emergence agitation
Conditions
Interventions
Control group:Conventional anesthesia management, not stellate ganglion block
Sponsors
Guangzhou Medical University Affiliated Women and Children's Medical Center
Eligibility
Sex/Gender
All
Age
2 Years to 6 Years
Inclusion criteria
Inclusion criteria: 1. Aged 24 to 72 months ; 2. Parents agree to participate in this study and sign the informed consent form; 3. ASA physical status I or II; 4. Patients undergoing adenotonsillectomy surgery in otorhinolaryngology.
Exclusion criteria
Exclusion criteria: 1.Sinus bradycardia; 2.The patient has a history of allergy to any medication involved in this study; 3.Coagulation disorders; 4.Broken or infected skin at the piercing site; 5.Children with a history of psychological or neurological disorders, psychotropic drugs or anticonvulsant use; 6.Children with developmental delay and attention deficit disorder.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of emergence agitation; | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence of postoperative nausea and vomiting;pediatric anesthesia emergence delirium scale,PAED peak scores ;Satisfaction of parents;Side effects ;FLACC pain scores;sufentanil consumption ;laryngeal spasm;Propofol consumption ; low oxygen saturation (SPO2<94%);electroencephalogram; | — |
Countries
China
Contacts
Public ContactMo xiaofei
Guangzhou Medical University Affiliated Women and Children's Medical Center
Outcome results
None listed