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Fibrinogen Panel
0030137
Ordering Recommendation
Mnemonic
FIB PAN
Methodology
Electromagnetic Mechanical Clot Detection/Radial Immunodiffusion
Performed
Sun-Sat
Reported
2-4 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
Lt. blue (sodium citrate). Refer to Specimen Handling at aruplab.com for hemostasis/thrombosis specimen handling guidelines.  
Specimen Preparation
Transfer 2 mL platelet-poor plasma to an ARUP Standard Transport Tube. (Min: 1.5 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: 4 hours; Refrigerated: Unacceptable; Frozen: 1 month  
Reference Interval
Test Number
Components
Reference Interval
0030135Fibrinogen Antigen149-353 mg/dL
0030130Fibrinogen150-430 mg/dL
 Fibrinogen Antigen/Functional Ratio0.59-1.23

Interpretive Data
A Fibrinogen Antigen/Functional Ratio of greater than 1.23 is suggestive of a dysfibrinogenaemia.


Note
CPT Code(s)
85384; 85385
Components
Component Test Code*Component Chart NameLOINC
0030130Fibrinogen3255-7
0030135Fibrinogen Ag3256-5
0030138Fibrinogen Ratio Ag/Functional31158-9
* 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
  • Dysfibrinogenemia
  • Factor I
  • Fibrinogen Antigen
  • Functional Fibrinogen