Evidence map›Paper›PMID 25766941›Full record

Trial reportJournal of the American College of Cardiology2015

Randomized trial of complete versus lesion-only revascularization in patients undergoing primary percutaneous coronary intervention for STEMI and multivessel disease: the CvLPRIT trial.

Anthony H Gershlick, Jamal Nasir Khan, Damian J Kelly, John P Greenwood, Thiagarajah Sasikaran, Nick Curzen, Daniel J Blackman, Miles Dalby, Kathryn L Fairbrother, Winston Banya and 9 more

6 registry-linked trialsAbstract readComparative StudyMulticenter 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. It is linked to 6 registered trials, which are not on this map. Cited by 270 papers, 22 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
270citing papers in PubMed, 22 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.

NCT02637440 phase3unknown statusnot on this map

Multi Centre Open Label Randomised Controlled Parallel-group Three Arm Trial To Compare The Use Of Fractional Flow Reserve (FFR) Guided and Angiographically Guided Revascularization To The Treatment Of Infarct Related Artery Only In Patients With STEMI And Multivessel Disease

TypeinterventionalSponsorUniversity of LimerickRan2015 to 2019Enrolled560ConditionsMultivessel Coronary Artery Disease, STEMI, FFR Guided PCIArmsFFR guided PCI, Angio guided PCI
NCT03135275 nacompletednot on this mapstarted 2016, after this paper: background citation

MULTivessel Immediate Versus STAged RevaScularization in Acute Myocardial Infarction - The MULTISTARS AMI Trial

TypeinterventionalSponsorUniversity of ZurichRan2016 to 2023Enrolled840ConditionsST-elevation Myocardial Infarction, Multivessel Coronary DiseaseArmsStaged complete PCI, Immediate complete PCI, Synergy™ stent
NCT03138473 completednot on this mapstarted 2018, after this paper: background citation

Impact of Residual Syntax Score and Syntax Revascularization Index on Outcomes of Acute Coronary Syndrome Patients With Multi-Vessel Disease

TypeobservationalSponsorAssiut UniversityRan2018 to 2021Enrolled149ConditionsSTEMI - ST Elevation Myocardial Infarction, Multi Vessel Coronary Artery Disease, NSTEMI - Non-ST Segment Elevation MI, ACS - Acute Coronary SyndromeArmsResidual SYNTAX Score, SYNTAX Revascularization Index
NCT03621501 naactive not recruitingnot on this mapstarted 2018, after this paper: background citation

Percutaneous Complete Revascularization Strategies Using Sirolimus Eluting Biodegradable Polymer Coated Stents in Patients Presenting With Acute Coronary Syndrome and Multivessel Disease

TypeinterventionalSponsorErasmus Medical CenterRan2018 to 2026Enrolled1,525ConditionsAcute Coronary SyndromeArmsPercutaneous coronary intervention
NCT04743154 nacompletednot on this mapstarted 2018, after this paper: background citation

In-hospital Versus After-discharge Complete Revascularization in STEMI Patients With Multivessel Disease.

TypeinterventionalSponsorHospital General Universitario de ValenciaRan2018 to 2022Enrolled250ConditionsSTEMI - ST Elevation Myocardial Infarction, Multivessel Coronary Artery DiseaseArmsIn-hospital nonculprit-lesions percutaneous coronary intervention (PCI), After-discharge nonculprit-lesions percutaneous coronary intervention (PCI)
NCT05231226 naunknown statusnot on this mapstarted 2022, after this paper: background citation

Timing of Complete Revascularization in Patients With ST-segment Elevation Myocardial Infarction And Multivessel Disease-A Multi-center Randomized Controlled Trial

TypeinterventionalSponsorBeijing Anzhen HospitalRan2022 to 2024Enrolled426ConditionsST-elevation Myocardial Infarction, Multivessel Coronary DiseaseArmsImmediately CR, Staged (within 45 days) CR
3 · Its place in the literature

Who cites it

270 citing papers in PubMed, 22 syntheses or guidelines pooled it.

