Wang Yu-Ting, Chen Jo-Hsin, Liao Shu-Fen, Chen Yu-Jen, Lip Gregory Y H, Yeh Jong-Shiuan
Department of Pharmacy, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan.
School of Public Health, College of Public Health, Taipei Medical University, Taipei, Taiwan.
Eur J Clin Invest. 2024 Jan;54(1):e14086. doi: 10.1111/eci.14086. Epub 2023 Aug 27.
Oral anticoagulation therapy with warfarin or direct oral anticoagulants (DOACs) is the mainstay for stroke prevention in patients with non-valvular atrial fibrillation (AF). The DOACs might have a lower risk of declining renal function than warfarin. This study aimed to compare renal outcomes among rivaroxaban, edoxaban, dabigatran, and warfarin.
This cohort study identified 2203 adults with AF who started anticoagulation therapy between 1 July 2013 and 31 December 2020, in a clinical database at a single centre. Inverse probability of treatment weighting was adopted to balance baseline characteristics among four anticoagulants treatment groups. The primary outcome was a composite of cardiac and renal outcomes, involving a ≥30% decline in estimated glomerular filtration rate (eGFR), renal failure and cardiovascular death.
After propensity score weighting, dabigatran was associated with significantly lower risks of a ≥30% decline in eGFR (hazard ratio [HR]: .69, 95% confidence interval [CI]: .497-.951, p = .0237), doubling of the serum creatinine level (HR: .49, 95% CI: .259-.927, p = .0282) and the cardiac and renal outcome composite (HR: .67, 95% CI: .485-.913, p = .0115) than warfarin. Rivaroxaban and edoxaban did not show significant protective effects on renal outcomes compared to warfarin.
In this study, patients treated with dabigatran had significantly reduced risks of declining renal function and composite cardiac and renal events than those treated with warfarin. However, rivaroxaban and edoxaban were not associated with lower risks of any renal outcomes than warfarin. More studies are warranted to investigate and compare the impact of renal function between different DOACs in patients with AF.
使用华法林或直接口服抗凝剂(DOACs)进行口服抗凝治疗是预防非瓣膜性心房颤动(AF)患者中风的主要方法。DOACs导致肾功能下降的风险可能低于华法林。本研究旨在比较利伐沙班、依度沙班、达比加群和华法林的肾脏结局。
这项队列研究在一个单一中心的临床数据库中,识别出2203名在2013年7月1日至2020年12月31日期间开始抗凝治疗的AF成年患者。采用治疗权重的逆概率来平衡四个抗凝治疗组之间的基线特征。主要结局是心脏和肾脏结局的综合指标,包括估计肾小球滤过率(eGFR)下降≥30%、肾衰竭和心血管死亡。
在倾向评分加权后,与华法林相比,达比加群发生eGFR下降≥30%(风险比[HR]:0.69,95%置信区间[CI]:0.497 - 0.951,p = 0.0237)、血清肌酐水平翻倍(HR:0.49,95% CI:0.259 - 0.927,p = 0.0282)以及心脏和肾脏结局综合指标(HR:0.67,95% CI:0.485 - 0.913,p = 0.0115)的风险显著更低。与华法林相比,利伐沙班和依度沙班对肾脏结局未显示出显著的保护作用。
在本研究中,与接受华法林治疗的患者相比,接受达比加群治疗的患者肾功能下降以及心脏和肾脏事件综合指标的风险显著降低。然而,与华法林相比,利伐沙班和依度沙班并未降低任何肾脏结局的风险。有必要开展更多研究来调查和比较不同DOACs对AF患者肾功能的影响。