Evidence map›Paper›PMID 32894227›Full record

Trial reportEuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology2021

Culprit lesion location and outcomes in patients with multivessel disease and infarct-related cardiogenic shock: a core laboratory analysis of the CULPRIT-SHOCK trial.

Marie Hauguel-Moreau, Olvier Barthélémy, Serdar Farhan, Kurt Huber, Stéphanie Rouanet, Michel Zeitouni, Paul Guedeney, Georges Hage, Eric Vicaut, Uwe Zeymer and 3 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01927549 (Prospective Randomized Multicenter Study Comparing Immediate Multivessel Revascularization by PCI Versus Culprit Lesion PCI With Staged Non-culprit Lesion Revascularization in Patients With Acute Myocardial Infarction Complicated by Cardiogenic Shock), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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.

NCT01927549 phase4completednot on this map

Prospective Randomized Multicenter Study Comparing Immediate Multivessel Revascularization by PCI Versus Culprit Lesion PCI With Staged Non-culprit Lesion Revascularization in Patients With Acute Myocardial Infarction Complicated by Cardiogenic Shock

TypeinterventionalSponsorUniversity of LuebeckRan2013 to 2017Enrolled706ConditionsCardiogenic Shock, Acute Myocardial Infarction, ComplicationsArmsImmediate multivessel PCI, Culprit Lesion only PCI
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Observational
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

13 authors.

Marie Hauguel-MoreauSorbonne Université, ACTION Study Group, INSERM UMRS 1166, Institut de Cardiologie (AP-HP), Paris, France.
Olvier Barthélémy
Serdar Farhan
Kurt Huber
Stéphanie Rouanet
Michel Zeitouni
Paul Guedeney
Georges Hage
Eric Vicaut
Uwe Zeymer
Steffen Desch
Holger Thiele
Gilles Montalescot

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCritical culprit lesion locations (CCLL) such as left main (LM) and proximal left anterior descending (LAD) are associated with worse clinical outcome in myocardial infarction without cardiogenic shock (CS).

aimsWe aimed to assess whether CCLL identify a subgroup of patients with poorer prognosis when presenting with CS.

methodsIn the CULPRIT-SHOCK trial, a core laboratory reviewed all coronary angiograms to identify CCLL. A CCLL was defined as a culprit lesion with a >70% diameter stenosis of the LM, LM equivalent (>70% diameter stenosis of both proximal LAD and proximal circumflex), proximal LAD or last remaining vessel. We evaluated the primary study endpoint of the CULPRIT-SHOCK trial according to CCLL.

resultsA total of 269 (43%) out of 626 patients eligible for this analysis had a CCLL. Death or renal replacement therapy within 30 days, death within 30 days and death within one year were significantly higher in the CCLL than in the non-CCLL group (58.4% vs 43.4%, p<0.001, 55.8% vs 39.5%, p<0.001, 61.0% vs 44.5%, p<0.001, respectively). This was consistent after adjustment for baseline and angiographic characteristics. No interaction with the randomisation group (culprit lesion-only or immediate multivessel PCI) was found.

conclusionsCCLL is frequent in CS and independently associated with worse clinical outcomes irrespective of the revascularisation strategy.

trial registrationwww.clinicaltrials.gov NCT01927549.

Indexed as

Myocardial InfarctionPercutaneous Coronary InterventionCoronary AngiographyHumansLaboratoriesShock, CardiogenicTreatment Outcome

Identifiers

PMID32894227
PMCPMC9725066

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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.