Albumin, Body Fluid

0050024
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Example Reports
Abnormal
Normal

Ordering Recommendation

Aids in the evaluation of ascites.

Mnemonic

ALB-BF

Methodology

Quantitative Immunoturbidimetry/Quantitative Spectrophotometry

Performed

Sun-Sat

Reported

1-3 days

New York DOH Approval Status

This test is New York DOH approved.

Specimen Required

Patient Preparation
Collect

Body fluid.

Specimen Preparation

Centrifuge and separate to remove cellular material. Transfer 1 mL body fluid to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Storage/Transport Temperature

Refrigerated.

Unacceptable Conditions

Contaminated or grossly hemolyzed specimens. Needle sent with specimen.

Remarks

Indicate source on the test request form.

Stability

After separation from cellular material: Ambient: Unacceptable; Refrigerated: 1 month; Frozen: 1 month (avoid repeated freeze/thaw cycles)

Reference Interval

Not established

Interpretive Data



Compliance Category

FDA

Note

Hotline History

View Hotline History

 

Hotline History

Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
05/16/2022
X
02/16/2021
X
X
X
N/A

CPT Codes

82042

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Components

Component Test Code* Component Chart Name LOINC
0050024 Albumin, Body Fluid 1747-5
0097114 SR Source 31208-2
* 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

  • ALB
Albumin, Body Fluid