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.
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 language | English |
|---|---|
| Article number | 105012 |
| Number of pages | 8 |
| Journal | International Journal of Drug Policy |
| Volume | 145 |
| Early online date | 16 Sept 2025 |
| DOIs | |
| Publication status | Published - 1 Nov 2025 |
Bibliographical note
Publisher Copyright:© 2025
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Research Groups and Themes
- GEM-B
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