At a Glance
Hepatitis C is caused by infection with the hepatitis C virus (HCV), which was first identified in 1989. HCV is transmitted through contact with infected blood and blood products. HCV is one of the major causes of liver failure and transplant in the developed world1.
Initial (acute) infection with HCV is largely asymptomatic, with mild illness occurring in less than 25% of those infected2. Some infected individuals recover from their infection, but 75-85% progress to the chronic (carrier) state3. In these individuals, up to 20% will develop cirrhosis of the liver, often after two or more decades without symptoms. Due to its “silent” nature, approximately one-third of chronically infected individuals are unaware of their infection, increasing the risk that they could transmit the virus to others4. Currently, there is no vaccine for HCV.
Currently, injection drug use (IDU) is the dominant risk factor for HCV transmission in Canada (due to sharing of needles, syringes, and other injection equipment), and is implicated in 70-80% of recent HCV cases in Canada. Sharing of equipment for inhalation drug use (e.g. crack pipes, straws, etc.) has also been associated with HCV transmission. In larger Canadian cities, travel or residence in a HCV-endemic region is also a common risk factor, because of the higher rate of health care-acquired HCV infections in these areas. Sexual and perinatal (mother-to-child) transmission is inefficient and occurs uncommonly. Elevated risk is associated with tattooing or body piercing with contaminated equipment, or the sharing of personal hygiene items (e.g. razors, toothbrushes) with someone infected with HCV. While there have been cases of HCV transmission via contaminated blood transfusions, the enhanced screening procedures of Canada’s blood supply since 1990 has virtually eliminated this risk4.
The purpose of this document is to examine the prevalence and risk factors for HCV infections among injecting drug users (IDU) in Canada. Information presented is based on data collected during Phase 1 of I-Track, a multicentre, enhanced surveillance system that describes changing patterns in drug injecting practices, sexual risk behaviours, HIV and HCV prevalence and testing behaviours among IDU in Canada5. Phase 1 of I-Track was completed between October 2003 and May 2005. In this phase, there were 3031 participants recruited from seven sites (Victoria, Edmonton, Regina, Winnipeg, Sudbury, Toronto, and the SurvUDI sites (Abitibi-Témiscamingue, Estrie, Mauricie / Centre du Québec, Montérégie, Montréal, Ottawa, Outaouais, Québec, Saguenay / Lac St-Jean]). For more information about Phase 1 of I-Track, please refer to the Enhanced Surveillance of Risk Behaviours among Injecting Drug Users in Canada report which can be retrieved at http://www.phac-aspc.gc.ca/i-track/sr-re-1/index-eng.php.
Unless otherwise stated, the analyses presented here are restricted to those IDU participating in I-Track who consented to provide blood for HCV testing and who had definitive HCV results (n = 2,842).
HCV prevalence: Almost two-thirds of IDU were HCV positive.
HCV demographics: Older IDU were more likely to be infected with HCV.
Compared to those under the age of 20, IDU aged 40+ years were nearly thirty times as likely to be HCV positive (Table 1).
Total (n) | HCV+ (%) | OR (95% CI) | p-value | |
Gender | ||||
Male | 1982 | 1292 (65.2) | Ref | |
Female | 843 | 549 (65.1) | 1 (0.8-1.2) | 0.97 |
Age group | ||||
<20 years | 101 | 12 (11.9) | Ref | |
20-29 years* | 747 | 362 (48.5) | 6.9 (3.8-13.0) | <0.0001 |
30-39 years* | 942 | 641 (68.1) | 15.8 (8.5-29.3) | <0.0001 |
40-49 years* | 824 | 658 (79.9) | 29.4 (15.7-55.0 | <0.0001 |
50+ years* | 206 | 165 (80.1) | 29.8 (14.9-59.7) | <0.0001 |
Level of education | ||||
Completed less than high school level | 2111 | 1363 (64.6) | 0.92 (0.8-1.1) | 0.37 |
Completed high school or more | 703 | 467 (66.4) | Ref | |
Ethnicity | ||||
Aboriginal | 746 | 490 (65.7) | 1.03 (0.9-1.2) | 0.73 |
Non-aboriginal | 2059 | 1338 (65.0) | Ref |
Drug use and injecting practices: IDU who had injected cocaine or crack and cocaine in the last six months, who had injected in a public place in the last six months and who had injected more than one or two times per week in the last month were more likely to be infected with HCV (Table 2).
