British Society of Gastroenterology guidelines on the diagnosis and management of patients at risk of gastric adenocarcinoma
Gastric adenocarcinoma carries a poor prognosis, in part due to the late stage of diagnosis. Risk factors include Helicobacter pylori infection, family history of gastric cancer—in particular, hereditary diffuse gastric cancer and pernicious anaemia. The stages in the progression to cancer include c...
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Veröffentlicht in: | Gut 2019-09, Vol.68 (9), p.1545-1575 |
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creator | Banks, Matthew Graham, David Jansen, Marnix Gotoda, Takuji Coda, Sergio di Pietro, Massimiliano Uedo, Noriya Bhandari, Pradeep Pritchard, D Mark Kuipers, Ernst J Rodriguez-Justo, Manuel Novelli, Marco R Ragunath, Krish Shepherd, Neil Dinis-Ribeiro, Mario |
description | Gastric adenocarcinoma carries a poor prognosis, in part due to the late stage of diagnosis. Risk factors include Helicobacter pylori infection, family history of gastric cancer—in particular, hereditary diffuse gastric cancer and pernicious anaemia. The stages in the progression to cancer include chronic gastritis, gastric atrophy (GA), gastric intestinal metaplasia (GIM) and dysplasia. The key to early detection of cancer and improved survival is to non-invasively identify those at risk before endoscopy. However, although biomarkers may help in the detection of patients with chronic atrophic gastritis, there is insufficient evidence to support their use for population screening. High-quality endoscopy with full mucosal visualisation is an important part of improving early detection. Image-enhanced endoscopy combined with biopsy sampling for histopathology is the best approach to detect and accurately risk-stratify GA and GIM. Biopsies following the Sydney protocol from the antrum, incisura, lesser and greater curvature allow both diagnostic confirmation and risk stratification for progression to cancer. Ideally biopsies should be directed to areas of GA or GIM visualised by high-quality endoscopy. There is insufficient evidence to support screening in a low-risk population (undergoing routine diagnostic oesophagogastroduodenoscopy) such as the UK, but endoscopic surveillance every 3 years should be offered to patients with extensive GA or GIM. Endoscopic mucosal resection or endoscopic submucosal dissection of visible gastric dysplasia and early cancer has been shown to be efficacious with a high success rate and low rate of recurrence, providing that specific quality criteria are met. |
doi_str_mv | 10.1136/gutjnl-2018-318126 |
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Risk factors include Helicobacter pylori infection, family history of gastric cancer—in particular, hereditary diffuse gastric cancer and pernicious anaemia. The stages in the progression to cancer include chronic gastritis, gastric atrophy (GA), gastric intestinal metaplasia (GIM) and dysplasia. The key to early detection of cancer and improved survival is to non-invasively identify those at risk before endoscopy. However, although biomarkers may help in the detection of patients with chronic atrophic gastritis, there is insufficient evidence to support their use for population screening. High-quality endoscopy with full mucosal visualisation is an important part of improving early detection. Image-enhanced endoscopy combined with biopsy sampling for histopathology is the best approach to detect and accurately risk-stratify GA and GIM. Biopsies following the Sydney protocol from the antrum, incisura, lesser and greater curvature allow both diagnostic confirmation and risk stratification for progression to cancer. Ideally biopsies should be directed to areas of GA or GIM visualised by high-quality endoscopy. There is insufficient evidence to support screening in a low-risk population (undergoing routine diagnostic oesophagogastroduodenoscopy) such as the UK, but endoscopic surveillance every 3 years should be offered to patients with extensive GA or GIM. Endoscopic mucosal resection or endoscopic submucosal dissection of visible gastric dysplasia and early cancer has been shown to be efficacious with a high success rate and low rate of recurrence, providing that specific quality criteria are met.