Heinz Katja C, Beaudart Charlotte, Willems Damon, Wiethoff Isabell, Hiligsmann Mickaël
Department of Health Services Research, Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, The Netherlands.
Pharmacoeconomics. 2023 Nov;41(11):1415-1435. doi: 10.1007/s40273-023-01293-4. Epub 2023 Jul 1.
Numerous therapies have recently emerged for treatment of patients with atopic dermatitis (AD), a common skin disease, and understanding their cost-effectiveness is of high importance for policy makers. This systematic literature review (SLR) aimed to provide an overview of full economic evaluations that assessed cost-effectiveness of emerging AD treatments.
The SLR was conducted in Medline, Embase, UK National Health Service Economic Evaluation Database and EconLit. Reports published by the National Institute for Health and Care Excellence, the Institute for Clinical and Economic Review and the Canadian Agency for Drugs and Technologies in Health were manually searched. Economic evaluations published from 2017 to September 2022 that compared emerging AD treatments with any comparator were included. Quality assessment was conducted by using the Consensus on Health Economic Criteria list.
A total of 1333 references were screened after removing duplicates. Among those references, 15 that conducted a total of 24 comparisons were included. Most studies were from the USA, UK or Canada. Seven different emerging treatments were compared, mostly with usual care. In 15 comparisons (63%), the emerging treatment was cost-effective, and 11 out of 14 dupilumab comparisons (79%) reported that dupilumab was cost-effective. Upadacitinib was the only emerging therapy that was never classified as cost-effective. On average, 13 out of 19 quality criteria (68%) per reference were rated as fulfilled while manuscripts and health technology reports received generally higher quality assessment scores than published abstracts.
This study revealed some discrepancies in the cost-effectiveness of emerging therapies for AD. A variety of designs and guidelines made comparison difficult. Therefore, we recommend that future economic evaluations use more similar modelling approaches to improve comparability of results.
The protocol was published in PROSPERO (ID: CRD42022343993).
特应性皮炎(AD)是一种常见的皮肤病,近年来出现了多种治疗方法,了解这些治疗方法的成本效益对政策制定者至关重要。本系统文献综述(SLR)旨在概述评估新兴AD治疗方法成本效益的全面经济评估。
在Medline、Embase、英国国家卫生服务经济评估数据库和EconLit中进行了SLR。对英国国家卫生与临床优化研究所、临床与经济审查研究所和加拿大卫生技术评估署发布的报告进行了人工检索。纳入了2017年至2022年9月发表的将新兴AD治疗方法与任何对照进行比较的经济评估。使用卫生经济标准共识清单进行质量评估。
去除重复项后,共筛选了1333篇参考文献。其中,15篇进行了总共24次比较的文献被纳入。大多数研究来自美国、英国或加拿大。比较了七种不同的新兴治疗方法,大多与常规治疗进行比较。在15次比较(63%)中,新兴治疗具有成本效益,在14次度普利尤单抗比较中的11次(79%)报告度普利尤单抗具有成本效益。乌帕替尼是唯一一种从未被归类为具有成本效益的新兴疗法。每份参考文献平均19项质量标准中的13项(68%)被评定为符合,而手稿和卫生技术报告的质量评估得分总体上高于发表的摘要。
本研究揭示了新兴AD治疗方法在成本效益方面的一些差异。各种设计和指南使得比较变得困难。因此,我们建议未来的经济评估使用更相似的建模方法,以提高结果的可比性。
该方案已发表在PROSPERO(标识符:CRD42022343993)。