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Published on: December 6, 2016
Sleep-disordered breathing in children with Chiari malformation type II and myelomeningocele
Muslim M Alsaadi1, Shaikh M Iqbal, Essam A Elgamal
1Division of Pediatric Respiratory Medicine, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Insights
Sleep-disordered breathing (SDB) is common in children with Chiari malformation type II (CM-II) and neural tube defects (NTD). This underreported condition requires greater attention for timely diagnosis and treatment in affected children.
Area of Science:
- Pediatric Neurology
- Sleep Medicine
- Medical Genetics
Background:
- Chiari malformation type II (CM-II) is associated with neural tube defects (NTD).
- The prevalence of sleep-disordered breathing (SDB) in children with CM-II is not well-documented.
- Potential brainstem compression in CM-II may lead to respiratory dysfunction during sleep.
Purpose of the Study:
- To assess the prevalence of SDB in pediatric patients with CM-II.
- To identify potential predictive factors for SDB in this population.
Main Methods:
- Retrospective review of pediatric patients with documented CM-II.
- Referral from Neurosurgery to a University Sleep Disorders Centre.
- Full overnight polysomnography (PSG) performed on all included patients.
- Descriptive statistical analysis of polysomnographic data.
Main Results:
- Sixteen children (mean age 4.7 years) with CM-II were studied.
- The mean apnea-hypopnea index (AHI) was 6.3/h, with 31.3% of patients having AHI >5/h.
- A significant prevalence of central SDB was observed (mean central AHI 5.9/h), while obstructive SDB was minimal (mean obstructive AHI 0.4/h).
Conclusions:
- The study confirms the link between CM-II, NTD, and sleep-disordered breathing.
- SDB is highly prevalent in children with CM-II associated with NTD.
- SDB in these patients is likely underreported and undertreated, necessitating increased clinical awareness.
Background:
The prevalence of sleep-disordered breathing (SDB) in children with Chiari malformation type II (CM-II), a known association of neural tube defects (NTD), has not been well documented. The aim of the present study was to assess the prevalence and possible predictive factors of SDB in patients with CM-II.
Methods:
The study included all patients with documented CM-II who were routinely referred from the Neurosurgery Clinic to the University Sleep Disorders Centre at King Khalid University Hospital, Riyadh, Saudi Arabia, between January 2002 and July 2009. Overnight full polysomnography (PSG) was performed in all patients. Polysomnographic data were analyzed using descriptive statistics.
Results:
Sixteen children (11 boys, five girls) were included in the study; their mean age was 4.7 years (range, 0.8-10 years) and their mean body mass index was 18.05 kg/m(2) (range, 15.4-25.4 kg/m(2) ). For the whole group, the mean apnea-hypopnea index (AHI) was 6.3/h (range, 0.2-24.5/h), with AHI recorded as >5/h in five patients (31.3%) and ≥ 10/h in three patients (18.8%). The mean central apnea-hypopnea index was 5.9/h (range, 0-24.5/h) and the mean obstructive apnea-hypopnea index was 0.4/h (range, 0-2.9/h). The mean arousal index was 15.1/h (range, 5-34/h).
Conclusion:
The major assumption linking CM-II and NTD with potential brainstem compression and respiratory dysfunction during sleep was confirmed. Indeed, SDB is highly prevalent, and clearly underreported and undertreated in patients with CM-II associated with NTD.
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