</description><identifier>ISSN: 0017-5749</identifier><identifier>EISSN: 1468-3288</identifier><identifier>DOI: 10.1136/gutjnl-2018-318126</identifier><identifier>PMID: 31278206</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and British Society of Gastroenterology</publisher><subject>Adenocarcinoma ; Adenocarcinoma - diagnosis ; Adenocarcinoma - microbiology ; Adenocarcinoma - surgery ; Agreements ; Anemia ; Atrophy ; Biomarkers, Tumor - blood ; Biopsy ; Diagnosis ; Disease Management ; Disease Progression ; Dysplasia ; Early Detection of Cancer - methods ; Endoscopy ; Evidence-Based Medicine - methods ; gastric adenocarcinoma ; Gastric cancer ; gastric pre-cancer ; Gastritis ; Gastritis, Atrophic - diagnosis ; Gastritis, Atrophic - microbiology ; Gastritis, Atrophic - surgery ; Gastroenterology ; Gastroscopy - methods ; Guidelines ; Helicobacter Infections - complications ; Helicobacter Infections - drug therapy ; Helicobacter pylori ; helicobacter pylori-gastritis ; Humans ; Intestine ; Medical research ; Metaplasia ; Mucosa ; Pernicious anemia ; Precancerous Conditions - diagnosis ; Precancerous Conditions - microbiology ; Precancerous Conditions - surgery ; Quality ; Risk Assessment - methods ; Risk factors ; Stomach Neoplasms - diagnosis ; Stomach Neoplasms - microbiology ; Stomach Neoplasms - surgery ; Surveillance ; University colleges</subject><ispartof>Gut, 2019-09, Vol.68 (9), p.1545-1575</ispartof><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2019 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b573t-3c0a06a9f19a799a4e635cf97066381e299508b80973958abb41e36c30a755723</citedby><cites>FETCH-LOGICAL-b573t-3c0a06a9f19a799a4e635cf97066381e299508b80973958abb41e36c30a755723</cites><orcidid>0000-0003-0645-564X ; 0000-0002-9137-2779</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709778/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709778/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31278206$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Banks, Matthew</creatorcontrib><creatorcontrib>Graham, David</creatorcontrib><creatorcontrib>Jansen, Marnix</creatorcontrib><creatorcontrib>Gotoda, Takuji</creatorcontrib><creatorcontrib>Coda, Sergio</creatorcontrib><creatorcontrib>di Pietro, Massimiliano</creatorcontrib><creatorcontrib>Uedo, Noriya</creatorcontrib><creatorcontrib>Bhandari, Pradeep</creatorcontrib><creatorcontrib>Pritchard, D Mark</creatorcontrib><creatorcontrib>Kuipers, Ernst J</creatorcontrib><creatorcontrib>Rodriguez-Justo, Manuel</creatorcontrib><creatorcontrib>Novelli, Marco R</creatorcontrib><creatorcontrib>Ragunath, Krish</creatorcontrib><creatorcontrib>Shepherd, Neil</creatorcontrib><creatorcontrib>Dinis-Ribeiro, Mario</creatorcontrib><title>British Society of Gastroenterology guidelines on the diagnosis and management of patients at risk of gastric adenocarcinoma</title><title>Gut</title><addtitle>Gut</addtitle><addtitle>Gut</addtitle><description>Gastric adenocarcinoma carries a poor prognosis, in part due to the late stage of diagnosis. Risk factors include Helicobacter pylori infection, family history of gastric cancer—in particular, hereditary diffuse gastric cancer and pernicious anaemia. The stages in the progression to cancer include chronic gastritis, gastric atrophy (GA), gastric intestinal metaplasia (GIM) and dysplasia. The key to early detection of cancer and improved survival is to non-invasively identify those at risk before endoscopy. However, although biomarkers may help in the detection of patients with chronic atrophic gastritis, there is insufficient evidence to support their use for population screening. High-quality endoscopy with full mucosal visualisation is