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PHESP<br />

9021<br />

products (ie, blood transfusion, sharing of needles by drug addicts). The virus is found in virtually every<br />

type of human body fluid and also is spread through oral and genital contact. HBV can be transmitted<br />

from mother to child during delivery through contact with blood and vaginal secretions, but it is not<br />

commonly transmitted transplacentally. Infection of the infant can occur if the mother is a chronic<br />

hepatitis B surface antigen carrier or has an acute HBV infection at the time of delivery. Transmission is<br />

rare if an acute infection occurs in either the first or second trimester of pregnancy.<br />

Useful For: Screening pregnant women for chronic hepatitis B virus (HBV) infection Determining the<br />

level of infectivity in pregnant women with chronic HBV infection<br />

Interpretation: Hepatitis B surface antigen (HBsAg) is the first serologic marker appearing in the<br />

serum 6 to 16 weeks following hepatitis B virus (HBV) infection. A positive result for HBsAg is<br />

diagnostic of acute or chronic HBV infection. In acute cases, HBsAg usually disappears 1 to 2 months<br />

after the onset of symptoms. Persistence of HBsAg for more than 6 months indicates development of<br />

either a chronic carrier state or chronic liver disease. Hepatitis B surface antibody (anti-HBs) appears with<br />

the resolution of HBV infection after the disappearance of HBsAg. Hepatitis B envelope antigen (HBeAg)<br />

appears at approximately the same time as HBsAg and indicates that the virus is replicating and the<br />

individual is infectious. Appearance of hepatitis Be antibody (anti-HBe) after the disappearance of<br />

HBsAg and HBeAg usually indicates recovery and loss of infectivity. If HBsAg is positive and the<br />

patient's condition warrants, consider testing for hepatitis B core antigen (anti-HBc) IgM, HBV-DNA, and<br />

anti-hepatitis delta virus (HDV) to evaluate viral replication and infectivity.<br />

Reference Values:<br />

Negative<br />

See Viral Hepatitis Serologic Profiles in Special Instructions.<br />

Clinical References: Vranckx R, Alisjahbana A, Meheus A: Hepatitis B virus vaccination and<br />

antenatal transmission of HBV markers to neonates. J Viral Hepat 1999;6:135-139<br />

Previous Hepatitis Exposure Profile<br />

Clinical Information: Hepatitis A Hepatitis A virus (HAV) is an RNA virus (enterovirus) that<br />

accounts for 20% to 25% of the viral hepatitis in United States adults. HAV infection is spread by the<br />

oral/fecal route and produces acute hepatitis that follows a benign, self-limited course. Spread of the<br />

disease is usually associated with contaminated food or water caused by poor sanitary conditions.<br />

Outbreaks frequently occur in overcrowded situations and in institutions or high density centers such as<br />

prisons and health care centers. Epidemics may occur following floods or other disaster situations.<br />

Chronic carriers of HAV have never been observed. Hepatitis B Hepatitis B virus (HBV) is a DNA virus<br />

that is endemic throughout the world. The infection is spread primarily through percutaneous contact with<br />

infected blood products (eg, blood transfusion, sharing of needles by drug addicts). The virus is also found<br />

in virtually every type of human body fluid and is known to be spread through oral and genital contact.<br />

HBV can be transmitted from mother to child during delivery through contact with blood and vaginal<br />

secretions; it is not commonly transmitted transplacentally. After a course of acute illness, HBV persists<br />

in approximately 10% of patients; some of these chronic carriers are asymptomatic. Hepatitis C Hepatitis<br />

C virus (HCV) is an RNA virus that is a significant cause of morbidity and mortality worldwide. HCV is<br />

transmitted through contaminated blood or blood products or through other close, personal contacts. It is<br />

recognized as the cause of most cases of post transfusion hepatitis. HCV shows a high rate of progression<br />

(>50%) to chronic disease. In the United States, HCV infection is quite common, with an estimated 3.5 to<br />

4 million chronic HCV carriers. Cirrhosis and hepatocellular carcinoma are sequelae of chronic HCV.<br />

Publications: -Advances in the Laboratory Diagnosis of Hepatitis C (2002) The following algorithms are<br />

available in Special Instructions: -HBV Infection-Diagnostic Approach and Management Algorithm<br />

-Recommended Approach to the Diagnosis of Hepatitis C -Alternative Approaches to the Diagnosis of<br />

Hepatitis C<br />

Useful For: Determining if an individual has been infected following exposure to an unknown type of<br />

hepatitis Obtaining baseline serologic markers of an individual exposed to a source with an unknown type<br />

of hepatitis Determining immunity to hepatitis A and B viral infections<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 1470

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