{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,19]],"date-time":"2026-10-19T23:26:07Z","timestamp":1792452367414,"version":"4.5.0"},"reference-count":18,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2014,11,7]],"date-time":"2014-11-07T00:00:00Z","timestamp":1415318400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Haemophilia"],"published-print":{"date-parts":[[2015,5]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Recurrent gastrointestinal bleeding is one of the most challenging complications encountered in the management of patients with von Willebrand disease (<jats:styled-content style=\"fixed-case\">VWD<\/jats:styled-content>). The commonest cause is angiodysplasia, but often no cause is identified due to the difficulty in making the diagnosis. The optimal treatment to prevent recurrences remains unknown. We performed a retrospective study of <jats:styled-content style=\"fixed-case\">VWD<\/jats:styled-content> patients with occult or angiodysplastic bleeding within the setting of the von Willebrand Disease Prophylaxis Network (<jats:styled-content style=\"fixed-case\">VWD PN<\/jats:styled-content>) to describe diagnostic and treatment strategies. Centres participating in the <jats:styled-content style=\"fixed-case\">VWD PN<\/jats:styled-content> recruited subjects under their care with a history of congenital <jats:styled-content style=\"fixed-case\">VWD<\/jats:styled-content> and gastrointestinal (<jats:styled-content style=\"fixed-case\">GI<\/jats:styled-content>) bleeding due to angiodysplasia, or cases in which the cause was not identified despite investigation. Patients with acquired von Willebrand syndrome or those for whom the <jats:styled-content style=\"fixed-case\">GI<\/jats:styled-content> bleeding was due to another cause were excluded. Forty\u2010eight patients from 18 centres in 10 countries were recruited. Seven individuals had a family history of <jats:styled-content style=\"fixed-case\">GI<\/jats:styled-content> bleeding and all <jats:styled-content style=\"fixed-case\">VWD<\/jats:styled-content> types except 2N were represented. Angiodysplasia was confirmed in 38%, with video capsule endoscopy and <jats:styled-content style=\"fixed-case\">GI<\/jats:styled-content> tract endoscopies being the most common methods of making the diagnosis. Recurrent <jats:styled-content style=\"fixed-case\">GI<\/jats:styled-content> bleeding in <jats:styled-content style=\"fixed-case\">VWD<\/jats:styled-content> is associated with significant morbidity and required hospital admission on up to 30 occasions. Patients were treated with multiple pharmacological agents with prophylactic von Willebrand factor concentrate being the most efficient in preventing recurrence of the <jats:styled-content style=\"fixed-case\">GI<\/jats:styled-content> bleeding. The diagnosis and treatment of recurrent <jats:styled-content style=\"fixed-case\">GI<\/jats:styled-content> bleeding in congenital <jats:styled-content style=\"fixed-case\">VWD<\/jats:styled-content> remains challenging and is associated with significant morbidity. Prophylactic treatment with von Willebrand factor concentrate was the most effective method of preventing recurrent bleeding but its efficacy remains to be confirmed in a prospective study.<\/jats:p>","DOI":"10.1111\/hae.12571","type":"journal-article","created":{"date-parts":[[2014,11,8]],"date-time":"2014-11-08T03:03:21Z","timestamp":1415415801000},"page":"338-342","source":"Crossref","is-referenced-by-count":48,"title":["The natural history of occult or angiodysplastic gastrointestinal bleeding in von Willebrand disease"],"prefix":"10.1111","volume":"21","author":[{"given":"M.","family":"Makris","sequence":"first","affiliation":[{"name":"Sheffield Haemophilia and Thrombosis Centre Royal Hallamshire Hospital Sheffield UK"},{"name":"Department of Cardiovascular Science University of Sheffield Sheffield UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A. B.","family":"Federici","sequence":"additional","affiliation":[{"name":"Hematology and Transfusion Medicine L.SACCO University Hospital University of Milan Milan Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P. M.","family":"Mannucci","sequence":"additional","affiliation":[{"name":"Scientific Direction IRCCS Ca' Granda Maggiore Policlinico Hospital Foundation Milan Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P. H. B.","family":"Bolton\u2010Maggs","sequence":"additional","affiliation":[{"name":"SHOT Office Manchester Blood Centre Plymouth Grove Manchester UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T. 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