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基于 2020 年欧洲心脏病学会指南的高敏心肌肌钙蛋白检测与非侵入性检测、临床结局和医疗质量结局的一致性。

Agreement among high-sensitivity cardiac troponin assays and non-invasive testing, clinical outcomes, and quality-of-care outcomes based on the 2020 European Society of Cardiology Guidelines.

机构信息

Cardiovascular Imaging Research Center, Massachusetts General Hospital, Harvard Medical School, 165 Cambridge St Suite 400, Boston, MA 02114, USA.

Heart and Vascular Center, Semmelweis University, 9-11 Gaál József Street, Budapest 1122, Hungary.

出版信息

Eur Heart J Acute Cardiovasc Care. 2024 Feb 9;13(1):15-23. doi: 10.1093/ehjacc/zuad146.

DOI:10.1093/ehjacc/zuad146
PMID:38001050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10853690/
Abstract

AIMS

Quality-of-care and safety of patients with suspected acute coronary syndrome (ACS) would benefit if management was independent of which high-sensitivity cardiac troponin (hs-cTn) assay was used for risk stratification. We aimed to determine the concordance of hs-cTn assays to risk-stratify patients with suspected ACS according to the European Society of Cardiology (ESC) 2020 Guidelines.

METHODS AND RESULTS

Blood samples were obtained at arrival and at 2 h from patients with suspected ACS using four hs-cTn assays. The patients were classified into rule-out/observe/rule-in strata based on the ESC 2020 Guidelines. Concordance was determined among the assays for rule-out/observe/rule-in strata. The prevalences of significant underlying disease (≥50% stenosis on coronary computed tomography or inducible myocardial ischaemia on stress testing) and adjudicated ACS, plus quality-of-care outcomes, were compared. Among 238 patients (52.7 ± 8.0 years; 40.3% female), the overall concordance across assays to classify patients into rule-out/observe/rule-in strata was 74.0% (176/238). Platforms significantly differed for rule-out (89.9 vs. 76.5 vs. 78.6 vs. 86.6%, P < 0.001) and observe strata (6.7 vs. 20.6 vs. 17.7 vs. 9.2%, P < 0.001), but not for rule-in strata (3.4 vs. 2.9 vs. 3.8 vs. 4.2%, P = 0.62). Among patients in ruled-out strata, 19.1-21.6% had significant underlying disease and 3.3-4.2% had ACS. The predicted disposition of patients and cost-of-care differed across the assays (all P < 0.001). When compared with observed strata, conventional troponin-based management and predicted quality-of-care outcomes significantly improved with hs-cTn-based strategies (direct discharge: 21.0 vs. 80.3-90.8%; cost-of-care: $3889 ± 4833 vs. $2578 ± 2896-2894 ± 4371, all P < 0.001).

CONCLUSION

Among individuals with suspected ACS, patient management may differ depending on which hs-cTn assay is utilized. More data are needed regarding the implications of inter-assay differences.

TRAIL REGISTRATION

NCT01084239.

摘要

目的

如果管理独立于用于风险分层的高敏心肌肌钙蛋白(hs-cTn)检测方法,则疑似急性冠状动脉综合征(ACS)患者的治疗质量和安全性将得到改善。本研究旨在根据 2020 年欧洲心脏病学会(ESC)指南确定 hs-cTn 检测方法在风险分层方面对疑似 ACS 患者的一致性。

方法和结果

使用四种 hs-cTn 检测方法在疑似 ACS 患者到达时和 2 小时时采集血样。根据 ESC 2020 指南,患者被分为排除/观察/确诊分层。确定了检测方法在排除/观察/确诊分层中的一致性。比较了有意义的基础疾病(冠状动脉计算机断层扫描≥50%狭窄或应激试验诱导性心肌缺血)和确定的 ACS 的发生率以及治疗质量结果。在 238 名患者(52.7±8.0 岁;40.3%为女性)中,检测方法在将患者分为排除/观察/确诊分层中的总体一致性为 74.0%(176/238)。平台在排除(89.9%比 76.5%比 78.6%比 86.6%,P<0.001)和观察(6.7%比 20.6%比 17.7%比 9.2%,P<0.001)分层方面差异显著,但在确诊分层方面差异不显著(3.4%比 2.9%比 3.8%比 4.2%,P=0.62)。在排除分层的患者中,19.1%-21.6%有明显的基础疾病,3.3%-4.2%有 ACS。不同检测方法之间患者的预测处理方式和治疗质量结果存在差异(均 P<0.001)。与观察分层相比,基于 hs-cTn 的策略显著改善了传统肌钙蛋白管理和预测的治疗质量结果(直接出院:21.0%比 80.3%-90.8%;治疗费用:$3889±4833 比 $2578±2896-2894±4371,均 P<0.001)。

结论

在疑似 ACS 患者中,患者的管理可能取决于使用的 hs-cTn 检测方法。需要更多关于检测方法差异影响的数据。

临床试验注册

NCT01084239。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da06/10853844/18be29fcf8b2/zuad146_ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da06/10853844/18be29fcf8b2/zuad146_ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da06/10853844/18be29fcf8b2/zuad146_ga1.jpg

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