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Sleep-related breathing disorders in infants with spina bifida repaired prenatally and postnatally
Katherine G Stark1, Rachel Y Wang2, Kathryn A Smith2,3
1Neuroscience, Dornsife College of Letters Arts and Science, University of Southern California, Los Angeles, California.
Insights
Prenatal repair of myelomeningocele shows no difference in respiratory outcomes compared to postnatal repair. Infants with spina bifida, regardless of repair timing, experience sleep-disordered breathing and hypoxemia.
Area of Science:
- Pediatric Surgery
- Neonatal Care
- Respiratory Medicine
Background:
- Prenatal repair of myelomeningocele has advanced, but respiratory outcomes data are limited.
- Spina bifida repair timing may impact various organ systems, necessitating respiratory assessment.
Purpose of the Study:
- To investigate respiratory outcomes in infants with spina bifida based on prenatal versus postnatal surgical repair.
- To determine if prenatal repair impacts sleep-disordered breathing or oxygenation compared to postnatal repair.
Main Methods:
- Retrospective study of 46 infants under 1 year with spina bifida.
- Collected data on demographics, closure timing, neonatal course, Chiari II malformation, shunts, polysomnography, and oxygen needs.
- Analyzed data using unpaired t-tests and chi-squared tests.
Main Results:
- No significant differences in polysomnography findings (apnea indices, oxygen saturation, end-tidal CO2) between prenatal and postnatal repair groups.
- Similar rates of central and obstructive sleep apnea and supplemental oxygen use were observed.
- A higher rate of ventriculoperitoneal shunt placement was noted in the postnatal repair group (60% vs. 23%).
Conclusions:
- Infants with spina bifida repaired prenatally or postnatally exhibit persistent sleep-disordered breathing and hypoxemia.
- The timing of neural tube defect closure does not appear to influence the frequency or severity of these respiratory issues.
Study Objectives:
Advances in prenatal repair of myelomeningocele have improved outcomes involving different organ systems. There are limited data on respiratory outcomes following prenatal surgical repair. We hypothesize there is no difference in respiratory outcomes between patients with spina bifida who have undergone prenatal vs postnatal repair.
Methods:
We performed a retrospective study of 46 infants < 1 year with spina bifida seen at Children's Hospital Los Angeles from 2004-2022. Demographic data, timing of closure, neonatal course, Chiari II malformation, ventriculoperitoneal shunt, polysomnography results, and need for supplemental oxygen were collected. Unpaired t test and χ2 test were used to analyze results.
Results:
A total of 31/46 had prenatal repair of myelomeningocele; average age at repair was 27 weeks postconception. Average age at postnatal repair was 37 weeks postconception. There was no difference in age at polysomnography. There was no difference in Chiari II malformation presence (P = .61). Sixty pecent of patients with postnatal repair and 23% in the prenatal group underwent ventriculoperitoneal shunt placement (P = .01). There was no difference in polysomnography findings between the 2 groups: central apnea index (P = .11), obstructive apnea-hypopnea index (P = .64), average oxygen saturation baseline (P = .91), average oxygen saturation nadir (P = .17), average end-tidal carbon dioxide baseline (P = .87), and average end-tidal carbon dioxide maximum (P = .54). There were no significant differences in the proportion of patients on supplemental oxygen (P = .25), central sleep apnea or obstructive sleep apnea between groups.
Conclusions:
Patients with spina bifida who have undergone closure of neural tube defect have persistent central apneas, obstructive apneas, and significant hypoxemia. There were no differences in the frequency or severity of sleep-disordered breathing in those with prenatal repair vs postnatal repair.
Citation:
Stark KG, Wang RY, Smith KA. Sleep-related breathing disorders in infants with spina bifida repaired prenatally and postnatally. J Clin Sleep Med. 2024;20(10):1579-1583.
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