Hansen J F
Department of Cardiology, Hvidovre Hospital, Denmark.
J Cardiovasc Pharmacol. 1991;18 Suppl 6:S20-5.
The effect of verapamil on death and reinfarction after an acute myocardial infarction was studied in two double-blind, randomized, placebo-controlled multicenter trials, the Danish Verapamil Infarction Trials I and II (DAVIT I and II). The studies demonstrated that verapamil 360 mg/day from the 2nd week after an acute myocardial infarction, prevented death and reinfarction. Meta-analyses of the results of DAVITs I and II resulted in a reduction of pooled ratios of 22% (95% confidence limits 1-37, p = 0.04) for death, 21% (5-35, p = 0.02) for first major events (first reinfarction or death), and 27% (6-43, p = 0.02) for first reinfarctions. The effect of verapamil was to prevent myocardial ischemia and reduce sudden death and reinfarction. It is concluded that long-term treatment with verapamil after an acute myocardial infarction may be recommended with the object of reducing overall mortality, major events and reinfarction.
在两项双盲、随机、安慰剂对照的多中心试验——丹麦维拉帕米梗死试验I和II(DAVIT I和II)中,研究了维拉帕米对急性心肌梗死后死亡和再梗死的影响。研究表明,急性心肌梗死后第2周起每日服用360毫克维拉帕米可预防死亡和再梗死。对DAVIT I和II的结果进行的荟萃分析显示,死亡的合并比率降低了22%(95%置信区间1 - 37,p = 0.04),首次重大事件(首次再梗死或死亡)的合并比率降低了21%(5 - 35,p = 0.02),首次再梗死的合并比率降低了27%(6 - 43,p = 0.02)。维拉帕米的作用是预防心肌缺血并减少猝死和再梗死。结论是,为降低总体死亡率、重大事件和再梗死发生率,急性心肌梗死后可推荐使用维拉帕米进行长期治疗。