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Diagnostic accuracy of single baseline measurement of Elecsys Troponin T high-sensitive assay for diagnosis of acute myocardial infarction in emergency department: systematic review and meta-analysis

机译:Elecsys肌钙蛋白T高灵敏测定法单基线测量对急诊科急性心肌梗死的诊断准确性:系统评价和荟萃分析

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摘要

>Objective To obtain summary estimates of the accuracy of a single baseline measurement of the Elecsys Troponin T high-sensitive assay (Roche Diagnostics) for the diagnosis of acute myocardial infarction in patients presenting to the emergency department.>Design Systematic review and meta-analysis of diagnostic test accuracy studies.>Data sources Medline, Embase, and other relevant electronic databases were searched for papers published between January 2006 and December 2013.>Study selection Studies were included if they evaluated the diagnostic accuracy of a single baseline measurement of Elecsys Troponin T high-sensitive assay for the diagnosis of acute myocardial infarction in patients presenting to the emergency department with suspected acute coronary syndrome.>Study appraisal and data synthesis The first author screened all titles and abstracts identified through the searches and selected all potentially relevant papers. The screening of the full texts, the data extraction, and the methodological quality assessment, using the adapted QUADAS-2 tool, were conducted independently by two reviewers with disagreements being resolved through discussion or arbitration. If appropriate, meta-analysis was conducted using the hierarchical bivariate model.>Results Twenty three studies reported the performance of the evaluated assay at presentation. The results for 14 ng/L and 3-5 ng/L cut-off values were pooled separately. At 14 ng/L (20 papers), the summary sensitivity was 89.5% (95% confidence interval 86.3% to 92.1%) and the summary specificity was 77.1% (68.7% to 83.7%). At 3-5 ng/L (six papers), the summary sensitivity was 97.4% (94.9% to 98.7%) and the summary specificity was 42.4% (31.2% to 54.5%). This means that if 21 of 100 consecutive patients have the target condition (21%, the median prevalence across the studies), 2 (95% confidence interval 2 to 3) of 21 patients with acute myocardial infarction will be missed (false negatives) if 14 ng/L is used as a cut-off value and 18 (13 to 25) of 79 patients without acute myocardial infarction will test positive (false positives). If the 3-5 ng/L cut-off value is used, <1 (0 to 1) patient with acute myocardial infarction will be missed and 46 (36 to 54) patients without acute myocardial infarction will test positive.>Conclusions The results indicate that a single baseline measurement of the Elecsys Troponin T high-sensitive assay could be used to rule out acute myocardial infarction if lower cut-off values such as 3 ng/L or 5 ng/L are used. However, this method should be part of a comprehensive triage strategy and may not be appropriate for patients who present less than three hours after symptom onset. Care must also be exercised because of the higher imprecision of the evaluated assay and the greater effect of lot-to-lot reagent variation at low troponin concentrations.>Systematic review registration PROSPERO registration number CRD42013003926.
机译:>目的:获得用于急诊科患者的急性心肌梗死的Elecsys肌钙蛋白T高灵敏测定法(Roche Diagnostics)的单次基线测量的准确性的汇总估算。 > Design 系统分析和诊断测试准确性研究的荟萃分析。>数据来源检索了2006年1月至2013年12月发表的论文,Medline,Embase和其他相关电子数据库。 >研究选择,如果研究评估了以Elecsys肌钙蛋白T高灵敏测定法为诊断为急性冠状动脉综合征的急诊患者的急性心肌梗死的诊断,其单基线测量的诊断准确性。 strong>研究评估和数据综合:第一位作者筛选了通过搜索确定的所有标题和摘要,并选择了所有潜在内容有关文件。由两位审稿人使用经过改进的QUADAS-2工具对全文进行筛选,数据提取和方法学质量评估,这是由两名审阅者独立进行的,分歧之处通过讨论或仲裁解决。适当时,使用分层双变量模型进行荟萃分析。>结果有23项研究报告了演示文稿评估分析的性能。分别合并14 ng / L和3-5 ng / L临界值的结果。在14 ng / L(20篇论文)下,摘要敏感性为89.5%(95%置信区间86.3%至92.1%),摘要特异性为77.1%(68.7%至83.7%)。在3-5 ng / L(六篇论文)下,汇总敏感性为97.4%(94.9%至98.7%),汇总特异性为42.4%(31.2%至54.5%)。这意味着,如果连续100例患者中有21例达到目标病情(21%,研究中位患病率),如果发生以下情况,将漏诊21例急性心肌梗死患者中的2例(95%置信区间2到3)(假阴性) 14 ng / L作为临界值,在79例无急性心肌梗死的患者中,有18例(13至25)将检测为阳性(假阳性)。如果使用3-5 ng / L的临界值,则会漏诊<1(0至1)急性心肌梗死患者,而46(36至54)例无急性心肌梗死的患者会呈阳性。>结论结果表明,如果使用较低的临界值(例如3 ng / L或5 ng / L),则可以使用Elecsys肌钙蛋白T高灵敏测定的单个基线测量值来排除急性心肌梗塞。但是,此方法应作为综合分类策略的一部分,可能不适用于症状发作后少于三个小时的患者。在低肌钙蛋白浓度下,评估的测定方法的准确性更高,批次间试剂变化的影响更大,因此也必须格外小心。>系统评价注册 PROSPERO注册编号CRD42013003926。

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