Efficacy of ultrasound guided superior laryngeal nerve block on sedation for delayed extubation in maxillofacial surgery with free flap reconstruction

被引:0
作者
Wang, Xiao-Dong [1 ]
Zhou, Yi [1 ]
Guo, Zi-Jian [1 ]
Jiao, Liang [1 ]
Han, Fang [1 ]
Yang, Xu-Dong [1 ]
机构
[1] Peking Univ, Dept Anesthesiol, Sch & Hosp Stomatol, 22 Zhongguancun South Ave, Beijing 100081, Peoples R China
关键词
Ultrasound guided superior laryngeal nerve block; Sedation; Delayed extubation; Maxillofacial surgery; Free flap reconstruction; TRACHEAL EXTUBATION; RISK-FACTORS; INTUBATION; MANAGEMENT; ANESTHESIA; AIRWAY; HEAD;
D O I
10.1016/j.jormas.2023.101589
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Superior laryngeal nerve block (SLNB) is a regional anesthesia technique for addressing airway response. However, SLNB on the efficacy of sedation in patients with delayed extubation is unknown, particularly for maxillofacial surgery (MS). The aim of the study was to assess whether ultrasound guided (UG) SLNB reduces the incidence of moderate to severe cough for delayed extubation in MS with free flap reconstruction. Methods: 60 patients were randomly assigned to the GEA group (control group) and the SLNB group (UGSLNB postoperatively, study group). During the initial two postoperative hours, the incidence of moderate and severe cough, agitation, and the number of patients requiring rescue propofol and flurbiprofen were recorded. Additionally, the time spent under the target level of sedation, postoperative hemodynamics, and the total does of propofol during the postoperative 24 h were recorded. Results: The data showed the SLNB group had a significantly lower incidence of moderate to severe cough and agitation (p < 0.05), and a longer sedation time (p < 0.05). The number of patients required rescue propofol and flurbiprofen, as well as the hemodynamic changes, were significantly different between the two groups (p < 0.05). Conclusion: The use of UG-SLNB is associated with reduced incidence of postoperative cough. Moreover, SLNB can enhance the efficacy of postoperative sedation with need of fewer agents postoperatively. Clinical Trial Registration: ChiCTR2000039982 (c) 2023 The Authors. Published by Elsevier Masson SAS. This is an open access article under the CC BY-NC-ND license (999://creativecommons.olgIlicense99999.9nd/4.0/)
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页数:6
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