bih.button.backtotop.text
BROWSE BY TEST NAME
#
%
1
2
3
5
8
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
Clear
 
Test Code (รหัสการทดสอบ):
090-70-1450

Order Name (ชื่อการทดสอบ):
Gastrointestinal Pathogen Panel (GPP) by Film array, Stool

 
Specimen / Container (สิ่งส่งตรวจ/ภาชนะ):
Stool/ Clean container
 
Turnaround Time (ระยะเวลารอผล):
Specimen is received during 8.00 am to 8.00 pm, the result will be reported within 3 hours.
*If specimen is received after 8.00 pm, the result will be reported at 10.00 am in the next day.
 
Useful For (ประโยชน์การทดสอบ):
The test is capable of the simultaneous detection and identification of nucleic acids from multiple bacteria, viruses, and parasites directly from stool samples obtained from individuals with signs and/or symptoms of gastrointestinal infection.
 
Methodology (วิธีการทดสอบ):
  1. Multiplex and Nested Polymerase Chain Reaction (PCR)
  2. High Resolution Melting Analysis
 
Test List In Profile (การทดสอบใน Profile):
Campylobacter (C. jejuni/C. coli/C. upsaliensis)
Clostridium difficile toxin A/B
Plesiomonas shigelloides
Salmonella
Vibrio (V. parahaemolyticus/V. vulnificus/ V. cholerae)
Vibrio cholera
Yersinia enterocolitica
Enteroaggregative E. coli (EAEC)
Enteropathogenic E. coli (EPEC)
Enterotoxigenic E. coli (ETEC)
Shiga-like toxin-producing E. coli (STEC) 
E. coli O157
Shigella/ Enteroinvasive E. coli (EIEC) 
Cryptosporidium
Cyclospora cayetanensis
Entamoeba histolytica
Giardia lamblia   

Adenovirus F 40/41
Astrovirus
Norovirus GI/GII
Rotavirus A
Sapovirus
 
AliasesName (ชื่อเรียกอื่นๆ) :
GPP
GI panel by film array
FilmArray Gastrointestinal (GI) Panel
Gastrointestinal Infections
 
 
 
 
Test Code (รหัสการทดสอบ):
090-70-1450

Order Name (ชื่อการทดสอบ):
Gastrointestinal Pathogen Panel (GPP) by Film array, Stool

 
Collection Specimen Or Container (สิ่งส่งตรวจ/ภาชนะ):
Stool/ Clean container
 
Specimen Testing Type (สิ่งส่งตรวจที่ใช้ในการทดสอบ):
Stool/ liquid Cary Blair medium (Copan FecalSwab collection)
 
Sub Mission Container (ภาชนะส่งตรวจ):
Liquid Cary Blair medium
 
Rejection Criteria (เกณฑ์ปฏิเสธสิ่งส่งตรวจ):
  1. Stool older than 24 hr.
  2. Stool collected in liquid Cary Blair medium older than 96 hours.
 
Specimen Stabillity (ความคงตัวของสิ่งส่งตรวจ):
Specimen Type Temperature Time
Stool collected in liquid Cary Blair medium Room temperature or Refrigerated, 2oC to 8oC  96 hours
 
 
 
Test Code (รหัสการทดสอบ):
090-70-1450

Order Name (ชื่อการทดสอบ):
Gastrointestinal Pathogen Panel (GPP) by Film array, Stool

 
Method detail (วิธีการทดสอบ):
1. Multiplex and Nested Polymerase Chain Reaction (PCR)
2. High Resolution Melting Analysis
 
Turnaround Time (ระยะเวลารอผล):
Specimen is received during 8.00 am to 8.00 pm, the result will be reported within 3 hours.
*If specimen is received after 8.00 pm, the result will be reported at 10.00 am in the next day.
 
Performing Location (หน่วยงานที่ทำการทดสอบ):
Molecular biology & Genetics, Laboratory Department Tel.14168
 
Specimen Retention Time (ระยะเวลาเก็บสิ่งส่งตรวจ):
7 days
 
 
 
Test Code (รหัสการทดสอบ):
090-70-1450

Order Name (ชื่อการทดสอบ):
Gastrointestinal Pathogen Panel (GPP) by Film array, Stool

 
 
Clinical Information (ข้อมูลทางคลินิก):
Despite advances in food safety, sanitation, and medical treatment, infectious gastroenteritis remains a significant problem in industrialized countries among all age groups. Globally, infectious diarrheal illness is a significant cause of mortality in young children resulting in an estimated 800,000 deaths per year in children under the age of 5. In addition to this significant morbidity and mortality, diarrhea in children contributes to malnutrition, increased susceptibility to other infections, and may lead to delays in growth and intellectual development. The FilmArray GI Panel simultaneously tests for 22 pathogens from stool specimens. Results from the FilmArray GI Panel test are available within about one hour.
 
Reference Value (ค่าอ้างอิง):
Test Reference Value
Campylobacter (C. jejuni/C. coli/C. upsaliensis)  Not Detected
Clostridium difficile toxin A/B  Not Detected
Plesiomonas shigelloides  Not Detected
Salmonella  Not Detected
Vibrio (V. parahaemolyticus/V. vulnificus/ V. cholerae)  Not Detected
Vibrio cholera  Not Detected
Yersinia enterocolitica  Not Detected
Enteroaggregative E. coli (EAEC)   Not Detected
Enteropathogenic E. coli (EPEC)  Not Detected
Enterotoxigenic E. coli (ETEC)  Not Detected
Shiga-like toxin-producing E. coli (STEC)  Not Detected
E. coli O157     Not Detected
Shigella/ Enteroinvasive E. coli (EIEC)   Not Detected
Cryptosporidium  Not Detected
Cyclospora cayetanensis  Not Detected
Entamoeba histolytica  Not Detected
Giardia lamblia  Not Detected
Adenovirus F 40/41  Not Detected
Astrovirus   Not Detected
Norovirus GI/GII  Not Detected
Rotavirus A  Not Detected
Sapovirus   Not Detected
 
Interpretation (การแปลผล):
This test is a qualitative test and does not provide a quantitative value for the organism(s) in the sample. Virus, bacteria, and parasite nucleic acid may persist in vivo independently of organism viability. Additionally, some organisms may be carried asymptomatically. Detection of organism targets does not imply that the corresponding organisms are infectious or are the causative agents for clinical symptoms. Results from this test must be correlated with the clinical history, epidemiological data, and other data available to the clinician evaluating the patient. Due to high rates of asymptomatic carriage of Clostridium difficile, especially in very young children and hospitalized patients, the detection of toxigenic C. difficile should be interpreted within the context of guidelines developed by the testing facility or other experts (e.g., guidelines/policy statements published by The American Academy of Pediatrics or the Society for Healthcare Epidemiology of America and the Infectious Disease Society of America). The performance of this test has not been established for monitoring treatment of infection with any of the panel organisms.
 
Clinical Reference (เอกสารอ้างอิง):
Manufacturer’s package inserts. FilmArray Gastrointestinal (GI) Panel, June 2017, BioFire Diagnostis, Salt Lake City, UT 84108, USA.