Beta-hydroxy-beta-methylbutyrate supplementation and functional outcomes in multitrauma patients: A pilot randomized controlled trial.

beta-hydroxy-beta-methylbutyrate critical illness enteral nutrition muscle mass nutrition therapy

Journal

JPEN. Journal of parenteral and enteral nutrition
ISSN: 1941-2444
Titre abrégé: JPEN J Parenter Enteral Nutr
Pays: United States
ID NLM: 7804134

Informations de publication

Date de publication:
Nov 2023
Historique:
revised: 21 05 2023
received: 19 01 2023
accepted: 24 05 2023
medline: 7 11 2023
pubmed: 26 6 2023
entrez: 25 6 2023
Statut: ppublish

Résumé

Beta-hydroxy-beta-methylbutyrate (HMB) is a nutrition supplement that may attenuate muscle wasting from critical illness. This trial aimed to determine feasibility of administering a blinded nutrition supplement in the intensive care unit (ICU) and continuing it after ICU discharge. Single-center, parallel-group, blinded, placebo-controlled, randomized feasibility trial. After traumatic injury necessitating admission to ICU, participants were randomized to receive an enteral study supplement of 3 g of HMB (intervention) or placebo daily for 28 days or until hospital discharge. Primary outcome was feasibility of administering the study supplement, quantified as protocol adherence. Secondary outcomes included change in quadriceps muscle thickness, measured weekly until day 28 or hospital discharge by using ultrasound and analyzed by using a linear mixed model. Fifty randomized participants (intervention, n = 26; placebo, n = 24) showed comparable baseline characteristics. Participants received 862 (84.3%) of the 1022 prescribed supplements during hospitalization with 543 (62.8%) delivered via an enteral feeding tube. The median (IQR) number of study supplements successfully administered per participant was 19.5 (13.0-24.0) in the intervention group and 16.5 (8.5-23.5) in the placebo group. Marked loss of quadriceps muscle thickness occurred in both groups, with the point estimate favoring attenuated muscle loss with the intervention, albeit with wide CIs (mean intervention difference after 28 days, 0.26 cm [95% CI, -0.13 to 0.64]). A blinded, placebo-controlled, randomized clinical trial of daily enteral HMB supplementation for up to 28 days in hospital is feasible. Any effect of HMB supplementation to attenuate muscle wasting after traumatic injury remains uncertain.

Sections du résumé

BACKGROUND BACKGROUND
Beta-hydroxy-beta-methylbutyrate (HMB) is a nutrition supplement that may attenuate muscle wasting from critical illness. This trial aimed to determine feasibility of administering a blinded nutrition supplement in the intensive care unit (ICU) and continuing it after ICU discharge.
METHODS METHODS
Single-center, parallel-group, blinded, placebo-controlled, randomized feasibility trial. After traumatic injury necessitating admission to ICU, participants were randomized to receive an enteral study supplement of 3 g of HMB (intervention) or placebo daily for 28 days or until hospital discharge. Primary outcome was feasibility of administering the study supplement, quantified as protocol adherence. Secondary outcomes included change in quadriceps muscle thickness, measured weekly until day 28 or hospital discharge by using ultrasound and analyzed by using a linear mixed model.
RESULTS RESULTS
Fifty randomized participants (intervention, n = 26; placebo, n = 24) showed comparable baseline characteristics. Participants received 862 (84.3%) of the 1022 prescribed supplements during hospitalization with 543 (62.8%) delivered via an enteral feeding tube. The median (IQR) number of study supplements successfully administered per participant was 19.5 (13.0-24.0) in the intervention group and 16.5 (8.5-23.5) in the placebo group. Marked loss of quadriceps muscle thickness occurred in both groups, with the point estimate favoring attenuated muscle loss with the intervention, albeit with wide CIs (mean intervention difference after 28 days, 0.26 cm [95% CI, -0.13 to 0.64]).
CONCLUSION CONCLUSIONS
A blinded, placebo-controlled, randomized clinical trial of daily enteral HMB supplementation for up to 28 days in hospital is feasible. Any effect of HMB supplementation to attenuate muscle wasting after traumatic injury remains uncertain.

Identifiants

pubmed: 37357015
doi: 10.1002/jpen.2527
doi:

Substances chimiques

beta-hydroxyisovaleric acid 3F752311CD
Valerates 0

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

983-992

Subventions

Organisme : This project is supported by the Mary Elizabeth Watson Early Career Research Fellowship provided by the Melbourne Health foundation, which provides $30,000 per year over 2 years

Informations de copyright

© 2023 American Society for Parenteral and Enteral Nutrition.

Références

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Auteurs

Kym Wittholz (K)

Department of Allied Health (Clinical Nutrition), The Royal Melbourne Hospital, Melbourne, Australia.
Department of Critical Care, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.

Kate Fetterplace (K)

Department of Allied Health (Clinical Nutrition), The Royal Melbourne Hospital, Melbourne, Australia.
Department of Critical Care, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.

Amalia Karahalios (A)

Center of Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Australia.

Yasmine Ali Abdelhamid (Y)

Department of Critical Care, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.
Department of Intensive Care, The Royal Melbourne Hospital, Melbourne, Australia.

Lisa Beach (L)

Department of Allied Health (Physiotherapy), The Royal Melbourne Hospital, Melbourne, Australia.

David Read (D)

Department of Trauma and General Surgery, The Royal Melbourne Hospital, Melbourne, Australia.

René Koopman (R)

Department of Anatomy and Physiology, Center for Muscle Research, The University of Melbourne, Melbourne, Australia.

Jeffrey J Presneill (JJ)

Department of Critical Care, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.
Department of Intensive Care, The Royal Melbourne Hospital, Melbourne, Australia.

Adam M Deane (AM)

Department of Critical Care, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.
Department of Intensive Care, The Royal Melbourne Hospital, Melbourne, Australia.

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