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Test Code (รหัสการทดสอบ):
090-70-8501-01

Order Name (ชื่อการทดสอบ):
ANA (ANF),  (IFA method)

 
Specimen / Container (สิ่งส่งตรวจ/ภาชนะ):
Blood/ Plain blood (Red top) 6 mL, 1 tube
 
Turnaround Time (ระยะเวลารอผล):
Received specimen to reported within 2 days
 
Useful For (ประโยชน์การทดสอบ):
Diagnosis of a systemic rheumatic disease in the suspected patient.
 
Methodology (วิธีการทดสอบ):
Indirect immunofluorescence assay
 
AliasesName (ชื่อเรียกอื่นๆ) :
ANA (Antinuclear Antibodies)
Antinuclear Antibodies (ANA), HEp-2 substrate, Serum
Antinuclear Antibody, Serum
FANA (fluorescent antinuclear antibodies)
ANA IFA
ANA IF
 
 
 
Test Code (รหัสการทดสอบ):
090-70-8501-01

Order Name (ชื่อการทดสอบ):
ANA (ANF),  (IFA method)

 
Collection Specimen Or Container (สิ่งส่งตรวจ/ภาชนะ):
Blood/ Plain blood (Red top) 6 mL, 1 tube
 
Specimen Testing Type (สิ่งส่งตรวจที่ใช้ในการทดสอบ):
Serum, minimum volume 0.5 mL
 
Sub Mission Container (ภาชนะส่งตรวจ):
Plastic tube
 
Rejection Criteria (เกณฑ์ปฏิเสธสิ่งส่งตรวจ):
Hemolysis: N/A
Lipemia: N/A
Icterus: N/A
Other: Heat-treated specimen will be reject.
 
Specimen Stabillity (ความคงตัวของสิ่งส่งตรวจ):
Speciment Type Temperature Time
Serum Refrigerated, 2oC to 8oC 14 days
 
 
 
Test Code (รหัสการทดสอบ):
090-70-8501-01

Order Name (ชื่อการทดสอบ):
ANA (ANF),  (IFA method)

 
Method detail (วิธีการทดสอบ):
Indirect immunofluorescence assay
 
Schedule (ตารางการทดสอบ):
Test daily, at 03:00 p.m.
 
Turnaround Time (ระยะเวลารอผล):
Received specimen to reported within 2 days
 
Performing Location (หน่วยงานที่ทำการทดสอบ):
Molecular biology & Genetics, Laboratory Department Tel.14168
 
Specimen Retention Time (ระยะเวลาเก็บสิ่งส่งตรวจ):
7 days
 
 
 
Test Code (รหัสการทดสอบ):
090-70-8501-01

Order Name (ชื่อการทดสอบ):
ANA (ANF),  (IFA method)

 
 
Clinical Information (ข้อมูลทางคลินิก):
The detection of antinuclear antibodies (ANAs) by indirect immunofluorescence are nowadays predominantly tested using for screening in the patients suspected of having an autoimmune disease, particularly of the rheumatic form.

Autoantibodies against nuclear antigens occur in many disease such as systemic lupus erythematosus (SLE), Sharp's syndrome, rheumatoid arthritis, progressive systemic sclerosis, polymyositis/dermatomyositis.  The diagnosis of a systemic rheumatic disease is based primarily on the presence of compatible clinical signs and symptoms. The results of tests for autoantibodies including ANA and specific autoantibodies are ancillary. Additional diagnostic criteria include consistent histopathology or specific radiographic findings.
 
Reference Value (ค่าอ้างอิง):
Negative
 
Interpretation (การแปลผล):
The frequency (prevalence) of anti-nuclear antibodies in inflammatory rheumatic disease is between 20% and 100%, the lowest occuring in rheumatoid arthritis at between 20% and 40%. Therefore, differential antibody diagnostics against nuclear antigens is indispensible for the identification of individual rheumatic diseases and their differentiation from other autoimmune disease.  At times, antibodies against nuclear antigens are detectable in subjectively healthy individuals, usually at a low titer.  This finding is more common in women than men and the frequency of a detectable ANA in healthy women over 40 years of age may approach 15% to 20%. ANA may be detectable after viral illnesses, in chronic infections, or in patients treated with some kind of medications.  A diagnosis should not be made on a single test result. The clinical symptoms of the patient should alway be taken into account along with the serological results by the physician.  
 
Clinical Reference (เอกสารอ้างอิง):
Manufacturer’s package insert, Mosaic HEp-20-10/Liver (Monkey) Instruction for the indirect immunofluorescencetest, January 2017, EUROIMMUN, D-23560 Lübeck Germany.