Test Code UBT Helicobacter pylori Breath Test
Additional Codes
MAYO Code: UBT
Meditech Mnemonic:
HPYLORIBREATH
Aliases:
H. Pylori Urea Breath Test
Helicobacter Pylori Breath Test
Pylori, Helicobactor Breath Test
Ulcer Breath Test
Urea Breath Test
UBT
(13)C Urea Breath Test
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
For more information see Helicobacter pylori Diagnostic Algorithm.
Performing Laboratory
Mayo Clinic Laboratories in RochesterSpecimen 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.
Specimen Required
Patient Preparation:
1. Patient should be fasting for 1 hour.
2. Do not administer this test if this list of instructions is not followed, as test results may be inaccurate:
a. Do not administer this test if patient is allergic to citric acid.
Note: Product contains aspartame.
b. Patients should not take proton-pump inhibitors (eg, Prilosec, Prevacid, Aciphex, Protonix, and Nexium) or bismuth compounds (eg, Pepto-Bismol) for 2 weeks prior to testing.
c. Patients should not take antibiotics for 4 weeks prior to testing.
d. Histamine 2-receptor antagonists (H2RA), such as Pepcid, Tagamet, Axid, or Zantac may impact the sensitivity of the test and, if possible, should be discontinued for 2 weeks prior to testing.
3. 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 BreathID (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 daysReject Due To
No specimen should be rejected.Method Name
Qualitative Spectrophotometry
Forms
If not ordering electronically, complete, print, and send 1 of the following forms with the specimen:
-Infectious Disease Serology Test Request (T916)
-Gastroenterology and Hepatology Test Request (T728)
-Microbiology Test Request (T244)
-General Request (T239)