Influencing Factors of Health Technology Assessment to Orphan Drugs: Empirical Evidence in England, Scotland, Canada, and Australia.

consistency analysis correspondence analysis health insurance reimbursement health technology assessment (HTA) orphan drugs

Journal

Frontiers in public health
ISSN: 2296-2565
Titre abrégé: Front Public Health
Pays: Switzerland
ID NLM: 101616579

Informations de publication

Date de publication:
2022
Historique:
received: 24 01 2022
accepted: 23 05 2022
entrez: 5 7 2022
pubmed: 6 7 2022
medline: 7 7 2022
Statut: epublish

Résumé

This study summarizes the intrinsic criteria for the recommendation of orphan drugs in England, Scotland, Canada, and Australia with the aim of understanding the rationale for the variability in decision-making and to provide a reference for the establishment of criteria in the process of access to health insurance for orphan drugs in different countries and the construction of national uniform criteria. A comparative analysis of 60 health technology assessment (HTA) guidelines of 15 drug-indication pairs appraised by four countries (England, Scotland, Canada, and Australia) from 2017 to 2018 was done, including an in-depth analysis of a case study. Agreement levels were measured using kappa scores. Associations were explored through correspondence analysis. The four countries possess some homogeneity in the assessment, but each has its own preferences. Poor agreement exists between England, Scotland, and Canada (-0.41 < kappa score < 0.192). In the correspondence analysis, England placed more emphasis on treatment methods in terms of control type when making recommendations. Canada and Scotland focused more on trial type with Canada placing more emphasis on phase III and open-label trials and on cost-utility analysis, while Australia was less studied in terms of economic models. Different countries have different goals when establishing HTA decisions for orphan drugs due to their different degrees of orphan drug coverage. Different countries should not only combine their unique values of clinical benefit and cost-effectiveness in the assessment of orphan drugs but also give different weights during the HTA process, after considering account the development of the country itself.

Identifiants

pubmed: 35784205
doi: 10.3389/fpubh.2022.861067
pmc: PMC9247336
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

861067

Informations de copyright

Copyright © 2022 Zhou, Ji, Li, Hu, Xie, Feng and Yuan.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Value Health. 2017 Mar;20(3):320-328
pubmed: 28292476
Orphanet J Rare Dis. 2018 Jan 30;13(1):27
pubmed: 29382371
Int J Technol Assess Health Care. 2008 Fall;24(4):511-7
pubmed: 18828948
Br J Haematol. 2018 Jul;182(1):29-45
pubmed: 29741753
Health Policy. 2012 Dec;108(2-3):167-77
pubmed: 23088802
Malays Fam Physician. 2008 Apr 30;3(1):14-20
pubmed: 25606106
Front Med (Lausanne). 2022 Feb 17;9:820757
pubmed: 35252257

Auteurs

Na Zhou (N)

Department of Social Medicine, School of Public Health, Dalian Medical University, Dalian, China.
Department of Health Policy and Management, School of Public Health, Peking University, Beijing, China.

Hong Ji (H)

Department of Pediatrics, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

Zheng Li (Z)

Department of Social Medicine, School of Public Health, Dalian Medical University, Dalian, China.

Jun Hu (J)

Shanghai Medical Products Administration, Shanghai, China.

Jia-Hua Xie (JH)

Department of Social Medicine, School of Public Health, Dalian Medical University, Dalian, China.

Yu-Heng Feng (YH)

Department of Social Medicine, School of Public Health, Dalian Medical University, Dalian, China.

Ni Yuan (N)

Department of Social Medicine, School of Public Health, Dalian Medical University, Dalian, China.

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