Cryptococcal Meningitis Screening and Community-based Early Adherence Support in People With Advanced Human Immunodeficiency Virus Infection Starting Antiretroviral Therapy in Tanzania and Zambia: A Cost-effectiveness Analysis.


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:
10 04 2020
Historique:
received: 22 02 2019
accepted: 30 05 2019
pubmed: 1 6 2019
medline: 7 1 2021
entrez: 1 6 2019
Statut: ppublish

Résumé

A randomized trial demonstrated that among people living with late-stage human immunodeficiency virus (HIV) infection initiating antiretroviral therapy, screening serum for cryptococcal antigen (CrAg) combined with adherence support reduced all-cause mortality by 28%, compared with standard clinic-based care. Here, we present the cost-effectiveness. HIV-infected adults with CD4 count <200 cells/μL were randomized to either CrAg screening plus 4 weekly home visits to provide adherence support or to standard clinic-based care in Dar es Salaam and Lusaka. The primary economic outcome was health service care cost per life-year saved as the incremental cost-effectiveness ratio (ICER), based on 2017 US dollars. We used nonparametric bootstrapping to assess uncertainties and univariate deterministic sensitivity analysis to examine the impact of individual parameters on the ICER. Among the intervention and standard arms, 1001 and 998 participants, respectively, were enrolled. The annual mean cost per participant in the intervention arm was US$339 (95% confidence interval [CI], $331-$347), resulting in an incremental cost of the intervention of US$77 (95% CI, $66-$88). The incremental cost was similar when analysis was restricted to persons with CD4 count <100 cells/μL. The ICER for the intervention vs standard care, per life-year saved, was US$70 (95% CI, $43-$211) for all participants with CD4 count up to 200 cells/μL and US$91 (95% CI, $49-$443) among those with CD4 counts <100 cells /μL. Cost-effectveness was most sensitive to mortality estimates. Screening for cryptococcal antigen combined with a short period of adherence support, is cost-effective in resource-limited settings.

Sections du résumé

BACKGROUND
A randomized trial demonstrated that among people living with late-stage human immunodeficiency virus (HIV) infection initiating antiretroviral therapy, screening serum for cryptococcal antigen (CrAg) combined with adherence support reduced all-cause mortality by 28%, compared with standard clinic-based care. Here, we present the cost-effectiveness.
METHODS
HIV-infected adults with CD4 count <200 cells/μL were randomized to either CrAg screening plus 4 weekly home visits to provide adherence support or to standard clinic-based care in Dar es Salaam and Lusaka. The primary economic outcome was health service care cost per life-year saved as the incremental cost-effectiveness ratio (ICER), based on 2017 US dollars. We used nonparametric bootstrapping to assess uncertainties and univariate deterministic sensitivity analysis to examine the impact of individual parameters on the ICER.
RESULTS
Among the intervention and standard arms, 1001 and 998 participants, respectively, were enrolled. The annual mean cost per participant in the intervention arm was US$339 (95% confidence interval [CI], $331-$347), resulting in an incremental cost of the intervention of US$77 (95% CI, $66-$88). The incremental cost was similar when analysis was restricted to persons with CD4 count <100 cells/μL. The ICER for the intervention vs standard care, per life-year saved, was US$70 (95% CI, $43-$211) for all participants with CD4 count up to 200 cells/μL and US$91 (95% CI, $49-$443) among those with CD4 counts <100 cells /μL. Cost-effectveness was most sensitive to mortality estimates.
CONCLUSIONS
Screening for cryptococcal antigen combined with a short period of adherence support, is cost-effective in resource-limited settings.

Identifiants

pubmed: 31149704
pii: 5509363
doi: 10.1093/cid/ciz453
pmc: PMC7146002
doi:

Substances chimiques

Antigens, Fungal 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1652-1657

Subventions

Organisme : Medical Research Council
ID : MR/R010161/1
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

Godfather Dickson Kimaro (GD)

Muhimbili Medical Research Centre, National Institute of Medical Research, Dar es Salaam, United Republic of Tanzania.
Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, United Kingdom.

Lorna Guinness (L)

Department of Global Health and Development, London School of Hygiene and Tropical Medicine, United Kingdom.

Tinevimbo Shiri (T)

Department of International Public Health, Liverpool School of Tropical Medicine, United Kingdom.

Sokoine Kivuyo (S)

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

Duncan Chanda (D)

University Teaching Hospital, Lusaka Apex Medical University, Zambia.

Christian Bottomley (C)

Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, United Kingdom.

Tao Chen (T)

Department of International Public Health, Liverpool School of Tropical Medicine, United Kingdom.

Amos Kahwa (A)

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

Neil Hawkins (N)

Department of Global Health and Development, London School of Hygiene and Tropical Medicine, United Kingdom.

Peter Mwaba (P)

Department of Internal Medicine and Directorate of Research and Postgraduate Studies, Lusaka Apex Medical University, Zambia.

Sayoki Godfrey Mfinanga (SG)

Muhimbili Medical Research Centre, National Institute of Medical Research, Dar es Salaam, United Republic of Tanzania.
Department of International Public Health, Liverpool School of Tropical Medicine, United Kingdom.

Thomas S Harrison (TS)

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

Shabbar Jaffar (S)

Department of International Public Health, Liverpool School of Tropical Medicine, United Kingdom.

Louis W Niessen (LW)

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

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