Trouver des sites
Pour les horaires, les examens sans rendez-vous ou avec rendez-vous.Synonyms
- Human Calicivirus
- Norwalk Virus
Expected Turnaround Time
4 - 5 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
Related Documents
Specimen Requirements
Specimen
Stool
Volume
1 mL
Minimum Volume
0.2 mL (Note: This volume does not allow for repeat testing.)
Container
Sterile container or Para-Pak® Orange
Storage Instructions
Refrigerate. Samples in Cary-Blair medium (Para-Pak® Orange) can be kept at room temperature.
Stability Requirements
| Temperature | Period |
|---|---|
| Room temperature | Sterile container: 7 days; Cary-Blair medium: 5 days |
| Refrigerated | Sterile container: 7 days; Cary-Blair medium: 14 days |
| Frozen | Sterile container: 7 days; Cary-Blair medium: Unstable |
Causes for Rejection
Quantity not sufficient for analysis; specimen too old; leaking or broken tube; frozen sample in Cary-Blair medium (Para-Pak® Orange)
Test Details
Use
This test is intended to be used as an aid in the diagnosis of infections caused by noroviruses, and to differentiate viruses belonging to Norovirus genogroup 1 (eg, Norwalk virus) and from those belonging to Norovirus genogroup 2 (e.g., Snow Mountain agent).
|
This test is intended to be used as an aid in the diagnosis of infections caused by noroviruses, and to differentiate viruses belonging to Norovirus genogroup 1 (eg, Norwalk virus) and from those belonging to Norovirus genogroup 2 (e |
|
This test is intended to be used as an aid in the diagnosis of infections caused by noroviruses, and to differentiate viruses belonging to Norovirus genogroup 1 (eg, Norwalk virus) and from those belonging to Norovirus genogroup 2 (e.g., Snow Mountain agent). |
Limitations
This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.
|
|
|
This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration. |
Methodology
Real-time reverse transcriptase polymerase chain reaction (RT-PCR)
LOINC® Map
© 2021 Laboratory Corporation of America® Holdings and Lexi-Comp Inc. All Rights Reserved.
CPT Statement/Profile Statement
The LOINC® codes are copyright © 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Permission is granted in perpetuity, without payment of license fees or royalties, to use, copy, or distribute the LOINC® codes for any commercial or non-commercial purpose, subject to the terms under the license agreement found at https://loinc.org/license/. Additional information regarding LOINC® codes can be found at LOINC.org, including the LOINC Manual, which can be downloaded at LOINC.org/downloads/files/LOINCManual.pdf