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Joint ESPGHAN/NASPGHAN Guidelines for the Management of <i>Helicobacter pylori</i> in Children and Adolescents (Update 2016)

Nicola L. JonesDivision of Gastroenterology, Hepatology and Nutrition Cell Biology Program Sickkids Toronto Departments of Paediatrics and Physiology University of Toronto Toronto CanadaSibylle KoletzkoDivision of Gastroenterology and Hepatology Dr. von Hauner Children's Hospital Ludwig Maximilians University Munich GermanyKaren J. GoodmanDepartment of Medicine and School of Public Health Centre of Excellence for Gastrointestinal Inflammation and Immunity Research University of Alberta Edmonton Alberta CanadaPatrick BontemsPaediatric Gastroenterology Department Hôpital Universitaire des Enfants Reine FabiolaSamy CadranelDepartment of Paediatric Gastroenterology Queen Fabiola University Children's Hospital Université Libre de Bruxelles Brussels BelgiumThomas CasswallPediatric Gastroenterology, Hepatology, and Nutrition CLINTEC Karolinska Institutet and Karolinska University Hospital Stockholm SwedenSteve CzinnDepartment of Pediatrics University of Maryland School of Medicine Baltimore MDBenjamin D. GoldChildren's Center for Digestive Healthcare, LLC Gi Care for Kids, LLC Children's Healthcare of AtlantaJeannette GuarnerDepartment of Pathology and Laboratory Medicine Emory University Atlanta GAYoram ElitsurDepartment of Pediatrics Gastroenterology Division Marshall University School of Medicine Huntington WVMatjaž HomanFaculty of Medicine Department of Gastroenterology, Hepatology and Nutrition University Children's Hospital Ljubljana Ljubljana SloveniaNicolas KalachSaint Antoine Pediatric Clinic Saint Vincent de Paul Hospital Groupement de l’Institut Catholique de Lille (GH‐ICL) Catholic University Lille FranceMichal KoriKaplan Medical Center Hadassah Medical School Hebrew University Jerusalem IsraelArmando MadrazoPediatric Gastroenterology Division Hospital de Pediatría Centro Medico Nacional Siglo XXI I.M.S.S. Mexico City MexicoFrançis MégraudLaboratoire de Bactériologie Université de Bordeaux Bordeaux FranceAlexandra PapadopoulouDivision of Gastroenterology, Hepatology and Nutrition First Department of Pediatrics University of Athens Children's Hospital “Ag. Sofia” Athens GreeceMarion RowlandSchool of Medicine University College Dublin Dublin IrelandESPGHAN, NASPGHAN
2017en
ABI

Аннотация

BACKGROUND: Because of the changing epidemiology of Helicobacter pylori infection and low efficacy of currently recommended therapies, an update of the European Society for Paediatric Gastroenterology Hepatology and Nutrition/North American Society for Pediatric Gastroenterology, Hepatology and Nutrition recommendations for the diagnosis and management of H pylori infection in children and adolescents is required. METHODS: A systematic review of the literature (time period: 2009-2014) was performed. Representatives of both societies evaluated the quality of evidence using GRADE (Grading of Recommendation Assessment, Development, and Evaluation) to formulate recommendations, which were voted upon and finalized using a Delphi process and face-to-face meeting. RESULTS: The consensus group recommended that invasive diagnostic testing for H pylori be performed only when treatment will be offered if tests are positive. To reach the aim of a 90% eradication rate with initial therapy, antibiotics should be tailored according to susceptibility testing. Therapy should be administered for 14 days, emphasizing strict adherence. Clarithromycin-containing regimens should be restricted to children infected with susceptible strains. When antibiotic susceptibility profiles are not known, high-dose triple therapy with proton pump inhibitor, amoxicillin, and metronidazole for 14 days or bismuth-based quadruple therapy is recommended. Success of therapy should be monitored after 4 to 8 weeks by reliable noninvasive tests. CONCLUSIONS: The primary goal of clinical investigation is to identify the cause of upper gastrointestinal symptoms rather than H pylori infection. Therefore, we recommend against a test and treat strategy. Decreasing eradication rates with previously recommended treatments call for changes to first-line therapies and broader availability of culture or molecular-based testing to tailor treatment to the individual child.

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