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经导管主动脉瓣置换术后的抗栓策略:一项网状荟萃分析

Antithrombotic strategies after transcatheter aortic valve replacement a network meta-analysis.

作者信息

Shi Mengxiao, Wu Ying, Zhou Qing

机构信息

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.

出版信息

Front Cardiovasc Med. 2025 May 9;12:1496334. doi: 10.3389/fcvm.2025.1496334. eCollection 2025.

Abstract

UNLABELLED

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.

SYSTEMATIC REVIEW REGISTRATION

identifier, PROSPERO registration number: CRD42024584735.

摘要

未标注

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。

系统评价注册

标识符,PROSPERO注册号:CRD42024584735。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4839/12098576/1f83fc34650a/fcvm-12-1496334-g001.jpg

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