Spontaneous Intestinal Perforation in Extremely Premature Infants Exposed to Early Low-Dose Hydrocortisone

Gilles Cambonie1,2, Anais Jouffrey1, Benoit Tessier3,4

  • 1Department of Neonatal Medicine, Pediatric Intensive Care and Pediatric Emergency Transport Service, Arnaud de Villeneuve Hospital, Montpellier University Hospital Centre, University of Montpellier, Montpellier, France.

Insights

Early hydrocortisone and ibuprofen treatment in premature infants (<28 weeks) increases the risk of spontaneous intestinal perforation (SIP). This combination therapy requires careful consideration due to potential adverse outcomes in extremely preterm neonates.

Area of Science:

  • Neonatalogy
  • Pediatric Surgery
  • Pharmacology

Background:

  • Bronchopulmonary dysplasia (BPD) and persistent ductus arteriosus (PDA) are common in infants <28 weeks gestational age (GA).
  • Early low-dose hydrocortisone (ELH) is used to prevent BPD, while ibuprofen treats PDA.
  • The combined effect of ELH and ibuprofen on spontaneous intestinal perforation (SIP) risk is not fully understood.

Purpose of the Study:

  • To evaluate the incidence of SIP in infants <28 weeks GA exposed to ELH.
  • To assess the risk of SIP in infants exposed to both ELH and early ibuprofen treatment for PDA.

Main Methods:

  • Observational study comparing infants exposed and non-exposed to ELH.
  • Matching on key neonatal factors (delivery mode, GA, birthweight, sex).
  • Multivariate logistic regression analysis to determine risk factors for SIP.

Main Results:

  • Infants exposed to ELH had a higher SIP rate (8.1% vs. 2.9%).
  • Concomitant treatment with ELH and ibuprofen further increased SIP risk (11.8% vs. 3.8%).
  • Logistic regression confirmed increased SIP risk with combined ELH and ibuprofen (OR 2.93 [1.24-6.93]).

Conclusions:

  • Early concomitant treatment with ELH and ibuprofen is associated with a significantly increased risk of SIP.
  • This finding highlights a potential safety concern for this combination therapy in extremely preterm infants.
  • Further research may be needed to optimize treatment strategies for BPD and PDA while minimizing SIP risk.
Abstract

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