Cost-Effectiveness of Amphotericin B Deoxycholate Versus Itraconazole for Induction Therapy of Talaromycosis in Human Immunodeficiency Virus-Infected Adults in Vietnam.
dc.contributor.author | Buchanan, James | |
dc.contributor.author | Altunkaya, James | |
dc.contributor.author | Van Kinh, Nguyen | |
dc.contributor.author | Van Vinh Chau, Nguyen | |
dc.contributor.author | Trieu Ly, Vo | |
dc.contributor.author | Thi Thanh Thuy, Pham | |
dc.contributor.author | Hai Vinh, Vu | |
dc.contributor.author | Thi Hong Hanh, Doan | |
dc.contributor.author | Thuy Hang, Nguyen | |
dc.contributor.author | Phuong Thuy, Tran | |
dc.contributor.author | van Doorn, Rogier | |
dc.contributor.author | Thwaites, Guy | |
dc.contributor.author | Gray, Alastair | |
dc.contributor.author | Le, Thuy | |
dc.date.accessioned | 2021-08-18T18:10:49Z | |
dc.date.available | 2021-08-18T18:10:49Z | |
dc.date.issued | 2021-07-05 | |
dc.date.updated | 2021-08-18T18:10:49Z | |
dc.description.abstract | BackgroundTalaromycosis (penicilliosis) is an invasive fungal infection and a major cause of human immunodeficiency virus (HIV)-related deaths in Southeast Asia. Guidelines recommend induction therapy with amphotericin B deoxycholate; however, treatment with itraconazole has fewer toxic effects, is easier to administer, and is less expensive. Our recent randomized controlled trial in Vietnam found that amphotericin B was superior to itraconazole with respect to 6-month mortality. We undertook an economic evaluation alongside this trial to determine whether the more effective treatment is cost-effective.MethodsResource use, direct and indirect costs, and health and quality-of-life outcomes (measured using quality-adjusted life-years [QALYs]) were evaluated for 405 trial participants from 2012 to 2016. Both a Vietnamese health service and a broader societal costing perspective were considered. Mean costs and QALYs were combined to calculate the within-trial cost-effectiveness of amphotericin vs itraconazole from both perspectives.ResultsFrom a Vietnamese health service perspective, amphotericin increases costs but improves health outcomes compared to itraconazole, at a cost of $3013/QALY gained. The probability that amphotericin is cost-effective at a conventional (World Health Organization CHOICE) threshold of value for money is 46%. From a societal perspective, amphotericin is cost-reducing and improves outcomes compared to itraconazole, and is likely to be a cost-effective strategy at any value for money threshold greater than $0.ConclusionsOur analysis indicates that induction therapy with amphotericin is a cost-effective treatment strategy for HIV-infected adults diagnosed with talaromycosis in Vietnam. These results provide the evidence base for health care providers and policy makers to improve access to and use of amphotericin. | |
dc.identifier | ofab357 | |
dc.identifier.issn | 2328-8957 | |
dc.identifier.issn | 2328-8957 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Oxford University Press (OUP) | |
dc.relation.ispartof | Open forum infectious diseases | |
dc.relation.isversionof | 10.1093/ofid/ofab357 | |
dc.subject | HIV | |
dc.subject | amphotericin B | |
dc.subject | cost-effectiveness | |
dc.subject | itraconazole | |
dc.subject | talaromycosis | |
dc.title | Cost-Effectiveness of Amphotericin B Deoxycholate Versus Itraconazole for Induction Therapy of Talaromycosis in Human Immunodeficiency Virus-Infected Adults in Vietnam. | |
dc.type | Journal article | |
duke.contributor.orcid | Le, Thuy|0000-0002-3393-6580 | |
pubs.begin-page | ofab357 | |
pubs.issue | 7 | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Molecular Genetics and Microbiology | |
pubs.organisational-group | Duke Global Health Institute | |
pubs.organisational-group | Medicine, Infectious Diseases | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | University Institutes and Centers | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Clinical Science Departments | |
pubs.publication-status | Published | |
pubs.volume | 8 |
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