Children's Oxygen Administration Strategies And Nutrition Trial (COAST-Nutrition): a protocol for a phase II randomised controlled trial.
Sarah KiguliPeter Olupot-OlupotFlorence AlarokerCharles EngoruRobert O OpokaAbner TagoolaMainga M HamalubaHellen MnjallaAyub MpoyaChristabel MogakaDamalie NalwangaEva NabawanukaDavid James NokesCharles N AgotiAndré BriendJob B M van WoenselRichard GrieveZia SadiqueThomas N WilliamsKaren ThomasDavid A HarrisonKathryn RowanKathryn MaitlandPublished in: Wellcome open research (2021)
Background: To prevent poor long-term outcomes (deaths and readmissions) the integrated global action plan for pneumonia and diarrhoea recommends under the 'Treat' element of Protect, Prevent and Treat interventions the importance of continued feeding but gives no specific recommendations for nutritional support. Early nutritional support has been practiced in a wide variety of critically ill patients to provide vital cell substrates, antioxidants, vitamins, and minerals essential for normal cell function and decreasing hypermetabolism. We hypothesise that the excess post-discharge mortality associated with pneumonia may relate to the catabolic response and muscle wasting induced by severe infection and inadequacy of the diet to aid recovery. We suggest that providing additional energy-rich, protein, fat and micronutrient ready-to-use therapeutic feeds (RUTF) to help meet additional nutritional requirements may improve outcome. Methods: COAST-Nutrition is an open, multicentre, Phase II randomised controlled trial in children aged 6 months to 12 years hospitalised with suspected severe pneumonia (and hypoxaemia, SpO 2 <92%) to establish whether supplementary feeds with RUTF given in addition to usual diet for 56-days (experimental) improves outcomes at 90-days compared to usual diet alone (control). Primary endpoint is change in mid-upper arm circumference (MUAC) at 90 days and/or as a composite with 90-day mortality. Secondary outcomes include anthropometric status, mortality, readmission at days 28 and 180. The trial will be conducted in four sites in two countries (Uganda and Kenya) enrolling 840 children followed up to 180 days. Ancillary studies include cost-economic analysis, molecular characterisation of bacterial and viral pathogens, evaluation of putative biomarkers of pneumonia, assessment of muscle and fat mass and host genetic studies. Discussion: This study is the first step in providing an option for nutritional support following severe pneumonia and will help in the design of a large Phase III trial. Registration: ISRCTN10829073 (6 th June 2018) PACTR202106635355751 (2 nd June 2021).
Keyphrases
- phase ii
- phase iii
- clinical trial
- open label
- physical activity
- study protocol
- double blind
- placebo controlled
- community acquired pneumonia
- weight loss
- cardiovascular events
- randomized controlled trial
- skeletal muscle
- young adults
- respiratory failure
- risk factors
- adipose tissue
- body mass index
- sars cov
- single cell
- early onset
- stem cells
- insulin resistance
- gene expression
- type diabetes
- gram negative
- fatty acid
- pulmonary embolism
- body composition
- amino acid
- metabolic syndrome
- extracorporeal membrane oxygenation
- dna methylation
- bone marrow
- cross sectional
- cardiovascular disease
- data analysis
- intensive care unit
- mechanical ventilation
- clinical practice
- mesenchymal stem cells