Scaling Up Hepatitis C Prevention and Treatment Interventions for Achieving Elimination in the United States: A Rural and Urban Comparison.


Journal

American journal of epidemiology
ISSN: 1476-6256
Titre abrégé: Am J Epidemiol
Pays: United States
ID NLM: 7910653

Informations de publication

Date de publication:
01 08 2019
Historique:
received: 20 07 2018
revised: 02 04 2019
accepted: 02 04 2019
pubmed: 1 6 2019
medline: 21 3 2020
entrez: 1 6 2019
Statut: ppublish

Résumé

In the United States, hepatitis C virus (HCV) transmission is rising among people who inject drugs (PWID). Many regions have insufficient prevention intervention coverage. Using modeling, we investigated the impact of scaling up prevention and treatment interventions on HCV transmission among PWID in Perry County, Kentucky, and San Francisco, California, where HCV seroprevalence among PWID is >50%. A greater proportion of PWID access medication-assisted treatment (MAT) or syringe service programs (SSP) in urban San Francisco (established community) than in rural Perry County (young, expanding community). We modeled the proportion of HCV-infected PWID needing HCV treatment annually to reduce HCV incidence by 90% by 2030, with and without MAT scale-up (50% coverage, both settings) and SSP scale-up (Perry County only) from 2017. With current MAT and SSP coverage during 2017-2030, HCV incidence would increase in Perry County (from 21.3 to 22.6 per 100 person-years) and decrease in San Francisco (from 12.9 to 11.9 per 100 person-years). With concurrent MAT and SSP scale-up, 5% per year of HCV-infected PWID would need HCV treatment in Perry County to achieve incidence targets-13% per year without MAT and SSP scale-up. In San Francisco, a similar proportion would need HCV treatment (10% per year) irrespective of MAT scale-up. Reaching the same impact by 2025 would require increases in treatment rates of 45%-82%. Achievable provision of HCV treatment, alongside MAT and SSP scale-up (Perry County) and MAT scale-up (San Francisco), could reduce HCV incidence.

Identifiants

pubmed: 31150044
pii: 5509380
doi: 10.1093/aje/kwz097
pmc: PMC7415256
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1539-1551

Subventions

Organisme : Department of Health
ID : RP-PG-0616-20008
Pays : United Kingdom
Organisme : NIDA NIH HHS
ID : R01 DA024598
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA016017
Pays : United States
Organisme : Department of Health
ID : RP-DG-0610-10055
Pays : United Kingdom
Organisme : NIAID NIH HHS
ID : P30 AI036214
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA033862
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA037773
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Hannah Fraser (H)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

Claudia Vellozzi (C)

Division of Medical Affairs, Grady Health System, Atlanta, Georgia.

Thomas J Hoerger (TJ)

RTI International, Research Triangle Park, Raleigh, North Carolina.

Jennifer L Evans (JL)

Institute for Global Health Sciences, University of California San Francisco, San Francisco, California.

Alex H Kral (AH)

RTI International, Research Triangle Park, Raleigh, North Carolina.

Jennifer Havens (J)

Center on Drug and Alcohol Research, Department of Behavioral Science, University of Kentucky College of Medicine, Lexington, Kentucky.

April M Young (AM)

Center on Drug and Alcohol Research, Department of Behavioral Science, University of Kentucky College of Medicine, Lexington, Kentucky.
Department of Epidemiology, University of Kentucky College of Public Health, Lexington, Kentucky.

Jack Stone (J)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

Senad Handanagic (S)

Division of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia.

Susan Hariri (S)

Division of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia.

Carolina Barbosa (C)

RTI International, Research Triangle Park, Raleigh, North Carolina.

Matthew Hickman (M)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

Alyssa Leib (A)

Department of Chemistry, University of Colorado, Denver, Colorado.

Natasha K Martin (NK)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California San Diego, San Diego, California.

Lina Nerlander (L)

Division of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia.

Henry F Raymond (HF)

Center for Public Health Research, Population Health Division, San Francisco Department of Public Health, San Francisco, California.

Kimberly Page (K)

Department of Internal Medicine, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, New Mexico.

Jon Zibbell (J)

RTI International, Research Triangle Park, Raleigh, North Carolina.

John W Ward (JW)

Division of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia.
Coalition for Global Hepatitis Elimination, Task Force for Global Health, Decatur, Georgia.

Peter Vickerman (P)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

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