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

Introduction 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 My...

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Published in:BMJ Global Health
Main Authors: Peter Vickerman, Natasha K Martin, Adriane Wynn, Lara K Marquez, Antoine Chaillon, Kyi Pyar Soe, Derek C Johnson, Jean-Marc Zosso, Andrea Incerti, Anne Loarec, Aude Nguyen, Josephine G Walker, Nyashadzaishe Mafirakureva, Vincent Lo Re III, Craig McIntosh, Susan M Kiene, Stephanie Brodine, Richard S Garfein
Format: Article
Language:English
Published: BMJ Publishing Group 2021-02-01
Online Access:https://gh.bmj.com/content/6/2/e004181.full
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author Peter Vickerman
Natasha K Martin
Adriane Wynn
Lara K Marquez
Antoine Chaillon
Kyi Pyar Soe
Derek C Johnson
Jean-Marc Zosso
Andrea Incerti
Anne Loarec
Aude Nguyen
Josephine G Walker
Nyashadzaishe Mafirakureva
Vincent Lo Re III
Craig McIntosh
Susan M Kiene
Stephanie Brodine
Richard S Garfein
author_facet Peter Vickerman
Natasha K Martin
Adriane Wynn
Lara K Marquez
Antoine Chaillon
Kyi Pyar Soe
Derek C Johnson
Jean-Marc Zosso
Andrea Incerti
Anne Loarec
Aude Nguyen
Josephine G Walker
Nyashadzaishe Mafirakureva
Vincent Lo Re III
Craig McIntosh
Susan M Kiene
Stephanie Brodine
Richard S Garfein
author_sort Peter Vickerman
collection DOAJ
container_title BMJ Global Health
description Introduction 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).Methods 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.Results 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).Conclusions 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.
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spelling doaj-art-2bc809cc04474c6eae04bf3b01cf0b652025-08-20T01:24:12ZengBMJ Publishing GroupBMJ Global Health2059-79082021-02-016210.1136/bmjgh-2020-004181Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in MyanmarPeter Vickerman0Natasha K Martin1Adriane Wynn2Lara K Marquez3Antoine Chaillon4Kyi Pyar Soe5Derek C Johnson6Jean-Marc Zosso7Andrea Incerti8Anne Loarec9Aude Nguyen10Josephine G Walker11Nyashadzaishe Mafirakureva12Vincent Lo Re III13Craig McIntosh14Susan M Kiene15Stephanie Brodine16Richard S Garfein174 Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UKFaculty of Public Health and Policy, London School of Hygiene and Tropical Medicine, London, UKUniversity of California San Diego, La Jolla, California, USADivision of Infectious Diseases and Global Public Health, University of California San Diego, La Jolla, California, USADivision of Infectious Diseases and Global Public Health, University of California San Diego, La Jolla, California, USAMedical Department, Dawei Project, Doctors Without Borders, Dawei, MyanmarMedical Department, Myanmar Project, Doctors Without Borders, Yangon, MyanmarFinance Department, Myanmar Project, Doctors Without Borders, Yangon, MyanmarMedical Department, Doctors Without Borders, Geneva Operational Center, Geneva, SwitzerlandEpidemiology, Epicentre, Paris, Île-de-France, FranceMedical Department, Doctors Without Borders, Geneva Operational Center, Geneva, SwitzerlandPopulation Health Sciences, University of Bristol, Bristol, UKScHARR, The University of Sheffield, Sheffield, UKDivision of Infectious Diseases, Department of Medicine, Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USASchool of Global Policy and Strategy, University of California San Diego, La Jolla, California, USAEpidemiology and Biostatistics, San Diego State University College of Health and Human Services School of Public Health, San Diego, California, USASchool of Public Health, San Diego State University, San Diego, California, USAHerbert Wertheim School of Public Health and Human Longevity Science, University of California San Diego, La Jolla, California, USAIntroduction 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).Methods 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.Results 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).Conclusions 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.https://gh.bmj.com/content/6/2/e004181.full
spellingShingle Peter Vickerman
Natasha K Martin
Adriane Wynn
Lara K Marquez
Antoine Chaillon
Kyi Pyar Soe
Derek C Johnson
Jean-Marc Zosso
Andrea Incerti
Anne Loarec
Aude Nguyen
Josephine G Walker
Nyashadzaishe Mafirakureva
Vincent Lo Re III
Craig McIntosh
Susan M Kiene
Stephanie Brodine
Richard S Garfein
Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar
title Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar
title_full Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar
title_fullStr Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar
title_full_unstemmed Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar
title_short Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar
title_sort cost and cost effectiveness of a real world hcv treatment program among hiv infected individuals in myanmar
url https://gh.bmj.com/content/6/2/e004181.full
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