EC Nutrition

Research Article Volume 18 Issue 4 - 2023

A Prospective Pilot Study to Monitor the Impact of a High Fiber ‘Enteral Formula with Food-Derived Ingredients’ on Fecal Short-Chain Fatty Acid Concentrations in Children Admitted to Intensive Care with Sepsis

Graeme O'Connor1*, Yuxin Sun2, Breeana Gardiner1, Grace Audu3, Mona Bajaj-Elliott2 and Simon Eaton4

1Great Ormond Street Hospital, Dietetics Department, London, United Kingdom
2Infection, Immunity and Inflammation Department, Institute of Child Health, University College London, United Kingdom
3Infection, Immunity and Inflammation Department, Great Ormond Street Institute of Child Health, University College London, United Kingdom
4Developmental Biology and Cancer Department, UCL Great Ormond Street Institute of Child Health, University College London, United Kingdom

*Corresponding Author: Dr Graeme O'Connor, Great Ormond Street Hospital, Dietetics Department, London, United Kingdom.
Received: April 01, 2023; Published: April 11, 2023



Background: Dietary fiber undergoes fermentation by the microbiota to produce intestinal short-chain fatty acids (SCFA). The synergistic relationship between the host and SCFA inhibits the colonization of pathogenic microorganisms. Sepsis is the leading cause of mortality in hospitalized children. Paradoxically, antibiotic management of sepsis can increase infections by causing dysbiosis. This study assessed the impact of an ‘enteral formula with food-derived ingredients’ on feed tolerance and fecal SCFA concentrations in children admitted to intensive care with sepsis.

Methods: Children were switched to Compleat®Paediatric, which contains 1g fiber/100 ml (Nestle Health Science). Stool consistency and frequency were monitored. Stool samples were collected at baseline before the formula switch and weekly thereafter to measure SCFA concentrations (acetate, butyrate, and propionate). A Wilcoxon Signed-Rank test was used to measure the change in SCFA concentrations.

Results: Twenty children switched to a high-fiber enteral formula containing food-derived ingredients. All children were prescribed at least one antibiotic, with 25% of children treated with more than two antibiotics. After the formula switch stool frequency reduced from 2.6 (± 1.08SD) at baseline to 1.2 (± 0.45SD) (p < 0.004). Similarly, stool consistency significantly improved from 6.6 (± 0.4SD) at baseline compared to 3.6 (± 0.4SD) (p < 0.001). Fecal propionate and butyrate concentrations were maintained during the children’s time in intensive care.

Conclusion: Children admitted to intensive care with sepsis may benefit from a high fiber ‘enteral formula with food-derived ingredients’, which may mitigate the gastrointestinal symptoms associated with antibiotic dysbiosis by preserving intestinal SCFA concentrations.

Keywords: Pediatric Intensive Care Unit; Sepsis; Enteral Formula with Food-Derived Ingredients; Enteral Feed Intolerance; Short-Chain Fatty Acids

