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Anatomical deadspace during resuscitation of infants with congenital diaphragmatic hernia
Emma E Williams1, Theodore Dassios2, Vadivelam Murthy3
1Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Science and Medicine, King's College London, SE5 9RS, United Kingdom.
Insights
Congenital diaphragmatic hernia (CDH) survivors had greater anatomical deadspace, indicating less severe lung hypoplasia. Fetal tracheal occlusion (FETO) also increased anatomical deadspace in these infants.
Area of Science:
- Neonatal Medicine
- Pediatric Surgery
- Respiratory Physiology
Background:
- Congenital diaphragmatic hernia (CDH) is associated with significant mortality and morbidity due to pulmonary hypoplasia.
- Pulmonary hypoplasia in CDH infants leads to respiratory complications and increased mortality rates.
Purpose of the Study:
- To investigate if surviving CDH infants exhibit greater anatomical deadspace, suggesting less severe pulmonary hypoplasia.
- To determine if fetal tracheal occlusion (FETO) influences anatomical deadspace in CDH infants.
Main Methods:
- Volumetric capnography was used to measure anatomical deadspace in infants with CDH.
- Measurements were taken during resuscitation immediately after delivery, with infants intubated and ventilated.
- The study included 30 infants diagnosed with CDH antenatally, with 11 having undergone FETO.
Main Results:
- Infants who survived to discharge had significantly higher anatomical deadspace (2.9 mls/kg) compared to those who died (2.2 mls/kg).
- Infants who underwent FETO demonstrated increased anatomical deadspace (3.0 mls/kg) compared to those without FETO (2.8 mls/kg).
- Anatomical deadspace was a strong predictor of survival to discharge, with an AUC of 0.90.
Conclusions:
- Larger anatomical deadspace in surviving CDH infants suggests less severe pulmonary hypoplasia.
- FETO may lead to increased anatomical deadspace, potentially due to distension of conducting airways.
Background:
Congenital diaphragmatic hernia (CDH) has a high mortality and morbidity related to pulmonary hypoplasia.
Aims:
To test the hypothesis that CDH infants who survived would have a greater anatomical deadspace reflecting less severe pulmonary hypoplasia. Furthermore, infants with CDH who had undergone feto-tracheal occlusion (FETO) would have a greater anatomical deadspace.
Study Design:
Infants were studied during resuscitation in the delivery suite. They were all intubated immediately at delivery, given a neuromuscular blocking agent and underwent respiratory monitoring. The anatomical deadspace was calculated from volumetric capnography measurements.
Subjects:
Thirty infants born at 32 weeks of gestation or greater and diagnosed antenatally with a CDH were studied. Eleven had undergone FETO and overall five died.
Outcome Measures:
Anatomical deadspace (VdANA) and survival to discharge.
Results:
The median (IQR) gestational age of the infants was 38.1 (35.2-39.3) weeks and birthweight 2.8 (2.3-3.3) kg. The anatomical deadspace was higher in those infants who survived (2.9 (2.8-3.3) mls/kg) compared to those who died (2.2 (2.1-2.7) mls/kg; p = 0.003) and was higher in those who had undergone FETO (3.0 (2.8-3.8) mls/kg) compared to those who had not (2.8 (2.4-3.0) mls/kg; p = 0.032). In predicting survival to discharge, the anatomical deadspace had an AUC of 0.90 (p = 0.006).
Conclusions:
CDH infants who survived had a larger anatomical deadspace than those who died suggesting they had less lung hypoplasia. In addition, infants who had undergone FETO had greater anatomical deadspace possibly reflecting distension of the conducting airways.
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