This randomized controlled trial aims to compare the effectiveness and safety of 6% versus 8% sevoflurane inhalation induction in pediatric patients undergoing minor ophthalmic surgery. The primary outcome is emergence agitation assessed using the Pediatric Anesthesia Emergence Delirium (PAED) scale. Secondary outcomes include hemodynamic parameters, induction time, recovery time, and adverse events.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
80
Sevoflurane inhalation anesthesia was used for induction and maintenance of general anesthesia in pediatric patients undergoing minor ophthalmic surgery.
Joint Shantou International Eye Center of Shantou University and The Chinese University of Hong Kong
Shantou, Guangdong, China
RECRUITINGPAED score
Measured using the Pediatric Anesthesia Emergence Delirium (PAED) scale. The PAED scale ranges from 0 to 20, with higher scores indicating more severe emergence delirium (worse outcome).
Time frame: Within 30 minutes after recovery
Induction time
Time from face mask placement to loss of eyelash reflex, measured in seconds.
Time frame: Immediately after anesthesia induction
Recovery time
Time from discontinuation of sevoflurane to full recovery of consciousness, measured in minutes.
Time frame: Immediately after anesthesia discontinuation
Minimum alveolar concentration (MAC)
Minimum alveolar concentration (MAC) values recorded during anesthesia maintenance.
Time frame: Perioperatively
Respiratory depression
Incidence of respiratory depression recorded during the perioperative period.
Time frame: Perioperatively
Hypoxia
Incidence of hypoxia recorded during the perioperative period.
Time frame: Perioperatively
Cough
Incidence of cough recorded during the perioperative period.
Time frame: Perioperatively
Nausea and vomiting
Incidence of nausea and vomiting recorded during the postoperative recovery period.
Time frame: Immediately after anesthesia until discharge
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