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低风险人群急诊科单次肌钙蛋白检测的应用及结果

Utilization and outcomes of single-troponin discharge from the emergency department in a low-risk population.

作者信息

Zhou Zhengqiu, Heier Kory, Spindel Jeffrey F, Harris Austin, Slade Emily, McCowan Weston, Samadi Dealla, Kim Joshua, Moore James D, Stearley Seth T, Gupta Vedant

机构信息

Department of Emergency Medicine, HCA Florida North Florida, USA.

Department of Graduate Medical Education, Gainesville, FL, USA.

出版信息

Glob Cardiol Sci Pract. 2025 Feb 28;2025(1):e202508. doi: 10.21542/gcsp.2025.8.

Abstract

There is emerging data supporting rapid triage of low-risk chest pain patients to help facilitate Emergency Department (ED) throughput. We assessed an algorithm for accelerated rule-out of acute coronary syndrome in low-risk patients with an undetectable initial high sensitivity cardiac troponin (hs-cTn assays; Roche Diagnostics) in a real-world clinical setting. All adults presenting with chief complaint of non-traumatic chest pain to our tertiary care ED with HEART score ≤3 with at least one hs-cTn and EKG obtained were included in our study. Data and outcomes were compared three months before and after implementation of our updated Acute Chest Pain Optimal Care Pathway that allowed discharge of patients with an initial troponin below detectable range (<6ng/L). The primary outcome was acute coronary syndrome at presentation or major adverse cardiovascular events within 30 days. Secondary outcomes included ED length of stay, cardiology consultations, and hospital admissions. Of the 229 patients fitting our criteria with a low-risk heart score (≤3) and undetectable initial troponin, zero patients were diagnosed with ACS and one major adverse cardiac event occurred post-implementation (0.8%). There were no significant differences in median ED length of stay pre- (4.5 h, IQR 3.8-6.6) versus post-implementation (4.6 h, IQR 3.5-5.7;  = 0.448), number of cardiology consults ( = 0.305) and hospital admissions ( = 0.261). However, protocol adherence was poor (50%). In a subgroup analysis post-implementation, patients whose care aligned with the algorithm ( = 64, 50.0%) had significantly shorter ED stays (median 4.1 h, IQR 3.3-4.9 vs 5.2 h, IQR 4.4-6.9, ¡0.001), fewer admissions ( = 0.001) but not fewer cardiology consults ( = 0.440). Our study supports current data regarding the safety of accelerated rule out strategy with hs-cTn. However, our conclusions are limited due to its small sample size and retrospective design.

摘要

越来越多的数据支持对低风险胸痛患者进行快速分诊,以帮助提高急诊科(ED)的诊疗效率。我们在真实临床环境中评估了一种算法,用于在初始高敏心肌肌钙蛋白(hs-cTn检测;罗氏诊断)检测不到的低风险患者中加速排除急性冠状动脉综合征。所有因非创伤性胸痛为主诉前来我们三级医疗急诊科就诊、HEART评分≤3且至少进行了一次hs-cTn检测和心电图检查的成年人纳入我们的研究。在实施我们更新的急性胸痛最佳护理路径(允许初始肌钙蛋白低于可检测范围[<6ng/L]的患者出院)前后三个月,对数据和结果进行比较。主要结局是就诊时的急性冠状动脉综合征或30天内的主要不良心血管事件。次要结局包括急诊科住院时间、心脏病学会诊和住院情况。在符合我们标准的229例低风险心脏评分(≤3)且初始肌钙蛋白检测不到的患者中,零例患者被诊断为急性冠状动脉综合征,实施后发生了1例主要不良心脏事件(0.8%)。实施前(4.5小时,IQR 3.8 - 6.6)与实施后(4.6小时,IQR 3.5 - 5.7;P = 0.448)的急诊科住院时间中位数、心脏病学会诊次数(P = 0.305)和住院情况(P = 0.261)均无显著差异。然而,方案依从性较差(50%)。在实施后的亚组分析中,护理符合该算法的患者(n = 64,50.0%)的急诊科住院时间显著更短(中位数4.1小时,IQR 3.3 - 4.9对比5.2小时,IQR 4.4 - 6.9,P<0.001),住院次数更少(P = 0.001),但心脏病学会诊次数没有减少(P = 0.440)。我们的研究支持目前关于使用hs-cTn进行加速排除策略安全性的数据。然而,由于样本量小和回顾性设计,我们的结论有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/12085921/28dd6f96b322/gcsp-2025-1-e202508-g001.jpg

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