Icodextrin use for peritoneal dialysis in Australia: A cohort study using Australia and New Zealand Dialysis and Transplant Registry.


Journal

Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis
ISSN: 1718-4304
Titre abrégé: Perit Dial Int
Pays: United States
ID NLM: 8904033

Informations de publication

Date de publication:
03 2020
Historique:
pubmed: 18 2 2020
medline: 15 5 2021
entrez: 18 2 2020
Statut: ppublish

Résumé

Icodextrin is a high molecular weight, starch-derived glucose polymer that is used as an osmotic agent in peritoneal dialysis (PD) to promote ultrafiltration. There has been wide variation in its use across Australia and the rest of the world, but it is unclear whether these differences are due to patient- or centre-related factors. Using the Australia and New Zealand Dialysis and Transplant Registry, all adult patients (>18 years) who started PD in Australia between 1 January 2007 and 31 December 2014 were included. The primary outcome was icodextrin use at PD commencement. Hierarchical logistic regression clustered around the treatment centre was applied to determine the patient- and centre-related characteristics associated with icodextrin use. The impact of centre-level practice pattern variability on icodextrin uptake was estimated using the intra-cluster correlation coefficient (ICC). Of 5948 patients starting on PD in 58 centres during the study period, 2002 (33.7%) received icodextrin from the outset. Overall uptake of icodextrin increased from 29% in 2010 to 42.5% in 2014. Patient-level characteristics associated with an increased likelihood of commencing PD with icodextrin included male sex (adjusted odds ratio (OR) 1.55, 95% confidence interval (CI) 1.35-1.77; Icodextrin use in incident Australian PD patients is increasing variable and associated with both patient and centre characteristics. Centre-related factors explained 25% of variability in icodextrin use.

Sections du résumé

BACKGROUND
Icodextrin is a high molecular weight, starch-derived glucose polymer that is used as an osmotic agent in peritoneal dialysis (PD) to promote ultrafiltration. There has been wide variation in its use across Australia and the rest of the world, but it is unclear whether these differences are due to patient- or centre-related factors.
METHODS
Using the Australia and New Zealand Dialysis and Transplant Registry, all adult patients (>18 years) who started PD in Australia between 1 January 2007 and 31 December 2014 were included. The primary outcome was icodextrin use at PD commencement. Hierarchical logistic regression clustered around the treatment centre was applied to determine the patient- and centre-related characteristics associated with icodextrin use. The impact of centre-level practice pattern variability on icodextrin uptake was estimated using the intra-cluster correlation coefficient (ICC).
RESULTS
Of 5948 patients starting on PD in 58 centres during the study period, 2002 (33.7%) received icodextrin from the outset. Overall uptake of icodextrin increased from 29% in 2010 to 42.5% in 2014. Patient-level characteristics associated with an increased likelihood of commencing PD with icodextrin included male sex (adjusted odds ratio (OR) 1.55, 95% confidence interval (CI) 1.35-1.77;
CONCLUSIONS
Icodextrin use in incident Australian PD patients is increasing variable and associated with both patient and centre characteristics. Centre-related factors explained 25% of variability in icodextrin use.

Identifiants

pubmed: 32063201
doi: 10.1177/0896860819894058
doi:

Substances chimiques

Dialysis Solutions 0
Icodextrin 2NX48Z0A9G

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

209-219

Auteurs

Dharshan Rangaswamy (D)

Department of Nephrology, Kasturba Hospital and Medical College, Manipal Academy of Higher Education, Manipal, Udupi, India.

Vasudeva Guddattu (V)

Department of Statistics, Prasanna School of Public Health, Manipal Academy of Higher Education, Manipal, Udupi, India.

Angela C Webster (AC)

Centre for Transplant and Renal Research, Westmead Hospital, Westmead, Australia.
Sydney School of Public Health, The University of Sydney, Sydney, Australia.

Monique Borlace (M)

Central Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, Adelaide, Australia.

Neil Boudville (N)

Medical School, University of Western Australia, Australia.

Philip Clayton (P)

Central Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, Adelaide, Australia.
Australia and New Zealand Dialysis and Transplant (ANZDATA) Registry, Adelaide, Australia.
School of Medicine, Faculty of Health Sciences, University of Adelaide, Adelaide, Australia.

Sunil Badve (S)

Australia and New Zealand Dialysis and Transplant (ANZDATA) Registry, Adelaide, Australia.
Department of Nephrology, St George Hospital, Sydney, Australia.

David W Johnson (DW)

Australia and New Zealand Dialysis and Transplant (ANZDATA) Registry, Adelaide, Australia.
Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia.
Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
Translational Research Institute, Brisbane, Australia.

Kamal Sud (K)

Australia and New Zealand Dialysis and Transplant (ANZDATA) Registry, Adelaide, Australia.
Departments of Renal Medicine, Nepean and Westmead Hospitals, Sydney, Australia.
The University of Sydney Medical School, Sydney, Australia.

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