AI Article Synopsis

  • The study examines whether superior laryngeal nerve block (SLNB) can reduce coughing and improve sedation in patients undergoing maxillofacial surgery with delayed extubation.
  • 60 patients were divided into two groups: one received standard anesthesia (control group) and the other received ultrasound-guided SLNB postoperatively (study group).
  • Results showed that the SLNB group experienced less coughing and agitation, needed less rescue sedation, and enjoyed longer sedation periods, indicating SLNB improves postoperative outcomes.

Article Abstract

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 (UG-SLNB 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.

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Source
http://dx.doi.org/10.1016/j.jormas.2023.101589DOI Listing

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