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dc.contributor.authorJazayeri, SMHM
dc.contributor.authorOstadrahimi, A
dc.contributor.authorSafaiyan, A
dc.contributor.authorHashemzadeh, S
dc.contributor.authorSalehpour, F
dc.date.accessioned2018-08-26T07:25:43Z
dc.date.available2018-08-26T07:25:43Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/46694
dc.description.abstractBackground: Despite advances on nutrition in Intensive Care Unit (ICU), effects of different nutritional treatments and methods on inflammatory markers are still controversial in critically ill patients. This study was designed to examine the effects of four different methods of enteral feeding on serum levels of tumor necrosis factor-alpha (TNF-alpha) and high sensitive C-reactive protein (hs-CRP) in surgical ICU patients. Methods: In a double blinded, randomized controlled trial, 25critically ill patients were recruited. They randomly divided to four groups regarding enteral feeding: early closed (EC), delayed closed (DC), early opened (EO) and delayed opened (DO). Blood samples were obtained to measure TNF-alpha and hs-CRP on day 1st, 3rd, 5th and 7th by using ELISA method. Results: Monitoring of TNF-alpha and hs-CRP revealed a significant elevation of these inflammatory factors at 3rd day of ICU admission (P< 0.001) and a significant decrease on 5th and 7thdays (P< 0.001) in all groups. The inflammatory factors were controlled in early closed (EC) group more efficiently than other groups. Conclusion: Early closed (EC) enteral feeding can efficiently reduce both TNF-alpha and hs-CRP in ICU patients more than other methods of enteral feeding. Early initiation of closed enteral feeding has to be considered in critically ill patients.
dc.language.isoEnglish
dc.relation.ispartofPROGRESS IN NUTRITION
dc.subjectenteral feedings
dc.subjectalbumin
dc.subjectnutritional intake
dc.titleEffects of four different enteral feeding methods on tumor Necrosis Factor-alpha (TNF-alpha) and high sensitive C-Reactive Protein (hs-CRP) in critically Ill Patients: double blinded, randomized controlled trial
dc.typeArticle
dc.citation.volume18
dc.citation.issue3
dc.citation.spage236
dc.citation.epage241
dc.citation.indexWeb of science


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