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dc.contributor.authorHill, Aen_US
dc.contributor.authorHeyland, DKen_US
dc.contributor.authorElke, Gen_US
dc.contributor.authorSchaller, SJen_US
dc.contributor.authorStocker, Ren_US
dc.contributor.authorHaberthür, Cen_US
dc.contributor.authorvon Loeffelholz, Cen_US
dc.contributor.authorSuchner, Uen_US
dc.contributor.authorPuthucheary, ZAen_US
dc.contributor.authorBear, DEen_US
dc.contributor.authorNey, Jen_US
dc.contributor.authorClasen, KCen_US
dc.contributor.authorMeybohm, Pen_US
dc.contributor.authorLindau, Sen_US
dc.contributor.authorLaurentius, Ten_US
dc.contributor.authorStoppe, Cen_US
dc.date.accessioned2020-08-11T12:56:01Z
dc.date.available2020-07-06en_US
dc.date.issued2020-12en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/66203
dc.description.abstractWhile medical nutrition therapy is an essential part of the care for critically ill patients, uncertainty exists about the right form, dosage, timing and route in relation to the phases of critical illness. As enteral nutrition (EN) is often withheld or interrupted during the intensive care unit (ICU) stay, combined EN and parenteral nutrition (PN) may represent an effective and safe option to achieve energy and protein goals as recommended by international guidelines. We hypothesise that critically ill patients at high nutritional risk may benefit from such a combined approach during their stay on the ICU. Therefore, we aim to test if an early combination of EN and high-protein PN (EN+PN) is effective in reaching energy and protein goals in patients at high nutritional risk, while avoiding overfeeding. This approach will be tested in the here-presented EFFORTcombo trial. Nutritionally high-risk ICU patients will be randomised to either high (≥2·2 g/kg per d) or low protein (≤1·2 g/kg per d). In the high protein group, the patients will receive EN+PN; in the low protein group, patients will be given EN alone. EN will be started in accordance with international guidelines in both groups. Efforts will be made to reach nutrition goals within 48-96 h. The efficacy of the proposed nutritional strategy will be tested as an innovative approach by functional outcomes at ICU and hospital discharge, as well as at a 6-month follow-up.en_US
dc.format.extent312 - 320en_US
dc.languageengen_US
dc.relation.ispartofNutr Res Reven_US
dc.rightsThis article has been published in a revised form in Nutrition Research Reviews https://doi.org/10.1017/S0954422420000165. This version is free to view and download for private research and study only. Not for re-distribution or re-use. © copyright holder.
dc.subjectCritical illnessen_US
dc.subjectEnteral nutritionen_US
dc.subjectHigh-protein dieten_US
dc.subjectMalnutritionen_US
dc.subjectNutrition therapyen_US
dc.subjectNutritional statusen_US
dc.subjectParenteral nutritionen_US
dc.titleMeeting nutritional targets of critically ill patients by combined enteral and parenteral nutrition: review and rationale for the EFFORTcombo trial.en_US
dc.typeArticle
dc.identifier.doi10.1017/S0954422420000165en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/32669140en_US
pubs.issue2en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume33en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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