Small bowel injury in low-dose aspirin users
The use of low-dose aspirin (LDA) is well known to be associated with an increased risk of serious upper gastrointestinal complications, such as peptic ulceration and bleeding. Until recently, attention was mainly focused on aspirin-induced damage of the stomach and duodenum. However, recently, ther...
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Veröffentlicht in: | Journal of gastroenterology 2015-04, Vol.50 (4), p.378-386 |
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description | The use of low-dose aspirin (LDA) is well known to be associated with an increased risk of serious upper gastrointestinal complications, such as peptic ulceration and bleeding. Until recently, attention was mainly focused on aspirin-induced damage of the stomach and duodenum. However, recently, there has been growing interest among gastroenterologists on the adverse effects of aspirin on the small bowel, especially as new endoscopic techniques, such as capsule endoscopy (CE) and balloon-assisted endoscopy, have become available for the evaluation of small bowel lesions. Preliminary CE studies conducted in healthy subjects have shown that short-term administration of LDA can induce mild mucosal inflammation of the small bowel. Furthermore, chronic use of LDA results in a variety of lesions in the small bowel, including multiple petechiae, loss of villi, erosions, and round, irregular, or punched-out ulcers. Some patients develop circumferential ulcers with stricture. In addition, to reduce the incidence of gastrointestinal lesions in LDA users, it is important for clinicians to confirm the differences in the gastrointestinal toxicity between different types of aspirin formulations in clinical use. Some studies suggest that enteric-coated aspirin may be more injurious to the small bowel mucosa than buffered aspirin. The ideal treatment for small bowel injury in patients taking LDA would be withdrawal of aspirin, however, LDA is used as an antiplatelet agent in the majority of patients, and its withdrawal could increase the risk of cardiovascular/cerebrovascular morbidity and mortality. Thus, novel means for the treatment of aspirin-induced enteropathy are urgently needed. |
doi_str_mv | 10.1007/s00535-014-1028-x |
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Until recently, attention was mainly focused on aspirin-induced damage of the stomach and duodenum. However, recently, there has been growing interest among gastroenterologists on the adverse effects of aspirin on the small bowel, especially as new endoscopic techniques, such as capsule endoscopy (CE) and balloon-assisted endoscopy, have become available for the evaluation of small bowel lesions. Preliminary CE studies conducted in healthy subjects have shown that short-term administration of LDA can induce mild mucosal inflammation of the small bowel. Furthermore, chronic use of LDA results in a variety of lesions in the small bowel, including multiple petechiae, loss of villi, erosions, and round, irregular, or punched-out ulcers. Some patients develop circumferential ulcers with stricture. In addition, to reduce the incidence of gastrointestinal lesions in LDA users, it is important for clinicians to confirm the differences in the gastrointestinal toxicity between different types of aspirin formulations in clinical use. Some studies suggest that enteric-coated aspirin may be more injurious to the small bowel mucosa than buffered aspirin. The ideal treatment for small bowel injury in patients taking LDA would be withdrawal of aspirin, however, LDA is used as an antiplatelet agent in the majority of patients, and its withdrawal could increase the risk of cardiovascular/cerebrovascular morbidity and mortality. Thus, novel means for the treatment of aspirin-induced enteropathy are urgently needed.