Hepatitis C

The Hepatitis C virus (HCV) is the most common bloodborne infection in the US. This
RNA virus is predominantly transmitted through contact with contaminated blood and
blood products via injection drug use. Sexual and perinatal transmission of HCV appears
to occur less frequently. People at risk include: anyone who has had a blood transfusion
prior to 1989, IV drug users, hemodialysis patients, infants born to infected mothers,
those with multiple sexual partners, health care workers who suffer needle-stick
accidents, and people with tattoos or body-piercing. However, an estimated 30% have no
identifiable history of exposure to the virus. Household or familial contact is not
considered a risk factor for the transmission of hepatitis C. There is no vaccine
available for HCV and vaccines for hepatitis A and B do not provide immunity against
hepatitis C.
Symptoms of acute infections can include jaundice, fatigue, anorexia, nausea, or
vomiting; however, up to 85% of acute infections have mild or no symptoms and usually
go undetected. After acute infection, 15%-25% of persons appear to resolve their
infection without sequelae as defined by sustained absence of HCV RNA in serum and
normalization of ALT levels. Chronic HCV infection develops in most persons (75%-85%)
with persistent or fluctuating ALT elevations indicating active liver diseases
developing in 60%-70% of chronically infected persons. In the remaining 30%-40% of
chronically infected persons, ALT levels are normal. No clinical or epidemiologic features
among patients with acute infection have been found to be predictive of either persistent
infection or chronic liver disease [1]. Most studies have reported that medical
complications occur decades after initial infection including cirrhosis, liver failure,
and hepatic cancer.
ACDC uses the CDC/CSTE criteria for acute hepatitis C to standardize surveillance of
this infection. The criteria include discrete onset of symptoms and: 1. A positive HCV
test (antibody test EIA) confirmed by a more specific test (RIBA or detection of the
HCV-RNA antigen by polymerase-chain reaction [PCR]) or an EIA signal to cutoff ratio
of >3.8; and 2. Serum alanine aminotransferase (ALT) greater than 7 times the upper
limit of normal; and 3. No evidence of either acute hepatitis A or B disease. The
purpose of standardizing surveillance is to allow ACDC to more accurately monitor
trends in hepatitis C, compare local data with state and national data, and improve
identification of risk groups.
Presentations
Additional Resources
Publications & Archives
- MMWR:
Hepatocellular Carcinoma - United States, 2001-2006
- MMWR:
Surveillance for Acute Viral Hepatitis - United States, 2007
- MMWR:
Transmission of Hepatitis B and C Viruses in Outpatient Settings -
New York, Oklahoma, and Nebraska, 2000-2002
- MMWR: Acute Hepatitis C Virus Infections
Attributed to Unsafe Injection Practices at an Endoscopy Clinic
--- Nevada, 2007
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MMWR: Guidelines of Laboratory Testing and Result Reporting of Antibody to Hepatitis C
Virus Vol. 52, No RR-3, 2/7/03
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MMWR: Transmission of Hepatitis C Virus Infection Associated With Home Infusion Therapy for Hemophilia
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MMWR: Recommendations for Prevention and Control of Hepatitis C Virus (HCV) Infection
and HCV-Related Chronic Disease
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MMWR: Hepatitis C Virus Infection Among Firefighters, Emergency Medical Technicians,
and Paramedics --- Selected Locations, United States, 1991—2000
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More MMWR Publications Focusing on Viral Hepatitis