Leatham E W, Holt D W, McKenna W J
Department of Cardiological Sciences, St George's Hospital Medical School, London, England.
Drug Saf. 1993 Dec;9(6):450-62. doi: 10.2165/00002018-199309060-00008.
Class III (Vaughan-Williams classification) antiarrhythmic drugs prolong the cardiac action potential without affecting depolarisation. The 3 class III drugs currently in general use are amiodarone, sotalol and bretylium. The presenting features of acute toxicity are different for each agent and are, therefore, discussed separately. Several new class III antiarrhythmic agents are under development, including dofetilide and d-sotalol, but specific data on overdoses of these potent class III drugs are not yet available. Amiodarone toxicity following acute overdose is rare because poor bioavailability and a large volume of distribution limit the peak serum concentration. Toxicity is low even if high serum concentrations are reached. The major risks from acute overdose are hypotension (intravenous administration only) and arrhythmia if other factors, such as hypokalaemia or additional antiarrhythmic agents are present. Management is chiefly directed at reducing absorption with activated charcoal or cholestyramine, and monitoring for arrhythmia. Sotalol is a beta-blocker with additional class III activity. Oral bioavailability is high, and overdosed patients can present with bradycardia, hypotension and major haemodynamic collapse. The combination of bradycardia and prolongation of the QT interval is associated with malignant arrhythmias such as torsade de pointes. Management principles include observation and correction of bradycardia with endocardial pacing, intravenous adrenergic drugs and glucagon. The risk of arrhythmia can be substantially reduced by intravenous potassium and magnesium supplements. d-Sotalol is a potent class III drug devoid of beta-blocking activity and may be expected to share the proarrhythmic affects of the racemic mixture in overdose, without pronounced hypotension and bradycardia. Intravenous bretylium in overdose causes an initial hypertensive effect, followed by profound hypotension from systemic vasodilation. Management is directed at controlling hypotension with volume expansion and norepinephrine (noradrenaline).
Ⅲ类( Vaughan - Williams分类法)抗心律失常药物可延长心脏动作电位而不影响去极化。目前普遍使用的3种Ⅲ类药物是胺碘酮、索他洛尔和溴苄铵。每种药物急性中毒的表现各不相同,因此分别进行讨论。几种新型Ⅲ类抗心律失常药物正在研发中,包括多非利特和d - 索他洛尔,但关于这些强效Ⅲ类药物过量的具体数据尚未可得。急性过量服用胺碘酮后中毒情况罕见,因为其生物利用度差且分布容积大,限制了血清峰值浓度。即使达到高血清浓度,毒性也较低。急性过量的主要风险是低血压(仅静脉给药时)以及如果存在其他因素如低钾血症或额外的抗心律失常药物时出现心律失常。处理主要是用活性炭或考来烯胺减少吸收,并监测心律失常。索他洛尔是一种兼具Ⅲ类活性的β受体阻滞剂。口服生物利用度高,过量服用的患者可出现心动过缓、低血压和严重的血流动力学崩溃。心动过缓和QT间期延长共同作用与恶性心律失常如尖端扭转型室速相关。处理原则包括观察并用心内膜起搏、静脉注射肾上腺素能药物和胰高血糖素纠正心动过缓。静脉补充钾和镁可大幅降低心律失常的风险。d - 索他洛尔是一种强效Ⅲ类药物,无β受体阻滞活性,预计在过量服用时会出现与消旋体混合物相同的促心律失常作用,但不会有明显的低血压和心动过缓。过量服用静脉注射溴苄铵会引起初始的高血压效应,随后因全身血管扩张导致严重低血压。处理方法是通过扩容和去甲肾上腺素(去甲肾上腺素)控制低血压。