The clinic opens 1 October 2026
Breath test

SIBO

SIBO is typically investigated with a hydrogen and methane breath test. The test may support an assessment of bacterial overgrowth in the small intestine, but must always be interpreted together with symptoms and clinical context.

Important to know

This page contains general patient information and is not an individual diagnosis or treatment plan. A breath-test result must always be interpreted by a doctor in the overall clinical context — symptoms, medical history and risk factors alone cannot determine whether you have SIBO.

General patient information

The breath test: what is measured, and what the numbers mean

Here you can read the thresholds used in international consensus documents. You cannot enter your own measurements here and receive an individual interpretation - results are interpreted by the doctor together with your symptoms and the rest of your assessment.

Thresholds (static presentation, North American Consensus)

  • Hydrogen (H₂): a rise of at least 20 ppm above baseline within 90 minutes may support a positive finding.
  • Methane (CH₄): a value of at least 10 ppm at any point may support a positive finding.
  • Hydrogen sulphide (H₂S): a research area with no universally accepted threshold.
  • The thresholds are consensus-based and have known limitations. A result may support a suspicion, but it does not prove SIBO and cannot be interpreted in isolation.

How the test is performed

  • Preparation with dietary and medication restrictions is agreed in advance.
  • The substrate is glucose or lactulose. Fructose is used for fructose malabsorption and is not a SIBO substrate.
  • The test consists of repeated breath samples over roughly 2-3 hours.

When a breath test may be relevant to discuss

  • With dysmotility, previous gastrointestinal surgery, relevant anatomical changes, systemic sclerosis or signs of malabsorption.
  • Bloating or meal-related symptoms alone do not make a breath test indicated.
  • The breath test is not a routine part of an IBS assessment.

Clearly marked example - fictional

Fictional example: a baseline H₂ of 6 ppm and a highest H₂ of 31 ppm at 75 minutes corresponds to a rise of 25 ppm, which is above the consensus threshold and may support a suspicion. The example is constructed for illustration and is not an interpretation of your numbers.

Book a consultation

Interpretation of your own measurements always takes place in a medical consultation - not in a web tool.

This page contains general information only. No results are calculated, no treatment or medication is suggested and no data is stored.

What is SIBO?

Small Intestinal Bacterial Overgrowth (SIBO) describes a condition where the small intestine has an abnormally elevated number and/or an altered composition of bacteria compared with the normal, relatively bacteria-sparse environment.[1],[2]

SIBO is most often investigated with a breath test. This is an indirect investigation that measures microbially produced hydrogen and methane in exhaled breath. The result may support an assessment of SIBO or intestinal methanogen overgrowth (IMO), but cannot be interpreted in isolation — it always forms part of an overall medical assessment.[3],[4]

Symptoms of suspected SIBO — bloating, flatulence, irregular bowel habits, abdominal pain and early satiety — are non-specific and occur in many other conditions. Symptoms alone therefore cannot be used to make or exclude a diagnosis of SIBO.[1],[5]

What can the breath test — and what can it not — show?

Professional societies do not agree on how much diagnostic value the breath test has. The ACG Clinical Guideline, the AGA Clinical Practice Update and the North American Consensus describe the test as a useful, non-invasive tool when used in patients with relevant clinical suspicion.[1],[2],[3] Established consensus

Conversely, more recent critical reviews and the European guideline point out that the test has significant limitations: both false positive and false negative results occur, and the test's value depends heavily on how likely the diagnosis is beforehand (pre-test probability) and on the clinical context.[5],[4] Debated

The time it takes for the test substrate to reach the caecum from the stomach (oral-caecal transit time) especially affects the lactulose test, because lactulose passes through the entire small intestine and on to the colon. The test can therefore be significantly affected by transit time and by fermentation in the colon, which can produce false positive results.[3],[4]

Glucose is mainly absorbed proximally in the small intestine and so may be less sensitive to overgrowth further down the small bowel. On the other hand, the glucose test may have higher specificity than the lactulose test in certain populations. The two substrates each have different strengths and weaknesses, and the choice depends on the clinical question.[3],[1]

How can overgrowth arise? A multifactorial picture

SIBO is not simply a matter of colonic bacteria migrating up into the small intestine. It is thought to reflect an interplay between several systems: gut motility (including the migrating motor complex), anatomical factors, secretory barriers (gastric acid, bile, pancreatic enzymes), immune function and changes in the local microbiota.[1],[2]

  • Motility: Reduced function of the migrating motor complex (MMC), which normally sweeps food residue and bacteria down into the colon between meals, can contribute to overgrowth.
  • Anatomy: Structural factors such as diverticula, strictures or previous gastrointestinal surgery (e.g. Roux-en-Y) can create stasis.
  • Secretion: Low gastric acid (e.g. with long-term PPI use), reduced biliary secretion or exocrine pancreatic insufficiency can weaken the chemical barriers against bacteria.
  • Immune function and microbiota: Changes in gut immune defences and in the composition of the wider microbiota may also play a role.

