Quality of postoperative recovery
Conditions
Interventions
Combined atomization group1:Combined atomization group 1: After the operation, the same dose of saline was given intravenously as a placebo control,give 1µg/kg dextrometomidine atomization inhalation
Combined atomization group 2:Combined atomization group 2: After the operation, the same dose of saline was given intravenously as a placebo control,give 0.5µg/kg dextrometomidine atomization inhalati
Intravenous control group:Intravenous control group: 1µg/kg dextrometomidine was given intravenously after the operation, and the same dose of physiological saline was atomized and inhaled after extub
Sponsors
The First Affiliated Hospital of Anhui Medical University
Eligibility
Sex/Gender
All
Age
6 Years to 15 Years
Inclusion criteria
Inclusion criteria: 1. Signed informed consent; 2. Children with elective day tonsillectomy surgery; 3. Age 6-15 years old; ASA grade I~II.
Exclusion criteria
Exclusion criteria: 1. Children with increased intracranial pressure or intraocular pressure; 2. Those who have any emotional disorders or mental illnesses; 3. Bradycardia or with heart block; 4. Those who have contraindications to the test drug and other anesthetic drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Throat pain score 24h after surgery; | — |
Secondary
| Measure | Time frame |
|---|---|
| Degree of postoperative sedation;Delirium during awakening from anesthesia in children;Incidence of adverse events in 24 hours;Operation time;Anesthesia time;Wake-up time;Extubation time;PACU duration;Eating time;Length of hospitalization;Incidence of nausea and vomiting;Incidence of hypoxemia (SpO2<94%);Incidence of laryngeal spasm;Incidence of laryngeal spasm; | — |
Countries
China
Contacts
Public ContactCheng Xinqi
The First Affiliated Hospital of Anhui Medical University
Outcome results
None listed