Vestergaard Ane Emilie Friis, Jensen Simon Kok, Heide-Jørgensen Uffe, Adelborg Kasper, Birn Henrik, Carrero Juan-Jesus, Christiansen Christian Fynbo
Department of Clinical Epidemiology, Department of Clinical Medicine, Aarhus University and Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Biochemistry, Gødstrup Regional Hospital, Gødstrup, Denmark.
Clin Kidney J. 2023 Oct 3;17(1):sfad252. doi: 10.1093/ckj/sfad252. eCollection 2024 Jan.
Direct oral anticoagulants (DOACs) are recommended as first-line treatment of atrial fibrillation. Whether DOAC use is associated with lower risks of kidney complications compared with vitamin K antagonists (VKAs) remains unclear. We examined this association in a nationwide, population-based cohort study.
We conducted a cohort study including patients initiating oral anticoagulant treatment within 3 months after an atrial fibrillation diagnosis in Denmark during 2012-18. Using routinely collected creatinine measurements from laboratory databases, we followed patients in an intention-to-treat approach for acute kidney injury (AKI) and chronic kidney disease (CKD) progression. We used propensity-score weighting to balance baseline confounders, computed weighted risks and weighted hazard ratios (HRs) with 95% confidence intervals (CIs) comparing DOACs with VKAs. We performed several subgroup analyses and a per-protocol analysis.
We included 32 781 persons with atrial fibrillation initiating oral anticoagulation (77% initiating DOACs). The median age was 75 years, 25% had a baseline estimated glomerular filtration rate <60 mL/min/1.73 m, and median follow-up was 2.3 (interquartile range 1.1-3.9) years. The weighted 1-year risks of AKI were 13.6% in DOAC users and 15.0% in VKA users (HR 0.86, 95% CI 0.82; 0.91). The weighted 5-year risks of CKD progression were 13.9% in DOAC users and 15.4% in VKA users (HR 0.85, 95% CI 0.79; 0.92). Results were similar across subgroups and in the per-protocol analysis.
Initiation of DOACs was associated with a decreased risk of AKI and CKD progression compared with VKAs. Despite the potential limitations of observational studies, our findings support the need for increased clinical awareness to prevent kidney complications among patients who initiate oral anticoagulants.
直接口服抗凝剂(DOACs)被推荐作为心房颤动的一线治疗药物。与维生素K拮抗剂(VKAs)相比,使用DOACs是否与较低的肾脏并发症风险相关仍不清楚。我们在一项全国性的基于人群的队列研究中对此关联进行了研究。
我们进行了一项队列研究,纳入了2012年至2018年期间在丹麦房颤诊断后3个月内开始口服抗凝治疗的患者。利用实验室数据库中常规收集的肌酐测量值,我们采用意向性分析方法对患者进行急性肾损伤(AKI)和慢性肾脏病(CKD)进展情况的随访。我们使用倾向评分加权来平衡基线混杂因素,计算加权风险和加权风险比(HRs)以及95%置信区间(CIs),以比较DOACs与VKAs。我们进行了多项亚组分析和一项符合方案分析。
我们纳入了32781例开始口服抗凝治疗的房颤患者(77%开始使用DOACs)。中位年龄为75岁,25%的患者基线估计肾小球滤过率<60 mL/min/1.73 m²,中位随访时间为2.3年(四分位间距1.1 - 3.9年)。DOAC使用者的加权1年AKI风险为13.6%,VKA使用者为15.0%(HR 0.86,95% CI 0.82;0.91)。DOAC使用者的加权5年CKD进展风险为13.9%,VKA使用者为15.4%(HR 0.85,95% CI 0.79;0.92)。亚组分析和符合方案分析的结果相似。
与VKAs相比,开始使用DOACs与AKI和CKD进展风险降低相关。尽管观察性研究存在潜在局限性,但我们的研究结果支持提高临床意识,以预防开始口服抗凝剂治疗的患者发生肾脏并发症。