust and Norwich Medical School, University of East Anglia, Norwich, United Kingdom.
Howard SwantonDepartment of Cardiology, Heart Hospital, University College London Hospitals, London, United Kingdom.
Anthony H GershlickDepartment of Cardiovascular Sciences, University of Leicester and the National Institute of Health Research (NIHR) Leicester Cardiovascular Biomedical Research Unit, University Hospitals of Leicester National Health Service (NHS) Trust, Glenfield Hospital, Leicester, United Kingdom.

Funding

Medical Research Council MC_G1002675
6 · The paper itself

Abstract

backgroundComplete revascularization may improve outcomes compared with an infarct-related artery (IRA)-only strategy in patients being treated with primary percutaneous coronary intervention (PPCI) who have multivessel disease presenting with ST-segment elevation myocardial infarction (STEMI). However, there is concern that non-IRA PCI may cause additional non-IRA myocardial infarction (MI).

objectivesThis study sought to determine whether in-hospital complete revascularization was associated with increased total infarct size compared with an IRA-only strategy.

methodsThis multicenter prospective, randomized, open-label, blinded endpoint clinical trial evaluated STEMI patients with multivessel disease having PPCI within 12 h of symptom onset. Patients were randomized to either IRA-only PCI or complete in-hospital revascularization. Contrast-enhanced cardiovascular magnetic resonance (CMR) was performed following PPCI (median day 3) and stress CMR at 9 months. The pre-specified primary endpoint was infarct size on pre-discharge CMR. The study had 80% power to detect a 4% difference in infarct size with 100 patients per group.

resultsOf the 296 patients in the main trial, 205 participated in the CMR substudy, and 203 patients (98 complete revascularization and 105 IRA-only) completed the pre-discharge CMR. The groups were well-matched. Total infarct size (median, interquartile range) was similar to IRA-only revascularization: 13.5% (6.2% to 21.9%) versus complete revascularization, 12.6% (7.2% to 22.6%) of left ventricular mass, p = 0.57 (95% confidence interval for difference in geometric means 0.82 to 1.41). The complete revascularization group had an increase in non-IRA MI on the pre-discharge CMR (22 of 98 vs. 11 of 105, p = 0.02). There was no difference in total infarct size or ischemic burden between treatment groups at follow-up CMR.

conclusionsMultivessel PCI in the setting of STEMI leads to a small increase in CMR-detected non-IRA MI, but total infarct size was not significantly different from an IRA-only revascularization strategy. (Complete Versus Lesion-Only Primary PCI Pilot Study [CvLPRIT]; ISRCTN70913605).

Indexed as

ElectrocardiographyCoronary AngiographyFemaleHumansMagnetic Resonance Imaging, CineMaleMiddle AgedMyocardial InfarctionMyocardiumPercutaneous Coronary InterventionPilot ProjectsProspective StudiesTreatment OutcomeCMRcomplete revascularizationmultivessel diseasePPCISTEMI

Identifiers

PMID26700834
PMCPMC4681843

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Registered trials

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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.