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评估使用心脏型脂肪酸结合蛋白和高敏肌钙蛋白I的双重标志物方法作为连续采样诊断急性心肌梗死的替代方法。

Evaluation of Dual Marker Approach Using Heart-Type Fatty Acid Binding Protein and High Sensitivity Troponin-I as an Alternative to Serial Sampling for Diagnosis of Acute Myocardial Infarction.

作者信息

Raj Kulshrestha Manish, Raj Apurva, Tiwari Vandana, Chandra Subrat, Tiwari Bhuwan Chandra, Jha Ashish

机构信息

Department of Biochemistry, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.

Department of Pathology, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.

出版信息

EJIFCC. 2022 Apr 11;33(1):43-55. eCollection 2022 Apr.

Abstract

OBJECTIVE

An early rule in (high specificity and high PPV) and early rule out (high sensitivity and high NPV) is essential for diagnosing acute myocardial infarction (AMI) to provide better utilization of resources, cost-effectiveness, and to reduce mortality.

METHODS

Consecutive chest pain patients (n=80) with symptoms indicative of coronary artery disease reported to the emergency room within 6 hours after onset of symptoms. An alternate Dual Marker Approach (DMA; both Heart-type Fatty Acid Binding Protein (H-FABP) and High sensitive Troponin-I (hsTnI) at 0 h) was compared to the Double Sampling approach (DSA; hsTnI at 0 h and 3 h (ESC guidelines)).

RESULTS

If both biomarkers were increased (n=17; 77.5%: 11 STEMI and 6 NSTEMI) above their respective cut-off value (HFABP 6.3 ng/mL and hsTnI 20.24 ng/L) at presentation, AMI ensued (100% PPV). Also, if both the markers were below their respective cut-offs at presentation, AMI was safely ruled out (n=41; with only 1 false negative). However, among the patients with either of these markers above their respective cut-off at presentation (n=22), DSA was required to find remaining AMI cases (n=4). Overall, DMA stands best for rule out (sensitivity 95.5%, NPV 97.6%) while DSA is superior for rule in (98.2% specificity, 95.2% PPV).

CONCLUSION

With the use of the proposed DMA, 58/80 (72.5%) patients with acute chest pain were reliably ruled in/ruled out for AMI at the presentation itself, while the remaining patients still required serial monitoring (DSA) for confirmation.

摘要

目的

早期诊断(高特异性和高阳性预测值)和早期排除(高敏感性和高阴性预测值)对于急性心肌梗死(AMI)的诊断至关重要,有助于更好地利用资源、提高成本效益并降低死亡率。

方法

连续纳入80例胸痛患者,这些患者在症状发作后6小时内被送往急诊室,症状提示冠状动脉疾病。将一种替代双标志物方法(DMA;发病0小时时检测心脏型脂肪酸结合蛋白(H-FABP)和高敏肌钙蛋白I(hsTnI))与双重采样方法(DSA;按照欧洲心脏病学会(ESC)指南在发病0小时和3小时检测hsTnI)进行比较。

结果

如果就诊时两种生物标志物均高于各自的临界值(H-FABP为6.3 ng/mL,hsTnI为20.24 ng/L)(n = 17;77.5%:11例ST段抬高型心肌梗死和6例非ST段抬高型心肌梗死),则随后发生AMI(阳性预测值为100%)。此外,如果就诊时两种标志物均低于各自的临界值,则可安全排除AMI(n = 41;仅有1例假阴性)。然而,在就诊时其中一种标志物高于各自临界值的患者中(n = 22),需要采用DSA来发现其余的AMI病例(n = 4)。总体而言,DMA在排除诊断方面表现最佳(敏感性为95.5%,阴性预测值为97.6%),而DSA在诊断方面更具优势(特异性为98.2%,阳性预测值为95.2%)。

结论

使用所提出的DMA方法,80例急性胸痛患者中有58例(72.5%)在就诊时就能可靠地被诊断为AMI或排除AMI,而其余患者仍需要进行系列监测(DSA)以确诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/933d/9092720/caa251e724ea/ejifcc-33-043-g001.jpg

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