High incidence of permanent pacemaker after Cox-maze IV and mitral valve surgery: A nationwide registry-based study.

0 CARDIAC & CARDIOVASCULAR SYSTEMS
Torbjörn Ivert, Gabriella Boano, Farkas Vanky, Fredrik Gadler, Anders Holmgren, Lena Jidéus, Birgitta Johansson, Göran Kennebäck, Shahab Nozohoor, Henrik Scherstén, Johan Sjögren, Anders Wickbom, Örjan Friberg, Anders Albåge
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Abstract

Objectives: This study evaluated the long-term risk of permanent pacemaker implantation following Cox-maze IV (CMIV) and concurrent mitral valve surgery.

Methods: A retrospective, nationwide, registry-based analysis was conducted on postoperative permanent pacemaker implantation in 397 patients with symptomatic mitral valve insufficiency and atrial fibrillation who underwent CMIV and mitral valve surgery in Sweden between 2009 and 2017. They were compared to a registry group of 346 patients with atrial fibrillation who underwent mitral valve surgery without surgical ablation during 2014-2017. The follow-up ended on September 30, 2022.

Results: CMIV patients were on average four years younger and had lower surgical risk than registry patients. More CMIV patients underwent early (<30 days) pacemaker implantation (13.3% vs 5.5%, p = 0.002). CMIV patients had a doubled adjusted risk of requiring a pacemaker compared to registry patients after 8 years [HR 1.96, 95% CI 1.27-3.04]. In the CMIV group, 22% (95% CI 18-26%) had a pacemaker by 5 years, increasing to 27% (95% CI 22-31%) by 8 years, compared to 13% (95% CI 10-17%) at both time intervals in the registry group. Atrioventricular block II/III accounted for >60% of early pacemaker indications in both groups, and sinus node dysfunction was the indication for late pacemaker implantation in 48% in the CMIV group.

Conclusions: Patients undergoing CMIV concomitant with mitral valve surgery have a higher rate of postoperative pacemaker implantation compared to patients with atrial fibrillation undergoing mitral valve surgery alone. Sinus node dysfunction was the main indication for late pacemaker among CMIV patients.

Cox-maze IV和二尖瓣手术后永久性起搏器的高发病率:一项全国性的基于登记的研究。
目的:本研究评估Cox-maze IV (CMIV)合并二尖瓣手术后永久性起搏器植入的长期风险。方法:回顾性分析2009年至2017年在瑞典接受CMIV和二尖瓣手术的397例有症状的二尖瓣功能不全和心房颤动患者术后永久起搏器植入情况,并在全国范围内进行登记分析。将他们与2014-2017年期间接受二尖瓣手术但未手术消融的346例房颤患者进行比较。后续工作于2022年9月30日结束。结果:CMIV患者比登记患者平均年轻4岁,手术风险较低。在两组中,更多的CMIV患者接受了早期起搏器适应症(60%),在CMIV组中,窦结功能障碍是晚期起搏器植入的适应症(48%)。结论:CMIV合并二尖瓣手术的心房颤动患者术后起搏器植入率高于单纯二尖瓣手术的心房颤动患者。窦结功能障碍是CMIV患者晚期起搏器的主要指征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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