Helicobacter pylori (H. pylori) is a common bacterium that infects the stomach's lining and is implicated in various gastrointestinal diseases, including ulcers and gastritis. Despite its prevalence, detecting and managing H. pylori infections remains challenging.
This article aims to provide healthcare practitioners with a detailed overview of the diagnostic methods available for identifying H. pylori, ranging from noninvasive tests to invasive procedures. By understanding these techniques, practitioners can better diagnose and treat infections, potentially preventing more serious gastrointestinal diseases.
[signup]
What is H. pylori and What Are Its Health Implications?
H. pylori is a gram-negative bacterium that infects the stomach lining and has been implicated in numerous gastrointestinal diseases. It is highly prevalent globally, affecting up to 50% of people.
Although carriers of H. pylori can be asymptomatic, some infections can lead to inflammation and diseases such as gastritis, peptic ulcer disease, duodenal ulcer disease, gastric cancer, and MALT lymphoma (18,20).
Transmission of H. pylori occurs through numerous routes, including oral-oral and oral-fecal, and thus commonly occurs between family members and in areas where adequate sanitation is not accessible (20).
H. pylori is well suited to infect and survive the gastric environment in humans. It releases a compound called urease, which alters the pH in the area directly surrounding the bacterium, effectively buffering against the stomach's acidity, which would otherwise cause damage (18).
It has a small "tail" called a flagella that allows it to propel itself toward the cells of the stomach lining, where it attaches and colonizes, leading to infection. Once attached, H. pylori releases toxins that damage local tissues (20), leading to inflammation and disease development.
Symptoms of Infection
Although many carriers of H. pylori do not experience symptoms, symptoms can occur once the infection leads to inflammation. These include:
Diagnostic Tests for H. pylori
Testing for H. pylori may involve invasive tests that require an endoscopy or noninvasive tests that rely on stool, breath, or blood samples (17).
Noninvasive Tests
Urea Breath Test (UBT)
The urea breath test (UBT) has been used for over 30 years and is the most reliable noninvasive testing option for H. pylori. To perform this test, a patient ingests a urea solution in pill or liquid form and undergoes a breath test 15 minutes later.
H. pylori metabolizes the urea and releases carbon dioxide as a byproduct, which is then measured to determine if infection is present. The UBT is highly accurate, with a 95% sensitivity and specificity rate (22).
Medications such as proton-pump inhibitors (PPIs), bismuth, antibiotics, and herbal antibiotics can lead to inaccuracies in testing, so they should be avoided for 2-4 weeks before testing. Additionally, gastrointestinal bleeding from ulcers can interfere with UBT results, and it is recommended to delay testing until bleeding has resolved.
Stool Antigen Test (SAT)
The SAT uses fecal samples to look for H. pylori antigens. It is highly sensitive and specific for detecting H. pyloriinfections and does not involve costly or invasive procedures.
Like the UBT, the accuracy of the SAT can be affected by recent antibiotic or PPI use and upper gastrointestinal bleeding and should be delayed in the presence of these. Irregular bowel movements may also affect accuracy (22).
In addition to SAT, it is possible to test for H. pylori in the stool using PCR techniques that detect the presence of bacterial DNA and can provide more detailed genetic information about the specific genotypes of the bacteria present (22).
Serology
Blood tests that detect the presence of anti-H pylori IgG antibodies can also indicate present or recent H. pylori infection.
However, because IgG antibodies can persist in the bloodstream well after an infection has resolved, the serology tests cannot distinguish between past and current infections, making it less desirable than the UBT and SAT for clinical diagnostic purposes.
The advantage of the H. pylori blood test is that it is unaffected by gastrointestinal bleeding and PPI, antibiotic, or bismuth use (22).
Invasive Tests
Endoscopy with Biopsy
All invasive testing starts with an endoscopy, a procedure in which an instrument is inserted into the stomach and duodenum of the small intestine to visualize the gastrointestinal lining.
Biopsies (small tissue samples) are taken from the gastric mucosa during this procedure. These samples are then further examined and tested for the presence of H. pylori using PCR testing or one or more of the methods below.
Because endoscopies are invasive and costly, they are generally reserved for testing for more severe manifestations of H. pylori infection, such as gastrointestinal bleeding, suspected peptic or duodenal ulcers, gastric cancer, and MALT lymphoma (17,22).
When assessing for H. pylori infection, most biopsy samples are taken from the antrum and corpus of the stomach (22).
