Evidence map›Paper›PMID 35166427›Full record

ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine2022

Major adverse cardiac event rates in moderate-risk patients: Does prior coronary disease matter?

Henderson D McGinnis, Nicklaus P Ashburn, Brennan E Paradee, James C O'Neill, Anna C Snavely, Jason P Stopyra, Simon A Mahler

Abstract read
In one paragraph

Article in Academic emergency medicine : official journal of the Society for Academic Emergency Medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

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

1 citing paper in PubMed.

  1. Major adverse cardiac event rates in moderate-risk patients: Does prior coronary disease matter?Academic emergency medicine : official journal of the Society for Academic Emergency Medicine · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Henderson D McGinnisDepartment of Emergency Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0003-4684-4455
Nicklaus P AshburnDepartment of Emergency Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0002-3466-8813
Brennan E ParadeeDepartment of Emergency Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
James C O'NeillDepartment of Emergency Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Anna C SnavelyDepartment of Biostatistics and Data Science, Department of Emergency Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Jason P StopyraDepartment of Emergency Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0001-7457-3969
Simon A MahlerDepartment of Emergency Medicine, Department of Implementation Science, Department of Epidemiology and Prevention, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0003-2199-4078

Funding

CVD Epidemiology Training ProgramT32HL076132 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DAVID McLeod HERRINGTON · 2004 to 2026
$8.4M
NHLBI NIH HHS L30 HL120008NHLBI NIH HHS T32 HL076132
6 · The paper itself

Abstract

backgroundDespite negative troponins and nonischemic electrocardiograms (ECGs), patients at moderate risk for acute coronary syndrome (ACS) are frequently admitted. The objective of this study was to describe the major adverse cardiac event (MACE) rate in moderate-risk patients and how it differs based on history of coronary artery disease (CAD).

methodsA secondary analysis of the HEART Pathway implementation study was conducted. This prospective interrupted time-series study accrued adults with possible ACS from three sites (November 2013-January 2016). This analysis excluded low-risk patients determined by emergency providers' HEART Pathway assessments. Non-low-risk patients were further classified as high risk, based on elevated troponin measures or ischemic ECG findings or as moderate risk, based on HEAR score ≥ 4, negative troponin measures, and a nonischemic ECG. Moderate-risk patients were then stratified by the presence or absence of prior CAD (MI, revascularization, or ≥70% coronary stenosis). MACE (death, myocardial infarction, or revascularization) at 30 days was determined from health records, insurance claims, and death index data. MACE rates were compared among groups using a chi-square test and likelihood ratios (LRs) were calculated.

resultsAmong 4,550 patients with HEART Pathway assessments, 24.8% (1,130/4,550) were high risk and 37.7% (1715/4550) were moderate risk. MACE at 30 days occurred in 3.1% (53/1,715; 95% confidence interval [CI] = 2.3% to 4.0%) of moderate-risk patients. Among moderate-risk patients, MACE occurred in 7.1% (36/508, 95% CI = 5.1% to 9.8%) of patients with known CAD versus 1.4% (17/1,207, 95% CI = 0.9% to 2.3%) in patients without known prior CAD (p < 0.0001). The negative LR for 30-day MACE among moderate-risk patients without prior CAD was 0.08 (95% CI = 0.05 to 0.12).

conclusionMACE rates at 30 days were low among moderate-risk patients but were significantly higher among those with prior CAD.

Indexed as

Acute Coronary SyndromeCoronary Artery DiseaseAdultChest PainElectrocardiographyHumansProspective StudiesRisk AssessmentRisk FactorsTroponinTroponinacute coronary syndromechest painheart diseaseHEART Pathwayrisk stratification

Identifiers

PMID35166427
PMCPMC9232933

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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.