  1. Marchesi JR., et al. “The gut microbiota and host health: a new clinical frontier”. Gut2 (2016): 330-910.
  2. Kindon S., et al. “Participatory action research approaches and methods: connecting people, participation and place”. Routledge Studies in Human Geography London (2007).
  3. McDonnell L., et al. “Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis”. Gut Microbes1 (2021): 1-1810.
  4. Feng W., et al. “Dietary compounds in modulation of gut microbiota-derived metabolites”. Frontiers in Nutrition (2022): 910.
  5. Morrison DJ and Preston T. “Formation of short chain fatty acids by the gut microbiota and their impact on human metabolism”. Gut Microbes3 (2016): 189-200.
  6. Lattimer JM and Haub MD. “Effects of Dietary Fiber and Its Components on Metabolic Health”. Nutrients12 (2010): 1266-1289.
  7. Macfarlane GT and Macfarlane S. “Bacteria, colonic fermentation, and gastrointestinal health”. Journal of AOAC International1 (2012): 50-60.
  8. Ríos-Covián D., et al. “Intestinal Short Chain Fatty Acids and their Link with Diet and Human Health”. Frontiers in Microbiology 7 (2016): 18510.
  9. Corrêa-Oliveira R., et al. “Regulation of immune cell function by short-chain fatty acids”. Clinical and Translational Immunology4 (2016): e7310.
  10. Kim CH. “Control of lymphocyte functions by gut microbiota-derived short-chain fatty acids”. Cellular and Molecular Immunology5 (2021): 1161-7110.
  11. Moron R., et al. “The Importance of the Microbiome in Critically Ill Patients: Role of Nutrition”. Nutrients12 (2019): 10.
  12. Zaborin A., et al. “Membership and behavior of ultra-low-diversity pathogen communities present in the gut of humans during prolonged critical illness”. mBio5 (2014): e01361-e01410.
  13. Bhalodi AA., et al. “Impact of antimicrobial therapy on the gut microbiome”. Journal of Antimicrobial Chemotherapy1 (2019): i6-i1510.
  14. Shah T., et al. “The Intestinal Microbiota: Impacts of Antibiotics Therapy, Colonization Resistance, and Diseases”. International Journal of Molecular Sciences12 (2021): 6597.
  15. Chouraqui JP and Michard-Lenoir AP. “[Feeding infants and young children with acute diarrhea]”. Archives de Pediatrie: Organe Officiel de la Societe Francaise de Pediatrie3 (2007): S176-8010.
  16. Schmitz É PCR., et al. “Blenderized tube feeding for children: an integrative review”. Revista Paulista de Pediatria: Orgao oficial da Sociedade de Pediatria de Sao Paulo 40 (2021): e202041910.
  17. O'Connor G., et al. “Monitor gastrointestinal tolerance in children who have switched to an "enteral formula with food-derived ingredients A national, multicenter retrospective chart review (RICIMIX study)”. Nutrition in Clinical Practice: Official Publication of the American Society for Parenteral and Enteral Nutrition4 (2022): 929-3410.
  18. McFarland LV. “Epidemiology, risk factors and treatments for antibiotic-associated diarrhea”. Digestive Diseases5 (1998): 292-307.
  19. De la Cuesta-Zuluaga J., et al. “Higher Fecal Short-Chain Fatty Acid Levels Are Associated with Gut Microbiome Dysbiosis, Obesity, Hypertension and Cardiometabolic Disease Risk Factors”. Nutrients1 (2019): 51.
  20. Huysentruyt K., et al. “The Brussels Infant and Toddler Stool Scale: A Study on Interobserver Reliability”. Journal of Pediatric Gastroenterology and Nutrition2 (2019): 207-1310.
  21. Bernard AC., et al. “Defining and Assessing Tolerance in Enteral Nutrition”. Nutrition in Clinical Practice5 (2004): 481-610.
  22. Heaton KW and O'Donnell LJ. “An office guide to whole-gut transit time. Patients' recollection of their stool form”. Journal of Clinical Gastroenterology1 (1994): 28-301.
  23. Russo M., et al. “Functional Chronic Constipation: Rome III Criteria Versus Rome IV Criteria”. Journal of Neurogastroenterology and Motility1 (2019): 123-810.
  24. Cole TJ. “The development of growth references and growth charts”. Annals of Human Biology5 (2012): 382-9410.
  25. WHO Child Growth Standards based on length/height, weight and age”. Acta Paediatrica 450 (2006): 76-8510.
  26. Hengst JM. “The role of C-reactive protein in the evaluation and management of infants with suspected sepsis”. Advances in Neonatal Care: Official Journal of the National Association of Neonatal Nurses1 (2003): 3-131.
  27. Den Besten G., et al. “The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism”. Journal of Lipid Research9 (2013): 2325-4010.
  28. Chandrasekar N., et al. “Exploring Clinical Outcomes and Feasibility of Blended Tube Feeds in Children”. JPEN Journal of Parenteral and Enteral Nutrition4 (2021): 685-9810.
  29. Klosterbuer A., et al. “Benefits of dietary fiber in clinical nutrition”. Nutrition in Clinical Practice: Official Publication of the American Society for Parenteral and Enteral Nutrition5 (2011): 625-3510.
  30. Coad J., et al. “Blended foods for tube-fed children: a safe and realistic option? A rapid review of the evidence”. Archives of Disease in Childhood3 (2017): 27410.
  31. Samela K., et al. “Transition to a Tube Feeding Formula with Real Food Ingredients in Pediatric Patients with Intestinal Failure”. Nutrition in Clinical Practice: Official Publication of the American Society for Parenteral and Enteral Nutrition2 (2017): 277-8110.
  32. Kamarul Zaman M., et al. “Fiber and prebiotic supplementation in enteral nutrition: A systematic review and meta-analysis”. World Journal of Gastroenterology17 (2015): 5372-8110.
  33. Majid HA., et al. “Additional oligofructose/inulin does not increase faecal bifidobacteria in critically ill patients receiving enteral nutrition: a randomised controlled trial”. Clinical Nutrition6 (2014): 966-7210.
  34. Hayakawa M., et al. “Dramatic changes of the gut flora immediately after severe and sudden insults”. Digestive Diseases and Sciences8 (2011): 2361-2510.
  35. Wijeyesekera A., et al. “Multi-Compartment Profiling of Bacterial and Host Metabolites Identifies Intestinal Dysbiosis and Its Functional Consequences in the Critically Ill Child”. Critical Care Medicine9 (2019): e727-e3410.
  36. Valdés-Duque BE., et al. “Stool Short-Chain Fatty Acids in Critically Ill Patients with Sepsis”. Journal of the American College of Nutrition8 (2020): 706-1210.
  37. Vincent JL., et al. “International study of the prevalence and outcomes of infection in intensive care units”. The Journal of the American Medical Association21 (2009): 2323-2910.
  38. Rooney AM., et al. “Each Additional Day of Antibiotics Is Associated with Lower Gut Anaerobes in Neonatal Intensive Care Unit Patients”. Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America12 (2020): 2553-6010.
  39. Lankelma JM., et al. “Critically ill patients demonstrate large interpersonal variation in intestinal microbiota dysregulation: a pilot study”. Intensive Care Medicine1 (2017): 59-6810.

Graeme O’Connor., et al. "A Prospective Pilot Study to Monitor the Impact of a High Fiber ‘Enteral Formula with Food-Derived Ingredients’ on Fecal Short-Chain Fatty Acid Concentrations in Children Admitted to Intensive Care with Sepsis". EC Nutrition 18.4 (2023): 17-27.