医学
心脏再同步化治疗
心脏病学
内科学
植入式心律转复除颤器
心房颤动
窦性心律
心力衰竭
入射(几何)
置信区间
导管消融
烧蚀
射血分数
光学
物理
作者
Maurizio Gasparini,Axel Kloppe,Maurizio Lunati,Frédéric Anselme,Maurizio Landolina,José Martínez-Ferrer,Alessandro Proclemer,Giovanni Morani,Mauro Biffi,Renato Pietro Ricci,Roberto Rordorf,Lorenza Mangoni,Laura Manotta,Andrea Grammatico,Francisco Leyva,Giuseppe Boriani
摘要
Aims We sought to determine whether atrioventricular junction ablation (AVJA) in patients with cardiac resynchronization therapy (CRT) implantable cardioverter‐defibrillator (ICD) and with permanent atrial fibrillation (AF) has a positive impact on ICD shocks and hospitalizations compared with rate‐slowing drugs. Methods and results This is a pooled analysis of data from 179 international centres participating in two randomized trials and one prospective observational research. The co‐primary endpoints were all‐cause ICD shocks and all‐cause hospitalizations. Out of 3358 CRT‐ICD patients (2720 male, 66.6 years), 2694 (80%) were in sinus rhythm (SR) and 664 (20%) had permanent AF—262 (8%) treated with AVJA (AF + AVJA) and 402 (12%) treated with rate‐slowing drugs (AF + Drugs). Median follow‐up was 18 months. The mean (95% confidence intervals) annual rate of all‐cause ICD shocks per 100 patient years was 8.0 (5.3–11.9) in AF + AVJA, 43.6 (37.7–50.4) in AF + Drugs, and 34.4 (32.5–36.5) in SR patients, resulting in incidence rate ratio (IRR) reductions of 0.18 (0.10–0.32) for AF + AVJA vs. AF + Drugs ( P < 0.001) and 0.48 (0.35–0.66) for AF + AVJA vs. SR ( P < 0.001). These reductions were driven by significant reductions in both appropriate ICD shocks [IRR 0.23 (0.13–0.40), P < 0.001, vs. AF + Drugs] and inappropriate ICD shocks [IRR 0.09 (0.04–0.21), P < 0.001, vs. AF + Drugs]. Annual rate of all‐cause hospitalizations was significantly lower in AF + AVJA vs. AF + Drugs [IRR 0.57 (0.41–0.79), P < 0.001] and SR [IRR 0.85 (073–0.98), P = 0.027]. Conclusion In AF patients treated with CRT, AVJA results in a lower incidence and burden of all‐cause, appropriate and inappropriate ICD shocks, as well as to fewer all‐cause and heart failure hospitalizations. Clinical Trial Registration: NCT00147290, NCT00617175, NCT01007474.
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