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Delayed Progression to Dialysis with Early and Intensive Management of Predialysis Chronic Kidney Disease: A Case-Based Approach

In addition to hypertension and diabetes, disorders in mineral metabolism and bone disease (e.g. affecting phosphorus, calcium, parathyroid hormone, and vitamin D) are common complications of chronic kidney disease (CKD) and contribute to morbidity and mortality. Consequently, CKD requires multifact...

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Autor principal: Thomsen, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3808807/
https://www.ncbi.nlm.nih.gov/pubmed/24167516
http://dx.doi.org/10.1159/000353265
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author Thomsen, Stephen
author_facet Thomsen, Stephen
author_sort Thomsen, Stephen
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description In addition to hypertension and diabetes, disorders in mineral metabolism and bone disease (e.g. affecting phosphorus, calcium, parathyroid hormone, and vitamin D) are common complications of chronic kidney disease (CKD) and contribute to morbidity and mortality. Consequently, CKD requires multifactorial treatment to slow CKD progression and avoid end-stage renal disease. CKD progression and treatment outcomes are monitored by measuring the estimated glomerular filtration rate (eGFR), which decreases by 2–12 ml/min/1.73 m(2) per year depending on the stage of CKD and comorbidities, such as diabetes. This paper presents representative case studies illustrating the delay and reversal of CKD progression with comprehensive, individualized treatment regimens, including non-calcium phosphate binders, antihypertensives, lipid-lowering drugs, calcimimetics, and other drugs as required, to treat each component of CKD including CKD-mineral and bone disorder. Four patients are included, with an average age of 70–81 years and CKD stage 3 or 4 accompanied by various comorbidities, most notably diabetes and hypertension. The range of treatment and follow-up durations was 6–7 years. In each case, there was evidence of slowing or prevention of CKD progression, according to eGFR and serum creatinine, regardless of the patient's age or CKD stage. Despite a baseline eGFR of <20 ml/min/1.73 m(2) in 1 female patient, after 6 years of follow-up, her eGFR had stabilized and was maintained at >15 ml/min/1.73 m(2). These observations reinforce the value of early nephrology referral and comprehensive management of CKD and underlying conditions (hypertension and diabetes) beginning at eGFR <60 ml/min/1.73 m(2).
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spelling pubmed-38088072013-10-28 Delayed Progression to Dialysis with Early and Intensive Management of Predialysis Chronic Kidney Disease: A Case-Based Approach Thomsen, Stephen Case Rep Nephrol Urol Published online: June, 2013 In addition to hypertension and diabetes, disorders in mineral metabolism and bone disease (e.g. affecting phosphorus, calcium, parathyroid hormone, and vitamin D) are common complications of chronic kidney disease (CKD) and contribute to morbidity and mortality. Consequently, CKD requires multifactorial treatment to slow CKD progression and avoid end-stage renal disease. CKD progression and treatment outcomes are monitored by measuring the estimated glomerular filtration rate (eGFR), which decreases by 2–12 ml/min/1.73 m(2) per year depending on the stage of CKD and comorbidities, such as diabetes. This paper presents representative case studies illustrating the delay and reversal of CKD progression with comprehensive, individualized treatment regimens, including non-calcium phosphate binders, antihypertensives, lipid-lowering drugs, calcimimetics, and other drugs as required, to treat each component of CKD including CKD-mineral and bone disorder. Four patients are included, with an average age of 70–81 years and CKD stage 3 or 4 accompanied by various comorbidities, most notably diabetes and hypertension. The range of treatment and follow-up durations was 6–7 years. In each case, there was evidence of slowing or prevention of CKD progression, according to eGFR and serum creatinine, regardless of the patient's age or CKD stage. Despite a baseline eGFR of <20 ml/min/1.73 m(2) in 1 female patient, after 6 years of follow-up, her eGFR had stabilized and was maintained at >15 ml/min/1.73 m(2). These observations reinforce the value of early nephrology referral and comprehensive management of CKD and underlying conditions (hypertension and diabetes) beginning at eGFR <60 ml/min/1.73 m(2). S. Karger AG 2013-06-11 /pmc/articles/PMC3808807/ /pubmed/24167516 http://dx.doi.org/10.1159/000353265 Text en Copyright © 2013 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published online: June, 2013
Thomsen, Stephen
Delayed Progression to Dialysis with Early and Intensive Management of Predialysis Chronic Kidney Disease: A Case-Based Approach
title Delayed Progression to Dialysis with Early and Intensive Management of Predialysis Chronic Kidney Disease: A Case-Based Approach
title_full Delayed Progression to Dialysis with Early and Intensive Management of Predialysis Chronic Kidney Disease: A Case-Based Approach
title_fullStr Delayed Progression to Dialysis with Early and Intensive Management of Predialysis Chronic Kidney Disease: A Case-Based Approach
title_full_unstemmed Delayed Progression to Dialysis with Early and Intensive Management of Predialysis Chronic Kidney Disease: A Case-Based Approach
title_short Delayed Progression to Dialysis with Early and Intensive Management of Predialysis Chronic Kidney Disease: A Case-Based Approach
title_sort delayed progression to dialysis with early and intensive management of predialysis chronic kidney disease: a case-based approach
topic Published online: June, 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3808807/
https://www.ncbi.nlm.nih.gov/pubmed/24167516
http://dx.doi.org/10.1159/000353265
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