Histology
Histology is considered the gold standard for direct H. pylori testing. Once tissue samples are obtained by biopsy, they are treated with specific stains that make it easier to visualize the presence of H. pylori cells. These samples are then examined under a microscope to detect infection.
Like the UBT and SAT, histological examination is vulnerable to the recent use of PPIs and antibiotics, so these medications should be avoided for at least 2-4 weeks before the biopsy samples are taken.
Additionally, H. pylori infections are often distributed unevenly throughout the stomach lining. So, these cells can only be detected if biopsies are taken in H. pylori-concentrated areas (22).
Culture
Culturing H. pylori involves placing a biopsy sample into a growth media and incubating it to assess for H. pylori cell growth. Although culture studies can be more susceptible to human and laboratory error, they have the distinct advantage of being able to test for antibiotic sensitivity to help guide treatment options. Culture and sensitivity studies are recommended in areas where clarithromycin resistance exceeds 20% (22).
Rapid Urease Test (RUT)
RUT is a quick, inexpensive, and reliable method of identifying H. pylori infections in tissue samples. This test uses a urea test reagent that converts to ammonia in the presence of H. pylori, causing a notable increase in pH levels, detected using a pH monitor.
The main disadvantage of an RUT is its poor accuracy in the presence of gastric bleeding, so it should not be the sole indicator used in these cases (22).
How to Choose the Right Diagnostic Test
With a multitude of options to choose from, it can take time to determine which test is most appropriate for a patient. Due to the ease, accuracy, and noninvasive nature of the UBT and SAT, these tests can be helpful in pediatric patients when endoscopies are not otherwise warranted.
The UBT and SAT are also appropriate for testing in adults when symptoms are not severe and more serious diseases such as bleeding ulcers, gastric cancer, and MALT lymphoma are not suspected or have been previously ruled out (22). However, endoscopies are required for diagnostic workup if these diseases are suspected.
Additionally, the UBT and SAT are often employed to monitor treatment efficacy to ensure that H. pylori eradication is complete. For these purposes, waiting 2-4 weeks post antibiotic, bismuth, and PPI use is essential to enhance testing accuracy (20).
How to Treat H. pylori Based on Diagnosis
If testing confirms an active H. pylori infection in the presence of symptoms, treatment of the infection is often recommended. First-line treatment options are focused on the eradication of H. pylori and include a combination of antibiotics, PPIs, and sometimes bismuth taken together or sequentially:
- Clarithromycin triple therapy: The standard first-line treatment for H. pylori, this therapy combines PPI, clarithromycin, amoxicillin, and metronidazole for 14 days. It should only be undertaken when clarithromycin resistance is less than 15%.
- Bismuth quadruple therapy: PPI, bismuth, tetracycline, and nitroimidazole in combination for 10-14 days. This treatment option is suitable for those with penicillin allergies and high clarithromycin resistance.
- Concomitant therapy: PPI, clarithromycin, amoxicillin, and nitroimidazole taken together for 10-14 days. Evidence suggests that this therapy has the highest eradication rates among the conventional first-line treatment options.
Including culture antibiotic sensitivity analysis in the diagnostic workup can help guide which antibiotics would be most effective for treatment and which would likely lead to resistance.
Follow-up testing via a UBT or SAT is often performed to ensure that a prescribed treatment effectively eradicates the H. pylori infection (20).
[signup]
Key Takeaways
Accurate diagnosis of H. pylori is essential for effective patient management, as it guides appropriate treatment strategies that can prevent severe gastrointestinal complications.
Healthcare practitioners should prioritize staying updated with the latest diagnostic technologies and guidelines developments.
This commitment to continual learning will enhance their ability to detect H. pylori accurately and improve overall clinical outcomes for their patients.
Helicobacter pylori (H. pylori) is a common bacterium that affects the stomach's lining and is associated with various gastrointestinal issues, including ulcers and gastritis. Despite its prevalence, identifying and managing H. pylori can be complex.
This article aims to provide healthcare practitioners with an overview of the diagnostic methods available for identifying H. pylori, ranging from noninvasive tests to invasive procedures. By understanding these techniques, practitioners can better diagnose and manage infections, potentially supporting gastrointestinal health.
[signup]
What is H. pylori and What Are Its Health Implications?
H. pylori is a gram-negative bacterium that affects the stomach lining and is linked to numerous gastrointestinal issues. It is highly prevalent globally, affecting up to 50% of people.
