Associations of neutral pH, low GDP peritoneal dialysis solutions with patient survival, transfer to haemodialysis, and peritonitis.

dialysis solutions mortality peritoneal dialysis peritonitis transfer to haemodialysis

Journal

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
ISSN: 1460-2385
Titre abrégé: Nephrol Dial Transplant
Pays: England
ID NLM: 8706402

Informations de publication

Date de publication:
10 Jul 2023
Historique:
medline: 11 7 2023
pubmed: 11 7 2023
entrez: 10 7 2023
Statut: aheadofprint

Résumé

Peritoneal dialysis (PD) solutions containing low levels of glucose degradation products (GDPs) are associated with attenuation of peritoneal membrane injury and vascular complications. However, clinical benefits associated with neutral pH, low GDP (N-pH/L-GDP) solutions remain unclear. Using data from the Australia and New Zealand Dialysis and Transplant Registry, we examined the associations between N-pH/L-GDP solutions and all-cause mortality, cause-specific mortality, transfer to haemodialysis (TTH) for ≥ 30 days, and PD peritonitis in adult incident PD patients in Australia and New Zealand between January 1, 2005, and December 31, 2020, using adjusted Cox regression analyses. Of 12 814 incident PD patients, 2282 (18%) were on N-pH/L-GDP solutions. The proportion of patients on N-pH/L-GDP solutions each year increased from 11% in 2005 to 33% in 2017. During the study period, 5330 (42%) patients died, 4977 (39%) experienced TTH, and 5502 (43%) experienced PD peritonitis. Compared to use of conventional solutions only, use of any form of N-pH/L-GDP solution was associated with reduced risks of all-cause mortality (adjusted hazard ratio [aHR] 0.67, 95% confidence interval [CI] 0.61-0.74), cardiovascular mortality (aHR 0.65, 95%CI 0.56-0.77), infection-related mortality (aHR 0.62, 95%CI 0.47-0.83) and TTH (aHR 0.79, 95%CI 0.72-0.86), but an increased risk of PD peritonitis (aHR 1.16, 95%CI 1.07-1.26). Patients who received N-pH/L-GDP solutions had decreased risks of all-cause and cause-specific mortality despite an increased risk of PD peritonitis. Studies assessing the causal relationships are warranted to determine the clinical benefits of N-pH/L-GDP solutions.

Sections du résumé

BACKGROUND BACKGROUND
Peritoneal dialysis (PD) solutions containing low levels of glucose degradation products (GDPs) are associated with attenuation of peritoneal membrane injury and vascular complications. However, clinical benefits associated with neutral pH, low GDP (N-pH/L-GDP) solutions remain unclear.
METHODS METHODS
Using data from the Australia and New Zealand Dialysis and Transplant Registry, we examined the associations between N-pH/L-GDP solutions and all-cause mortality, cause-specific mortality, transfer to haemodialysis (TTH) for ≥ 30 days, and PD peritonitis in adult incident PD patients in Australia and New Zealand between January 1, 2005, and December 31, 2020, using adjusted Cox regression analyses.
RESULTS RESULTS
Of 12 814 incident PD patients, 2282 (18%) were on N-pH/L-GDP solutions. The proportion of patients on N-pH/L-GDP solutions each year increased from 11% in 2005 to 33% in 2017. During the study period, 5330 (42%) patients died, 4977 (39%) experienced TTH, and 5502 (43%) experienced PD peritonitis. Compared to use of conventional solutions only, use of any form of N-pH/L-GDP solution was associated with reduced risks of all-cause mortality (adjusted hazard ratio [aHR] 0.67, 95% confidence interval [CI] 0.61-0.74), cardiovascular mortality (aHR 0.65, 95%CI 0.56-0.77), infection-related mortality (aHR 0.62, 95%CI 0.47-0.83) and TTH (aHR 0.79, 95%CI 0.72-0.86), but an increased risk of PD peritonitis (aHR 1.16, 95%CI 1.07-1.26).
CONCLUSIONS CONCLUSIONS
Patients who received N-pH/L-GDP solutions had decreased risks of all-cause and cause-specific mortality despite an increased risk of PD peritonitis. Studies assessing the causal relationships are warranted to determine the clinical benefits of N-pH/L-GDP solutions.

Identifiants

pubmed: 37429598
pii: 7222382
doi: 10.1093/ndt/gfad153
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the ERA.

Auteurs

Jenny H C Chen (JHC)

Department of Renal Medicine, Wollongong Hospital, Wollongong, Australia.
School of Medicine, University of Wollongong, Wollongong, Australia.

David W Johnson (DW)

Department of Kidney and Transplant Services, Princess Alexandra Hospital, Brisbane, Australia.
Centre for Health Services Research, University of Queensland, Brisbane, Australia.
Translational Research Institute, Brisbane, Australia.
Australasian Kidney Trials Network, Brisbane, Australia.

Yeoungjee Cho (Y)

Department of Kidney and Transplant Services, Princess Alexandra Hospital, Brisbane, Australia.
Centre for Health Services Research, University of Queensland, Brisbane, Australia.
Australasian Kidney Trials Network, Brisbane, Australia.

Melissa Cheetham (M)

Centre for Health Services Research, University of Queensland, Brisbane, Australia.
Department of Nephrology, Sunshine Coast University Hospital, Sunshine Coast, Australia.
Sunshine Coast Health Institute, Birtinya, Australia.

Kamal Sud (K)

Nepean Kidney Research Centre, Department of Renal Medicine, Nepean Hospital, Sydney, Australia.
Faculty of Medicine and Health, University of Sydney, Sydney, Australia.

Ashik Hayat (A)

Department of Kidney and Transplant Services, Princess Alexandra Hospital, Brisbane, Australia.
Centre for Health Services Research, University of Queensland, Brisbane, Australia.
Australasian Kidney Trials Network, Brisbane, Australia.

Belinda Stallard (B)

Department of Nephrology, Tweed Hospital, Tweed Heads, Australia.

Philip Clayton (P)

Department of Nephrology, Royal Adelaide Hospital, Adelaide, Australia.
Australia & New Zealand Dialysis and Transplant (ANZDATA) Registry, Adelaide, Australia.
Adelaide Medical School, University of Adelaide, Adelaide, Australia.

Christopher E Davies (CE)

Australia & New Zealand Dialysis and Transplant (ANZDATA) Registry, Adelaide, Australia.
Adelaide Medical School, University of Adelaide, Adelaide, Australia.

Monique Borlace (M)

Department of Nephrology, Royal Adelaide Hospital, Adelaide, Australia.

Neil Boudville (N)

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

Classifications MeSH