Cost and cost-effectiveness of a real-world HCV treatment program among HIV-infected individuals in Myanmar.
HIV
health economics
viral hepatitis
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
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.
Références
J Biomed Inform. 2009 Apr;42(2):377-81
pubmed: 18929686
United European Gastroenterol J. 2019 May;7(4):507-516
pubmed: 31065368
Lancet Infect Dis. 2016 Jul;16(7):797-808
pubmed: 26922272
JAMA. 2012 Dec 26;308(24):2584-93
pubmed: 23268517
Hepatology. 2014 Jul;60(1):98-105
pubmed: 24615981
Hepatology. 2005 Apr;41(4):779-89
pubmed: 15800956
BMC Infect Dis. 2018 Dec 14;18(1):657
pubmed: 30547747
J Hepatol. 2015 Jul;63(1):199-236
pubmed: 25911336
BMC Gastroenterol. 2016 Aug 05;16(1):91
pubmed: 27492396
PLoS One. 2017 May 17;12(5):e0176503
pubmed: 28520728
Clin Infect Dis. 2009 Nov 15;49(10):1605-15
pubmed: 19842982
J Hepatol. 2009 Nov;51(5):964-6
pubmed: 19775770
AIDS. 2006 Jan 2;20(1):49-57
pubmed: 16327319
AIDS. 2011 Apr 24;25(7):899-904
pubmed: 21330908
Clin Drug Investig. 2017 Jul;37(7):635-646
pubmed: 28409482
AIDS. 2008 Oct 1;22(15):1979-91
pubmed: 18784461
Lancet Glob Health. 2015 Nov;3(11):e712-23
pubmed: 26475018
N Engl J Med. 2015 Dec 31;373(27):2599-607
pubmed: 26571066
Drugs. 2017 Feb;77(2):131-144
pubmed: 28074358
AIDS. 2014 Jan;28 Suppl 1:S35-46
pubmed: 24468945
J Viral Hepat. 2016 Sep;23(9):677-86
pubmed: 26996144
Hepatology. 2011 Aug;54(2):396-405
pubmed: 21520194
J Viral Hepat. 2008 Jun;15(6):427-33
pubmed: 18221303
Clinicoecon Outcomes Res. 2017 Oct 03;9:595-607
pubmed: 29042803
Ann Intern Med. 2013 Mar 5;158(5 Pt 1):329-37
pubmed: 23460056
PLoS One. 2019 Jun 6;14(6):e0217964
pubmed: 31170246
Hepatology. 2013 Nov;58(5):1598-609
pubmed: 23553643
AIDS Rev. 2016 Apr-Jun;18(2):68-80
pubmed: 27196354
Ann Intern Med. 2013 Jan 15;158(2):114-23
pubmed: 23437439
Int J Epidemiol. 2018 Apr 1;47(2):550-560
pubmed: 29309592
Glob Public Health. 2015;10(3):296-317
pubmed: 25469976