</description><identifier>ISSN: 0944-1174</identifier><identifier>EISSN: 1435-5922</identifier><identifier>DOI: 10.1007/s00535-014-1028-x</identifier><identifier>PMID: 25501289</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject><![CDATA[Abdominal Surgery ; Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Anti-Inflammatory Agents, Non-Steroidal - adverse effects ; Aspirin ; Aspirin - administration & dosage ; Aspirin - adverse effects ; Capsule Endoscopy ; Colorectal Surgery ; Dosage and administration ; Drug Administration Schedule ; Endoscopy ; Gastroenterology ; Gastrointestinal Hemorrhage - chemically induced ; Gastrointestinal Hemorrhage - prevention & control ; Hepatology ; Humans ; Intestinal Diseases - chemically induced ; Intestinal Diseases - prevention & control ; Intestine, Small - drug effects ; Medicine ; Medicine & Public Health ; Peptic ulcer ; Platelet Aggregation Inhibitors - administration & dosage ; Platelet Aggregation Inhibitors - adverse effects ; Review ; Surgical Oncology ; Ulcer - chemically induced ; Ulcer - prevention & control]]></subject><ispartof>Journal of gastroenterology, 2015-04, Vol.50 (4), p.378-386</ispartof><rights>Springer Japan 2014</rights><rights>COPYRIGHT 2015 Springer</rights><rights>Springer Japan 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c576t-dd0bec48ca38ae69b41e830c6ee71fa8cab0979df666901509fb16fc4d35cf1f3</citedby><cites>FETCH-LOGICAL-c576t-dd0bec48ca38ae69b41e830c6ee71fa8cab0979df666901509fb16fc4d35cf1f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00535-014-1028-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00535-014-1028-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25501289$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Endo, Hiroki</creatorcontrib><creatorcontrib>Sakai, Eiji</creatorcontrib><creatorcontrib>Kato, Takayuki</creatorcontrib><creatorcontrib>Umezawa, Shotaro</creatorcontrib><creatorcontrib>Higurashi, Takuma</creatorcontrib><creatorcontrib>Ohkubo, Hidenori</creatorcontrib><creatorcontrib>Nakajima, Atsushi</creatorcontrib><title>Small bowel injury in low-dose aspirin users</title><title>Journal of gastroenterology</title><addtitle>J Gastroenterol</addtitle><addtitle>J Gastroenterol</addtitle><description>The use of low-dose aspirin (LDA) is well known to be associated with an increased risk of serious upper gastrointestinal complications, such as peptic ulceration and bleeding. Until recently, attention was mainly focused on aspirin-induced damage of the stomach and duodenum. However, recently, there has been growing interest among gastroenterologists on the adverse effects of aspirin on the small bowel, especially as new endoscopic techniques, such as capsule endoscopy (CE) and balloon-assisted endoscopy, have become available for the evaluation of small bowel lesions. Preliminary CE studies conducted in healthy subjects have shown that short-term administration of LDA can induce mild mucosal inflammation of the small bowel. Furthermore, chronic use of LDA results in a variety of lesions in the small bowel, including multiple petechiae, loss of villi, erosions, and round, irregular, or punched-out ulcers. Some patients develop circumferential ulcers with stricture. In addition, to reduce the incidence of gastrointestinal lesions in LDA users, it is important for clinicians to confirm the differences in the gastrointestinal toxicity between different types of aspirin formulations in clinical use. Some studies suggest that enteric-coated aspirin may be more injurious to the small bowel mucosa than buffered aspirin. The ideal treatment for small bowel injury in patients taking LDA would be withdrawal of aspirin, however, LDA is used as an antiplatelet agent in the majority of patients, and its withdrawal could increase the risk of cardiovascular/cerebrovascular morbidity and mortality. Thus, novel means for the treatment of aspirin-induced enteropathy are urgently needed.</description><subject>Abdominal Surgery</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - adverse effects</subject><subject>Aspirin</subject><subject>Aspirin - administration & dosage</subject><subject>Aspirin - adverse effects</subject><subject>Capsule Endoscopy</subject><subject>Colorectal Surgery</subject><subject>Dosage and administration</subject><subject>Drug Administration Schedule</subject><subject>Endoscopy</subject><subject>Gastroenterology</subject><subject>Gastrointestinal Hemorrhage - chemically induced</subject><subject>Gastrointestinal Hemorrhage - prevention & control</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Intestinal Diseases - chemically