an important part of improving early detection. Image-enhanced endoscopy combined with biopsy sampling for histopathology is the best approach to detect and accurately risk-stratify GA and GIM. Biopsies following the Sydney protocol from the antrum, incisura, lesser and greater curvature allow both diagnostic confirmation and risk stratification for progression to cancer. Ideally biopsies should be directed to areas of GA or GIM visualised by high-quality endoscopy. There is insufficient evidence to support screening in a low-risk population (undergoing routine diagnostic oesophagogastroduodenoscopy) such as the UK, but endoscopic surveillance every 3 years should be offered to patients with extensive GA or GIM. Endoscopic mucosal resection or endoscopic submucosal dissection of visible gastric dysplasia and early cancer has been shown to be efficacious with a high success rate and low rate of recurrence, providing that specific quality criteria are met.</description><subject>Adenocarcinoma</subject><subject>Adenocarcinoma - diagnosis</subject><subject>Adenocarcinoma - microbiology</subject><subject>Adenocarcinoma - surgery</subject><subject>Agreements</subject><subject>Anemia</subject><subject>Atrophy</subject><subject>Biomarkers, Tumor - blood</subject><subject>Biopsy</subject><subject>Diagnosis</subject><subject>Disease Management</subject><subject>Disease Progression</subject><subject>Dysplasia</subject><subject>Early Detection of Cancer - methods</subject><subject>Endoscopy</subject><subject>Evidence-Based Medicine - methods</subject><subject>gastric adenocarcinoma</subject><subject>Gastric cancer</subject><subject>gastric pre-cancer</subject><subject>Gastritis</subject><subject>Gastritis, Atrophic - diagnosis</subject><subject>Gastritis, Atrophic - microbiology</subject><subject>Gastritis, Atrophic - surgery</subject><subject>Gastroenterology</subject><subject>Gastroscopy - methods</subject><subject>Guidelines</subject><subject>Helicobacter Infections - complications</subject><subject>Helicobacter Infections - drug therapy</subject><subject>Helicobacter pylori</subject><subject>helicobacter pylori-gastritis</subject><subject>Humans</subject><subject>Intestine</subject><subject>Medical research</subject><subject>Metaplasia</subject><subject>Mucosa</subject><subject>Pernicious anemia</subject><subject>Precancerous Conditions - diagnosis</subject><subject>Precancerous Conditions - microbiology</subject><subject>Precancerous Conditions - surgery</subject><subject>Quality</subject><subject>Risk Assessment - methods</subject><subject>Risk factors</subject><subject>Stomach Neoplasms - diagnosis</subject><subject>Stomach Neoplasms - microbiology</subject><subject>Stomach Neoplasms - surgery</subject><subject>Surveillance</subject><subject>University colleges</subject><issn>0017-5749</issn><issn>1468-3288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>ACMMV</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkUtv1DAUhS0EotPCH2CBLLFhk-LHxI8NEq1oQarEAlhbN46T8ZDYg50gjcSPx1HK8FggVrbv_c7RvT4IPaPkklIuXvXztA9DxQhVFaeKMvEAbehWlBdT6iHaEEJlVcutPkPnOe8JIUpp-hidccqkYkRs0Per5Cefd_hjtN5NRxw7fAt5StGFyaU4xP6I-9m3bvDBZRwDnnYOtx76ELPPGEKLRwjQu7EoFvkBJl-upTXh5POXpdYvlt5iaF2IFpL1IY7wBD3qYMju6f15gT7fvP10_a66-3D7_vrNXdXUkk8VtwSIAN1RDVJr2DrBa9tpSYTgijqmdU1Uo4iWXNcKmmZLHReWE5B1LRm_QK9X38PcjK61ZboEgzkkP0I6mgje_NkJfmf6-M0IWTylKgYv7w1S_Dq7PJnRZ-uGAYKLczaM1eXLNa95QV_8he7jnEJZr1BCK6GYpoViK2VTzDm57jQMJWYJ16zhmiVcs4ZbRM9_X-Mk-ZlmAaoVaMb9_xle_uJPY_5D8ANzKMCL</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Banks, Matthew</creator><creator>Graham, David</creator><creator>Jansen, Marnix</creator><creator>Gotoda, Takuji</creator><creator>Coda, Sergio</creator><creator>di Pietro, Massimiliano</creator><creator>Uedo, Noriya</creator><creator>Bhandari, Pradeep</creator><creator>Pritchard, D Mark</creator><creator>Kuipers, Ernst J</creator><creator>Rodriguez-Justo, Manuel</creator><creator>Novelli, Marco