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Updated: May 23, 2026

Drug-Induced Sleep Endoscopy (DISE) with Target Controlled Infusion (TCI) and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
[Effects of obstructive sleep apnea hypopnea syndrome in children on multiple systems]
Xiao-hong Cai1, Xiu-cui Li, Mei-li Li
1Department of Pulmonology, The 2nd Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical College, Wenzhou 325027, China.
Insights
Obstructive sleep apnea-hypopnea syndrome (OSAHS) in children is linked to craniofacial issues and impacts growth. This condition can also lead to higher blood pressure, altered blood viscosity, and changes in cardiac structure.
Area of Science:
- Pediatric Pulmonology
- Sleep Medicine
- Cardiology
Context:
- Obstructive sleep apnea-hypopnea syndrome (OSAHS) is associated with significant comorbidities in adults, including hypertension and diabetes.
- Limited research exists on the effects of OSAHS in pediatric populations.
- Understanding OSAHS's impact on children's development is crucial for early intervention.
Purpose:
- To investigate the multifaceted effects of OSAHS on various physiological systems in children.
- To compare clinical and physiological data between children with OSAHS and healthy controls.
Summary:
- A study of 89 children with snoring found OSAHS is associated with craniofacial malformations like adenoid face and abnormal occlusion.
- Children with OSAHS exhibited slower growth (lower weight and height), elevated blood pressure and viscosity, and altered lipid profiles (lower HDL-C, higher LDL-C).
- Echocardiography revealed changes in cardiac structure, including decreased right ventricular diameter and increased main pulmonary artery diameter and right ventricular wall thickness in children with OSAHS.
Impact:
- OSAHS in children may contribute to impaired physical development and increased cardiovascular risk.
- Findings highlight the importance of screening for OSAHS in children with craniofacial abnormalities.
- Early diagnosis and management of pediatric OSAHS can potentially mitigate long-term health consequences.
Objective:
Obstructive sleep apnea-hypopnea syndrome (OSAHS) may cause serious morbidities, such as systemic hypertension, diabetes, and cor pulmonale. However, currently no many reports on study of OSAHS in children are available. This study aimed to explore the effects of OSAHS on children's multiple systems.
Method:
A total of 89 cases of children who came to the Sleep Treatment Center in the authors' hospital from March 2009 to December 2010 with snoring were tested with overnight polysomnography (PSG). They were classified into mild OSAHS group (n = 59, mean age of 5.71, SD = 2.46) and moderate to severe group (n = 30, mean age of 5.30, SD = 2.73) based on the PSG results, and 100 healthy children were selected as the control group (n = 100, mean age of 6 years, SD = 2.98). Data including height, weight, body mass index and blood pressure, peripheral blood routine, blood lipids, glucose and insulin, electrocardiogram and echocardiography were collected. Patients' adenoid face and abnormal occlusion were also recorded. Comparisons of the data were made among those groups.
Result:
Mild OSAHS and moderate to severe group had significantly higher prevalence of adenoid face (23.7%, 26.7%), and abnormal occlusion (74.6%, 60.0%) than that in control group (0, 40%) (P < 0.05). There were no significant differences in terms of BMI between the OSAHS group and the control group, but the weight (kg) and height (cm) in the mild OSAHS group (23.3 ± 10.1, 114.9 ± 16.2) and moderate to severe group (21.9 ± 8.4, 110.8 ± 13.3) were lower than those of the control group (31.8 ± 10.1, 136.1 ± 15.1) (all P < 0.05). Compared with the control group, the level of HDL-C (mmol/L)and insulin (mU/L) in moderate and severe group decreased [(1.20 ± 0.30) vs. (1.40 ± 0.27), 2.79 (0.84 - 16.16) vs. 4.92 (0.76 - 16.80), P < 0.05], while the LDL-C (mmol/L) increased [(2.61 ± 0.75) vs. (2.32 ± 0.62), P < 0.05]. The red blood cell counts (× 10(12)/L) and the blood platelet counts (× 10(9)/L) in the mild OSAHS (4.93 ± 0.37, 292.92 ± 75.64) and moderate and severe OSAHS group (5.23 ± 0.22, 292.50 ± 63.05) were significantly higher in contrast to the control group (4.70 ± 0.31, 255.60 ± 69.12) (all P < 0.05), systolic blood pressure (mmHg) in mild group (98.54 ± 10.44) and moderate to severe group (99.13 ± 19.13) was significantly higher compared to control group (87.88 ± 11.37), and the heart rate (beats/min) in moderate to severe group (94.43 ± 10.64) was higher than those in control group (87.12 ± 16.20) (all P < 0.05). The mild OSAHS and moderate and severe OSAHS group had decreased right ventricular internal diameter [(14.24 ± 1.64) mm, (13.17 ± 2.07) mm ], increased main pulmonary artery diameter [(17.05 ± 3.33) mm, (16.33 ± 3.14) mm] and the thickness of right ventricular wall [(3.43 ± 0.26) mm, (3.57 ± 0.20) mm] compared to control group [ (16.10 ± 2.96) mm, (14.11 ± 2.52) mm, (3.32 ± 0.25) mm] (all P < 0.05).
Conclusion:
OSAHS in children may be associated with craniofacial malformations, and may contribute to slow growth and development, elevated blood viscosity and blood pressure, metabolic abnormalities, and change cardiac structure.
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