Inoue Hiroshi, Atarashi Hirotsugu, Okumura Ken, Yamashita Takeshi, Fukuzawa Masayuki, Shiosakai Kazuhito, Kimura Tetsuya
Saiseikai Toyama Hospital, Toyama, Japan.
Department of Internal Medicine, Nippon Medical School Tama-Nagayama Hospital, Tokyo, Japan.
J Cardiol. 2017 Jan;69(1):293-301. doi: 10.1016/j.jjcc.2016.05.012. Epub 2016 Jun 28.
β-Blockers are used to control heart rate (HR) in patients with atrial fibrillation (AF). However, the appropriate dosage and efficacy of carvedilol in Japanese AF patients are yet to be clarified.
In this multicenter, randomized, double-blind study, Japanese patients with persistent or permanent AF received carvedilol for 6 weeks in the following three dosage-regimen groups: 5-mg fixed-dose (n=42), 10-mg dose-escalation (n=42), or 20-mg dose-escalation (n=43). To evaluate the efficacy of each dosage regimen and the dose-response relationship, changes in 24-h mean HR (mHR) on Holter electrocardiograms from baseline to weeks 2, 4, and 6 were determined as primary endpoints. The effects on circadian changes in HR, the proportion of patients achieving target HR, clinical symptoms, and adverse events were also examined.
After 2 weeks, carvedilol 5mg decreased 24-h mHR significantly [6.6 (95% CI: 5.2-8.0)beats/min, p<0.0001]. After 6 weeks, carvedilol showed a trend of dose-dependent HR reduction (p=0.0638): 7.6 (5.4-9.8) in the 5-mg fixed-dose group; 8.9 (6.7-11.1) in the 10-mg dose-escalation group; and 10.6 (8.4-12.8)beats/min in the 20-mg dose-escalation group. There were no serious adverse events related to carvedilol.
In Japanese patients with persistent or permanent AF, carvedilol at 5mg once daily demonstrated a significant HR reduction, and step-wise dose escalation from 5mg to 20mg showed a trend of dose-dependent HR reduction.
β受体阻滞剂用于控制心房颤动(AF)患者的心率(HR)。然而,卡维地洛在日本AF患者中的合适剂量及疗效尚待阐明。
在这项多中心、随机、双盲研究中,日本持续性或永久性AF患者被分入以下三个剂量方案组,接受卡维地洛治疗6周:5毫克固定剂量组(n = 42)、10毫克剂量递增组(n = 42)或20毫克剂量递增组(n = 43)。为评估各剂量方案的疗效及剂量反应关系,将24小时动态心电图平均心率(mHR)从基线到第2、4和6周的变化确定为主要终点。还检查了对心率昼夜变化、达到目标心率的患者比例、临床症状及不良事件的影响。
2周后,5毫克卡维地洛显著降低24小时mHR[6.6(95%CI:5.2 - 8.0)次/分钟,p < 0.0001]。6周后,卡维地洛呈现剂量依赖性心率降低趋势(p = 0.0638):5毫克固定剂量组为7.6(5.4 - 9.8);10毫克剂量递增组为8.9(6.7 - 11.1);20毫克剂量递增组为10.6(8.4 - 12.8)次/分钟。未出现与卡维地洛相关的严重不良事件。
在日本持续性或永久性AF患者中,每日一次服用5毫克卡维地洛可显著降低心率,从5毫克逐步递增至20毫克显示出剂量依赖性心率降低趋势。