Evidence map›Paper›PMID 42716566›Full record

ArticleOpen heart2026

Does increasing model complexity improve HEART-based chest pain risk stratification? A multicentre development and held-out emergency department validation study.

Hao Wang, Jenna R Williamson, Hunter Scarborough, Devin Sandlin

Abstract readMulticenter StudyValidation Study
In one paragraph

Article in Open heart, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hao WangDepartment of Emergency Medicine, JPS Health Network, Fort Worth, Texas, USA hwang@ies.healthcare.ORCID http://orcid.org/0000-0002-5105-0951
Jenna R WilliamsonAnne Burnett Marion School of Medicine, Texas Christian University, Fort Worth, Texas, USA.
Hunter ScarboroughDepartment of Emergency Medicine, JPS Health Network, Fort Worth, Texas, USA.ORCID http://orcid.org/0009-0005-4808-6258
Devin SandlinDepartment of Emergency Medicine, JPS Health Network, Fort Worth, Texas, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe History, ECG, Age, Risk factors and Troponin (HEART) score is widely used for emergency department (ED) chest pain risk stratification, but its fixed-point structure may not optimally represent relationships between its components and major adverse cardiac events (MACE). We evaluated whether increasingly flexible modelling approaches improve prediction when restricted to the same five HEART components.

methodsWe conducted a retrospective multicentre cohort study of 47 853 adult ED patients with chest pain and documented HEART scores across six EDs from 2021 to 2023. Data from five EDs (n=39 587) were used for model development and one geographically held-out ED (n=8266) was used for validation. The conventional HEART score was compared with categorical cross-validated logistic regression (CVLR) and extreme gradient boosting (XGBoost) for predicting 30-day MACE. Performance was assessed using the area under the receiver operating characteristic (AUROC), the area under the precision-recall curve (AUPRC), the Brier score, paired bootstrap comparisons and clinical performance at comparable-sensitivity operating points.

resultsIn the held-out validation cohort, 267 patients (3.23%) experienced 30-day MACE. AUROCs were similar for HEART (0.855), CVLR (0.857) and XGBoost (0.856; pairwise p>0.05). In contrast, both data-driven models demonstrated significantly higher AUPRC than HEART: CVLR (0.237 vs 0.187; Δ=0.050, p<0.001) and XGBoost (0.244 vs 0.187; Δ=0.057, p<0.001) with no significant difference between CVLR and XGBoost (p=0.305). At comparable-sensitivity operating points, HEART, CVLR and XGBoost classified 63.74%, 59.39% and 61.58% of patients as low risk, respectively, with corresponding low-risk MACE rates of 0.53%, 0.51% and 0.57%.

conclusionsData-driven reweighting of HEART components improved precision-recall performance and risk ranking compared with fixed HEART scoring. However, XGBoost provided no incremental benefit over categorical CVLR, and neither approach expanded low-risk classification at comparable sensitivity.

Indexed as

Chest PainEmergency Service, HospitalAgedElectrocardiographyFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisReproducibility of ResultsRetrospective StudiesRisk AssessmentRisk FactorsAcute Coronary SyndromeChest PainTranslational Medical Research

Identifiers

PMID42716566
PMCPMC13560967

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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.