Test ID: Anti- HAV Total
|
Hepatitis A Total Antibody
|
Detection of HAV Antibody (total) in Blood
|
Useful For
|
Aid in diagnosis of Hepatitis A infection; detection of previous exposure to HAV and long-lasting acquired immunity.
|
Method name and description
|
Indirect sandwich chemiluminescence immunoassay (CLIA)
In the presence of complimentary antigen and antibody, the antibody binds to the antigen to form an antigen-antibody or an immune complex.The light signal, the amount of isoluminol-antibody conjugate, is measured by a photomultiplier as relative light units (RLU) and is indicative of analyte concentration present in calibrators, samples or controls.
|
Clinical information
|
The hepatitis A virus is a Heparnavirus of the Picornaviridae family causing Hepatitis A infection. The virus, which is transmitted primarily by the foecal-oral route, is spread by close person-to-person contact and by food- and water-borne epidemics. There is little or no evidence of transplacental transmission from mother to fetus or transmission to newborn during delivery. Common symptoms include malaise, loss of appetite, nausea and icterus. Symptoms, which are often mild and even subclinical, usually resolve within two to four weeks of onset. Recovery is complete, with no chronic sequelae, and long-lasting, usually lifelong, immunity results. The hepatitis A antigen (HAV antigen) is present in stool about one to two weeks before onset of clinical symptoms and for about one week afterwards. After HAV antigen is no longer detectable in stool, antibodies to HAV antigen (anti-HAV) are found in serum and persist for the life of the patient, conferring long-lasting immunity to HAV reinfection.
|
|
Specimen type / Specimen volume / Specimen container
|
Specimen type: Serum, Plasma
Minimum volume of sample: 1 mL
Serum: Plain tube (red or yellow top)
Plasma: Li-Heparin tube
|
Collection instructions / Special Precautions / Timing of collection
|
Collect blood by standard venipuncture techniques as per specimen requirements. When processing samples in primary tubes (sample collection systems), follow the instructions of the tube manufacturer.
Do not use plasma specimens obtained with CPD (citrate + phosphate + dextrose) as an anticoagulant.
|
Storage and transport instructions
|
Storage: 7 days at 2 – 8°C;
Transport: 2-25°C
|
Specimen Rejection Criteria
|
Grossly hemolyzed, icteric and lipemic samples, wrong collection container, insufficient sample and heat‑inactivated samples.
|
|
Biological reference intervals and clinical decision values
|
Unit |
Result |
Result Message |
Interpretation / Further steps |
Index Value |
>=1.1 |
Negative |
Negative for Anti-HAV, No further testing needed |
Index Value |
>=0.9 to < 1.1 |
Equivocal |
Equivocal samples should be verified as equivocal & comment will be added automatically by system |
Index Value |
<0.9 |
Positive |
Postive for Anti-HAV, if suspected acute infection HAV IgM should be performed |
|
Turnaround time / Days and times test performed / Specimen retention time
|
Daily (24/7)
Turn-around time:
Routine: One working day
Specimen Retention: 4 days
|
|
|