Although carriers of H. pylori can be asymptomatic, some infections can lead to inflammation and issues such as gastritis, peptic ulcer disease, duodenal ulcer disease, gastric cancer, and MALT lymphoma (18,20).
Transmission of H. pylori occurs through numerous routes, including oral-oral and oral-fecal, and thus commonly occurs between family members and in areas where adequate sanitation is not accessible (20).
H. pylori is well suited to survive the gastric environment in humans. It releases a compound called urease, which alters the pH in the area directly surrounding the bacterium, effectively buffering against the stomach's acidity, which would otherwise cause damage (18).
It has a small "tail" called a flagella that allows it to move toward the cells of the stomach lining, where it attaches and colonizes, potentially leading to infection. Once attached, H. pylori releases substances that may affect local tissues (20), which can contribute to inflammation and health issues.
Symptoms of Infection
Although many carriers of H. pylori do not experience symptoms, symptoms can occur once the infection leads to inflammation. These include:
Diagnostic Tests for H. pylori
Testing for H. pylori may involve invasive tests that require an endoscopy or noninvasive tests that rely on stool, breath, or blood samples (17).
Noninvasive Tests
Urea Breath Test (UBT)
The urea breath test (UBT) has been used for over 30 years and is considered a reliable noninvasive testing option for H. pylori. To perform this test, a patient ingests a urea solution in pill or liquid form and undergoes a breath test 15 minutes later.
H. pylori metabolizes the urea and releases carbon dioxide as a byproduct, which is then measured to determine if infection is present. The UBT is noted for its accuracy, with a 95% sensitivity and specificity rate (22).
Medications such as proton-pump inhibitors (PPIs), bismuth, antibiotics, and herbal antibiotics can lead to inaccuracies in testing, so they should be avoided for 2-4 weeks before testing. Additionally, gastrointestinal bleeding from ulcers can interfere with UBT results, and it is recommended to delay testing until bleeding has resolved.
Stool Antigen Test (SAT)
The SAT uses fecal samples to look for H. pylori antigens. It is noted for its sensitivity and specificity for detecting H. pylori and does not involve costly or invasive procedures.
Like the UBT, the accuracy of the SAT can be affected by recent antibiotic or PPI use and upper gastrointestinal bleeding and should be delayed in the presence of these. Irregular bowel movements may also affect accuracy (22).
In addition to SAT, it is possible to test for H. pylori in the stool using PCR techniques that detect the presence of bacterial DNA and can provide more detailed genetic information about the specific genotypes of the bacteria present (22).
Serology
Blood tests that detect the presence of anti-H pylori IgG antibodies can also indicate present or recent H. pylori exposure.
However, because IgG antibodies can persist in the bloodstream well after an infection has resolved, the serology tests cannot distinguish between past and current infections, making it less desirable than the UBT and SAT for clinical diagnostic purposes.
The advantage of the H. pylori blood test is that it is unaffected by gastrointestinal bleeding and PPI, antibiotic, or bismuth use (22).
Invasive Tests
Endoscopy with Biopsy
All invasive testing starts with an endoscopy, a procedure in which an instrument is inserted into the stomach and duodenum of the small intestine to visualize the gastrointestinal lining.
Biopsies (small tissue samples) are taken from the gastric mucosa during this procedure. These samples are then further examined and tested for the presence of H. pylori using PCR testing or one or more of the methods below.
Because endoscopies are invasive and costly, they are generally reserved for testing for more severe manifestations of H. pylori infection, such as gastrointestinal bleeding, suspected peptic or duodenal ulcers, gastric cancer, and MALT lymphoma (17,22).
When assessing for H. pylori, most biopsy samples are taken from the antrum and corpus of the stomach (22).
Histology
Histology is considered a standard method for direct H. pylori testing. Once tissue samples are obtained by biopsy, they are treated with specific stains that make it easier to visualize the presence of H. pylori cells. These samples are then examined under a microscope to detect infection.
Like the UBT and SAT, histological examination is vulnerable to the recent use of PPIs and antibiotics, so these medications should be avoided for at least 2-4 weeks before the biopsy samples are taken.
Additionally, H. pylori is often distributed unevenly throughout the stomach lining. So, these cells can only be detected if biopsies are taken in H. pylori-concentrated areas (22).
