Sign in →

Test ID NBLD0653 Bile Acids, Bowel Dysfunction, 48 Hour, Feces

Useful For

Aids in evaluation of patients suspected of having irritable bowel syndrome-diarrhea symptoms due to bile acid malabsorption

Specimen Type

Fecal


Ordering Guidance


This test is for evaluation of bowel dysfunction or confirmatory testing for bile acid malabsorption using a 48-hour fecal collection.

 

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:

1. The patient should be on a fat-controlled diet (100-150 g fat per day) for 3 days before and during the collection period.

2. Patient should not use:

 a. Antibiotics for 7 days before or during specimen collection

 b. Statins for 5 days before or during specimen collection

 c. Laxatives (particularly mineral oil and castor oil) for 3 days before or during specimen collection.

 d. Bile acid sequestrants for 24 hours before or during specimen collection

 e. Synthetic fat substitutes (eg, Olestra) or fat-blocking nutritional supplements for 24 hours before or during the specimen collection

3. If the patient has used barium, it is recommended to wait at least 48 hours before collecting the specimen.

 

Supplies: Stool Containers - 24, 48, 72 Hour Kit (T291)

Collection Container/Tube: Stool container that complies with shipping requirements

Specimen Volume: Entire 48-hour collection

Collection Instructions:

1. Do not use other containers.

2. Freeze immediately.

3. All containers must be sent together.

4. The entire collection must contain at least 5 g of feces.

5. The number of containers sent should be indicated on the labels (1 of 4, for example).

Additional Information:

1. The patient may store specimen at refrigerate temperature during the collection period, but it must be frozen immediately after completion.

2. If additional tests are ordered, aliquot and separate sample prior to freezing to allow 1 container per test.


Reject Due To

  All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Specimen Minimum Volume

5 g

Specimen Stability Information

Specimen Type Temperature Time
Fecal Frozen 30 days

Day(s) Performed

Wednesday

Report Available

2 to 9 days

Method Name

Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

82542

Reporting Name

Bile Acids, Bowel Dysfunc, 48 Hr, F

Reference Values

≥ to 18 years:

Sum of cholic acid and chenodeoxycholic acid ≤9.7%

Total bile acids ≤2619 mcmoles/48 h

 

Reference values have not been established for patients who are younger than 18 years of age

Test 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.

Forms

If not ordering electronically, complete, print, and send a Gastroenterology and Hepatology Test Request (T728) with the specimen.

Testing Algorithm

For information see Bile Acid-Associated Tests Ordering Guide

Secondary ID

607368
Sanford Laboratories - Sioux Falls/Rapid City Additional Information:

SANFORD LABORATORY INTERFACE BUILD INFORMATION

 Result Code     Result Code Description   
 27007     Bile Acids, % CDCA + CA, F   
 27008     Total Bile Acid, F   
 27009     Stool Weight