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在患有传统起搏器系统的高龄患者中使用无导线起搏器:一项为期两年的随访病例系列研究,在高风险情况下未进行发生器拔除

Utilizing Leadless Pacemakers in Extremely Elderly Patients With a Conventional Pacemaker System: A Two-Year Follow-Up Case Series Without Generator Extraction in High-Risk Scenarios.

作者信息

Chu Man Fong, Tam Weng Chio, Lam Kuok Wun, Chan Chon Hou, Évora Màrio, Lam U Po

机构信息

Cardiology, Centro Hospitalar Conde São Januário, Macau, MAC.

Dermatology, Centro Hospitalar Conde São Januário, Macau, MAC.

出版信息

Cureus. 2024 Aug 16;16(8):e67003. doi: 10.7759/cureus.67003. eCollection 2024 Aug.

DOI:10.7759/cureus.67003
PMID:39286713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11403653/
Abstract

Background and objectives Leadless pacemakers, known for their safer clinical profile, offer significant advantages for elderly patients at a higher risk of complications associated with transvenous pacemaker procedures, particularly those susceptible to high-risk bleeding and infections related to cardiac implantable electronic device interventions. This study explores an alternative use of leadless pacemakers without removing existing transvenous systems, deviating from conventional generator replacement and lead re-interventions. Methods This study was conducted with full approval from the Institutional Review Board, Medical Ethical Committee, Centro Hospitalar Conde São Januário, Macau. Between January 2018 and December 2021, we conducted a retrospective case series involving extremely elderly individuals (aged 85 years or older) at a high risk of complications, necessitating either generator replacement or lead re-implantation. The study considered implanting a leadless pacemaker (Micra; Medtronic, Minneapolis, MN, USA) without removing the transvenous generator. For the primary endpoints, we evaluated procedure-related complications and clinical outcomes during hospitalization. Secondary endpoints included the stability of parameters and any unexpected interference or interactions between the two systems during the two-year follow-up. Results Eleven patients (aged 86-101) were enrolled, most receiving antiplatelet or anticoagulation therapy. Leadless pacemaker implantation proceeded without major complications or adverse clinical outcomes during hospitalization. Regular follow-up was conducted every three to six months for adjusting pacemaker parameters and interrogating each patient. Over two years, three patients died from non-cardiac causes: two from infection and one from spontaneous intracranial hemorrhage, while eight completed regular follow-ups. We didn't detect any episodes of ventricular arrhythmias or intracardiac capture from the transvenous pacemaker system. We observed the stability in both the longevity and the voltage of the conventional generator battery, maintaining similar parameters without significant depletion (mean voltage decline: -0.07V/year). Parameters of the leadless pacemaker remained consistently normal without interference with existing pacing systems. Conclusion Implanting leadless pacemakers without removing transvenous pacemaker generators appears safe and effective for extremely elderly patients who are at high risk of complications. Comprehensive two-year follow-up supports the safety and viability of this approach. Opting for this approach instead of conventional generator replacement, with or without additional lead implantation, may be reasonable in this population. However, further research within this patient cohort, such as exploring long-term outcomes beyond two years or comparing clinical outcomes with conventional strategies, may be necessary.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bf4/11403653/537035b6ad70/cureus-0016-00000067003-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bf4/11403653/48a43ac0703c/cureus-0016-00000067003-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bf4/11403653/537035b6ad70/cureus-0016-00000067003-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bf4/11403653/48a43ac0703c/cureus-0016-00000067003-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bf4/11403653/537035b6ad70/cureus-0016-00000067003-i02.jpg
摘要

背景与目的 无导线起搏器以其更安全的临床特征而闻名,对于与经静脉起搏器手术相关并发症风险较高的老年患者具有显著优势,尤其是那些易发生与心脏植入式电子设备干预相关的高风险出血和感染的患者。本研究探索了在不移除现有经静脉系统的情况下无导线起搏器的另一种使用方式,这与传统的发生器更换和导线再次干预不同。

方法 本研究在澳门圣若热医院中心医院伦理委员会和机构审查委员会的完全批准下进行。在2018年1月至2021年12月期间,我们进行了一项回顾性病例系列研究,涉及并发症风险高的极度老年个体(85岁及以上),这些个体需要进行发生器更换或导线重新植入。该研究考虑在不移除经静脉发生器的情况下植入无导线起搏器(Micra;美敦力公司,美国明尼阿波利斯)。对于主要终点,我们评估了住院期间与手术相关的并发症和临床结果。次要终点包括参数的稳定性以及在两年随访期间两个系统之间的任何意外干扰或相互作用。

结果 招募了11名患者(年龄86 - 101岁),大多数患者接受抗血小板或抗凝治疗。住院期间,无导线起搏器植入过程未出现重大并发症或不良临床结果。每三到六个月进行一次定期随访,以调整起搏器参数并询问每位患者。在两年多的时间里,3名患者死于非心脏原因:2名死于感染,1名死于自发性颅内出血,而8名患者完成了定期随访。我们未检测到经静脉起搏器系统出现任何室性心律失常或心内捕获事件。我们观察到传统发生器电池的寿命和电压均保持稳定,参数相似且无明显损耗(平均电压下降:-0.07V/年)。无导线起搏器的参数始终保持正常,未对现有的起搏系统造成干扰。

结论 对于并发症风险高的极度老年患者,在不移除经静脉起搏器发生器的情况下植入无导线起搏器似乎是安全有效的。全面的两年随访支持了这种方法的安全性和可行性。在这一人群中,选择这种方法而非传统的发生器更换(无论是否额外植入导线)可能是合理的。然而,可能需要在这一患者队列中进行进一步研究,例如探索两年以上的长期结果或与传统策略比较临床结果。

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本文引用的文献

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End-of-service program compulsory ventricular pacing by the transvenous pacemaker remaining after implantation of a leadless pacemaker.无导线起搏器植入后,经静脉起搏器进行的服务终止程序强制性心室起搏。
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