The 2012 Chitranjan Ranawat Award: Intraarticular Analgesia After TKA Reduces Pain: A Randomized, Double-blinded, Placebo-controlled, Prospective Study

被引:46
作者
Goyal, Nitin [3 ]
McKenzie, James [1 ,2 ]
Sharkey, Peter F. [1 ,2 ]
Parvizi, Javad [1 ,2 ]
Hozack, William J. [1 ,2 ]
Austin, Matthew S. [1 ,2 ]
机构
[1] Thomas Jefferson Univ Hosp, Dept Orthopaed Surg, Philadelphia, PA 19107 USA
[2] Rothman Inst, Philadelphia, PA 19107 USA
[3] Anderson Orthopaed Clin, Alexandria, VA 22306 USA
关键词
TOTAL KNEE; POSTOPERATIVE PAIN; TOTAL HIP; NERVE BLOCK; ARTHROPLASTY; MANAGEMENT; ANESTHESIA; ROPIVACAINE; BUPIVACAINE; REPLACEMENT;
D O I
10.1007/s11999-012-2596-9
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Postoperative pain after total knee arthroplasty remains one of the most important challenges facing patients undergoing this surgery. Providing a balance of adequate analgesia while limiting the functional impact of regional anesthesia and minimizing opioid side effects is critical to minimize adverse events and improve patient satisfaction. We asked whether bupivacaine delivered through an elastomeric device decreases the (1) patients' perception of pain after TKA; (2) narcotic consumption; and (3) narcotic-related side effects as compared with a placebo. In this prospective, double-blind, placebo-controlled study, all patients received standardized regional anesthesia, a preemptive and multimodal analgesic protocol, and a continuous intraarticular infusion at 5 mL/hour through an elastomeric infusion pump. The patients were randomized to receive either an infusion pump filled with (1) 300 mL of 0.5% bupivacaine, the experimental group (n = 75); or (2) 300 mL of 0.9% normal saline solution, the control group (n = 75). Data concerning postoperative pain levels through a visual analog scale, postoperative opioid consumption, opioid-related side effects, and complications were collected and analyzed. Patients in the experimental group receiving the bupivacaine reported a reduction in pain levels in highest, lowest, and current visual analog scale scores compared with the placebo group on the first postoperative day and highest visual analog scale score on postoperative Day 2 along with a 33% reduction in opioid consumption on postoperative Day 2 and a 54% reduction on postoperative Day 3. In patients undergoing TKA, continuous intraarticular analgesia provided an effective adjunct for pain relief in the immediate postoperative period without the disadvantages encountered with other analgesic methods. Level I, therapeutic study. See Guidelines for Authors for a complete description of levels of evidence.
引用
收藏
页码:64 / 75
页数:12
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