Wu Sijin, Jin Yuanhao, Lu Wenzhao, Chen Zhongli, Dai Yan, Chen Keping
State Key Laboratory of Cardiovascular Disease, Arrhythmia Center, National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100037, China.
J Clin Med. 2023 Mar 27;12(7):2512. doi: 10.3390/jcm12072512.
Leadless pacemakers with an atrioventricular synchrony algorithm represent a novel technology for patients qualified for VDD pacing. The current evidence of their performance is limited to several small-scale observational studies. This systematic review and meta-analysis aimed to evaluate the efficacy and safety of this new technology. We systematically searched the PubMed, Embase, and Cochrane library databases from their inception to 12 September 2022. The primary efficacy outcome was atrioventricular synchrony after implantation, whereas the secondary efficacy outcome was the change in cardiac output represented by the left ventricular outflow tract velocity time integral (LVOT-VTI). The primary safety outcome was major complications related to the procedures and the algorithm. Means or mean differences with 95% confidence interval (95% CI) were combined using a random-effects model or a fixed-effects model. Finally, 8 published studies with 464 participants were included in the qualitative analysis. The pooled atrioventricular synchrony proportion was 78.9% (95% CI 71.9-86.0%), and a further meta-regression did not screen factors that contributed significantly to the heterogeneity. Additionally, a significant increase in atrioventricular synchrony of 11.3% (95% CI 7.0-15.7%, < 0.01) was achieved in patients experiencing programming optimization. LVOT-VTI was significantly increased by 1.9 cm (95% CI 1.2-2.6, < 0.01), compared with the VVI pacing mode. The overall incidence of complications was approximately 6.3%, with major complications related to the algorithm being extremely low. Overall, leadless pacemakers with atrioventricular synchronous pacing demonstrated favorable safety and efficacy. Future data on their long-term performance are required to facilitate their widespread adoption in clinical practice.
具备房室同步算法的无导线起搏器是为适合VDD起搏的患者研发的一项新技术。目前关于其性能的证据仅限于几项小规模观察性研究。本系统评价和荟萃分析旨在评估这项新技术的有效性和安全性。我们系统检索了PubMed、Embase和Cochrane图书馆数据库,检索时间从建库至2022年9月12日。主要疗效指标为植入后的房室同步,次要疗效指标是以左心室流出道速度时间积分(LVOT-VTI)表示的心输出量变化。主要安全指标是与手术及算法相关的严重并发症。采用随机效应模型或固定效应模型合并95%置信区间(95%CI)的均值或均值差。最终,8项发表的研究、464名参与者纳入定性分析。汇总的房室同步比例为78.9%(95%CI 71.9-86.0%),进一步的Meta回归未筛查出对异质性有显著贡献的因素。此外,进行程控优化的患者房室同步显著增加11.3%(95%CI 7.0-15.7%,<0.01)。与VVI起搏模式相比,LVOT-VTI显著增加1.9 cm(95%CI 1.2-2.6,<0.01)。并发症总发生率约为6.3%,与算法相关的严重并发症极低。总体而言,具备房室同步起搏功能的无导线起搏器显示出良好的安全性和有效性。需要有关其长期性能的未来数据,以促进其在临床实践中的广泛应用。