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Fibrin/Fibrinogen Degradation Split Products (INACTIVE as of 07/05/2016: Refer to 2006491)
0030140
Ordering Recommendation
Mnemonic
FDP
Methodology
Latex Agglutination
Performed
Sun-Sat
Reported
1-2 days
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
ARUP Consult®
Disease Topics
Specimen Required
Patient Preparation
 
Collect
Whole blood drawn into tube with Thrombin/Soybean trypsin inhibitor. (ARUP supply #16496) Available online through eSupply using ARUP Connect™ or contact ARUP Client Services at (800) 522-2787. 
Specimen Preparation
Transfer 1 mL serum 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
Plasma. Specimens not collected in Thrombin/Soybean trypsin inhibitor or that have not clotted. 
Remarks
 
Stability
Ambient: 2 hours; Refrigerated: Unacceptable; Frozen: 1 month 
Reference Interval
By report (reports may vary based on instrumentation)
Interpretive Data


Note
Some hemolysis of the specimen may be seen. This will not affect the ability of Thrombo-Wellco test to detect FDP in the specimen, and will not lead to false-positive results.
CPT Code(s)
85362
Components
Component Test Code*Component Chart NameLOINC
0030140Fibrin Degradation Products29991-7
* 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
  • Fibrinogen Degradation Products (FDP), Plasma
  • FSP