Department of Vascular Surgery, Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou 310005, China.
Department of Vascular Surgery, Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou 310005, China
Biosci Rep. 2018 Nov 13;38(6). doi: 10.1042/BSR20180423. Print 2018 Dec 21.
To compare the efficacy and safety of rivaroxaban, apixaban and enoxaparin for thromboprophylaxis after arthroplastic surgery.
We conducted a meta-analysis containing a wide range of randomized controlled trials about efficiency and safety of rivaroxaban, apixaban and enoxaparin for thromboprophylaxis after arthroplastic surgery in the recent decade from January 2006 to June 2018. The present study separately analyzed the following key components: the different efficiency and safety for rivaroxaban and enoxaparin; apixaban and enoxaparin; and enoxaparin and other new developed anticoagulants.
Sixteen studies containing 58885 patients were included. In results of efficacy outcomes, total events occurred in 4.89% patients of rivaroxaban group and 9.55% patients of the control group; however, no significant difference was observed in apixaban groups of their efficacy outcomes. Primary events didn't show significant difference when comparing apixaban with the control or comparing enoxaparin with the control. In analysis of safety outcomes, bleeding events occurred in 3.41% patients of rivaroxaban group compared with 2.84% patients of the control groups; bleeding events in apixaban groups were 4.09% compared with the control groups 4.64%. Bleeding events occurred in 3.51% patients of enoxaparin group, slightly lower than 5.82% of the control group.
Direct oral anticoagulant, rivaroxaban might have better efficacy outcomes in thromboprophylaxis after arthroplastic surgery; however, apixaban showed no significantly different efficacy outcomes compared with enoxaparin, and enoxaparin may have equal or even better safety outcomes compared with direct oral anticoagulants.
比较利伐沙班、阿哌沙班和依诺肝素预防关节成形术后血栓形成的疗效和安全性。
我们对 2006 年 1 月至 2018 年 6 月近十年内发表的关于利伐沙班、阿哌沙班和依诺肝素预防关节成形术后血栓形成的疗效和安全性的随机对照试验进行了荟萃分析。本研究分别分析了以下关键组成部分:利伐沙班和依诺肝素的不同疗效和安全性;阿哌沙班和依诺肝素;以及依诺肝素和其他新开发的抗凝剂。
纳入了 16 项研究,共 58885 例患者。在疗效结果方面,利伐沙班组总事件发生率为 4.89%,对照组为 9.55%;但阿哌沙班组疗效结果未见显著差异。与对照组相比,阿哌沙班与对照组比较的主要事件无显著差异,依诺肝素与对照组比较的主要事件也无显著差异。在安全性结果分析中,利伐沙班组出血事件发生率为 3.41%,对照组为 2.84%;阿哌沙班组出血事件发生率为 4.09%,对照组为 4.64%。依诺肝素组出血事件发生率为 3.51%,略低于对照组的 5.82%。
直接口服抗凝剂利伐沙班在关节成形术后血栓预防中可能具有更好的疗效,但阿哌沙班与依诺肝素相比,疗效无显著差异,依诺肝素与直接口服抗凝剂相比,安全性可能相当或更好。