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一种用于识别无肌钙蛋白的极低风险急诊科患者策略的多中心验证

Multisite Validation of a Strategy to Identify Very Low Risk Emergency Department Patients Without Troponin.

作者信息

Ashburn Nicklaus P, Snavely Anna C, Villenthi Akalya, Hashemian Tara, Supples Michael W, Mahler Simon A

机构信息

Department of Emergency Medicine, Wake Forest University School of Medicine (WFUSM), Winston-Salem, North Carolina, USA.

Department of Emergency Medicine, Wake Forest University School of Medicine (WFUSM), Winston-Salem, North Carolina, USA; Department of Biostatistics and Data Science, WFUSM, Winston-Salem, North Carolina, USA.

出版信息

JACC Adv. 2025 Jun 18;4(7):101913. doi: 10.1016/j.jacadv.2025.101913.

Abstract

BACKGROUND

Patients with chest pain who are very low risk, defined by a History, Electrocardiogram, Age, and Risk factors (HEAR) score ≤1, may not require troponin testing.

OBJECTIVES

The aim of this study was to determine whether troponin testing is needed in patients with HEAR scores ≤1 in a multisite U.S.

METHODS

We conducted an observational cohort study using the Wake Forest Chest Pain Registry. Patients ≥18 years old with HEART Pathway assessments and high-sensitivity troponin testing were accrued from 5 U.S. emergency departments (November 1, 2020-July 7, 2022). HEAR scores were prospectively completed by the treating clinician for patients with no known coronary artery disease and a nonischemic electrocardiogram. The outcome was 30-day major adverse cardiovascular events (MACE) (death, myocardial infarction [MI], and revascularization). The proportion of patients with HEAR scores ≤1 with MACE within 30 days was determined, and test characteristics were calculated. The net reclassification improvement index for troponin testing among patients with HEAR scores ≤1 was determined.

RESULTS

Among 9,105 patients, 17.2% (1,565/9,105) had a HEAR score ≤1. At 30 days, MACE occurred in 0.7% (11/1,565; 95% CI: 0.4-1.3), with 3 deaths, 8 MIs, and 1 revascularization. The sensitivity and negative predictive value for 30-day MACE in patients with a HEAR score ≤1 were 97.9% (95% CI: 96.2-98.9) and 99.3% (95% CI: 98.7-99.6). Troponin testing correctly reclassified 8 with death, MI, or revascularization. Troponin was elevated among 74 without MACE, yielding a nonsignificant net reclassification improvement index of 0.7% (95% CI: -0.4 to 1.8).

CONCLUSIONS

Patients with no known coronary artery disease, a nonischemic electrocardiogram, and a HEAR score ≤1 had a missed MACE rate <1%. Troponin testing identified additional patients with MACE but did not significantly improve risk stratification accuracy.

摘要

背景

根据病史、心电图、年龄和风险因素(HEAR)评分≤1定义为极低风险的胸痛患者可能不需要进行肌钙蛋白检测。

目的

本研究的目的是确定在美国多中心,HEAR评分≤1的患者是否需要进行肌钙蛋白检测。

方法

我们使用维克森林胸痛登记处进行了一项观察性队列研究。从美国5个急诊科(2020年11月1日至2022年7月7日)招募了年龄≥18岁且进行了心脏通路评估和高敏肌钙蛋白检测的患者。对于无已知冠状动脉疾病且心电图无缺血表现的患者,治疗医生前瞻性地完成HEAR评分。结局为30天主要不良心血管事件(MACE)(死亡、心肌梗死[MI]和血运重建)。确定HEAR评分≤1的患者在30天内发生MACE的比例,并计算检验特征。确定HEAR评分≤1的患者中肌钙蛋白检测的净重新分类改善指数。

结果

在9105例患者中,17.2%(1565/9105)的HEAR评分≤1。在30天时,MACE发生率为0.7%(11/1565;95%CI:0.4-1.3),其中3例死亡,8例MI,1例血运重建。HEAR评分≤1的患者30天MACE的敏感性和阴性预测值分别为97.9%(95%CI:96.2-98.9)和99.3%(95%CI:98.7-99.6)。肌钙蛋白检测正确地将8例有死亡、MI或血运重建的患者重新分类。74例无MACE的患者肌钙蛋白升高,净重新分类改善指数为0.7%,无统计学意义(95%CI:-0.4至1.8)。

结论

无已知冠状动脉疾病、心电图无缺血表现且HEAR评分≤1的患者漏诊MACE率<1%。肌钙蛋白检测识别出了更多有MACE的患者,但未显著提高风险分层的准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b561/12219363/01bf5f960386/ga1.jpg

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