Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34321
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dc.contributor.authorChapman, Brooke-
dc.contributor.authorWong, Darren-
dc.contributor.authorWhitcher, Bethany-
dc.contributor.authorSinclair, Marie-
dc.contributor.authorGow, Paul J-
dc.contributor.authorMajumdar, Avik-
dc.contributor.authorTestro, Adam G-
dc.date2023-
dc.date.accessioned2023-12-01T02:13:36Z-
dc.date.available2023-12-01T02:13:36Z-
dc.date.issued2023-11-13-
dc.identifier.citationNutrients 2023-11-13; 15(22)en_US
dc.identifier.issn2072-6643-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34321-
dc.description.abstractMalnutrition is ubiquitous in cirrhotic patients presenting for liver transplant (LT). Providing an appropriate energy prescription is fundamental to effective nutrition therapy. We aimed to compare measured energy expenditure (mEE) with predicted energy expenditure (pEE) in patients awaiting LT and determine clinical factors associated with mEE. In this prospective observational study, energy expenditure was measured by indirect calorimetry in 110 adult patients referred for LT and predicted by commonly utilized equations (Harris-Benedict, Schofield, and EASL guidelines). Nutritional status, anthropometry, muscle function, biochemical and clinical data were also collected. The median model for end-stage liver disease (MELD) was 19 (IQR 13, 25), and the majority were Child-Pugh B (51%) or C (37%). Malnutrition was evident in 85%. Median mEE by calorimetry was 1756 (1531, 2104) kcal/d and significantly higher than pEE as per Harris-Benedict 1480 (1322, 1722) kcal/d and Schofield 1474 (1349, 1723) kcal/d (both p < 0.001), but lower than EASL guidelines (35 kcal/kg) when an activity factor was applied to mEE; 2283 (1990, 2735) kcal/d versus 2590 (2178, 3010) kcal/d (p < 0.001). Hypermetabolism (mEE:pEE > 1.2) was evident in 48% of the cohort. Multivariate analysis found MELD, Child-Pugh class, diuretic use, and severe malnutrition to be independent predictors of hypermetabolism. A new liver-specific predictive model has been developed, showing superior agreement with mEE than common predictive equations. In conclusion, there is a poor correlation between mEE and pEE in patients awaiting LTs, and hypermetabolism is common. Relying on historical predictive equations in this patient population may result in significant under or over-feeding. A tailored energy prescription based on indirect calorimetry or a liver-specific predictive model is recommended for LT candidates.en_US
dc.language.isoeng-
dc.subjectcirrhosisen_US
dc.subjectenergy requirementsen_US
dc.subjectindirect calorimetryen_US
dc.subjectliver transplanten_US
dc.subjectmalnutritionen_US
dc.titleRedefining Nutritional Requirements in End-Stage Liver Disease: Towards a Personalized Approach.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleNutrientsen_US
dc.identifier.affiliationNutrition and Dieteticsen_US
dc.identifier.affiliationVictorian Liver Transplant Uniten_US
dc.identifier.affiliationSchool of Medicine, Dentistry and Health Sciences, The University of Melbourne, Melbourne, VIC 3010, Australia.en_US
dc.identifier.doi10.3390/nu15224770en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-7251-8314en_US
dc.identifier.orcid0000-0003-1490-0547en_US
dc.identifier.orcid0000-0003-0657-3048en_US
dc.identifier.pubmedid38004164-
dc.description.volume15-
dc.description.issue22-
dc.subject.meshtermssecondaryEnergy Metabolism/physiology-
dc.subject.meshtermssecondaryMalnutrition/etiology-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptNutrition and Dietetics-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
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