Testing Patterns for CKD-MBD Abnormalities in a Sample US Population.

25D chronic kidney disease mineral/bone disorder parathyroid hormone phosphorus

Journal

Kidney international reports
ISSN: 2468-0249
Titre abrégé: Kidney Int Rep
Pays: United States
ID NLM: 101684752

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 23 09 2020
revised: 22 12 2020
accepted: 29 12 2020
entrez: 29 4 2021
pubmed: 30 4 2021
medline: 30 4 2021
Statut: epublish

Résumé

Patterns of testing, treatment, and retesting following treatment for disorders of chronic kidney disease mineral bone disorder (CKD-MBD) have not been explored using a large electronic database. To determine concordance with CKD-MBD management guidelines, we used 2010 to 2019 data from an electronic health record (>50 million patients) to create cohorts of incident CKD stage 3, 4, and 5 patients using diagnosis codes and estimated glomerular filtration rates. The CKD-MBD test ordering and relevant drug prescribing were assessed during follow-up. We estimated cumulative incidence of posttreatment retesting (death as competing risk). We used multivariable Cox regression to examine baseline characteristics and pretreatment test results as predictors of retesting. For 215,553 stage 3, 43,576 stage 4, and 11,407 stage 5 CKD patients, the mean follow-up was 2.3, 1.7, and 0.6 years, respectively. Only 46% of stage 4 and 41% of stage 5 patients underwent parathyroid hormone (PTH) testing, 74% and 73% had phosphorus testing, and 38% and 25% had 25D testing. By 1 year after vitamin D sterol treatment, only 50%, 53%, and 60% of stage 3, 4, and 5 patients had been retested for PTH. By 1 year after treatment with ergocalciferol or cholecalciferol, only 46%, 49%, and 55% had 25D reassessed. Pretreatment levels of PTH and 25D were not associated in a graded fashion with likelihood of retesting after treatment. Rates of retesting were not highest for patients with the highest and lowest pre-treatment PTH and 25D levels, respectively. Frequency of testing for CKD-MBD abnormalities and posttreatment retesting appears to be suboptimal.

Identifiants

pubmed: 33912763
doi: 10.1016/j.ekir.2020.12.036
pii: S2468-0249(20)31870-2
pmc: PMC8071625
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1141-1150

Informations de copyright

© 2021 International Society of Nephrology. Published by Elsevier Inc.

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Auteurs

James B Wetmore (JB)

Chronic Disease Research Group, Hennepin Healthcare Research Institute, Minneapolis, Minnesota, USA.
Division of Nephrology, Hennepin County Medical Center and Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.

Yuanyuan Ji (Y)

Chronic Disease Research Group, Hennepin Healthcare Research Institute, Minneapolis, Minnesota, USA.

Akhtar Ashfaq (A)

OPKO Pharmaceuticals, Miami, Florida.

David T Gilbertson (DT)

Chronic Disease Research Group, Hennepin Healthcare Research Institute, Minneapolis, Minnesota, USA.

Nicholas S Roetker (NS)

Chronic Disease Research Group, Hennepin Healthcare Research Institute, Minneapolis, Minnesota, USA.

Classifications MeSH