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Published on: December 6, 2016
Outcomes of pediatric mild sleep-disordered breathing
Alex Gileles-Hillel1, Leah Korchemny2, Shmuel Goldberg3
1Faculty of Medicine, Hebrew University, Jerusalem, Israel; Pediatric Pulmonary and Sleep Unit, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Insights
Many children with mild obstructive sleep apnea (OSA) experience persistent symptoms, underscoring the need for ongoing monitoring. Follow-up is crucial for those with comorbidities or specific risk factors.
Area of Science:
- Pediatric Sleep Medicine
- Respiratory Disorders
- Child Health Outcomes
Background:
- Sleep-disordered breathing (SDB), including obstructive sleep apnea (OSA), is prevalent in children and can lead to long-term health issues.
- Management guidelines for mild pediatric OSA remain unclear, with options including surgery, medication, or watchful waiting.
Purpose of the Study:
- To investigate the persistence of symptoms in children diagnosed with mild SDB.
- To evaluate the effectiveness of different treatment strategies for mild pediatric SDB.
Main Methods:
- Children with mild SDB (apnea-hypopnea index 2-5/h) diagnosed via polysomnography (PSG) were assessed 1-2 years later.
- Symptom persistence was evaluated using the Pediatric Sleep Questionnaire (PSQ).
Main Results:
- Of 78 children, 40% reported persistent symptoms (positive PSQ).
- Persistent symptoms were linked to background morbidities, prematurity, higher BMI, and higher respiratory rate during PSG.
- Initial treatment offered included surgery for 33% of children.
Conclusions:
- A significant proportion of children with mild OSA exhibit persistent symptoms, highlighting the need for continued follow-up.
- Proactive monitoring is recommended for children with comorbidities, prematurity, elevated BMI, ongoing complaints, or high respiratory rates on PSG.
Objectives:
Sleep-disordered breathing disorders (SDB) ranging from snoring to obstructive sleep apnea (OSA), are common in children and have long-term consequences. However, guidelines for mild OSA are unclear with possible early surgery, pharmacotherapy, or watchful waiting. The current study aimed to investigate the persistence of symptoms in children with polysomnographic (PSG) diagnosis of mild SDB and the different treatment strategies carried out.
Methods:
Children diagnosed with mild SDB at two tertiary medical centers were contacted 1-2 years following PSG diagnosis of mild SDB and assessed for symptom persistence using the Pediatric Sleep Questionnaire (PSQ).
Results:
A total of 78 children (38 female) were enrolled. The mean age at PSG was 5.45 (±3.98) years, the baseline apnea-hypopnea index (AHI) 2-5/h. The PSQ was completed at a mean age of 7.37 (±4.11) years and was positive in 31 (40 %) children. Twenty-six (33 %) children were initially offered surgical treatment, two-thirds of whom went through with surgery. A positive PSQ was associated with the presence of any background morbidity (including asthma, trisomy 21, prematurity, developmental delay, attention deficit disorder, chronic lung disease, congenital heart disease, etc.), prematurity, the BMI, having had no change in complaints, and high respiratory rate on PSG (p ≤ 0.05) but not the type of intervention provided.
Conclusions:
We identified a high rate of persistent SDB symptoms in children previously diagnosed with mild OSA, emphasizing the importance of continued follow-up of these children. Proactive follow-up should be considered in children with background morbidities, prematurity, higher BMI z scores, persistent complaints, or high respiratory rates on the PSG.
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