中国糖尿病肾病标准治疗中加入达格列净和恩格列净的成本-效果

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Tingting Qiu, Ping Li, Dan Yan
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引用次数: 0

摘要

背景:达格列净和恩格列净正在成为糖尿病肾病(DKD)的有希望的治疗选择。目的:本研究旨在评估将达格列净和恩格列净纳入中国DKD标准治疗的成本效益。方法:建立马尔可夫模型,从保健角度评价达格列净和恩格列净联合标准治疗与单独标准治疗对DKD的成本-效果。成本和效用数据来自中国背景下发表的文献。主要结局包括总成本、质量调整生命年(QALYs)和增量成本-效果比(ICER)。以2023年中国人均GDP(89,358元)作为支付意愿阈值。结果:与单纯接受标准治疗相比,加用达格列净或依帕格列净的总费用高于单纯接受标准治疗的患者(分别为+¥19,203.56和+¥9496.92)。然而,dapagliflozin和empagliflozin也产生了更多的生命年(+1.72 vs +1.40)和质量年(+1.40 vs +0.88)。达格列净的ICER / life-year和ICER / QALY分别为¥11,178.52和¥18,192.50,恩格列净为¥6773.10和¥10,811.64。达格列净和恩格列净的增量净货币效益分别为75,120.54日元和68,994.90日元。敏感性分析支持基本病例分析的主要发现,因为达格列净或恩格列净的成本-效果在参数值的最合理范围内是持续的。结论:考虑到ICER低于预先设定的支付意愿阈值,在中国,将达格列净和恩格列净纳入DKD的标准治疗可能是一种具有成本效益的策略。
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 of Adding Dapagliflozin and Empagliflozin to Standard Treatment for Diabetic Kidney Disease in China.

Background: Dapagliflozin and empagliflozin are emerging as promising treatment options for diabetic kidney disease (DKD).

Objective: This study sought to evaluate the cost effectiveness of incorporating dapagliflozin and empagliflozin into the standard treatment for DKD in China.

Methods: A Markov model was constructed to evaluate the cost-effectiveness of dapagliflozin and empagliflozin plus standard treatment versus standard treatment alone for DKD treatment from a healthcare perspective. Costs and utility data was obtained from published literatures within the Chinese context. The primary outcome included total cost, quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratio (ICER). GDP per capita of 2023 in China (¥89,358) was utilized as the willingness-to-pay threshold.

Results: Compared to standard treatment alone, add-on therapy of dapagliflozin or empagliflozin resulted in a higher total cost than those solely receiving standard treatment (+¥19,203.56 and +¥9496.92, respectively). However, both dapagliflozin and empagliflozin also yielded more life-years (+1.72 vs. +1.40) and QALYs (+1.40 vs. +0.88). The ICER per life-year and ICER per QALY was ¥11,178.52 and ¥18,192.50 for dapagliflozin and ¥6773.10 and ¥10,811.64 for empagliflozin, respectively. The incremental net monetary benefit was ¥75,120.54 and ¥68,994.90 for dapagliflozin and empagliflozin, respectively. Sensitivity analysis supported the main findings of the base-case analysis as the cost-effectiveness of dapagliflozin or empagliflozin was sustained for most plausible ranges of parameter values.

Conclusions: Considering that the ICER falls below the predefined willingness-to-pay threshold, incorporating dapagliflozin and empagliflozin into standard treatment for DKD is likely to be a cost-effective strategy in China.

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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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