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Test Code LAB177 Albumin, Body Fluid


Ordering Guidance


For cerebrospinal fluid (CSF) specimens, order ALBSF / Albumin, Spinal Fluid. Testing will be changed to ALBSF if this test is ordered on that specimen type.



Necessary Information


1. Date and time of collection are required.

2. Specimen source is required.



Specimen Required


Specimen Type: Body fluid

Preferred Source:

-Peritoneal fluid (peritoneal, abdominal, ascites, paracentesis)

-Pleural fluid (pleural, chest, thoracentesis)

-Drain fluid (drainage, JP drain)

Acceptable Source: Write in source name with source location (if appropriate)

Collection Container/Tube: Sterile container

Submission Container/Tube: Plastic vial

Specimen Volume: 1 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.


Secondary ID

60622

Useful For

Aiding in identifying the cause of ascites

 

Aiding in differentiating exudative and transudative pleural effusions

Method Name

Colorimetric

Reporting Name

Albumin, BF

Specimen Type

Body Fluid

Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time
Body Fluid Refrigerated (preferred) 7 days
  Frozen  30 days
  Ambient  24 hours

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Gross Icterus Reject
Anticoagulant or additive
Breast milk
Nasal secretions
Gastric secretions
Bronchoalveolar lavage (BAL) or bronchial washings
Colostomy/ostomy
Feces
Urine
Saliva
Sputum
Vitreous fluid
Reject

Reference Values

An interpretive report will be provided

Cautions

Serum and ascitic fluid for determination of serum-albumin ascites gradient should be collected on the same day.

 

In very rare cases of gammopathy, in particular type IgM (Waldenstrom macroglobulinemia), (may cause unreliable results.

 

Colorimetric methods used for the determination of albumin may lead to falsely elevated test results in patients suffering from renal failure or insufficiency due to interference with other proteins. Immunoturbidimetric methods are less affected.

Day(s) Performed

Monday through Sunday

Report Available

Same day/1 to 2 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test 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

82042

LOINC Code Information

Test ID Test Order Name Order LOINC Value
ALBFL Albumin, BF 1747-5

 

Result ID Test Result Name Result LOINC Value
ALBF Albumin, BF 1747-5
797FL Fluid Type, Albumin 14725-6

NY State Approved

Yes