Thoracoscopic wedge resection was performed
Conditions
Interventions
Experimental Group:The method of anesthesia in this study was rapid induction of double-lumen endotracheal intubation and intravenous inhalation combined anesthesia. Sublobar resection (wedge or segme
Control group:The control group was treated with a common intravenous analgesia pump consisting of opioids (sufentanil 0.8µg/kg) and central antiemetic (palonosetron 0.5 mg), nalbuphine 0.8 mg/kg, and
Single compression volume: 0.5 mL. Nalbuphine 1 mg was given 20 min before the end of surgery, and then the postoperative intravenous analgesia pump was continuously pumped. In the experimental group,
Sponsors
The Affiliated Hospital of Guizhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Patients scheduled for pulmonary surgery under general anesthesia with double-lumen bronchial intubation; 2.Age >= 18 years old; 3. American Society of Anesthesiologists Health Classification (ASA Surgical Classification) Grade I/II/III; 4.Those who can participate in cognitive function assessment and obtain informed consent.
Exclusion criteria
Exclusion criteria: 1.Patients with missing case data: 2. Patients with a preoperative Mini-Mental State Examination (MMSE) score of less than 20 points; 3.Patients with a history of psychosocial disorders or the use of psychotropic drugs; 4. Patients with any central nervous system diseases; 5. Those who are unable to communicate due to aphasia, severe hearing impairment or other difficulties; 6. Those with neurological and mental disorders such as dementia, language disorders, or psychological problems that prevent them from collaborating with the survey participants; 7. Those with a history of alcohol abuse or acetylcholine use; 8. Severe circulatory system diseases (such as severe arrhythmia, hypertension, coronary artery disease, heart failure) and history of cardiac surgery; 9. Severe respiratory system diseases (respiratory failure, severe chronic obstructive pulmonary disease);
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative NRS pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Hamilton Depression Scale score;Hamilton Anxiety Scale score; | — |
Countries
China
Contacts
Public ContactTan li
The Affiliated Hospital of Guizhou Medical University
Outcome results
None listed