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Updated: May 14, 2026

A Structured Approach to Extubation in Mechanically Ventilated Rats
Published on: July 18, 2025
The effect of deep vs. awake extubation on respiratory complications in high-risk children undergoing
Britta S von Ungern-Sternberg1, Kylie Davies, Mary Hegarty
1Department of Anaesthesia and Pain Management, Princess Margaret Hospital for Children, Subiaco, WA 6008, Australia. britta.regli-vonungern@health.wa.gov.au
Insights
Tracheal extubation timing in children undergoing adenotonsillectomy showed no significant difference in overall respiratory complications. Both deep and awake extubation are viable options with close postoperative monitoring for high-risk pediatric patients.
Area of Science:
- Anesthesiology
- Pediatric Surgery
- Respiratory Medicine
Background:
- Debate exists on optimal tracheal extubation timing in children at high risk for perioperative respiratory adverse events, especially after adenotonsillectomy.
- Risk factors include recent respiratory infections, eczema, wheezing, cough, asthma history, and passive smoking.
Purpose of the Study:
- To compare perioperative respiratory adverse events in children undergoing elective adenotonsillectomy.
- To evaluate outcomes between deep anesthesia extubation and awake extubation.
Main Methods:
- Prospective, randomized controlled trial involving 100 children (<16 years) with risk factors for respiratory events.
- Participants were randomized to either deep or awake extubation.
- Adverse events monitored included laryngospasm, bronchospasm, coughing, airway obstruction, and desaturation.
Main Results:
- No significant difference in the overall incidence of perioperative respiratory adverse events between deep and awake extubation groups.
- Awake extubation was associated with more persistent coughing (60% vs. 35%).
- Deep extubation showed a higher incidence of airway obstruction requiring intervention (26% vs. 8%).
Conclusions:
- The overall incidence of perioperative respiratory adverse events did not differ significantly between deep and awake extubation in high-risk children.
- Both extubation strategies are acceptable for adenotonsillectomy in these children.
- Close postoperative monitoring is crucial regardless of the extubation technique used.
Context:
There is ongoing debate regarding the optimal timing for tracheal extubation in children at increased risk of perioperative respiratory adverse events, particularly following adenotonsillectomy.
Objective:
To assess the occurrence of perioperative respiratory adverse events in children undergoing elective adenotonsillectomy extubated under deep anaesthesia or when fully awake.
Design:
Prospective, randomised controlled trial.
Setting:
Tertiary paediatric hospital.
Patients:
One hundred children (<16 years), with at least one risk factor for perioperative respiratory adverse events (current or recent upper respiratory tract infection in the past 2 weeks, eczema, wheezing in the past 12 months, dry nocturnal cough, wheezing on exercise, family history of asthma, eczema or hay fever as well as passive smoking).
Intervention:
Deep or awake extubation.
Main Outcome Measure:
The occurrence of perioperative respiratory adverse events (laryngospasm, bronchospasm, persistent coughing, airway obstruction, desaturation <95%).
Results:
There were no differences between the two groups with regard to age, medical and surgical parameters. The overall incidence of complications did not differ between the two groups; tracheal extubation in fully awake children was associated with a greater incidence of persistent coughing (60 vs. 35%, P = 0.028), whereas the incidence of airway obstruction relieved by simple airway manoeuvres in children extubated while deeply anaesthetised was greater (26 vs. 8%, P = 0.03). There was no difference in the incidence of oxygen desaturation lasting more than 10 s.
Conclusion:
There was no difference in the overall incidence of perioperative respiratory adverse events. Both extubation techniques may be used in high-risk children undergoing adenotonsillectomy provided that the child is monitored closely in the postoperative period.
Trial Registration:
Australian New Zealand Clinical Trials Registry: ACTRN12609000387224.
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