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Health-related quality of life across all stages of autosomal dominant polycystic kidney disease

BACKGROUND: A limited number of studies have assessed health-related quality of life (HRQoL) in autosomal dominant polycystic kidney disease (ADPKD). Results to date have been conflicting and studies have generally focused on patients with later stages of the disease. This study aimed to assess HRQo...

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Autores principales: Eriksson, Daniel, Karlsson, Linda, Eklund, Oskar, Dieperink, Hans, Honkanen, Eero, Melin, Jan, Selvig, Kristian, Lundberg, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5837636/
https://www.ncbi.nlm.nih.gov/pubmed/27662885
http://dx.doi.org/10.1093/ndt/gfw335
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author Eriksson, Daniel
Karlsson, Linda
Eklund, Oskar
Dieperink, Hans
Honkanen, Eero
Melin, Jan
Selvig, Kristian
Lundberg, Johan
author_facet Eriksson, Daniel
Karlsson, Linda
Eklund, Oskar
Dieperink, Hans
Honkanen, Eero
Melin, Jan
Selvig, Kristian
Lundberg, Johan
author_sort Eriksson, Daniel
collection PubMed
description BACKGROUND: A limited number of studies have assessed health-related quality of life (HRQoL) in autosomal dominant polycystic kidney disease (ADPKD). Results to date have been conflicting and studies have generally focused on patients with later stages of the disease. This study aimed to assess HRQoL in ADPKD across all stages of the disease, from patients with early chronic kidney disease (CKD) to patients with end-stage renal disease. METHODS: A study involving cross-sectional patient-reported outcomes and retrospective clinical data was undertaken April–December 2014 in Denmark, Finland, Norway and Sweden. Patients were enrolled into four mutually exclusive stages of the disease: CKD stages 1–3; CKD stages 4–5; transplant recipients; and dialysis patients. RESULTS: Overall HRQoL was generally highest in patients with CKD stages 1–3, followed by transplant recipients, patients with CKD stages 4–5 and patients on dialysis. Progressive disease predominately had an impact on physical health, whereas mental health showed less variation between stages of the disease. A substantial loss in quality of life was observed as patients progressed to CKD stages 4–5. CONCLUSIONS: Later stages of ADPKD are associated with reduced physical health. The value of early treatment interventions that can delay progression of the disease should be considered.
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spelling pubmed-58376362018-03-09 Health-related quality of life across all stages of autosomal dominant polycystic kidney disease Eriksson, Daniel Karlsson, Linda Eklund, Oskar Dieperink, Hans Honkanen, Eero Melin, Jan Selvig, Kristian Lundberg, Johan Nephrol Dial Transplant ORIGINAL ARTICLES BACKGROUND: A limited number of studies have assessed health-related quality of life (HRQoL) in autosomal dominant polycystic kidney disease (ADPKD). Results to date have been conflicting and studies have generally focused on patients with later stages of the disease. This study aimed to assess HRQoL in ADPKD across all stages of the disease, from patients with early chronic kidney disease (CKD) to patients with end-stage renal disease. METHODS: A study involving cross-sectional patient-reported outcomes and retrospective clinical data was undertaken April–December 2014 in Denmark, Finland, Norway and Sweden. Patients were enrolled into four mutually exclusive stages of the disease: CKD stages 1–3; CKD stages 4–5; transplant recipients; and dialysis patients. RESULTS: Overall HRQoL was generally highest in patients with CKD stages 1–3, followed by transplant recipients, patients with CKD stages 4–5 and patients on dialysis. Progressive disease predominately had an impact on physical health, whereas mental health showed less variation between stages of the disease. A substantial loss in quality of life was observed as patients progressed to CKD stages 4–5. CONCLUSIONS: Later stages of ADPKD are associated with reduced physical health. The value of early treatment interventions that can delay progression of the disease should be considered. Oxford University Press 2017-12 2016-09-23 /pmc/articles/PMC5837636/ /pubmed/27662885 http://dx.doi.org/10.1093/ndt/gfw335 Text en © The Author 2016. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle ORIGINAL ARTICLES
Eriksson, Daniel
Karlsson, Linda
Eklund, Oskar
Dieperink, Hans
Honkanen, Eero
Melin, Jan
Selvig, Kristian
Lundberg, Johan
Health-related quality of life across all stages of autosomal dominant polycystic kidney disease
title Health-related quality of life across all stages of autosomal dominant polycystic kidney disease
title_full Health-related quality of life across all stages of autosomal dominant polycystic kidney disease
title_fullStr Health-related quality of life across all stages of autosomal dominant polycystic kidney disease
title_full_unstemmed Health-related quality of life across all stages of autosomal dominant polycystic kidney disease
title_short Health-related quality of life across all stages of autosomal dominant polycystic kidney disease
title_sort health-related quality of life across all stages of autosomal dominant polycystic kidney disease
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5837636/
https://www.ncbi.nlm.nih.gov/pubmed/27662885
http://dx.doi.org/10.1093/ndt/gfw335
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