Peters R W, Byington R P, Barker A, Yusuf S
Department of Medicine, VA Medical Center, Baltimore, Maryland 21218.
J Clin Epidemiol. 1990;43(2):167-72. doi: 10.1016/0895-4356(90)90180-w.
In the Beta Blocker Heart Attack Trial (BHAT), 3837 patients were randomized to propranolol (180-240 mg/day) or placebo 5-21 days after a documented myocardial infarction and were followed in a double blind manner for a mean period of 25 months. Twelve lead electrocardiograms were routinely obtained at the time of randomization (baseline electrocardiogram) and at 12 and 24 months of follow-up. There was a positive correlation between baseline QTc interval prolongation (but not QT prolongation) and mortality and sudden death that was independent of treatment group. The data for non-sudden death and non-fatal reinfarction exhibit similar trends. We conclude that: (1) QTc prolongation identifies a high risk subset of post myocardial infarction patients. (2) The relative benefit of propranolol is similar in patients with normal and prolonged QTc.
在β受体阻滞剂心肌梗死试验(BHAT)中,3837例患者在确诊心肌梗死后5 - 21天被随机分为普萘洛尔组(180 - 240毫克/天)或安慰剂组,并以双盲方式随访平均25个月。在随机分组时(基线心电图)以及随访12个月和24个月时常规获取12导联心电图。基线QTc间期延长(而非QT延长)与死亡率和猝死之间存在正相关,且与治疗组无关。非猝死和非致命性再梗死的数据呈现相似趋势。我们得出结论:(1)QTc延长可识别出心肌梗死后高危患者亚组。(2)在QTc正常和延长的患者中,普萘洛尔的相对获益相似。