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Leukocyte Adhesion Deficiency Panel
Test Code38576
CPT Codes
86356 (x3)<br>This test is not available for New York patient testing<br>Limited Access Code
Preferred Specimen
5 mL whole blood collected in a sodium or lithium heparin (green-top) tube
Minimum Volume
1 mL
Instructions
Specimen must be analyzed within 48 hours.
Follow client direct ship process.
Follow client direct ship process.
Transport Temperature
Refrigerated (cold packs)
Specimen Stability
Room temperature: Unacceptable
Refrigerated: 48 hours
Frozen: Unacceptable
Refrigerated: 48 hours
Frozen: Unacceptable
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Clotted or hemolyzed specimens
Methodology
Semi-Quantitative Flow Cytometry
FDA Status
This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, the FDA has determined that such clearance or approval is not necessary.
Setup Schedule
Set up: Daily; Report available: 2-5 days
Reference Range
%CD11b: 93-100%
%CD15: 91-100%
%CD18: 98-100%
%CD15: 91-100%
%CD18: 98-100%
Clinical Significance
Aids in the diagnosis of type I and II leukocyte adhesion deficiency. Panel measures CD11b, CD15, and CD18 on neutrophils.