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Osmotic Fragility, Erythrocytes
Test CodeCPT Codes
85555, 85557<br>Restricted Client Code
Preferred Specimen
4 mL whole blood collected in EDTA (lavender-top) tube, and
2nd specimen (for Control):
4 mL whole blood collected in EDTA (lavender-top) tube
Minimum Volume
Instructions
Both a whole blood EDTA specimen and a shipping control specimen are required.
Patient's age is required.
1. Collect a shipping control specimen from a normal (healthy), unrelated, nonsmoking person at the same time as the patient.
2. Clearly hand write "normal control" on the outermost label.
3. Refrigerate specimen immediately after collection.
4. Send control specimen in original tube. Do not aliquot.
5. Rubber band patient specimen and control vial together. The control and patient specimen must be handled in the same manner from specimen collection to receipt in the testing laboratory.
Specimens must arrive within 72 hours of collection.
If not ordering electronically, complete, print, and send a Benign Hematology Test Request (T755) with specimen.
Note: **Specimens cannot be collected at a PSC**
Transport Temperature
Specimen Stability
Refrigerated: 72 hours
Frozen: Unacceptable
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Methodology
Osmotic Lysis
FDA Status
This test was developed, and its performance characteristics 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.
Setup Schedule
Reference Range
0.50 g/dL NaCl (unincubated): 3-53% hemolysis
0.60 g/dL NaCl (incubated): 14-74% hemolysis
0.65 g/dL NaCl (incubated): 4-40% hemolysis
0.75 g/dL NaCl (incubated): 1-11% hemolysis
Clinical Significance
Reference
1. Palek J, Jarolin P: Hereditary spherocytosis. In: Williams WJ, Beutler E, Erslev AJ, Lichtman MA, eds. Hematology. 4th ed. Mcgraw-Hill Book Company; 1990:558-569
2. King MJ, Garcon L, Hoyer JD, et al: International Council for Standardization in Haematology. ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders. Int J Lab Hematol. 2015 Jun;37 (3):304-325