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ข้อมูลทั่วไป Specimen
ข้อมูลสิ่งส่งตรวจ Performance
ข้อมูลการทดสอบ Clinical & Interpretation
ข้อมูลทางคลินิก

Test Code (รหัสการทดสอบ):

090-70-0061

Order Name (ชื่อการทดสอบ):

HPV Genotype (Cervix)

Specimen / Container (สิ่งส่งตรวจ/ภาชนะ):

Cervical cells/ PreservCyt^® (ThinPrep liquid PAP vial) 20 mL, 1 vial

Turnaround Time (ระยะเวลารอผล):

Received specimen to reported within 4 days.

Useful For (ประโยชน์การทดสอบ):

Use for the detection of human papillomaviruses DNA of 19 high-risk and 9 low-risk types in liquid based cytology

Methodology (วิธีการทดสอบ):

Multiplex real-time polymerase chain reaction (PCR) and Melting Temperature Analysis

AliasesName (ชื่อเรียกอื่นๆ) :

Human Papillomavirus (HPV) Genotyping
HPV (Human Papillomavirus) PCR
High Risk HPV
Low Risk HPV

Test Code (รหัสการทดสอบ):

090-70-0061

Order Name (ชื่อการทดสอบ):

HPV Genotype (Cervix)

Collection Specimen Or Container (สิ่งส่งตรวจ/ภาชนะ):

Cervical cells/ PreservCyt^® (ThinPrep liquid PAP vial) 20 mL, 1 vial

Specimen Testing Type (สิ่งส่งตรวจที่ใช้ในการทดสอบ):

Cervical cells in PreservCyt^®solution, minimum volume 3 mL

Sub Mission Container (ภาชนะส่งตรวจ):

Plastic tube

Rejection Criteria (เกณฑ์ปฏิเสธสิ่งส่งตรวจ):

Specimen volume less than 3 mL will be reject.

Specimen Stabillity (ความคงตัวของสิ่งส่งตรวจ):

Specimen Type	Temperature	Time
Cervical cells in PreservCyt^®solution	Room temperature or Refrigerated, 2^oC to 8^oC	90 days

Test Code (รหัสการทดสอบ):

090-70-0061

Order Name (ชื่อการทดสอบ):

HPV Genotype (Cervix)

Method detail (วิธีการทดสอบ):

Multiplex real-time polymerase chain reaction (PCR) and Melting Temperature Analysis

Schedule (ตารางการทดสอบ):

Thursday and Sunday, at 09:00 a.m.

Turnaround Time (ระยะเวลารอผล):

Received specimen to reported within 4 days.

Performing Location (หน่วยงานที่ทำการทดสอบ):

Molecular biology & Genetics, Laboratory Department Tel.14168

Specimen Retention Time (ระยะเวลาเก็บสิ่งส่งตรวจ):

30 days

Test Code (รหัสการทดสอบ):

090-70-0061

Order Name (ชื่อการทดสอบ):

HPV Genotype (Cervix)

Clinical Information (ข้อมูลทางคลินิก):

Human Papilloma Virus (HPV) infection is linked with cervical cancer. HPV can be divided into “high-risk (HR)” and “low-risk (LR)” groups on the basis of their association with cervical lesions. Therefore, it is very important to know which type of HPV is infected in patients to prevent cancer development and transmission of disease. Cervical cancer, which progresses from the precancerous stage to invasive cancer, has 7-20 years of precancerous stage; consequently early diagnosis is possible when HPV infection is suspected. High-risk HPV group may lead to the development of cervical cancer; especially, HPV16 and 18 are associated with 70% of cervical cancer case. On the other hands, low-risk HPV group including HPV6 and 11 may cause genital warts.

Reference Value (ค่าอ้างอิง):

Negative

Interpretation (การแปลผล):

This test can identify 19 high-risk HPV types (16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 69, 73, 82) and also detect for 9 low-risk HPV types (6, 11, 40, 42, 43, 44, 54, 61, 70)
Reliable results are dependent on adequate specimen collection, transport, storage and processing procedures.
The detection of HPV is dependent on the number of organisms present in the specimen and may be affected by specimen collection methods, patient factors and stage of infection.
Mutations or polymorphisms in primer- or probe-binding regions may affect detection of HPV DNA, resulting in a false negative result.

Clinical Reference (เอกสารอ้างอิง):

Manufacturer’s package insert, Anyplex^TM II HPV28 Detection, January 2019, Seegene, Inc. 138-050 Seoul, Korea