With prolonged, marked overgrowth, bacteria may deconjugate bile salts, which can impair fat absorption and contribute to reduced absorption of the fat-soluble vitamins A, D, E and K. The bacteria may also consume some of the patient's vitamin B12, while bacterial synthesis can simultaneously produce elevated folate levels. Such findings should always be assessed together with the overall clinical picture.

PPI use has been reported in observational studies as an associated factor for SIBO, but the association is not necessarily causal, and long-term PPI use is not on its own an indication for a breath test. The need for investigation always depends on the overall symptom picture and clinical assessment.[1],[5]

SIBO and IBS — a debated overlap

Studies have reported a higher rate of positive breath tests in some IBS populations, but estimates vary considerably depending on patient selection, substrate and diagnostic criteria. A positive breath test does not by itself demonstrate that SIBO is the cause of the IBS symptoms.[5],[6],[8] Debated

IBS is defined in the Rome criteria as a condition with recurrent abdominal pain linked to altered bowel habit, without requiring a positive breath test.[7]

Gas types: what they can tell us — and what they cannot

It is not possible to determine which gas predominates from symptoms alone. Symptom-based classification into "hydrogen type", "methane type" and "H₂S type" is not used as a diagnostic method — only the breath test's own gas measurements can say anything about which gases are present.[3],[5]

  • Methane is associated in studies with slower gut transit and constipation, but a symptom picture of constipation cannot on its own be used to diagnose methane overgrowth.[1] Conditional recommendation
  • Hydrogen sulphide (H₂S): Hydrogen sulphide measurement is a newer method. There is not yet a universally accepted diagnostic threshold or standardised treatment algorithm.[2] New or non-standardised method

The ACG Clinical Guideline primarily covers hydrogen-based SIBO and methane/IMO. This is not a matter of three equally established microbiological phenotypes.[1]

When is a breath test relevant?

A breath test is relevant in selected symptomatic patients — particularly with documented or suspected dysmotility, relevant anatomical changes, previous gastrointestinal surgery, systemic sclerosis, significant malabsorption or other concrete clinical suspicion. The test is not a routine investigationand is not recommended without an independent clinical suspicion — the result is always interpreted together with the overall clinical picture.[1],[2],[4],[5]

Schematic overview

SIBO — possible contributing factors
Clinical suspicion
Relevant symptom picture + risk factor
Mechanical / motor
May support suspicion of overgrowth
Known or suspected dysmotility
Anatomical stasis / diverticula
Previous GI surgery (e.g. RYGB)
Reduced ileocaecal valve function
Systemic / secretory
Should be assessed in clinical context
Systemic sclerosis
Long-term PPI use
Diabetic autonomic neuropathy
Exocrine pancreatic insufficiency

These factors may be consistent with an increased risk of SIBO, but do not determine the diagnosis on their own. The breath-test result is always assessed together with the overall clinical picture.

The breath test in practice

The patient drinks a standardised amount of substrate (glucose or lactulose) dissolved in water after fasting and a preparatory diet. Exhaled breath is then measured continuously over 2–3 hours.[3]

  • Hydrogen (H₂): A rise of at least 20 ppm above baseline within 90 minutes is used in the North American Consensus to support a positive result. The threshold is consensus-based and has known limitations.[3] Established consensus
  • Methane (CH₄ / IMO): A methane level of at least 10 ppm at any point may support a diagnosis of intestinal methanogen overgrowth in a relevantly symptomatic patient.[3],[1] Conditional recommendation
  • Lactulose: Lactulose passes through the small intestine and on to the colon. The test can therefore be significantly affected by oral-caecal transit time and fermentation in the colon.[4]
  • Glucose: Glucose is mainly absorbed proximally and so may be less sensitive to more distal overgrowth. The test may have higher specificity than lactulose in certain populations.[3]

None of these thresholds alone proves or diagnoses SIBO or IMO — they may support a clinical assessment, which is always made by the treating doctor.

Preparing for the breath test

When you book, you receive the clinic's written, standardised preparation guide. It generally follows these principles:

  • Avoid antibiotics for the period stated in the clinic's instructions before the test.
  • Avoid fermentable and slow-digesting foods the day before the test.
  • Fast overnight before the test.
  • No smoking, no vigorous exercise and no chewing gum on the morning of the test.
  • Brush your teeth before the test.

