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评估症状表现和3小时高敏肌钙蛋白以诊断和排除急性心肌梗死

Validation of presentation and 3 h high-sensitivity troponin to rule-in and rule-out acute myocardial infarction.

作者信息

Pickering John W, Greenslade Jaimi H, Cullen Louise, Flaws Dylan, Parsonage William, George Peter, Worster Andrew, Kavsak Peter A, Than Martin P

机构信息

Emergency Department, Christchurch Hospital, Christchurch, New Zealand Department of Medicine, University of Otago, Christchurch, New Zealand.

Department of Emergency Medicine, Royal Brisbane and Women's Hospital, and The University of Queensland and School of Public Health, Queensland University of Technology Brisbane, Brisbane, Australia.

出版信息

Heart. 2016 Aug 15;102(16):1270-8. doi: 10.1136/heartjnl-2015-308505. Epub 2016 Mar 8.

Abstract

OBJECTIVE

International guidelines to rule-in acute myocardial infarction (AMI) in patients presenting with chest pain to the emergency department (ED) recommend an algorithm using high-sensitivity cardiac troponin (hs-cTn) sampling on presentation and 3 h following presentation. We tested the diagnostic accuracy of this algorithm by pooling data from five distinct cohorts from three countries of prospectively recruited patients with independently adjudicated outcomes.

METHOD

We measured high-sensitivity cardiac troponin I (hs-cTnI) and high-sensitivity cardiac troponin T (hs-cTnT) on presentation (0 h) and 3 h post-presentation samples in adult patients attending an ED with possible AMI to validate the European Society of Cardiology (ESC) Working Group on Acute Cardiac Care rule-in algorithm (ESC-rule-in). Specifically, (i) in patients with a 0 h hs-cTn concentration ≤99th percentile and a 3 h hs-cTn >99th percentile, positive patients are those with an absolute change in troponin ≥50% of the 99th percentile, and (ii) in patients with a 0 and 3 h hs-cTn >99th percentile, positive patients are those with a relative change in troponin of ≥20%. We concurrently assessed the efficacy of the 0 and 3 h hs-cTn <99th percentile to rule-out AMI.

RESULTS

1061 patients with hs-cTnI and 985 with hs-cTnT were included. The ESC-rule-in positive predictive value (PPV) was 83.5% (95% CI 74.9% to 90.1%) for hs-cTnI and 72.0% (95% CI 62.1% to 80.5%) for hs-cTnT. Forty-six AMIs (34.9%) were not ruled in using hs-cTnI and 62 (46.2%) using hs-cTnT. The sensitivity of the 99th percentile to rule-out AMI was 93.2% (95% CI 87.5% to 96.8%) for hs-cTnI and 94.8% (95% CI 89.5% to 97.9%) for hs-cTnT.

CONCLUSIONS

The ESC-rule-in algorithm has good PPV with hs-cTnI and reasonable with hs-cTnT and can rule-in over 50% of AMIs. However, the sensitivity of the 99th percentile to rule-out AMI is too low for clinical use.

摘要

目的

针对急诊科(ED)中出现胸痛症状的患者,国际上用于诊断急性心肌梗死(AMI)的指南推荐了一种算法,即采用高敏心肌肌钙蛋白(hs-cTn)在就诊时及就诊后3小时进行采样检测。我们通过汇总来自三个国家的五个不同队列中前瞻性招募的、具有独立判定结果的患者数据,对该算法的诊断准确性进行了测试。

方法

我们对因可能患有AMI而前往ED就诊的成年患者在就诊时(0小时)及就诊后3小时的样本进行了高敏心肌肌钙蛋白I(hs-cTnI)和高敏心肌肌钙蛋白T(hs-cTnT)检测,以验证欧洲心脏病学会(ESC)急性心脏护理工作组的诊断算法(ESC诊断算法)。具体而言,(i)对于就诊时hs-cTn浓度≤第99百分位数且就诊后3小时hs-cTn>第99百分位数的患者,阳性患者为肌钙蛋白绝对变化≥第99百分位数的50%的患者;(ii)对于就诊时和就诊后3小时hs-cTn均>第99百分位数的患者,阳性患者为肌钙蛋白相对变化≥20%的患者。我们同时评估了就诊时和就诊后3小时hs-cTn<第99百分位数排除AMI的有效性。

结果

纳入了1061例检测hs-cTnI的患者和985例检测hs-cTnT的患者。对于hs-cTnI,ESC诊断算法的阳性预测值(PPV)为83.5%(95%CI 74.9%至90.1%);对于hs-cTnT,PPV为72.0%(95%CI 62.1%至80.5%)。使用hs-cTnI未能诊断出46例AMI(34.9%),使用hs-cTnT未能诊断出62例(4,6.2%)。对于排除AMI,第99百分位数的敏感性在hs-cTnI方面为93.2%(95%CI 87.5%至96.8%),在hs-cTnT方面为94.8%(95%CI 89.5%至97.9%)。

结论

ESC诊断算法在hs-cTnI方面具有良好的PPV,在hs-cTnT方面也较为合理,且能诊断出超过50%的AMI。然而,第99百分位数用于排除AMI的敏感性过低,不适合临床应用。

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