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对 preHEART 评分进行外部验证,并与当前临床风险评分进行比较,以评估疑似 NSTE-ACS 患者的院前风险。

External validation of the preHEART score and comparison with current clinical risk scores for prehospital risk assessment in patients with suspected NSTE-ACS.

机构信息

Department of Cardiology, Catharina Hospital, Eindhoven, The Netherlands.

GGD Brabant-Zuidoost, Eindhoven, The Netherlands.

出版信息

Emerg Med J. 2024 Sep 25;41(10):610-616. doi: 10.1136/emermed-2023-213866.

Abstract

BACKGROUND

Emergency Medical Services (EMS) studies have shown that prehospital risk stratification and triage decisions in patients with suspected non-ST-elevation acute coronary syndrome (NSTE-ACS) can be improved using clinical risk scores with point-of-care (POC) troponin. In current EMS studies, three different clinical risk scores are used in patients suspected of NSTE-ACS: the prehospital History, ECG, Age, Risk and Troponin (preHEART) score, History, ECG, Age, Risk and Troponin (HEART) score and Troponin-only Manchester Acute Coronary Syndromes (T-MACS). The preHEART score lacks external validation and there exists no prospective comparative analysis of the different risk scores within the prehospital setting. The aim of this analysis is to externally validate the preHEART score and compare the diagnostic performance of the these three clinical risk scores and POC-troponin.

METHODS

Prespecified analysis from a prospective, multicentre, cohort study in patients with suspected NSTE-ACS who were transported to an ED between April 2021 and December 2022 in the Netherlands. Risk stratification is performed by EMS personnel using preHEART, HEART, T-MACS and POC-troponin. The primary end point was the hospital diagnosis of NSTE-ACS. The diagnostic performance was expressed as area under the receiver operating characteristic (AUROC), sensitivity, specificity, negative predictive value (NPV) and positive predictive value (PPV).

RESULTS

A total of 823 patients were included for external validation of the preHEART score, final hospital diagnosis of NSTE-ACS was made in 29% (n=235). The preHEART score classified 27% as low risk, with a sensitivity of 92.8% (95% CI 88.7 to 95.7) and NPV of 92.3% (95% CI 88.3 to 95.1). The preHEART classified 9% of the patients as high risk, with a specificity of 98.5% (95% CI 97.1 to 99.3) and PPV of 87.7% (95% CI 78.3 to 93.4). Data for comparing clinical risk scores and POC-troponin were available in 316 patients. No difference was found between the preHEART score and HEART score (AUROC 0.83 (95% CI 0.78 to 0.87) vs AUROC 0.80 (95% CI 0.74 to 0.85), p=0.19), and both were superior compared with T-MACS (AUROC 0.72 (95% CI 0.66 to 0.79), p≤0.001 and p=0.03, respectively) and POC-troponin measurement alone (AUROC 0.71 (95% CI 0.64 to 0.78), p<0.001 and p=0.01, respectively).

CONCLUSION

On external validation, the preHEART demonstrates good overall diagnostic performance as a prehospital risk stratification tool. Both the preHEART and HEART scores have better overall diagnostic performance compared with T-MACS and sole POC-troponin measurement. These data support the implementation of clinical risk scores in prehospital clinical pathways.

TRIAL REGISTRATION NUMBER

NCT05243485.

摘要

背景

紧急医疗服务(EMS)研究表明,在疑似非 ST 段抬高型急性冠状动脉综合征(NSTE-ACS)患者中,使用床旁肌钙蛋白的临床风险评分可以改善院前风险分层和分诊决策。在当前的 EMS 研究中,在疑似 NSTE-ACS 的患者中使用了三种不同的临床风险评分:院前病史、心电图、年龄、风险和肌钙蛋白(preHEART)评分、病史、心电图、年龄、风险和肌钙蛋白(HEART)评分和肌钙蛋白仅曼彻斯特急性冠状动脉综合征(T-MACS)。preHEART 评分缺乏外部验证,并且在院前环境中尚未对不同风险评分进行前瞻性比较分析。本分析旨在对外科验证 preHEART 评分,并比较这些三种临床风险评分和床旁肌钙蛋白的诊断性能。

方法

这是一项在荷兰 2021 年 4 月至 2022 年 12 月期间疑似 NSTE-ACS 患者被送往急诊室的前瞻性、多中心队列研究的预设分析。EMS 人员使用 preHEART、HEART、T-MACS 和床旁肌钙蛋白进行风险分层。主要终点是医院诊断为 NSTE-ACS。诊断性能表示为接收者操作特征(AUROC)曲线下面积、灵敏度、特异性、阴性预测值(NPV)和阳性预测值(PPV)。

结果

共纳入 823 例患者对 preHEART 评分进行外部验证,最终医院诊断为 NSTE-ACS 的患者占 29%(n=235)。preHEART 评分将 27%的患者归类为低风险,其灵敏度为 92.8%(95%CI 88.7 至 95.7),NPV 为 92.3%(95%CI 88.3 至 95.1)。preHEART 将 9%的患者归类为高风险,特异性为 98.5%(95%CI 97.1 至 99.3),PPV 为 87.7%(95%CI 78.3 至 93.4)。有 316 例患者的数据可用于比较临床风险评分和床旁肌钙蛋白。preHEART 评分与 HEART 评分之间没有差异(AUROC 0.83(95%CI 0.78 至 0.87)与 AUROC 0.80(95%CI 0.74 至 0.85),p=0.19),并且与 T-MACS(AUROC 0.72(95%CI 0.66 至 0.79),p≤0.001 和 p=0.03,分别)和单独的床旁肌钙蛋白测量(AUROC 0.71(95%CI 0.64 至 0.78),p<0.001 和 p=0.01,分别)相比,均具有更好的总体诊断性能。

结论

在外部验证中,preHEART 作为一种院前风险分层工具,显示出良好的总体诊断性能。与 T-MACS 和单独的床旁肌钙蛋白测量相比,preHEART 和 HEART 评分的总体诊断性能均更好。这些数据支持在院前临床路径中实施临床风险评分。

试验注册

NCT05243485。

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