A Study on the Safety and Feasibility of Using Low-dose Muscle Relaxants in Bronchoscopy Interventional Surgery
The purpose of this clinical trial is to observe the use of low-dose muscle relaxants in bronchoscopy intervention surgeries, compared with no muscle relaxants, in terms of the satisfaction of tracheal tube insertion after anesthesia induction, the incidence of laryngospasm, the grading of intraoperative cough and movement, and the recovery of patients after surgery. The main questions it aims to answer are: * How safe and feasible is the use of low-dose muscle relaxants in bronchoscopy intervention surgeries? * Is the muscle relaxant regimen better than the no-muscle-relaxant regimen? Participants will: * During anesthesia induction, the experimental group will use low-dose muscle relaxants for anesthesia, while the control group will not use muscle relaxants for anesthesia. * Record the satisfaction of mask ventilation and the incidence of laryngospasm.
• Patients undergoing elective electronic bronchoscopic interventional surgery;
• Age 18 years or older;
• American Society of Anesthesiologists (ASA) I-III;
• The duration of bronchoscopic surgery \>=20min;
• Through pre-anesthesia assessment, the patient/family member has informed consent and signed the consent form;
• The general clinical information of the patient is complete.