Examining Consistency Across NICE Single Technology Appraisals: A Review of Appraisals for Paroxysmal Nocturnal Haemoglobinuria.

IF 4.4 3区 医学 Q1 ECONOMICS
PharmacoEconomics Pub Date : 2025-05-01 Epub Date: 2025-02-12 DOI:10.1007/s40273-025-01472-5
Jeremiah Donoghue, Matthew Youngs, Alex Reeve, Krishna Vydyula, Natalia Kunst, Roochi Trikha, Daniel Gallacher
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引用次数: 0

Abstract

In 2024, the National Institute for Health and Care Excellence (NICE) recommended two new health technologies for paroxysmal nocturnal haemoglobinuria. This review systematically compares the clinical and cost-effectiveness evidence considered within the NICE single technology appraisals of iptacopan, danicopan and pegcetacoplan, examines the consistency of the clinical evidence and economic modelling, and considers whether single technology appraisals are a suitable apparatus for consistent decision making. The studies used different follow-up lengths and used different definitions for reporting breakthrough haemolysis (BTH), but otherwise reported similar outcomes and found a significant benefit for their interventions. A lack of direct evidence and unreliable indirect comparisons meant that naïve comparisons across trials were carried into the economic modelling despite differences in their control arms. Approaches to modelling BTH and associated dose escalation differed across appraisals, despite information for pegcetacoplan coming from the same source in each appraisal, which had a large impact on the economic results. This review raises the question of whether NICE should implement multiple technology appraisals more frequently to reduce these inconsistences. Additionally, we recommend the development of a framework for revisiting positive recommendations when the implementation of health technologies deviates from assumptions made in the economic modelling to ensure cost-effective healthcare is preserved.

检查NICE单一技术评价的一致性:阵发性夜间血红蛋白尿评价综述。
2024年,国家健康与护理卓越研究所(NICE)推荐了两种治疗阵发性夜间血红蛋白尿的新健康技术。本综述系统地比较了NICE对伊普他科泮、达尼可泮和pegcetacoplan的单一技术评价中考虑的临床和成本效益证据,检查了临床证据和经济模型的一致性,并考虑了单一技术评价是否是一致决策的合适工具。这些研究使用了不同的随访时间和不同的定义来报告突破性溶血(BTH),但其他方面报告了相似的结果,并发现他们的干预措施有显著的益处。直接证据的缺乏和不可靠的间接比较意味着naïve试验之间的比较被带入经济模型,尽管它们的对照组存在差异。尽管每次评估中有关pegcetacoplan的信息来自相同的来源,但不同评估对BTH和相关剂量递增的建模方法不同,这对经济结果有很大影响。这篇综述提出了NICE是否应该更频繁地实施多种技术评估以减少这些不一致的问题。此外,我们建议制定一个框架,以便在卫生技术的实施偏离经济模型中的假设时重新审视积极的建议,以确保维持具有成本效益的医疗保健。
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
PharmacoEconomics
PharmacoEconomics 医学-药学
CiteScore
8.10
自引率
9.10%
发文量
85
审稿时长
6-12 weeks
期刊介绍: PharmacoEconomics is the benchmark journal for peer-reviewed, authoritative and practical articles on the application of pharmacoeconomics and quality-of-life assessment to optimum drug therapy and health outcomes. An invaluable source of applied pharmacoeconomic original research and educational material for the healthcare decision maker. PharmacoEconomics is dedicated to the clear communication of complex pharmacoeconomic issues related to patient care and drug utilization. PharmacoEconomics offers a range of additional features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand the scientific content and overall implications of the article.
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