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
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 or hemolyzed specimens.  
Remarks
  
Stability
Ambient: 4 hours; Refrigerated: Unacceptable; Frozen: 1 month  
Reference Interval
 
 
Test Number Components Reference Interval
0030135Fibrinogen Antigen 149-​353 mg/dL
0030130Fibrinogen 150-​430 mg/dL
 Fibrinogen Antigen/Functional Ratio 0.59-​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