Sociodemographic Disparities in Hepatitis B Treatment: A Real-World Analysis of 3 Safety-Net Health Systems in the United States.

antiviral disparities gender hepatitis B safety net

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Oct 2024
Historique:
received: 04 09 2024
accepted: 27 09 2024
medline: 16 10 2024
pubmed: 16 10 2024
entrez: 16 10 2024
Statut: epublish

Résumé

Timely treatment of chronic hepatitis B (CHB) reduces risks of cirrhosis and hepatocellular carcinoma. Gaps in timely treatment persist, especially among underserved safety-net populations. We aim to evaluate gaps and disparities in CHB treatment in the United States. Adults with treatment-naive CHB without human immunodeficiency virus were identified from 2010 to 2018 across 3 safety-net health systems. CHB treatment eligibility was assessed using American Association for the Study of Liver Diseases (AASLD) criteria and alternative criteria, including the Simplified Approach for Hepatitis B Algorithm. Differences in CHB treatment between groups were evaluated using χ Among 3749 patients with treatment-naive CHB (51.5% women, 38.7% White, 33.7% African American, 19.6% Asian, 24.6% cirrhosis), 30.0% were AASLD treatment eligible, among whom 31.0% were treated. Men were more likely than women to be treated (33.5% vs 26.6%, Among an ethnically diverse multicenter safety-net cohort of CHB patients, less than one-third of treatment-eligible patients received antiviral treatment. Significant disparities in CHB treatment were observed by sociodemographic characteristics.

Sections du résumé

Background UNASSIGNED
Timely treatment of chronic hepatitis B (CHB) reduces risks of cirrhosis and hepatocellular carcinoma. Gaps in timely treatment persist, especially among underserved safety-net populations. We aim to evaluate gaps and disparities in CHB treatment in the United States.
Methods UNASSIGNED
Adults with treatment-naive CHB without human immunodeficiency virus were identified from 2010 to 2018 across 3 safety-net health systems. CHB treatment eligibility was assessed using American Association for the Study of Liver Diseases (AASLD) criteria and alternative criteria, including the Simplified Approach for Hepatitis B Algorithm. Differences in CHB treatment between groups were evaluated using χ
Results UNASSIGNED
Among 3749 patients with treatment-naive CHB (51.5% women, 38.7% White, 33.7% African American, 19.6% Asian, 24.6% cirrhosis), 30.0% were AASLD treatment eligible, among whom 31.0% were treated. Men were more likely than women to be treated (33.5% vs 26.6%,
Conclusions UNASSIGNED
Among an ethnically diverse multicenter safety-net cohort of CHB patients, less than one-third of treatment-eligible patients received antiviral treatment. Significant disparities in CHB treatment were observed by sociodemographic characteristics.

Identifiants

pubmed: 39411222
doi: 10.1093/ofid/ofae571
pii: ofae571
pmc: PMC11475814
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofae571

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. R. J. W. has received research grants (to his institution) from Gilead Sciences, Exact Sciences, Theratechnologies, and Durect Corporation, and has served in consulting roles without compensation for Gilead Sciences. M. K. J. has received investigator-initiated grant funding from Gilead Sciences paid to her institution. G. T. has received funding from Gilead Sciences (to his institution) not related to this study. M. T. has received investigator-initiated grant funding from Gilead Sciences paid to her institution. All other authors report no potential conflicts.

Auteurs

Robert J Wong (RJ)

Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Palo Alto, California, USA.
Gastroenterology Section, Veterans Affairs Palo Alto Healthcare System, Palo Alto, California, USA.

Mamta K Jain (MK)

Division of Infectious Diseases, Department of Internal Medicine, University of Texas Southwestern and Parkland Health and Hospital System, Dallas, Texas, USA.

Bolin Niu (B)

Division of Gastroenterology and Hepatology, MetroHealth System, Cleveland, Ohio, USA.

George Therapondos (G)

Multi-Organ Transplant Institute, Ochsner Health System, New Orleans, Louisiana, USA.

Onkar Kshirsagar (O)

Medical Technology and Practice Patterns Institute, Bethesda, Maryland, USA.

Mae Thamer (M)

Medical Technology and Practice Patterns Institute, Bethesda, Maryland, USA.

Classifications MeSH