Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar
IntroductionOver 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 Mya...
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Published in | BMJ global health Vol. 6; no. 2; p. e004181 |
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Main Authors | , , , , , , , , , , , , , , , , , |
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BMJ Publishing Group LTD
01.02.2021
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Abstract | IntroductionOver 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).MethodsCosts (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.ResultsFrom 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 $316/DALY averted).ConclusionsUsing MSF programme data, the DAA treatment programme for HCV among HIV-coinfected individuals is cost-effective in Myanmar, and even more so with updated DAA prices. A simplified treatment protocol could enhance cost-effectiveness if further rollout demonstrates it is not associated with worse treatment outcomes. |
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AbstractList | Introduction Over half of those hepatitis C virus (HCV)/HIV coinfected live in low-income and middle-income countries, and many remain undiagnosed or untreated. In 2016, Médecins Sans Frontières (MSF) established a direct-acting antiviral (DAA) treatment programme for people HCV/HIV coinfected in Myanmar. The purpose of our study was to evaluate the real-world cost and cost-effectiveness of this programme, and potential cost-effectiveness if implemented by the Ministry of Health (MoH).Methods Costs (patient-level microcosting) and treatment outcomes were collected from the MSF prospective cohort study in Dawei, Myanmar. A Markov model was used to assess cost-effectiveness of the programme compared with no HCV treatment from a health provider perspective. Estimated lifetime and healthcare costs (in 2017 US$) 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 $316/DALY averted).Conclusions Using MSF programme data, the DAA treatment programme for HCV among HIV-coinfected individuals is cost-effective in Myanmar, and even more so with updated DAA prices. A simplified treatment protocol could enhance cost-effectiveness if further rollout demonstrates it is not associated with worse treatment outcomes. Over half of those hepatitis C virus (HCV)/HIV coinfected live in low-income and middle-income countries, and many remain undiagnosed or untreated. In 2016, Médecins Sans Frontières (MSF) established a direct-acting antiviral (DAA) treatment programme for people HCV/HIV coinfected in Myanmar. The purpose of our study was to evaluate the real-world cost and cost-effectiveness of this programme, and potential cost-effectiveness if implemented by the Ministry of Health (MoH). Costs (patient-level microcosting) and treatment outcomes were collected from the MSF prospective cohort study in Dawei, Myanmar. A Markov model was used to assess cost-effectiveness of the programme compared with no HCV treatment from a health provider perspective. Estimated lifetime and healthcare costs (in 2017 US$) 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 $316/DALY averted). Using MSF programme data, the DAA treatment programme for HCV among HIV-coinfected individuals is cost-effective in Myanmar, and even more so with updated DAA prices. A simplified treatment protocol could enhance cost-effectiveness if further rollout demonstrates it is not associated with worse treatment outcomes. IntroductionOver half of those hepatitis C virus (HCV)/HIV coinfected live in low-income and middle-income countries, and many remain undiagnosed or untreated. In 2016, Médecins Sans Frontières (MSF) established a direct-acting antiviral (DAA) treatment programme for people HCV/HIV coinfected in Myanmar. The purpose of our study was to evaluate the real-world cost and cost-effectiveness of this programme, and potential cost-effectiveness if implemented by the Ministry of Health (MoH).MethodsCosts (patient-level microcosting) and treatment outcomes were collected from the MSF prospective cohort study in Dawei, Myanmar. A Markov model was used to