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Transversus Abdominis Plane Block for Postoperative Analgesia in Living Donor Hepatectomy

Phase 4
Completed
Conditions
Acute Pain
Interventions
Drug: standard general anesthesia
Drug: 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
Inclusion Criteria
  • Liver transplantation donors
Exclusion Criteria
  • 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
GroupInterventionDescription
nonblockedstandard general anesthesiaPatients 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 blockTransversus Abdominis Plane BlockPatients 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
NameTimeMethod
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
NameTimeMethod
morphine consumptionpostoperatively at 24 hours

morphine consumption were measured in postoperatively 24 hours

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