The hepatitis C virus was identified in 1989 (Choo et al., 1989), with a specific test to detect the presence of the virus available in 1990 (Remis, 1998). Serologic tests for HCV are relatively recent, as such there are many areas relating to disease and transmission that are only now being realized (Mather and Crofts, 1999).
Although a restricted form of national reporting of HCV infection
in Canada started in 1992, it was not until January 01, 1999 that
all Canadian provinces and territories were reporting HCV cases
(LCDC, 1999). In 1997, a total of 19,571 cases were reported.
The prevalence of HCV infection in Canada is estimated at 0.8%
(240,000 persons) (Remis, 1998). Worldwide, it is estimated that
3%, or approximately 170 million people are chronic carriers (LCDC,
1999). Most newly or chronically infected persons have no symptoms
(approximately 70%), and as such are unaware of their infection
(LCDC, 1999; MRC, 1999). They remain a source of transmission
and are at risk for chronic liver disease, cirrhosis and liver
cancer (LCDC, 1999).
The lack of symptoms, as well as the absence of a test to distinguish
new cases from chronic cases, make it very difficult to estimate
the incidence of the disease. An enhanced surveillance system
to identify cases of acute HCV was established in four Canadian
cities in October 1998. The extrapolated results suggest that
911 cases of clinically recognized acute hepatitis C could be
identified in Canada. If infections without symptoms (70%) are
included in this estimate, the total number of new HCV infections
is estimated at 4,500 per year for Canada (Zou, Zhang, Tepper,
et al., 2000).
Because of the potentially long lag time between infection and
symptoms, a substantial increase in disease sequelae of HCV infection
is anticipated in Canada over the next decade (LCDC, 1999). It
has been predicted that by the year 2008, the incidence of cirrhosis
and end-stage liver disease will have doubled, the incidence of
liver cancer will have increased by 70% and liver deaths by 140%
(MRC, 1999).
The primary mode of transmission for HCV is through
exposure to blood and blood products. The major group infected and
at risk of infection is persons who share needles and other drug
paraphernalia. In numerous studies of this population, HCV antibody
positivity rates have been reported to be higher than 50%, and in
some populations, reaching close to 100% (Heintges and Wands, 1997).
In Canada, IDU accounts for approximately 70% of all HCV prevalent
infections (LCDC, 1999).
Before HCV antibody screening of donated blood became standard practice,
10-15% of individuals who had received multiple blood transfusions
or plasma products contracted the virus (LCDC, 1999). The introduction
of HCV antibody screening of blood products has led to a dramatic
decrease in HCV transmission through this method (Heintges and Wands,
1997). In Canada, the current risk is very low at about 1 in 103,000
units (LCDC, 1999). The Canadian Blood Services and HEMA Québec
are currently investigating a new blood screening method (Nucleic
Acid Amplification Testing or NAT) that is anticipated to further
decrease the risk of transmission to 1 in 500,000 units (Canadian
Blood Services, 1999).
Although sexual transmission of HCV infection has been demonstrated,
it is not a common mode of transmission. Research in the United
States and Europe has found low rates of infection, in the range
of 0% to 6%, in partners of individuals with chronic HCV infection.
The risk of infection through sexual intercourse with a carrier
has been estimated at 2.5% over 20 years (LCDC, 1999). There is
evidence to suggest that individuals who engage in frequent multi-partner
sexual activity, independent of other factors such as IDU and tattooing,
are at increased risk of contracting HCV (Dienstag, 1997).
Scully and colleagues (1993) examined the clinical and epidemiological
features of HCV virus infection in a gastroenterology/hepatology
practice in Ottawa, Canada. In this study, a retrospective chart
review was conducted on 63 consecutive patients identified as anti-HCV
positive. The results indicated that 48 (76%) had been exposed to
HCV through exposure to blood: 27 used intravenous drugs, and 21
had received blood or blood products. In addition, the long-term
sexual partners of 29 of these patients agreed to HCV antibody testing.
None of the sexual partners who were tested were anti-HCV positive.
The authors concluded that the majority of HCV cases, at least in
Ottawa, are acquired through exposure to blood (either through medical
treatment or sharing of needles) and that sexual transmission is
rare.
Mother to child transmission of HCV is fairly uncommon, occurring
in less than 5% of cases. Transmission rates are approximately three
times greater if the mother is co-infected with HCV and HIV (Zanetti
et al., 1999; Zanetti et al., 1995). There is no definite association
between transmission and type of delivery or breast-feeding (Patrick
et al., 2000). However, the Canadian Liver Foundation recommends
the suspension of breast-feeding if the mother's nipples are bleeding
or cracked (Canadian Liver Foundation, 1999).
In other countries, associations have been observed between the
use of unsterilized devices in activities that break the skin, such
as tattooing, ear or body piercing, or acupuncture, and HCV infection
(CDC, 1998). However, research in the US has failed to find a relationship
between these practices and HCV infection (CDC, 1998; Silverman
et al., 2000). Finally, approximately 10% of people with HCV infection
have no known risk factor (LCDC, 1999).
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