Management of epithelial precancerous conditions and lesions in the stomach (MAPS II): European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter and Microbiota Study Group (EHMSG), European Society of Pathology (ESP), and Sociedade Portuguesa de Endoscopia Digestiva (SPED) guideline update 2019
Main Recommendations Patients with chronic atrophic gastritis or intestinal metaplasia (IM) are at risk for gastric adenocarcinoma. This underscores the importance of diagnosis and risk stratification for these patients. High definition endoscopy with chromoendoscopy (CE) is better than high definit...
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Published in | Endoscopy Vol. 51; no. 4; pp. 365 - 388 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Stuttgart · New York
Georg Thieme Verlag KG
01.04.2019
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Subjects | |
Online Access | Get full text |
ISSN | 0013-726X 1438-8812 |
DOI | 10.1055/a-0859-1883 |
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Abstract | Main Recommendations
Patients with chronic atrophic gastritis or intestinal metaplasia (IM) are at risk for gastric adenocarcinoma. This underscores the importance of diagnosis and risk stratification for these patients. High definition endoscopy with chromoendoscopy (CE) is better than high definition white-light endoscopy alone for this purpose. Virtual CE can guide biopsies for staging atrophic and metaplastic changes and can target neoplastic lesions. Biopsies should be taken from at least two topographic sites (antrum and corpus) and labelled in two separate vials. For patients with mild to moderate atrophy restricted to the antrum there is no evidence to recommend surveillance. In patients with IM at a single location but with a family history of gastric cancer, incomplete IM, or persistent
Helicobacter pylori
gastritis, endoscopic surveillance with CE and guided biopsies may be considered in 3 years. Patients with advanced stages of atrophic gastritis should be followed up with a high quality endoscopy every 3 years. In patients with dysplasia, in the absence of an endoscopically defined lesion, immediate high quality endoscopic reassessment with CE is recommended. Patients with an endoscopically visible lesion harboring low or high grade dysplasia or carcinoma should undergo staging and treatment.
H. pylori
eradication heals nonatrophic chronic gastritis, may lead to regression of atrophic gastritis, and reduces the risk of gastric cancer in patients with these conditions, and it is recommended.
H. pylori
eradication is also recommended for patients with neoplasia after endoscopic therapy. In intermediate to high risk regions, identification and surveillance of patients with precancerous gastric conditions is cost-effective. |
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AbstractList | Main Recommendations
Patients with chronic atrophic gastritis or intestinal metaplasia (IM) are at risk for gastric adenocarcinoma. This underscores the importance of diagnosis and risk stratification for these patients. High definition endoscopy with chromoendoscopy (CE) is better than high definition white-light endoscopy alone for this purpose. Virtual CE can guide biopsies for staging atrophic and metaplastic changes and can target neoplastic lesions. Biopsies should be taken from at least two topographic sites (antrum and corpus) and labelled in two separate vials. For patients with mild to moderate atrophy restricted to the antrum there is no evidence to recommend surveillance. In patients with IM at a single location but with a family history of gastric cancer, incomplete IM, or persistent
Helicobacter pylori
gastritis, endoscopic surveillance with CE and guided biopsies may be considered in 3 years. Patients with advanced stages of atrophic gastritis should be followed up with a high quality endoscopy every 3 years. In patients with dysplasia, in the absence of an endoscopically defined lesion, immediate high quality endoscopic reassessment with CE is recommended. Patients with an endoscopically visible lesion harboring low or high grade dysplasia or carcinoma should undergo staging and treatment.
H. pylori
eradication heals nonatrophic chronic gastritis, may lead to regression of atrophic gastritis, and reduces the risk of gastric cancer in patients with these conditions, and it is recommended.
H. pylori
eradication is also recommended for patients with neoplasia after endoscopic therapy. In intermediate to high risk regions, identification and surveillance of patients with precancerous gastric conditions is cost-effective. Patients with chronic atrophic gastritis or intestinal metaplasia (IM) are at risk for gastric adenocarcinoma. This underscores the importance of diagnosis and risk stratification for these patients. High definition endoscopy with chromoendoscopy (CE) is better than high definition white-light endoscopy alone for this purpose. Virtual CE can guide biopsies for staging atrophic and metaplastic changes and can target neoplastic lesions. Biopsies should be taken from at least two topographic sites (antrum and corpus) and labelled in two separate vials. For patients with mild to moderate atrophy restricted to the antrum there is no evidence to recommend surveillance. In patients with IM at a single location but with a family history of gastric cancer, incomplete IM, or persistent gastritis, endoscopic surveillance with CE and guided biopsies may be considered in 3 years. Patients with advanced stages of atrophic gastritis should be followed up with a high quality endoscopy every 3 years. In patients with dysplasia, in the absence of an endoscopically defined lesion, immediate high quality endoscopic reassessment with CE is recommended. Patients with an endoscopically visible lesion harboring low or high grade dysplasia or carcinoma should undergo staging and treatment. eradication heals nonatrophic chronic gastritis, may lead to regression of atrophic gastritis, and reduces the risk of gastric cancer in patients with these conditions, and it is recommended. eradication is also recommended for patients with neoplasia after endoscopic therapy. In intermediate to high risk regions, identification and surveillance of patients with precancerous gastric conditions is cost-effective. |
