Very early diagnosis and risk stratification of patients admitted with suspected acute myocardial infarction by the combined evaluation of a single serum value of cardiac troponin-T, myoglobin, and creatine kinase MBmass

被引:39
作者
Jurlander, B
Clemmensen, P
Wagner, GS
Grande, P
机构
[1] Univ Copenhagen, HS Rigshosp, Ctr Heart, DK-2100 Copenhagen O, Denmark
[2] Duke Univ, Div Cardiol, Durham, NC 27706 USA
关键词
myocardial infarction; diagnosis; prognosis; myoglobin; troponin-T; creatine kinase MBmass;
D O I
10.1053/euhj.1999.1760
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims The diagnostic and prognostic capacity of biochemical markers of acute myocardial infarction in the emergency department were evaluated in consecutive patients (n = 155) with suspected acute myocardial infarction. Methods and Results Serum myoglobin greater than or equal to 110 mu g. 1(-1) and creatine kinase MBmass greater than or equal to 5 mu g.1(-1) had a high accuracy (0.77-0.85) (ns) for acute myocardial infarction diagnosis in patients presenting >2 h after symptom onset. Troponin-T (greater than or equal to 0.10 mu g . 1(-1)) had a lower accuracy (0.53-0.70) for acute myocardial infarction diagnosis, but was the most important 1-year prognostic marker (cardiac death or non-fatal acute myocardial infarction). In patients without ST elevation, combined analysis of two biochemical tests would accurately identify an additional 20% of acute myocardial infarction patients (predictive value of a positive test = 0.82) and also identify those without acute myocardial infarction (predictive value of a negative test = 0.80). One-year event-free survival was excellent (96%) for patients with two negative biochemical tests, intermediate (74%) for those with discordant tests, and only 53% for patients with two positive biochemical tests. Conclusion Analysis of biochemical tests in the emergency department prior to hospital admission could accurately identify approximately 20% additional acute myocardial infarction patients. The prognosis of these patients is poor, and they may be a target for primacy PTCA or new early initiated aggressive medical therapies. (C) 2000 The European Society of Cardiology.
引用
收藏
页码:382 / 389
页数:8
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