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. 2023 Sep;26(9):e26168.
doi: 10.1002/jia2.26168.

Sexual and drug use risk behaviour trajectories among people treated for recent HCV infection: the REACT study

Affiliations

Sexual and drug use risk behaviour trajectories among people treated for recent HCV infection: the REACT study

Joanne M Carson et al. J Int AIDS Soc. 2023 Sep.

Abstract

Introduction: Exploration of sexual and drug use behaviours following treatment for recent hepatitis C virus (HCV) is limited. This analysis modelled behavioural trajectories following treatment for recent HCV and assessed reinfection.

Methods: Participants treated for recent HCV in an international trial (enrolled 2017-2019) were followed at 3-monthly intervals for up to 2 years to assess longitudinal behaviours. Population-averaged changes were assessed using generalized estimating equations. Distinct behavioural trajectories were identified using group-based trajectory modelling. HCV reinfection incidence was calculated using person-years (PY) of observation.

Results: During the follow-up of 212 participants (84% gay and bisexual men [GBM]; 69% HIV; 26% current injecting drug use [IDU]), behavioural trajectories for IDU and stimulant use (past month) did not change. However, population-averaged decreases in the likelihood of daily IDU (adjusted odds ratio [AOR] 0.83; 95% CI 0.72, 0.95) and opioid use (AOR 0.84; 95% CI 0.75, 0.93) were observed. Among GBM, behavioural trajectories for chemsex did not change. Population-averaged decreases in condomless anal intercourse with casual male partners (CAI-CMP) (AOR 0.95; 95% CI 0.90, 0.99) and group-sex (AOR 0.86; 95% CI 0.80, 0.93) were observed, but masked distinct trajectories. While a proportion had a decreased probability of CAI-CMP (23%) and group-sex (59%) post-treatment, a substantial proportion retained a high probability of these behaviours. High HCV reinfection incidence was observed for the sustained high probability IDU (33.0/100 PY; 95% CI 17.7, 61.3) and chemsex (23.3/100 PY; 95% CI 14.5, 37.5) trajectories.

Conclusions: Limited sexual and drug use behavioural change was observed following treatment for recent HCV, supporting access to surveillance and (re)treatment.

Trial registration: ClinicalTrials.gov NCT02625909.

Keywords: GBM; HCV; HIV; PWID; STI; reinfection.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Proportion of participants reporting drug use and sexual risk behaviours. Proportion of participants reporting (A) injecting drug use and (B) type of drug used and opioid agonist treatment before, during and following treatment for recent HCV infection. Proportion of gay and bisexual men reporting (C) sexual risk behaviour and (D) STI diagnosis before, during and following treatment of recent HCV infection. Abbreviations: BSL, baseline; CAI‐CMP, condomless anal intercourse with casual male partner; ETR, end or treatment; FU, follow‐up; SCR, screening; STI, sexually transmitted infection; SVR12, sustained virological response 12‐weeks post treatment.
Figure 2
Figure 2
Group‐based trajectory modelling behavioural outcomes. Behavioural trajectories for (A) injecting drug use, (B) stimulant use and (C) opioid use before, during and following treatment for recent HCV infection in the overall population; behavioural trajectories for (D) condomless anal intercourse with casual male partners, (E) group‐sex and (F) chemsex before, during and following treatment for recent HCV infection among gay and bisexual men. Abbreviations: BSL, baseline; CAI‐CMP, condomless anal intercourse with casual male partner; ETR, end or treatment; FU, follow‐up; SCR, screening; SVR12, sustained virological response 12‐weeks post treatment.
Figure 3
Figure 3
Cumulative hazards curves for behavioural trajectories. Cumulative hazard of HCV reinfection for (A) injecting drug use and (B) chemsex behavioural trajectories, and, of sexually transmitted infections for (C) group‐sex and (D) chemsex behavioural trajectories.

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