Chapman Andrew R, Fujisawa Takeshi, Lee Kuan Ken, Andrews Jack Patrick, Anand Atul, Sandeman Dennis, Ferry Amy V, Stewart Stacey, Marshall Lucy, Strachan Fiona E, Gray Alasdair, Newby David E, Shah Anoop S V, Mills Nicholas L
BHF Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
Department of Emergency Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK.
Heart. 2019 Apr;105(8):616-622. doi: 10.1136/heartjnl-2018-314093. Epub 2018 Nov 15.
High-sensitivity cardiac troponin assays enable the early risk stratification of patients with suspected acute coronary syndrome to identify those at low risk of myocardial infarction or cardiac death. We evaluated the performance of a novel high-sensitivity cardiac troponin I assay in early rule out pathways.
In 1920 patients with suspected acute coronary syndrome, cardiac troponin was measured using the Siemens Atellica high-sensitivity cardiac troponin I assay (99th centile: 34 ng/L women, 53 ng/L men). We evaluated three pathways which use either low risk-stratification thresholds of cardiac troponin (ensitivityroponin in the valuation of patients with cute oronary yndrome (High-STEACS) and the European Society of Cardiology (ESC) 1 hour pathway) or the 99th centile diagnostic threshold (ESC 3 hour pathway) to rule out myocardial infarction.
The primary outcome of myocardial infarction or cardiac death at 30 days occurred in 14.4% (277/1920). The High-STEACS pathway ruled out 63% of patients (1218/1920), with five missed events for a negative predictive value (NPV) of 99.5% (95% CI (CI) 99.1% to 99.8%). Similar performance was observed for the ESC 1 hour pathway with an NPV of 99.0% (97.6% to 99.8%). In contrast, the ESC 3 hour pathway ruled out 65% of patients (1248/1920), but missed 25 events for an NPV of 98.0% (97.1% to 98.7%).
A novel high-sensitivity cardiac troponin I assay can safely identify patients at low risk of myocardial infarction or cardiac death. Diagnostic pathways that use low cardiac troponin concentrations for risk stratification miss fewer events than those that rely on the 99th centile to rule out myocardial infarction.
NCT1852123.
高敏心肌肌钙蛋白检测可对疑似急性冠状动脉综合征患者进行早期风险分层,以识别心肌梗死或心源性死亡低风险患者。我们评估了一种新型高敏心肌肌钙蛋白I检测在早期排除途径中的性能。
在1920例疑似急性冠状动脉综合征患者中,使用西门子Atellica高敏心肌肌钙蛋白I检测法(第99百分位数:女性34 ng/L,男性53 ng/L)检测心肌肌钙蛋白。我们评估了三种途径,这些途径使用心肌肌钙蛋白的低风险分层阈值(急性冠状动脉综合征患者评估中的高敏肌钙蛋白(High-STEACS)和欧洲心脏病学会(ESC)1小时途径)或第99百分位数诊断阈值(ESC 3小时途径)来排除心肌梗死。
30天时心肌梗死或心源性死亡的主要结局发生率为14.4%(277/1920)。High-STEACS途径排除了63%的患者(1218/1920),有5例假阴性事件,阴性预测值(NPV)为99.5%(95%置信区间(CI)99.1%至99.8%)。ESC 1小时途径观察到类似的性能,NPV为99.0%(97.6%至99.8%)。相比之下,ESC 3小时途径排除了65%的患者(1248/1920),但有25例假阴性事件,NPV为98.0%(97.1%至98.7%)。
一种新型高敏心肌肌钙蛋白I检测可安全地识别心肌梗死或心源性死亡低风险患者。使用低心肌肌钙蛋白浓度进行风险分层的诊断途径比依赖第99百分位数来排除心肌梗死的途径漏诊事件更少。
NCT1852123。