Culture
Culturing H. pylori involves placing a biopsy sample into a growth media and incubating it to assess for H. pylori cell growth. Although culture studies can be more susceptible to human and laboratory error, they have the distinct advantage of being able to test for antibiotic sensitivity to help guide treatment options. Culture and sensitivity studies are recommended in areas where clarithromycin resistance exceeds 20% (22).
Rapid Urease Test (RUT)
RUT is a quick, inexpensive, and reliable method of identifying H. pylori in tissue samples. This test uses a urea test reagent that converts to ammonia in the presence of H. pylori, causing a notable increase in pH levels, detected using a pH monitor.
The main disadvantage of an RUT is its poor accuracy in the presence of gastric bleeding, so it should not be the sole indicator used in these cases (22).
How to Choose the Right Diagnostic Test
With a multitude of options to choose from, it can take time to determine which test is most appropriate for a patient. Due to the ease, accuracy, and noninvasive nature of the UBT and SAT, these tests can be helpful in pediatric patients when endoscopies are not otherwise warranted.
The UBT and SAT are also appropriate for testing in adults when symptoms are not severe and more serious issues such as bleeding ulcers, gastric cancer, and MALT lymphoma are not suspected or have been previously ruled out (22). However, endoscopies are required for diagnostic workup if these issues are suspected.
Additionally, the UBT and SAT are often employed to monitor management efficacy to ensure that H. pylori is no longer present. For these purposes, waiting 2-4 weeks post antibiotic, bismuth, and PPI use is essential to enhance testing accuracy (20).
How to Approach H. pylori Based on Diagnosis
If testing confirms an active H. pylori presence in the presence of symptoms, management of the presence is often considered. First-line management options are focused on addressing H. pylori and include a combination of antibiotics, PPIs, and sometimes bismuth taken together or sequentially:
- Clarithromycin triple therapy: The standard first-line approach for H. pylori, this therapy combines PPI, clarithromycin, amoxicillin, and metronidazole for 14 days. It should only be undertaken when clarithromycin resistance is less than 15%.
- Bismuth quadruple therapy: PPI, bismuth, tetracycline, and nitroimidazole in combination for 10-14 days. This approach is suitable for those with penicillin allergies and high clarithromycin resistance.
- Concomitant therapy: PPI, clarithromycin, amoxicillin, and nitroimidazole taken together for 10-14 days. Evidence suggests that this approach has the highest rates of addressing H. pylori among the conventional first-line options.
Including culture antibiotic sensitivity analysis in the diagnostic workup can help guide which antibiotics would be most effective for management and which would likely lead to resistance.
Follow-up testing via a UBT or SAT is often performed to ensure that a prescribed approach effectively addresses the H. pylori presence (20).
[signup]
Key Takeaways
Accurate identification of H. pylori is essential for effective patient management, as it guides appropriate strategies that can support gastrointestinal health.
Healthcare practitioners should prioritize staying updated with the latest diagnostic technologies and guidelines developments.
This commitment to continual learning will enhance their ability to detect H. pylori accurately and improve overall clinical outcomes for their patients.
Adelman, M. (2024, February 9). Acid Reducers and Nutrient Absorption: What You Need to Know. Rupa Health. https://www.rupahealth.com/post/acid-reducers-and-nutrient-absorption-what-you-need-to-know
Bertagna, B. (2024, January 24). Can Diet Play A Role In Heartburn Relief? Rupa Health. https://www.rupahealth.com/post/can-diet-play-a-role-in-heartburn-relief
Chey, W. D., Leontiadis, G. I., Howden, C. W., & Moss, S. F. (2017). ACG Clinical Guideline: Treatment of Helicobacter pylori Infection. American Journal of Gastroenterology, 112(2), 212–239. https://doi.org/10.1038/ajg.2016.563
