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Table 4 Treatment outcomes (7 studies)

From: Hepatitis C virus infection in Irish drug users and prisoners – a scoping review

 

Date and author

Setting

Sample (n)

Data collection

Design

Main results

[50]

2005 Keating et al

Dublin Multi-site 5 drug treatment centres

PWID mono-infected with HCV (496; m = 341; 2 years follow up = 127)

Jan 1997- Nov 2001 Repeat follow up testing in 2003

Cross-sectional prospective study on HCV clearance

HCV RNA:

• Negative = 38% (self-clearance) (f = 47.4%; m = 34.5%)

• Follow up (2 yrs) = 82.2% sustained viral clearance

• Overall viral clearance = 31.1%

• Genotype distribution (1 = 48.8%; 3 = 48.5%)

[76]

2006 Hopkins

Single site Hospital

Co-infected with HIV and HCV patients with CD4 counts > 200 cells/mL

(45; m = 39; PWID = 58%)

June 2001–2003

Open-label, prospective study

SVR = 53%

• Genotype 2 and 3 patients had a significantly higher SVR (75%) than genotype 1 (19%)

• Adverse events occurred frequently

[74]

2011 Kieran et al

Dublin Single-site Hospital Integrated HIV/HCV clinic

Co-infected attendees (386; m = 278)

October 2008–January 2009

Retrospective chart review

202/386 – referred to co-infected clinic, with 107 completing treatment

• SVR = 44% (similar outcomes for PWID compared to patients with other transmission risks)

Associations with missed appointments

• younger age

• active IDU

• advanced HIV infection

Dedicated co-infection clinics lower the threshold for treatment and improve management of liver disease in co-infected patients

[75]

2011 Lowry et al

Dublin Single-site Hospital

HCV mono-infected patients referred (588 individuals (repeat referrals = 742 cases); m = 388; PWID = 74%)

2000–2007

Retrospective chart review

SVR = 74%

• History of IDU was not a significant predictor of lower therapy completion rate or achievement of SVR

In total, 451 (61%) dropouts occurred

• 141 (19%) failed to attend their initial appointment

• 180 dropped out from early outpatient management

• 29 failed to attend liver biopsy

• 81 defected from subsequent outpatient follow-up.

Statistically significant associations with history of injection drug use

• dropout immediately after the referral (P < 0.001)

• dropout from early outpatient management (P < 0.001)

• dropout over entire span of disease management (P < 0.001)

Male sex was also associated with dropout from disease management (P < 0.05)

[52]

2012 Kelly and Kelly

Dublin Single site GP

PWID (82; m = 62%)

1985–2010

Longitudinal cohort study

Anti-HCV = 33% at 10 yrs. (survivors)

Anti-HCV = 40% at 25 yrs. (survivors)

• 63% of the cohort had died by 2010, of which 26 were attributed to HIV disease

• Median survival time for those ant-HCV = 21 years (95% CI 15.5–26.5) which was significantly lower than the median survival time for drug users with a negative hepatitis C status. (p = 0.006)

[77]

2017 Elsherif et al

Dublin Single-site Hospital

HCV infected patients (1000; Former PWID (> 6 months) = 608; Recent PWID (< 6 months) = 85; Non-drug users = 307)

2002–2012

Retrospective chart review

SVR in PWID = 64.2%

• No significant compared to non-PWID (60.9%) [RR = 1.05, 95% CI 0.95 ± 1.17]

• There was no significant difference in SVR rates between the groups controlling for genotype (48.4% vs 48.4% for genotype 1; 74.9 vs 73.3% for genotype 3).

• No significant difference in treatment non-adherence between the groups (8.4% in PWID vs 6.8% in non-PWIDs; RR = 1.23, CI 0.76 ± 1.99)

• Former and recent PWID had similar adherence rates.