Global Mapping of National Health Economic Evaluation Guidelines: Evidence from 40 Countries.

IF 4.7 Q2 PHARMACOLOGY & PHARMACY
Pharmaceutical Medicine Pub Date : 2026-11-01 Epub Date: 2026-08-18 DOI:10.1007/s40290-026-00618-w
Thu Anh Do, Tung Hoang
{"title":"Global Mapping of National Health Economic Evaluation Guidelines: Evidence from 40 Countries.","authors":"Thu Anh Do, Tung Hoang","doi":"10.1007/s40290-026-00618-w","DOIUrl":null,"url":null,"abstract":"<p><p>Health economic evaluation (HEE) guidelines play an important role in health technology assessment (HTA) by supporting the consistent and transparent use of economic evidence in decision making. As countries continue updating their guidelines, substantial methodological variation persists. This review aimed to provide an updated global comparison of national HEE guidelines. National HEE guidelines were identified from the ISPOR and GEAR repositories and supplemented by hand-searching and searches of governmental and institutional sources. Two reviewers independently extracted data across 23 methodological domains, including analytical perspective, comparators, cost categories, outcome measures, modeling, discounting, evidence synthesis, and uncertainty analysis. Forty national guidelines were identified (25 high-income countries, 9 upper-middle-income countries, and 6 lower-middle-income countries). Most guidelines had been updated between 2015 and 2025. Forty-eight percent were recommendatory, 43% mandatory, and 10% voluntary. Cost-utility analysis was preferred in 48% of guidelines, and quality-adjusted life-years (QALYs) were recommended in 53%. Systematic review and the use of real-world evidence was commonly emphasized. Discount rates ranged from 1.5 to 5%, largely reflecting national economic conditions. Nearly all guidelines required clear reporting of assumptions, parameter values, and sensitivity analyses. Variation remained in preferred perspectives, comparator selection, inclusion of indirect costs, and utility measurement methods. This review provides an updated global overview of national HEE guidelines, highlighting areas of convergence in analytical methods, evidence requirements, and approaches to uncertainty. Persistent differences across countries and income settings underscore the need for context-specific but methodologically robust guidance to support HTA and healthcare decision making.</p>","PeriodicalId":19778,"journal":{"name":"Pharmaceutical Medicine","volume":" ","pages":"485-501"},"PeriodicalIF":4.7000,"publicationDate":"2026-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutical Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s40290-026-00618-w","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/18 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Health economic evaluation (HEE) guidelines play an important role in health technology assessment (HTA) by supporting the consistent and transparent use of economic evidence in decision making. As countries continue updating their guidelines, substantial methodological variation persists. This review aimed to provide an updated global comparison of national HEE guidelines. National HEE guidelines were identified from the ISPOR and GEAR repositories and supplemented by hand-searching and searches of governmental and institutional sources. Two reviewers independently extracted data across 23 methodological domains, including analytical perspective, comparators, cost categories, outcome measures, modeling, discounting, evidence synthesis, and uncertainty analysis. Forty national guidelines were identified (25 high-income countries, 9 upper-middle-income countries, and 6 lower-middle-income countries). Most guidelines had been updated between 2015 and 2025. Forty-eight percent were recommendatory, 43% mandatory, and 10% voluntary. Cost-utility analysis was preferred in 48% of guidelines, and quality-adjusted life-years (QALYs) were recommended in 53%. Systematic review and the use of real-world evidence was commonly emphasized. Discount rates ranged from 1.5 to 5%, largely reflecting national economic conditions. Nearly all guidelines required clear reporting of assumptions, parameter values, and sensitivity analyses. Variation remained in preferred perspectives, comparator selection, inclusion of indirect costs, and utility measurement methods. This review provides an updated global overview of national HEE guidelines, highlighting areas of convergence in analytical methods, evidence requirements, and approaches to uncertainty. Persistent differences across countries and income settings underscore the need for context-specific but methodologically robust guidance to support HTA and healthcare decision making.

国家卫生经济评价指南全球制图:来自40个国家的证据。
卫生经济评价(HEE)指南通过支持在决策中一致和透明地使用经济证据,在卫生技术评价(HTA)中发挥重要作用。随着各国继续更新其指导方针,大量的方法差异仍然存在。本综述旨在提供最新的全球HEE指南比较。从ISPOR和GEAR存储库中确定国家HEE指南,并通过手工检索和政府和机构来源的检索进行补充。两位审稿人独立提取了23个方法学领域的数据,包括分析视角、比较、成本类别、结果测量、建模、贴现、证据综合和不确定性分析。确定了40个国家指南(25个高收入国家,9个中高收入国家和6个中低收入国家)。大多数指南都是在2015年至2025年间更新的。48%是推荐性的,43%是强制性的,10%是自愿性的。48%的指南推荐成本效用分析,53%的指南推荐质量调整生命年(QALYs)。系统评价和使用真实世界的证据被普遍强调。贴现率从1.5%到5%不等,主要反映了国家的经济状况。几乎所有的指南都要求清楚地报告假设、参数值和敏感性分析。在偏好视角、比较国选择、间接成本和效用测量方法方面仍然存在差异。本综述提供了最新的国家医疗卫生指导方针的全球概述,突出了分析方法、证据要求和不确定性处理方法方面的趋同领域。不同国家和收入环境之间的持续差异突出表明,需要针对具体情况提供方法上可靠的指导,以支持HTA和卫生保健决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Pharmaceutical Medicine
Pharmaceutical Medicine PHARMACOLOGY & PHARMACY-
CiteScore
5.10
自引率
4.00%
发文量
36
期刊介绍: Pharmaceutical Medicine is a specialist discipline concerned with medical aspects of the discovery, development, evaluation, registration, regulation, monitoring, marketing, distribution and pricing of medicines, drug-device and drug-diagnostic combinations. The Journal disseminates information to support the community of professionals working in these highly inter-related functions. Key areas include translational medicine, clinical trial design, pharmacovigilance, clinical toxicology, drug regulation, clinical pharmacology, biostatistics and pharmacoeconomics. The Journal includes:Overviews of contentious or emerging issues.Comprehensive narrative reviews that provide an authoritative source of information on topical issues.Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by PRISMA statement.Original research articles reporting the results of well-designed studies with a strong link to wider areas of clinical research.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 Pharmaceutical Medicine 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 important medical advances.All manuscripts are subject to peer review by international experts. Letters to the Editor are welcomed and will be considered for publication.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书