Hepatitis C screening and linkage to care with a mobile clinic in Southern Denmark.


Journal

The International journal on drug policy
ISSN: 1873-4758
Titre abrégé: Int J Drug Policy
Pays: Netherlands
ID NLM: 9014759

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 14 04 2023
revised: 25 08 2023
accepted: 25 08 2023
medline: 27 11 2023
pubmed: 16 9 2023
entrez: 15 9 2023
Statut: ppublish

Résumé

Knowing the prevalence of hepatitis C (HCV) in risk groups is essential for elimination. The aim of the study was to assess HCV prevalence among people with different risk profiles and the feasibility of linking people with HCV to care. In Southern Denmark we tested people who were using shelters, cafés, and facilities for marginalized populations and the general population. We established a mobile clinic for HCV testing offering point-of-care HCV-antibody (HCV-Ab), point-of-care HCV RNA testing, and dried blood spot (DBS) testing. People with HCV infection were linked to care. Among 802 tested persons, we found an HCV-Ab /HCV RNA prevalence of 13% (n = 101) /3% (n = 24). We found a prevalence of 20% (n = 97)/5% (n = 24) among 475 persons tested at locations attended by people who inject drugs but 0%/0% when testing the general population. Of 24 people who were HCV RNA positive, 83% (n = 20) initiated treatment, 13% (n = 3) spontaneously cleared their infection, and one was lost to follow-up. General population testing has limited utility while focus on settings attended by people with increased HCV risk is more feasible. Linkage of people with a current HCV infection to care is feasible.

Sections du résumé

BACKGROUND BACKGROUND
Knowing the prevalence of hepatitis C (HCV) in risk groups is essential for elimination. The aim of the study was to assess HCV prevalence among people with different risk profiles and the feasibility of linking people with HCV to care.
METHODS METHODS
In Southern Denmark we tested people who were using shelters, cafés, and facilities for marginalized populations and the general population. We established a mobile clinic for HCV testing offering point-of-care HCV-antibody (HCV-Ab), point-of-care HCV RNA testing, and dried blood spot (DBS) testing. People with HCV infection were linked to care.
RESULTS RESULTS
Among 802 tested persons, we found an HCV-Ab /HCV RNA prevalence of 13% (n = 101) /3% (n = 24). We found a prevalence of 20% (n = 97)/5% (n = 24) among 475 persons tested at locations attended by people who inject drugs but 0%/0% when testing the general population. Of 24 people who were HCV RNA positive, 83% (n = 20) initiated treatment, 13% (n = 3) spontaneously cleared their infection, and one was lost to follow-up.
CONCLUSION CONCLUSIONS
General population testing has limited utility while focus on settings attended by people with increased HCV risk is more feasible. Linkage of people with a current HCV infection to care is feasible.

Identifiants

pubmed: 37714009
pii: S0955-3959(23)00227-X
doi: 10.1016/j.drugpo.2023.104180
pii:
doi:

Substances chimiques

RNA, Viral 0
Hepatitis C Antibodies 0
Antiviral Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104180

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest S.D. has received travel support and speaker fees from Gilead, Abbott, and AbbVie, and research grants from Gilead, all unrelated to the current study. P.B.C. has received research grants from Gilead, AbbVie, and MSD unrelated to the current study. ALHØ has received research grants from Gilead and speaker fees and travel support from Gilead, AbbVie, and MSD unrelated to the current study. D.H. and B.R. have no conflicts of interest.

Auteurs

Sandra Dröse (S)

Department of Infectious Diseases, Odense University Hospital, J. B. Winsloews Vej 4, Indgang 18 Penthouse 2. sal, DK-5000 Odense C, Denmark; Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Winsløwparken 19, 3. sal, DK-5000 Odense, Denmark; OPEN, Odense Patient data Explorative Network, Odense University Hospital, Odense. Electronic address: Sandra.Droese@rsyd.dk.

Anne Lindebo Holm Øvrehus (ALH)

Department of Infectious Diseases, Odense University Hospital, J. B. Winsloews Vej 4, Indgang 18 Penthouse 2. sal, DK-5000 Odense C, Denmark; Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Winsløwparken 19, 3. sal, DK-5000 Odense, Denmark.

Dorte Kinggaard Holm (DK)

Department of Clinical Immunology, Odense University Hospital, J. B. Winsloews Vej 4, DK-5000 Odense C Odense, Denmark.

Birgit Thorup Røge (BT)

Department of Medicine, Lillebaelt Hospital, Sygehusvej 24, DK-6000 Kolding, Denmark.

Peer Brehm Christensen (PB)

Department of Infectious Diseases, Odense University Hospital, J. B. Winsloews Vej 4, Indgang 18 Penthouse 2. sal, DK-5000 Odense C, Denmark; Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Winsløwparken 19, 3. sal, DK-5000 Odense, Denmark.

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