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HomeLab Services GuideTests
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Overview
ข้อมูลทั่วไป Specimen
ข้อมูลสิ่งส่งตรวจ Performance
ข้อมูลการทดสอบ Clinical & Interpretation
ข้อมูลทางคลินิก
 
Test Code (รหัสการทดสอบ):
090-70-1420-04
Order Name (ชื่อการทดสอบ):
STD, PCR, Vaginal Swab
 
Specimen / Container (สิ่งส่งตรวจ/ภาชนะ):
Vaginal swab/ Universal Transport Media (UTM) 1 mL, 1 tube
 
Turnaround Time (ระยะเวลารอผล):
Received specimen to reported within 3 days.
 
Useful For (ประโยชน์การทดสอบ):
Use for the detection of C. trachomatis (CT), N. gonorrhoeae (NG), M. genitalium (MG), M. hominis (MH), U. urealyticum (UU), U. parvum (UP), and T. vaginalis (TV) from urine and genital swab specimens.
 
Methodology (วิธีการทดสอบ):
Multiplex real-time polymerase chain reaction (PCR)
 
Test List In Profile (การทดสอบใน Profile):
Ureaplasma urealyticum
Neisseria gonorrhoeae
Mycoplasma hominis
Mycoplasma genitalium
Ureaplasma parvum
Chlamydia trachomatis
Trichomonas vaginalis
 
AliasesName (ชื่อเรียกอื่นๆ) :
PCR for Sexual transmitted disease (STD)
STD by PCR
Sexually transmitted infections (STI) assay
PCR for STI
PCR for STD (Vaginal swab)
 
 
 
Test Code (รหัสการทดสอบ):
090-70-1420-04
Order Name (ชื่อการทดสอบ):
STD, PCR, Vaginal Swab
 
Collection Specimen Or Container (สิ่งส่งตรวจ/ภาชนะ):
Vaginal swab/ Universal Transport Media (UTM) 1 mL, 1 tube
 
Specimen Testing Type (สิ่งส่งตรวจที่ใช้ในการทดสอบ):
Vaginal swab/ Universal Transport Media (UTM) 1 mL, 1 tube
 
Sub Mission Container (ภาชนะส่งตรวจ):
Universal Transport Media (UTM) tube
 
Specimen Stabillity (ความคงตัวของสิ่งส่งตรวจ):
Specimen Type Temperature Time
Swab specimen collected in UTM tube Refrigerated, 2oC to 8oC 1 week
 
 
 
Test Code (รหัสการทดสอบ):
090-70-1420-04
Order Name (ชื่อการทดสอบ):
STD, PCR, Vaginal Swab
 
Method detail (วิธีการทดสอบ):
Multiplex real-time polymerase chain reaction (PCR)
 
Schedule (ตารางการทดสอบ):
Monday, Wednesday and Friday, at 09:00 a.m.
 
Turnaround Time (ระยะเวลารอผล):
Received specimen to reported within 3 days.
 
Performing Location (หน่วยงานที่ทำการทดสอบ):
Molecular biology & Genetics, Laboratory Department Tel.14168
 
Specimen Retention Time (ระยะเวลาเก็บสิ่งส่งตรวจ):
7 days
 
 
 
Test Code (รหัสการทดสอบ):
090-70-1420-04
Order Name (ชื่อการทดสอบ):
STD, PCR, Vaginal Swab
 
 
Clinical Information (ข้อมูลทางคลินิก):
The term sexually transmitted diseases (STDs) is used to refer to a variety of clinical syndromes caused by pathogens that can be acquired and transmitted through sexual activity. More than 30 bacterial, viral, and parasitic pathogens are transmissible sexually and constitute a group of infections called to as sexually transmitted infections (STIs). Some STIs can increase the risk of HIV acquisition three-fold or more. STIs can have serious consequences beyond the immediate impact of the infection itself, through mother-to-child transmission of infections and chronic diseases. Further complicating STI diagnosis is that different pathogens can cause similar symptoms, but the antibiotic treatment regimen may differ depending upon the pathogen. This complexity of issues makes simultaneous and accurate STI detection a major key to cost-effective patient care.
 
Reference Value (ค่าอ้างอิง):
Test Reference Value
Ureaplasma urealyticum Not detected
Neisseria gonorrhoeae Not detected
Mycoplasma hominis Not detected
Mycoplasma genitalium Not detected
Ureaplasma parvum Not detected
Chlamydia trachomatis Not detected
Trichomonas vaginalis Not detected
 
Interpretation (การแปลผล):
  1. Reliability of the results depends on adequate specimen collection, storage, transport and processing procedure.
  2. The detection result is dependent on the number of organisms present in the specimen and may be affected by specimen collection methods, patient factors (i.e., age, history of STD, presence of symptoms), stage of infection and/or infecting pathogen strains.
  3. Ureaplasmas and M. hominis should be considered primarily as commensals when detected in the lower genital tract. Although the diagnosis of Ureaplasma spp. and M. hominis in cervical samples is important because these microorganisms could be pathogenic and could be associated with adverse pregnancy outcomes, postpartum sepsis, neonatal systemic inflammatory response syndrome and bronchopulmonary dysplasia.
  4. Interfering substances may affect the detection of this test therefore, the results must be used in conjunction with clinical presentation and other laboratory markers.
 
Clinical Reference (เอกสารอ้างอิง):
Manufacturer’s package insert, AllplexTM STI Essential Assay, January 2019, Seegene, Inc. Seoul 138-050, Korea.