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Post Surgical Outcomes in Paediatric Adenotonsillar Hypertrophy with Obstructive Sleep Apnea: Subjective and
Ravi Roy1, Sween Banger1, S K Singh2
1Department of ENT HNS, Army Hospital Research and Referral, New Delhi, 110010 India.
Insights
Pediatric adenotonsillar hypertrophy with obstructive sleep apnea (OSA) significantly improves after surgery, as shown by portable polysomnography (PSG) and quality of life scores. The OSA 18 questionnaire is a viable alternative for monitoring outcomes when PSG is unavailable.
Area of Science:
- Pediatric Otolaryngology
- Sleep Medicine
- Respiratory Medicine
Background:
- Adenotonsillar hypertrophy is a common cause of obstructive sleep apnea (OSA) in children.
- Surgical intervention is the primary treatment for pediatric OSA due to adenotonsillar hypertrophy.
- Assessing post-surgical outcomes requires objective and subjective measures.
Purpose of the Study:
- To evaluate post-surgical outcomes in pediatric patients with adenotonsillar hypertrophy and OSA.
- To compare objective polysomnography (PSG) findings with subjective OSA 18 questionnaire scores.
- To assess the impact of surgery on quality of life (QoL) in these children.
Main Methods:
- A prospective, single-arm study involving 30 children aged 3-12 years with symptomatic adenotonsillar hypertrophy and suspected OSA.
- Portable polysomnography (PSG) and the OSA 18 questionnaire were administered pre- and 6 weeks post-surgery.
- Statistical analysis using the Wilcoxon signed rank test was performed to assess changes in PSG indices, OSA 18 scores, and QoL.
Main Results:
- Significant improvement was observed in the apnea-hypopnea index (AHI), respiratory disturbance index (RDI), and oxygen desaturation index (ODI) post-surgery (p < 0.05).
- Total symptom scores (TSS) and QoL scores also showed statistically significant improvements post-treatment (p < 0.05).
- No significant correlation was found between PSG and OSA 18 questionnaire scores pre- or post-surgery.
Conclusions:
- Surgery effectively improves objective sleep apnea metrics and subjective QoL in children with adenotonsillar hypertrophy and OSA.
- Portable PSG is valuable for objectively monitoring treatment effectiveness.
- The OSA 18 questionnaire serves as a suitable alternative for outcome assessment when PSG is not feasible.
Abstract:
The aim of the study was to determine the post surgical outcomes in pediatric adenotonsillar hypertrophy with OSA using portable polysomnography (PSG), OSA 18 Questionnaire and Quality of life (QoL) scores. Secondly to correlate the subjective outcomes with objective scores of polysomonography. A prospective, single-arm, nonrandomized, single center study was performed at a tertiary care centre on children aged 3-12 years (n = 30) with adenoid hypertrophy/ tonsillar hypertrophy/adenotonsillar hypertrophy and symptoms suggestive of OSA. All subjects underwent appropriate surgical intervention. A portable PSG and OSA 18 questionnaire evaluation was performed pre surgery and 06 weeks post surgery to assess objective and clinical assessment for OSA. The mean age of children enrolled in the study was 8.68 ± 3 years. The mean pre treatment AHI was 12.56 ± 13.16 which improved to 1.72 ± 1.53 post surgery and was statistically significant (p < 0.05, Wilcoxon signed rank test). There was a statistically significant improvement in other PSG indices such as RDI and ODI post surgery also. The mean total symptom score (TSS) and QoL score also showed a statistically significant improvement post treatment (p < 0.05). However there was no correlation between the PSG and OSA 18 questionnaire scores pre and post surgery. Children with OSA like symptoms can undergo a portable polysomnography pre and post surgery to demonstrate severity of OSA and objectively monitor improvement in OSA post treatment. In the absence of availability of PSG, OSA 18 questionnaire is a suitable alternative to monitor disease severity and outcomes. Further studies may plan to include impact of paediatric OSA on other function such as the cardiac, dentition & malocclusion and neurocognitive function.
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