Author | Kikuste, Ilze Marcos-Pinto, Ricardo Leja, Marcis Megraud, Francis Kuipers, Ernst J. Barros, Rita Dumonceau, Jean-Marc Matysiak-Budnik, Tamara van Hooft, Jeanin E. Fléjou, Jean-François Areia, Miguel Annibale, Bruno Dinis-Ribeiro, Mario Pimentel-Nunes, Pedro Esposito, Gianluca Libânio, Diogo Garrido, Monica Carneiro, Fátima |
Author_xml | – sequence: 1 givenname: Pedro surname: Pimentel-Nunes fullname: Pimentel-Nunes, Pedro organization: Gastroenterology Department – sequence: 2 givenname: Diogo surname: Libânio fullname: Libânio, Diogo organization: Center for Research in Health Technologies and Information Systems (CINTESIS), Faculty of Medicine, Porto, Portugal – sequence: 3 givenname: Ricardo surname: Marcos-Pinto fullname: Marcos-Pinto, Ricardo organization: Department of Gastroenterology, Porto University Hospital Centre, Institute of Biomedical Sciences, University of Porto (ICBAS/UP), Portugal – sequence: 4 givenname: Miguel surname: Areia fullname: Areia, Miguel organization: Gastroenterology Department, Portuguese Oncology Institute of Coimbra, Portugal – sequence: 5 givenname: Marcis surname: Leja fullname: Leja, Marcis organization: Institute of Clinical and Preventive Medicine, University of Latvia, Digestive Diseases Center, GASTRO, Riga, Latvia – sequence: 6 givenname: Gianluca surname: Esposito fullname: Esposito, Gianluca organization: Department of Medicine, Surgery and Translational Medicine University Hospital Sant’Andrea, University Sapienza Roma, Rome, Italy – sequence: 7 givenname: Monica surname: Garrido fullname: Garrido, Monica organization: Department of Gastroenterology, Porto University Hospital Centre, Institute of Biomedical Sciences, University of Porto (ICBAS/UP), Portugal – sequence: 8 givenname: Ilze surname: Kikuste fullname: Kikuste, Ilze organization: Institute of Clinical and Preventive Medicine, University of Latvia, Digestive Diseases Center, GASTRO, Riga, Latvia – sequence: 9 givenname: Francis surname: Megraud fullname: Megraud, Francis organization: INSERM U1053, Université de Bordeaux and CHU Pellegrin, Laboratoire de Bacteriologie, Bordeaux, France – sequence: 10 givenname: Tamara surname: Matysiak-Budnik fullname: Matysiak-Budnik, Tamara organization: IMAD, Hepato-Gastroenterology and Digestive Oncology, CHU de Nantes, University of Nantes, France – sequence: 11 givenname: Bruno surname: Annibale fullname: Annibale, Bruno organization: Department of Medicine, Surgery and Translational Medicine University Hospital Sant’Andrea, University Sapienza Roma, Rome, Italy – sequence: 12 givenname: Jean-Marc surname: Dumonceau fullname: Dumonceau, Jean-Marc organization: Gedyt Endoscopy Center, Buenos Aires, Argentina – sequence: 13 givenname: Rita surname: Barros fullname: Barros, Rita organization: Instituto de Investigação e Inovação em Saúde (i3S), University of Porto, Porto, Portugal – sequence: 14 givenname: Jean-François surname: Fléjou fullname: Fléjou, Jean-François organization: Service d’Anatomie Pathologique, Hôpital Saint-Antoine, AP-HP, Faculté de Médecine Sorbonne Université, Paris, France – sequence: 15 givenname: Fátima surname: Carneiro fullname: Carneiro, Fátima organization: Pathology Department, Centro Hospitalar de São João and Faculty of Medicine, Porto, Portugal – sequence: 16 givenname: Jeanin E. surname: van Hooft fullname: van Hooft, Jeanin E. organization: Department of Gastroenterology and Hepatology, Amsterdam UMC, University of Amsterdam, The Netherlands – sequence: 17 givenname: Ernst J. surname: Kuipers fullname: Kuipers, Ernst J. organization: Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands – sequence: 18 givenname: Mario surname: Dinis-Ribeiro fullname: Dinis-Ribeiro, Mario organization: Center for Research in Health Technologies and Information Systems (CINTESIS), Faculty of Medicine, Porto, Portugal |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30841008$$D View this record in MEDLINE/PubMed |
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PublicationTitle | Endoscopy |
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Patients with chronic atrophic gastritis or intestinal metaplasia (IM) are at risk for gastric adenocarcinoma. This underscores the... Patients with chronic atrophic gastritis or intestinal metaplasia (IM) are at risk for gastric adenocarcinoma. This underscores the importance of diagnosis and... |
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SubjectTerms | Biopsy - methods Endoscopy, Gastrointestinal - methods Europe Gastritis, Atrophic - diagnosis Gastritis, Atrophic - pathology Gastritis, Atrophic - therapy Guideline Helicobacter Infections - diagnosis Helicobacter Infections - therapy Humans Metaplasia - pathology Metaplasia - therapy Patient Care Management - methods Patient Care Management - standards Precancerous Conditions - diagnosis Precancerous Conditions - pathology Precancerous Conditions - therapy Risk Assessment - methods Stomach Neoplasms - diagnosis Stomach Neoplasms - pathology Stomach Neoplasms - therapy |
Title | Management of epithelial precancerous conditions and lesions in the stomach (MAPS II): European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter and Microbiota Study Group (EHMSG), European Society of Pathology (ESP), and Sociedade Portuguesa de Endoscopia Digestiva (SPED) guideline update 2019 |
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