R</creator><creator>Ragunath, Krish</creator><creator>Shepherd, Neil</creator><creator>Dinis-Ribeiro, Mario</creator><general>BMJ Publishing Group Ltd and British Society of Gastroenterology</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0645-564X</orcidid><orcidid>https://orcid.org/0000-0002-9137-2779</orcidid></search><sort><creationdate>20190901</creationdate><title>British Society of Gastroenterology guidelines on the diagnosis and management of patients at risk of gastric adenocarcinoma</title><author>Banks, Matthew ; Graham, David ; Jansen, Marnix ; Gotoda, Takuji ; Coda, Sergio ; di Pietro, Massimiliano ; Uedo, Noriya ; Bhandari, Pradeep ; Pritchard, D Mark ; Kuipers, Ernst J ; Rodriguez-Justo, Manuel ; Novelli, Marco R ; Ragunath, Krish ; Shepherd, Neil ; Dinis-Ribeiro, Mario</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b573t-3c0a06a9f19a799a4e635cf97066381e299508b80973958abb41e36c30a755723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adenocarcinoma</topic><topic>Adenocarcinoma - diagnosis</topic><topic>Adenocarcinoma - microbiology</topic><topic>Adenocarcinoma - surgery</topic><topic>Agreements</topic><topic>Anemia</topic><topic>Atrophy</topic><topic>Biomarkers, Tumor - blood</topic><topic>Biopsy</topic><topic>Diagnosis</topic><topic>Disease Management</topic><topic>Disease Progression</topic><topic>Dysplasia</topic><topic>Early Detection of Cancer - methods</topic><topic>Endoscopy</topic><topic>Evidence-Based Medicine - methods</topic><topic>gastric adenocarcinoma</topic><topic>Gastric cancer</topic><topic>gastric pre-cancer</topic><topic>Gastritis</topic><topic>Gastritis, Atrophic - diagnosis</topic><topic>Gastritis, Atrophic - microbiology</topic><topic>Gastritis, Atrophic - surgery</topic><topic>Gastroenterology</topic><topic>Gastroscopy - methods</topic><topic>Guidelines</topic><topic>Helicobacter Infections - complications</topic><topic>Helicobacter Infections - drug therapy</topic><topic>Helicobacter pylori</topic><topic>helicobacter pylori-gastritis</topic><topic>Humans</topic><topic>Intestine</topic><topic>Medical research</topic><topic>Metaplasia</topic><topic>Mucosa</topic><topic>Pernicious anemia</topic><topic>Precancerous Conditions - diagnosis</topic><topic>Precancerous Conditions - microbiology</topic><topic>Precancerous Conditions - surgery</topic><topic>Quality</topic><topic>Risk Assessment - methods</topic><topic>Risk factors</topic><topic>Stomach Neoplasms - diagnosis</topic><topic>Stomach Neoplasms - microbiology</topic><topic>Stomach Neoplasms - surgery</topic><topic>Surveillance</topic><topic>University colleges</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Banks, Matthew</creatorcontrib><creatorcontrib>Graham, David</creatorcontrib><creatorcontrib>Jansen, Marnix</creatorcontrib><creatorcontrib>Gotoda, Takuji</creatorcontrib><creatorcontrib>Coda, Sergio</creatorcontrib><creatorcontrib>di Pietro, Massimiliano</creatorcontrib><creatorcontrib>Uedo, Noriya</creatorcontrib><creatorcontrib>Bhandari, Pradeep</creatorcontrib><creatorcontrib>Pritchard, D Mark</creatorcontrib><creatorcontrib>Kuipers, Ernst J</creatorcontrib><creatorcontrib>Rodriguez-Justo, Manuel</creatorcontrib><creatorcontrib>Novelli, Marco R</creatorcontrib><creatorcontrib>Ragunath, Krish</creatorcontrib><creatorcontrib>Shepherd, Neil</creatorcontrib><creatorcontrib>Dinis-Ribeiro, Mario</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Gut</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Banks, Matthew</au><au>Graham, David</au><au>Jansen, Marnix</au><au>Gotoda, Takuji</au><au>Coda, Sergio</au><au>di Pietro, Massimiliano</au><au>Uedo, Noriya</au><au>Bhandari, Pradeep</au><au>Pritchard, D Mark</au><au>Kuipers, Ernst J</au><au>Rodriguez-Justo, Manuel</au><au>Novelli, Marco R</au><au>Ragunath, Krish</au><au>Shepherd, Neil</au><au>Dinis-Ribeiro, Mario</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>British Society of Gastroenterology guidelines on the diagnosis and management of patients at risk of gastric