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Clear
 
Test Code (รหัสการทดสอบ):
090-70-0080

Order Name (ชื่อการทดสอบ):
Dengue, PCR

 
Specimen / Container (สิ่งส่งตรวจ/ภาชนะ):
Blood/ K3 EDTA (Lavender Top) 3 mL, 2 tubes
 
Turnaround Time (ระยะเวลารอผล):
Received specimen to reported within 3 hours
 
Useful For (ประโยชน์การทดสอบ):
The assay is intended for the in vitro detection and typing of dengue virus serotypes 1, 2, 3 and 4 in human peripheral blood.
 
Methodology (วิธีการทดสอบ):
Multiplex real-time, reverse transcriptase polymerase chain reaction (RT-PCR) assay
 
AliasesName (ชื่อเรียกอื่นๆ) :
Dengue Fever
Mosquito-borne infection
Dengue, PCR
 
 
 
Test Code (รหัสการทดสอบ):
090-70-0080

Order Name (ชื่อการทดสอบ):
Dengue, PCR

 
Collection Specimen Or Container (สิ่งส่งตรวจ/ภาชนะ):
Blood/ K3 EDTA (Lavender Top) 3 mL, 2 tubes
 
Specimen Testing Type (สิ่งส่งตรวจที่ใช้ในการทดสอบ):
Plasma EDTA, minimum volume 0.5 mL 
Separate plasma within 8 hours of collection.
 
Sub Mission Container (ภาชนะส่งตรวจ):
Plastic tube
 
Rejection Criteria (เกณฑ์ปฏิเสธสิ่งส่งตรวจ):
Gross Hemolysis
Gross Lipemia
Gross Icterus
Heparin blood
 
Specimen Stabillity (ความคงตัวของสิ่งส่งตรวจ):
Specimen Type Temperature Time
Plasma, EDTA Room temperature 8 hours
Refrigerated, 2oC to 8oC 7 days
 
 
 
Test Code (รหัสการทดสอบ):
090-70-0080

Order Name (ชื่อการทดสอบ):
Dengue, PCR

 
Method detail (วิธีการทดสอบ):
Multiplex real-time, reverse transcriptase polymerase chain reaction (RT-PCR) assay
 
Schedule (ตารางการทดสอบ):
24 hours service 
 
Turnaround Time (ระยะเวลารอผล):
Received specimen to reported within 3 hours
 
Performing Location (หน่วยงานที่ทำการทดสอบ):
Molecular biology & Genetics, Laboratory Department Tel.14168
 
Specimen Retention Time (ระยะเวลาเก็บสิ่งส่งตรวจ):
2 months
 
 
 
Test Code (รหัสการทดสอบ):
090-70-0080

Order Name (ชื่อการทดสอบ):
Dengue, PCR

 
 
Clinical Information (ข้อมูลทางคลินิก):
Dengue fever (DF) is an acute, self limiting, viral disease that is characterized by fever, headache, body pains, rash, lymphadenopathy, and prostration. In its most severe form, dengue hemorrhagic fever (DHF), infected patients will experience severe fever and renal failure leading to the often fatal dengue shock syndrome (DSS). There are 4 strains of dengue virus, each serologically distinct. Infection with 1 strain does not protect the host from infection by the others. DHF and DSS occur most commonly in individuals that have been infected previously by another strain. The presence of circulating, non-neutralizing, cross-reactive DV antibody may act as an immune infection enhancement factor. Both dengue virus-specific immunoglobulin G (IgG) and IgM antibodies are usually found in the sera from patients with acute primary infections, while the IgM response may be low or sometimes even absent in secondary dengue fever. Furthermore, a strong cross-reactivity exists among the flavivirus family. As a result, the antibody response may be difficult to interpret with regard to an acute dengue fever, if other flavivirus infections cannot be excluded by clinical, laboratory, or epidemiological means. More recently real-time RT-PCR methods have been developed to detect Dengue virus in the patients’ blood. The detection of dengue virus RNA by reverse transcriptase PCR (RT-PCR) in human blood samples is highly indicative of acute dengue fever. Dengue virus can be detected in the blood from patients for approximately the first 5 days of symptoms.
 
Reference Value (ค่าอ้างอิง):
Not detected
 
Interpretation (การแปลผล):
  1. The detection result is dependant upon proper sample specimen collection, handling, transportation, storage, and preparation, including extraction.
  2. All results from this tests must be correlated with the clinical history, epidemiological data and other data available to the clinician evaluating the patient.
  3. As with other tests, negative results do not rule out dengue virus infections.
  4. False-negative results may occur when the infecting organism has genomic mutations, insertions, deletions, or rearrangements or when performed very early in the course of illness.
  5. False-negative results may occur if inadequate numbers of organisms are present in the specimen due to improper collection, transport or handling.
  6. This test cannot rule out diseases caused by other viral or bacterial pathogens.
 
Clinical Reference (เอกสารอ้างอิง):
Manufacturer’s packages insert, STANDARD™ Arbovirus Panel, April 2023, SD Biosensor Inc, Chungcheongbuk-do 27915, Korea.