Assessing Molecular Point-of-Care Testing and Dried Blood Spot for Hepatitis C Virus Screening in People Who Inject Drugs

Author:

Chevaliez Stéphane12,Wlassow Mélanie12,Volant Johann3,Roudot-Thoraval Françoise24,Bachelard Antoine5,Poiteau Lila12,Trabut Jean-Baptiste26,Hézode Christophe24,Bourdel Anne7,Dominguez Stéphanie5

Affiliation:

1. National Reference Center for Viral Hepatitis B, C, and D, Department of Virology, Hôpital Henri Mondor, Université Paris-Est, Créteil, France

2. INSERM U955, Créteil, France

3. Médecin du Monde, Paris, France

4. Department of Hepatology, Hôpital Henri Mondor, Université Paris-Est, Créteil, France

5. Department of Infectious Diseases, Hôpital Henri Mondor, Université Paris-Est, Créteil, France

6. Service d’Addictologie, Hôpital Henri Mondor, Université Paris-Est, Créteil, France

7. CSAPA EGO, Association Aurore, Paris, France

Abstract

Abstract Background Injecting drug use is a major driver of hepatitis C virus (HCV) spread worldwide, and the World Health Organization (WHO) has identified people who inject drugs (PWID) as a key population to target for HCV screening and care. Point-of-care (POC) hepatitis C tests and dried blood spot (DBS) sampling offer benefits for the management of patients with HCV infection by increasing HCV testing and linkage to care in different nonclinical settings. The aims of this prospective study were to evaluate the feasibility and the acceptability of use HCV ribonucleic acid (RNA) POC and fingerstick DBS testing in social-medical risk-reduction centers and to describe the cascade of care among PWID in France. Methods Between June 2018 and February 2019, 89 consecutive HCV-seropositive PWID attending 2 drug treatment services and 1 supervised consumption room in inner Paris were invited to participate in further evaluation, undergoing a clinical review with a liver assessment and blood tests including fingerstick capillary whole blood POC HCV RNA testing and fingerstick DBS sampling. Results Of the 89 participants enrolled, HCV RNA was detected in 34 (38.6%) participants. Fingerstick whole blood POC RNA testing and HCV RNA detection from DBS sample were feasible and acceptable among PWID with no major difference in terms of HCV RNA detection rate. Overall, 16 participants received pan-genotypic antiviral treatment. The proportion of PWID with sustained virologic response at 12 weeks was 81.2%, with data for 3 patients still pending. Conclusions One-step screening strategy based on the detection of HCV RNA would engage people in care for treatment scale-up and HCV elimination.

Funder

Regional Agency for Health

Gilead Sciences

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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