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Test Code C2CMPM C2 Complement, Functional, with Reflex, Serum

Additional Codes

MAYO Test ID

C2

EPIC Test ID

LAB5438

Reporting Name

C2 Complement,Functional,w/Reflex,S

Useful For

Investigation of a patient with a low (absent) hemolytic complement, with reflex testing to C3 and C4, if appropriate

Reflex Tests

Test ID Reporting Name Available Separately Always Performed
C4 Complement C4, S Yes No
C3 Complement C3, S Yes No

Testing Algorithm

If the C2 result is less than 15 U/mL, then complement C3 and C4 will be performed at an additional charge.

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Serum


Ordering Guidance


This test is for assessment of complement C2 and includes assessment of C3 and C4 as reflex testing. Unless a deficiency has already been identified, initial assessment should begin with the total complement assay (COM / Complement, Total, Serum), which is a screen for suspected complement deficiencies and should be performed before ordering individual complement component assays. A deficiency of an individual component of the complement cascade will result in an undetectable total complement level.



Specimen Required


Patient Preparation: Fasting preferred

Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Submission Container/Tube: Plastic vial

Specimen Volume: 1 mL

Collection Instructions:

1. Immediately after specimen collection, place the tube on wet ice and allow specimen to clot.

2. Centrifuge at 4° C and aliquot serum into a plastic vial.

3. Within 30 minutes of centrifugation, freeze specimen. Sample must be placed on dry ice if not frozen immediately.

NOTE: If a refrigerated centrifuge is not available, it is acceptable to use a room temperature centrifuge, provided the specimen is kept on ice before centrifugation, and immediately afterward, the serum aliquoted and frozen.


Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Frozen 21 days

Reference Values

25-47 U/mL

Day(s) Performed

Monday through Friday

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

86161

86160 x 2 (if appropriate)

LOINC Code Information

Test ID Test Order Name Order LOINC Value
C2 C2 Complement,Functional,w/Reflex,S 93977-7

 

Result ID Test Result Name Result LOINC Value
C2FX C2 Complement,Functional,S 93977-7
INT53 Interpretation 69048-7

Report Available

1 to 3 days

Reject Due To

Gross hemolysis OK
Gross lipemia Reject
Gross icterus OK

Method Name

Automated Liposome Lysis Assay