Marks C, Dews I, Gould S E, Stephens J, VandenBurg M
Department of Cardiology, Oldchurch Hospital, Romford, Essex, UK.
Cardiovasc Drugs Ther. 1990 Jan;4 Suppl 1:93-5. doi: 10.1007/BF00053436.
Ketanserin is a serotonin S2-receptor antagonist that lowers blood pressure and inhibits platelet aggregation. Ketanserin treatment is also associated with prolongation of the corrected QT interval. The recently reported Prevention of Atherosclerotic Complications with Ketanserin (PACK) trial confirmed this prolongation of QT and also revealed a significant excess of deaths in patients receiving ketanserin together with potassium-losing diuretics. The investigators suggested that this excess of deaths may have been attributable to exacerbation of hypokalemia-induced ventricular arrhythmias by the repolarization-prolonging effect of ketanserin. However, drugs that prolong the QT interval may affect ventricular ectopic activity beneficially, and our study was designed to evaluate the effects of ketanserin on ventricular ectopic activity. Twenty patients (18 male, 2 female) aged 42-73 years were studied, each having at least 15 ventricular ectopic beats/hour. The study design was a double-blind, crossover comparison of ketanserin, 40 mg twice daily, and placebo, both given for 1 week. Ventricular ectopic activity was assessed by 48-hour Holter electrocardiogram (ECG) tapes at the end of each treatment period. Ketanserin treatment was associated with prolongation of repolarization, as reflected by the significant mean increases in both QT interval (+30 ms; p less than 0.001) and corrected QT interval (+20 ms; p less than 0.05). The mean overall degree of ventricular ectopic activity, as represented by a score based on the Lown classification, was significantly reduced (p less than 0.05). This was associated with a concordant improvement in the individual indices of ectopic activity. Our results show that ketanserin significantly suppressed ventricular ectopic activity in our normokalemic patients.(ABSTRACT TRUNCATED AT 250 WORDS)
酮色林是一种血清素S2受体拮抗剂,可降低血压并抑制血小板聚集。酮色林治疗还与校正QT间期延长有关。最近报道的酮色林预防动脉粥样硬化并发症(PACK)试验证实了QT间期的这种延长,并且还显示接受酮色林与排钾利尿剂联合治疗的患者死亡显著增多。研究人员认为,这种死亡过多可能归因于酮色林的复极延长作用加剧了低钾血症诱发的室性心律失常。然而,延长QT间期的药物可能对室性异位活动产生有益影响,我们的研究旨在评估酮色林对室性异位活动的影响。研究了20名年龄在42至73岁之间的患者(18名男性,2名女性),每人每小时至少有15次室性早搏。研究设计为双盲、交叉比较,每日两次给予40毫克酮色林和安慰剂,均给药1周。在每个治疗期结束时,通过48小时动态心电图(ECG)磁带评估室性异位活动。酮色林治疗与复极延长有关,QT间期(+30毫秒;p小于0.001)和校正QT间期(+20毫秒;p小于0.05)均显著平均增加即反映了这一点。以基于洛恩分类的评分表示的室性异位活动的平均总体程度显著降低(p小于0.05)。这与异位活动的各个指标的一致改善相关。我们的结果表明,酮色林在我们的正常血钾患者中显著抑制了室性异位活动。(摘要截短为250字)