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

INTRODUCTION: 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. METHODS: To determine concordance with CKD-MBD management guidelines, we used 2010 to 2019...

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Autores principales: Wetmore, James B., Ji, Yuanyuan, Ashfaq, Akhtar, Gilbertson, David T., Roetker, Nicholas S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071625/
https://www.ncbi.nlm.nih.gov/pubmed/33912763
http://dx.doi.org/10.1016/j.ekir.2020.12.036
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author Wetmore, James B.
Ji, Yuanyuan
Ashfaq, Akhtar
Gilbertson, David T.
Roetker, Nicholas S.
author_facet Wetmore, James B.
Ji, Yuanyuan
Ashfaq, Akhtar
Gilbertson, David T.
Roetker, Nicholas S.
author_sort Wetmore, James B.
collection PubMed
description INTRODUCTION: 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. METHODS: 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. RESULTS: 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. CONCLUSION: Frequency of testing for CKD-MBD abnormalities and posttreatment retesting appears to be suboptimal.
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spelling pubmed-80716252021-04-27 Testing Patterns for CKD-MBD Abnormalities in a Sample US Population Wetmore, James B. Ji, Yuanyuan Ashfaq, Akhtar Gilbertson, David T. Roetker, Nicholas S. Kidney Int Rep Clinical Research INTRODUCTION: 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. METHODS: 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. RESULTS: 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. CONCLUSION: Frequency of testing for CKD-MBD abnormalities and posttreatment retesting appears to be suboptimal. Elsevier 2021-01-06 /pmc/articles/PMC8071625/ /pubmed/33912763 http://dx.doi.org/10.1016/j.ekir.2020.12.036 Text en © 2021 International Society of Nephrology. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Clinical Research
Wetmore, James B.
Ji, Yuanyuan
Ashfaq, Akhtar
Gilbertson, David T.
Roetker, Nicholas S.
Testing Patterns for CKD-MBD Abnormalities in a Sample US Population
title Testing Patterns for CKD-MBD Abnormalities in a Sample US Population
title_full Testing Patterns for CKD-MBD Abnormalities in a Sample US Population
title_fullStr Testing Patterns for CKD-MBD Abnormalities in a Sample US Population
title_full_unstemmed Testing Patterns for CKD-MBD Abnormalities in a Sample US Population
title_short Testing Patterns for CKD-MBD Abnormalities in a Sample US Population
title_sort testing patterns for ckd-mbd abnormalities in a sample us population
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071625/
https://www.ncbi.nlm.nih.gov/pubmed/33912763
http://dx.doi.org/10.1016/j.ekir.2020.12.036
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