Vaage-Nilsen M, Rasmussen V, Hansen J F, Hagerup L, Sørensen M B, Bjergaard O P, Mellemgaard K, Holländer N H, Nielsen I, Sigurd B
Department of Cardiology, Hvidovre University Hospital, Denmark.
J Cardiovasc Pharmacol. 1991;18 Suppl 6:S26-9.
This article is a review of presented subsets of the Danish Verapamil Infarction Trial II (DAVIT II) regarding the effect of verapamil on postinfarction ischemia, ventricular arrhythmias, and heart rate (HR), and the prognostic implications of these findings. Patients underwent Holter monitoring for 24-48 h at 1 week, i.e., before randomization to long-term treatment with placebo or verapamil, and after 1 month and about 1 year of study treatment. Ischemia: 18% of the patients had transient ST-segment deviation before randomization; 24% of the placebo- and 8% of the verapamil-treated patients (p = 0.04) showed ischemia after 1 month; and after 1 year, the figures were 26 and 4%, respectively (p = 0.02). The 18-month major event rate, i.e., first reinfarction or death, in patients with ischemia before randomization were 40 and 23.8% in patients without ischemia (p = 0.06). Arrhythmias: In the placebo group the prevalence and incidence of many ventricular ectopic beats (VEBs), i.e., more than 10 VEBs/h, increased significantly during the first years after infarction; this was not the case in the verapamil patients group. The mean HR was significantly reduced by verapamil treatment after 1 month and after 16 months of treatment. Multivariate analysis demonstrated the presence of more than 10 VEBs/h only early (i.e., 1 week) but not late (i.e., 1 month) after infarction, to be an independent predictor of major events during 18 months' follow-up observation. A HR above 80 beats/min independently predicted major events when appearing both early and late after infarction.(ABSTRACT TRUNCATED AT 250 WORDS)
本文是对丹麦维拉帕米梗死试验II(DAVIT II)特定子集的综述,内容涉及维拉帕米对梗死后缺血、室性心律失常及心率(HR)的影响,以及这些研究结果的预后意义。患者在1周时,即随机接受安慰剂或维拉帕米长期治疗前,以及研究治疗1个月和约1年后,接受24 - 48小时的动态心电图监测。缺血情况:18%的患者在随机分组前有短暂ST段偏移;1个月后,安慰剂组24%的患者和维拉帕米治疗组8%的患者出现缺血(p = 0.04);1年后,这一数字分别为26%和4%(p = 0.02)。随机分组前有缺血的患者18个月主要事件发生率,即首次再梗死或死亡,在无缺血患者中为40%,有缺血患者中为23.8%(p = 0.06)。心律失常:在安慰剂组,梗死后头几年许多室性早搏(VEB),即每小时超过10次室性早搏的发生率和患病率显著增加;维拉帕米治疗组则不然。治疗1个月和16个月后,维拉帕米治疗使平均心率显著降低。多因素分析表明,仅在梗死后早期(即1周)而非晚期(即1个月)每小时有超过10次室性早搏是18个月随访观察期间主要事件的独立预测因素。梗死后早期和晚期心率高于80次/分钟均独立预测主要事件。(摘要截选于250字)