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ESC 0/1h-hs-cTnT 算法观测区的新标准。

Novel Criteria for the Observe-Zone of the ESC 0/1h-hs-cTnT Algorithm.

机构信息

Cardiovascular Research Institute Basel and Department of Cardiology (P.L.-A., T.N., J.B., L.K., P.D.R., I.S., J.G., S.M., J.W., E.M., R.T., C.M.), University Hospital Basel, University of Basel, Switzerland.

Global Research on Acute Conditions Team Network, Rome, Italy (P.L.-A., T.N., J.B., L.K., P.D.R., I.S., J.G., J.W., M.R.G., O.M., B.L.-B., F.J.M.-S., R.T., C.M.).

出版信息

Circulation. 2021 Sep 7;144(10):773-787. doi: 10.1161/CIRCULATIONAHA.120.052982. Epub 2021 Aug 11.

Abstract

BACKGROUND

The non-ST-segment-elevation myocardial infarction (NSTEMI) guidelines of the European Society of Cardiology (ESC) recommend a 3h cardiac troponin determination in patients triaged to the observe-zone of the ESC 0/1h-algorithm; however, no specific cutoff for further triage is endorsed. Recently, a specific cutoff for 0/3h high-sensitivity cardiac troponin T (hs-cTnT) change (7 ng/L) was proposed, warranting external validation.

METHODS

Patients presenting with acute chest discomfort to the emergency department were prospectively enrolled into an international multicenter diagnostic study. Final diagnoses were centrally adjudicated by 2 independent cardiologists applying the fourth universal definition of myocardial infarction, on the basis of complete cardiac workup, cardiac imaging, and serial hs-cTnT. Hs-cTnT concentrations were measured at presentation, after 1 hour, and after 3 hours. The objective was to externally validate the proposed cutoff, and if necessary, derive and internally as well as externally validate novel 0/3h-criteria for the observe-zone of the ESC 0/1h-hs-cTnT-algorithm in an independent multicenter cohort.

RESULTS

Among 2076 eligible patients, application of the ESC 0/1h-hs-cTnT-algorithm triaged 1512 patients (72.8%) to either rule out or rule in NSTEMI, leaving 564 patients (27.2%) in the observe-zone (adjudicated NSTEMI prevalence, 120/564 patients, 21.3%). The suggested 0/3h-hs-cTnT-change of <7 ng/L triaged 517 patients (91.7%) toward rule-out, resulting in a sensitivity of 33.3% (95% CI, 25.5-42.2), missing 80 patients with NSTEMI, and ≥7 ng/L triaged 47 patients toward rule-in (8.3%), resulting in a specificity of 98.4% (95% CI, 96.8-99.2). Novel derived 0/3h-criteria for the observe-zone patients ruled out NSTEMI with a 3h hs-cTnT concentration <15 ng/L and a 0/3h-hs-cTnT absolute change <4 ng/L, triaging 138 patients (25%) toward rule-out, resulting in a sensitivity of 99.2% (95% CI, 96.0-99.9), missing 1 patient with NSTEMI. A 0/3h-hs-cTnT absolute change ≥6 ng/L triaged 63 patients (11.2%) toward rule-in, resulting in a specificity of 98% (95% CI, 96.2-98.9) Thereby, the novel 0/3h-criteria reduced the number of patients in the observe zone by 36%s and the number of type 1 myocardial infarction by 50%. Findings were confirmed in both internal and external validation.

CONCLUSIONS

A combination of a 3h-hs-cTnT concentration (<15 ng/L) and a 0/3h absolute change (<4 ng/L) is necessary to safely rule out NSTEMI in patients remaining in the observe-zone of the ESC 0/1h-hs-cTnT-algorithm. Registration: URL: https://clinicaltrials.gov; Unique identifier: NCT00470587.

摘要

背景

欧洲心脏病学会(ESC)的非 ST 段抬高型心肌梗死(NSTEMI)指南建议对 ESC 0/1h 算法分诊到观察区的患者在 3 小时内测定心脏肌钙蛋白;然而,没有推荐具体的界值用于进一步分诊。最近,提出了一种特定的 0/3 小时高敏心肌肌钙蛋白 T(hs-cTnT)变化(7ng/L)的界值,需要进行外部验证。

方法

将出现急性胸痛的患者前瞻性纳入一项国际多中心诊断研究。最终诊断由 2 位独立的心脏病专家根据第四版心肌梗死通用定义,在进行全面心脏检查、心脏成像和连续 hs-cTnT 检测的基础上进行中心裁决。在就诊时、1 小时后和 3 小时后测量 hs-cTnT 浓度。目的是在独立的多中心队列中外部验证建议的界值,如果有必要,还可以推导和内部及外部验证 ESC 0/1h-hs-cTnT 算法观察区的新的 0/3 小时标准。

结果

在 2076 名合格患者中,ESC 0/1h-hs-cTnT 算法将 1512 名患者(72.8%)分诊为排除或确诊 NSTEMI,将 564 名患者(27.2%)分诊到观察区(观察区裁决的 NSTEMI 患病率为 120/564 例,21.3%)。建议的 0/3 小时 hs-cTnT 变化<7ng/L 将 517 名患者(91.7%)分诊为排除,敏感性为 33.3%(95%CI,25.5-42.2),漏诊了 80 例 NSTEMI 患者,≥7ng/L 将 47 名患者分诊为确诊(8.3%),特异性为 98.4%(95%CI,96.8-99.2%)。新推导的观察区患者的 0/3 小时标准,以 3 小时 hs-cTnT 浓度<15ng/L 和 0/3 小时 hs-cTnT 绝对变化<4ng/L 排除 NSTEMI,将 138 名患者(25%)分诊为排除,敏感性为 99.2%(95%CI,96.0-99.9),漏诊了 1 例 NSTEMI 患者。0/3 小时 hs-cTnT 绝对变化≥6ng/L 将 63 名患者(11.2%)分诊为确诊,特异性为 98%(95%CI,96.2-98.9)。因此,新的 0/3 小时标准将观察区的患者数量减少了 36%,将 1 型心肌梗死的数量减少了 50%。内部和外部验证都证实了这些发现。

结论

在 ESC 0/1h-hs-cTnT 算法分诊到观察区的患者中,要安全地排除 NSTEMI,需要同时使用 3 小时 hs-cTnT 浓度(<15ng/L)和 0/3 小时绝对变化(<4ng/L)。

登记

网址:https://clinicaltrials.gov;唯一标识符:NCT00470587。

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