Lung tumor
Conditions
Interventions
The ropivacaine erector spinae plane block group (Group A) :For group A patients, 30 ml of 0.375% ropivacaine was administered immediately after the surgery under ultrasound guidance for spinal muscle
The oxycodone combined with ropivacaine erector spinae plane block group (Group B):For group B patients, 30 ml of a mixture of 5 mg oxycodone and 0.375% ropivacaine was given immediately after the sur
Sponsors
Xuzhou Cancer Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Subjects must meet all of the following inclusion criteria to be enrolled in this study: 1. Undergoing minimally invasive thoracoscopic lobectomy, aged 18 years or older; 2. American Society of Anesthesiologists (ASA) classification of grade I or II; 3. Having surgical indications, having signed the informed consent form and willing to accept follow-up.
Exclusion criteria
Exclusion criteria: Any of the following conditions would disqualify a participant from being included in this study: 1. Obese patients with a BMI greater than 30 kg/m2; 2. Patients with obvious cardiac, pulmonary, liver, kidney and brain functional abnormalities before the surgery; 3. Patients with cognitive or mental disorders or those who cannot cooperate; 4. Patients with COPD before the surgery or those with pulmonary infections within one month. 5. Abnormal platelet and coagulation function or electrolyte and acid-base imbalance; 6. Damaged or infected puncture site, BMI greater than 30 kg/m2, etc.; 7. Complicated with neuromuscular system diseases; 8. Long-term use of analgesic drugs or history of drug abuse; 9. Chronic pain diseases; 10. Previous history of heavy drinking; 11. Allergic to opioid drugs, local anesthetic drugs, or having an allergic constitution and not suitable for oxycodone.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The VAS score for coughing at 24 hours after the operation; | — |
Secondary
| Measure | Time frame |
|---|---|
| The duration of erector spinae plane block resolution;The VAS scores at rest and during coughing at other time points;The time of the first press of the postoperative analgesic pump;The proportion of patients who pressed the pain relief pump more than 3 times;The cumulative dosage of oxycodone over 48 hours;Pain relief satisfaction score;The incidence of postoperative pulmonary complications;Severity grading and ratio of postoperative pulmonary complications;QoR-40 Recovery Scale;The incidence rate of adverse reactions such as nausea and vomiting within 48 hours after the operation;Complications related to thoracic erector spinae plane block;Postoperative recovery-related indicators; | — |
Countries
China
Contacts
Public ContactWenwen Ma
Xuzhou Cancer Hospital
Outcome results
None listed