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  3. 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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  14. Multivessel versus culprit-only PCI in STEMI patients with multivessel disease: meta-analysis of randomized controlled trials.Clinical research in cardiology : official journal of the German Cardiac Society · 2020
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210 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Anthony H GershlickDepartment of Cardiovascular Sciences, University of Leicester and National Institute of Health Research Leicester Cardiovascular Biomedical Research Unit, Glenfield Hospital, Leicester, United Kingdom. Electronic address: agershlick@aol.com.
Jamal Nasir KhanDepartment of Cardiovascular Sciences, University of Leicester and National Institute of Health Research Leicester Cardiovascular Biomedical Research Unit, Glenfield Hospital, Leicester, United Kingdom.
Damian J KellyDepartment of Cardiology, Royal Derby Hospital, Derby, United Kingdom.
John P GreenwoodMultidisciplinary Cardiovascular Research Centre and the Division of Cardiovascular and Diabetes Research, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, United Kingdom; Department of Cardiology, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Thiagarajah SasikaranClinical Trials and Evaluation Unit, Royal Brompton & Harefield NHS Foundation Trust and Imperial College London, London, United Kingdom.
Nick CurzenUniversity Hospital Southampton and Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Daniel J BlackmanDepartment of Cardiology, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Miles DalbyRoyal Brompton & Harefield NHS Trust, London, United Kingdom.
Kathryn L FairbrotherUniversity Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Winston BanyaNational Institute for Health Research Cardiovascular Biomedical Research Unit, Royal Brompton & Harefield NHS Trust, London, United Kingdom.
Duolao WangDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Marcus FlatherNorfolk and Norwich University Hospitals NHS Foundation Trust and Norwich Medical School, University of East Anglia Norwich, United Kingdom.
Simon L HetheringtonKettering General Hospital, Kettering, United Kingdom.
Andrew D KelionOxford Heart Centre, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, United Kingdom.
Suneel TalwarRoyal Bournemouth Hospital, Bournemouth, United Kingdom.
Mark GunningRoyal Stoke University Hospital, University Hospitals of North Midlands NHS Trust, Stoke-on-Trent, Staffordshire, United Kingdom.
Roger HallNorfolk and Norwich University Hospitals NHS Foundation Trust and Norwich Medical School, University of East Anglia Norwich, United Kingdom.
Howard SwantonThe Heart Hospital, University College London Hospitals, London, United Kingdom.
Gerry P McCannDepartment of Cardiovascular Sciences, University of Leicester and National Institute of Health Research Leicester Cardiovascular Biomedical Research Unit, Glenfield Hospital, Leicester, United Kingdom.

Funding

British Heart Foundation SP/10/001/28194Department of Health CDF-2014-07-045Medical Research Council MC_G1002675
6 · The paper itself

Abstract

backgroundThe optimal management of patients found to have multivessel disease while undergoing primary percutaneous coronary intervention (P-PCI) for ST-segment elevation myocardial infarction is uncertain.

objectivesCvLPRIT (Complete versus Lesion-only Primary PCI trial) is a U.K. open-label randomized study comparing complete revascularization at index admission with treatment of the infarct-related artery (IRA) only.

methodsAfter they provided verbal assent and underwent coronary angiography, 296 patients in 7 U.K. centers were randomized through an interactive voice-response program to either in-hospital complete revascularization (n = 150) or IRA-only revascularization (n = 146). Complete revascularization was performed either at the time of P-PCI or before hospital discharge. Randomization was stratified by infarct location (anterior/nonanterior) and symptom onset (≤ 3 h or >3 h). The primary endpoint was a composite of all-cause death, recurrent myocardial infarction (MI), heart failure, and ischemia-driven revascularization within 12 months.

resultsPatient groups were well matched for baseline clinical characteristics. The primary endpoint occurred in 10.0% of the complete revascularization group versus 21.2% in the IRA-only revascularization group (hazard ratio: 0.45; 95% confidence interval: 0.24 to 0.84; p = 0.009). A trend toward benefit was seen early after complete revascularization (p = 0.055 at 30 days). Although there was no significant reduction in death or MI, a nonsignificant reduction in all primary endpoint components was seen. There was no reduction in ischemic burden on myocardial perfusion scintigraphy or in the safety endpoints of major bleeding, contrast-induced nephropathy, or stroke between the groups.

conclusionsIn patients presenting for P-PCI with multivessel disease, index admission complete revascularization significantly lowered the rate of the composite primary endpoint at 12 months compared with treating only the IRA. In such patients, inpatient total revascularization may be considered, but larger clinical trials are required to confirm this result and specifically address whether this strategy is associated with improved survival.

Indexed as

AgedCoronary AngiographyFemaleHeart FailureHumansKaplan-Meier EstimateMaleMiddle AgedMyocardial InfarctionMyocardial RevascularizationPercutaneous Coronary Interventioncomplete revascularizationnon-infarct-related lesionprimary percutaneous coronary angioplasty

Identifiers

PMID25766941
PMCPMC4359051

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.