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心肌梗死患者使用缓释普鲁卡因酰胺。

Sustained release procainamide in patients with myocardial infarction.

作者信息

Birkhead J, Evans T, Mumford P, Martinez E, Jewitt D

出版信息

Br Heart J. 1976 Jan;38(1):77-80. doi: 10.1136/hrt.38.1.77.

Abstract

Sustained release procainamide tablets were administered to 34 patients 48 hours after the onset of an acute myocardial infarct. Therapeutic blood levels of procainamide in the range of 4 to 8 mug/ml were consistently achieved using an 8-hourly maintenance dose of 1.5g after an initial loading dose of 2g. In contrast conventional procainamide capsules administered to 21 comparable patients repeatedly failed to produce plasma concentrations in the therapeutic range, despite the administration of a maintenance dose of 375 mg 3 hourly, after a loading dose of 1g. It is suggested that when the oral administration of procainamide is indicated for the management of ventricular arrhythmias after myocardial infarction, a sustained release preparation should be used.

摘要

在急性心肌梗死发作48小时后,对34例患者给予了缓释普鲁卡因胺片。在初始负荷剂量2g后,使用1.5g的8小时维持剂量,始终能达到4至8μg/ml范围内的治疗性血药浓度。相比之下,对21例情况相当的患者给予常规普鲁卡因胺胶囊,尽管在负荷剂量1g后每3小时给予375mg的维持剂量,但反复未能使血浆浓度达到治疗范围。建议在心肌梗死后需要口服普鲁卡因胺来治疗室性心律失常时,应使用缓释制剂。

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