# Respiratory Support Strategies for Surgical Neonates: A Review

**Authors:** Piero Alberti, Niyi Ade-Ajayi, Anne Greenough

PMC · DOI: 10.3390/children12030273 · Children · 2025-02-24

## TL;DR

This review discusses respiratory support strategies for neonates with surgical conditions affecting lung function.

## Contribution

The paper provides an updated overview of respiratory management strategies for four specific neonatal surgical conditions.

## Key findings

- Conventional ventilation may improve outcomes in CDH infants compared to high-frequency ventilation.
- Echocardiographic assessment is crucial for CDH infants with pulmonary hypertension.
- Lung-protective ventilation may reduce postoperative complications in CLM infants.

## Abstract

Neonates with congenital conditions which require surgical management frequently experience respiratory distress. This review discusses the management of pulmonary complications and the respiratory support strategies for four conditions: oesophageal atresia-tracheoesophageal fistula (OA-TOF), congenital diaphragmatic hernia (CDH), congenital lung malformations (CLM), and anterior abdominal wall defects (AWD). Mechanical ventilation techniques which can reduce the risk of ventilator-induced lung injury (VILI) are discussed, as well as the use of non-invasive respiratory support modes. While advances in perioperative respiratory support have improved outcomes in infants with OA-TOF, managing respiratory distress in premature OA-TOF neonates remains a challenge. In CDH infants, a randomised trial has suggested that conventional ventilation may improve outcomes compared to high-frequency ventilation. Echocardiographic assessment is essential in the management of CDH infants with pulmonary hypertension. Lung-protective ventilation settings may lower the rate of postoperative complications in symptomatic CLM infants, but there remains debate regarding the choice of expectant versus surgical management in neonates with asymptomatic CLMs. Infants with AWDs can require ventilation due to pulmonary hypoplasia, but the effects of this on their long-term respiratory health are poorly understood. As surgical techniques continue to evolve and novel ventilation techniques become available, prospective multi-centre studies will be required to define the optimal respiratory support strategies for neonatal surgical conditions that affect lung function.

## Linked entities

- **Diseases:** congenital diaphragmatic hernia (MONDO:0005711), pulmonary hypertension (MONDO:0005149), pulmonary hypoplasia (MONDO:0800133)

## Full-text entities

- **Diseases:** OA-TOF (MESH:C531835), CLM (MESH:C562992), tracheoesophageal fistula (MESH:D014138), pulmonary complications (MESH:D008171), CDH (MESH:D065630), pulmonary hypertension (MESH:D006976), oesophageal atresia (MESH:D000077277), AWD (MESH:D046449), conditions (MESH:D020763), VILI (MESH:D055397), respiratory distress (MESH:D012128)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11941308/full.md

## References

204 references — full list in the complete paper: https://tomesphere.com/paper/PMC11941308/full.md

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Source: https://tomesphere.com/paper/PMC11941308