waking period restlessness
Conditions
Interventions
Esketamine group (Group E):Group E was given esketamine 0.5mg/kg before skin incision, and then esketamine 4ug/kg/min
Control group (group C):total intravenous anesthesia
Sponsors
The Second Affiliated Hospital of Anhui Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Gender is not limited, age 18-65 years old, ASA classification ?~? 2. Voluntarily accept the use of postoperative analgesic pump 3. Thoracoscopic partial lung resection (lung segment, wedge, bullae) 4. Voluntary subjects and signed informed consent
Exclusion criteria
Exclusion criteria: 1. History of allergy to local anesthetics or non-steroidal anti-inflammatory drugs 2. Known coagulation disorders 3. Infection near the puncture 4. History of chronic pain or frequent use of analgesics 5. Patients with communication disorders or other reasons not applicable to this study were excluded 6. There are symptoms of high intracranial pressure or a history of glaucoma.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| RSS Agitation Score and Ramsay Sedation Score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Extubation quality score;Intraoperative opioid use;Pain score at 0.5h,1h,2h, 4h, 8h, 12h, 24h, 48h after operation;Occurrence of adverse reactions;Analgesic pump use; | — |
Countries
China
Contacts
Public ContactChenqi
The Second Affiliated Hospital of Anhui Medical University
Outcome results
None listed