Transversus Abdominis Plane Block for Postoperative Analgesia in Living Donor Hepatectomy
- Conditions
- Acute Pain
- Interventions
- Drug: standard general anesthesiaDrug: Transversus Abdominis Plane Block
- Registration Number
- NCT02645903
- Lead Sponsor
- Inonu University
- Brief Summary
Living donor organ transplantation has increased in recent years due to an increased need for organs. The objective of this study was to investigate the effects of a TAP block on postoperative analgesia and opioid consumption in liver transplantation donors in whom a right lateral extending upper mid-line abdominal incision was used.
- Detailed Description
This prospective randomized controlled double-blinded study was conducted with 50 liver transplantation donors between 18-65 years who were scheduled to undergo right hepatectomy surgery. Cases to whom TAP block with ultrasound was applied after standard general anesthesia were determined as Group 1 and cases to whom only standard general anesthesia was applied, were determined as Group 2.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 50
- Liver transplantation donors
- Patients with a history of allergy to the drugs used in the study protocol, coagulation pathology, opioid tolerance
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description nonblocked standard general anesthesia Patients who received standard general anesthesia alone made up Group 2. Postoperative analgesia was administered through a morphine the patient-controlled analgesia device. transversus abdominis plane block Transversus Abdominis Plane Block Patients who received a tranversus abdominis plane block with ultrasound after standard general anesthesia represented Group 1. The tranversus abdominis plane block was performed bilaterally by obtaining an image with real time ultrasound guidance with a 6-13 MHz linear probe. The block was placed with a 22 G 80 mm needle while obtaining real-time images via an in-plane technique. Two 20 mL syringes were prepared after preparing a local anesthetic concentration of 1.5 mg/kg of 0.5% bupivacaine to 40 mL with saline. These were administered to the left and right abdominal walls. Postoperative analgesia was administered through a morphine the patient-controlled analgesia device.
- Primary Outcome Measures
Name Time Method pain scores (at movement and at rest) postoperatively at 24 hours Pain scores were assessed using a visual analog scale (0: No pain, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10: Excruciating pain).
- Secondary Outcome Measures
Name Time Method morphine consumption postoperatively at 24 hours morphine consumption were measured in postoperatively 24 hours