Estimated costs for the delivery of safer conception strategies for HIV-discordant couples in Zimbabwe: a cost analysis.


Journal

BMC health services research
ISSN: 1472-6963
Titre abrégé: BMC Health Serv Res
Pays: England
ID NLM: 101088677

Informations de publication

Date de publication:
12 Oct 2020
Historique:
received: 05 06 2020
accepted: 30 09 2020
entrez: 13 10 2020
pubmed: 14 10 2020
medline: 3 2 2021
Statut: epublish

Résumé

In recent years, safer conception strategies have been developed to help HIV-serodiscordant couples conceive a child without transmitting HIV to the seronegative partner. The SAFER clinical trial assessed implementation of these strategies in Zimbabwe. As a part of the SAFER study, we estimated the costs (in 2017 $US) associated with individual and combination strategies, in the trial setting and real-world practice, from a healthcare system perspective. Safer conception strategies included: 1) ART with frequent viral load testing until achieving undetectable viral load (ART-VL); 2) daily oral pre-exposure prophylaxis (PrEP); 3) semen-washing with intrauterine insemination; and 4) manual self-insemination at home. For costs in the trial, we used a micro-costing approach, including a time and motion study to quantify personnel effort, and estimated the cost per couple for individual and combination strategies for a mean of 6 months of safer services. For real-world practice, we modeled costs for three implementation scenarios, representing differences from the trial in input prices (paid by the Ministry of Health and Child Care [MOHCC]), intervention intensity, and increments to current HIV prevention and treatment practices and guidelines. We used one-way sensitivity analyses to assess the impact of uncertainty in input variables. Individual strategy costs were $769-$1615 per couple in the trial; $185-$563 if using MOHCC prices. Under the target intervention intensity and using MOHCC prices, individual strategy costs were $73-$360 per couple over and above the cost of current HIV clinical practices. The cost of delivering the most commonly selected combination, ART-VL plus PrEP, ranged from $166-$517 per couple under the three real-world scenarios. Highest costs were for personnel, lab tests, and strategy-specific consumables, in variable proportions by clinical strategy and analysis scenario. Total costs were most affected by uncertainty in the price of PrEP, number of semen-washing attempts, and scale-up of semen-washing capacity. Safer conception methods have costs that may be affordable in many low-resource settings. These cost data will help implementers and policymakers add safer conception services. Cost-effectiveness analysis is needed to assess value for money for safer conception services overall and for safer strategy combinations. Registry Name: Clinicaltrials.gov. NCT03049176 . Registration date: February 9, 2017.

Sections du résumé

BACKGROUND BACKGROUND
In recent years, safer conception strategies have been developed to help HIV-serodiscordant couples conceive a child without transmitting HIV to the seronegative partner. The SAFER clinical trial assessed implementation of these strategies in Zimbabwe.
METHODS METHODS
As a part of the SAFER study, we estimated the costs (in 2017 $US) associated with individual and combination strategies, in the trial setting and real-world practice, from a healthcare system perspective. Safer conception strategies included: 1) ART with frequent viral load testing until achieving undetectable viral load (ART-VL); 2) daily oral pre-exposure prophylaxis (PrEP); 3) semen-washing with intrauterine insemination; and 4) manual self-insemination at home. For costs in the trial, we used a micro-costing approach, including a time and motion study to quantify personnel effort, and estimated the cost per couple for individual and combination strategies for a mean of 6 months of safer services. For real-world practice, we modeled costs for three implementation scenarios, representing differences from the trial in input prices (paid by the Ministry of Health and Child Care [MOHCC]), intervention intensity, and increments to current HIV prevention and treatment practices and guidelines. We used one-way sensitivity analyses to assess the impact of uncertainty in input variables.
RESULTS RESULTS
Individual strategy costs were $769-$1615 per couple in the trial; $185-$563 if using MOHCC prices. Under the target intervention intensity and using MOHCC prices, individual strategy costs were $73-$360 per couple over and above the cost of current HIV clinical practices. The cost of delivering the most commonly selected combination, ART-VL plus PrEP, ranged from $166-$517 per couple under the three real-world scenarios. Highest costs were for personnel, lab tests, and strategy-specific consumables, in variable proportions by clinical strategy and analysis scenario. Total costs were most affected by uncertainty in the price of PrEP, number of semen-washing attempts, and scale-up of semen-washing capacity.
CONCLUSIONS CONCLUSIONS
Safer conception methods have costs that may be affordable in many low-resource settings. These cost data will help implementers and policymakers add safer conception services. Cost-effectiveness analysis is needed to assess value for money for safer conception services overall and for safer strategy combinations.
TRIAL REGISTRATION BACKGROUND
Registry Name: Clinicaltrials.gov.
TRIAL REGISTRATION NUMBER BACKGROUND
NCT03049176 . Registration date: February 9, 2017.

Identifiants

pubmed: 33046066
doi: 10.1186/s12913-020-05784-4
pii: 10.1186/s12913-020-05784-4
pmc: PMC7552466
doi:

Substances chimiques

Anti-HIV Agents 0

Banques de données

ClinicalTrials.gov
['NCT03049176']

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

940

Subventions

Organisme : National Institutes of Health (US)
ID : K01MH100994

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Auteurs

Carolyn Smith Hughes (CS)

Institute for Global Health Sciences, University of California, 550 16th Street, 3rd Floor, San Francisco, 94158, USA. carolyn.smithhughes@ucsf.edu.

Joelle Brown (J)

Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, USA.
Department of Epidemiology and Biostatistics, University of California, San Francisco, USA.

Caroline Murombedzi (C)

College of Health Sciences Clinical Trials Research Centre, University of Zimbabwe, Harare, Zimbabwe.

Thandiwe Chirenda (T)

College of Health Sciences Clinical Trials Research Centre, University of Zimbabwe, Harare, Zimbabwe.

Gift Chareka (G)

College of Health Sciences Clinical Trials Research Centre, University of Zimbabwe, Harare, Zimbabwe.

Felix Mhlanga (F)

College of Health Sciences Clinical Trials Research Centre, University of Zimbabwe, Harare, Zimbabwe.

Bismark Mateveke (B)

Harare Central Hospital, Harare, Zimbabwe.

Serah Gitome (S)

Centre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.

Tinei Makurumure (T)

Mercy-Care Fertility Centre, Harare, Zimbabwe.

Allen Matubu (A)

College of Health Sciences Clinical Trials Research Centre, University of Zimbabwe, Harare, Zimbabwe.

Nyaradzo Mgodi (N)

College of Health Sciences Clinical Trials Research Centre, University of Zimbabwe, Harare, Zimbabwe.

Zvavahera Chirenje (Z)

College of Health Sciences Clinical Trials Research Centre, University of Zimbabwe, Harare, Zimbabwe.

James G Kahn (JG)

Department of Epidemiology and Biostatistics, University of California, San Francisco, USA.
Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, San Francisco, USA.

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Classifications MeSH