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HBAB<br />

8254<br />

variability in HBIG dosage required to achieve desirable serum anti-HBs levels among transplant<br />

recipients during the first few weeks to months after transplantation. Patients who were hepatitis B<br />

envelope (HBe) antigen positive before transplantation usually require more HBIG to achieve the target<br />

anti-HBs levels, especially in the first week after transplantation. Duration of HBIG therapy varies from 6<br />

months to indefinite among different US liver transplant programs. Protocols providing 500 mIU/mL during the first week after transplantation, >250<br />

mIU/mL during weeks 2 to 12, and >100 mIU/mL after week 12. See HBV Infection-Monitoring Before<br />

and After Liver Transplantation in Special Instructions.<br />

Reference Values:<br />

Negative<br />

Clinical References: 1. Samuel D: Management of hepatitis B in liver transplant patients. Semin<br />

Liver Dis 2004;24(suppl 1):55-62 2. Terrault NA, Vyas G: Hepatitis B immune globulin preparations and<br />

use in liver transplantation. Clin Liver Dis 2003;7:537-550 3. Lok AS: Prevention of recurrent hepatitis B<br />

post-liver transplantation. Liver Transpl 2002;8:S67-S73<br />

Hepatitis B Surface Antibody, Qualitative/Quantitative, Serum<br />

Clinical Information: Hepatitis B virus (HBV) infection, also known as serum hepatitis, is endemic<br />

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

products, eg, blood transfusion and sharing of needles by drug addicts. The virus is also found in virtually<br />

every type of human body fluid and has been known to be spread through oral and genital contact. HBV<br />

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

secretions, but is not commonly transmitted via the transplacental route. The incubation period for HBV<br />

infection averages 60 to 90 days (range of 45-180 days). Common symptoms include malaise, fever,<br />

gastroenteritis, and jaundice (icterus). After acute infection, HBV infection becomes chronic in 30% to<br />

90% of infected children or =5 years of age.<br />

Some of these chronic carriers are asymptomatic, while others progress to chronic liver disease, including<br />

cirrhosis and hepatocellular carcinoma. Hepatitis B surface antigen (HBsAg) is the first serologic marker,<br />

appearing in the serum 6 to 16 weeks following HBV infection. In acute cases, HBsAg usually disappears<br />

1 to 2 months after the onset of symptoms with the appearance of hepatitis B surface antibody (anti-HBs).<br />

Anti-HBs also appears as the immune response following hepatitis B vaccination. See The Laboratory<br />

Approach to the Diagnosis and Monitoring of Hepatitis B Infection in Publications and HBV<br />

Infection–Diagnostic Approach and Management Algorithm in Special Instructions.<br />

Useful For: Identifying previous exposure to hepatitis B virus Determining adequate immunity from<br />

hepatitis B vaccination<br />

Interpretation: This assay provides both qualitative and quantitative results. Positive results usually<br />

indicate recovery from acute or chronic hepatitis B virus (HBV) infection, or acquired immunity from<br />

HBV vaccination. Positive results (quantitative hepatitis B surface antibody [anti-HBs] levels of > or =12<br />

mIU/mL) indicate an adequate immunity to hepatitis B from previous HBV infection or HBV vaccination.<br />

Negative results (quantitative anti-HBs levels of or =5-12 mIU/mL) indicate inability to determine if<br />

anti-HBs is present at levels consistent with recovery or immunity. Repeat testing is recommended in 1 to<br />

3 months. See The Laboratory Approach to the Diagnosis and Monitoring of Hepatitis B Infection in<br />

Publications and HBV Infection-Diagnostic Approach and Management Algorithm in Special<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 891

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