Fibrinogen Degradation Products (FDP), Plasma
Also known as: FDP, Plasma
Use
This assay is used to detect and semi quantitatively measure the presence of FDP in plasma.
Special Instructions
If a patient's hematocrit exceeds 55%, adjust the citrate volume in the collection tube as necessary following the coagulation collection procedures. Ensure proper blood collection techniques to obtain an accurate blood-to-anticoagulant ratio to avoid delays in turnaround time.
Limitations
Increased FDP levels are not specific to any single condition and are seen in various disorders such as DIC, primary fibrinolysis, liver diseases, eclampsia, and thrombotic episodes. The test is not diagnostic on its own and must be interpreted in conjunction with other clinical findings.
Methodology
Immunoassay (IHC)
Biomarkers
LOINC Codes
- 30226-5
- 30226-5
Result Turnaround Time
2-3 days
Related Documents
For more information, please review the documents below
Specimen
Plasma
Volume
1 mL
Minimum Volume
Not provided
Container
Blue-top (sodium citrate) tube
Collection Instructions
Blood should be collected in a blue-top tube containing 3.2% buffered sodium citrate. Evacuated collection tubes must be filled to ensure a proper blood-to-anticoagulant ratio. Mix immediately by gentle inversion six times. If using a winged collection set, draw a discard tube first. Submit separate frozen specimens for multiple tests.
Storage Instructions
Freeze