Rapid diagnosis of acute myocardial infarction

P. L. Ayala, S. Shrestha, C. Mueller
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Abstract

Over the last decade, intense collaboration between physician scientists and the diagnostic industry has enabled game-changing innovation in the rapid diagnosis of acute myocardial infarction (AMI). (1–12) High sensitivity cardiac troponin (hs-cTn) assays enable reliable measurement of cardiac troponin (cTn) concentrations in the normal range, thereby increasing substantially the diagnostic accuracy for AMI already with the first blood drawn at presentation to the emergency department (ED). (1–12) This was a prerequisite for the development and maturation of early rule-out and rulein strategies for AMI into clinical practice worldwide. While the first iteration was complex and required the combination of a biomarker panel, the electrocardiogram, and a clinical risk score, allowing the safe ruleout of AMI in only 10% of patients with acute chest pain, the latest iterations including the European Society of Cardiology (ESC) 0/1h-algorithm are simple, as they are based on hs-cTn concentrations only, and allow the safe rule-out AND/OR rule-in of AMI in about 75% of patients. (13-21) The ESC 0/1h-algorithm is a combination of the single measurement approach with the original 0/1halgorithm. (5, 7, 22–25) It has all the advantages of the single measurement approach (speed and simplicity), but further extends the number of patients eligible for triage towards rule-out of AMI to those patients with low hs-cTnT/I concentrations at presentation and NO relevant change (rise AND/OR fall) in hs-cTnT/I concentrations after 1 h. It also adds the possibility to triage patients towards rule-in of AMI using high initial hs-cTnT/I concentrations and/or relevant changes in hs-cTnT/I after 1 h. The ESC 0/1h-algorithm has been derived and validated for all currently available hs-cTnT/I assays, with unique data-driven cut-off values for each assay to achieve a sensitivity and negative predictive value of 99% or higher. (5, 7, 22–26) It is recommended by the ESC guideline for the management of acute coronary syndromes in patients without
急性心肌梗死的快速诊断
在过去的十年中,医师科学家和诊断行业之间的密切合作使急性心肌梗死(AMI)的快速诊断成为可能。(1-12)高灵敏度心肌肌钙蛋白(hs-cTn)检测能够在正常范围内可靠地测量心肌肌钙蛋白(cTn)浓度,从而大大提高急诊(ED)患者首次抽血诊断AMI的准确性。(1-12)这是AMI早期排除和排除策略在全球范围内进入临床实践的发展和成熟的先决条件。虽然第一次迭代很复杂,需要结合生物标志物小组、心电图和临床风险评分,仅允许10%的急性胸痛患者安全排除AMI,但最新的迭代包括欧洲心脏病学会(ESC) 0/ h算法很简单,因为它们仅基于hs-cTn浓度,并且允许大约75%的患者安全排除和/或AMI规则。(13-21) ESC 0/1h算法是单一测量方法与原始0/1算法的结合。(5,7,22 - 25)它具有单一测量方法的所有优点(速度快,简单),但进一步将符合AMI排除分类的患者数量扩大到那些在就诊时hs-cTnT/I浓度较低且1小时后hs-cTnT/I浓度没有相关变化(上升和/或下降)的患者。它还增加了使用高初始hs-cTnT/I浓度和/或1小时后hs-cTnT/I相关变化来分类AMI患者的可能性。ESC 0/1h算法已经推导并验证了所有目前可用的hs-cTnT/I检测。具有独特的数据驱动的截止值为每个分析实现灵敏度和阴性预测值99%或更高。(5,7,22 - 26) ESC指南推荐对无血管内皮细胞的急性冠状动脉综合征患者进行治疗
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