Global Innovative Pharma Business Clinical Pharmacology and Clinical Sciences, Pfizer Inc., Groton, Connecticut, USA.
Global Clinical Affairs, Proteus Digital Health Inc., Redwood City, California, USA.
Clin Transl Sci. 2017 Jul;10(4):260-270. doi: 10.1111/cts.12471. Epub 2017 May 23.
We carried out a dose-response model-based meta-analysis to assess venous thromboembolism (VTE) and bleeding with factor Xa (FXa) inhibitors (apixaban, edoxaban, rivaroxaban) and a thrombin inhibitor (dabigatran) compared with European (EU) (40 mg q.d.) and North American (NA) (30 mg Q12H) dose regimens of a low molecular weight heparin (enoxaparin) following orthopedic surgery. Statistically significant differences in both VTE and bleeding outcomes were found between the NA and EU doses of enoxaparin, with odds ratios (95% confidence interval) for the NA vs. EU dose of 0.73 (0.71-0.76) and 1.20 (1.14-1.29) for total VTE and major bleeding, respectively. At approved doses, estimated odds ratios vs. both doses of enoxaparin for the three FXa inhibitors (range: 0.35-0.75 for VTE; 0.76-1.09 for bleeding) compared with those for dabigatran (range: 0.66-1.21 for VTE; 1.10-1.38 for bleeding) suggested generally greater efficacy and less bleeding for the FXa inhibitors.
我们进行了一项基于剂量反应模型的荟萃分析,以评估在骨科手术后,与欧洲(EU)(40mgqd)和北美(NA)(30mgQ12H)剂量方案的低分子肝素(依诺肝素)相比,Xa 因子(FXa)抑制剂(阿哌沙班、依度沙班、利伐沙班)和凝血酶抑制剂(达比加群)的静脉血栓栓塞症(VTE)和出血风险。在依诺肝素的 NA 和 EU 剂量之间,VTE 和出血结局均存在统计学显著差异,NA 与 EU 剂量的比值比(95%置信区间)分别为 0.73(0.71-0.76)和 1.20(1.14-1.29),总 VTE 和主要出血的比值比分别为 0.73(0.71-0.76)和 1.20(1.14-1.29)。在批准剂量下,与依诺肝素的两种剂量相比,三种 FXa 抑制剂(VTE 的比值比范围为 0.35-0.75;出血的比值比范围为 0.76-1.09)的估计比值比与达比加群(VTE 的比值比范围为 0.66-1.21;出血的比值比范围为 1.10-1.38)相比,表明 FXa 抑制剂通常具有更高的疗效和更少的出血风险。