The impact of peritoneal dialysis on oxypurinol and urate elimination in people with gout

Author:

Wilson Luke C.1ORCID,Ward Jacob1,Wright Daniel F. B.23ORCID,Green Suetonia C.4ORCID,Stocker Sophie L.356,Putt Tracey L.1ORCID,Schollum John B. W.1,Walker Robert J.1ORCID

Affiliation:

1. Department of Medicine Dunedin School of Medicine Dunedin New Zealand

2. School of Pharmacy University of Otago Dunedin New Zealand

3. Sydney Pharmacy School University of Sydney Sydney New South Wales Australia

4. Department of Medicine University of Otago Christchurch New Zealand

5. Department of Clinical Pharmacology & Toxicology St Vincent's Hospital Sydney Sydney New South Wales Australia

6. Sydney Musculoskeletal Health Univ. of Sydney Sydney New South Wales Australia

Abstract

AbstractGout affects 15%–30% of individuals with advanced kidney disease. Allopurinol which is rapidly and extensively metabolised to an active metabolite, oxypurinol, is the most commonly prescribed urate‐lowering therapy. Oxypurinol is almost entirely eliminated by the kidneys (>95%) and has an elimination half‐life of 18–30 h in those with normal kidney function. However, oxypurinol pharmacokinetics are poorly understood in individuals with kidney failure on peritoneal dialysis. This study characterised the elimination of oxypurinol and urate in people with gout receiving peritoneal dialysis. Oxypurinol steady‐state oral clearance (CL/F), elimination half‐life as well as kidney (CLk) and peritoneal (CLpd) clearances for oxypurinol and urate were calculated from the plasma, urine and dialysate concentration data for each individual. Our results demonstrate that oxypurinol and urate are removed by peritoneal dialysis, accounting for more than 50% of oxypurinol and urate clearances. An allopurinol dose about 50%–60% lower than the usual dose used for a patient with normal kidney function will provide adequate urate‐lowering therapy.

Funder

Otago Medical Research Foundation

Publisher

Wiley

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