Agency for Care Effectiveness, Ministry of Health Singapore, Singapore, Singapore.
Department of Rheumatology, Allergy and Immunology, Tan Tock Seng Hospital, Singapore, Singapore.
J Med Econ. 2020 Aug;23(8):838-847. doi: 10.1080/13696998.2020.1757456. Epub 2020 May 13.
Allopurinol is the most common urate lowering therapy (ULT) used to treat gout but may cause life-threatening severe cutaneous adverse reactions (SCAR) in a small number of patients. Risk of SCAR is increased for patients with the HLA-B58:01 genotype. When alternative ULT is required, febuxostat or probenecid are recommended. The aim of this study was to conduct a cost-utility analysis of sequential ULT treatment strategies for gout, including strategies with and without HLA-B58:01 genotyping prior to treatment initiation, with a view to inform optimal gout management in Singapore. A Markov model was developed from the Singapore healthcare payer perspective. Reflecting local practice, 12 different treatment strategies containing at least one ULT (allopurinol, febuxostat, probenecid) were evaluated in adults with gout. Response rates (SUA < 6mg/dL) were derived from an in-house network meta-analysis and from published literature. Incremental cost-effectiveness ratios (ICERs) were calculated over a 30-year time horizon, with costs and benefits discounted at 3% per annum. Sensitivity analyses were conducted to explore uncertainties. Sequential treatment of allopurinol 300 mg/day-allopurinol 600 mg/day-probenecid ("standard of care") was cost-effective compared to no ULT, with an ICER of SGD1,584/QALY. Allopurinol300-allopurinol600-probenecid-febuxostat sequence compared to allopurinol300-allopurinol600-probenecid had an ICER of SGD11,400/QALY. All other treatment strategies were dominated by preceding strategies. Treatment strategies incorporating HLA-B*58:01 genotyping before ULT use were dominated by the corresponding non-genotyping strategy. Current standard of care (allopurinol300-allopurinol 600-probenecid) for gout is cost-effective compared with no ULT in the local context. Febuxostat is unlikely to be cost-effective in Singapore at current prices unless it is used last-line.
别嘌醇是最常用的降尿酸治疗药物(ULT),用于治疗痛风,但在少数患者中可能会引起危及生命的严重皮肤不良反应(SCAR)。对于 HLA-B58:01 基因型的患者,SCAR 的风险增加。当需要替代 ULT 时,建议使用非布司他或丙磺舒。本研究旨在对痛风的序贯 ULT 治疗策略进行成本效用分析,包括治疗前是否进行 HLA-B58:01 基因分型,以期为新加坡的痛风最佳管理提供信息。从新加坡医疗保健支付者的角度出发,建立了一个马尔可夫模型。考虑到当地的实践情况,评估了 12 种不同的治疗策略,这些策略都包含至少一种 ULT(别嘌醇、非布司他、丙磺舒),用于治疗痛风成人患者。反应率(SUA < 6mg/dL)来自内部网络荟萃分析和已发表的文献。在 30 年的时间范围内计算增量成本效益比(ICER),成本和效益按每年 3%贴现。进行敏感性分析以探索不确定性。与不使用 ULT 相比,300mg/天-600mg/天别嘌醇-丙磺舒(“标准治疗”)序贯治疗是具有成本效益的,ICER 为 SGD1584/QALY。300mg 别嘌醇-600mg 别嘌醇-丙磺舒-非布司他序贯治疗与 300mg 别嘌醇-600mg 别嘌醇-丙磺舒相比,ICER 为 SGD11400/QALY。其他所有治疗策略均被先前的策略所主导。在使用 ULT 之前纳入 HLA-B*58:01 基因分型的治疗策略,均被相应的非基因分型策略所主导。在当地背景下,目前痛风的标准治疗(300mg 别嘌醇-600mg 别嘌醇-丙磺舒)与不使用 ULT 相比是具有成本效益的。除非最后一线使用,否则非布司他在新加坡的价格不太可能具有成本效益。