Test Code BFLA1 Lipid Analysis, Body Fluid
Reporting Name
Lipid Analysis, BFPerforming Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Distinguishing between chylous and nonchylous effusions
Method Name
Colorimetry/Spectrophotometry (SP)/Electrophoresis
Necessary Information
1. Date and time of collection are required.
2. Specimen source is required.
Specimen Required
Specimen Type: Body fluid
Preferred Sources:
-Peritoneal fluid (peritoneal, abdominal, ascites, paracentesis)
-Pleural fluid (pleural, chest, thoracentesis)
-Drain fluid (drainage, JP drain)
-Pericardial
Acceptable Source:
Collection Container/Tube: Sterile container, no additive
Submission Container/Tube: Plastic vial
Specimen Volume: 3 mL
Collection Instructions:
1. Centrifuge to remove any cellular material and transfer into a plastic vial.
2. Indicate the specimen source and source location on label.
Specimen Type
Body FluidSpecimen Minimum Volume
2.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Body Fluid | Frozen (preferred) | 30 days | |
Refrigerated | 7 days | ||
Ambient | 24 hours |
Reject Due To
Gross hemolysis | OK |
Gross lipemia | OK |
Gross icterus | OK |
Breast milk Nasal secretions Gastric secretions Bronchoalveolar lavage (BAL or bronchial washings) Colostomy/ostomy Amniotic fluid Feces Saliva Sputum Urine Spinal fluid Synovial fluid Vitreous fluid |
Reject |
Reference Values
An interpretive report will be provided.
Interpretation
Pleural Fluid:
Pleural fluid cholesterol concentrations 46 to 65 mg/dL are consistent with exudative effusions.
Cholesterol concentrations greater than 200 mg/dL suggest pseudochylous effusion.
Triglyceride concentrations greater than 110 mg/dL are consistent with chylous effusions.
Triglyceride concentrations less than 50 mg/dL are usually not due to chylous effusions.
Peritoneal Fluid:
Peritoneal fluid triglyceride concentrations greater than 187 mg/dL are most consistent with chylous effusion.
Cholesterol concentrations 33 to 70 mg/dL suggest malignant causes of ascites.
Day(s) Performed
Monday through Friday
Report Available
3 to 4 daysTest Classification
This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
82664-Electrophoretic technique, not elsewhere specified (Chylomicrons and lipoproteins)
84311-Spectrophotometry, analyte not specified (Cholesterol)
84478-Triglycerides
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
BFLA1 | Lipid Analysis, BF | 94872-9 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
FLD28 | Fluid Type: | 14725-6 |
BFCHO | Cholesterol, BF | 12183-0 |
BFTRG | Triglycerides, BF | 12228-3 |
BFCMT | Comment | 21025-2 |