Meinertz T, Kasper W, Stengel E, Waldecker B, Löllgen H, Jähnchen E, Bechtold H, Just J
Z Kardiol. 1982 Jan;71(1):35-8.
In a blind cross-over study, 12 patients with ventricular arrhythmias (VPC's; Lown Grades II-IVB) resistant to a daily dose of quinidine 1.2 g, disopyramide 0.8 g, N-propyl-ajmaline 0.1 g were randomly given, each dose for one week, placebo (PL), mexiletine (MEX; 400, 600, 800 mg daily) and lorcainide (LOR; 200, 300, 400 mg daily). On the last day of each treatment period, patients were evaluated by 24-h continuous ambulatory monitoring, 6-channel surface ECG, plasma concentrations and side-effects. During PL I (before) and PL II (after drug treatment), the mean number of VPCs per hour was 670 and 701. VPCs were reduced in 5 of the 12 patients with MEX by 43% (400 mg), 74% (600 mg) and 91% (800 mg). VPCs were reduced in 10 patients with LOR by 60% (200 mg), 78% (300 mg) and 93% (400 mg). Log. lin. plasma conc. effect relationships were constructed for MEX and LOR. Vomiting, nausea, and abdominal pain were seen in 2 patients with MEX; insomnia and feeling heat in 10 patients with LOR. At the end of the LOR-treatment, these side-effects were less in 5 and absent in 5 patients. In this study, LOR seems superior to MEX in refractory ventricular arrhythmias.
在一项双盲交叉研究中,12例对每日剂量1.2 g奎尼丁、0.8 g丙吡胺、0.1 g N-丙基阿马林耐药的室性心律失常(室性早搏;洛恩分级II-IVB级)患者被随机给予,每种剂量服用一周,分别为安慰剂(PL)、美西律(MEX;每日400、600、800 mg)和劳卡尼(LOR;每日200、300、400 mg)。在每个治疗期的最后一天,通过24小时连续动态监测、6通道体表心电图、血浆浓度和副作用对患者进行评估。在PL I(用药前)和PL II(药物治疗后)期间,每小时室性早搏的平均数量分别为670次和701次。12例服用MEX的患者中有5例室性早搏减少,减少幅度分别为43%(400 mg)、74%(600 mg)和91%(800 mg)。10例服用LOR的患者室性早搏减少,减少幅度分别为60%(200 mg)、78%(300 mg)和93%(400 mg)。构建了MEX和LOR的对数线性血浆浓度-效应关系。2例服用MEX的患者出现呕吐、恶心和腹痛;10例服用LOR的患者出现失眠和发热感。在LOR治疗结束时,5例患者这些副作用减轻,5例患者副作用消失。在本研究中,在难治性室性心律失常方面,LOR似乎优于MEX。