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Incidence, risk factors, and prevention of hepatitis C reinfection: a population-based cohort study

Incidence, risk factors, and prevention of hepatitis C reinfection: a population-based cohort study
Incidence, risk factors, and prevention of hepatitis C reinfection: a population-based cohort study
Background: People remain at risk of reinfection with hepatitis C virus (HCV), even after clearance of the primary infection. We identified factors associated with HCV reinfection risk in a large population-based cohort study in British Columbia, Canada, and examined the association of opioid substitution therapy and mental health counselling with reinfection.
Methods: We obtained data from the British Columbia Hepatitis Testers Cohort, which includes all individuals tested for HCV or HIV at the British Columbia Centre for Disease Control Public Health Laboratory during 1990–2013 (when data were available). We defined cases of HCV reinfection as individuals with a positive HCV PCR test after either spontaneous clearance (two consecutive negative HCV PCR tests spaced ≥28 days apart without treatment) ora sustained virological response (SVR; two consecutive negative HCV PCR tests spaced ≥28 days apart 12 weeks after completing interferon-based treatment). We calculated incidence rates of HCV reinfection (per 100 person-years of follow-up) and corresponding 95% C Is assuming a Poisson distribution, and used a multivariable Cox proportional hazards model to examine reinfection risk factors (age, birth cohort, sex, year of HCV diagnosis, HCV clearance type, HIV co-infection, number of mental health counselling visits, levels of material and social deprivation, and alcohol and injection drug use), and the association of opioid substitution therapy and mental health counselling with HCV reinfection among people who inject drugs (PWID).
Findings: 5915 individuals with HCV were included in this study after clearance (3690 after spontaneous clearance and 2225 after SVR). 452 (8%) patients developed reinfection; 402 (11%) after spontaneous clearance and 50 (2%) who had achieved SVR. Individuals were followed up for a median of 5·4 years (IQR 2·9–8·7), and the median time to reinfection was 3·0 years (1·5–5·4). The overall incidence rate of reinfection was 1·27 (95% CI 1·15–1·39) per 100 person-years of follow-up over a total of 35 672 person-years, with signifi cantly higher rates in the spontaneous clearance group (1·59, 1·44–1·76) than in the SVR group (0·48, 0·36–0·63). With the adjusted Cox proportional hazards model, we noted higher reinfection risks in the spontaneous clearance group (adjusted hazard ratio [HR] 2·71, 95% CI 2·00–3·68), individuals co-infected with HIV (2·25, 1·78–2·85), and PWID (1·53, 1·21–1·92) than with other reinfection risk factors. Among the 1604 PWID with a current history of injection drug use, opioid substitution therapy was significantly associated with a lower risk of reinfection (adjusted HR 0·73, 95% CI 0·54–0·98), as was engagement with mental health counselling services (0·71, 0·54–0·92).
Interpretation: The incidence of HCV reinfection was higher among HIV co-infected individuals, those whospontaneously cleared HCV infection, and PWID. HCV treatment complemented with opioid substitution therapy and mental health counselling could reduce HCV reinfection risk among PWID. These findings support policies of post-clearance follow-up of PWID, and provision of harm-reduction services to minimise HCV reinfectionand transmission.
200-210
Islam, Nazrul
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Krajden, Mel
fb93cecf-2505-40c1-9343-0ede5373ecaf
Shoveller, Jean
1a898825-76fa-4774-a7f3-294da0bcfa34
Gustafson, Paul
60034910-45eb-4b4f-8380-482bb5caca1b
Gilbert, Mark
f1d12608-a0ff-46f3-8aff-fdd08b27031c
Buxton, Jane A
823e92fe-9123-4eff-a81a-93e359815de0
Wong, Jason
ed99d02f-3c83-47e7-818e-f66dbe495221
Tyndall, Mark W
cff7ce94-7b04-4954-a395-f5b233c4c384
Janjua, Naveed Z
63d9071c-cc94-4379-a317-c5de234b9de0
Islam, Nazrul
e5345196-7479-438f-b4f6-c372d2135586
Krajden, Mel
fb93cecf-2505-40c1-9343-0ede5373ecaf
Shoveller, Jean
1a898825-76fa-4774-a7f3-294da0bcfa34
Gustafson, Paul
60034910-45eb-4b4f-8380-482bb5caca1b
Gilbert, Mark
f1d12608-a0ff-46f3-8aff-fdd08b27031c
Buxton, Jane A
823e92fe-9123-4eff-a81a-93e359815de0
Wong, Jason
ed99d02f-3c83-47e7-818e-f66dbe495221
Tyndall, Mark W
cff7ce94-7b04-4954-a395-f5b233c4c384
Janjua, Naveed Z
63d9071c-cc94-4379-a317-c5de234b9de0

Islam, Nazrul, Krajden, Mel, Shoveller, Jean, Gustafson, Paul, Gilbert, Mark, Buxton, Jane A, Wong, Jason, Tyndall, Mark W and Janjua, Naveed Z (2016) Incidence, risk factors, and prevention of hepatitis C reinfection: a population-based cohort study. The Lancet Gastroenterology & Hepatology, 2 (3), 200-210. (doi:10.1016/ S2468-1253(16)30182-0).

