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普罗帕酮抗心律失常作用与血清浓度及传导时间的关系(作者译)

[Antiarrhythmic effect of propafenone in relation to serum concentration and conduction time (author's transl)].

作者信息

Meyer-Estorf G, Keller K, Beck O A, Hochrein H

出版信息

Z Kardiol. 1978 May;67(5):353-6.

PMID:654420
Abstract

7 patients with stable cardiac dysrhythmias (ectopic beats of ventricular origin) received a single oral dose of 900 mg Propafenone. Besides the antiarrhythmic effect of propafenone the effect on changes of PQ- and QRS duration as well as the corresponding serum concentration was measured. A significant correlation between changes of PQ-time and serum concentration (r = 0.6810, p less than 0.001) was found. The half-life of serum level was 3.6 +/- 0.2 h, that of PQ-time prolongation 3.8 +/- 0.6 h. A complete suppression of all ectopic beats has been achieved in all treated patients for 6--8 hours.

摘要

7例患有稳定型心律失常(室性异位搏动)的患者单次口服900毫克普罗帕酮。除了测量普罗帕酮的抗心律失常作用外,还测量了其对PQ间期和QRS时限变化以及相应血清浓度的影响。发现PQ间期变化与血清浓度之间存在显著相关性(r = 0.6810,p < 0.001)。血清水平的半衰期为3.6±0.2小时,PQ间期延长的半衰期为3.8±0.6小时。所有接受治疗的患者在6 - 8小时内实现了所有异位搏动的完全抑制。

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