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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.
Aim:
To assess the occurrence of spontaneous intestinal perforation (SIP) in < 28 weeks' gestational age (GA) infants exposed to early low-dose hydrocortisone (ELH) to reduce the risk of bronchopulmonary dysplasia (BPD). Additionally, the risk of SIP was assessed in infants exposed to early concomitant treatment with ibuprofen for persistent ductus arteriosus (PDA).
Methods:
Observational study in a tertiary neonatal centre preceding and following hydrocortisone implementation. Exposed and non-exposed infants were compared after matching on delivery mode, multiple pregnancy, GA, birthweight, sex and using multivariate logistic regression analysis.
Results:
Among 653 infants, 259 (40%) had been exposed to hydrocortisone, and 210 from each group could be paired. Exposed infants had a higher rate of SIP (8.1% vs. 2.9%, OR [95% CI] 2.99 [1.15-7.74]). Early ibuprofen was provided to 110 exposed (52%) and 105 nonexposed (50%). The rate of SIP was higher in exposed infants cotreated with ibuprofen (11.8% vs. 3.8%, OR 3.38 [1.07-10.73]). Logistic regression analysis in the whole cohort confirmed the risk of SIP in infants exposed to concomitant treatment (OR [95% CI] 2.93 [1.24-6.93]).
Conclusion:
Early concomitant treatment with ELH and ibuprofen is associated with an increased risk of SIP in infants born < 28 weeks.
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