Cost effectiveness of simplified HCV screening-and-treatment interventions for people who inject drugs in Dar-es-Salaam, Tanzania.


Journal

The International journal on drug policy
ISSN: 1873-4758
Titre abrégé: Int J Drug Policy
Pays: Netherlands
ID NLM: 9014759

Informations de publication

Date de publication:
01 2022
Historique:
received: 10 12 2020
revised: 19 08 2021
accepted: 03 09 2021
pubmed: 9 10 2021
medline: 27 1 2022
entrez: 8 10 2021
Statut: ppublish

Résumé

Compared to other countries in sub-Saharan Africa, Tanzania has a relatively progressive illicit drug harm reduction (HR) policy, through a predominantly opioid substitution therapy-based programme. However, access to hepatitis C virus (HCV) diagnosis and curative direct acting antiviral therapy remains elusive. We developed a cost-effectiveness model to evaluate a simplified HCV screening-and-treatment intervention amongst PWID in Dar-es-Salaam, Tanzania. A decision tree and Markov state transition model compared existing practice (no access to HCV viral confirmation and treatment) with the integration of point-of-care HCV screening and treatment within (1) existing HR services and (2) expansion to include PWID not currently engaged in HR. Outcome measures were screening, treatment, HR and disease-related costs per PWID, quality-adjusted life years (QALY) and disability adjusted life years (DALY). Cost-effectiveness was evaluated from a healthcare payer's perspective over a 30-year time horizon over a range of willingness-to-pay thresholds (USD$273 to USD$1,050). Both deterministic and probabilistic sensitivity analyses have been conducted. Assuming a chronic HCV prevalence of 18.8%, screening-and-treatment in existing HR settings resulted in an ICER per QALY-gained and DALY averted of USD$633 and USD$1,161, respectively. Expanding to include an outreach programme for unengaged PWID yielded an ICER per QALY-gained and DALY-averted of USD$4,091 and USD$10,288. Factors affecting the sensitivity of the ICER value included the cost of HR and the health utility of non-cirrhotic disease states. Simplified HCV screening and treatment of PWID has the potential to be cost-effective in Dar-es-Salaam, Tanzania. In practice, synergism of human and financial resources with established health programmes may offer a pragmatic solution to minimise operational costs.

Sections du résumé

BACKGROUND
Compared to other countries in sub-Saharan Africa, Tanzania has a relatively progressive illicit drug harm reduction (HR) policy, through a predominantly opioid substitution therapy-based programme. However, access to hepatitis C virus (HCV) diagnosis and curative direct acting antiviral therapy remains elusive. We developed a cost-effectiveness model to evaluate a simplified HCV screening-and-treatment intervention amongst PWID in Dar-es-Salaam, Tanzania.
METHODS
A decision tree and Markov state transition model compared existing practice (no access to HCV viral confirmation and treatment) with the integration of point-of-care HCV screening and treatment within (1) existing HR services and (2) expansion to include PWID not currently engaged in HR. Outcome measures were screening, treatment, HR and disease-related costs per PWID, quality-adjusted life years (QALY) and disability adjusted life years (DALY). Cost-effectiveness was evaluated from a healthcare payer's perspective over a 30-year time horizon over a range of willingness-to-pay thresholds (USD$273 to USD$1,050). Both deterministic and probabilistic sensitivity analyses have been conducted.
RESULTS
Assuming a chronic HCV prevalence of 18.8%, screening-and-treatment in existing HR settings resulted in an ICER per QALY-gained and DALY averted of USD$633 and USD$1,161, respectively. Expanding to include an outreach programme for unengaged PWID yielded an ICER per QALY-gained and DALY-averted of USD$4,091 and USD$10,288. Factors affecting the sensitivity of the ICER value included the cost of HR and the health utility of non-cirrhotic disease states.
CONCLUSION
Simplified HCV screening and treatment of PWID has the potential to be cost-effective in Dar-es-Salaam, Tanzania. In practice, synergism of human and financial resources with established health programmes may offer a pragmatic solution to minimise operational costs.

Identifiants

pubmed: 34624732
pii: S0955-3959(21)00363-7
doi: 10.1016/j.drugpo.2021.103458
pii:
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

103458

Subventions

Organisme : Medical Research Council
ID : MR/R015600/1
Pays : United Kingdom

Informations de copyright

Crown Copyright © 2021. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declarations of Interest All authors have no conflict of interest to declare in relation to this study.

Auteurs

Zameer Mohamed (Z)

Department of Metabolism, Digestion and Reproduction, Imperial College London, London, United Kingdom. Electronic address: zm204@ic.ac.uk.

Nick Scott (N)

Burnet Institute, Melbourne, Australia; Monash University, Melbourne, Australia.

Shevanthi Nayagam (S)

Department of Metabolism, Digestion and Reproduction, Imperial College London, London, United Kingdom; MRC Centre for Global Infectious Disease Analysis, Imperial College London, United Kingdom.

John Rwegasha (J)

Muhimbili National Hospital, Dar es Salaam, Tanzania.

Jessie Mbwambo (J)

Muhimbili National Hospital, Dar es Salaam, Tanzania.

Mark R Thursz (MR)

Department of Metabolism, Digestion and Reproduction, Imperial College London, London, United Kingdom.

Ashley S Brown (AS)

Department of Metabolism, Digestion and Reproduction, Imperial College London, London, United Kingdom.

Margaret Hellard (M)

Burnet Institute, Melbourne, Australia; Monash University, Melbourne, Australia; The Alfred and Monash University, Melbourne, Australia; Peter Doherty Institute for Infection and Immunity, Parkville, Australia; University of Melbourne, Parkville, Australia.

Maud Lemoine (M)

Department of Metabolism, Digestion and Reproduction, Imperial College London, London, United Kingdom.

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