Overview

Definition:
-Helicobacter pylori (H
-pylori) is a gram-negative bacterium that infects the gastric mucosa, commonly causing gastritis and peptic ulcer disease
-In children, infection can be asymptomatic or manifest with various gastrointestinal symptoms
-It is a significant cause of chronic gastritis and is associated with an increased risk of peptic ulcer disease and gastric adenocarcinoma in adults, though the latter is rare in children.
Epidemiology:
-The prevalence of H
-pylori infection in children varies significantly worldwide, generally being lower in developed countries and higher in developing nations, often acquired in childhood through fecal-oral or oral-oral transmission
-In India, seroprevalence studies show varying rates, with some indicating a significant burden of infection even in younger age groups, influenced by socioeconomic factors and hygiene practices.
Clinical Significance:
-Prompt diagnosis and effective eradication of H
-pylori in symptomatic children are crucial to prevent long-term complications such as peptic ulcer disease, growth retardation, and iron deficiency anemia
-Understanding current diagnostic strategies and evidence-based treatment regimens is essential for pediatricians preparing for DNB and NEET SS examinations, impacting patient outcomes and preventing recurrence.

Clinical Presentation

Symptoms:
-Many children with H
-pylori are asymptomatic
-Symptomatic children may present with: Epigastric pain, often described as burning or gnawing, which may be worse on an empty stomach or at night
-Nausea and vomiting
-Early satiety
-Loss of appetite
-Abdominal distension
-Unexplained weight loss or failure to thrive
-Vomiting of blood (hematemesis) or passing black, tarry stools (melena) are alarming signs of upper GI bleeding.
Signs:
-Physical examination may reveal: Epigastric tenderness on palpation
-In cases of significant bleeding, pallor may be present
-Signs of malnutrition or growth failure in chronic, symptomatic infections
-In most cases, the physical examination is non-specific.
Diagnostic Criteria:
-There are no strict diagnostic criteria for H
-pylori infection itself in children, but rather guidelines for when to test based on symptoms and risk factors
-The diagnosis is confirmed by detecting the bacteria or its products using validated methods
-Current international guidelines (e.g., ESPGHAN) provide recommendations for testing and management.

Diagnostic Approach

History Taking:
-Key history points include: Duration, character, and timing of abdominal pain
-Association with meals, time of day, or nocturnal symptoms
-Presence of nausea, vomiting, early satiety, or anorexia
-History of weight loss or failure to thrive
-Previous diagnoses of PUD, gastritis, or H
-pylori infection
-Family history of H
-pylori, peptic ulcers, or gastric cancer
-Medications, especially NSAIDs
-Red flags: Hematemesis, melena, unexplained weight loss, severe persistent vomiting, dysphagia, or iron deficiency anemia unresponsive to iron supplementation.
Physical Examination:
-A thorough abdominal examination is essential, focusing on: Inspection for distension or scars
-Palpation for tenderness (especially epigastric), masses, or organomegaly
-Auscultation for bowel sounds
-Assessment of growth parameters (height, weight, BMI) and signs of anemia or malnutrition.
Investigations:
-Non-invasive testing is preferred in children when indicated
-Invasive testing (biopsy) is usually reserved for children undergoing endoscopy for other reasons: Non-invasive: Urea Breath Test (UBT) - highly sensitive and specific, involves ingesting a labeled urea compound and measuring labeled CO2 in exhaled breath
-Stool Antigen Test (SAT) - detects H
-pylori antigen in stool, good sensitivity and specificity
-Serology (IgG antibodies) - less reliable for active infection diagnosis, as antibodies can persist for months after eradication
-more useful for epidemiological studies or historical infection status
-Invasive: Endoscopic biopsy with rapid urease testing (RUT), histology, or PCR - gold standard but requires endoscopy
-Culture is rarely used due to low sensitivity and difficulty in rapid results.
Differential Diagnosis:
-Conditions to consider in children with abdominal pain or dyspepsia include: Functional dyspepsia (most common)
-Gastroesophageal reflux disease (GERD)
-Peptic ulcer disease (if H
-pylori positive or other causes)
-Esophagitis
-Gastritis (non-H
-pylori)
-Irritable bowel syndrome
-Lactose intolerance
-Constipation
-Pancreatitis
-Malabsorption syndromes.

When To Test

Indications For Testing:
-Testing for H
-pylori in children is generally recommended in the presence of: Documented peptic ulcer disease (gastric or duodenal ulcer)
-Unexplained iron deficiency anemia unresponsive to iron therapy, particularly in older children and adolescents
-Chronic or recurrent abdominal pain with alarm symptoms (as listed in history taking)
-A strong family history of gastric cancer
-Children with certain conditions like Henoch-Schönlein purpura or chronic urticaria have also been considered, but indications are evolving.
Timing Of Test:
-Testing should ideally be performed when the child is not on proton pump inhibitors (PPIs) or antibiotics for at least 2 weeks, as these can lead to false-negative results
-Bismuth compounds should be avoided for at least 4 weeks prior to testing
-For UBT and stool antigen tests, the absence of PPIs and antibiotics is crucial.

