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Protein supplementation versus standard feeds in underweight critically ill children: A pilot dual-centre randomised controlled trial protocol

Wong, Judith Ju Ming; Ong, Jacqueline Soo May; Ong, Chengsi; Allen, John Carsen; Gandhi, Mihir; Fan, Lijia; Taylor, Ryan; Lim, Joel Kian Boon; Poh, Pei Fen; Chiou, Fang Kuan; Lee, Jan Hau (2022-01-04)

 
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Wong, Judith Ju Ming
Ong, Jacqueline Soo May
Ong, Chengsi
Allen, John Carsen
Gandhi, Mihir
Fan, Lijia
Taylor, Ryan
Lim, Joel Kian Boon
Poh, Pei Fen
Chiou, Fang Kuan
Lee, Jan Hau
04.01.2022

BMJ Open
e047907
doi:10.1136/bmjopen-2020-047907
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202203222662

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Peer reviewed
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<p>Introduction Protein-energy malnutrition, increased catabolism and inadequate nutritional support leads to loss of lean body mass with muscle wasting and delayed recovery in critical illness. However, there remains clinical equipoise regarding the risks and benefits of protein supplementation. This pilot trial will determine the feasibility of performing a larger multicentre trial to determine if a strategy of protein supplementation in critically ill children with body mass index (BMI) z-score ≤-2 is superior to standard enteral nutrition in reducing the length of stay in the paediatric intensive care unit (PICU). Methods and analysis This is a randomised controlled trial of 70 children in two PICUs in Singapore. Children with BMI z-score ≤-2 on PICU admission, who are expected to require invasive mechanical ventilation for more than 48 hours, will be randomised (1:1 allocation) to protein supplementation of ≥1.5 g/kg/day in addition to standard nutrition, or standard nutrition alone for 7 days after enrolment or until PICU discharge, whichever is earlier. Feasibility outcomes for the trial include effective screening, satisfactory enrolment rate, timely protocol implementation (within first 72 hours) and protocol adherence. Secondary outcomes include mortality, PICU length of stay, muscle mass, anthropometric measurements and functional outcomes. Ethics and dissemination The trial protocol was approved by the institutional review board of both participating centres (Singhealth Centralised Institutional Review Board and National Healthcare Group Domain Specific Review Board) under the reference number 2020/2742. Findings of the trial will be disseminated through peer-reviewed journals and scientific conferences. Trial registration number NCT04565613.</p>
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TekijätNimekkeetTiedekunta (2019 -)Tiedekunta (- 2018)Tutkinto-ohjelmat ja opintosuunnatAvainsanatJulkaisuajatKokoelmat

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Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste