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Intra-articular morphine and/or bupivacaine in the management of pain after total knee arthroplasty
Affiliation:1. Miller Orthopaedic Clinic, Charlotte, North Carolina, USA;2. Orthopaedic Surgery Department, Carolinas Medical Center, Charlotte, North Carolina, USA;3. Southeast Pain Care, Charlotte, North Carolina, USA;1. Center for Tobacco Control Research and Education, University of California, San Francisco, USA;2. IFT Institut für Therapieforschung, München, Germany;3. Institute for Biological and Medical Imaging, Helmholtz Zentrum München, München, Germany;4. Centre for Social Research on Alcohol and Drugs (SoRAD), Stockholm University, Stockholm, Sweden;1. Cleveland Clinic Orthopaedic and Rheumatologic Institute, Cleveland, Ohio;2. Cleveland Clinic Quantitative Health Sciences, Cleveland, Ohio;1. School of Pharmacy and Bioengineering, Keele University, Keele, Staffordshire, ST5 5BG, UK;2. The Robert Jones and Agnes Hunt Orthopaedic Hospital NHS Foundation Trust, Oswestry, Shropshire, SY10 7AG, UK;3. Department of Orthopaedics, Erasmus MC University Medical Center, 3000 CA Rotterdam, Netherlands
Abstract:The purpose of this study was to determine if intra-articular injection of morphine or bupivacaine significantly decreased postoperative pain as well as the use of intravenous narcotics for pain relief in patients undergoing total knee arthroplasty (TKA). In a prospective, double-blind, randomized fashion, 105 patients undergoing TKA were divided into the following 4 groups defined by the intra-articular injection they received: group 1 (n = 27) received saline solution, group 2 (n = 26) received morphine sulfate (5 mg), group 3 (n = 24) received bupivacaine (50 mg), and group 4 (n = 28) received a combination of morphine sulfate and bupivacaine. The injections were administered immediately after wound closure by the Hemovac drainage tubing that remained clamped for 45 minutes after surgery to allow for absorption. Before surgery and at 2, 4, 6, 24, and 48 hours after surgery, pain intensity was recorded using a visual analog scale. Postoperative supplemental intravenous morphine and/or meperidine was administered via a patient-controlled analgesia device, and 24-hour drug usage was tabulated. Results were suggestive of a modest short-term reduction in pain scores in the morphine and bupivacaine treatment groups compared with placebo (saline); however, results were statistically significant only at 4 hours because of the great variability in the pain score data. The total amount of postoperative pain medication used in the first 24 hours after surgery was not statistically significant between the 4 treatment groups. Thus, the results put into question the benefit of postoperative intraarticular administration of morphine or bupivacaine in patients undergoing TKA.
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