Treatment as prevention effect of direct-acting antivirals on primary hepatitis C virus incidence: Findings from a multinational cohort between 2010 and 2019

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van Santen, Daniela, K | Sacks-Davis, Rachel | Stewart, Ashleigh | Boyd, Anders | Young, Jim | van der Valk, Marc | Smit, Colette | Rauch, Andri | Braun, Dominique, L | Jarrin, Inmaculada | Berenguer, Juan | Lazarus, Jeffrey, V | Lacombe, Karine | Requena, Maria-Bernarda | Wittkop, Linda | Leleux, Olivier | Salmon, Dominique | Bonnet, Fabrice | Matthews, Gail | Doyle, Joseph, S | Spelman, Tim | Klein, Marina, B | Prins, Maria | Asselin, Jason | Stoové, Mark, A | Hellard, Margaret

Edité par CCSD ; Elsevier -

International audience. Background Broad direct-acting antiviral (DAA) access may reduce hepatitis C virus (HCV) incidence through a "treatment as prevention" (TasP) effect. We assessed changes in primary HCV incidence following DAA access among people living with HIV (PLHIV). Methods We used pooled individual-level data from six cohorts from the International Collaboration on Hepatitis C Elimination in HIV Cohorts (InCHEHC). Follow-up started from the first recorded negative HCV antibody test date and ended at last negative antibody test or estimated infection date. Follow-up was restricted to 2010-2019. We used segmented Poisson regression to model trends across pre-, limited-(i.e., restrictions on access) and broad-DAA access periods. Findings Overall, 45,942 participants had at least one HCV antibody negative result and follow-up between 2010 and 2019. We observed 2042 incident HCV infections over 248,189 person-years (PY). Pooled incidence decreased from 0.91 per 100 PY in 2015 to 0.41 per 100 PY in 2019. Compared to the average pre-DAA period incidence (0.90 per 100 PY), average incidence was similar during the limited-DAA access period (Incidence rate ratio [IRR] = 0.98; 95% CI = 0.87, 1.11), and 52% lower during the broad-DAA access period (IRR = 0.48; 95%CI = 0.42, 0.52). The

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