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Can hepatitis C elimination targets be sustained among people who inject drugs post-2030?
Lanièce Delaunay, Charlotte; Godin, Arnaud; Kronfli, Nadine; Panagiotoglou, Dimitra; Cox, Joseph; Alary, Michel; Klein, Marina B; Maheu-Giroux, Mathieu.
Afiliação
  • Lanièce Delaunay C; Department of Epidemiology, Biostatistics, and Occupational Health, School of Population and Global Health, Faculty of Medicine, McGill University, 1020 Avenue des Pins Ouest, H3A 1A2, Montréal (QC), Canada; Centre for Outcomes Research and Evaluation, Research Institute of the McGill University Hea
  • Godin A; Department of Epidemiology, Biostatistics, and Occupational Health, School of Population and Global Health, Faculty of Medicine, McGill University, 1020 Avenue des Pins Ouest, H3A 1A2, Montréal (QC), Canada.
  • Kronfli N; Department of Medicine, Division of Infectious Disease and Chronic Viral Illness Service, McGill University Health Centre, 1001 Boulevard Décarie, H4A 3J1, Montréal (QC), Canada; Centre for Outcomes Research and Evaluation, Research Institute of the McGill University Health Centre, 5252 Boulevard de
  • Panagiotoglou D; Department of Epidemiology, Biostatistics, and Occupational Health, School of Population and Global Health, Faculty of Medicine, McGill University, 1020 Avenue des Pins Ouest, H3A 1A2, Montréal (QC), Canada.
  • Cox J; Department of Epidemiology, Biostatistics, and Occupational Health, School of Population and Global Health, Faculty of Medicine, McGill University, 1020 Avenue des Pins Ouest, H3A 1A2, Montréal (QC), Canada; Department of Medicine, Division of Infectious Disease and Chronic Viral Illness Service, Mc
  • Alary M; Département de Médecine Sociale et Préventive, Université Laval, 1050 Avenue de la Médecine, G1V 016, Québec (QC), Canada; Axe Santé des Populations et Pratiques Optimales en Santé, Centre de recherche du CHU de Québec-Université Laval, 1050 Chemin Sainte-Foy, G1S 4L8, Québec (QC), Canada; Institut
  • Klein MB; Department of Epidemiology, Biostatistics, and Occupational Health, School of Population and Global Health, Faculty of Medicine, McGill University, 1020 Avenue des Pins Ouest, H3A 1A2, Montréal (QC), Canada; Department of Medicine, Division of Infectious Disease and Chronic Viral Illness Service, Mc
  • Maheu-Giroux M; Department of Epidemiology, Biostatistics, and Occupational Health, School of Population and Global Health, Faculty of Medicine, McGill University, 1020 Avenue des Pins Ouest, H3A 1A2, Montréal (QC), Canada. Electronic address: mathieu.maheu-giroux@mcgill.ca.
Int J Drug Policy ; 96: 103343, 2021 10.
Article em En | MEDLINE | ID: mdl-34215459
ABSTRACT

BACKGROUND:

In high-income countries, people who inject drugs (PWID) are a priority population for eliminating hepatitis C virus (HCV) by 2030. Despite evidence informing micro-elimination strategies, little is known regarding efforts needed to maintain elimination targets in populations with ongoing acquisition risks. This model-based study investigates post-elimination transmission dynamics of HCV and HIV among PWID under different scenarios where harm reduction interventions and HCV testing and treatment are scaled-down.

METHODS:

We calibrated a dynamic compartmental model of concurrent HCV and HIV transmission among PWID in Montréal (Canada) to epidemiological data (2003-2018). We then simulated achieving the World Health Organization elimination targets by 2030. Finally, we assessed the impact of four post-elimination scenarios (2030-2050) 1) scaling-down testing, treatment, opioid agonist therapy (OAT), and needle and syringe programs (NSP) to pre-2020 levels; 2) only scaling-down testing and treatment; 3) suspending testing and treatment, while scaling down OAT and NSP to pre-2020 levels; 4) suspending testing and treatment and maintaining OAT and NSP coverage required for elimination.

RESULTS:

Scaling down interventions to pre-2020 levels (scenario 1) leads to a modest rebound in chronic HCV incidence from 2.4 to 3.6 per 100 person-years by 2050 (95% credible interval - CrI 0.8-7.2). When only scaling down testing and treatment (scenario 2), chronic HCV incidence continues to decrease. In scenario 3 (suspending treatment and scaling down OAT and NSP), HCV incidence and mortality rapidly increase to 11.4 per 100 person-years (95%CrI 7.4-15.5) and 3.2 per 1000 person-years (95%CrI 2.4-4.0), respectively. HCV resurgence was mitigated in scenario 4 (maintaining OAT and NSP) as compared to scenario 3. All scenarios lead to decreases in the proportion of reinfections among incident cases and have little impact on HIV incidence and HIV-HCV coinfection prevalence.

CONCLUSION:

Despite ongoing transmission risks, HCV incidence rebounds slowly after 2030 under pre-2020 testing and treatment levels. This is heightened by maintaining high-coverage harm reduction interventions. Overall, sustaining elimination would require considerably less effort than achieving it.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Preparações Farmacêuticas / Abuso de Substâncias por Via Intravenosa / Hepatite C Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Preparações Farmacêuticas / Abuso de Substâncias por Via Intravenosa / Hepatite C Idioma: En Ano de publicação: 2021 Tipo de documento: Article