Meinertz T, Kasper W, Kersting F, Bechtold H, Just H, Jähnchen E
Arzneimittelforschung. 1980;30(9):1593-5.
The effect of oral N-(4-chlorophenyl)-N-[1-(1-methylethyl)-4-piperidinyl]benzene acetamide (lorcainide) was studied in 12 patients with frequent and stable ventricular arrhythmias resistant to a number of other antiarrhythmic agents. Ambulatory electrocardiograms were obtained before and during treatment with lorcainide and in some patients after discontinuation of the drug. Lorcainide suppressed ventricular premature contractions by more than 90% in all but one patient. The daily doses were 200 mg (N = 8), 300 mg (N = 1), 400 mg (N = 1)and 600 mg (N = 2). Plasma concentrations of lorcainide and of the dealkylated metabolite ranged from 0.13 to 0.27 microgram/ml and 0.25 to 0.95 microgram/ml, respectively. Side effects such as insomnia and excessive perspiration were seen in 7 and 3 patients, respectively. Lorcainide is an effective antiarrhythmic agent against ventricular arrhythmias otherwise difficult to treat.
对12例频发且稳定的室性心律失常患者进行了研究,这些患者对多种其他抗心律失常药物耐药。研究口服N-(4-氯苯基)-N-[1-(1-甲基乙基)-4-哌啶基]苯乙酰胺(劳卡尼)的效果。在服用劳卡尼治疗前和治疗期间以及部分患者停药后进行了动态心电图检查。除1例患者外,劳卡尼在所有患者中均使室性早搏抑制率超过90%。每日剂量分别为200mg(8例)、300mg(1例)、400mg(1例)和600mg(2例)。劳卡尼及其脱烷基代谢物的血浆浓度分别为0.13至0.27μg/ml和0.25至0.95μg/ml。分别有7例和3例患者出现失眠和多汗等副作用。劳卡尼是一种治疗其他方法难以治疗的室性心律失常的有效抗心律失常药物。