Pulse Brain · Growing Health Evidence Index
Tier 2 — RCT / large cohortPeer-reviewed

Effect of intermittent or continuous feeding and amino acid concentration on urea‐to‐creatinine ratio in critical illness

Luke Flower, Ryan W. Haines, Angela McNelly, Danielle E. Bear, Kiran V.K. Koelfat, Steven W.M. Olde Damink, Nicholas Hart, Hugh Montgomery, John R. Prowle, Zudin Puthucheary

Journal of Parenteral and Enteral Nutrition · 2021

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Summary

This secondary analysis of a multicentre UK intensive care trial found that intermittent feeding produced a flatter urea-to-creatinine ratio trajectory compared with continuous feeding, suggesting mitigation of catabolism in critically ill patients. Notably, neither total protein intake nor serum essential amino acid concentrations were independently correlated with the urea-to-creatinine ratio, suggesting that feeding pattern rather than absolute amino acid dose may influence protein metabolism during critical illness.

UK applicability

Findings are directly applicable to UK intensive care practice, derived from a multicentre UK trial. Results may inform clinical nutrition protocols for managing muscle catabolism in critically ill patients receiving parenteral or enteral support.

Key measures

Serum urea-to-creatinine ratio (mmol/mmol) measured from day 0 to day 10; essential amino acid concentrations; protein intake; trajectory clustering of urea-to-creatinine ratio

Outcomes reported

The study measured serum urea-to-creatinine ratio trajectories over 10 days in critically ill patients randomised to intermittent or continuous feeding, as a marker of muscle catabolism. Metabolic phenotypes were identified through clustering analysis of urea-to-creatinine ratio trajectories, and associations between amino acid concentrations and this ratio were modelled.

Theme
Nutrition & health
Subject
Dietary patterns & chronic disease
Study type
Research
Study design
Secondary analysis of a multicentre randomised controlled trial
Source type
Peer-reviewed study
Status
Published
Geography
United Kingdom
System type
Human clinical
DOI
10.1002/jpen.2258
Catalogue ID
BFmou2m94m-rai2z3

Topic tags

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