The Cardiovascular Institute, Tokyo, Japan.
Pharmacovigilance Division, Ono Pharmaceutical Co., Ltd., Osaka, Japan.
J Cardiol. 2019 Nov;74(5):418-425. doi: 10.1016/j.jjcc.2019.05.012. Epub 2019 Jun 26.
Atrial fibrillation and atrial flutter occur commonly in patients with heart failure. Ultrashort-acting β-blockers, including landiolol, can rapidly control heart rate. As part of postmarketing surveillance for landiolol in Japan, a real-world drug-use survey (AF-CHF landiolol survey) was established for the treatment of atrial fibrillation and atrial flutter in patients with heart failure. We report the safety and effectiveness of landiolol from this survey, focusing on adverse events/adverse drug reactions.
Consecutive patients with cardiac dysfunction who received landiolol (continuous intravenous infusion, starting at 1μg/kg/min) for atrial fibrillation or atrial flutter in routine clinical practice in Japan were enrolled between June 2014 and May 2016. Safety variables included adverse events and adverse drug reactions (number of patients and events, incidence rate, types, seriousness). Effectiveness variables included the proportion of patients with a ≥20% decrease in heart rate.
Data were available for 1121 patients (safety analysis set); 888 patients were evaluable for effectiveness parameters. Mean (± standard deviation) patient age was 72.5±13.5 years, 57.2% were male. Most patients (84.2%) received landiolol for atrial fibrillation. Overall, 174 adverse events occurred in 140 patients (12.5%), including 105 serious adverse events. The most common type of adverse events was cardiac (60 events). Seventy-five events in 63 patients were categorized as adverse drug reactions (5.6% of patients). Mean heart rate decreased substantially after treatment with landiolol, by ≥20% in 77.5% of patients.
In a real-world setting in Japan, landiolol for the treatment of atrial fibrillation or atrial flutter with heart failure was acceptable without new safety concerns, and most patients achieved effective heart rate control during their arrhythmias.
心房颤动和心房扑动在心力衰竭患者中很常见。超短效β受体阻滞剂,包括拉地洛尔,可以快速控制心率。作为拉地洛尔在日本上市后监测的一部分,进行了一项真实世界的药物使用调查(AF-CHF 拉地洛尔调查),以治疗心力衰竭患者的心房颤动和心房扑动。我们报告了这项调查中拉地洛尔的安全性和有效性,重点关注不良事件/药物不良反应。
连续入选 2014 年 6 月至 2016 年 5 月在日本常规临床实践中接受拉地洛尔(连续静脉输注,起始剂量为 1μg/kg/min)治疗心房颤动或心房扑动的心脏功能障碍患者。安全性变量包括不良事件和药物不良反应(患者和事件数量、发生率、类型、严重程度)。有效性变量包括心率降低≥20%的患者比例。
1121 例患者(安全性分析集)的数据可用;888 例患者可评估有效性参数。患者平均(±标准差)年龄为 72.5±13.5 岁,57.2%为男性。大多数患者(84.2%)因心房颤动接受拉地洛尔治疗。总体而言,140 例患者(12.5%)发生 174 例不良事件,包括 105 例严重不良事件。最常见的不良事件类型为心脏(60 例事件)。63 例患者的 75 例事件被归类为药物不良反应(5.6%的患者)。使用拉地洛尔治疗后,平均心率显著降低,77.5%的患者心率降低≥20%。
在日本的真实环境中,拉地洛尔治疗心力衰竭伴心房颤动或心房扑动没有新的安全性问题,大多数患者在心律失常期间实现了有效的心率控制。