Important: Prescribed medication — including PPIs and antibiotics — must never be stopped without prior agreement with the treating doctor. Any adjustment of medication as part of preparing for the test must always be agreed individually.

Testing for fructose malabsorption

Fructose is not part of the SIBO breath test. Suspected fructose malabsorption is investigated as a separate question with a fructose breath test, where there is clinically relevant suspicion of it.

Duodenal aspiration with culture

A more invasive method is aspiration of small-intestinal content during gastroscopy, with culture of bacterial counts. The method is used less often in clinical practice because of its invasiveness and variation in cut-off values between laboratories.[1]

Next steps after the breath test

A breath-test result is assessed together with symptoms, risk factors, previous surgery, medication and other possible explanations. A positive result does not automatically lead to antibiotic treatment. The treating doctor assesses whether there is sufficient clinical indication and whether an underlying cause should be investigated or treated.[1],[2]

A low-FODMAP diet may give some patients temporary symptom relief, but the diet does not eradicate any bacterial overgrowth and does not prevent relapse.[6] Low certainty evidence

For healthcare professionals

About rifaximin

Rifaximin has documentation for IBS-D in international studies and guidelines, but treatment of IBS-D and SIBO is off-label in Denmark. Any use requires individual medical assessment of indication, contraindications, side effects and antibiotic use.[9],[6],[10]

Rifaximin and a time-limited low-FODMAP intervention are two different treatment options in IBS-D. There is insufficient evidence for a general recommendation to start them at the same time. The choice and the sequence depend on an individual medical assessment.[6]

Prognosis

Relapse occurs in some patients, particularly if the underlying cause has not been clarified or corrected. With irreversible anatomical changes or severe dysmotility, SIBO is more often seen as a condition that requires ongoing follow-up and an individually tailored plan, determined by the treating doctor.[1],[2]

Book your SIBO test

Frequently asked questions

SIBO — your questions answered

References

These references support the professional points on this page. They do not replace an individual medical assessment.

  1. 1.Pimentel M, Saad RJ, Long MD, Rao SSC. ACG Clinical Guideline: Small Intestinal Bacterial Overgrowth. Am J Gastroenterol. 2020;115(2):165-178. PMID 32023228
  2. 2.Quigley EMM, Murray JA, Pimentel M. AGA Clinical Practice Update on Small Intestinal Bacterial Overgrowth: Expert Review. Gastroenterology. 2020;159(4):1526-1532. PMID 32679220
  3. 3.Rezaie A, Buresi M, Lembo A, et al. Hydrogen and Methane-Based Breath Testing in Gastrointestinal Disorders: The North American Consensus. Am J Gastroenterol. 2017;112(5):775-784. PMID 28323273
  4. 4.Hammer HF, Fox MR, Keller J, et al. European guideline on indications, performance, and clinical impact of hydrogen and methane breath tests in adult and pediatric patients: ESNM, ESPGHAN and EAGEN consensus. United European Gastroenterol J. 2022;10(1):15-40. PMID 34431620
  5. 5.Kashyap P, Moayyedi P, Quigley EMM, Simren M, Vanner S. Critical appraisal of the SIBO hypothesis and breath testing: A clinical practice update endorsed by the European Society of Neurogastroenterology and Motility (ESNM) and the American Neurogastroenterology and Motility Society (ANMS). Neurogastroenterol Motil. 2024;36(8):e14817. PMID 38798120
  6. 6.Lacy BE, Pimentel M, Brenner DM, et al. ACG Clinical Guideline: Management of Irritable Bowel Syndrome. Am J Gastroenterol. 2021;116(1):17-44. PMID 33315591
  7. 7.Corsetti M, et al. Bowel Disorders. Gastroenterology. 2026;170(6):1261-1282. PMID 41713703
  8. 8.Ford AC, Sperber AD, Corsetti M, Camilleri M. Irritable bowel syndrome. Lancet. 2020;396(10263):1675-1688. PMID 33049223
  9. 9.Pimentel M, Lembo A, Chey WD, et al. Rifaximin therapy for patients with irritable bowel syndrome without constipation. N Engl J Med. 2011;364(1):22-32. PMID 21208106
  10. 10.Lægemiddelstyrelsen / produktresume.dk. Produktresumé for Xifaxan (rifaximin) - godkendte indikationer i Danmark (hepatisk encefalopati og rejsediarré). IBS-D og SIBO er ikke godkendte indikationer; anvendelse er dermed off-label i Danmark. Link