BCH Order Code LAB572 Helicobacter pylori Breath Test
Additional Codes
Mayo Test ID |
---|
UBT |
Reporting Name
H. pylori C Urea Breath TestUseful For
Diagnostic testing for Helicobacter pylori infection in patients suspected to have active H pylori infection
Monitoring response to therapy
This test is not appropriate for asymptomatic people.
Testing Algorithm
See Helicobacter pylori Diagnostic Algorithm in Special Instructions
Performing Laboratory

Specimen Type
BreathOrdering Guidance
An alternative test for the diagnosis of active Helicobacter pylori infection in patients is the HPFRP / Helicobacter pylori with Clarithromycin Resistance Prediction, Molecular Detection, PCR, Feces, which requires a different collection.
Necessary Information
Specimen Required
Patient Preparation:
1. Patient should be fasting for 1 hour.
2. Patients should not have taken bismuth/Tritec, antimicrobials, proton-pump inhibitors (eg, Prilosec, Prevacid, Aciphex, Protonix, and Nexium) or bismuth preparations (eg, Pepto-Bismol) for 2 weeks prior to testing. If these instructions are not followed, test results may be inaccurate. Do not administer this test.
3. Histamine 2-receptor antagonists (H2RA) such as Pepcid, Tagamet, Axid, or Zantac should be discontinued for 24 to 48 hours before the BreathTek UBT test is administered. If these instructions are not followed, test results may be inaccurate. Do not administer this test.
4. Carafate (sucralfate) does not interfere with the test. Use of antacids does not affect the accuracy of this assay.
Supplies: H. Pylori Breath Kit - Meridian Breath ID (T906: fees apply)
Collection Instructions:
1. Do not collect if patient is younger than 3 years of age.
2. Follow instructions included with kit.
3. Mixing the (13)C-Urea Tablet
a. Dissolve the Citrica and the (13)C-enriched urea tablet in 150 to 200 mL (5.1 to 6.8 oz.) of tap water in the provided drinking cup.
b. Close the lid firmly using both hands. Place fingers over lid and shake thoroughly for a few minutes, until the Citrica Powder and the urea tablet are completely dissolved.
Note: Tiny particles may remain visible after thorough mixing. However, if more substantial particulate matter is still present after five minutes of mixing, discard the solution and repeat the procedure with a new kit.
Specimen Minimum Volume
Bag of ’’breath’’ must be full
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Breath | Ambient | 14 days | BREATH TEST BAG |
Special Instructions
Reference Values
Negative
Reference values apply to all ages.
Day(s) Performed
Monday through Friday, Sunday
Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
83013
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
UBT | H. pylori C Urea Breath Test | 29891-9 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
81590 | H. pylori C Urea Breath Test | 29891-9 |
Report Available
Same day/1 to 2 daysMethod Name
Qualitative Spectrophotometry (SP)
Forms
If not ordering electronically, complete, print, and send 1 of the following forms with the specimen:
-Microbiology Test Request (T244)