Clinical Efficacy and Safety of Ibutilide in Cardioversion of Atrial Fibrillation or Flutter in Indian Patients: A Multicenter Study.

IF 1.5 Q3 CRITICAL CARE MEDICINE
Bhupesh Dewan, Sanjaykumar Navale, Siddheshwar Shinde, Janaki Chaudhary
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引用次数: 0

Abstract

Aim and background: To assess the efficacy and safety of Ibutilide infusion for cardioversion of atrial fibrillation (AF) or flutter (AFL) to sinus rhythm.

Materials and methods: This open-label, multicenter phase IV study was conducted at six sites across India. The study enrolled 120 patients (108 with AF, 12 with AFL), each receiving up to two, 10-minute intravenous doses of 1.0 mg Ibutilide. The primary endpoints were the proportion of patients achieving cardioversion and the mean time taken to achieve cardioversion. Secondary endpoints included the proportion of patients maintaining sinus rhythm at 24 hours and the incidence of adverse events.

Results: The cardioversion rate at 4 hours post-Ibutilide infusion among 120 patients was 65.83% (n = 79), with an average conversion time of 35.12 ± 36.71 minutes. At 24 hours, 85 patients (70.8%) had successful cardioversion, with a mean time of 107.24 minutes. The majority of patients (71.76%) had achieved cardioversion within 30 minutes. Of the 85 patients who achieved successful conversion, 82 (68.3%) maintained sinus rhythm at 24 hours. A total of 66 patients (55%) achieved cardioversion with the first bolus whereas 19 (15.8%) needed a second bolus. Atrial fibrillation patients had a higher conversion rate (75%) compared to AFL patients (33%). A total of 10 adverse events were recorded in eight patients (6.67%), including nausea, headache, palpitations, and bradycardia. Three severe cardiac events, one case of ventricular tachycardia, and two of tachycardia necessitated discontinuation of Ibutilide. No fatalities or serious adverse events (SAE) were reported.

Conclusion: Ibutilide was found to be effective and well-tolerated for rapid restoration of sinus rhythm in patients with AF or AFL.

Clinical trial registry of india: CTRI/2018/01/011248.

How to cite this article: Dewan B, Navale S, Shinde S, Chaudhary J. Clinical Efficacy and Safety of Ibutilide in Cardioversion of Atrial Fibrillation or Flutter in Indian Patients: A Multicenter Study. Indian J Crit Care Med 2025;29(1):45-51.

伊布利特在印度患者房颤或扑动复律中的临床疗效和安全性:一项多中心研究
目的与背景:评价静脉输注伊布利特对心房颤动(AF)或扑动(AFL)转窦性心律的疗效和安全性。材料和方法:这项开放标签、多中心的IV期研究在印度的6个地点进行。该研究招募了120名患者(108名AF患者,12名AFL患者),每位患者接受两次静脉注射1.0 mg伊布利特,每次10分钟。主要终点是实现心律转复的患者比例和实现心律转复所需的平均时间。次要终点包括24小时维持窦性心律的患者比例和不良事件的发生率。结果:120例患者输注伊布利特后4 h心律转复率为65.83% (n = 79),平均转复时间为35.12±36.71 min。24小时时,85例(70.8%)患者心脏复律成功,平均时间107.24分钟。大多数患者(71.76%)在30分钟内实现了心律转复。在85例成功转换的患者中,82例(68.3%)在24小时内保持窦性心律。总共66例(55%)患者通过第一次注射获得了心律转复,而19例(15.8%)患者需要第二次注射。心房颤动患者的转换率(75%)高于AFL患者(33%)。8例患者(6.67%)共发生恶心、头痛、心悸、心动过缓等10项不良事件。3例严重心脏事件,1例室性心动过速,2例心动过速需要停用伊布利特。无死亡或严重不良事件(SAE)报告。结论:伊布利特对房颤或AFL患者窦性心律的快速恢复是有效且耐受性良好的。印度临床试验注册:CTRI/2018/01/011248。Dewan B, Navale S, Shinde S, Chaudhary J.伊布利特治疗心房颤动或扑动的临床疗效和安全性:一项多中心研究。中华检验医学杂志,2015;29(1):45-51。
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来源期刊
CiteScore
3.50
自引率
10.00%
发文量
299
期刊介绍: Indian Journal of Critical Care Medicine (ISSN 0972-5229) is specialty periodical published under the auspices of Indian Society of Critical Care Medicine. Journal encourages research, education and dissemination of knowledge in the fields of critical and emergency medicine.
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