Dabrowski R, Skrabucha B, Kunicki P K, Kowalik I, Skorykow-Sapińska A, Sitkiewicz D, Sadowski Z
Klinika Choroby Wieńcowej Instytutu Kardiologii w Warszawie.
Pol Arch Med Wewn. 1998 Apr;99(4):323-30.
We prospectively evaluated reaching of steady state and clinical efficacy of propafenone (PPF), class Ic antiarrhythmic agent, in 16 patients (pts) (age 46-69, mean 57 years) with symptomatic ventricular arrhythmias (Low class II and IV). The majority (13 pts) had coronary artery disease. Drug was administered for 7 days (daily dose: 3 x 150 mg). Efficacy was defined as > 80% reduction of ventricular premature complexes (VPC) and class IV elimination in 24-hours Holter recording. Responders were continued on PPF for 3 weeks, in non-responders dose was titrated to 900 mg a day for the next 7 days. After second Holter evaluation the treatment was continued for 2 weeks in responders group. The non-responders were switched to other drug. After 4 weeks final Holter monitoring was performed. Serum concentration of PPF and its 2 metabolites: 5-hydroxy PPF and N-depropyl PPF were determined in 2, 3, 4, 5, 6, 7th day, just before the morning dose (3 x 150 mg/day) in 9 pts.
Trough serum concentrations of PPF differed in high degree: 0-226 ng/ml (2nd day), 22-438 ng/ml (4th day), 42-614 ng/ml (6-7 day). An increasing tendency of serum concentrations of PPF was observed, so steady-state was not reached. This great dispersion of concentration values is because of non-linear metabolism and individual differences. Defined efficacy critetion was achieved in 62% pts, 56% for lower dose. Mean frequency of VPC was reduced by 86% in 24-hour Holter recording and per hour (p = 0.0011). Reduction of couplets/24 h was 87% (p = 0.0175). Significant prolongation of PQ (14%, p = 0.009) and QRS (13%, p = 0.0052) were observed. Changes of QT interval were not significant. One case of proarrhythmia was the cause of stopping the treatment.
Serum concentrations' values undermine common opinion, that steady state can be reached after 1-2 days of treatment. High dispersion of serum levels is the result of nonlinear metabolism of PPF and individual differences. In spite of this the study showed defined antiarrhythmic efficacy in 62.5% pts. In this group 90% success rate was achieved after lower dose 3 x 150 mg.
我们前瞻性评估了Ⅰc类抗心律失常药物普罗帕酮(PPF)在16例有症状室性心律失常(低Ⅱ级和Ⅳ级)患者(年龄46 - 69岁,平均57岁)中的稳态达到情况及临床疗效。大多数患者(13例)患有冠状动脉疾病。药物给药7天(每日剂量:3×150mg)。疗效定义为24小时动态心电图记录中室性早搏(VPC)减少>80%且Ⅳ级消除。有反应者继续服用PPF 3周,无反应者在接下来7天将剂量滴定至每日900mg。第二次动态心电图评估后,有反应者组继续治疗2周。无反应者换用其他药物。4周后进行最终的动态心电图监测。在9例患者的第2、3、4、5、6、7天,即晨服(3×150mg/天)前测定PPF及其2种代谢物:5 - 羟基PPF和N - 去丙基PPF的血清浓度。
PPF的谷血清浓度差异很大:第2天为0 - 226ng/ml,第4天为22 - 438ng/ml,第6 - 7天为42 - 614ng/ml。观察到PPF血清浓度有上升趋势,因此未达到稳态。浓度值的这种巨大差异是由于非线性代谢和个体差异。62%的患者达到了定义的疗效标准,低剂量组为56%。24小时动态心电图记录中VPC的平均频率每小时降低了86%(p = 0.0011)。每24小时成对室性早搏减少87%(p = 0.0175)。观察到PQ间期显著延长(14%,p = 0.009)和QRS间期显著延长(13%,p = 0.0052)。QT间期变化不显著。1例促心律失常是停止治疗的原因。
血清浓度值推翻了通常认为治疗1 - 2天后可达到稳态的观点。血清水平的高度分散是PPF非线性代谢和个体差异的结果。尽管如此,该研究显示62.5%的患者有明确的抗心律失常疗效。在该组中,较低剂量3×150mg后成功率达到90%。