Ordering Recommendation

Detect M. pneumoniae bacteria.

New York DOH Approval Status

This test is New York state approved.

Specimen Required

Patient Preparation
Collect

Respiratory specimen: Bronchoalveolar lavage (BAL), bronchial brushings, nasopharyngeal swab, sputum, tracheal aspirates, or pleural fluid.
OR CSF.

Specimen Preparation

CSF: Transfer 1 mL CSF to a sterile container. (Min: 0.5 mL).
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(TM) or contact ARUP Client Services at 800-522-2787
Swabs: Place in viral transport media. Place each specimen in an individually sealed bag.

Storage/Transport Temperature

Preferred transport temp: Frozen.

Unacceptable Conditions

Tissues in optimal cutting temperature compound.

Remarks

Specimen source required .

Stability

Room temperature: 1 day; Refrigerated: 5 days; Frozen: 1 year.

Methodology

Qualitative Polymerase Chain Reaction (PCR)

Performed

Mon, Wed, Fri

Reported

1-4 days

Reference Interval

Interpretive Data



Compliance Category

Laboratory Developed Test (LDT)

Note

Hotline History

N/A

CPT Codes

87581

Components

Component Test Code* Component Chart Name LOINC
0060256 Mycoplasma pneumoniae by PCR 29257-3
0060259 Mycoplasma pneumoniae Source 31208-2
* 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

  • Mycoplasma by PCR
  • Mycoplasma pneumoniae DNA PCR
Mycoplasma pneumoniae by PCR