CKD Progression in Medicare Beneficiaries With Nonvalvular Atrial Fibrillation Treatead with Apixaban Versus Warfarin

被引:16
|
作者
Wetmore, James B. [1 ,2 ,3 ]
Yan, Heng [1 ]
Herzog, Charles A. [1 ,3 ,4 ]
Weinhandl, Eric [1 ]
Reyes, Jorge L. [5 ]
Roetker, Nicholas S. [1 ]
机构
[1] Hennepin Healthcare Res Inst, Chron Dis Res Grp, 701 Pk Ave,Suite S4-100, Minneapolis, MN 55415 USA
[2] Univ Minnesota, Hennepin Cty Med Ctr, Div Nephrol, Minneapolis, MN 55415 USA
[3] Univ Minnesota, Dept Med, Box 736 UMHC, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Hennepin Cty Med Ctr, Div Cardiol, Minneapolis, MN 55415 USA
[5] Hennepin Cty Med Ctr, Dept Internal Med, Minneapolis, MN 55415 USA
关键词
GROSS HEMATURIA; RENAL-FUNCTION; VITAMIN-K; RISK; ANTICOAGULANTS; EFFICACY; INSIGHTS; CLAIMS;
D O I
10.1053/j.ajkd.2020.12.004
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Rationale & Objective: Comparing kidney disease progression among patients treated with direct oral anticoagulants (DOACs) versus warfarin has not been well studied. We hypothesized that apixaban would be associated with lower risks of progression of chronic kidney disease (CKD) and progression to incident kidney failure than warfarin in patients with atrial fibrillation (AF). Study Design: Retrospective cohort study. Setting & Participants: Medicare recipients with stage 3, 4, or 5 CKD and incident AF who received a new prescription for apixaban or warfarin from 2013 through 2017. Exposure: Apixaban or warfarin. Outcomes: Progression to incident kidney failure or, separately, to a more advanced stage of CKD. Analytical Approach: Marginal structural causes-specific proportional hazards models with inverse probability weighting to estimate marginal hazard ratios (HRs) for each outcome. HRs compared apixaban to warfarin in intention-to-treat and censored-at-drug-switch analyses. Results: 12,816 individuals met inclusion criteria (50.3% received apixaban; 49.7% received warfarin). After weighting, the mean age of the cohort was 80 +/- 7 years, 51 % were women, and 88% were White. Approximately 84% had stage 3, 15% had stage 4, and 1% had stage 5 CKD. In the intention-to-treat analysis, apixaban, relative to warfarin, was associated with an HR of developing incident kidney failure of 0.98 (95% confidence interval [CI], 0.79-1.22) and of CKD stage progression of 0.90 (95% CI, 0.82-0.99). Corresponding HRs for censored-at-drug-switch analyses were 0.81 (95% CI, 0.56-1.17) and 0.81 (95% CI, 0.70-0.92). Results were similar for a series of subgroup and sensitivity analyses. Limitations: CKD was defined based on diagnosis codes from claims; findings may not be generalizable to non-Medicare CKD populations. Conclusions: Apixaban, compared with warfarin, was associated with lower risk of CKD stage progression, but not with incident kidney failure.
引用
收藏
页码:180 / 189
页数:10
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