Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar.


Journal

BMJ global health
ISSN: 2059-7908
Titre abrégé: BMJ Glob Health
Pays: England
ID NLM: 101685275

Informations de publication

Date de publication:
02 2021
Historique:
received: 12 10 2020
revised: 16 01 2021
accepted: 30 01 2021
entrez: 25 2 2021
pubmed: 26 2 2021
medline: 25 6 2021
Statut: ppublish

Résumé

Over half of those hepatitis C virus (HCV)/HIV coinfected live in low-income and middle-income countries, and many remain undiagnosed or untreated. In 2016, Médecins Sans Frontières (MSF) established a direct-acting antiviral (DAA) treatment programme for people HCV/HIV coinfected in Myanmar. The purpose of our study was to evaluate the real-world cost and cost-effectiveness of this programme, and potential cost-effectiveness if implemented by the Ministry of Health (MoH). Costs (patient-level microcosting) and treatment outcomes were collected from the MSF prospective cohort study in Dawei, Myanmar. A Markov model was used to assess cost-effectiveness of the programme compared with no HCV treatment from a health provider perspective. Estimated lifetime and healthcare costs (in 2017 US$) and health outcomes (in disability-adjusted life-years (DALYs)) were simulated to calculate the incremental cost-effectiveness ratio (ICER), compared with a willingness-to-pay threshold of per capita Gross Domestic Product in Myanmar ($1250). We evaluated cost-effectiveness with updated quality-assured generic DAA prices and potential cost-effectiveness of a proposed simplified treatment protocol with updated DAA prices if implemented by the MoH. From November 2016 to October 2017, 122 with HIV/HCV-coinfected patients were treated with DAAs (46% with cirrhosis), 96% (n=117) achieved sustained virological response. Mean treatment costs were $1229 (without cirrhosis) and $1971 (with cirrhosis), with DAA drugs being the largest contributor to cost. Compared with no treatment, the program was cost-effective (ICER $634/DALY averted); more so with updated prices for quality-assured generic DAAs (ICER $488/DALY averted). A simplified treatment protocol delivered by the MoH could be cost-effective if associated with similar outcomes (ICER $316/DALY averted). Using MSF programme data, the DAA treatment programme for HCV among HIV-coinfected individuals is cost-effective in Myanmar, and even more so with updated DAA prices. A simplified treatment protocol could enhance cost-effectiveness if further rollout demonstrates it is not associated with worse treatment outcomes.

Identifiants

pubmed: 33627360
pii: bmjgh-2020-004181
doi: 10.1136/bmjgh-2020-004181
pmc: PMC7908309
pii:
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAAA NIH HHS
ID : K01 AA027733
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI036214
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI147490
Pays : United States
Organisme : NIDA NIH HHS
ID : T32 DA023356
Pays : United States

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: NM has received unrestricted research grants and honoraria from Gilead and Merck, outside the submitted work. PV has received unrestricted research grants from Gilead, outside the submitted work.

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Auteurs

Lara K Marquez (LK)

Division of Infectious Diseases and Global Public Health, University of California San Diego, La Jolla, California, USA lkusnezo@health.ucsd.edu.
School of Public Health, San Diego State University, San Diego, California, USA.

Antoine Chaillon (A)

Division of Infectious Diseases and Global Public Health, University of California San Diego, La Jolla, California, USA.

Kyi Pyar Soe (KP)

Medical Department, Dawei Project, Doctors Without Borders, Dawei, Myanmar.

Derek C Johnson (DC)

Medical Department, Myanmar Project, Doctors Without Borders, Yangon, Myanmar.

Jean-Marc Zosso (JM)

Finance Department, Myanmar Project, Doctors Without Borders, Yangon, Myanmar.

Andrea Incerti (A)

Medical Department, Doctors Without Borders, Geneva Operational Center, Geneva, Switzerland.

Anne Loarec (A)

Epidemiology, Epicentre, Paris, Île-de-France, France.

Aude Nguyen (A)

Medical Department, Doctors Without Borders, Geneva Operational Center, Geneva, Switzerland.
Department of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.

Josephine G Walker (JG)

Population Health Sciences, University of Bristol, Bristol, UK.

Nyashadzaishe Mafirakureva (N)

Population Health Sciences, University of Bristol, Bristol, UK.

Vincent Lo Re Iii (V)

Division of Infectious Diseases, Department of Medicine, Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Adriane Wynn (A)

Division of Infectious Diseases and Global Public Health, University of California San Diego, La Jolla, California, USA.

Craig McIntosh (C)

School of Global Policy and Strategy, University of California San Diego, La Jolla, California, USA.

Susan M Kiene (SM)

School of Public Health, San Diego State University, San Diego, California, USA.

Stephanie Brodine (S)

School of Public Health, San Diego State University, San Diego, California, USA.

Richard S Garfein (RS)

Department of Family Medicine and Public Health, University of California San Diego, La Jolla, CA, USA.

Peter Vickerman (P)

Population Health Sciences, University of Bristol, Bristol, UK.

Natasha K Martin (NK)

Division of Infectious Diseases and Global Public Health, University of California San Diego, La Jolla, California, USA.

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