Woo J, Lacbawan F L, Sunheimer R, LeFever D, McCabe J B
Department of Pathology, State University of New York Health Science Center, Syracuse 13210, USA.
Am J Clin Pathol. 1995 Jun;103(6):725-9. doi: 10.1093/ajcp/103.6.725.
The authors evaluated the usefulness of a rapid fluorometric enzyme immunoassay for myoglobin (Myo) for early diagnosis of acute myocardial infarction (AMI) in patients in the emergency department. The rapid fluorometric enzyme immunoassay for myoglobin was performed on timed blood samples collected previously for serial CK and CKMB determinations from 41 patients who initially presented to the ED with chest pain and were subsequently admitted to patient care units. Twenty-two patients were AMI positive and 19 were AMI negative. In 12 patients who were AMI positive, Myo increased rapidly and significantly peaking at 6.53 +/- 5.45 hours, whereas in the other 10 patients who were AMI positive, only the declining slopes of Myo were observed due to late AMI presentation. In the AMI negative group, Myo values were within reference range in 8 and persistently elevated in 11. Using the initial rate of Myo release of 20 ng/mL per hour as criteria of discrimination, this assay has a sensitivity of 90.1% and a specificity of 74%. Available samples for the two patients who were false negative were past the window of Myo release for AMI detection. All five patients who were false positive were associated with various degrees of muscular trauma or renal disorder. The authors conclude that the initial rate of Myo release demonstrates good utility both at early detection and early exclusion of AMI. However, its tissue nonspecificity may not permit AMI recognition in the presence of muscular injury.
作者评估了一种用于检测肌红蛋白(Myo)的快速荧光酶免疫测定法在急诊科患者急性心肌梗死(AMI)早期诊断中的实用性。对41例最初因胸痛就诊于急诊科并随后被收治到病房的患者,针对先前采集的用于系列肌酸激酶(CK)和肌酸激酶同工酶(CKMB)测定的定时血样,进行了肌红蛋白快速荧光酶免疫测定。22例患者AMI呈阳性,19例呈阴性。在12例AMI阳性患者中,Myo迅速且显著升高,在6.53±5.45小时达到峰值,而在另外10例AMI阳性患者中,由于AMI出现较晚,仅观察到Myo的下降斜率。在AMI阴性组中,8例患者的Myo值在参考范围内,11例患者的Myo值持续升高。以每小时20 ng/mL的Myo初始释放速率作为判别标准,该测定法的灵敏度为90.1%,特异性为74%。两名假阴性患者的可用样本已过AMI检测的Myo释放窗口期。所有五例假阳性患者均与不同程度的肌肉创伤或肾脏疾病有关。作者得出结论,Myo的初始释放速率在AMI的早期检测和早期排除方面均显示出良好的效用。然而,其组织非特异性可能在存在肌肉损伤时无法实现AMI的识别。