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Safety of Adenotonsillectomy in Children with Genetic Syndromes
Comert Sen1, Ömer Orak1, Tülay Günsay1
1Department of Otorhinolaryngology - Head and Neck Surgery, Istanbul Faculty of Medicine, Istanbul University, Türkiye.
Insights
Adenotonsillectomy (AT) is safe for children with genetic syndromes, including Down syndrome (DS). This procedure shows low complication rates, making it a viable option for these high-risk patients.
Area of Science:
- Pediatric Otolaryngology
- Genetics
- Surgical Safety
Background:
- Children with genetic syndromes, particularly Down syndrome (DS), are considered high-risk for adenotonsillectomy (AT) due to unique anatomical and comorbidity profiles.
- Evaluating the safety of AT in this population is crucial for informed clinical decision-making.
Purpose of the Study:
- To assess the safety and complication rates of adenotonsillectomy (AT) in pediatric patients with Down syndrome (DS) and other genetic syndromes (OS).
Main Methods:
- Retrospective review of 62 pediatric patients (<18 years) with genetic syndromes (46 DS, 16 OS) who underwent AT or tonsillectomy with or without ventilation tube insertion between 2010-2025.
- Data collected included demographics, comorbidities, surgical details, complications, and hospital stay duration.
Main Results:
- The primary indications for surgery were sleep-disordered breathing (82.3%) and recurrent tonsillitis (25.8%).
- The overall complication rate was low at 8.1%, with no emergency admissions or perioperative mortality. Specific complications included bleeding (1.6%), respiratory events (1.6%), and poor oral intake (4.8%).
- Most patients (93.5%) were discharged within 1 day, though 2 OS patients required planned ICU admission.
Conclusions:
- Adenotonsillectomy (AT) is a safe surgical procedure for children with genetic syndromes, including Down syndrome (DS).
- The study demonstrates low complication rates and short hospital stays, supporting the use of AT in this patient group.
Objectives:
Children with genetic syndromes, especially Down syndrome (DS), are considered high-risk candidates for adenotonsillectomy (AT) due to anatomical abnormalities and comorbidities. This study aimed to evaluate the safety of AT in patients with DS and other genetic syndromes (OS).
Methods:
This retrospective study included 62 syndromic patients (46 DS, 16 OS) under 18 years of age who underwent tonsillectomy ± adenoidectomy ± ventilation tube (VT) insertion between 2010 and 2025. Demographics, comorbidities, surgical details, complications, and hospital stays were reviewed.
Results:
Indications included sleep-disordered breathing (51/62, 82.3%) and recurrent tonsillitis (16/62, 25.8%). Procedures performed were AT (51/62, 82.3%) or tonsillectomy alone (11/62, 17.7%) ± VT insertion (16/62, 25.8%). Median hospital stay was 1 day (IQR: 1-1), with 93.5% (58/62) discharged after 1 day. Two-day stays occurred in 18.75% of OS patients (3/16) and 2.2% of DS patients (1/46). Planned intensive care unit admission was required in 2 OS patients (3.2%). No emergency admissions or perioperative mortality occurred. Overall complication rate was 8.1% (5/62)-8.7% in DS and 6.3% in OS (P = 1.00)-including bleeding requiring reoperation (1/62, 1.6%), respiratory event (1/62, 1.6%), and insufficient oral intake (3/62, 4.8%).
Conclusion:
AT appears to be safe in children with genetic syndromes, with low rates of complications.
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