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Recommendations when to order or not order the test. May include related or preferred tests.
Aids in the evaluation of liver function and intrahepatic cholestasis of pregnancy. Use to monitor patients on bile acid therapy. This assay is not useful for the diagnosis of inborn errors of bile acid metabolism.
New York DOH Approval Status
Indicates whether a test has been approved by the New York State Department of Health.
This test is New York state approved.
Specimen Required
Patient PreparationInstructions patient must follow before/during specimen collection.
Fasting for a minimum of eight hours prior to specimen collection is recommended.
CollectSpecimen type to collect. May include collection media, tubes, kits, etc.
Plain red or serum separator tube.
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
After clot formation, centrifuge specimen and pour off serum into a transport tube. Transfer 1 mL serum to an ARUP standard transport tube. (Min: 0.2 mL)
Storage/Transport TemperaturePreferred temperatures for storage prior to and during shipping to ARUP. See Stability for additional info.
Refrigerated. Store specimen refrigerated or frozen.
Unacceptable ConditionsCommon conditions under which a specimen will be rejected.
RemarksAdditional specimen collection, transport, or test submission information.
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry
Performed
Days of the week the test is performed.
Tue, Thu, Sat
Reported
Expected turnaround time for a result, beginning when ARUP has received the specimen.
1-6 days
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
7 years and older: Cholic acid (CA) 0-1.9 µmol/L Chenodeoxycholic acid (CDC) 0-3.4 µmol/L Deoxycholic acid (DCA) 0-2.5 µmol/L Ursodeoxycholic acid (UDC) 0-1.0 µmol/L Total 0-7.0 µmol/L
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
The reference intervals were established in fasting individuals. Mild elevation of bile acids could be secondary to nonfasting. For a more accurate interpretation of the results, a fasting specimen is recommended for this test.
Compliance Category
Laboratory Developed Test (LDT)
Note
Additional information related to the test.
Reference intervals were derived using samples obtained after an overnight fast.
Hotline History
N/A
CPT Codes
The American Medical Association Current Procedural Terminology (CPT) codes published in ARUP's Laboratory Test Directory are provided for informational purposes only. The codes reflect our interpretation of CPT coding requirements based upon AMA guidelines published annually. CPT codes are provided only as guidance to assist clients with billing. ARUP strongly recommends that clients confirm CPT codes with their Medicare administrative contractor, as requirements may differ. CPT coding is the sole responsibility of the billing party. ARUP Laboratories assumes no responsibility for billing errors due to reliance on the CPT codes published.
* 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.