Chlamydia IgM and IgG Panel, Immunofluorescence, Serum - Mayo Clinic Laboratories Extended Catalog

Ordering Guidance

For suspected Chlamydia trachomatis infection, order either CTRNA / Chlamydia trachomatis, Nucleic Acid Amplification, Varies or CGRNA / Chlamydia trachomatis and Neisseria gonorrhoeae, Nucleic Acid Amplification, Varies.

Specimen Required

Collection Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Submission Container/Tube: Plastic vial

Specimen Volume: 0.6 mL

Collection Instructions: Centrifuge and aliquot serum into a plastic vial.

Reporting Name

Chlamydia IgM/IgG Panel, IFA, S

Specimen Type

Serum

Specimen Stability Information

Specimen Type	Temperature	Time
Serum	Refrigerated (preferred)	30 days
	Frozen	30 days

Report Available

Same day/1 to 4 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

LOINC Code Information

Test ID	Test Order Name	Order LOINC Value
CHLAP	Chlamydia IgM/IgG Panel, IFA, S	77166-7

Result ID	Test Result Name	Result LOINC Value
619392	C. pneumoniae IgG	In Process
619390	C. pneumoniae IgM	In Process
619391	C. psittaci IgM	In Process
619393	C. psittaci IgG	In Process

Forms

If not ordering electronically, complete, print, and send an Infectious Disease Serology Test Request (T916) with the specimen.

Useful For

Aiding in the clinical diagnosis of Chlamydia pneumoniae or Chlamydia psittaci infection

Day(s) Performed

Monday

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

86632 x 2

86631 x 2

Specimen Minimum Volume

0.3 mL

Reference Values

Chlamydia pneumoniae

IgM: <1:10

IgG: <1:64

Chlamydia psittaci