Total (n) | HCV+ (%) | OR (95% CI) | p-value | |
Injected cocaine in the last 6 months* | ||||
Yes | 2346 | 1590 (67.8) | 1.9 (1.5-2.3) | <0.0001 |
No | 492 | 260 (52.9) | Ref | |
Injected crack and cocaine in the last 6 months* | ||||
Yes | 2432 | 1640 (67.4) | 1.9 (1.6-2.4) | <0.0001 |
No | 406 | 210 (51.7) | Ref | |
Frequency of injection in the last month* | ||||
Regularly. more than one or two times per week | 2021 | 1362 (67.3) | 1.4 (1.2-1.7) | <0.0001 |
Sometimes or never | 821 | 490 (59.7) | Ref | |
Injected in a public place in the last 6 months* | ||||
Yes | 2591 | 1709 (66.0) | 1.5 (1.2-2.0) | 0.0024 |
No | 222 | 124 (55.9) | Ref | |
Most frequent place of injection | ||||
Public | 684 | 448 (65.6) | 1.02 (0.9-1.2) | 0.81 |
Others | 2097 | 1363 (65.0) | Ref |
Sharing of needles and injecting equipment: Needle exchange program (NEP) users and those who had borrowed needles in the last six months were more likely to be infected with HCV (Table 3).
Total | HCV+ (%) | OR (95% CI) | p-value | |
Any Needle Exchange Program use* | ||||
Yes | 2530 | 1722 (68.1) | 3.13 (2.4-4.0) | <0.0001 |
No | 301 | 122 (40.5) | Ref | |
Borrowed needles in the last 6 months* | ||||
Yes | 578 | 418 (72.3) | 1.51 (1.2-1.8) | <0.0001 |
No | 2223 | 1409 (63.4) | Ref | |
Borrowed equipment in the last 6 months | ||||
Yes | 856 | 551 (64.4) | 0.95 (0.8-1.1) | 0.52 |
No | 1947 | 1278 (65.6) | Ref | |
Borrowed needles in the last month | ||||
Yes | 1501 | 974 (64.9) | 1.01 (0.9-1.2) | 0.87 |
No | 1180 | 762 (64.6) | Ref | |
Borrowed equipment in the last month | ||||
Yes | 1479 | 962 (65.0) | 1.01 (0.9-1.2) | 0.93 |
No | 1170 | 759 (64.9) | Ref |
Sexual behaviours: Female IDU who were sex trade workers in the last six months were 1.7 times more likely to be infected with HCV than female IDU who had not been involved in sex trade work in the past 6 months (Table 4).
Total (n) | HCV+ (%) | OR (95% CI) | p-value | |
Sex trade worker in the last 6 months (female)* | ||||
Yes | 250 | 182 (72.8) | 1.7 (1.2-2.3) | 0.0022 |
No | 589 | 364 (64.8) | Ref | |
Sex with male sex partners in the last 6 months (male) | ||||
Yes | 186 | 119 (64.0) | 0.9 (0.7-1.3) | 0.7 |
No | 1776 | 1161 (65.4) | Ref |
Testing behaviours: The vast majority of IDU reported a previous testing history for HCV (Table 5).
Time of previous HCV test | Total (%) N=2,374 |
Within six months | 883 (37.4) |
Between six & twelve months | 361 (15.2) |
Between one & two years | 344 (14.5) |
More than two years | 786 (33.1) |
Accessing care: More than a half of IDU who knew their positive HCV infection status reported accessing care.
Results from Phase 1 I-Track indicate that HCV prevalence remains unacceptably high among IDU in this study population at 65.7% when compared to the estimated HCV prevalence of 0.8% in the general Canadian population. Approximately 1 in 7 (14%) of IDU were co-infected with HCV and HIV. Older (and more likely established) IDU were more likely to be HCV-infected relative to their younger counterparts. Like other studies, risk factors such as cocaine and crack use, borrowing needles and frequency of injection were independently associated with HCV prevalence (data not shown). Although NEP attendance was positively associated with a positive HCV status, published reports suggest that NEPs attract higher risk IDU 6,7,8. This observation provides one explanation for the higher proportion of HCV positive participants among NEP users and also suggests that these venues provide a good opportunity to reach and provide prevention and care services to these higher-risk individuals. One third of HCV positive IDU had been tested for HCV within the past six months and of those testing positive, nearly one half accessed care within the previous six months. Given the rapidly changing drug culture in urban and semi-urban centres across Canada, it is important for prevention, treatment, and care services to be responsive to the local needs. It is also important not to overlook the social and contextual factors that may be associated with HCV transmission.
I-Track is possible as a result of collaboration between the Public Health Agency of Canada and researchers, provincial and local health authorities and community based organisations from participating sites across Canada; coordination is provided by the Surveillance and Risk Assessment Division, and HCV and HIV testing is performed by the National HIV and Retrovirology Laboratory. Special thanks to the I-Track study participants. Further information on I-Track may be obtained at http://www.phac-aspc.gc.ca/aids-side/about/itrack-eng.php.
For more information on Hepatitis C, please contact:
Surveillance and Epidemiology Section
Community Acquired Infections Division
Centre for Communicable Disease and Infection Control
Tunney’s Pasture
Postal Locator: 0603B
Ottawa, Ontario K1A 0K9
Fax: (613) 941-9813