Cost-effectiveness analysis of romosozumab for severe postmenopausal osteoporosis at very high risk of fracture in Mexico.

IF 2.6 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES PLoS ONE Pub Date : 2025-02-07 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0299673
Juan Pablo Diaz Martinez, Therese Aubry de Maraumont, Elly Natty Sánchez, Luis Miguel Camacho Cordero, Eric Yeh
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Abstract

Introduction: This study aims to assess the cost effectiveness of romosozumab versus teriparatide, both sequenced to denosumab, for the treatment of severe postmenopausal osteoporosis at very high risk of fractures in Mexican women.

Methods: A Markov model was used to assess the relative cost effectiveness of 1 year of romosozumab versus 2 years of teriparatide, both sequenced to denosumab for a total treatment duration of 5 years. Outcomes for a cohort of women with a mean age of 74 years, a T-score ≤-2.5 and a previous fragility fracture were simulated over a lifetime horizon. The analysis was conducted from the perspective of the Mexican healthcare system and used a discount rate of 5% per annum. To inform relative fracture incidence, the bone mineral density (BMD) advantage of romosozumab over teriparatide was translated into relative risks of fracture, using relationships provided by a meta-regression of osteoporosis therapy trials. Outcomes were assessed in terms of lifetime costs (2023 Mexican pesos), quality-adjusted life years (QALYs) and life-years gained (LYs).

Results: Base case results showed that, compared with teriparatide/ denosumab, romosozumab/ denosumab reduced costs by $51,363 MXN per patient and yielded 0.03 additional QALYs and 0.01 LYs. Scenario analyses and probabilistic sensitivity analyses confirmed that results are robust to uncertainty in model assumptions and inputs.

Conclusions: Results show that romosozumab/ denosumab produces greater health benefits at a lower total cost than teriparatide/ denosumab.

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在墨西哥,romosozumab治疗绝经后骨质疏松症的成本-效果分析。
简介:本研究旨在评估romosozumab与teriparatide的成本效益,两者均为denosumab测序,用于治疗墨西哥妇女严重绝经后骨质疏松症,骨折风险极高。方法:采用Markov模型评估1年romosozumab与2年teriparatide的相对成本效益,两者均按denosumab排序,总治疗时间为5年。对平均年龄为74岁、t评分≤-2.5、既往脆性骨折的女性进行终身模拟。分析是从墨西哥医疗保健系统的角度进行的,并使用每年5%的贴现率。为了了解相对骨折发生率,利用骨质疏松治疗试验提供的关系,将romosozumab优于teriparatide的骨密度(BMD)优势转化为骨折的相对风险。根据终身成本(2023墨西哥比索)、质量调整生命年(QALYs)和获得生命年(LYs)对结果进行评估。结果:基础病例结果显示,与特立帕肽/ denosumab相比,romosozumab/ denosumab为每位患者降低了51,363 MXN美元的成本,并产生了0.03个额外的qaly和0.01个LYs。情景分析和概率敏感性分析证实,结果对模型假设和输入的不确定性具有鲁棒性。结论:结果显示,与特立帕肽/地诺单抗相比,romosozumab/ denosumab以更低的总成本产生了更大的健康益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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