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dc.contributor.author Csontos, Ágnes Anna
dc.contributor.author Molnár, Andrea
dc.contributor.author Piri Z
dc.contributor.author Pálfi, Erzsébet
dc.contributor.author Miheller, Pál
dc.date.accessioned 2017-06-09T08:27:47Z
dc.date.available 2017-06-09T08:27:47Z
dc.date.issued 2017
dc.identifier.citation pagination=26-32; journalVolume=109; journalIssueNumber=1; journalTitle=REVISTA ESPANOLA DE ENFERMEDADES DIGESTIVAS;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4401
dc.identifier.uri doi:10.17235/reed.2016.4557/2016
dc.description.abstract The purpose of malnutrition screening is to predict the probability of a worse outcome due to nutritional factors. The Malnutrition Universal Screening Tool (MUST) can be used for screening in inflammatory bowel disease (IBD); however, it does not provide details about body composition. Our aim was to assess the body composition and combine this with the MUST method to screen risk of malnutrition and sarcopenia. A total of 173 IBD outpatients were enrolled in this cross-sectional study. The MUST scale indicated 21.4% of IBD patients to be at risk of malnutrition. A risk of sarcopenia was detected in 27.7%. However, one third of these patients were not considered to be at risk by their MUST score. Furthermore, Crohn's disease (CD) patients had a strongly unfavorable fat-free mass index (FFMI) value compared to ulcerative colitis (UC) patients, and these differences were significant among men (FFMI: 18.62 +/- 2.16 vs 19.85 +/- 2.22, p = 0.02, in CD and UC males, respectively). As sarcopenia is a relevant prognostic factor, the MUST method should be expanded to include body composition analysis to detect more IBD patients at risk of malnutrition and sarcopenia in order to start their nutritional therapy immediately.
dc.relation.ispartof urn:issn:1130-0108
dc.title Malnutrition risk questionnaire combined with body composition measurement in malnutrition screening in inflammatory bowel disease.
dc.type Journal Article
dc.date.updated 2017-06-09T08:24:43Z
dc.language.rfc3066 en
dc.identifier.mtmt 3153446
dc.identifier.pubmed 27931104


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