Pickering T G, Goulding L
Br Heart J. 1978 Aug;40(8):851-5. doi: 10.1136/hrt.40.8.851.
The antiarrhythmic effects of perhexiline were investigated in 13 of 20 patients with frequent and long standing ventricular extrasystoles in a double blind crossover trial using 24-hour electrocardiograph tape recordings, routine electrocardiograms, and treadmill exercise testing. With a dose of 300 to 400 mg per day, there was a significant decrease (mean 41%) in the number of ventricular extrasystoles per 24 hours. There were large differences in the individual responses to perhexiline, which were significantly related to the diurnal variations of ventricular extrasystoles: those patients whose ventricular extrasystoles disappeared spontaneously during sleep were less likely to respond to perhexiline than those whose ventricular extrasystoles persisted throughout the night. Suppression of ventricular extrasystoles was also apparent from the routine electrocardiogram and the exercise tests. Side effects (dizziness and unsteadiness) were troublesome in 5 of 20 patients. It is concluded that in selected patients perhexiline is an effective antiarrhythmic drug, and is likely to be most useful in patients with coexisting angina and ventricular extrasystoles. Because of its potential toxicity, it should not be used as a drug of first choice.
在一项双盲交叉试验中,使用24小时心电图磁带记录、常规心电图和跑步机运动试验,对20例频发且长期存在室性期前收缩的患者中的13例进行了哌克昔林抗心律失常作用的研究。每日剂量为300至400毫克时,每24小时室性期前收缩的数量显著减少(平均41%)。个体对哌克昔林的反应存在很大差异,这与室性期前收缩的昼夜变化显著相关:那些在睡眠期间室性期前收缩自发消失的患者对哌克昔林产生反应的可能性低于那些室性期前收缩整夜持续存在的患者。常规心电图和运动试验也显示出室性期前收缩受到抑制。20例患者中有5例出现了令人困扰的副作用(头晕和不稳)。得出的结论是,在特定患者中,哌克昔林是一种有效的抗心律失常药物,并且可能对合并心绞痛和室性期前收缩的患者最为有用。由于其潜在毒性,它不应作为首选药物使用。