Shi Mengxiao, Wu Ying, Zhou Qing
Department of Cardio-Thoracic Surgery, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Department of Cardio-thoracic Surgery, Nanjing Drum Tower Hospital, Nanjing, China.
Front Cardiovasc Med. 2025 May 9;12:1496334. doi: 10.3389/fcvm.2025.1496334. eCollection 2025.
The optimal antithrombotic regimen for patients without an indication for oral anticoagulation (OAC) after transcatheter aortic valve replacement (TAVR) remains unclear. We conducted a network meta-analysis of randomized controlled trials to clarify the best postoperative antithrombotic regimen. We searched literature databases including PubMed/Medline and Cochrane up to June 2024. Safety endpoints included all-cause death, cardiovascular death, major/life-threatening bleeding, and minor bleeding during follow-up. Efficacy endpoints encompassed ischaemic stroke transient ischemic attack (TIA), systemic embolism, hypoattenuated leaflet thickening (HALT), and reduced leaflet motion (RELM). Outcomes were assessed during the follow-up period specified in each trial (range:3-24 months). The results were statistically analyzed using R 4.3.2 and Stata 16 software. The final analysis included seven randomized controlled trials. Single antiplatelet therapy (SAPT) showed a lower incidence of major/life-threatening bleeding compared to the direct oral anticoagulants (DOACs) group (OR: 0.68, 95% CI: 0.47-0.99, = 0.002) during the 3-24 month post-TAVR period. However, no significant differences were found in other safety or efficacy endpoints. SAPT is the preferred treatment strategy for TAVR patients without anticoagulation indications.
identifier, PROSPERO registration number: CRD42024584735.
经导管主动脉瓣置换术(TAVR)后无口服抗凝(OAC)指征患者的最佳抗栓方案仍不明确。我们进行了一项随机对照试验的网络荟萃分析,以明确最佳的术后抗栓方案。我们检索了截至2024年6月的文献数据库,包括PubMed/Medline和Cochrane数据库。安全性终点包括随访期间的全因死亡、心血管死亡、严重/危及生命的出血和轻微出血。疗效终点包括缺血性卒中、短暂性脑缺血发作(TIA)、系统性栓塞、瓣叶增厚低密度影(HALT)和瓣叶运动减弱(RELM)。在各试验规定的随访期内(范围:3 - 24个月)评估结果。使用R 4.3.2和Stata 16软件对结果进行统计分析。最终分析纳入了七项随机对照试验。在TAVR术后3 - 24个月期间,单药抗血小板治疗(SAPT)组的严重/危及生命出血发生率低于直接口服抗凝剂(DOACs)组(OR:0.68,95% CI:0.47 - 0.99,P = 0.002)。然而,在其他安全性或疗效终点方面未发现显著差异。对于无抗凝指征的TAVR患者,SAPT是首选的治疗策略。
标识符,PROSPERO注册号:CRD42024584735。