Anderson J L, Platt M L, Guarnieri T, Fox T L, Maser M J, Pritchett E L
Department of Medicine, University of Utah, Salt Lake City.
Am J Cardiol. 1994 Sep 15;74(6):578-84. doi: 10.1016/0002-9149(94)90747-1.
Flecainide has been shown to be effective in short-term, controlled studies for prevention of paroxysmal supraventricular tachycardia (SVT) and paroxysmal atrial fibrillation (AF). However, it is unknown whether this beneficial response is maintained during long-term chronic therapy. Forty-nine patients were studied who enrolled in double-blind, placebo-controlled, short-term studies of safety and efficacy and subsequently received long-term, open-label therapy for > or = 6 months (mean duration of therapy, 17 months). To evaluate chronic efficacy, events during long-term therapy were documented by a transtelephonic monitor for either 4 or 8 weeks, comparable to the corresponding 4- or 8-week placebo-baseline periods in the same patients. Results during chronic therapy were compared with those at baseline and after the initial (short-term) treatment period. Compared with placebo-baseline results, the number of patients free of arrhythmic attacks increased significantly for both patients with SVT (from 24% to 82%, p = 0.013, n = 17) and patients with AF (from 12% to 68%, p < 0.001, n = 25). Mean time to first attack and mean number of days between attacks also showed significant and parallel increases during the chronic efficacy period. In patients with paired short- and long-term efficacy evaluations with the same dose of flecainide, end points were maintained at equivalent levels or showed further improvement (i.e., mean rate of AF attacks decreased further with chronic therapy, p = 0.036). No proarrhythmic events, death, or myocardial infarction occurred.(ABSTRACT TRUNCATED AT 250 WORDS)
在预防阵发性室上性心动过速(SVT)和阵发性心房颤动(AF)的短期对照研究中,已证明氟卡尼是有效的。然而,这种有益反应在长期慢性治疗期间是否能维持尚不清楚。对49名患者进行了研究,这些患者参加了双盲、安慰剂对照的短期安全性和有效性研究,随后接受了≥6个月(平均治疗持续时间为17个月)的长期开放标签治疗。为了评估长期疗效,通过电话传输监测仪记录长期治疗期间4周或8周的事件,这与同一患者相应的4周或8周安慰剂基线期相当。将长期治疗结果与基线期及初始(短期)治疗期后的结果进行比较。与安慰剂基线结果相比,SVT患者(从24%增至82%,p = 0.013,n = 17)和AF患者(从12%增至68%,p < 0.001,n = 25)中无心律失常发作的患者数量均显著增加。在长期疗效期,首次发作的平均时间和发作间隔的平均天数也显示出显著且平行的增加。在使用相同剂量氟卡尼进行短期和长期疗效配对评估的患者中,终点维持在同等水平或有进一步改善(即慢性治疗使AF发作的平均发生率进一步降低,p = 0.036)。未发生促心律失常事件、死亡或心肌梗死。(摘要截短于250字)