Effect of continuous cuff pressure regulator on postoperative sore throat in patients undergoing laparoscopic cholecystectomy with H-LMA: a randomized controlled trial

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Abstract

Background: The aim of this study was to investigate the effect of continuous regulation of laryngeal mask cuff pressure on postoperative sore throat (POST) after laparoscopic cholecystectomy. Methods: Patients underwent laparoscopic cholecystectomy were randomly divided into group E or group C in a 1:1 ratio. Laryngeal mask was inserted after successful induction of general anaesthesia. The product of laryngeal mask used in this study was Hope laryngeal mask airway (H-LMA). Group E: the continuous cuff pressure regulator was used to continuously control the cuff pressure of the laryngeal mask at 40 cmH2O. Group C: without the continuous cuff pressure regulator. The primary outcome was the incidence of POST within 24 h of extubation. Secondary outcomes included other postoperative pharyngolaryngeal adverse events 30 min and 24 h after extubation. Results: A total of 100 adult patients completed the study. The incidence of POST 30 min and within 24 h of extubation was lower in group E than in group C (12% vs. 36%; P = 0.009) (10% vs. 32%; P = 0.013). The severity of POST 30 min and within 24 h after extubation was also lower in group E than in group C (all P<0.05). The incidence of dysphagia 30 min and within 24 h after extubation was lower in group E than in group C (all P<0.05). Conclusions: In conclusion, the incidence of POST can be reduced by continuously controlling the laryngeal mask cuff pressure at 40 cmH2O with the continuous cuff pressure regulator. Trial registration: Chinese Clinical Trial Registry identifier: ChiCTR2400093522. (Principal investigator: Gongchen Duan; registration date: 6 December 2024).

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He, R., Wu, C., Lan, H., Han, X., Wu, J., Jiang, J., & Duan, G. (2025). Effect of continuous cuff pressure regulator on postoperative sore throat in patients undergoing laparoscopic cholecystectomy with H-LMA: a randomized controlled trial. BMC Anesthesiology, 25(1). https://doi.org/10.1186/s12871-025-03435-x

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