Is HLA-B*58:01 genotyping cost effective in guiding allopurinol use in gout patients with chronic kidney disease?

Author:

Teng Gim Gee12ORCID,Tan-Koi Wei-Chuen3,Dong Di4,Sung Cynthia35ORCID

Affiliation:

1. Division of Rheumatology, University Medicine Cluster, National University Health System, Singapore, 119228

2. Chronic Program, Alexandra Hospital, National University Health System, Singapore, 159964

3. Vigilance & Compliance Branch, Health Sciences Authority, Singapore, 138667

4. Global Health Research Center, Duke Kunshan University, China, 215316

5. Health Services & Systems Research, Duke-NUS Medical School, Singapore, 169857

Abstract

Aim: Concerns for fatal severe cutaneous adverse reactions (SCARs) hamper allopurinol use. Methods and material: We adopted a health system perspective to evaluate the cost–effectiveness of HLA-B*58:01 genotyping before allopurinol initiation. A decision tree compared three treatment strategies in gout patients with chronic kidney disease who have higher risk for SCAR. They were standard allopurinol treatment followed by febuxostat in nonresponders, test-positive patients receive febuxostat while test-negative receive allopurinol and universal use of febuxostat. Results: The first strategy was the most cost effective. Genotyping dominated universal febuxostat use. Time horizon and SCAR incidence were the most influential factors on the incremental cost–effectiveness ratio. Conclusion: HLA-B*58:01 genotyping compared with standard allopurinol–febuxostat sequential treatment does not provide good value for money in gout with chronic kidney disease.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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