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Published on: December 5, 2025
Early use of Nasal-BiPAP in two infants with Congenital Central Hypoventilation syndrome
C Migliori1, A Cavazza, M Motta
1Division of Neonatology and Neonatal Intensive Care, Spedali Civili, Brescia, Italy. claudio.migliori@tin.it
Insights
Nasal Bilevel Positive Airway Pressure (N-BiPAP) effectively ventilated two infants with Congenital Central Hypoventilation syndrome (CCHS). This non-invasive approach improved oxygenation and reduced the need for prolonged intubation or tracheotomy.
Area of Science:
- Pediatric Pulmonology
- Neonatal Intensive Care
- Respiratory Physiology
Background:
- Congenital Central Hypoventilation syndrome (CCHS) often necessitates prolonged mechanical ventilation.
- Artificial ventilation in infants carries risks such as intubation-related complications and tracheotomy dependence.
Observation:
- Two term infants diagnosed with CCHS were treated with Nasal Bilevel Positive Airway Pressure (N-BiPAP).
- The infants received N-BiPAP at ages 53 and 31 days, with initial weights of 4030g and 3100g.
Findings:
- N-BiPAP significantly improved transcutaneous oxygen (tcPO2) and carbon dioxide (tcPCO2) levels during sleep in both infants.
- While minor complications like skin abrasion and reflux occurred, they did not require cessation of N-BiPAP therapy.
- The use of N-BiPAP successfully avoided prolonged intubation and tracheotomy in these CCHS patients.
Implications:
- Early implementation of N-BiPAP in CCHS infants can mitigate the adverse effects of invasive ventilation.
- Non-invasive ventilation strategies like N-BiPAP offer a promising alternative for managing CCHS.
- Careful monitoring is crucial for optimizing N-BiPAP therapy and managing potential side effects in infants with CCHS.
Aim:
To reduce the problems caused by prolonged artificial ventilation in babies with Congenital Central Hypoventilation syndrome (CCHS).
Methods:
Two term infants with CCHS, weighing 4030 g and 3100 g, respectively, at the beginning of treatment and aged 53 and 31 d, respectively, were successfully ventilated with a Nasal Bilevel Positive Airway Pressure (N-BiPAP) device.
Results:
In the first patient the tcPO2 recordings (mean +/- SD) during sleep were 46 +/- 12 mmHg before using N-BiPAP and 58 +/- 13 mmHg after using the device, while those for tcPCO2 were 75 +/- 9 mmHg and 49 +/- 11 mmHg, respectively. In the second patient tcPO2 during sleep was 42 +/- 3 mmHg before, and 55 +/- 5 after N-BiPAP, and for tcPCO2 the recordings were 119 +/- 24 mmHg and 55 +/- 6 mmHg, respectively, showing a significant improvement. One infant had persistent gastro-oesophageal reflux, and frontal skin abrasion caused by the face mask. Nevertheless, these complications did not necessitate the discontinuation of N-BiPAP ventilation, thus precluding prolonged use of intubation and tracheotomy.
Conclusion:
In infants with CCHS, early use of non-invasive, positive-pressure ventilation with N-BiPAP, in association with careful monitoring, can decrease problems caused by prolonged intubation and tracheotomy.
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