Test Details
Methodology
Visual observation of refrigerated samples
Result Turnaround Time
3 - 5 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
Use
Detect cryofibrinogen complexes in plasma1
Limitations
This test was developed, and its performance characteristics determined, by LabCorp. It has not been cleared or approved by the Food and Drug Administration.
Custom Additional Information
Cryofibrinogen is an abnormal complex of proteins that precipitate out of plasma as it is cooled.1 These cold, insoluble protein complexes can be composed of fibrin, fibrinogen, fibrin split products, along with other plasma proteins. Cryofibrinogen forms in refrigerated plasma, but not in refrigerated serum.1 Protein precipitate that forms in both refrigerated serum and refrigerated plasma is referred to as cryoglobulin. Testing for cryofibrinogen requires the collection of serum (see Cryoglobulin, Qualitative With Quantitative Reflex [001594]) in order to exclude the presence of cryoglobulin in the patient sample.1 Cryofibrinogen can occur spontaneously (ie, essential cryofibrinogenemia) or in association with other inflammatory conditions. Secondary cryofibrinogenemia has been reported in patients with malignancy, diabetes mellitus, collagen vascular disease, and active infection.1 Most individuals with cryofibrinogenemia are asymptotic.1 Morbidity associated with cryofibrinogenemia occurs as the result of thrombotic occlusion of the small to medium arteries by insoluble protein complexes. Cryofibrinogenemia can produce symptoms due to cutaneous ischemia including purpura, livedo reticularis, ecchymosis, ulcerations, or ischemic necrosis. These symptoms are typically observed in areas of the body that tend to be at lower temperature including the hands, feet, ears, nose, and buttocks.1 Less specific symptoms, such as malaise and fever, are also relatively common manifestations of the condition. In some rare cases, essential cryofibrinogenemia has been associated with cutaneous ulcers and gangrene.1 Cryofibrinogenemia has infrequently been associated with other conditions including cerebrovascular thrombosis; myocardial infarction; thrombophlebitis; obstruction of the aortic, ileac, or femoral artery; pulmonary emboli; mesenteric artery thrombosis; and retinal artery thrombosis.1 These thrombotic conditions can occasionally produce spontaneous bleeding due to depletion of clotting factors, similar to that seen in disseminated intravascular coagulation (DIC).1
Specimen Requirements
Specimen
Plasma
Volume
3 mL
Minimum Volume
1 mL
Container
Blue-top (sodium citrate) tube, lavender-top (EDTA) tube, or gray-top (sodium fluoride) tube
Collection Instructions
Specimen must be drawn in a prewarmed tube and kept at 37°C. Separate plasma from cells immediately, and transfer the plasma into a clean transport tube. Label transport tube "Prewarmed."
Reference Range
None detected
Storage Instructions
Maintain specimen at room temperature.
Causes for Rejection
Heparinized plasma; whole blood received
Footnotes
LOINC® Map
Order Code | Order Code Name | Order Loinc | Result Code | Result Code Name | UofM | Result LOINC |
---|---|---|---|---|---|---|
080317 | Cryofibrinogen, Qualitative | 11043-7 | 080317 | Cryofibrinogen, Qualitative | 11043-7 | |
Order Code | 080317 | |||||
Order Code Name | Cryofibrinogen, Qualitative | |||||
Order Loinc | 11043-7 | |||||
Result Code | 080317 | |||||
Result Code Name | Cryofibrinogen, Qualitative | |||||
UofM | ||||||
Result LOINC | 11043-7 |