Christie, J. (2023, January 26). 5 Lab Test Can That Help Diagnose The Root Cause of Chronic Bloating. Rupa Health. https://www.rupahealth.com/post/5-lab-test-that-help-diagnose-the-root-cause-of-chronic-bloating
Cloyd, J. (2023a, February 21). A Functional Medicine GERD Protocol. Rupa Health. https://www.rupahealth.com/post/a-functional-medicine-gerd-protocol
Cloyd, J. (2023b, March 16). A Functional Medicine H. Pylori Treatment Protocol. Rupa Health. https://www.rupahealth.com/post/a-functional-medicine-h-pylori-treatment-protocol
Cloyd, J. (2023c, March 29). Top 5 Differential Diagnosis for Abdominal Pain and How to Treat With Functional Medicine. Rupa Health. https://www.rupahealth.com/post/top-5-differential-diagnoses-for-abdominal-pain-and-how-to-treat-with-functional-medicine
Cloyd, J. (2023d, April 5). Treatment of Antibiotic Resistance Through Functional Medicine. Rupa Health. https://www.rupahealth.com/post/treatment-of-antibiotic-resistance-through-functional-medicine
Cloyd, J. (2023e, April 13). A Functional Medicine Protocol for Peptic Ulcers. Rupa Health. https://www.rupahealth.com/post/a-functional-medicine-protocol-for-peptic-ulcers
Cloyd, J. (2023f, June 20). A Functional Medicine H-Pylori Protocol: Testing, Diagnoses, and Treatment. Rupa Health. https://www.rupahealth.com/post/a-functional-medicine-h-pylori-protocol-testing-diagnoses-and-treatment
Cloyd, J. (2023g, July 3). The Importance of Comprehensive Stool Testing in Functional Medicine. Rupa Health. https://www.rupahealth.com/post/the-importance-of-comprehensive-stool-testing-in-functional-medicine
Cloyd, J. (2023h, July 26). A Functional Medicine Iron Deficiency Anemia Protocol: Comprehensive Testing, Therapeutic Diet, and Supplements. Rupa Health. https://www.rupahealth.com/post/a-functional-medicine-iron-deficiency-anemia-protocol-comprehensive-testing-therapeutic-diet-and-supplements
Cloyd, J. (2023i, December 29). How to Use An H Pylori Test to Diagnose and Treat. Rupa Health. https://www.rupahealth.com/post/how-to-use-an-h-pylori-test-to-diagnose-and-treat
Endoscopy: Procedure, Types, What To Expect. (n.d.). Cleveland Clinic. Retrieved May 1, 2024, from https://my.clevelandclinic.org/health/diagnostics/25126-endoscopy
H. pylori IgG. (n.d.). Rupa Health. Retrieved May 28, 2024, from https://www.rupahealth.com/biomarkers/h-pylori-igg
Hooi, J. K. Y., Lai, W. Y., Ng, W. K., Suen, M. M. Y., Underwood, F. E., Tanyingoh, D., Malfertheiner, P., Graham, D. Y., Wong, V. W. S., Wu, J. C. Y., Chan, F. K. L., Sung, J. J. Y., Kaplan, G. G., & Ng, S. C. (2017). Global Prevalence of Helicobacter pylori Infection: Systematic Review and Meta-Analysis. Gastroenterology, 153(2), 420–429. https://doi.org/10.1053/j.gastro.2017.04.022
Iannone, A., Giorgio, F., Russo, F., Riezzo, G., Girardi, B., Pricci, M., Palmer, S. C., Barone, M., Principi, M., Strippoli, G. F., Leo, A. D., & Ierardi, E. (2018). New fecal test for noninvasive Helicobacter pylori detection: A diagnostic accuracy study. World Journal of Gastroenterology, 24(27), 3021–3029. https://doi.org/10.3748/wjg.v24.i27.3021
Kao, C.-Y., Sheu, B.-S., & Wu, J.-J. (2016). Helicobacter pylori infection: An overview of bacterial virulence factors and pathogenesis. Biomedical Journal, 39(1), 14–23. https://doi.org/10.1016/j.bj.2015.06.002
Lee, H. J. (2015). Concomitant therapy achieved the best eradication rate forHelicobacter pyloriamong various treatment strategies. World Journal of Gastroenterology, 21(1), 351. https://doi.org/10.3748/wjg.v21.i1.351
Parikh, N. S., & Ahlawat, R. (2022, August 8). Helicobacter Pylori. PubMed; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK534233/
Perera, H. (2024, May 23). Labs to Test for H. pylori Infection: A Comprehensive Guide. Rupa Health. https://www.rupahealth.com/post/labs-test-h-pylori
Wang, Y.-K. (2015). Diagnosis ofHelicobacter pyloriinfection: Current options and developments. World Journal of Gastroenterology, 21(40), 11221. https://doi.org/10.3748/wjg.v21.i40.11221
Weinberg, J. (2022, September 23). An Integrative Medicine Approach to Gastritis. Rupa Health. https://www.rupahealth.com/post/6-natural-treatments-for-gastritis