Integrating hepatitis C care for at-risk groups (HepLink): baseline data from a multicentre feasibility study in primary and community care

Author:

Nic An Riogh Eithne1,Swan Davina1,McCombe Geoff1,O’Connor Eileen12,Avramovic Gordana12,Macías Juan3,Oprea Cristiana45,Story Alistair6,Surey Julian7,Vickerman Peter8,Ward Zoe8,Lambert John S12,Tinago Willard1,Ianache Irina4,Iglesias Maria3,Cullen Walter1

Affiliation:

1. School of Medicine, University College Dublin, Dublin, Ireland

2. Mater Misericordiae University Hospital, Dublin, Ireland

3. Unidad de Enfermedades Infecciosas y Microbiología, Hospital Universitario de Valme, Seville, Spain

4. Victor Babes Clinical Hospital for Infectious and Tropical Diseases, Bucharest, Romania

5. Carol Davila University of Medicine and Pharmacy, Bucharest, Romania

6. Find and Treat, NHS, London, UK

7. Institute of Global Health, University College London, London, UK

8. Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK

Abstract

Abstract Objectives To examine HCV prevalence and management among people who inject drugs (PWID) attending primary care and community-based health services at four European sites using baseline data from a multicentre feasibility study of a complex intervention (HepLink). Methods Primary care and community-based health services in Dublin, London, Bucharest and Seville were recruited from the professional networks of the HepLink consortium. Patients were eligible to participate if aged ≥18 years, on opioid substitution treatment or at risk of HCV (i.e. injecting drug use, homeless or incarcerated), and attended the service. Data on patient demographics and prior HCV management were collected on participants at baseline. Results Twenty-nine primary care and community-based health services and 530 patients were recruited. Baseline data were collected on all participants. Participants’ mean age ranged from 35 (Bucharest) to 51 years (London), with 71%–89% male. Prior lifetime HCV antibody testing ranged from 65% (Bucharest) to 95% (Dublin) and HCV antibody positivity among those who had been tested ranged from 78% (Dublin) to 95% (Bucharest). Prior lifetime HCV RNA testing among HCV antibody-positive participants ranged from 17% (Bucharest) to 84% (London). Among HCV antibody- or RNA-positive participants, prior lifetime attendance at a hepatology/infectious disease service ranged from 6% (London) to 50% (Dublin) and prior lifetime HCV treatment initiation from 3% (London) to 33% (Seville). Conclusions Baseline assessment of the HCV cascade of care among PWID attending primary care and community-based health services at four European sites identified key aspects of the care cascade at each site that need to be improved.

Funder

European Commission

EU Third Health Programme

Ireland’s Health Services Executive

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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