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0030137
Fibrinogen Panel
FIB PAN
Ordering Recommendation
Assist in diagnosing dysfibrinogenemia.
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 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, grossly lipemic, or hemolyzed specimens.
Remarks
Stability
Ambient: 4 hours; Refrigerated: Unacceptable; Frozen: 1 month
Methodology
Electromagnetic Mechanical Clot Detection/Immunoturbidimetry
Performed
Sun-Sat
Reported
2-5 days
Reference Interval
| Test Number |
Components |
Reference Interval |
|---|---|---|
| Fibrinogen | 150-430 mg/dL | |
| Fibrinogen Ag | 149-353 mg/dL | |
| Fibrinogen Ratio Ag/Functional | 0.59-1.23 ratio |
Interpretive Data
A Fibrinogen Antigen/Functional Ratio of greater than 1.23 is suggestive of a dysfibrinogenaemia.
Compliance Category
Modified FDA
Note
Hotline History
N/A
CPT Codes
85384; 85385
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 0030130 | Fibrinogen | 3255-7 |
| 0030135 | Fibrinogen Ag | 3256-5 |
| 0030138 | Fibrinogen Ratio Ag/Functional | 31158-9 |
* 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
- Factor I
- Fibrinogen Antigen
- Functional Fibrinogen
- Dysfibrinogenemia
Fibrinogen Panel
