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Differential risk for Hepatitis C And HIV among People Who Inject Drugs in Kenya: a latent class analysis signaling needs for innovation in service delivery

Hannah Manley, Lindsey Riback, Chenshu Zhang, Peter T Vickerman, Jack Stone, Josephine G Walker, Mercy Nyakowa, Rose Wafula, Nazila Ganatra, Matthew Akiyama*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

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Abstract

Background:
Subgroups of people who inject drugs (PWID) may experience differential exposure to HIV and hepatitis C (HCV). This study analyzes behavioral risk profiles associated with HIV and HCV infection among PWID, with the aim of identifying subgroups at highest risk and guiding future interventions.

Methods:
We recruited PWID in Kenya using respondent driven sampling. Participants completed behavioral surveys and point-of-care HCV, HIV, and hepatitis B (HBV) testing. We used latent class (LC) analysis to divide the sample into mutually exclusive classes based on nine risk- and service access-related measures.

Results:
Among the 3152 participants enrolled, one-fifth (N = 610, 19.4 %) were HCV antibody-positive, one-tenth were HIV-positive (N = 306, 9.7 %), and 1.3 % (N = 40) were HBV-positive. We obtained three LCs: LC1 – long-term, high-frequency PWID with large networks, high access to NSP services, and moderate access to OAT (N = 1522, 48.3 %), LC2 – newer, high-frequency PWID with large networks, moderate access to NSP services, and moderate access to OAT (N = 878, 27.8 %), and LC3 – long-term, low-frequency PWID with small networks, high access to NSP, and moderate access to OAT (N = 752, 23.9 %). HIV and HCV prevalence and risk behaviors differed between the classes, and classes differed in demographic characteristics as well.

Conclusion:
Subgroups of PWID in Kenya have different risk for HIV and HCV, influenced by duration of injection, network size, service access, and other behavioral risk factors. Targeted interventions to meet each subgroup’s needs are essential to prevent ongoing HCV and HIV epidemics among PWID.
Original languageEnglish
Article number105012
Number of pages8
JournalInternational Journal of Drug Policy
Volume145
Early online date16 Sept 2025
DOIs
Publication statusPublished - 1 Nov 2025

Bibliographical note

Publisher Copyright:
© 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Groups and Themes

  • GEM-B

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