改善肾移植受者骨矿物质密度的地诺单抗与阿仑膦酸钠的成本效益分析:一项比较研究

IF 3.4 Q2 PHARMACOLOGY & PHARMACY
Mona Alshahawey, May A Shawki, Sherihan Ahmed Sayed, Ahmad Elseasi, Lamia ElWakeel
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引用次数: 0

摘要

背景德诺单抗和阿仑膦酸钠对肾移植后骨矿物质密度(BMD)的保存有积极影响。然而,这些药物在肾移植中的成本效益在很大程度上仍未得到探讨。我们进行了一项成本效益分析,比较了在肾移植受者标准治疗(维生素 D 和钙)的基础上,每 6 个月皮下注射 (SC) 60 毫克地诺单抗与每周口服 70 毫克阿仑膦酸钠的成本和临床效果。研究调查了这两种药物对改善 BMD t 分数和预防骨折的影响。结果成本效益分析表明,就改善 BMD 和预防骨折而言,阿仑膦酸钠加用标准疗法是最具成本效益的方案,其增量成本效益比 (ICER) 为 154 美元/患者/年。单向敏感性分析确定了阿仑膦酸钠零售单价提高 25% 和 50% 或地诺单抗零售单价降低 25% 和 50% 时成本效益的变化。该模型对骨折预防概率和达到预期结果概率的不确定性(95% 置信区间)非常敏感。结论该模型表明,就 RTR 患者 BMD 改善和骨折预防而言,每周口服一次阿仑膦酸钠作为标准疗法的附加疗法似乎比每年两次 SC 地诺单抗更具成本效益。为了验证这些数据,有必要使用更长的时间跨度模型,对骨折风险和不良事件进行更长时间的随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cost-effectiveness analysis of denosumab versus alendronate for improving bone mineral density in renal transplant recipients: a comparative study

Background

Denosumab and alendronate had a positive impact on bone mineral density (BMD) preservation after kidney transplantation. However, the cost-effectiveness of these agents in the context of kidney transplantation remains largely unexplored. We have conducted a cost-effectiveness analysis to compare the cost and the clinical outcomes of adding subcutaneous (SC) 60 mg denosumab every 6 months vs. oral weekly 70 mg Alendronate, to the standard care therapy (vitamin D and calcium) in renal transplant recipients (RTRs). The impact of both drugs on BMD t-score improvement and fracture prevention was investigated. A decision-analysis model from a health care payer perspective was applied.

Results

The cost-effectiveness analysis has shown that alendronate add-on to the standard therapy was the most cost-effective regimen, in terms of BMD improvement and fracture prevention with an incremental cost-effectiveness ratio (ICER) of $154/patient/year. The one-way sensitivity analyses have delineated the change in cost-effectiveness when alendronate retail unit price was increased by 25% and 50%, or when denosumab retail unit price was decreased by 25% and 50%. The model was sensitive to the uncertainties (95% confidence interval) in the probabilities of fracture prevention and the probabilities of attaining the desired outcome.

Conclusion

The model suggests that oral once weekly alendronate add-on regimen to standard therapy seems to be substantially more cost effective than twice yearly SC denosumab in terms of BMD improvement and fracture prevention in RTRs. Longer time horizon models with longer follow-up periods for fracture risks and adverse events are warranted to validate these data.

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来源期刊
自引率
0.00%
发文量
44
审稿时长
23 weeks
期刊介绍: Future Journal of Pharmaceutical Sciences (FJPS) is the official journal of the Future University in Egypt. It is a peer-reviewed, open access journal which publishes original research articles, review articles and case studies on all aspects of pharmaceutical sciences and technologies, pharmacy practice and related clinical aspects, and pharmacy education. The journal publishes articles covering developments in drug absorption and metabolism, pharmacokinetics and dynamics, drug delivery systems, drug targeting and nano-technology. It also covers development of new systems, methods and techniques in pharmacy education and practice. The scope of the journal also extends to cover advancements in toxicology, cell and molecular biology, biomedical research, clinical and pharmaceutical microbiology, pharmaceutical biotechnology, medicinal chemistry, phytochemistry and nutraceuticals.
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