Test Code MYCO Mycoplasma pneumoniae Antibodies, IgG and IgM, Serum
Additional Codes
Torrance Memorial Laboratories Test Code: 62873039
Ordering Guidance
Detection of IgM or IgG class antibodies to Mycoplasma pneumoniae provides exposure information. The preferred method of diagnosis of acute M pneumoniae infection is by molecular detection; order MPRP / Mycoplasma pneumoniae, Molecular Detection, PCR, Varies.
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Useful For
Screening for recent or past exposure to Mycoplasma pneumoniae
This test should not be used as a screening procedure for the general population.
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
MYCOG | M. pneumoniae Ab, IgG, S | No | Yes |
MYCOM | M. pneumoniae Ab, IgM, S | No | Yes |
MYCON | M. pneumoniae Ab Interpretation | No | Yes |
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
MMYCO | M. pneumoniae Ab, IgM, S by IFA | No | No |
Testing Algorithm
If the Mycoplasma pneumoniae IgM result is reactive or equivocal, then M pneumoniae IgM by indirect immunofluorescence assay will be performed at an additional charge.
Method Name
MYCOG, MYCOM: Enzyme Immunoassay (EIA)
MMYCO: Indirect Immunofluorescence Assay (IFA)
MYCON: Interpretation
Reporting Name
M. pneumoniae Ab, IgG and IgM, SSpecimen Type
SerumSpecimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 14 days | |
Frozen | 14 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Heat inactivated specimen | Reject |
Reference Values
IgG: Negative
IgM: Negative
IgM by indirect immunofluorescence: Negative
Day(s) Performed
Monday through Friday
Report Available
Same day/1 to 3 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
86738 x 2-Mycoplasma pneumoniae by EIA
86738-Mycoplasma pneumoniae by indirect IFA (if appropriate)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
MYCO | M. pneumoniae Ab, IgG and IgM, S | 58733-7 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
MYCOG | M. pneumoniae Ab, IgG, S | 45224-3 |
MYCOM | M. pneumoniae Ab, IgM, S | 5257-1 |
MYCON | M. pneumoniae Ab Interpretation | 69048-7 |
Forms
If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.