Ropivacaine wound infusion for postoperative pain control in living donors of liver transplantation
Postoperative pain control in living donors of liver transplantation : A comparison of ropivacaine wound infusion vs. intrathecal morphine with intravenous patient controlled analgesia
Soo Joo Choi
19 participants
Nov 30, 2010
Interventional
Conditions
Summary
We evaluated the efficacy and safety of ropivacaine continuous infusion (Painbuster) in liver donors compared to intrathecal morphine (ITM) with intravenous patient controlled analgesia (IV PCA). Adult donors were randomly allocated into 2 groups: ITM + IV PCA group, Painbuster + rescue IV PCA group. Donors in Painbuster + rescue IV PCA group were placed a catheter in the wound and 0.5% ropivacaine was infused for postoperative 72 hours at a rate of 4ml/hr. Donors in ITM + IV PCA group received morphine sulfate (400ug) and fentanyl IV PCA postoperatively . The visual analogue scale (VAS) at rest and coughing, and IV PCA fentanyl and meperidine consumptions were assessed for 72 hours postoperatively. Side effects including sedation, dizziness, nausea, vomiting, pruritis, respiratory depression, wound seroma or hematoma, and bowel recovery time were recorded.
Eligibility
Inclusion Criteria1
- All living liver donors
Exclusion Criteria2
- A known allergy to eggs, propofol or any of the drugs used in the study.
- Bleeding diathesis, neurologic dysfunction (preexisting lower limb neurological deficit), recent systemic or local infections, insufficient comprehension to use the PCA device, history of drug use, or under treatment with opioids because of chronic pain.
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Interventions
Local anesthetic (0.5% Ropivacaine) wound instillation device, Painbuster 4ml/hr, for postoperative 72 hours Painbuster is an elastometric pump with catheters that have multiorifice holes through which local anesthetics can be delivered at a constant rate 4ml/hr if the catheters are placed at the wound are. As for a rescue analgesics, fentanyl intravenous patient controlled analgeisa (IV PCA) was applied at the end of surgery with a regimen of 1500 ug of fentanyl in normal saline 100 mL (15 ug/mL), programmed for 1ml bolus, 15 minutes lockout time without a basal infusion.
Locations(1)
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ACTRN12612000530820