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Drug-Induced Sleep Endoscopy (DISE) with Target Controlled Infusion (TCI) and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
Impaired blood pressure control in children with obstructive sleep apnea
Lisa M Walter1, Stephanie R Yiallourou, Anna Vlahandonis
1The Ritchie Centre, Monash Institute of Medical Research, Monash University, Melbourne, Australia. lisa.walter@monash.edu
Insights
Children with obstructive sleep apnea (OSA) show impaired baroreflex sensitivity (BRS) and increased blood pressure variability (BPV). This suggests altered autonomic control in pediatric OSA, warranting further investigation into treatment effects.
Area of Science:
- Pediatric cardiology
- Sleep medicine
- Autonomic nervous system function
Background:
- Obstructive sleep apnea (OSA) in adults is linked to hypertension, reduced baroreflex sensitivity (BRS), delayed heart rate response (HPD), and increased blood pressure variability (BPV).
- While children with OSA have higher blood pressure, data on their BRS, BPV, and HPD are limited.
- Impaired BRS may contribute to hypertension by affecting blood pressure control, leading to increased BPV and HPD.
Purpose of the Study:
- To investigate baroreflex sensitivity (BRS), heart period delay (HPD), and blood pressure variability (BPV) in children with obstructive sleep apnea (OSA).
- To compare these cardiovascular autonomic parameters between children with OSA and non-snoring controls.
Main Methods:
- 105 children (ages 7-12) referred for OSA assessment and 36 controls underwent overnight polysomnography (PSG) with continuous blood pressure monitoring.
- Subjects were categorized into primary snoring (PS), mild OSA, and moderate/severe (MS) OSA based on their obstructive apnea-hypopnea index (OAHI).
- BRS and HPD were calculated using cross-spectral analysis, and BPV using power spectral analysis.
Main Results:
- Children with OSA exhibited significantly lower BRS and longer HPD compared to controls.
- The moderate/severe (MS) OSA group showed higher BPV across all frequencies (low and high) than control and primary snoring groups.
- These findings indicate reduced baroreflex function in children with OSA.
Conclusions:
- Pediatric obstructive sleep apnea (OSA) is associated with reduced baroreflex sensitivity (BRS), prolonged heart period delay (HPD), and elevated blood pressure variability (BPV).
- These results suggest altered baroreflex function in children with OSA.
- Longitudinal studies are needed to determine if OSA treatment can reverse these changes in baroreflex response.
Background:
Obstructive sleep apnea (OSA) in adults has been associated with hypertension, low baroreflex sensitivity (BRS), a delayed heart rate response to changing blood pressure (heart period delay [HPD]), and increased blood pressure variability (BPV). Poor BRS may contribute to hypertension by impairing the control of blood pressure (BP), with increased BPV and HPD. Although children with OSA have elevated BP, there are scant data on BRS, BPV, or HPD in this group.
Methods:
105 children ages 7-12 years referred for assessment of OSA and 36 nonsnoring controls were studied. Overnight polysomnography (PSG) was performed with continuous BP monitoring. Subjects were assigned to groups according to their obstructive apnea-hypopnea index (OAHI): primary snoring (PS) (OAHI ≤1event/h), mild OSA (OAHI>1- ≤5events/h) and moderate/severe (MS) OSA (OAHI>5events/h). BRS and HPD were calculated using cross spectral analysis and BPV using power spectral analysis.
Results:
Subjects with OSA had significantly lower BRS (p<.05 for both) and a longer HPD (PS and MS OSA, p<.01; mild OSA, p<.05) response to spontaneous BP changes compared with controls. In all frequencies of BPV, the MS group had higher power compared with the control and PS groups (low frequency [LF], p<.05; high frequency [HF], p<.001).
Conclusions:
Our study demonstrates reduced BRS, longer HPD, and increased BPV in subjects with OSA compared to controls. This finding suggests that children with OSA have altered baroreflex function. Longitudinal studies are required to ascertain if this dampening of the normal baroreflex response can be reversed with treatment.
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