Healthcare Costs and Life-years Gained From Treatments Within the Advancing Cryptococcal Meningitis Treatment for Africa (ACTA) Trial on Cryptococcal Meningitis: A Comparison of Antifungal Induction Strategies in Sub-Saharan Africa.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
01 08 2019
Historique:
received: 10 09 2018
accepted: 25 11 2018
pubmed: 14 3 2019
medline: 17 6 2020
entrez: 14 3 2019
Statut: ppublish

Résumé

Mortality from cryptoccocal meningitis remains high. The ACTA trial demonstrated that, compared with 2 weeks of amphotericin B (AmB) plus flucystosine (5FC), 1 week of AmB and 5FC was associated with lower mortality and 2 weeks of oral flucanozole (FLU) plus 5FC was non-inferior. Here, we assess the cost-effectiveness of these different treatment courses. Participants were randomized in a ratio of 2:1:1:1:1 to 2 weeks of oral 5FC and FLU, 1 week of AmB and FLU, 1 week of AmB and 5FC, 2 weeks of AmB and FLU, or 2 weeks of AmB and 5FC in Malawi, Zambia, Cameroon, and Tanzania. Data on individual resource use and health outcomes were collected. Cost-effectiveness was measured as incremental costs per life-year saved, and non-parametric bootstrapping was done. Total costs per patient were US $1442 for 2 weeks of oral FLU and 5FC, $1763 for 1 week of AmB and FLU, $1861 for 1 week of AmB and 5FC, $2125 for 2 weeks of AmB and FLU, and $2285 for 2 weeks of AmB and 5FC. Compared to 2 weeks of AmB and 5FC, 1 week of AmB and 5FC was less costly and more effective and 2 weeks of oral FLU and 5FC was less costly and as effective. The incremental cost-effectiveness ratio for 1 week of AmB and 5FC versus oral FLU and 5FC was US $208 (95% confidence interval $91-1210) per life-year saved. ISRCTN45035509. Both 1 week of AmB and 5FC and 2 weeks of Oral FLU and 5FC are cost-effective treatments.

Sections du résumé

BACKGROUND
Mortality from cryptoccocal meningitis remains high. The ACTA trial demonstrated that, compared with 2 weeks of amphotericin B (AmB) plus flucystosine (5FC), 1 week of AmB and 5FC was associated with lower mortality and 2 weeks of oral flucanozole (FLU) plus 5FC was non-inferior. Here, we assess the cost-effectiveness of these different treatment courses.
METHODS
Participants were randomized in a ratio of 2:1:1:1:1 to 2 weeks of oral 5FC and FLU, 1 week of AmB and FLU, 1 week of AmB and 5FC, 2 weeks of AmB and FLU, or 2 weeks of AmB and 5FC in Malawi, Zambia, Cameroon, and Tanzania. Data on individual resource use and health outcomes were collected. Cost-effectiveness was measured as incremental costs per life-year saved, and non-parametric bootstrapping was done.
RESULTS
Total costs per patient were US $1442 for 2 weeks of oral FLU and 5FC, $1763 for 1 week of AmB and FLU, $1861 for 1 week of AmB and 5FC, $2125 for 2 weeks of AmB and FLU, and $2285 for 2 weeks of AmB and 5FC. Compared to 2 weeks of AmB and 5FC, 1 week of AmB and 5FC was less costly and more effective and 2 weeks of oral FLU and 5FC was less costly and as effective. The incremental cost-effectiveness ratio for 1 week of AmB and 5FC versus oral FLU and 5FC was US $208 (95% confidence interval $91-1210) per life-year saved.
CLINICAL TRIALS REGISTRATION
ISRCTN45035509.
CONCLUSIONS
Both 1 week of AmB and 5FC and 2 weeks of Oral FLU and 5FC are cost-effective treatments.

Identifiants

pubmed: 30863852
pii: 5377300
doi: 10.1093/cid/ciy971
pmc: PMC6669289
doi:

Substances chimiques

Antifungal Agents 0
Flucytosine D83282DT06

Banques de données

ISRCTN
['ISRCTN45035509']

Types de publication

Clinical Trial, Phase III Comparative Study Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

588-595

Subventions

Organisme : FIC NIH HHS
ID : D43 TW010060
Pays : United States
Organisme : Medical Research Council
ID : G1100814
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : 100504
Pays : United Kingdom

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.

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Auteurs

Tao Chen (T)

Liverpool School of Tropical Medicine, United Kingdom.

Lawrence Mwenge (L)

Zambart, Health Economics Unit, Lusaka Apex Medical University, Zambia.

Shabir Lakhi (S)

University Teaching Hospital, Lusaka Apex Medical University, Zambia.

Duncan Chanda (D)

Institute for Medical Research and Training, University Teaching Hospital, Lusaka Apex Medical University, Zambia.

Peter Mwaba (P)

Department of Internal Medicine and Directorate of Research and Post-Graduate Studies, Lusaka Apex Medical University, Zambia.

Síle F Molloy (SF)

Centre for Global Health, Institute for Infection and Immunity, St George's University of London, United Kingdom.

Adrian Gheorghe (A)

London School of Hygiene and Tropical Medicine, United Kingdom.

Ulla K Griffiths (UK)

London School of Hygiene and Tropical Medicine, United Kingdom.

Robert S Heyderman (RS)

Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre.
College of Medicine, University of Malawi, Blantyre.
University College London, United Kingdom.

Cecilia Kanyama (C)

University of North Carolina Project-Malawi, Kamuzu Central Hospital, Lilongwe.

Charles Kouanfack (C)

Hôpital Central Yaoundé/Site Agence Nationale de Recherche sur le Sida Cameroun, Yaoundé Hopitaux de Paris, France.
University of Dschang, Cameroon.

Sayoki Mfinanga (S)

Liverpool School of Tropical Medicine, United Kingdom.
National Institute for Medical Research, Muhimbili Medical Research Centre, Dar Es Salaam, United Republic of Tanzania.

Adrienne K Chan (AK)

Dignitas International, Zomba Central Hospital, Malawi.
Division of Infectious Diseases, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Ontario, Canada.

Elvis Temfack (E)

Douala General Hospital, Cameroon.
Institut Pasteur, Molecular Mycology Unit, Paris, France.

Sokoine Kivuyo (S)

National Institute for Medical Research, Muhimbili Medical Research Centre, Dar Es Salaam, United Republic of Tanzania.

Mina C Hosseinipour (MC)

University of North Carolina Project-Malawi, Kamuzu Central Hospital, Lilongwe.
University of North Carolina, Chapel Hill.

Olivier Lortholary (O)

Institut Pasteur, Molecular Mycology Unit, Paris, France.
Paris Descartes University, Necker Pasteur Center for Infectious Diseases and Tropical Medicine, Imagine Institute, Assistance Publique - Hopitaux de Paris, France.

Angela Loyse (A)

Centre for Global Health, Institute for Infection and Immunity, St George's University of London, United Kingdom.

Shabbar Jaffar (S)

Liverpool School of Tropical Medicine, United Kingdom.

Thomas S Harrison (TS)

Centre for Global Health, Institute for Infection and Immunity, St George's University of London, United Kingdom.

Louis W Niessen (LW)

Liverpool School of Tropical Medicine, United Kingdom.
Department of International Health, Johns Hopkins School of Public Health, Baltimore, Maryland.

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