Test Code BA48F Bile Acids, Bowel Dysfunction, 48 Hour, Feces
Reporting Name
Bile Acids, Bowel Dysfunc, 48 Hr, FPerforming Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Aids to evaluate patients suspected of having irritable bowel syndrome-diarrhea (IBS-D) symptoms due to bile acid malabsorption
Method Name
Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)
Ordering Guidance
This test is for evaluation of bowel dysfunction.
For evaluation of hepatobiliary dysfunction, order BILEA / Bile Acids, Total, Serum.
For evaluation of patients treated with urso or cholate, order BAFS / Bile Acids, Fractionated and Total, Serum.
For evaluation of inborn errors of metabolism, order BAIPD / Bile Acids for Peroxisomal Disorders, Serum.
Specimen Required
Patient Preparation:
For 3 days prior to and during the collection period:
1. Patient should be on a fat-controlled diet (100-150 g fat per day)
2. No laxatives (particularly mineral oil and castor oil)
3. No synthetic fat substitutes (eg, Olestra) or fat-blocking nutritional supplements
Supplies: Stool Containers - 24, 48, 72 Hours Kit (T291)
Collection Container/Tube: Stool container (T291); complies with shipping requirements, do not use other containers
Specimen Volume: Entire 48-hour collection
Collection Instructions:
1. Do not use other containers.
2. All containers must be sent together.
3. The entire collection must contain at least 5 g of feces.
4. The number of containers sent should be indicated on the labels (1 of 4, for example).
Additional Information:
1. Patient may store sample at refrigerate temperature during collection period.
2. Barium interferes with test procedure; a waiting period of 48 hours before stool collection analysis is recommended.
Specimen Type
FecalSpecimen Minimum Volume
5 g
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Fecal | Frozen | 30 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability. |
Reference Values
≥ to 18 years:
Sum of cholic acid and chenodeoxycholic acid ≤9.7%
Total bile acids ≤2619 mcmoles/48 hours
Reference values have not been established for patients who are <18 years of age
Interpretation
Elevated total fecal bile acid or percent cholic acid plus chenodeoxycholic acid is consistent with the diagnosis of bile acid malabsorption.
Pharmacological treatment with bile acid sequestrants has been shown to improve symptoms in some patients.
Day(s) Performed
Wednesday
Report Available
2 to 9 daysTest Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
82542
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
BA48F | Bile Acids, Bowel Dysfunc, 48 Hr, F | 93338-2 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
36968 | Bile Acids, % CDCA + CA, F | 93337-4 |
36969 | Total Bile Acids, F | 93336-6 |
610285 | Stool Weight | 30078-0 |
Forms
If not ordering electronically, complete, print, and send a Gastroenterology and Hepatology Test Request (T728) with the specimen.