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International variation in the management of mineral bone disorder in patients with chronic kidney disease: Results from CKDopps

医学 肾脏疾病 肾病科 内科学 维生素D与神经学 透析 甲状旁腺激素 磷酸盐粘合剂 血液透析 内分泌学 胃肠病学 前瞻性队列研究 高磷血症
作者
Sophie Liabeuf,Keith McCullough,Eric W. Young,Ronald L. Pisoni,Jarcy Zee,Helmut Reichel,Roberto Pecoits‐Filho,Friedrich K. Port,Bénédicte Stengel,Philipp Csomor,Marie Metzger,Bruce Robinson,Ziad A. Massy
出处
期刊:Bone [Elsevier]
卷期号:129: 115058-115058 被引量:12
标识
DOI:10.1016/j.bone.2019.115058
摘要

Chronic kidney disease (CKD) is commonly associated with mineral and bone metabolism disorders, but these are less frequently studied in non-dialysis CKD patients than in dialysis patients. We examined and described international variation in mineral and bone disease (MBD) markers and their treatment and target levels in Stage 3–5 CKD patients. Prospective cohort study of 7658 adult patients with eGFR <60 mL/min/1.73 m2, excluding dialysis or transplant patients, participating in the Chronic Kidney Disease Outcomes and Practice Patterns Study (CKDopps) in Brazil, France, Germany, and the US. CKD-MBD laboratory markers included serum levels of phosphorus (P), calcium (Ca), intact parathyroid hormone (iPTH), and 25-hydroxyvitamin D (25-D). MBD treatment data included phosphate binders and vitamin D (nutritional and active). Nephrologist survey data were collected on target MBD marker levels. Over two-thirds of the patients had MBD markers measured at time intervals in line with practice guidelines. P and iPTH increased and Ca decreased gradually from eGFR 60–20 mL/min/1.73m2 and more sharply for eGFR<20. 25-D showed no relation to eGFR. Nephrologist survey data indicated marked variation in upper target P and iPTH levels. Among patients with P > 5.5 mg/dL, phosphate binder use was 14% to 43% across the four countries. Among patients with PTH >300 pg/mL, use of active (calcitriol and related analogs) vitamin D was 12%–51%, and use of any (active or nutritional) vitamin D was 60%–87%. Although monitoring of CKD-MBD laboratory markers by nephrologists in CKDopps countries is consistent with guidelines, target levels vary notably and prescription of medications to treat abnormalities in these laboratory markers is generally low in these cross-sectional analyses. While there are opportunities to increase treatment of hyperphosphatemia, hyperparathyroidism, and vitamin D deficiency in advanced CKD, the effect on longer-term complications of these conditions requires study.

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