Feeding intolerance after pediatric cardiac surgery is associated with dysbiosis, barrier dysfunction, and reduced

Jacob Owens1, Haowen Qiu2, Cole Knoblich1

  • 1Department of Pediatrics, University of Nebraska Medical Center, Omaha, Nebraska, United States.

Insights

Postoperative feeding intolerance in pediatric congenital heart disease is linked to gut microbiome changes, reduced beneficial short-chain fatty acids (SCFAs), and intestinal barrier dysfunction. Addressing these gut issues may improve patient outcomes after cardiac surgery.

Area of Science:

  • Gastroenterology
  • Pediatric Cardiology
  • Microbiome Research

Background:

  • Congenital heart disease (CHD) affects ~40,000 US infants annually, with 30-42% experiencing malnutrition and feeding intolerance (FI).
  • Cardiopulmonary bypass (CPB) surgery for CHD can trigger inflammation, gut dysbiosis, and intestinal epithelial barrier dysfunction (EBD), potentially causing postoperative FI.
  • FI in CHD patients is associated with prolonged hospitalization and increased mortality, highlighting the need to understand its underlying mechanisms.

Purpose of the Study:

  • To investigate the relationship between postoperative FI and the intestinal microbiome, short-chain fatty acids (SCFAs), and EBD in pediatric CHD patients.
  • To identify specific microbial shifts and metabolic changes associated with FI following cardiac surgery with CPB.

Main Methods:

  • Prospective study of 26 pediatric patients (0-15 years) undergoing cardiac surgery with CPB.
  • Collection of preoperative and postoperative samples for gut microbiome analysis, plasma EBD markers, SCFAs, and cytokines.
  • Clinical data collection to calculate FI scores and assess patient status.

Main Results:

  • Patients who developed FI (n=13) exhibited distinct microbial shifts, notably reduced SCFA-producing bacteria like Rothia and Clostridium innocuum.
  • FI was associated with elevated plasma markers of EBD, including claudin-2, claudin-3, and fatty acid-binding protein.
  • Patients with FI showed decreased plasma and stool SCFA levels, with mediation analysis linking microbiome changes to reduced butyric and propionic acid.

Conclusions:

  • Novel evidence suggests intestinal dysbiosis, EBD markers, and SCFA depletion are significantly associated with postoperative FI in pediatric CHD.
  • These findings highlight the gut microbiome's role in post-cardiac surgery outcomes and suggest potential therapeutic targets.
  • Improving the intestinal milieu may enhance nutrition and clinical outcomes for pediatric patients undergoing cardiac surgery.

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