Incremental Versus Standard (Full-Dose) Peritoneal Dialysis.

incremental dialysis patient-centered care peritoneal dialysis personalized medicine quality of life

Journal

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

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 15 09 2021
revised: 08 11 2021
accepted: 15 11 2021
entrez: 14 2 2022
pubmed: 15 2 2022
medline: 15 2 2022
Statut: epublish

Résumé

Incremental peritoneal dialysis (PD), defined as less than "standard dose" PD prescription, has a number of possible benefits, including better preservation of residual kidney function (RKF), reduced risk of peritonitis, lower peritoneal glucose exposure, lesser environmental impact, and reduced costs. Patients commencing PD are often new to kidney replacement therapy and possess substantial RKF, which may allow safe delivery of an incremental prescription, often in the form of lower frequency or duration of PD. This has the potential to help improve quality of life (QOL) and life participation through reducing time requirements and burden of treatment. Alternatively, incremental PD could potentially contribute to reduced small solute clearance, fluid overload, or patient reluctance to increase dialysis prescription when later needed. This review discusses the definition, rationale, uptake, potential advantages and disadvantages, and clinical trial evidence pertaining to the use of incremental PD.

Identifiants

pubmed: 35155856
doi: 10.1016/j.ekir.2021.11.019
pii: S2468-0249(21)01542-4
pmc: PMC8820986
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

165-176

Informations de copyright

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

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Auteurs

Melissa S Cheetham (MS)

Department of Nephrology, Sunshine Coast University Hospital, Birtinya, Australia.
Faculty of Medicine, The University of Queensland, Brisbane, Australia.

Yeoungjee Cho (Y)

Faculty of Medicine, The University of Queensland, Brisbane, Australia.
Australasian Kidney Trials Network at the University of Queensland, Brisbane, Australia.
Translational Research Institute, Brisbane, Australia.
Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia.

Rathika Krishnasamy (R)

Department of Nephrology, Sunshine Coast University Hospital, Birtinya, Australia.
Faculty of Medicine, The University of Queensland, Brisbane, Australia.
Australasian Kidney Trials Network at the University of Queensland, Brisbane, Australia.

Arsh K Jain (AK)

Schulich School of Medicine & Dentistry, Department of Epidemiology & Biostatistics, Western University, London, Canada.

Neil Boudville (N)

Medical School, University of Western Australia, Perth, Australia.
Department of Renal Medicine, Sir Charles Gairdner Hospital, Perth, Australia.

David W Johnson (DW)

Faculty of Medicine, The University of Queensland, Brisbane, Australia.
Australasian Kidney Trials Network at the University of Queensland, Brisbane, Australia.
Translational Research Institute, Brisbane, Australia.
Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia.

Louis L Huang (LL)

Department of Renal Medicine, Eastern Health Clinical School, Monash University, Melbourne, Australia.

Classifications MeSH