泰国痛风患者HLA-B*58:01基因型检测预防严重别嘌呤醇超敏反应的最新经济评价

IF 2.8 Q2 RHEUMATOLOGY
Piyameth Dilokthornsakul, Worawit Louthrenoo, Jirawit Yadee, Boonjing Siripaitoon, Kanon Jatuworapruk, Suda Vannaprasaht, Ticha Rerkpattanapipat, Apinya Chungcharoenpanich, Wimolsiri Iamsumang, Nilawan Upakdee, Supinya Dechanont, Suppachai Lawanaskol, Bodin Butthum, Parawee Chevaisrakul, Patapong Towiwat
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引用次数: 0

摘要

目的:人类白细胞抗原(HLA),特别是HLA- b *58:01,在泰国的痛风患者开始使用别嘌呤醇之前检测是具有成本效益的。然而,在泰国有几种药物可用于治疗痛风,因此更新的成本效益分析是有必要的。本研究旨在更新泰国痛风患者别嘌呤醇起始治疗前HLA-B*58:01检测的成本效益。方法:从社会视角出发,建立决策树模型和马尔可夫模型的混合模型。将HLA-B*58:01检测与护理标准比较为无检测。评估了总医疗费用和质量调整生命年(QALYs)。通过全面的文献综述、回顾性数据分析和前瞻性数据收集来确定模型的输入。计算增量成本-效果比分析。结果:HLA-B*58:01检测可避免1.554例Stevens-Johnson综合征和中毒性表皮坏死,每1000例患者可挽救0.140例患者的生命。与不检测相比,它可以增加0.002个生命年和0.004个质量年。然而,它需要更高的生命周期成本(4,690泰铢),导致增量成本效益比为1,093,068泰铢/QALY(每个QALY 31,404美元)。结论:在泰国痛风患者开始使用别嘌呤醇前进行HLA-B*58:01检测不具有成本效益,目前每次检测价格为1,000 THB。然而,如果对于HLA-B*58:01结果阳性的患者,只有probenecid作为替代治疗,那么HLA-B*58:01检测将是具有成本效益的。该结果可为卫生当局、政策决策者和医生组织提供在开始使用别嘌呤醇前进行HLA-B*58:01检测的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An Updated Economic Evaluation of HLA-B*58:01 Genotype Testing in Gouty Patients for Preventing Severe Allopurinol Hypersensitivity in Thailand.

An Updated Economic Evaluation of HLA-B*58:01 Genotype Testing in Gouty Patients for Preventing Severe Allopurinol Hypersensitivity in Thailand.

An Updated Economic Evaluation of HLA-B*58:01 Genotype Testing in Gouty Patients for Preventing Severe Allopurinol Hypersensitivity in Thailand.

An Updated Economic Evaluation of HLA-B*58:01 Genotype Testing in Gouty Patients for Preventing Severe Allopurinol Hypersensitivity in Thailand.

Objective: Human Leukocyte Antigen (HLA), specifically HLA-B*58:01, testing before allopurinol initiation in patients with gout in Thailand was previously shown to be cost-effective. However, several drugs are available in the treatment of gout in Thailand, so the updated cost-effectiveness analysis is warranted. This study aimed to update the cost-effectiveness of HLA-B*58:01 testing before allopurinol initiation in patients with gout in Thailand.

Methods: A hybrid model consisting of a decision tree and a Markov model with a lifetime horizon from a societal perspective was undertaken. The HLA-B*58:01 testing was compared to the standard of care as no testing. Total health care costs and quality-adjusted life years (QALYs) were assessed. A comprehensive literature review along with retrospective data analysis and prospective data collection were conducted to determine inputs to inform the model. The incremental cost-effectiveness ratio analysis was calculated.

Results: HLA-B*58:01 testing could avoid 1.554 Stevens-Johnson syndrome and toxic epidermal necrosis cases, resulting in a saving of 0.140 patients' lives per 1,000 patients. It could gain 0.002 life-years and 0.004 QALYs compared to no testing. However, it required a higher lifetime cost of 4,690 Thai baht (THB), resulting in an incremental cost-effectiveness ratio of 1,093,068 THB/QALY (31,404 US dollars per QALY).

Conclusion: HLA-B*58:01 testing was not cost-effective before allopurinol initiation in Thai patients with gout at the current price of 1,000 THB per test. However, HLA-B*58:01 testing would be cost-effective if only probenecid was the alternative treatment for patients with positive HLA-B*58:01 results. This result would be useful for health authorities, policy decision-makers, and physicians' organizations in providing the recommendation for HLA-B*58:01 testing before initiation of allopurinol.

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