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Exploration of muscle loss and metabolic state during prolonged critical illness: Implications for intervention?

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posted on 2020-05-14, 14:34 authored by L Wandrag, SJ Brett, GS Frost, V Bountziouka, M Hickson
Background Muscle wasting in the critically ill is up to 2% per day and delays patient recovery and rehabilitation. It is linked to inflammation, organ failure and severity of illness. The aims of this study were to understand the relationship between muscle depth loss, and nutritional and inflammatory markers during prolonged critical illness. Secondly, to identify when during critical illness catabolism might decrease, such that targeted nutritional strategies may logically be initiated. Methods This study was conducted in adult intensive care units in two large teaching hospitals. Patients anticipated to be ventilated for >48 hours were included. Serum C-reactive protein (mg/L), urinary urea (mmol/24h), 3-methylhistidine (μmol/24h) and nitrogen balance (g/24h) were measured on days 1, 3, 7 and 14 of the study. Muscle depth (cm) on ultrasound were measured on the same days over the bicep (bicep and brachialis muscle), forearm (flexor compartment of muscle) and thigh (rectus femoris and vastus intermedius). Results Seventy-eight critically ill patients were included with mean age of 59 years (SD: 16) and median Intensive care unit (ICU) length of stay of 10 days (IQR: 6–16). Starting muscle depth, 8.5cm (SD: 3.2) to end muscle depth, 6.8cm (SD: 2.2) were on average significantly different over 14 days, with mean difference -1.67cm (95%CI: -2.3 to -1cm), p<0.0001. Protein breakdown and inflammation continued over 14 days of the study. Conclusion Our patients demonstrated a continuous muscle depth loss and negative nitrogen balance over the 14 days of the study. Catabolism remained dominant throughout the study period. No obvious ‘nutritional tipping point” to identify anabolism or recovery could be identified in our cohort. Our ICU patient cohort is one with a moderately prolonged stay. This group showed little consistency in data, reflecting the individuality of both disease and response. The data are consistent with a conclusion that a time based assumption of a tipping point does not exist. Trial registration International Standard Randomised Controlled Trial Number: ISRCTN79066838. Registration 25 July 2012.

Funding

The authors acknowledge support from the Department of Health and Social Care via the National Institute of Health Research (NIHR) who supported this work through the provision of a Clinical Doctoral Research Fellowship for LW. The research was further supported by the NIHR Comprehensive Biomedical Research Centre based at Imperial College Healthcare NHS Trust and Imperial College London.

History

Citation

PLOS ONE, 2019

Author affiliation

Department of Health Sciences

Version

  • VoR (Version of Record)

Published in

PLoS ONE

Volume

14

Issue

11

Pagination

e0224565

Publisher

Public Library of Science (PLoS)

eissn

1932-6203

Acceptance date

2019-10-16

Copyright date

2019

Publisher version

https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0224565#abstract0

Language

eng

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