adenocarcinoma</atitle><jtitle>Gut</jtitle><stitle>Gut</stitle><addtitle>Gut</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>68</volume><issue>9</issue><spage>1545</spage><epage>1575</epage><pages>1545-1575</pages><issn>0017-5749</issn><eissn>1468-3288</eissn><abstract>Gastric adenocarcinoma carries a poor prognosis, in part due to the late stage of diagnosis. Risk factors include Helicobacter pylori infection, family history of gastric cancer—in particular, hereditary diffuse gastric cancer and pernicious anaemia. The stages in the progression to cancer include chronic gastritis, gastric atrophy (GA), gastric intestinal metaplasia (GIM) and dysplasia. The key to early detection of cancer and improved survival is to non-invasively identify those at risk before endoscopy. However, although biomarkers may help in the detection of patients with chronic atrophic gastritis, there is insufficient evidence to support their use for population screening. High-quality endoscopy with full mucosal visualisation is an important part of improving early detection. Image-enhanced endoscopy combined with biopsy sampling for histopathology is the best approach to detect and accurately risk-stratify GA and GIM. Biopsies following the Sydney protocol from the antrum, incisura, lesser and greater curvature allow both diagnostic confirmation and risk stratification for progression to cancer. Ideally biopsies should be directed to areas of GA or GIM visualised by high-quality endoscopy. There is insufficient evidence to support screening in a low-risk population (undergoing routine diagnostic oesophagogastroduodenoscopy) such as the UK, but endoscopic surveillance every 3 years should be offered to patients with extensive GA or GIM. Endoscopic mucosal resection or endoscopic submucosal dissection of visible gastric dysplasia and early cancer has been shown to be efficacious with a high success rate and low rate of recurrence, providing that specific quality criteria are met.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and British Society of Gastroenterology</pub><pmid>31278206</pmid><doi>10.1136/gutjnl-2018-318126</doi><tpages>31</tpages><orcidid>https://orcid.org/0000-0003-0645-564X</orcidid><orcidid>https://orcid.org/0000-0002-9137-2779</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Adenocarcinoma - diagnosis Adenocarcinoma - microbiology Adenocarcinoma - surgery Agreements Anemia Atrophy Biomarkers, Tumor - blood Biopsy Diagnosis Disease Management Disease Progression Dysplasia Early Detection of Cancer - methods Endoscopy Evidence-Based Medicine - methods gastric adenocarcinoma Gastric cancer gastric pre-cancer Gastritis Gastritis, Atrophic - diagnosis Gastritis, Atrophic - microbiology Gastritis, Atrophic - surgery Gastroenterology Gastroscopy - methods Guidelines Helicobacter Infections - complications Helicobacter Infections - drug therapy Helicobacter pylori helicobacter pylori-gastritis Humans Intestine Medical research Metaplasia Mucosa Pernicious anemia Precancerous Conditions - diagnosis Precancerous Conditions - microbiology Precancerous Conditions - surgery Quality Risk Assessment - methods Risk factors Stomach Neoplasms - diagnosis Stomach Neoplasms - microbiology Stomach Neoplasms - surgery Surveillance University colleges |
title | British Society of Gastroenterology guidelines on the diagnosis and management of patients at risk of gastric adenocarcinoma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T16%3A33%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=British%20Society%20of%20Gastroenterology%20guidelines%20on%20the%20diagnosis%20and%20management%20of%20patients%20at%20risk%20of%20gastric%20adenocarcinoma&rft.jtitle=Gut&rft.au=Banks,%20Matthew&rft.date=2019-09-01&rft.volume=68&rft.issue=9&rft.spage=1545&rft.epage=1575&rft.pages=1545-1575&rft.issn=0017-5749&rft.eissn=1468-3288&rft_id=info:doi/10.1136/gutjnl-2018-318126&rft_dat=%3Cproquest_pubme%3E2269868291%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2269868291&rft_id=info:pmid/31278206&rfr_iscdi=true |