Long-Term Effects of Bupivacaine on Cartilage in a Rabbit Shoulder Model

被引:76
作者
Gomoll, Andreas H. [4 ]
Yanke, Adam B. [1 ]
Kang, Richard W. [1 ]
Chubinskaya, Susan [2 ]
Williams, James M. [3 ]
Bach, Bernard R. [1 ]
Cole, Brian J. [1 ,3 ]
机构
[1] Rush Univ, Med Ctr, Dept Orthoped Surg, Rush Med Coll, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Dept Biochem, Rush Med Coll, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Dept Anat & Cell Biol, Rush Med Coll, Chicago, IL 60612 USA
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Orthoped Surg, Boston, MA 02115 USA
关键词
shoulder arthroscopy; articular cartilage; bupivacaine toxicity; pain pump; ARTICULAR-CARTILAGE; SULFATED GLYCOSAMINOGLYCANS; REPAIR; PROTEOGLYCANS; QUANTITATION; ASSAY; BLUE;
D O I
10.1177/0363546508323748
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
100224 [整形外科学];
摘要
Background: Previous investigations have reported on the chondrotoxicity of bupivacaine in short-term in vivo and in vitro models. This study was designed to provide additional information on the long-term effects of bupivacaine infusion on articular cartilage in an established rabbit shoulder model. Hypothesis: Infusion of bupivacaine into the rabbit shoulder will have long-term deleterious effects on articular cartilage. Study Design: Controlled laboratory study. Methods: Thirty-six rabbits were randomized into 3 groups and were infused over 48 hours with saline (S), bupivacaine alone (B), or bupivacaine with epinephrine (B+E) into the glenohumeral joint. Animals were sacrificed after 3 months, and tissue samples were analyzed with live/dead cell assay, proteoglycan (PG) synthesis and content assays, and conventional histological evaluation. Results: No macroscopic or radiographic changes were detected in the infused shoulders. Sulfate uptake of infused shoulders relative to controls was elevated to 112% +/- 39% (S), 166% +/- 67% (B), and 210% +/- 127% (B+E). Statistical analysis of PG content demonstrated significantly increased levels in bupivacaine groups compared with saline. There were no significant differences among groups in cell count, percentage of living cells, or histological grade. Conclusions: No permanent impairment of cartilage function was detected 3 months after intra-articular infusion of bupivacaine. Cartilage metabolism was increased, indicating a possible reparative response. This suggests that, at least in the model used, articular cartilage has the ability to recover from the chondrotoxic effects of bupivacaine infusion. Before extrapolating these results to human cartilage, other factors including underlying cartilage injury or disease, decreased chondrocyte density, and increased bupivacaine dosing need to be taken into account. Clinical Relevance: Bupivacaine toxicity has recently been implicated in the development of chondrolysis after arthroscopic shoulder procedures, but these findings suggest that additional noxious stimuli might be required before permanent damage ensues.
引用
收藏
页码:72 / 77
页数:6
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