video-assisted thoracoscopic lobectomy
Conditions
Interventions
control group:general anesthesia and thoracoscopic-guided thoracic paravertebral block with placebo
PVB group:thoracoscopic-guided thoracic paravertebral block
Sponsors
Putian First Hospital, Fujian Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: The study enrolled 60 ASA I-III patients (18-65 years old, either gender, weighing 50-85 kg) who were scheduled to undergo elective thoracoscopic lobectomy. Patients undergoing elective general anesthesia and video-assisted thoracoscopic unilateral lobectomy had no history of cardiopulmonary disease, no sinus bradycardia, no functional lesions of the sinoatrial node, no serious arrhythmia, and no thoracic deformity. Surgery time was more than 2 hours.
Exclusion criteria
Exclusion criteria: Exclusion criteria: minimental state examination scores below 23 points; the history of dementia, psychosis, or other central nervous system disease or drug dependence and poor compliance; and those who did not complete video-assisted thoracoscopic lobectomy under general anesthesia or have to convert to thoracotomy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| intraoperative opioid consumption;total sufentanil dosages within the first 48h postoperatively;postoperative NRS scores; | — |
Secondary
| Measure | Time frame |
|---|---|
| Ramsay sedation scores;first use of patient-controlled analgesia (PCIA) intravenously;the pressing times of analgesic pumps;QoR-40 scores; | — |
Countries
China
Contacts
Public ContactYaohua Yu
Putian First Hospital, Fujian Medical University
Outcome results
None listed