Cardiovascular Imaging Research Center, Massachusetts General Hospital-Harvard Medical School, Boston, Massachusetts, USA; MTA-SE Cardiovascular Imaging Research Group, Heart and Vascular Center, Semmelweis University, Budapest, Hungary.
Cardiovascular Imaging Research Center, Massachusetts General Hospital-Harvard Medical School, Boston, Massachusetts, USA; School of Business Studies, Stralsund University of Applied Sciences, Stralsund, Germany.
J Am Coll Cardiol. 2021 Mar 30;77(12):1487-1499. doi: 10.1016/j.jacc.2021.01.046.
High-sensitivity cardiac troponin (hs-cTn) assays have different analytic characteristics.
The goal of this study was to quantify differences between assays for common analytical benchmarks and to determine whether they may result in differences in the management of patients with suspected acute coronary syndrome (ACS).
The authors included patients with suspected ACS enrolled in the ROMICAT (Rule Out Myocardial Infarction/Ischemia Using Computer Assisted Tomography) I and II trials, with blood samples taken at emergency department presentation (ROMICAT-I and -II) or at 2 and 4 h thereafter (ROMICAT-II). hs-cTn concentrations were measured using 3 assays (Roche Diagnostics, Elecsys 2010 platform; Abbott Diagnostics, ARCHITECT i2000SR; Siemens Diagnostics, HsVista). Per blood sample, we determined concordance across analytic benchmarks (<limit of detection [<LOD]/LOD-99th percentile/>99th percentile). Per-patient, the authors determined concordance of management recommendations (rule-out/observe/rule-in) per the 0/2-h algorithm, and their association with diagnostic test findings (coronary artery stenosis >50% on coronary computed tomography angiography or inducible ischemia on perfusion imaging) and ACS.
Among 1,027 samples from 624 patients (52.8 ± 10.0 years; 39.4% women), samples were classified as <LOD (56.3% vs. 10.4% vs. 41.2%; p < 0.001), LOD-99th percentile (36.5% vs. 83.5% vs. 52.6; p < 0.001), >99th percentile (7.2% vs. 6.0% vs. 6.2%) by Roche, Abbott, and Siemens, respectively. A total of 37.4% (n = 384 of 1,027) of blood samples were classified into the same analytical benchmark category, with low concordance across benchmarks (<LOD 11.1%; LOD-99th percentile 29.3%; >99th percentile 43.6%). Serial samples were available in 242 patients (40.1% women; mean age: 52.8 ± 8.0 years). The concordance of management recommendations across assays was 74.8% (n = 181 of 242) considering serial hs-cTn measurements. Of patients who were recommended to discharge, 19.6% to 21.1% had positive diagnostic test findings and 2.8% to 4.3% had ACS at presentation.
Caregivers should be aware that there are significant differences between hs-cTn assays in stratifying individual samples and patients with intermediate likelihood of ACS according to analytical benchmarks that may result in different management recommendations. (Rule Out Myocardial Infarction by Computer Assisted Tomography [ROMICAT]; NCT00990262) (Multicenter Study to Rule Out Myocardial Infarction by Cardiac Computed Tomography [ROMICAT-II]; NCT01084239).
高敏肌钙蛋白(hs-cTn)检测方法具有不同的分析特性。
本研究旨在量化不同检测方法在常见分析基准方面的差异,并确定这些差异是否可能导致疑似急性冠脉综合征(ACS)患者的管理方式发生改变。
本研究纳入了疑似 ACS 患者,这些患者来自 ROMICAT(使用计算机断层扫描排除心肌梗死/缺血)I 期和 II 期临床试验,在急诊科就诊时(ROMICAT-I 和 -II)或之后 2 小时和 4 小时(ROMICAT-II)采集血样。使用 3 种检测方法(罗氏诊断 Elecsys 2010 平台、雅培诊断 ARCHITECT i2000SR、西门子诊断 HsVista)检测 hs-cTn 浓度。对于每一份血样,我们根据分析基准(<检测限 [<LOD]/LOD-99 百分位值/>99 百分位值)确定一致性。对于每一位患者,我们根据 0/2 小时算法确定管理建议(排除/观察/纳入)的一致性,并评估其与诊断性检测结果(冠状动脉计算机断层扫描血管造影上存在>50%的狭窄或灌注成像上存在可诱导缺血)和 ACS 的相关性。
在 624 例患者的 1027 份样本中(52.8 ± 10.0 岁;39.4%为女性),罗氏、雅培和西门子分别将<LOD(56.3% vs. 10.4% vs. 41.2%;p<0.001)、LOD-99 百分位值(36.5% vs. 83.5% vs. 52.6%;p<0.001)、>99 百分位值(7.2% vs. 6.0% vs. 6.2%)归类为<LOD、LOD-99 百分位值和>99 百分位值。共有 37.4%(n=1027 份样本中的 384 份)的血样被归入相同的分析基准类别,不同基准之间的一致性较低(<LOD 为 11.1%;LOD-99 百分位值为 29.3%;>99 百分位值为 43.6%)。242 例患者(40.1%为女性;平均年龄:52.8 ± 8.0 岁)有连续的血样。考虑到连续 hs-cTn 测量值,3 种检测方法的管理建议一致性为 74.8%(n=242 份患者中的 181 份)。建议出院的患者中,19.6%至 21.1%的患者有阳性诊断性检测结果,2.8%至 4.3%的患者在就诊时患有 ACS。
医护人员应当意识到,hs-cTn 检测方法在根据分析基准对个体样本和疑似 ACS 可能性处于中间范围的患者进行分层时存在显著差异,这可能导致不同的管理建议。(通过计算机断层扫描排除心肌梗死研究 [ROMICAT];NCT00990262)(多中心通过心脏计算机断层扫描排除心肌梗死研究 [ROMICAT-II];NCT01084239)。