postoperative quality of recovery
Conditions
Interventions
Experimental group(total intravenous anesthesia group):Anesthesia was maintained with propofol dose of 4-12 mg · kg-1 · H-1 and remifentanil dose of 0.05-0.2 µ g · kg-1 · min-1
Control group (inhalation anesthesia group):Anesthesia was maintained with sevoflurane inhalation of 1.0-3.0% and remifentanil dose of 0.05-0.2 µ g · kg-1 · min-1
Sponsors
Guanyun people's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Aged 18-65 years, ASA grades I-III, elective retroperitoneal laparoscopic urological surgery (operation types include ureterolithotomy, renal cyst unroofing and decompression, and partial nephrectomy).
Exclusion criteria
Exclusion criteria: 1. Unplanned or emergency surgery; 2. Those with mental illness, abnormal cognitive function, chronic pain disease, long-term use of sedative and analgesic drugs or alcohol abuse; 3.Severe liver and kidney disease ; 4. Severe cardiopulmonary disease; 5. Pregnant and lactating women; 6. Those who have allergies or contraindications to the drugs used in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative quality of recovery score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative quality of recovery score;NRS pain score;Inflammatory factors;Hemodynamic indices at special moments in the perioperative period;Intraoperative end tidal carbon dioxide partial pressure;Intraoperative arterial blood gas partial pressure of carbon dioxide;Ramsay Sedation score on awakening;Awakening time;Extubation time of endotracheal tube;PACU Length of Stay;Incidence of adverse reactions 24 hours after operation (nausea and vomiting, headache, respiratory depression, hypoxemia, etc.); | — |
Countries
China
Contacts
Public ContactQian Long
Guanyun people's Hospital
Outcome results
None listed