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2006491
Fibrin/Fibrinogen Degradation Split Products, Plasma
FDP PLASMA
Ordering Recommendation
May be useful for the evaluation of rare disorders such as primary fibrinolysis. For evaluating coagulopathies (eg, disseminated intravascular coagulation), D-Dimer (0030057) is the preferred test.
New York DOH Approval Status
This test is New York state approved.
Specimen Required
Patient Preparation
Collect
Lt. blue (sodium citrate). Refer to Specimen Handling at aruplab.com for hemostasis/thrombosis specimen handling guidelines.
Specimen Preparation
Transfer 1 mL platelet-poor plasma to an ARUP standard transport tube. (Min: 0.5 mL)
Storage/Transport Temperature
CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.
Unacceptable Conditions
Serum. EDTA plasma, clotted or hemolyzed specimens.
Remarks
Stability
Ambient: 8 hours; Refrigerated: Unacceptable; Frozen: 3 months
Methodology
Latex Agglutination
Performed
Sun-Sat
Reported
1-2 days
Reference Interval
<5 ug/mL
Interpretive Data
Compliance Category
FDA
Note
Hotline History
Hotline History
Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
N/A
CPT Codes
85362
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 2006492 | Fibrin Degradation Products, Plasma | 30226-5 |
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
- FDP
- FDP/fdp (Fibrin/Fibrinogen Degradation Split Products)
- FSP
Fibrin/Fibrinogen Degradation Split Products, Plasma