assess cost-effectiveness of the programme compared with no HCV treatment from a health provider perspective. Estimated lifetime and healthcare costs (in 2017 US$) 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.ResultsFrom 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 $316/DALY averted).ConclusionsUsing MSF programme data, the DAA treatment programme for HCV among HIV-coinfected individuals is cost-effective in Myanmar, and even more so with updated DAA prices. A simplified treatment protocol could enhance cost-effectiveness if further rollout demonstrates it is not associated with worse treatment outcomes. Introduction Over half of those hepatitis C virus (HCV)/HIV coinfected live in low-income and middle-income countries, and many remain undiagnosed or untreated. In 2016, Médecins Sans Frontières (MSF) established a direct-acting antiviral (DAA) treatment programme for people HCV/HIV coinfected in Myanmar. The purpose of our study was to evaluate the real-world cost and cost-effectiveness of this programme, and potential cost-effectiveness if implemented by the Ministry of Health (MoH). Methods Costs (patient-level microcosting) and treatment outcomes were collected from the MSF prospective cohort study in Dawei, Myanmar. A Markov model was used to assess cost-effectiveness of the programme compared with no HCV treatment from a health provider perspective. Estimated lifetime and healthcare costs (in 2017 US$) 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. |
Author | Loarec, Anne Garfein, Richard S Lo Re III, Vincent Wynn, Adriane Martin, Natasha K Marquez, Lara K Johnson, Derek C Nguyen, Aude Zosso, Jean-Marc McIntosh, Craig Vickerman, Peter Chaillon, Antoine Soe, Kyi Pyar Brodine, Stephanie Incerti, Andrea Kiene, Susan M Mafirakureva, Nyashadzaishe Walker, Josephine G |
AuthorAffiliation | 1 Division of Infectious Diseases and Global Public Health , University of California San Diego , La Jolla , California , USA 4 Medical Department , Myanmar Project, Doctors Without Borders , Yangon , Myanmar 11 School of Global Policy and Strategy , University of California San Diego , La Jolla , California , USA 6 Medical Department , Doctors Without Borders, Geneva Operational Center , Geneva , Switzerland 3 Medical Department , Dawei Project, Doctors Without Borders , Dawei , Myanmar 7 Epidemiology , Epicentre , Paris , Île-de-France , France 9 Population Health Sciences , University of Bristol , Bristol , UK 5 Finance Department , Myanmar Project, Doctors Without Borders , Yangon , Myanmar 2 School of Public Health , San Diego State University , San Diego , California , USA 8 Department of Infectious Diseases , Geneva University Hospitals , Geneva , Switzerland 12 Department of Family Medicine and Public Health , University of California San Diego , La Jolla , CA , USA 10 Division of Infecti |
AuthorAffiliation_xml | – name: 4 Medical Department , Myanmar Project, Doctors Without Borders , Yangon , Myanmar – name: 7 Epidemiology , Epicentre , Paris , Île-de-France , France – name: 12 Department of Family Medicine and Public Health , University of California San Diego , La Jolla , CA , USA – name: 6 Medical Department , Doctors Without Borders, Geneva Operational Center , Geneva , Switzerland – name: 9 Population Health Sciences , University of Bristol , Bristol , UK – name: 10 Division of Infectious Diseases, Department of Medicine, Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine , University of Pennsylvania , Philadelphia , Pennsylvania , USA – name: 8 Department of Infectious Diseases , Geneva University Hospitals , Geneva , Switzerland – name: 3 Medical Department , Dawei Project, Doctors Without Borders , Dawei , Myanmar – name: 5 Finance Department , Myanmar Project, Doctors Without Borders , Yangon , Myanmar – name: 11 School of Global Policy and Strategy , University of California San Diego , La Jolla , California , USA – name: 2 School of Public Health , San Diego State University , San Diego , California , USA – name: 1 Division of Infectious Diseases and Global Public Health , University of California San Diego , La Jolla , California , USA |
