IF 2.7 3区 医学 Q2 RESPIRATORY SYSTEM
Kai-Michael Beeh, Jing Claussen, Dhvani Shah, Alan Martin, Robyn Kendall, Priyadarsini Dasari, Afisi S Ismaila, Stephen G Noorduyn
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引用次数: 0

摘要

目的:INTREPID试验表明,在现实世界的临床实践中,与非ellipta多吸入器三联治疗(MITT)相比,每日一次的糠酸氟替卡松、乌莫克利地铵和维兰特罗(FF/UMEC/VI)单吸入器三联治疗(SITT)在慢性阻塞性肺疾病(COPD)的治疗中具有临床益处。该分析从德国医疗保健的角度评估了SITT联合FF/UMEC/VI与非ellipta MITT治疗症状性COPD的成本效益。患者和方法:来自INTREPID试验的数据,包括基线特征、治疗效果(1秒用力呼气量和圣乔治呼吸问卷评分[源自探索性COPD评估测试评分图])、停药率,以及德国医疗资源和药物成本(2023欧元),用于填充GALAXY COPD模型。该分析是在整个生命周期内进行的,其结果包括生命年(LYs)、质量调整LYs (QALYs)和增量成本效用比。分析的稳健性通过情景分析、单向敏感性分析和概率分析进行评估。结果:与非ellipta MITT相比,FF/UMEC/VI的终生预后预测改善,每位患者额外的LYs为0.174(95%范围:0.065,0.322),QALYs为0.261(0.186,0.346),同时节省成本2,850欧元(3,517欧元,2,220欧元)。此外,接受FF/UMEC/VI治疗的患者预计会经历急性发作的减少(-0.063),突出其作为首选治疗方案的优势。这些发现在单向敏感性、情景分析和概率分析中保持一致,突出了FF/UMEC/VI作为德国COPD管理成本效益解决方案的稳健性。结论:与非ellipta MITT相比,FF/UMEC/VI具有临床益处和成本节约,表明它可能减轻德国COPD的负担,值得医生考虑作为首选治疗方案。
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 Single-Inhaler Versus Multiple-Inhaler Triple Therapy in COPD: A German Healthcare Perspective.

Purpose: The INTREPID trial showed that once-daily single-inhaler triple therapy (SITT) using fluticasone furoate, umeclidinium, and vilanterol (FF/UMEC/VI) offers clinical benefits versus non-ELLIPTA multiple-inhaler triple therapy (MITT) for the management of chronic obstructive pulmonary disease (COPD) in real-world clinical practice. This analysis evaluated the cost-effectiveness of SITT with FF/UMEC/VI versus non-ELLIPTA MITT for treating symptomatic COPD from a German healthcare perspective.

Patients and methods: Data from the INTREPID trial, including baseline characteristics, treatment effects (forced expiratory volume in 1 second and St. George's Respiratory Questionnaire score [derived from exploratory COPD assessment test score mapping]), and discontinuation rates, along with German healthcare resource and drug costs (2023 Euros), were used to populate the GALAXY COPD model. The analysis was conducted over a lifetime horizon, with outcomes including life years (LYs), quality-adjusted LYs (QALYs), and incremental cost-utility ratios. The robustness of the analysis was assessed using scenario, one-way sensitivity, and probabilistic analyses.

Results: Improved lifetime outcomes were predicted for FF/UMEC/VI versus non-ELLIPTA MITT, providing additional LYs of 0.174 (95% range: 0.065, 0.322) and QALYs of 0.261 (0.186, 0.346) per patient, together with cost savings of €2,850 (€3,517, €2,220). Additionally, patients receiving FF/UMEC/VI were predicted to experience a reduction in exacerbations (-0.063), highlighting its dominance as the preferred treatment option. These findings remained consistent across one-way sensitivity, scenario, and probabilistic analyses, highlighting the robustness of FF/UMEC/VI as a cost-effective solution for COPD management in Germany.

Conclusion: FF/UMEC/VI offers clinical benefits and cost savings compared with non-ELLIPTA MITT, suggesting that it may reduce the burden of COPD in Germany and warranting consideration as a preferred treatment option by physicians.

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来源期刊
CiteScore
4.80
自引率
10.70%
发文量
372
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal of therapeutics and pharmacology focusing on concise rapid reporting of clinical studies and reviews in COPD. Special focus will be given to the pathophysiological processes underlying the disease, intervention programs, patient focused education, and self management protocols. This journal is directed at specialists and healthcare professionals
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