An intervention to improve HCV testing, linkage to care, and treatment among people who use drugs in Tehran, Iran: The ENHANCE study.


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:
10 2019
Historique:
received: 01 04 2019
revised: 21 06 2019
accepted: 02 07 2019
pubmed: 16 7 2019
medline: 21 5 2020
entrez: 16 7 2019
Statut: ppublish

Résumé

Globally, HCV testing, linkage to care and treatment is sub-optimal among people who use drugs (PWUD). This study aimed to evaluate the impact of an innovative intervention to enhance HCV testing, linkage to care, and treatment initiation among PWUD in Tehran, Iran. ENHANCE is a non-randomized trial evaluating the effect of on-site rapid HCV antibody testing, venepuncture for HCV RNA testing (HCV antibody positive only), liver fibrosis assessment, and linkage to care to enhance direct-acting antiviral (DAA) therapy (sofosbuvir/daclatasvir) initiation for HCV among people with a history of drug use. Recruitment was from April 2018 and will continue to July 2019, through three opioid substitution treatment (OST) clinics, five community-based drop-in centres, and one homeless reception centre. Participants initiated DAA therapy at a specialist clinic (OST clinics) or on-site (other sites), with monitoring provided on-site or at the specialist clinic (for those with cirrhosis attending OST clinics). Among 632 participants enrolled (median age, 44 years), 97% were male, 28% had a history of injecting drug use, and 58% had used drugs within the previous year. HCV antibody prevalence was 27%; 62% and 15% among those with and without a history of injecting drug use. Among 170 HCV antibody positive participants, 168 had HCV RNA testing (99%), of whom 134 (80%) were positive. Among HCV RNA positive participants, treatment initiation was 84%: 100% (45/45), 96% (46/48) and 54% (22/41) in OST clinics, drop-in centres, and homeless reception settings, respectively. Following on-site HCV testing and linkage to care, HCV treatment uptake was extremely high among PWUD, apart from the homeless reception population. This intervention could be explored in other settings globally to enhance HCV scale-up and elimination efforts.

Sections du résumé

BACKGROUND
Globally, HCV testing, linkage to care and treatment is sub-optimal among people who use drugs (PWUD). This study aimed to evaluate the impact of an innovative intervention to enhance HCV testing, linkage to care, and treatment initiation among PWUD in Tehran, Iran.
METHODS
ENHANCE is a non-randomized trial evaluating the effect of on-site rapid HCV antibody testing, venepuncture for HCV RNA testing (HCV antibody positive only), liver fibrosis assessment, and linkage to care to enhance direct-acting antiviral (DAA) therapy (sofosbuvir/daclatasvir) initiation for HCV among people with a history of drug use. Recruitment was from April 2018 and will continue to July 2019, through three opioid substitution treatment (OST) clinics, five community-based drop-in centres, and one homeless reception centre. Participants initiated DAA therapy at a specialist clinic (OST clinics) or on-site (other sites), with monitoring provided on-site or at the specialist clinic (for those with cirrhosis attending OST clinics).
RESULTS
Among 632 participants enrolled (median age, 44 years), 97% were male, 28% had a history of injecting drug use, and 58% had used drugs within the previous year. HCV antibody prevalence was 27%; 62% and 15% among those with and without a history of injecting drug use. Among 170 HCV antibody positive participants, 168 had HCV RNA testing (99%), of whom 134 (80%) were positive. Among HCV RNA positive participants, treatment initiation was 84%: 100% (45/45), 96% (46/48) and 54% (22/41) in OST clinics, drop-in centres, and homeless reception settings, respectively.
CONCLUSION
Following on-site HCV testing and linkage to care, HCV treatment uptake was extremely high among PWUD, apart from the homeless reception population. This intervention could be explored in other settings globally to enhance HCV scale-up and elimination efforts.

Identifiants

pubmed: 31303262
pii: S0955-3959(19)30180-X
doi: 10.1016/j.drugpo.2019.07.002
pii:
doi:

Substances chimiques

Antiviral Agents 0
Carbamates 0
Drug Combinations 0
Hepatitis C Antibodies 0
Imidazoles 0
Pyrrolidines 0
Valine HG18B9YRS7
daclatasvir LI2427F9CI
Sofosbuvir WJ6CA3ZU8B

Types de publication

Clinical Trial Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

99-105

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Maryam Alavi (M)

Viral Hepatitis Clinical Research Program, The Kirby Institute, UNSW Sydney, Sydney, NSW 2052, Australia; Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran. Electronic address: msalehialavi@kirby.unsw.edu.au.

Hossein Poustchi (H)

Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran.

Shahin Merat (S)

Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran.

Soudeh Kaveh-Ei (S)

Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran.

Afarin Rahimi-Movaghar (A)

Iranian National Center for Addiction Studies, Tehran University of Medical Sciences, Tehran, Iran.

Behrang Shadloo (B)

Iranian National Center for Addiction Studies, Tehran University of Medical Sciences, Tehran, Iran.

Behzad Hajarizadeh (B)

Viral Hepatitis Clinical Research Program, The Kirby Institute, UNSW Sydney, Sydney, NSW 2052, Australia.

Jason Grebely (J)

Viral Hepatitis Clinical Research Program, The Kirby Institute, UNSW Sydney, Sydney, NSW 2052, Australia.

Gregory J Dore (GJ)

Viral Hepatitis Clinical Research Program, The Kirby Institute, UNSW Sydney, Sydney, NSW 2052, Australia.

Reza Malekzadeh (R)

Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran.

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Classifications MeSH