Chronic Disease Research Group, Hennepin Healthcare Research Institute, Minneapolis, MN (J.B.W., N.S.R., H.Y., C.A.H.).
Division of Nephrology (J.B.W.), Hennepin County Medical Center and Department of Medicine, University of Minnesota, Minneapolis.
Stroke. 2020 Aug;51(8):2364-2373. doi: 10.1161/STROKEAHA.120.028934. Epub 2020 Jul 9.
The comparative effectiveness of direct-acting oral anticoagulants, compared with warfarin, for risks of stroke/systemic embolism, major bleeding, or death have not been studied in Medicare beneficiaries with atrial fibrillation and nondialysis-dependent chronic kidney disease.
Medicare data from 2011 to 2017 were used to identify patients with stages 3, 4, or 5 chronic kidney disease and new atrial fibrillation who received a new prescription for warfarin, apixaban, rivaroxaban, or dabigatran. We estimated marginal hazard ratios with 95% CIs for the association of each direct-acting oral anticoagulant, compared with warfarin, for the outcomes of interest using inverse-probability-of-treatment weighted Cox proportional hazards models in as-treated and intention-to-treat analyses.
A total of 22 739 individuals met criteria (46.3% warfarin, 29.6% apixaban, 17.2% rivaroxaban, 6.9% dabigatran). Across the groups of anticoagulant users, mean age was 78.4 to 79.0 years; 50.3% to 51.4% were women, and 80.3% to 82.8% had stage 3 chronic kidney disease. In the as-treated analysis, for stroke/systemic embolism, hazard ratios, all compared with warfarin, were 0.70 (0.51-0.96) for apixaban, 0.80 (0.54-1.17) for rivaroxaban, and 1.15 (0.69-1.94) for dabigatran. For major bleeding, analogous hazard ratios were 0.47 (0.37-0.59) for apixaban, 1.05 (0.85-1.30) for rivaroxaban, and 0.95 (0.70-1.31) for dabigatran. There was no difference in the risk of all-cause mortality between the direct-acting oral anticoagulants and warfarin. Results of the intention-to-treat analysis were similar.
Apixaban, compared with warfarin, was associated with decreased risk of stroke/systemic embolism and major bleeding; risks for both outcomes with rivaroxaban and dabigatran did not differ from risks with warfarin.
在患有非透析依赖型慢性肾脏病且合并心房颤动的医疗保险受益人群中,尚未对直接作用的口服抗凝剂(与华法林相比)在卒中/全身性栓塞、大出血或死亡风险方面的疗效进行研究。
利用 2011 年至 2017 年的医疗保险数据,确定了新诊断为心房颤动且合并 3 期、4 期或 5 期慢性肾脏病的患者,并记录了这些患者开始使用华法林、阿哌沙班、利伐沙班或达比加群的新处方。我们使用逆概率治疗加权 Cox 比例风险模型在实际治疗和意向治疗分析中,估算了每个直接作用的口服抗凝剂与华法林相比,对上述感兴趣结局的边际风险比及其 95%可信区间。
共有 22739 名患者符合标准(华法林组 46.3%,阿哌沙班组 29.6%,利伐沙班组 17.2%,达比加群组 6.9%)。在抗凝剂使用者中,平均年龄为 78.4 岁至 79.0 岁;50.3%至 51.4%为女性,80.3%至 82.8%为 3 期慢性肾脏病。在实际治疗分析中,对于卒中/全身性栓塞,与华法林相比,阿哌沙班的风险比为 0.70(0.51 至 0.96),利伐沙班的风险比为 0.80(0.54 至 1.17),达比加群的风险比为 1.15(0.69 至 1.94)。对于大出血,相应的风险比分别为阿哌沙班 0.47(0.37 至 0.59),利伐沙班 1.05(0.85 至 1.30),达比加群 0.95(0.70 至 1.31)。直接作用的口服抗凝剂与华法林相比,全因死亡率的风险无差异。意向治疗分析的结果相似。
与华法林相比,阿哌沙班降低了卒中/全身性栓塞和大出血的风险;利伐沙班和达比加群的这两种结局风险与华法林无差异。