Evidence map›Paper›PMID 37167775›Full record

Observational studyJournal of critical care2023

Major adverse cardiovascular events (MACE) in patients with severe COVID-19 registered in the ISARIC WHO clinical characterization protocol: A prospective, multinational, observational study.

Luis Felipe Reyes, Esteban Garcia-Gallo, Srinivas Murthy, Yuli V Fuentes, Cristian C Serrano, Elsa D Ibáñez-Prada, James Lee, Amanda Rojek, Barbara Wanjiru Citarella, Bronner P Gonçalves and 10 more

Open access · hybridAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Journal of critical care, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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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

20 authors at 6 institutions in 5 countries.

Luis Felipe ReyesUniversidad de La Sabana, Chía, Colombia; Clínica Universidad de La Sabana, Cundinamarca, Colombia; Pandemic Sciences Institute, University of Oxford, Oxford, United Kingdom. Electronic address: luis.reyes5@unisabana.edu.co.
Esteban Garcia-GalloUniversidad de La Sabana, Chía, Colombia; Pandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Srinivas MurthyDepartment of Pediatrics, University of British Columbia, Vancouver, Canada.
Yuli V FuentesUniversidad de La Sabana, Chía, Colombia.
Cristian C SerranoUniversidad de La Sabana, Chía, Colombia; Clínica Universidad de La Sabana, Cundinamarca, Colombia.
Elsa D Ibáñez-PradaUniversidad de La Sabana, Chía, Colombia; Clínica Universidad de La Sabana, Cundinamarca, Colombia.
James LeePandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Amanda RojekPandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Barbara Wanjiru CitarellaPandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Bronner P GonçalvesPandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Jake DunningPandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Indrek RätsepPandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Andre Emilio Viñan-GarcesUniversidad de La Sabana, Chía, Colombia.
Christiana KartsonakiPandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Jordi RelloClinical Research/Epidemiology in Pneumonia & Sepsis (CRIPS), Vall d'Hebron Institute of Research (VHIR), Barcelona, Spain; Centro de Investigación Biomédica En Red de Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, Madrid, Spain.
Ignacio Martin-LoechesDepartment of Clinical Medicine, St James's Hospital, Multidisciplinary Intensive Care Research Organization (MICRO), Dublin, Ireland.
Manu Shankar-HariCentre for Inflammation Research, University of Edinburgh; 47 Little France Crescent, Edinburgh, Scotland, United Kingdom.
Piero L OlliaroPandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Laura MersonPandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
ISARIC Characterisation Group
University of Oxford · GBUniversidad de La Sabana · COSt. James's Hospital · IEUniversity of British Columbia · CAUniversity of Edinburgh · GBVall d'Hebron Institut de Recerca · ES

Funding

Cancer Research UK C18616/A25153Department of Health 200907Department of Health 200927Department of Health CO-CIN-01Department of Health ISBRC-1215-20013Department of Health NIHR201385Medical Research Council MC_PC_19059Wellcome Trust 215091/Z/18/ZWellcome Trust 220757/Z/20/ZWellcome Trust 222410/Z/21/ZWellcome Trust 225288/Z/22/Z
6 · The paper itself

Abstract

purposeTo determine its cumulative incidence, identify the risk factors associated with Major Adverse Cardiovascular Events (MACE) development, and its impact clinical outcomes. MATERIALS AND

methodsThis multinational, multicentre, prospective cohort study from the ISARIC database. We used bivariate and multivariate logistic regressions to explore the risk factors related to MACE development and determine its impact on 28-day and 90-day mortality.

results49,479 patients were included. Most were male 63.5% (31,441/49,479) and from high-income countries (84.4% [42,774/49,479]); however, >6000 patients were registered in low-and-middle-income countries. MACE cumulative incidence during their hospital stay was 17.8% (8829/49,479). The main risk factors independently associated with the development of MACE were older age, chronic kidney disease or cardiovascular disease, smoking history, and requirement of vasopressors or invasive mechanical ventilation at admission. The overall 28-day and 90-day mortality were higher among patients who developed MACE than those who did not (63.1% [5573/8829] vs. 35.6% [14,487/40,650] p < 0.001; 69.9% [6169/8829] vs. 37.8% [15,372/40,650] p < 0.001, respectively). After adjusting for confounders, MACE remained independently associated with higher 28-day and 90-day mortality (Odds Ratio [95% CI], 1.36 [1.33-1.39];1.47 [1.43-1.50], respectively).

conclusionsPatients with severe COVID-19 frequently develop MACE, which is independently associated with worse clinical outcomes.

Indexed as

Cardiovascular DiseasesCOVID-19FemaleHumansMaleProspective StudiesRisk FactorsWorld Health OrganizationComplicationsCOVID-19Major adverse cardiovascular events (MACE)Mortality

Identifiers

PMID37167775
PMCPMC10167415
OpenAlexW4376225657

What OpenQuestion holds

Textmetadata
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.