Adolescent scoliosis
Conditions
Interventions
Propofol monitoring group:none
Sponsors
Drum Tower Hospital
Eligibility
Sex/Gender
All
Age
10 Years to 18 Years
Inclusion criteria
Inclusion criteria: 1. Age >= 10 years old and <= 18 years old; 2. ASA classification I-III; 3. Scheduled to undergo spinal orthopedic surgery; 4. Need for intraoperative awakening; 5. Agree to participate in this research and sign the informed consent form;
Exclusion criteria
Exclusion criteria: 1. Refuse to participate in this research; 2. Severe liver dysfunction (Child-Pugh C grade); Severe renal dysfunction (preoperative dialysis was received); ASA classification >= IV grade; 3. The preoperative assessment indicated that the patient was unable to cooperate for the completion of intraoperative awakening or had language communication disorders. 4. Allergy to Propofol; 5. Other researchers or attending physicians consider that certain situations are not suitable for participation in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plasma concentration of propofol;Bispectral index; | — |
Secondary
| Measure | Time frame |
|---|---|
| The time from awakening and stopping medication during surgery to awakening;The dosage of anesthesia drugs used during surgery;Intraoperative wake-up quality score;Intraoperative awareness of incidence rate; | — |
Countries
China
Contacts
Public ContactJinhua Bo
Drum Tower Hospital
Outcome results
None listed