Volume 22, Issue 9 pp. 1519-1525

Directly observed therapy for the treatment of hepatitis C virus infection in current and former injection drug users

Jason Grebely

Corresponding Author

Jason Grebely

Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia,

Pender Community Health Center, Vancouver Coastal Health, Vancouver,

Dr Jason Grebely, Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia, 201-1200 Burrard Street, Vancouver, BC V6Z 2C7, Canada. Email: [email protected]Search for more papers by this author
Jesse D Raffa

Jesse D Raffa

Department of Statistics and Actuarial Science, University of Waterloo, Waterloo, and

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Caite Meagher

Caite Meagher

Cool Aid Community Health Center, Victoria, British Columbia, Canada

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Fiona Duncan

Fiona Duncan

Pender Community Health Center, Vancouver Coastal Health, Vancouver,

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Krista A Genoway

Krista A Genoway

Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia,

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Milan Khara

Milan Khara

Pender Community Health Center, Vancouver Coastal Health, Vancouver,

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Mark McLean

Mark McLean

Pender Community Health Center, Vancouver Coastal Health, Vancouver,

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Annabel Mead

Annabel Mead

Pender Community Health Center, Vancouver Coastal Health, Vancouver,

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Mark Viljoen

Mark Viljoen

Pender Community Health Center, Vancouver Coastal Health, Vancouver,

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Stanley DeVlaming

Stanley DeVlaming

Pender Community Health Center, Vancouver Coastal Health, Vancouver,

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Chris Fraser

Chris Fraser

Cool Aid Community Health Center, Victoria, British Columbia, Canada

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Brian Conway

Brian Conway

Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia,

Pender Community Health Center, Vancouver Coastal Health, Vancouver,

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First published: 15 August 2007
Citations: 58

Abstract

Background and Aim: There are few studies investigating the treatment of hepatitis C virus (HCV) infection in current and former drug users. With this in mind, we sought to evaluate the antiviral efficacy of interferon alpha-2b (IFN α-2b) or pegylated-interferon alpha-2b (PEG-IFN α-2b) and ribavirin (RBV) in injection drug users (IDU) enrolled in a directly observed therapy (DOT) program, as measured by sustained virologic response (SVR).

Methods: Viremic HCV-infected IDU, with alanine aminotransferase (ALT) >1.5× upper limit of normal (ULN) were offered 24–48 week (based on HCV genotype) therapy with RBV (800–1200 mg/day, based on weight) along with IFN α-2b (3 million IU thrice weekly) replaced by PEG-IFN α-2b (1.5 ìg/kg once weekly) as it became available. All injections were directly observed. The primary endpoint was SVR.

Results: Overall, 40 patients (33 males) received IFN α-2b (12) or PEG-IFN α-2b (28), 55% with HCV genotypes 2 or 3. Only 14 discontinued therapy, 5 due to toxicity, 6 due to illicit drug use and 3 did not achieve an early virologic response. In an intent-to-treat analysis, the overall SVR was 55% (22/40), 64% (14/22) in subjects with genotypes 2/3. There was no significant difference in response rates among those with >6 (50%) or ≤6 months (64%) drug abstinence (P = 0.51) or among those with (53%) and without (57%) intercurrent drug use (P = 0.99); however, frequent users (n = 9) had a decreased SVR (22%) when compared with occasional users (n = 10, 80%, P = 0.12).

Conclusion: Treatment of HCV in current and former IDU within a multidisciplinary DOT program can be successfully undertaken, resulting in SVR similar to those in randomized controlled trials.

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