Preferences and feasibility of long-acting technologies for treatment of hepatitis C virus in low- and middle-income countries: A survey of providers and policymakers.

hepatitis C long‐acting technologies low‐ and middle‐income countries treatment

Journal

Journal of viral hepatitis
ISSN: 1365-2893
Titre abrégé: J Viral Hepat
Pays: England
ID NLM: 9435672

Informations de publication

Date de publication:
28 Mar 2024
Historique:
revised: 15 12 2023
received: 16 10 2023
accepted: 10 01 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: aheadofprint

Résumé

Long-acting technologies (LATs) for hepatitis C virus (HCV) are under development as a strategy to improve linkage to care, treatment adherence and outcomes. We conducted a survey of HCV treatment prescribers and HCV policymakers in low- and middle-income countries (LMICs) regarding acceptability and feasibility of HCV LATs. We included one-time intramuscular injection, subdermal implant and transdermal patch as potential LAT options. We surveyed participants regarding optimal health system and patient characteristics, concerns, potential barriers, overall feasibility and preferences for HCV LAT as compared to daily oral medication. Overall, 122 providers and 50 policymakers from 42 LMICs completed the survey. Among providers, 93% (113/122) expressed willingness to prescribe LAT and 72% (88/120) of providers preferred LAT if provided at comparable efficacy, safety and cost as current oral treatments. Of providers preferring HCV LAT to daily oral medication, 67% (59/88) preferred injection, 24% (21/88) preferred patch and 9% (8/88) preferred implant. Only 20% (24/122) would prescribe LAT if it were more costly than oral treatment. In regression analysis, no provider characteristics were associated with preference for LAT over oral treatment. Policymakers reported high likelihood that LAT would be included in treatment guidelines (42/50; 84%) and national drug formularies (39/50; 78%) if efficacy, safety and cost were similar to oral treatment. HCV LATs could advance progress to HCV elimination in LMICs by diversifying treatment options to improve treatment coverage and outcomes. Provider preferences from LMICs are a critical consideration in the development of HCV LATs to ensure its early and equitable availability in LMICs.

Identifiants

pubmed: 38545826
doi: 10.1111/jvh.13921
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Unitaid
ID : 2020-38-LONGEVITY

Informations de copyright

© 2024 John Wiley & Sons Ltd.

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Auteurs

Neil Gupta (N)

Coalition for Global Hepatitis Elimination, The Task Force for Global Health, Decatur, Georgia, USA.

Susan Swindells (S)

Section of Infectious Diseases, Department of Internal Medicine, The University of Nebraska Medical Center, Omaha, Nebraska, USA.

Kimberly K Scarsi (KK)

Department of Pharmacy Practice and Science, College of Pharmacy, The University of Nebraska Medical Center, Omaha, Nebraska, USA.

Renae Furl (R)

Section of Infectious Diseases, Department of Internal Medicine, The University of Nebraska Medical Center, Omaha, Nebraska, USA.

David L Thomas (DL)

Division of Infectious Diseases, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Ethel D Weld (ED)

Division of Infectious Diseases, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Division of Clinical Pharmacology, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Joelle Dountio Ofimboudem (JD)

Treatment Action Group, New York, New York, USA.

Hailemichael Desalegn (H)

Medical Department, St. Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.

Saeed Hamid (S)

Section of Gastroenterology, Department of Medicine, Aga Khan University, Karachi, Pakistan.

Alethse de la Torre Rosas (AT)

Centro Nacional para la Prevención y el Control del VIH y el SIDA, Mexico City, Mexico.

Angelica E Miranda (AE)

Post-Graduation Program in Infectious Diseases, Federal University of Espirito Santo, Vitória, Brazil.

Andrew Owen (A)

Department of Pharmacology and Therapeutics, Centre of Excellence in Long acting Therapeutics (CELT), University of Liverpool, Liverpool, UK.

Steve Rannard (S)

Department of Chemistry, Centre of Excellence in Long acting Therapeutics (CELT), University of Liverpool, Liverpool, UK.

Lindsey Hiebert (L)

Coalition for Global Hepatitis Elimination, The Task Force for Global Health, Decatur, Georgia, USA.

Katherine Sun (K)

Coalition for Global Hepatitis Elimination, The Task Force for Global Health, Decatur, Georgia, USA.

John W Ward (JW)

Coalition for Global Hepatitis Elimination, The Task Force for Global Health, Decatur, Georgia, USA.

Classifications MeSH