• BMC anesthesiology · Oct 2023

    Randomized Controlled Trial

    Effect of superior laryngeal nerve block in alleviating sore throat after application of i-gel supraglottic airway: a randomized controlled trial.

    • Zhu Lv, Xinyi Huang, Jinxia Cai, Zijun Zhou, Linglin Gao, Weijian Wang, Jiehao Sun, and Yizhao Pan.
    • Department of Anesthesiology, 1st affiliated hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
    • BMC Anesthesiol. 2023 Oct 5; 23 (1): 333333.

    BackgroundPostoperative sore throat (POST) is a common complaint after supraglottic airway device (SAD) application. Internal branch of the superior laryngeal nerve (iSLN) block has the potential to alleviate POST. The aim of this trial was to explore the effect of iSLN block in alleviating sore throat, as well as to identify the potential risk factors for POST after SAD insertion.MethodsOne hundred thirty-four patients scheduled for elective gynecological surgery were randomized to either group T: tetracaine syrup (1%) for local lubrication on i-gel supraglottic device (n = 67) or group B: i-gel insertion with water based lubricant on it and followed by bilateral iSLN block (ropivacaine, 0.375%, 2 ml for each side) (n = 67). Under ultrasound guidance, iSLN was exposed below thyrohyoid membrane. The primary outcome was the intensity of sore throat at 6 h after surgery. In addition, POST score at 0.5 h and 24 h, the severity of postoperative swallowing discomfort, acoustic analysis and complications were measured.ResultsCompared with tetracaine syrup for local lubrication, iSLN block resulted in a reduced intensity of POST at 0.5 h (P = 0.044, OR = 1.99, 95%CI 1.02 to 3.88) and 6 h (P < 0.001, OR = 5.07, 95%CI 2.53 to 10.14) after surgery, as well as less severity of swallowing discomfort (P < 0.001, OR = 2.21, 95%CI 1.63 to 2.99) and cough (P = 0.039, OR = 1.97, 95%CI 1.04 to 3.73). The patients after iSLN block presented lower jitter and shimmer value in acoustic analysis at 6 h after surgery (P < 0.001).ConclusionsiSLN block was effective in alleviating POST, improving voice function, as well as reducing postoperative swallowing discomfort and coughing.Trial RegistrationChinese Clinical Trial Registry (ChiCTR2000037974) on 8th Sept 2020.© 2023. BioMed Central Ltd., part of Springer Nature.

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