Parainfluenza 1-4 by PCR

2006247
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Example Reports
Detected
Not Detected

Ordering Recommendation

Detect parainfluenza types 1-4.

Mnemonic

PARAFLUPCR

Methodology

Qualitative Polymerase Chain Reaction

Performed

Mon, Wed, Fri

Reported

1-5 days

New York DOH Approval Status

This test is New York DOH approved.

Specimen Required

Patient Preparation
Collect

Bronchoalveolar lavage (BAL), nasal wash, nasopharyngeal swab or sputum.

Specimen Preparation

Fluid: Transfer 2 mL respiratory specimen to a sterile container. (Min: 0.5 mL) Also acceptable: Transfer to viral transport media (ARUP supply #12884). Available online through eSupply using ARUP Connect™ or contact ARUP Client Services at (800) 522-2787. Swabs: Place in viral transport media.

Storage/Transport Temperature

Frozen.

Unacceptable Conditions
Remarks

Specimen source required.

Stability

Ambient: Unacceptable; Refrigerated: 4 days; Frozen: 1 month

Reference Interval

Interpretive Data

A negative result does not rule out the presence of PCR inhibitors in the patient specimen or test-specific nucleic acid in concentrations below the level of detection by this assay.

Compliance Category

Depends on Specimen/Source/Method

Note

Hotline History

View Hotline History

 

Hotline History

Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
08/16/2021
X
N/A

CPT Codes

87631

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Components

Component Test Code* Component Chart Name LOINC
2006248 Parainfluenza Source 31208-2
2006249 Parainfluenza 1 by PCR 29908-1
2006250 Parainfluenza 2 by PCR 29909-9
2006251 Parainfluenza 3 by PCR 29910-7
2006252 Parainfluenza 4 by PCR 41010-0
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • Paraflu 1-4 PCR
Parainfluenza 1-4 by PCR