Bile Acids, Fractionated and Total by LC-MS/MS
Also known as: BILE ACIDS
Use
This test aids in the evaluation of liver function and intrahepatic cholestasis of pregnancy. It is also used to monitor patients on bile acid therapy. The test is not useful for the diagnosis of inborn errors of bile acid metabolism. The reference intervals were established in fasting individuals to improve accuracy.
Special Instructions
Not provided.
Limitations
The test is not approved for diagnosing inborn errors of bile acid metabolism. Mild elevation of bile acids in non-fasting individuals can occur, which may affect result interpretation. For accurate interpretations, specimen fasting is recommended.
New York Approved
Methodology
Mass Spectrometry
Biomarkers
LOINC Codes
- 30518-5 - Cholate SerPl-sCnc
- 30520-1 - DO-cholate SerPl-sCnc
- 30519-3 - CDCAe SerPl-sCnc
- 14628-2 - Bile Ac SerPl-sCnc
- 55159-8 - Ursodeoxycholate SerPl-sCnc
Result Turnaround Time
1-6 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1 mL
Minimum Volume
0.2 mL
Container
ARUP standard transport tube
Collection Instructions
After clot formation, centrifuge specimen and pour off serum into a transport tube.
Patient Preparation
Fasting for a minimum of eight hours prior to specimen collection is recommended.
Storage Instructions
Store specimen refrigerated or frozen.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 8 hours |
| Refrigerated | 2 weeks |
| Frozen | 3 months |
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