Record type: Article

Abstract

Background: People remain at risk of reinfection with hepatitis C virus (HCV), even after clearance of the primary infection. We identified factors associated with HCV reinfection risk in a large population-based cohort study in British Columbia, Canada, and examined the association of opioid substitution therapy and mental health counselling with reinfection.
Methods: We obtained data from the British Columbia Hepatitis Testers Cohort, which includes all individuals tested for HCV or HIV at the British Columbia Centre for Disease Control Public Health Laboratory during 1990–2013 (when data were available). We defined cases of HCV reinfection as individuals with a positive HCV PCR test after either spontaneous clearance (two consecutive negative HCV PCR tests spaced ≥28 days apart without treatment) ora sustained virological response (SVR; two consecutive negative HCV PCR tests spaced ≥28 days apart 12 weeks after completing interferon-based treatment). We calculated incidence rates of HCV reinfection (per 100 person-years of follow-up) and corresponding 95% C Is assuming a Poisson distribution, and used a multivariable Cox proportional hazards model to examine reinfection risk factors (age, birth cohort, sex, year of HCV diagnosis, HCV clearance type, HIV co-infection, number of mental health counselling visits, levels of material and social deprivation, and alcohol and injection drug use), and the association of opioid substitution therapy and mental health counselling with HCV reinfection among people who inject drugs (PWID).
Findings: 5915 individuals with HCV were included in this study after clearance (3690 after spontaneous clearance and 2225 after SVR). 452 (8%) patients developed reinfection; 402 (11%) after spontaneous clearance and 50 (2%) who had achieved SVR. Individuals were followed up for a median of 5·4 years (IQR 2·9–8·7), and the median time to reinfection was 3·0 years (1·5–5·4). The overall incidence rate of reinfection was 1·27 (95% CI 1·15–1·39) per 100 person-years of follow-up over a total of 35 672 person-years, with signifi cantly higher rates in the spontaneous clearance group (1·59, 1·44–1·76) than in the SVR group (0·48, 0·36–0·63). With the adjusted Cox proportional hazards model, we noted higher reinfection risks in the spontaneous clearance group (adjusted hazard ratio [HR] 2·71, 95% CI 2·00–3·68), individuals co-infected with HIV (2·25, 1·78–2·85), and PWID (1·53, 1·21–1·92) than with other reinfection risk factors. Among the 1604 PWID with a current history of injection drug use, opioid substitution therapy was significantly associated with a lower risk of reinfection (adjusted HR 0·73, 95% CI 0·54–0·98), as was engagement with mental health counselling services (0·71, 0·54–0·92).
Interpretation: The incidence of HCV reinfection was higher among HIV co-infected individuals, those whospontaneously cleared HCV infection, and PWID. HCV treatment complemented with opioid substitution therapy and mental health counselling could reduce HCV reinfection risk among PWID. These findings support policies of post-clearance follow-up of PWID, and provision of harm-reduction services to minimise HCV reinfectionand transmission.

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More information

Published date: 22 December 2016
Additional Information: This online publication has been corrected. The corrected version first appeared at thelancet.com/gastrohep on February 8, 2017 Funding: The British Columbia Centre for Disease Control and the Canadian Institutes of Health Research.

Identifiers

Local EPrints ID: 471555
URI: http://eprints.soton.ac.uk/id/eprint/471555
PURE UUID: d29d99b7-fcc1-42d3-8ad7-c2b1a3c20845
ORCID for Nazrul Islam: ORCID iD orcid.org/0000-0003-3982-4325

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Date deposited: 11 Nov 2022 17:31
Last modified: 17 Mar 2024 04:15

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Contributors

Author: Nazrul Islam ORCID iD
Author: Mel Krajden
Author: Jean Shoveller
Author: Paul Gustafson
Author: Mark Gilbert
Author: Jane A Buxton
Author: Jason Wong
Author: Mark W Tyndall
Author: Naveed Z Janjua

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