Test Code LAB849 Cold Agglutinin Titer, Serum
Additional Codes
SQ: CAGGM
MAYO: CATTR
Ordering Guidance
The cold agglutinin test is not specific for Mycoplasma pneumoniae and is not recommended to diagnose M pneumoniae infections. To diagnose M pneumoniae infections, order MPRP / Mycoplasmoides pneumoniae, Molecular Detection, PCR, Varies. For screening recent or past exposure to M pneumoniae, order MYCO / Mycoplasma pneumoniae Antibodies, IgG and IgM, Serum.
Specimen Required
Collection Container/Tube: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 4 mL
Pediatric Volume: 1 mL
Collections Instructions:
1. Use a warm pack to keep specimen at 37° C prior to and after collecting.
2. Allow specimen to clot at 37° C.
3. Centrifuge at 37° C and aliquot serum into plastic vial immediately after blood clots or within one hour of collection.
4. Do not refrigerate prior to separation of serum from red cells.
Secondary ID
614034Useful For
Detection of cold agglutinins in patients with suspected cold agglutinin disease
This test is not recommended to diagnose Mycoplasma pneumoniae infections.
Method Name
Titration/Red Cell Agglutination
Reporting Name
Cold Agglutinin TiterSpecimen Type
Serum RedSpecimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum Red | Refrigerated (preferred) | 7 days | |
Frozen | 7 days | ||
Ambient | 72 hours |
Reject Due To
Gross hemolysis | OK |
Gross icterus | OK |
Reference Values
Titer results:
>64: Elevated
>1000: May be indicative of hemolytic anemia
Method Description
The titer is determined by making serial doubling dilutions of the patient's serum in 0.9% saline. Group O indicator red cells are added, and the serum-cell mixture is then incubated 60 to 120 minutes at 2 to 8° C. The titer end point range is determined by hemagglutination.(Cohn CS, Delaney M, Johnson ST, Katz LM, eds: Technical Manual. 20th ed. AABB; 2020)
Day(s) Performed
Monday through Friday, Sunday
Report Available
1 to 3 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest 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
86157
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
CATTR | Cold Agglutinin Titer | 14658-9 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
CATTR | Cold Agglutinin Titer | In Process |
Forms
If not ordering electronically, complete, print, and send an Benign Hematology Test Request (T755) with the specimen.