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妥卡尼对室性异位去极化的抑制作用。

Suppression of ventricular ectopic depolarizations by tocainide.

作者信息

Woosley R L, McDevitt D G, Nies A S, Smith R F, Wilkinson G R, Oates J A

出版信息

Circulation. 1977 Dec;56(6):980-4. doi: 10.1161/01.cir.56.6.980.

Abstract

In a previous clinical study we demonstrated that tocainide is effective in the suppression of ventricular ectopic depolarizations (VEDs) after single oral doses. This information provided the basis for evaluating this drug's antiarrhythmic efficacy after multiple dose administration according to a loading-maintenance regimen. Twelve patients with stable VEDs were given loading doses of tocainide (400-600 mg) with maintenance doses every 12 hours. Every 48 hours the dose was increased until either arrhythmia suppression to less than 25% of VED frequency during placebo administration or side effects occurred. Computer analysis of 12-hr telemetric ECGs taken 24-36 hr after each dosage increment documented effective suppression (76-95%) in 8 of 12 patients. Those subjects demonstrating suppression were randomly assigned to a cross-over study of placebo or active drug at the dosage found effective in the dose-ranging phase. Dosages for the cross-over stage ranged from 400 to 1100 mg every 12 hours. Comparison of the two five-day periods documented suppression in these patients (mean +/- SE = 83.3 +/- 4%). No serious side effects or undue drug accumulation occurred during the study. The data indicate that tocainide can effectively suppress VEDs for 8-12 hours in many patients and that continuous suppression could be possible on an 8-12 hr dosage regimen.

摘要

在之前的一项临床研究中,我们证明了妥卡尼单次口服给药后对室性异位去极化(VEDs)有抑制作用。这一信息为根据负荷 - 维持方案评估该药物多次给药后的抗心律失常疗效提供了基础。12例VEDs稳定的患者给予妥卡尼负荷剂量(400 - 600mg),每12小时给予维持剂量。每48小时增加一次剂量,直至心律失常抑制至安慰剂给药期间VED频率的25%以下或出现副作用。每次剂量增加后24 - 36小时采集的12小时遥测心电图的计算机分析记录显示,12例患者中有8例有效抑制(76 - 95%)。那些显示有抑制作用的受试者被随机分配到交叉研究中,在剂量范围研究阶段找到的有效剂量下给予安慰剂或活性药物。交叉阶段的剂量为每12小时400至1100mg。对两个五天周期的比较记录了这些患者的抑制情况(均值±标准误 = 83.3±4%)。研究期间未出现严重副作用或药物过度蓄积。数据表明,妥卡尼可在许多患者中有效抑制VEDs达8 - 12小时,并且采用8 - 12小时给药方案可能实现持续抑制。

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