H. pylori epidemiology and pathogenesis: gram-negative microaerophilic spiral bacterium colonizing gastric mucosa; global prevalence 50% (higher in developing countries). Transmission - oral-oral, fecal-oral; mostly acquired in childhood. Virulence factors - urease (acid neutralization), CagA (cytotoxin associated gene A; pro-inflammatory), VacA (vacuolating cytotoxin), BabA (adhesin). Pathology spectrum - chronic gastritis (100%), peptic ulcer (10-15%), gastric adenocarcinoma (1-3%, especially intestinal type), MALT lymphoma (<1%, often regresses with eradication), iron deficiency anemia, ITP.
Diagnosis: 1) Non-invasive - urea breath test (sensitivity 95%, specificity 95%; first choice; PPI off ≥2 weeks, antibiotic off ≥4 weeks); stool antigen test (similar performance, cheaper); serology (low specificity, only suggests prior exposure, not active); 2) Invasive (endoscopy) - histology (sensitivity 90-95%; gold standard with H&E + Giemsa staining), rapid urease test (CLO test; 5-10% false negative if PPI), culture (allows susceptibility testing; needed in refractory cases), molecular tests (PCR, FISH for clarithromycin resistance). Indications - PUD, MALT lymphoma, gastric cancer first-degree relatives, atrophic gastritis, ITP, iron deficiency, long-term NSAID/aspirin, dyspepsia (test-and-treat <60 yr).
Eradication regimens (Maastricht VI/Florence 2022): 1) First-line - bismuth quadruple therapy (BQT): PPI bid + bismuth subcitrate 240 mg qid + tetracycline 500 mg qid + metronidazole 500 mg tid, 14 days (eradication >90%); preferred in high clarithromycin resistance (>15%); 2) Alternative first-line - concomitant therapy: PPI bid + amoxicillin 1 g bid + clarithromycin 500 mg bid + metronidazole 500 mg bid, 14 days; only if low clarithromycin resistance; 3) Rescue - levofloxacin triple (PPI + amoxicillin + levofloxacin 500 mg/day), rifabutin triple (PPI + amoxicillin + rifabutin 150 mg bid); high-dose dual therapy (HDDT) - PPI qid + amoxicillin 1 g qid; vonoprazan-based regimens (potassium-competitive acid blocker) increasing in availability. Confirmation - urea breath test or stool antigen ≥4 weeks after eradication, ≥2 weeks off PPI.