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Test Code (รหัสการทดสอบ):
090-30-0780-01

Order Name (ชื่อการทดสอบ):
Toxoplasma IgG

 
Specimen / Container (สิ่งส่งตรวจ/ภาชนะ):
Blood/ Plain Blood (Red Top) 6 mL, 1 tube
 
Turnaround Time (ระยะเวลารอผล):
Specimen collected to reported within 2:00 Hours (120 Mins)
 
Useful For (ประโยชน์การทดสอบ):
Determine the quantitative of IgG antibodies to Toxoplasma gondii  in human serum.
 
Methodology (วิธีการทดสอบ):
Chemiluminescent Microparticle Immuno Assay (CMIA)
 
AliasesName (ชื่อเรียกอื่นๆ) :
Toxoplasma gondii IgG
Toxoplasma gondii IgG antibody
 
 
 
Test Code (รหัสการทดสอบ):
090-30-0780-01

Order Name (ชื่อการทดสอบ):
Toxoplasma IgG

 
Collection Specimen Or Container (สิ่งส่งตรวจ/ภาชนะ):
Blood/ Plain Blood (Red Top) 6 mL, 1 tube
 
Specimen Testing Type (สิ่งส่งตรวจที่ใช้ในการทดสอบ):
Serum, minimum volume 1 mL
 
Sub Mission Container (ภาชนะส่งตรวจ):
Plastic vial
 
Rejection Criteria (เกณฑ์ปฏิเสธสิ่งส่งตรวจ):
Hemolysis: 4+ reject
 
Specimen Stabillity (ความคงตัวของสิ่งส่งตรวจ):
Specimen Type Temperature Time
Serum (keep in original tube) Room temperature, 20oC to 28oC 8 hours
Serum Refrigerated, 2oC to 8oC 14 days
Frozen, -10oC 1 month
 
 
 
Test Code (รหัสการทดสอบ):
090-30-0780-01

Order Name (ชื่อการทดสอบ):
Toxoplasma IgG

 
Schedule (ตารางการทดสอบ):
Tested Daily (24 Hours)
 
Turnaround Time (ระยะเวลารอผล):
Specimen collected to reported within 2:00 Hours (120 Mins)
 
Performing Location (หน่วยงานที่ทำการทดสอบ):
Immunology, Laboratory Department Tel. 13227
 
Specimen Retention Time (ระยะเวลาเก็บสิ่งส่งตรวจ):
5 days
 
 
 
Test Code (รหัสการทดสอบ):
090-30-0780-01

Order Name (ชื่อการทดสอบ):
Toxoplasma IgG

 
 
Clinical Information (ข้อมูลทางคลินิก):
Toxoplasma gondii is an obligate intracellular protozoan parasite that infects most species of warm-blooded animals, including humans. Toxoplasmosis is primarily acquired by ingestion of undercooked, infected meat; via oocysts from fecally contaminated hands, food and water; and maternally through transplacental transmission. In addition, transmission associated with organ transplantation and during blood transfusion has been reported, although the risk of transmission through blood transfusion is extremely low.

Acquired infection with Toxoplasma gondii in healthy individuals is commonly asymptomatic, however 10-20 % of patients with acute infection may develop lymphadenopathy . Severe infections can occur in AIDS patients and adults immunocompromised by cancer chemotherapy or transplant recipients receiving immunosuppressive treatment. These infections can be fatal. Toxoplasmic encephalitis is the most common presentation and is the most frequent cause of focal central nervous system lesions in AIDS patients.

Primary infection during pregnancy can result in transplacental transmission of the parasite resulting in congenital infection. The risk of congenital infection is lowest (10-25%) if acute maternal infection occurs during the first trimester and highest (60-90%) if it occurs during the third trimester.  Severity of congenital infection is greatest when maternal infection is acquired early during pregnancy. Common outcomes of congenital
toxoplasmosis include chorioretinitis, intracranial calcifications  and hydrocephalus. The majority of infants infected later in pregnancy are asymptomatic at birth, with sequelae occurring later in life.

Early treatment after prenatal diagnosis of Toxoplasma gondii infection has been shown to reduce the frequency and severity of congenital toxoplasmosis6. Serological tests can be used to identify seronegative women who then should be monitored during pregnancy.

The presence of IgG antibodies to Toxoplasma gondii indicates that infection has occurred but does not distinguish between recent and past infection. IgM antibodies are detected in individuals with a recently acquired infection, but antibodies may persist for up to 18 months post-infection. To differentiate between a recently acquired and a past infection, IgM and IgG positive specimens should be tested for IgG avidity. A high avidity index for IgG antibodies is a strong indication that an infection took place more than 4 months ago.
 
Reference Value (ค่าอ้างอิง):
Non reactive
 
 
Clinical Reference (เอกสารอ้างอิง):
Manufacturer’s Reagent package insert, Architect Toxo IgG, November 2014, Abbott Laboratories, MAX-Planck-Ring 65205 Wiesbaden, Germany.