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非透析依赖性慢性肾脏病患者贫血管理的真实世界纵向研究:CKDopps 的跨国分析。

A real-world longitudinal study of anemia management in non-dialysis-dependent chronic kidney disease patients: a multinational analysis of CKDopps.

机构信息

Arbor Research Collaborative for Health, 3700 Earhart Road, Ann Arbor, MI, 48105, USA.

School of Medicine, Pontificia Universidade Catolica Do Parana, Curitiba, Brazil.

出版信息

Sci Rep. 2021 Jan 19;11(1):1784. doi: 10.1038/s41598-020-79254-6.

Abstract

Previously lacking in the literature, we describe longitudinal patterns of anemia prescriptions for non-dialysis-dependent chronic kidney disease (NDD-CKD) patients under nephrologist care. We analyzed data from 2818 Stage 3-5 NDD-CKD patients from Brazil, Germany, and the US, naïve to anemia medications (oral iron, intravenous [IV] iron, or erythropoiesis stimulating agent [ESA]) at enrollment in the CKDopps. We report the cumulative incidence function (CIF) of medication initiation stratified by baseline characteristics. Even in patients with hemoglobin (Hb) < 10 g/dL, the CIF at 12 months for any anemia medication was 40%, and 28% for ESAs. Patients with TSAT < 20% had a CIF of 26% and 6% for oral and IV iron, respectively. Heart failure was associated with earlier initiation of anemia medications. IV iron was prescribed to < 10% of patients with iron deficiency. Only 40% of patients with Hb < 10 g/dL received any anemia medication within a year. Discontinuation of anemia treatment was very common. Anemia treatment is initiated in a limited number of NDD-CKD patients, even in those with guideline-based indications to treat. Hemoglobin trajectory and a history of heart failure appear to guide treatment start. These results support the concept that anemia is sub-optimally managed among NDD-CKD patients in the real-world setting.

摘要

以前的文献中缺乏对接受肾病医生治疗的非透析依赖型慢性肾脏病(NDD-CKD)患者贫血处方的纵向模式的描述。我们分析了来自巴西、德国和美国的 2818 名 3-5 期 NDD-CKD 患者的数据,这些患者在进入 CKDopps 研究时对贫血药物(口服铁、静脉铁或红细胞生成刺激剂 [ESA])均无用药史。我们报告了按基线特征分层的药物起始累积发生率函数(CIF)。即使在血红蛋白(Hb)<10 g/dL 的患者中,任何贫血药物的 12 个月 CIF 为 40%,ESA 为 28%。转铁蛋白饱和度(TSAT)<20%的患者,口服铁和静脉铁的 CIF 分别为 26%和 6%。心力衰竭与贫血药物的更早起始相关。只有<10%的缺铁患者接受了静脉铁治疗。Hb<10 g/dL 的患者中,只有 40%在一年内接受了任何贫血药物治疗。贫血治疗的停药非常常见。即使有基于指南的治疗指征,贫血治疗也仅在少数 NDD-CKD 患者中开始。血红蛋白轨迹和心力衰竭史似乎指导着治疗的开始。这些结果支持了在真实世界环境中 NDD-CKD 患者贫血管理不理想的概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be4f/7815803/569604fb2649/41598_2020_79254_Fig1_HTML.jpg

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