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Published on: January 31, 2025
Diaphragmatic function in infants with surgically corrected anomalies
Gabriel Dimitriou1, Anne Greenough, Vasiliki Kavvadia
1Department of Child Health, Guy's, King's, and St Thomas' School of Medicine, Children Nationwide Regional Neonatal Intensive Care Centre, King's College London, SE5 9RS, United Kingdom.
Insights
Infants with congenital diaphragmatic hernia (CDH) or gastroschisis show impaired diaphragmatic function after surgery. This affects their breathing capacity, highlighting the need for further research into these conditions.
Area of Science:
- Pediatric Surgery
- Neonatology
- Respiratory Physiology
Background:
- Congenital anomalies like abdominal wall defects (AWD) and congenital diaphragmatic hernia (CDH) may lead to poor diaphragmatic function.
- In utero low intra-abdominal pressure might impair diaphragmatic development in affected infants.
Purpose of the Study:
- To compare postoperative diaphragmatic function in infants with CDH or AWD against gestational age-matched controls.
- To investigate the impact of CDH and AWD on diaphragmatic contractility and lung volumes.
Main Methods:
- Assessed diaphragmatic function via transdiaphragmatic pressure and maximal inspiratory pressure during crying.
- Measured transdiaphragmatic pressure from phrenic nerve stimulation (TwPdi) and functional residual capacity (FRC) using helium dilution.
Main Results:
- Infants with left-sided CDH had significantly lower left and right TwPdi and FRC compared to controls.
- Gastroschisis infants, unlike exomphalos infants, exhibited significantly lower left and right TwPdi.
- No significant differences were found in mouth-generated pressures between patient groups and controls.
Conclusions:
- Postoperative diaphragmatic function is impaired in infants diagnosed with CDH or gastroschisis.
- Specific congenital anomalies impact diaphragmatic contractility and lung volumes differently.
Abstract:
Infants with surgically correctable anomalies, abdominal wall defects (AWD) or congenital diaphragmatic hernia (CDH) may have poor postnatal diaphragmatic function, because the low intra-abdominal pressure experienced by such patients in utero could result in impaired diaphragmatic development. Our objective was to compare postoperative diaphragmatic function of infants with CDH or AWD to that of gestational age-matched controls. Diaphragmatic function was assessed by measurement of the transdiaphragmatic pressure and maximum inspiratory pressure at the mouth generated during crying against an occlusion. In addition, the transdiaphragmatic pressure produced by unilateral and/or bilateral magnetic stimulation of the phrenic nerves (TwPdi) was examined. Lung volume was assessed by measurement of functional residual capacity (FRC) using a helium gas dilution technique. Ten infants with CDH, 26 with AWD infants (19 gastroschisis, seven exomphalos), and 36 gestational age-matched controls were studied. Compared with their matched controls, the eight CDH infants with left-sided defects had significantly lower left (p < 0.01) and right (p < 0.05) TwPdi and FRC (p < 0.01), and the gastroschisis infants, but not those with exomphalos, had significantly lower left and right TwPdi (p < 0.05). There were no significant differences in transdiaphragmatic pressure and maximum inspiratory pressure at the mouth between the CDH or AWD infants and the controls. Diaphragmatic function postoperatively is impaired in infants with CDH or gastroschisis.
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