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


Journal

Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566

Informations de publication

Date de publication:
09 2023
Historique:
received: 22 01 2023
accepted: 23 08 2023
medline: 8 9 2023
pubmed: 7 9 2023
entrez: 7 9 2023
Statut: ppublish

Résumé

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

Identifiants

pubmed: 37675828
doi: 10.1002/jia2.26168
pmc: PMC10483502
doi:

Banques de données

ClinicalTrials.gov
['NCT02625909']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e26168

Subventions

Organisme : NIH HHS
Pays : United States

Informations de copyright

© 2023 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

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Auteurs

Joanne M Carson (JM)

Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.

Sebastiano Barbieri (S)

The Centre for Big Data Research in Health, UNSW Sydney, Sydney, New South Wales, Australia.

Evan Cunningham (E)

Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.

Eric Mao (E)

Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.

Marc van der Valk (M)

Division of Infectious Diseases, Amsterdam Infection and Immunity Institute, University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
Stichting HIV Monitoring, Amsterdam, The Netherlands.

Jürgen K Rockstroh (JK)

University Hospital Bonn, Bonn, Germany.

Margaret Hellard (M)

Burnet Institute, Melbourne, Victoria, Australia.
The Alfred Hospital, Melbourne, Victoria, Australia.

Arthur Kim (A)

Massachusetts General Hospital, Boston, Massachusetts, USA.

Sanjay Bhagani (S)

Royal Free Hospital, London, UK.

Jordan J Feld (JJ)

Toronto Centre for Liver Diseases, Toronto General Hospital, Toronto, Ontario, Canada.

Ed Gane (E)

Auckland City Hospital, Auckland, New Zealand.

Maria C Thurnheer (MC)

Department of Infectious Diseases, Bern Inselspital, Bern, Switzerland.

Julie Bruneau (J)

Research Center, Centre Hospitalier de l'Université de Montréal, Montréal, Quebec, Canada.

Elise Tu (E)

Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.

Gregory J Dore (GJ)

Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.

Gail V Matthews (GV)

Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.

Marianne Martinello (M)

Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.
Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.

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