Effect of Ultrasound-guided Bilateral Erector Spina Plan Block for Postoperative Analgesia in Patients Undergoing Multilevel Posterior Spinal Instrumentation.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Pain
- Sponsor
- Kahramanmaras Sutcu Imam University
- Enrollment
- 42
- Locations
- 1
- Primary Endpoint
- opioid consumption
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
Erector spinae plane (ESP) block is an interfacial plane block with visceral and somatic analgesic activity at paraspinal muscles. This study aims to examine the postoperative analgesic efficacy of ESP block in patients undergoing posterior spinal instrumentation
Detailed Description
Postoperative patient-controlled analgesia in the ESP group and control group will be compared with 24-hour morphine consumption and NRS scores at different time points. In addition, the need for rescue analgesics and patient satisfaction will be evaluated.
Investigators
Gökçe Gişi
Assistant Professor
Kahramanmaras Sutcu Imam University
Eligibility Criteria
Inclusion Criteria
- •ASA I-III patients
- •Agreed to participate in the study
Exclusion Criteria
- •Patients with infection at the injection site
- •Coagulopathy Allergy to amide-type local anesthetics
- •History of peripheral neuropathy
- •Hepatic and/or renal failure
- •Refusing the procedure
- •Patients with heart disease
- •Patients who have previously undergone surgery from the same area
Outcomes
Primary Outcomes
opioid consumption
Time Frame: up to 24 hour
The amount of morphine consumed in milligrams in the first 24 hours was determined with a patient-controlled analgesia pump.