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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.
Afiliación
  • Wong JJM; Children's Intensive Care Unit, KK Women's and Children's Hospital, Singapore.
  • Ong JSM; Duke-NUS Medical School, Singapore.
  • Ong C; Division of Paediatric Critical Care, National University Hospital, Singapore.
  • Allen JC; Department of Dietetics, KK Women's and Children's Hospital, Singapore.
  • Gandhi M; Duke-NUS Medical School, Singapore.
  • Fan L; Singapore Clinical Research Institute, Singapore.
  • Taylor R; Tampere University, Tampere, Finland.
  • Lim JKB; Division of Paediatric Critical Care, National University Hospital, Singapore.
  • Poh PF; Division of Paediatric Critical Care, National University Hospital, Singapore.
  • Chiou FK; Children's Intensive Care Unit, KK Women's and Children's Hospital, Singapore.
  • Lee JH; Children's Intensive Care Unit, KK Women's and Children's Hospital, Singapore.
BMJ Open ; 12(1): e047907, 2022 Jan 04.
Article en En | MEDLINE | ID: mdl-34983751
ABSTRACT

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 (11 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Delgadez / Enfermedad Crítica Tipo de estudio: Clinical_trials / Guideline Límite: Child / Humans Idioma: En Revista: BMJ Open Año: 2022 Tipo del documento: Article País de afiliación: Singapur

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Delgadez / Enfermedad Crítica Tipo de estudio: Clinical_trials / Guideline Límite: Child / Humans Idioma: En Revista: BMJ Open Año: 2022 Tipo del documento: Article País de afiliación: Singapur