induced</subject><subject>Intestinal Diseases - prevention & control</subject><subject>Intestine, Small - drug effects</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Peptic ulcer</subject><subject>Platelet Aggregation Inhibitors - administration & dosage</subject><subject>Platelet Aggregation Inhibitors - adverse effects</subject><subject>Review</subject><subject>Surgical Oncology</subject><subject>Ulcer - chemically induced</subject><subject>Ulcer - prevention & control</subject><issn>0944-1174</issn><issn>1435-5922</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kFtLAzEQhYMotlZ_gC9S8NWtM7vJbvJYijco-KA-h2w2KVv2UpMubf-9KVtvoMzDwJnvTDKHkEuECQJktx6AJSwCpBFCzKPtERkiDQoTcXxMhiBomGBGB-TM-yUAJsD4KRnEjAHGXAzJzUutqmqctxtTjctm2bldaOOq3URF681Y-VXpgtB54_w5ObGq8ubi0Efk7f7udfYYzZ8fnmbTeaRZlq6jooDcaMq1SrgyqcgpGp6ATo3J0Kqg5yAyUdg0TQUgA2FzTK2mRcK0RZuMyHW_d-Xa9874tVy2nWvCkxLTDIAjiuybWqjKyLKx7dopXZdey2mGlPFE0DhQkz-oUIWpS902xpZB_2XA3qBd670zVq5cWSu3kwhyH7vsY5chdrmPXW6D5-rw4S6vTfHl-Mw5AHEP-DBqFsb9uOjfrR-Cu4s3</recordid><startdate>20150401</startdate><enddate>20150401</enddate><creator>Endo, Hiroki</creator><creator>Sakai, Eiji</creator><creator>Kato, Takayuki</creator><creator>Umezawa, Shotaro</creator><creator>Higurashi, Takuma</creator><creator>Ohkubo, Hidenori</creator><creator>Nakajima, Atsushi</creator><general>Springer Japan</general><general>Springer</general><general>Springer Nature B.V</general><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>7RV</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20150401</creationdate><title>Small bowel injury in low-dose aspirin users</title><author>Endo, Hiroki ; 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Until recently, attention was mainly focused on aspirin-induced damage of the stomach and duodenum. However, recently, there has been growing interest among gastroenterologists on the adverse effects of aspirin on the small bowel, especially as new endoscopic techniques, such as capsule endoscopy (CE) and balloon-assisted endoscopy, have become available for the evaluation of small bowel lesions. Preliminary CE studies conducted in healthy subjects have shown that short-term administration of LDA can induce mild mucosal inflammation of the small bowel. Furthermore, chronic use of LDA results in a variety of lesions in the small bowel, including multiple petechiae, loss of villi, erosions, and round, irregular, or punched-out ulcers. Some patients develop circumferential ulcers with stricture. In addition, to reduce the incidence of gastrointestinal lesions in LDA users, it is important for clinicians to confirm the differences in the gastrointestinal toxicity between different types of aspirin formulations in clinical use. Some studies suggest that enteric-coated aspirin may be more injurious to the small bowel mucosa than buffered aspirin. The ideal treatment for small bowel injury in patients taking LDA would be withdrawal of aspirin, however, LDA is used as an antiplatelet agent in the majority of patients, and its withdrawal could increase the risk of cardiovascular/cerebrovascular morbidity and mortality. Thus, novel means for the treatment of aspirin-induced enteropathy are urgently needed.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>25501289</pmid><doi>10.1007/s00535-014-1028-x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abdominal Surgery Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Anti-Inflammatory Agents, Non-Steroidal - adverse effects Aspirin Aspirin - administration & dosage Aspirin - adverse effects Capsule Endoscopy Colorectal Surgery Dosage and administration Drug Administration Schedule Endoscopy Gastroenterology Gastrointestinal Hemorrhage - chemically induced Gastrointestinal Hemorrhage - prevention & control Hepatology Humans Intestinal Diseases - chemically induced Intestinal Diseases - prevention & control Intestine, Small - drug effects Medicine Medicine & Public Health Peptic ulcer Platelet Aggregation Inhibitors - administration & dosage Platelet Aggregation Inhibitors - adverse effects Review Surgical Oncology Ulcer - chemically induced Ulcer - prevention & control |
title | Small bowel injury in low-dose aspirin users |
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