L00149033_-2
L00149033_-2
DEPARTMENT OF IMMUNOLOGY
Test Name Result Unit Bio. Ref. Interval Method
HBsAg Australia Antigen ELISA) 0.061 AU/ml <1.0 Non Reactive CLIA
Sample:Serum >1.0 Reactive
Interpretation:
This is the initial detectable marker found in serum in the incubation period of HBV infection. The titer of HbsAg peaks at or
shortly after the on set of elevated serum enzymes. The clinical improvement and decrease in enzyme concentration is paralleled by
fall in HbsAg titers and subsequently disappearance. The duration of HbsAg Reactive is variable depending upon the clinical
course of disease. HbsAg is detected in serum a month after the exposure, peaking in the preicteric phase and disappearing 1 - 13
weeks after the onset of enzyme abnormalities. Persistence of HbsAg after the complete clinical recovery indicates a carrier state.
Vaccination against HBV does not cause HbsAg Reactive. Causes of HbsAg Reactive are acute HBV infection and reactivation of
chronic HBV infection. Results with value <0.178 will be given as Non Reactive.
Interpretation:
The hepatitis C virus HCV is now the cause of 90% post transfusion hepatitis it is also found in drug addicts and also contributes
to sporadic acute viral hepatitis –HCV is a RNA flavi virus and the incubation period may be short (1-4 weeks ) or long ( 6-12
weeks . chronicity of infection is reported in > 10 % . The frequency of post transfusion hepatitis can be definitely reduced with
help of serological assays available for HCV. Results with value <0.333 will be given as Non Reactive.
Note: - HCV RNA test by using PCR Assay is helpful as an additional or confirmatory test.
Interpretation:
1)A Non Reactive result implies that no Anti HIV – II antibodies have been detected in the sample by this method. This means that
either the patient has not been exposed to HIV-I or HIV-II infection or the sample has been tested during the “WINDOW
PHASE” (before the development of detectable levels of antibodies)
2)A Reactive result suggests the possibilities of HIV-I and / or HIV-II infection. However these results must be verified by a
confirmatory test (IFA / WESTERN BLOT I-II) before pronouncing the patient REACTIVEfor HIV-I and / r HIV-II infection.
Results with value <0.293 will be given as NON REACTIVE.
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SIN No:67894203
CHANDAN SPECIALITY LAB
Add: Biotech Park,Sec. G, Jankipuram, Lucknow
Ph: 7390005444,05226666600
CIN: U85110UP2003PLC193493
DEPARTMENT OF IMMUNOLOGY
Test Name Result Unit Bio. Ref. Interval Method
This report is not for medico legal purpose. If clinical correlation is not established, kindly repeat the test at no additional cost within seven days.
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SIN No:67894203