Peter T, Ross D, Duffield A, Luxton M, Harper R, Hunt D, Sloman G
Br Heart J. 1978 Dec;40(12):1356-60. doi: 10.1136/hrt.40.12.1356.
A prospective, randomised, open trial was performed in 150 patients to test for any beneficial effects on 2-year mortality of long-term antiarrhythmic therapy with phenytoin in patients with acute myocardial infarction. Patients were stratified according to age, sex, past history of myocardial infarction, and the presence of absence of electrical or mechanical complications in the course of acute infarction. They were then randomised to treatment or control groups (74 v. 76). The former received phenytoin in doses aimed at maintaining plasma phenytoin levels between 40 and 80 mumol/litre. All patients entered the study before discharge from the coronary care ward. Plasma phenytoin levels were in the therapeutic range in between 51 and 75 per cent of subjects at any follow up visit. There were 19 withdrawals from the treatment group, 10 of which were the result of side effects. There were 5 withdrawals from the control group. According to the original intention to treat, there were 18 deaths at 2 years in the treatment group and 14 deaths in the control group. There was no reduction in the incidence of instantaneous or sudden deaths. Deaths on treatment were not associated with a low phenytoin plasma level. Phenytoin treatment showed no beneficial effects on mortality and was associated with a high incidence of side effects.
对150例患者进行了一项前瞻性、随机、开放试验,以测试苯妥英钠长期抗心律失常治疗对急性心肌梗死患者2年死亡率的有益影响。患者根据年龄、性别、心肌梗死病史以及急性梗死过程中是否存在电或机械并发症进行分层。然后将他们随机分为治疗组和对照组(74例对76例)。治疗组接受苯妥英钠治疗,剂量旨在使血浆苯妥英水平维持在40至80微摩尔/升之间。所有患者在从冠心病监护病房出院前进入研究。在任何随访中,51%至75%的受试者血浆苯妥英水平处于治疗范围内。治疗组有19例退出,其中10例是副作用导致的。对照组有5例退出。根据最初的治疗意向分析,治疗组2年时有18例死亡,对照组有14例死亡。即时或猝死的发生率没有降低。治疗期间的死亡与苯妥英血浆水平低无关。苯妥英治疗对死亡率没有有益影响,且副作用发生率高。