Lumbar fusion
Conditions
Interventions
The control group:erector spinae plane block was performed with normal saline
The experimental group:erector spinae plane block was performed with ropivacaine
Sponsors
Taizhou Hospital of Zhejiang Province
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. For patients who underwent lumbar fusion; 2. Age range from 30 to 70 years; 3. The ASA I - II level; 4. Operation time is less than 3 hours.
Exclusion criteria
Exclusion criteria: 1. Spinal cord injury or multiple injuries; 2. Allergic to local anesthetic drugs; 3. Intracranial hypertension symptoms (headache, papillary edema, nausea and vomiting), previous history of cerebrovascular accident; 4. Puncture site has infection (i.e. swelling, heat and pain); 5. Combined with severe hypertension, long-term use of cortisol hormones; 6. Low blood volume, blood disease or abnormal coagulation function; 7. Body mass index >= 30kg/m2; 8. Liver function or renal insufficiency; 9. Having abnormal lung function (mainly with copd or uncontrolled asthma); 10. Pregnant women; 11. Communication with medical staff this study difficulty; 12. With psychosis or has serious anxiety or depression.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Nausea and vomiting and other adverse reactions;Anal exhaust time;Infusion volume, blood loss, body temperature; | — |
Primary
| Measure | Time frame |
|---|---|
| Nerve block range;Intraoperative blood pressure and heart rate at specific time points;VAS score;Consumption of analgesics; | — |
Countries
China
Contacts
Public ContactZhu Lijun
Department of Anesthesiology, Taizhou Hospital of Zhejiang Province
Outcome results
None listed