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Test Code (รหัสการทดสอบ):
CMVAB

Order Name (ชื่อการทดสอบ):
CMV 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):
Determination of IgG antibodies to Cytomegalovirus in human serum.
 
Methodology (วิธีการทดสอบ):
Chemiluminescent Microparticle Immuno Assay (CMIA)
 
AliasesName (ชื่อเรียกอื่นๆ) :
Cytomegalovirus Antibody IgG
Cytomegalovirus  IgG
 
 
 
Test Code (รหัสการทดสอบ):
CMVAB

Order Name (ชื่อการทดสอบ):
CMV IgG 

 
Collection Specimen Or Container (สิ่งส่งตรวจ/ภาชนะ):
Blood/ Plain Blood (Red Top) 6 mL, 1 tube
 
Specimen Testing Type (สิ่งส่งตรวจที่ใช้ในการทดสอบ):
Serum, minimum volume 2 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) Refrigerated, 2oC to 8oC 8 hours
Serum Refrigerated, 2oC to 8oC 14 days
Frozen, -20oC 1 month
 
 
 
Test Code (รหัสการทดสอบ):
CMVAB

Order Name (ชื่อการทดสอบ):
CMV IgG 

 
Method detail (วิธีการทดสอบ):
Chemiluminescent Microparticle Immuno Assay (CMIA)
 
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):
CMVAB

Order Name (ชื่อการทดสอบ):
CMV IgG 

 
 
Clinical Information (ข้อมูลทางคลินิก):
Infections with Cytomegalovirus (CMV), a member of the herpesvirus family, are common in man and are usually mild and asymptomatic. However, in pregnant women, newborns, and immunocompromised individuals CMV infections may pose a significant medical risk.

The provision of seronegative blood products to selected patients remains a vital consideration in patient management. Serologic tests can be used to identify seronegative individuals5 and seronegative donors of organs or blood products. In utero infection may result in sequelae of varying degree including mental retardation, chorioretinitis, hearing loss and neurologic problems. Since the risk of in utero virus transmission
and CMV related damage of the fetus is strongly increased during primary infection, reliable recognition of primary CMV infections is of high importance for pregnant women. Thus, the presence of CMV-specific IgG antibody does not assure protection from disease. An individual may undergo primary infection with CMV, reinfection with exogenous virus or reactivation of latent virus.

If primary infection needs to be excluded, CMV IgG reactive samples should be tested for CMV IgM and CMV IgG Avidity. A positive CMV IgM result in connection with low avidity result is a strong indicator of a primary CMV infection within the last 4 months.  A substantial rise in anti-CMV IgG concentrations in sequential
samples taken from an individual accompanied by the presence of anti-CMV IgM could also indicate serological evidence of active infection.
 
Reference Value (ค่าอ้างอิง):
Non reactive
 
Clinical Reference (เอกสารอ้างอิง):
Manufacturer’s Reagent package insert, Architect CMV IgM, March 2015, Abbott Ireland Diagnostics Division, Finisklin Business Park, Sligo, Ireland.