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Figure 2.
Sources
of Infection for Persons with Hepatitis C |
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* Hemodialysis;
health-care work; perinatal
Source: CDC |
Prior
to the mid-1980's there was a 7 percent to 10 percent risk
of non-A, non-B hepatitis (hepatitis C) from blood
transfusion. This risk declined by more than 50 percent
between 1985 and 1990 as a result of implementation of blood
donor screening for HIV and surrogate testing for non-A,
non-B hepatitis. In 1990, specific donor screening for HCV
was implemented and by 1992 the risk of HCV infection from a
unit of transfused blood was reduced to one in 100,000. As
of 2001, the risk of HCV infection from a unit of transfused
blood is less than one per million transfused units.
Clotting factor concentrates, which are plasma-derived
products used to treat individuals with hemophilia, posed a
high risk for HCV infection prior to the use of virus
inactivation procedures that were introduced in 1985 and
1987. Except for one outbreak of hepatitis C from a single
type of contaminated intravenous immunoglobulin, other
plasma-derived products, including immune globulin for
intramuscular administration, have not been associated with
the transmission of HCV in the United States. Currently, all
immune globulin products undergo a virus inactivation
procedure or test negative for HCV prior to release.
Sexual
exposures account for about 15 percent of cases of hepatitis
C. Although the risk for transmitting HCV infection through
sexual intercourse is low, sex is a common behavior in the
general population, a substantial proportion of the adult
population has had unprotected sex with multiple partners,
and there are a large number of persons with HCV infection.
While other types of exposures are more likely to transmit
HCV (e.g., transfusion from an infected donor), they account
for a smaller proportion of infections because of the
relatively small proportion of the population in whom these
exposures have occurred.
Exposures resulting from hemodialysis, employment in the
health care field, and birth to an HCV-infected mother
together account for about 5 percent of cases. About 10
percent of people with HCV infection have no recognized
source for their infection.
While
it is possible for HCV to be transmitted from any
percutaneous exposure to blood, exposures such as tattooing,
body piercing, or acupuncture have not been shown to place
people at increased risk for infection. Higher rates of HCV
infection are not found among persons with these exposures
alone and these exposures are rarely reported among new
cases of hepatitis C.
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HCV is most efficiently transmitted by exposures that
involve direct passage of blood through the
skin, i.e., a percutaneous exposure. |
Consequences of HCV infection. About 15 percent to 25
percent of persons with acute hepatitis C resolve their
infection without further problems. The remainder develop a
chronic infection and about 60 percent to 70 percent of
these persons develop chronic hepatitis. Cirrhosis of the
liver develops in 10 percent to 20 percent of persons with
chronic hepatitis C over a period of 20-30 years, and
hepatocellular carcinoma (liver cancer) in 1 percent to 5
percent. For individuals with cirrhosis, however, the rate
of development of liver cancer might be as high as 1 percent
to 4 percent per year.
Lower
rates of complications have been reported from studies of
persons who acquired infection as children. However, longer
term follow-up studies are needed to assess lifetime
consequences of chronic HCV infection in different
populations, especially among children.
Chronic liver disease is the tenth leading cause of death
among adults in the United States. It is estimated that 40
percent to 60 percent of chronic liver disease is due to
hepatitis C and another 10 percent to 15 percent is due to
chronic hepatitis B. HCV-associated chronic liver disease is
the most frequent indication for liver transplantation among
adults. Additionally, because alcohol use is one of the most
important contributing factors to progression of chronic
liver disease among persons with hepatitis C, it is
important to identify infected individuals as early as
possible so that they can be counseled to limit alcohol
consumption and be offered treatment if appropriate.
Treatment for hepatitis C. In 1997, an NIH Consensus
Development Conference established guidelines for the
medical management of hepatitis C1
,which have since been updated to reflect the evolving
nature of antiviral therapy. A combination of
alpha-interferon and ribavirin currently is the most
effective therapy and achieves the sustained elimination of
HCV infection for at least 6 months in 30 percent to 40
percent of patients.
However, 10 percent to 20 percent of treated patients do not
complete therapy because they experience significant side
effects. In addition, some patients may have conditions,
such as severe cirrhosis which prohibit treatment. Current
antiviral therapy is not licensed for patients below age 18
years.
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HCV-associated chronic liver disease is the most frequent
indication for liver transplantation among
adults. |
Persons with chronic hepatitis C who continue to abuse
alcohol are at risk for ongoing liver injury and antiviral
therapy may be ineffective. In addition, interferon therapy
can be associated with relapse in people with a previous
history of alcohol abuse; therefore, abstinence from alcohol
is recommended during antiviral therapy. Interferon therapy
should be considered with caution for patients who recently
stopped alcohol abuse, and these patients require the
support of alcohol treatment programs.
Patients with hepatitis C on methadone treatment have been
successfully treated with interferon. However, there is
limited experience with treatment of persons who are
recovered injection drug users or who are active injection
drug users. In addition, there is the concern that active
injection drug users are at risk for re-infection with HCV.
When patients with past or continuing substance abuse are
considered for antiviral treatment, such patients should
receive drug treatment or care from substance abuse
specialists or counselors.
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Drug treatment is an important adjunct to care for many
persons with hepatitis C. |
Persons with HCV-related liver disease should be vaccinated
against diseases that may produce further complications or
increase their risk of death. Susceptible persons with
chronic liver disease should receive hepatitis A vaccine
since they are at increased risk of death from liver failure
if they get hepatitis A. All persons with chronic liver
disease should be vaccinated annually against influenza and
should receive pneumoccocal vaccine. In addition, persons
with continued risk factors for HBV infection should receive
hepatitis B vaccine.
Co-infection.
Coinfection with HCV, HIV and/or HBV is currently recognized
as a serious problem and is more likely to be found among
injection drug users and persons treated for hemophilia
before the availability of inactivated clotting factor
concentrates. Deaths from chronic hepatitis C among patients
with HIV are expected to increase as advances with
antiretroviral therapy extend the life span of these
patients. Management of HIV infection in HCV co-infected
patients generally is similar to that for patients with HIV
alone, although there is some risk of liver toxicity from
the antiretroviral drugs. HCV co-infected patients should be
evaluated to determine if they are candidates for antiviral
treatment of their chronic liver disease. Because treatment
and medical management of co-infected patients is
complicated and rapidly evolving, such patients are best
managed by health care providers with experience in treating
both HIV and HCV infection. More research is needed to
determine the ideal management and treatment of co-infected
individuals.
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Deaths from chronic hepatitis C among patients
co-infected with HIV are expected to increase as
antiretroviral therapy extends their life spans. |
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