Postoperative analgesia after gynecological single-port surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: a. Age 18-65 years old, ASA classification I-II level b. Planned for elective gynecological single-port laparoscopic surgery (such as ovarian cystectomy, total hysterectomy, bilateral adnexectomy, etc.) c. Voluntarily sign the informed consent form
Exclusion criteria
Exclusion criteria: Exclusion criteria: a. History of local anesthetic allergy or opioid dependence; b. Coagulation dysfunction (INR > 1.4, PLT 3 months; d. Severe heart or lung diseases or liver and kidney dysfunction; e. Long-term use of opioids or glucocorticoids (> 3 months, prednisone = 5mg/d equivalent dose); f. Presence of cognitive impairment preventing the operation of PCIA equipment; g. Pregnant or lactating women; h. Surgery duration > 180 minutes.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total consumption of oxycodone (mg) 72 hours after surgery;Number of PCIA compressions and the time of the first compression (in postoperative hours); | — |
Secondary
| Measure | Time frame |
|---|---|
| The area under the curve of the resting/moving NRS score within 72 hours after the operation;The intraoperative dosage of remifentanil/sufentanil and the dosage of oxycodone in the recovery room (in µg/kg/h);The change gradient of the QoR-15 score at 24/48/72 hours;Dynamic changes in serum IL-6/TNF-a levels;First defecation/elimination time (hours);Abdominal distension score (0 - 10 points); | — |
Countries
China
Contacts
The First Affiliated Hospital of Nanjing Medical University, Jiangsu Provincial Hospital