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References | Ferreira, Tonin, Assis Jarek 2017; 37 Thein, Yi, Dore 2008; 22 Martin, Vickerman, Grebely 2013; 58 Lim, Qureshi, Mahmood 2018; 47 Chan, Patel, Naggie 2017; 77 de Lédinghen, Barreiro, Foucher 2008; 15 Lwin AA, Htun, Kyaw 2017; 29 López-Diéguez, Montes, Pascual-Pareja 2011; 25 Kim, Hutton, Raouf 2015; 10 De Nicola, Aghemo, Rumi 2009; 51 Feld, Jacobson, Hézode 2015; 373 Chou, Hartung, Rahman 2013; 158 Platt, Easterbrook, Gower 2016; 16 Lee, van Driel, Crawford 2017; 9 Aggarwal, Chen, Goel 2017; 12 Chromy, Mandorfer, Bucsics 2019; 7 Pineda, Romero-Gómez, Díaz-García 2005; 41 Merchante, Girón-González, González-Serrano 2006; 20 Chaillon, Mehta, Hoenigl 2019; 14 Chen, Ding, Seage Iii 2009; 49 Morgan, Baack, Smith 2013; 158 Ousley, Nesbitt, Kyaw 2018; 18 2015; 63 Salomon, Haagsma, Davis 2015; 3 Gray, O'Leary, Kieran 2016; 23 Harris, Taylor, Thielke 2009; 42 Martinello, Amin, Matthews 2016; 18 Kapol, Lochid-Amnuay, Teerawattananon 2016; 16 Martin, Devine, Eaton 2014; 28 Suppl 1 van der Meer, Veldt, Feld 2012; 308 Kanwal, Kramer, Ilyas 2014; 60 Dienstag, Ghany, Morgan 2011; 54 Lee (2024051500180146000_6.2.e004181.37) 2017; 9 Gray (2024051500180146000_6.2.e004181.36) 2016; 23 Lim (2024051500180146000_6.2.e004181.13) 2018; 47 Martinello (2024051500180146000_6.2.e004181.7) 2016; 18 2024051500180146000_6.2.e004181.18 2024051500180146000_6.2.e004181.19 2024051500180146000_6.2.e004181.15 Ferreira (2024051500180146000_6.2.e004181.34) 2017; 37 2024051500180146000_6.2.e004181.16 2024051500180146000_6.2.e004181.17 Chaillon (2024051500180146000_6.2.e004181.38) 2019; 14 2024051500180146000_6.2.e004181.39 2024051500180146000_6.2.e004181.10 2024051500180146000_6.2.e004181.32 2024051500180146000_6.2.e004181.35 2024051500180146000_6.2.e004181.30 2024051500180146000_6.2.e004181.31 Kim (2024051500180146000_6.2.e004181.11) 2015; 10 Aggarwal (2024051500180146000_6.2.e004181.12) 2017; 12 Martin (2024051500180146000_6.2.e004181.26) 2014; 28 Suppl 1 Ousley (2024051500180146000_6.2.e004181.8) 2018; 18 2024051500180146000_6.2.e004181.9 2024051500180146000_6.2.e004181.29 2024051500180146000_6.2.e004181.4 2024051500180146000_6.2.e004181.25 2024051500180146000_6.2.e004181.3 2024051500180146000_6.2.e004181.2 2024051500180146000_6.2.e004181.27 De Nicola (2024051500180146000_6.2.e004181.40) 2009; 51 2024051500180146000_6.2.e004181.1 2024051500180146000_6.2.e004181.28 2024051500180146000_6.2.e004181.21 2024051500180146000_6.2.e004181.22 2024051500180146000_6.2.e004181.6 2024051500180146000_6.2.e004181.23 2024051500180146000_6.2.e004181.5 2024051500180146000_6.2.e004181.24 2024051500180146000_6.2.e004181.20 Chromy (2024051500180146000_6.2.e004181.33) 2019; 7 Kapol (2024051500180146000_6.2.e004181.14) 2016; 16 |
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doi: 10.1080/17441692.2014.984742 contributor: fullname: Kim |
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Snippet | IntroductionOver half of those hepatitis C virus (HCV)/HIV coinfected live in low-income and middle-income countries, and many remain undiagnosed or untreated.... 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,... Introduction Over half of those hepatitis C virus (HCV)/HIV coinfected live in low-income and middle-income countries, and many remain undiagnosed or... INTRODUCTIONOver half of those hepatitis C virus (HCV)/HIV coinfected live in low-income and middle-income countries, and many remain undiagnosed or untreated.... Introduction Over half of those hepatitis C virus (HCV)/HIV coinfected live in low-income and middle-income countries, and many remain undiagnosed or... |
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SubjectTerms | Antiviral drugs Capital costs Clinical outcomes Cost analysis Cost control Counseling Global health Health administration Hepatitis Hepatitis C HIV Human immunodeficiency virus Infections Laboratories Liver cancer Liver cirrhosis Liver diseases Markov chains Medical equipment Original Research Patients Performance evaluation Pharmacy |
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Title | Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar |
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