口服抗凝治疗和肾脏疾病的风险——一项全国性的、基于人群的队列研究

NDT Plus Pub Date : 2023-10-03 DOI:10.1093/ckj/sfad252
Ane Emilie Friis Vestergaard, Kok SimonJensen, Uffe Heide-Jørgensen, Kasper Adelborg, Henrik Birn, Juan-Jesus Carrero, Christian Fynbo Christiansen
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摘要

背景:直接口服抗凝剂(DOACs)被推荐作为房颤的一线治疗。与维生素K拮抗剂(VKAs)相比,DOAC的使用是否与肾脏并发症风险较低有关尚不清楚。我们在一项全国性的、基于人群的队列研究中检验了这种关联。方法:我们进行了一项队列研究,包括2012 - 2018年丹麦房颤诊断后3个月内开始口服抗凝治疗的患者。使用从实验室数据库中常规收集的肌酐测量值,我们对急性肾损伤(AKI)和慢性肾病(CKD)进展的患者进行了意向治疗方法的随访。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(hr),比较doac和vka的95%置信区间(ci)。我们进行了几个亚组分析和每个方案分析。结果我们纳入了32781例心房颤动患者,其中77%的患者开始口服抗凝治疗。中位年龄为75岁,25%的患者基线肾小球滤过率为60 mL/min/1.73 m2,中位随访时间为2.3年(四分位数间隔1.1-3.9年)。DOAC使用者的加权1年AKI风险为13.6%,VKA使用者的加权1年AKI风险为15.0% (HR 0.86, 95% CI 0.82;0.91)。DOAC使用者CKD进展的5年加权风险为13.9%,VKA使用者为15.4% (HR 0.85, 95% CI 0.79;0.92)。各亚组和按方案分析的结果相似。结论:与vka相比,DOACs的启动与AKI和CKD进展的风险降低有关。尽管观察性研究存在潜在的局限性,但我们的研究结果支持提高临床意识以预防口服抗凝剂患者肾脏并发症的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral anticoagulant treatment and risk of kidney disease – a nationwide, population-based cohort study
ABSTRACT Background 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. Methods 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. Results 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 m2, 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. Conclusions 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.
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