Catheter Ablation vs Antiarrhythmic Drug Therapy for Treatment of Premature Ventricular Complexes

医学 胺碘酮 导管消融 心脏病学 射血分数 心肌病 不利影响 烧蚀 临床试验 动态心电图监护仪 随机对照试验 内科学 欧洲联盟 科克伦图书馆 心脏病 心力衰竭 心电图 心房颤动 业务 经济政策
作者
Kasun De Silva,Haris M. Haqqani,Rajiv Mahajan,Pierre Qian,W. Chik,Aleksandr Voskoboinik,P. Kistler,Geoffrey Lee,Nicholas Jackson,Saurabh Kumar
出处
期刊:JACC: Clinical Electrophysiology [Elsevier]
卷期号:9 (6): 873-885 被引量:2
标识
DOI:10.1016/j.jacep.2023.01.035
摘要

There is variability in treatment modalities for premature ventricular complexes (PVCs), including use of antiarrhythmic drug (AAD) therapy or catheter ablation (CA). This study reviewed evidence comparing CA vs AADs for the treatment of PVCs. A systematic review was performed from the Medline, Embase, and Cochrane Library databases, as well as the Australian and New Zealand Clinical Trials Registry, U.S. National Library of Medicine ClinicalTrials database, and the European Union Clinical Trials Register. Five studies (1 randomized controlled trial) enrolling 1,113 patients (57.9% female) were analyzed. Four of five studies recruited mainly patients with outflow tract PVCs. There was significant heterogeneity in AAD choice. Electroanatomic mapping was used in 3 of 5 studies. No studies documented intracardiac echocardiography or contact force–sensing catheter use. Acute procedural endpoints varied (2 of 5 targeted elimination of all PVCs). All studies had significant potential for bias. CA seemed superior to AADs for PVC recurrence, frequency, and burden. One study reported long-term symptoms (CA superior). Quality of life or cost-effectiveness was not reported. Complication and adverse event rates were 0% to 5.6% for CA and 9.5% to 21% for AADs. Future randomized controlled trials will assess CA vs AADs for patients with PVCs without structural heart disease (ECTOPIA [Elimination of Ventricular Premature Beats with Catheter Ablation versus Optimal Antiarrhythmic Drug Treatment]), with impaired LVEF (PAPS [Prospective Assessment of Premature Ventricular Contractions Suppression in Cardiomyopathy] Pilot), and with structural heart disease (CAT-PVC [Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contractions in Patients With Structural Heart Disease]). In conclusion, CA seems to reduce recurrence, burden, and frequency of PVCs compared with AADs. There is a lack of data on patient- and health care–specific outcomes such as symptoms, quality of life, and cost-effectiveness. Several upcoming trials will offer important insights for management of PVCs.
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