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Correlates and outcomes of warfarin initiation in kidney transplant recipients newly diagnosed with atrial fibrillation

机译:新诊断为心房颤动的肾移植受者中华法林起始的相关性和结果

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摘要

In the kidney transplant population with atrial fibrillation (AF), evidence regarding the effectiveness and safety of warfarin treatment is lacking. We used fee-for-service Medicare claims to identify kidney transplant recipients with newly diagnosed AF from the United States Renal Data System. Warfarin use within 30 days of AF diagnosis was ascertained from Medicare Part D prescription claims (2007–11) or using a validated algorithm (1997–2011). The study end points were (i) the composite of death, stroke or gastrointestinal bleed, (ii) death and (iii) death-censored graft failure. Warfarin user and non-user groups were balanced using inverse probability of treatment weighting and hazard ratios were (HRs) estimated using Cox regression. Among 718 subjects with an indication for anticoagulation, 24% initiated warfarin treatment within 30 days of AF diagnosis. Age was the only independent correlate of warfarin use [odds ratio = 1.02 per year; 95% confidence interval (95% CI) 1.01–1.04]. In the larger cohort of 6492 patients with AF, warfarin use [(23.5%) versus non-use (76.5%)] was associated with small and non-significant reductions in the composite of death, stroke or gastrointestinal bleed (HR = 0.92; 95% CI 0.83–1.02), death (HR = 0.92; 95% CI 0.82–1.02) and death-censored graft failure (HR = 0.90; 95% CI 0.76–1.08). Our study suggests the need for clinical trials of warfarin use in the kidney transplant population with AF.
机译:在患有房颤(AF)的肾脏移植人群中,缺乏有关华法林治疗有效性和安全性的证据。我们使用了有偿服务的Medicare索赔来确定来自美国肾脏数据系统的新诊断为AF的肾移植接受者。根据美国医疗保险D部分处方要求(2007-11)或使用经过验证的算法(1997-2011)确定房颤诊断后30天内使用华法林。研究终点为:(i)死亡,中风或胃肠道出血的综合;(ii)死亡;(iii)以死亡为前提的移植物衰竭。华法林使用者和非使用者组的治疗权重成反比,使用Cox回归估算危险比(HRs)。在718例有抗凝指征的受试者中,有24%的人在AF诊断后30天内开始了华法林治疗。年龄是华法林使用的唯一独立相关因素[比值比= 1.02 /年; 95%置信区间(95%CI)1.01–1.04]。在6492例患有AF的较大人群中,华法林使用[(23.5%)vs不使用(76.5%)]与死亡,中风或胃肠道出血的综合减少量较小且无明显减少有关(HR = 0.92; 95%CI 0.83–1.02),死亡(HR = 0.92; 95%CI 0.82–1.02)和死亡检查的移植失败(HR = 0.90; 95%CI 0.76-1.08)。我们的研究表明,在患有房颤的肾移植人群中需要使用华法林进行临床试验。

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