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阿哌沙班或华法林用于 On-X 机械主动脉瓣患者。

Apixaban or Warfarin in Patients with an On-X Mechanical Aortic Valve.

机构信息

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.

Cleveland Clinic, Cleveland.

出版信息

NEJM Evid. 2023 Jul;2(7):EVIDoa2300067. doi: 10.1056/EVIDoa2300067. Epub 2023 May 6.

Abstract

BACKGROUND

Vitamin K antagonists are the only oral anticoagulants approved to prevent valve thrombosis and valve-related thromboembolism in patients with mechanical heart valves. Whether patients with an On-X mechanical aortic valve can be safely anticoagulated with apixaban is unknown. METHODS: Patients with an On-X aortic valve implanted at least 3 months before enrollment were randomly assigned to receive apixaban 5 mg twice daily or warfarin (target international normalized ratio 2.0 to 3.0). The primary efficacy end point was the composite of valve thrombosis or valve-related thromboembolism with coprimary analyses comparing apixaban with warfarin for noninferiority and comparing the apixaban event rate with an objective performance criterion (OPC). RESULTS: The trial was stopped after 863 participants were enrolled owing to an excess of thromboembolic events in the apixaban group. Most (94%) participants took aspirin. A total of 26 primary end-point events occurred, 20 (in 16 participants) in the apixaban group (4.2%/patient-year; 95% confidence interval [CI], 2.3 to 6.0) and 6 (in 6 participants) in the warfarin group (1.3%/patient-year; 95% CI, 0.3 to 2.3). The difference in primary end-point rates between the apixaban and warfarin groups was 2.9 (95% CI, 0.8 to 5.0); noninferiority and OPC success criteria were not met. Major bleeding rates were 3.6%/patient-year with apixaban and 4.5%/patient-year with warfarin. CONCLUSIONS: Apixaban did not demonstrate noninferiority to warfarin and is less effective than warfarin for the prevention of valve thrombosis or thromboembolism in patients with an On-X mechanical aortic valve. (Funded by Artivion; ClinicalTrials.gov number, NCT04142658.)

摘要

背景

维生素 K 拮抗剂是唯一被批准用于预防机械心脏瓣膜患者的瓣膜血栓形成和与瓣膜相关的血栓栓塞的口服抗凝剂。患有 On-X 机械主动脉瓣的患者能否安全地使用阿哌沙班抗凝尚不清楚。

方法

至少在入组前 3 个月植入 On-X 主动脉瓣的患者被随机分配接受阿哌沙班 5mg,每日两次或华法林(目标国际标准化比值 2.0 至 3.0)。主要疗效终点是瓣膜血栓形成或与瓣膜相关的血栓栓塞的复合终点,主要分析比较阿哌沙班与华法林的非劣效性,并比较阿哌沙班的事件发生率与客观绩效标准(OPC)。

结果

由于阿哌沙班组的血栓栓塞事件过多,在纳入 863 名患者后试验停止。大多数(94%)参与者服用阿司匹林。共发生 26 例主要终点事件,阿哌沙班组 20 例(16 名参与者)(4.2%/患者年;95%置信区间[CI],2.3 至 6.0),华法林组 6 例(6 名参与者)(1.3%/患者年;95%CI,0.3 至 2.3)。阿哌沙班组和华法林组的主要终点发生率差异为 2.9(95%CI,0.8 至 5.0);未达到非劣效性和 OPC 成功标准。阿哌沙班的主要出血发生率为 3.6%/患者年,华法林为 4.5%/患者年。

结论

阿哌沙班与华法林相比不具有非劣效性,并且在预防 On-X 机械主动脉瓣患者的瓣膜血栓形成或血栓栓塞方面不如华法林有效。(由 Artivion 资助;ClinicalTrials.gov 编号,NCT04142658)。

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