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一项针对疑似急性冠脉综合征的1小时肌钙蛋白T检测方案的随机试验:急诊科高敏肌钙蛋白T快速评估可能的急性冠脉综合征(RAPID-TnT)研究的设计

A randomized trial of a 1-hour troponin T protocol in suspected acute coronary syndromes: Design of the Rapid Assessment of Possible ACS In the emergency Department with high sensitivity Troponin T (RAPID-TnT) study.

作者信息

Papendick Cynthia, Blyth Andrew, Seshadri Anil, Edmonds Michael J R, Briffa Tom, Cullen Louise, Quinn Stephen, Karnon Jon, Chuang Anthony, Nelson Adam J, Horsfall Matthew, Morton Erin, Chew Derek P

机构信息

School of Medicine, University of Adelaide, Adelaide, Australia.

South Australian Department of Health, Adelaide, Australia.

出版信息

Am Heart J. 2017 Aug;190:25-33. doi: 10.1016/j.ahj.2017.05.004. Epub 2017 May 18.

Abstract

BACKGROUND

Protocols incorporating high-sensitivity troponin to guide decision making in the disposition of patients with suspected acute coronary syndromes (ACS) in the emergency department have received a lot of attention. Traditionally, patients with chest pain have required long periods of observation in emergency department before being deemed safe for discharge. In an era of limited health service resources, a protocol that could discharge patients safely within an hour of presentation is extremely attractive. Unfortunately, despite incorporation into some guidelines, these protocols have not been subjected to randomized comparisons evaluating safety, effectiveness, and cost-effectiveness.

OBJECTIVE

This study is designed to provide the evidence required to allow key decision makers to implement these protocols: specifically, to provide evidence that a decision rule based on 0- and 1-hour high-sensitivity troponin T (hs-TnT) is safe, provides noninferior outcomes in all patients with suspected ACS, and that implementation of a rapid troponin protocol leads to efficient care.

DESIGN

This prospective pragmatic trial (n=5,400, 5 hospitals) randomly allocates patients with suspected ACS to either a 0/1-hour hs-TnT protocol as advocated in clinical guidelines, versus usual care of standard troponin reporting evaluated at 3 and 6hours. The primary effectiveness composite end points of this study are all-cause death and new/recurrent ACS within 30days. To evaluate cost-effectiveness, follow-up will determine clinical events, quality of life, and resource utilization within 12 months.

SUMMARY

Demonstrating that a 0/1-hour hs-TnT protocol improves the effectiveness and efficiency of care within a robust comparative study will fill an evidence gap that currently limits the translation of more precise hs-TnT testing into better patient and health service outcomes.

摘要

背景

在急诊科采用高敏肌钙蛋白来指导疑似急性冠脉综合征(ACS)患者处置决策的方案受到了广泛关注。传统上,胸痛患者在急诊科需要长时间观察,之后才能被认为可以安全出院。在卫生服务资源有限的时代,一种能在患者就诊后一小时内安全出院的方案极具吸引力。不幸的是,尽管这些方案已被纳入一些指南,但尚未进行随机对照比较来评估其安全性、有效性和成本效益。

目的

本研究旨在提供关键决策者实施这些方案所需的证据:具体而言,提供证据表明基于0小时和1小时高敏肌钙蛋白T(hs-TnT)的决策规则是安全的,在所有疑似ACS患者中能提供非劣效的结果,并且实施快速肌钙蛋白方案可实现高效医疗。

设计

这项前瞻性实用试验(n = 5400,5家医院)将疑似ACS患者随机分配至临床指南所倡导的0/1小时hs-TnT方案组,或常规的在3小时和6小时评估标准肌钙蛋白报告的常规治疗组。本研究的主要有效性复合终点是30天内的全因死亡和新发/复发ACS。为评估成本效益,随访将确定12个月内的临床事件、生活质量和资源利用情况。

总结

在一项严格的比较研究中证明0/1小时hs-TnT方案能提高医疗的有效性和效率,将填补目前限制将更精确的hs-TnT检测转化为更好的患者和卫生服务结局的证据空白。

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