Herlitz J, Waldenström J, Hjalmarson A
Department of Medicine, University of Göteborg, Sahlgren's Hospital, Sweden.
Cardiology. 1988;75(2):117-22. doi: 10.1159/000174358.
One of the secondary objectives of the MIAMI Trial which evaluated the role of the beta-1-selective blocker metoprolol in suspected acute myocardial infarction was to further assess whether early intervention with beta-blockade can limit infarct size. A total of 5,778 patients from 104 worldwide centres were randomized into the trial. Various enzymes such as aspartate aminotransferase (ASAT), creatine kinase (CK), CK MB, CK B, lactate dehydrogenase (LD) and LD isoenzyme I were analysed. All enzymes were used according to the clinical routine of the respective hospital, except ASAT which was analysed once daily for 3 days in the majority of cases and LD I which was analysed every 12 h for 72 h in a subsample. A consistent observation was the lower serum enzyme activity among patients receiving metoprolol and randomized early after onset of symptoms, whereas no difference between metoprolol and placebo was observed in patients treated later in the course. The results of the MIAMI Trial support previous observations that early institution of metoprolol therapy limits infarct size, as indicated by the maximum serum enzyme activity.
评估β1选择性阻滞剂美托洛尔在疑似急性心肌梗死中作用的迈阿密试验的次要目标之一是进一步评估早期β受体阻滞剂干预是否能限制梗死面积。来自全球104个中心的5778例患者被随机纳入该试验。分析了多种酶,如天冬氨酸转氨酶(ASAT)、肌酸激酶(CK)、CK MB、CK B、乳酸脱氢酶(LD)和LD同工酶I。除了在大多数情况下ASAT每天分析1次,共分析3天,以及在一个子样本中LD I每12小时分析1次,共分析72小时外,所有酶均按照各医院的临床常规进行检测。一个一致的观察结果是,在症状发作后早期随机接受美托洛尔治疗的患者中,血清酶活性较低,而在病程后期接受治疗的患者中,未观察到美托洛尔与安慰剂之间存在差异。迈阿密试验的结果支持了先前的观察结果,即如最大血清酶活性所示,早期使用美托洛尔治疗可限制梗死面积。