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Published on: February 5, 2021
Postnatal management of preterm infants with congenital diaphragmatic hernia
Emma E Williams1,2, Stephanie Lau2, Nimrah Abbasi3,4
1Division of Neonatology, The Hospital for Sick Children, Toronto, ON, Canada.
Insights
Management of preterm congenital diaphragmatic hernia (CDH) remains challenging. This study highlights high morbidity and mortality, emphasizing the need for standardized guidelines and further research in preterm CDH infants.
Area of Science:
- Neonatal Surgery
- Pediatric Surgery
- Critical Care Medicine
Background:
- Congenital diaphragmatic hernia (CDH) management in preterm infants is complex, especially with the rise of fetal endoluminal tracheal occlusion (FETO) therapy.
- Current clinical guidance for managing preterm CDH is limited, necessitating a review of existing practices.
- This study describes the experience of a single quaternary neonatal intensive care unit (NICU) in managing preterm CDH.
Purpose of the Study:
- To describe the clinical experience and outcomes of preterm infants with CDH managed at a single quaternary NICU.
- To identify challenges and inform potential improvements in the management of this vulnerable population.
Main Methods:
- Retrospective, single-center observational case series.
- Inclusion criteria: preterm infants (<37 weeks gestation) diagnosed with CDH (pre- or post-natally) between 2017 and 2024.
- Data collected on gestational age, birth weight, prenatal diagnosis, FETO, surgical repair timing, ventilation duration, and outcomes.
Main Results:
- Thirty-two preterm infants (median gestational age 33.9 weeks) were analyzed.
- Prenatal diagnosis occurred in 68.8%, with 43.8% undergoing antenatal FETO.
- Survival to discharge was 59.4%, with significant morbidity including intraventricular hemorrhage and need for home oxygen.
Conclusions:
- Preterm CDH is associated with high rates of morbidity and mortality.
- There is a critical need for robust clinical evidence, multicenter studies, and standardized guidelines to improve outcomes for preterm CDH patients.
- Further research is essential to optimize management strategies for this challenging patient group.
Introduction:
Congenital diaphragmatic hernia (CDH) in the preterm population is increasingly common in the current era of fetal endoluminal tracheal occlusion (FETO) therapy. There remains a lack of clinical guidance for clinicians and surgeons regarding optimal management strategies for such infants. We aimed to describe our experience in managing preterm CDH in a single quaternary neonatal intensive care unit (NICU).
Methods:
This was a retrospective single-center observational case series of preterm infants born between 2017 and 2024 at less than 37 weeks of gestation and diagnosed with CDH (pre- or post-natally).
Results:
Thirty-two infants with a median (range) gestational age of 33.9 (27.0-36.9) weeks and a birth weight of 1975 (1070-3290) grams. Twenty-two infants (68.8%) were diagnosed with CDH prenatally and 43.8% underwent antenatal FETO. The median time of surgical repair was at 10 (2-47) days of life. The duration of invasive mechanical ventilation was 11 (1-115) days. Nineteen infants (59.4%) survived to discharge with a median postmenstrual age at time of discharge of 40.6 (36.0-51.0) weeks. Two infants developed a grade 3 or 4 intraventricular hemorrhage. Five infants required home oxygen at discharge.
Conclusion:
Preterm CDH confers high morbidity and mortality. Robust clinical evidence, multicenter studies and standardized guidelines are needed to improve outcomes in this challenging patient population.
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