Management

Eradication Therapy Regimens:
-Treatment aims to eradicate H
-pylori and heal any associated pathology
-Standard triple therapy (Omeprazole, Clarithromycin, Amoxicillin/Metronidazole) is often used, but resistance is increasing
-Recommended first-line therapies often include a PPI, Amoxicillin, and Clarithromycin or Metronidazole, or a PPI with bismuth, Amoxicillin, and Metronidazole
-High-dose dual therapy (PPI + Amoxicillin) or sequential therapy are alternatives
-Recommended regimens for DNB/NEET SS preparation: 1
-Standard Triple Therapy: PPI (e.g., Omeprazole 1mg/kg/day divided BID) + Clarithromycin (15mg/kg/day divided BID) + Amoxicillin (25-50mg/kg/day divided BID) OR Metronidazole (20mg/kg/day divided BID) for 10-14 days
-2
-Bismuth-based Quadruple Therapy: PPI + Bismuth subsalicylate (e.g., 15mg/kg/day divided QID) + Amoxicillin (25-50mg/kg/day divided BID) + Metronidazole (20mg/kg/day divided BID) for 10-14 days
-Clarithromycin resistance rates influence choice
-if >20%, non-Clarithromycin regimens are preferred.
Duration And Doses:
-Therapy typically lasts for 10-14 days
-Doses are weight-based and may vary slightly between guidelines
-For Amoxicillin, doses up to 50mg/kg/day are common
-For Clarithromycin, up to 15mg/kg/day
-For Metronidazole, up to 20mg/kg/day
-PPI doses are usually 0.5-1mg/kg/day
-Bismuth doses are around 15mg/kg/day.
Follow Up Testing:
-Test-of-cure is recommended 4-8 weeks after completion of therapy, using UBT or stool antigen test, to confirm eradication
-Repeat testing is crucial as eradication rates can be suboptimal
-If initial therapy fails, salvage therapy with a different regimen, often guided by susceptibility testing if possible, is indicated
-Re-testing for H
-pylori is essential after failed treatment.

Complications

Peptic Ulcer Disease: Gastric or duodenal ulcers are the most common complication, leading to pain, bleeding, perforation, or obstruction.
Iron Deficiency Anemia: Chronic blood loss from gastritis or ulcers can cause or exacerbate iron deficiency anemia, especially in children.
Growth Retardation: In severe, chronic infections, malabsorption and poor nutritional intake can lead to impaired growth and failure to thrive.
Gastric Adenocarcinoma:
-While extremely rare in children, chronic H
-pylori infection is a known risk factor for gastric cancer in adults, highlighting the importance of eradication.
Prevention Strategies:
-Good hygiene practices, including hand washing and safe food and water, are key to preventing transmission
-Early diagnosis and treatment of symptomatic children are vital to prevent long-term complications.

Prognosis

Factors Affecting Prognosis:
-Prognosis is generally good with successful eradication of H
-pylori and resolution of associated complications
-Factors influencing outcome include the severity of initial infection, presence of complications (e.g., perforation), adherence to treatment, and bacterial resistance patterns.
Outcomes With Treatment:
-Successful eradication leads to symptom resolution, healing of ulcers, and improvement in anemia and growth parameters
-Eradication significantly reduces the risk of ulcer recurrence.
Long Term Follow Up:
-Children with a history of peptic ulcer disease or complications may require periodic follow-up to monitor for recurrence and ensure adequate growth
-Those with H
-pylori-related anemia usually show improvement after successful eradication and iron supplementation
-Long-term monitoring for gastric cancer risk is not generally recommended in children unless they have specific risk factors for other reasons.

Key Points

Exam Focus:
-DNB/NEET SS exam focus: Indications for testing in children (ulcers, IDA, chronic pain with alarm symptoms)
-Preferred non-invasive tests (UBT, stool antigen)
-Contraindications for testing (recent antibiotics/PPIs)
-First-line and alternative eradication regimens (PPI-based triple/quadruple therapy)
-Importance of test-of-cure
-Complications like PUD, IDA, growth failure.
Clinical Pearls:
-Always consider H
-pylori in children with unexplained iron deficiency anemia or persistent dyspeptic symptoms
-Eradication therapy requires strict adherence to the full course
-Always re-test for H
-pylori after treatment to confirm eradication
-Be aware of local antibiotic resistance patterns when selecting therapy.
Common Mistakes:
-Not testing for H
-pylori in indicated children
-Using serology for active infection diagnosis
-Failing to stop PPIs/antibiotics before testing
-Incomplete treatment courses or non-adherence
-Not performing test-of-cure
-Treating symptoms without confirming eradication.