Hepatitis C Treatment Initiation Among US Medicaid Enrollees.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 08 2023
Historique:
medline: 7 8 2023
pubmed: 4 8 2023
entrez: 4 8 2023
Statut: epublish

Résumé

Direct-acting antiviral (DAA) treatment for hepatitis C virus (HCV) infection is highly effective but remains underused. Understanding disparities in the delivery of DAAs is important for HCV elimination planning and designing interventions to promote equitable treatment. To examine variations in the receipt of DAA in the 6 months following a new HCV diagnosis. This retrospective cohort study used national Medicaid claims from 2017 to 2019 from 50 states, Washington DC, and Puerto Rico. Individuals aged 18 to 64 years with a new diagnosis of HCV in 2018 were included. A new diagnosis was defined as a claim for an HCV RNA test followed by an International Statistical Classification of Diseases and Related Health Problems, Tenth Revision (ICD-10) diagnosis code, after a 1-year lookback period. Outcome was receipt of a DAA prescription within 6 months of diagnosis. Logistic regression was used to examine demographic factors and ICD-10-identified comorbidities associated with treatment initiation. Among 87 652 individuals, 43 078 (49%) were females, 12 355 (14%) were age 18 to 29 years, 35 181 (40%) age 30 to 49, 51 282 (46%) were non-Hispanic White, and 48 840 (49%) had an injection drug use diagnosis. Of these individuals, 17 927 (20%) received DAAs within 6 months of their first HCV diagnosis. In the regression analyses, male sex was associated with increased treatment initiation (OR, 1.24; 95% CI, 1.16-1.33). Being age 18 to 29 years (OR, 0.65; 95% CI, 0.50-0.85) and injection drug use (OR, 0.84; 95% CI, 0.75-0.94) were associated with decreased treatment initiation. After adjustment for state fixed effects, Asian race (OR, 0.50; 95% CI, 0.40-0.64), American Indian or Alaska Native race (OR, 0.68; 95% CI, 0.55-0.84), and Hispanic ethnicity (OR, 0.81; 95% CI, 0.71-0.93) were associated with decreased treatment initiation. Adjustment for state Medicaid policy did not attenuate the racial or ethnic disparities. In this retrospective cohort study, HCV treatment initiation was low among Medicaid beneficiaries and varied by demographic characteristics and comorbidities. Interventions are needed to increase HCV treatment uptake among Medicaid beneficiaries and to address disparities in treatment among key populations, including younger individuals, females, individuals from minoritized racial and ethnic groups, and people who inject drugs.

Identifiants

pubmed: 37540513
pii: 2808080
doi: 10.1001/jamanetworkopen.2023.27326
pmc: PMC10403776
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2327326

Subventions

Organisme : NIDA NIH HHS
ID : K01 DA048172
Pays : United States
Organisme : NIDA NIH HHS
ID : P30 DA040500
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK123205
Pays : United States

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Auteurs

Shashi N Kapadia (SN)

Division of Infectious Diseases, Weill Cornell Medicine, New York, New York.
Department of Population Health Sciences, Weill Cornell Medicine, New York, New York.

Hao Zhang (H)

Department of Population Health Sciences, Weill Cornell Medicine, New York, New York.

Christopher J Gonzalez (CJ)

Division of General Internal Medicine, Weill Cornell Medicine, New York, New York.

Bisakha Sen (B)

Department of Health Policy and Organization, University of Alabama at Birmingham, Birmingham.

Ricardo Franco (R)

Division of Infectious Diseases, University of Alabama at Birmingham.

Kayla Hutchings (K)

Department of Population Health Sciences, Weill Cornell Medicine, New York, New York.

Elaine Wethington (E)

Department of Sociology and Department of Psychology, Cornell University, Ithaca, New York.

Andrew Talal (A)

Division of Gastroenterology, Hepatology, and Nutrition, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.

Audrey Lloyd (A)

Division of Infectious Diseases, University of Alabama at Birmingham.

Arpan Dharia (A)

Division of Gastroenterology, Hepatology, and Nutrition, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.

Martin Wells (M)

Department of Statistics and Data Science, Cornell University, Ithaca, New York.

Yuhua Bao (Y)

Department of Population Health Sciences, Weill Cornell Medicine, New York, New York.

Martin F Shapiro (MF)

Division of General Internal Medicine, Weill Cornell Medicine, New York, New York.

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