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Published on: November 6, 2019
[Comparison of two supraglottic airway devices on postoperative sore throat in children: a prospective randomized
Malika Hameed1, Khalid Samad1, Hameed Ullah1
1Aga Khan University Hospital, Department of Anesthesiology, Karachi, Pakistan.
Insights
Postoperative sore throat in children was similar between the Ambu laryngeal mask and I-gel airway devices. This study found no significant difference in sore throat frequency or severity between the two airway devices in pediatric patients.
Area of Science:
- Anesthesiology
- Pediatric Surgery
- Airway Management
Background:
- Postoperative sore throat is a common complaint in children after general anesthesia.
- Laryngeal mask airways are frequently used for airway management in pediatric surgery.
- Comparing different airway devices is crucial for optimizing patient outcomes.
Purpose of the Study:
- To compare the severity and frequency of postoperative sore throat in children using Ambu laryngeal mask airway versus I-gel®.
- To evaluate patient-reported outcomes regarding sore throat after elective surgery.
Main Methods:
- Seventy children (6-16 years) undergoing elective surgery were randomly assigned to Ambu laryngeal mask or I-gel®.
- Patients were interviewed postoperatively at 0, 1, 6, and 24 hours by a blinded observer.
- Data collected included self-reported sore throat severity and frequency.
Main Results:
- No statistically significant difference in the incidence of postoperative sore throat between the Ambu Group and I-gel Group at any time point (p > 0.28).
- Insertion duration was shorter for the Ambu laryngeal mask, while I-gel® was easier to insert (p=0.029).
- I-gel® demonstrated a higher oropharyngeal seal pressure than the Ambu laryngeal mask (p=0.001).
Conclusions:
- The choice between Ambu laryngeal mask and I-gel® does not significantly impact the severity or frequency of postoperative sore throat in children.
- Both devices are viable options for airway management in pediatric surgery, with considerations for insertion ease and seal pressure.
Background And Objective:
Sore throat is well recognized complaint after receiving general anesthesia. This study is conducted to compare the severity and frequency of postoperative sore throat in children undergoing elective surgery - following the use of Ambu laryngeal mask airway) or I-gel® - who are able to self-report postoperative sore throat.
Method:
Seventy children, 6 to 16 years-old, undergoing elective surgery randomly allocated to either Ambu laryngeal mask (Ambu Group) or I-gel® (I-gel Group). After the procedure, patients were interviewed in the recovery room immediately, after one hour, 6 and 24 hours postoperatively by an independent observer blinded to the device used intra-operatively.
Results:
On arrival in the recovery room 17.1% (n=6) of children of the Ambu Group complained of postoperative sore throat, against 5.7% in I-gel Group (n=2). After one hour, the results were similar. After 6 hours, postoperative sore throat was found in 8.6% (n=3) of the children in Ambu group vs. 2.9% (n=1) in I-gel Group. After 24hours, 2.9% (n=1) of the kids in Ambu Group compared to none in I-gel Group. There was no significant difference found in the incidence of postoperative sore throat in both devices on arrival (p=0.28); after 1 hour (p=0.28); after 6 hours (p=0.30); and after 24 hours (p=0.31). The duration of the insertion was shorter in Ambu Group and it was easier to insert the I-gel® (p=0.029). Oropharyngeal seal pressure of I-gel® was higher than that of Ambu laryngeal mask (p=0.001).
Conclusion:
The severity and frequency of postoperative sore throat in children is not statistically significant in the I-gel Group compared to Ambu Group.
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