Alias

Epic: 6391

Specimen Preparation

Location Specimen Preparation
Amery, Hudson, Lakeview, Methodist Hospital, Regions, Westfields, Hutchinson, Olivia Nasopharyngeal (NP) or nares swab in universal transport medial (UTM), viral transport media (VTM)
Health Partners Central Lab Nasopharyngeal (NP) or Nares swab in UTM, VTM or saline (PBS)

Unacceptable Conditions

Location Unacceptable Conditions
Amery, Hudson, Lakeview, Methodist Hospital, Regions, Westfields, Hutchinson, Olivia Cotton, calcium alginate or swabs with wooden shafts
Swabs without transport media, washes or Eswabs
Specimens collected with expired swabs, expired transport media or leaking containers
Health Partners Central Lab Samples collected with expired swabs or UTM
Specimens received >96 hours from collection

Storage/Transport Temperature

Location Storage/Transport
Amery, Hudson, Lakeview, Methodist Hospital, Regions, Westfields, Hutchinson, Olivia Room temperature: 24 hours; Refrigerated: 7 days
Ship specimens at 2-8 degrees Celsius
Health Partners Central Lab 2-8 degrees Celsius: 4 days
Ship specimens at 2-8 degrees Celsius

Reported

Same day

Notes

Performing Lab: Amery, Health Partners Central Lab, Hudson, Hutchinson Hospital, Lakeview, Methodist Hospital, Regions Hospital, Westfields

Reference Interval

No Influenza A or Influenza B RNA Detected
Results from the Influenza A/B assay should be interpreted in conjunction with other laboratory and clinical data available to the clinician.

Exceptions/Limitations:    
This test has not been evaluated for patients receiving intranasal administered influenza vaccine or for immunocompromised individuals.  
This test has not been evaluated for patients without signs or symptoms of influenza infection.
This test cannot rule out diseases caused by other bacterial or viral pathogens.
Detection of the corresponding virus(es) does not imply they are infectious or are the causative agents for clinical symptoms. Positive results do not rule out bacterial infection or co-infection with other viruses.
False negative results may occur if a specimen is incorrectly collected, transported or handled.  False negative results may occur if inadequate numbers of organisms are present in the specimen.

 

Methodology

Qualitative Real Time Polymerase Chain Reaction (PCR)
 

CPT Codes

87502
Collection

Alias

Epic: 6391

Specimen Preparation

Location Specimen Preparation
Amery, Hudson, Lakeview, Methodist Hospital, Regions, Westfields, Hutchinson, Olivia Nasopharyngeal (NP) or nares swab in universal transport medial (UTM), viral transport media (VTM)
Health Partners Central Lab Nasopharyngeal (NP) or Nares swab in UTM, VTM or saline (PBS)

Unacceptable Conditions

Location Unacceptable Conditions
Amery, Hudson, Lakeview, Methodist Hospital, Regions, Westfields, Hutchinson, Olivia Cotton, calcium alginate or swabs with wooden shafts
Swabs without transport media, washes or Eswabs
Specimens collected with expired swabs, expired transport media or leaking containers
Health Partners Central Lab Samples collected with expired swabs or UTM
Specimens received >96 hours from collection

Storage/Transport Temperature

Location Storage/Transport
Amery, Hudson, Lakeview, Methodist Hospital, Regions, Westfields, Hutchinson, Olivia Room temperature: 24 hours; Refrigerated: 7 days
Ship specimens at 2-8 degrees Celsius
Health Partners Central Lab 2-8 degrees Celsius: 4 days
Ship specimens at 2-8 degrees Celsius

Reported

Same day

Notes

Performing Lab: Amery, Health Partners Central Lab, Hudson, Hutchinson Hospital, Lakeview, Methodist Hospital, Regions Hospital, Westfields
Result Interpretation

Reference Interval

No Influenza A or Influenza B RNA Detected
Results from the Influenza A/B assay should be interpreted in conjunction with other laboratory and clinical data available to the clinician.

Exceptions/Limitations:    
This test has not been evaluated for patients receiving intranasal administered influenza vaccine or for immunocompromised individuals.  
This test has not been evaluated for patients without signs or symptoms of influenza infection.
This test cannot rule out diseases caused by other bacterial or viral pathogens.
Detection of the corresponding virus(es) does not imply they are infectious or are the causative agents for clinical symptoms. Positive results do not rule out bacterial infection or co-infection with other viruses.
False negative results may occur if a specimen is incorrectly collected, transported or handled.  False negative results may occur if inadequate numbers of organisms are present in the specimen.

 

Methodology

Qualitative Real Time Polymerase Chain Reaction (PCR)
 
Administrative

CPT Codes

87502