Gomoll Andreas H, Kang Richard W, Williams James M, Bach Bernard R, Cole Brian J
Department of Orthopedic Surgery, Rush University Medical Center, Rush Medical College, Chicago, Illinois 60612, USA.
Arthroscopy. 2006 Aug;22(8):813-9. doi: 10.1016/j.arthro.2006.06.006.
Postoperative pain pumps are increasingly used to deliver a continuous infusion of local anesthetic into the surgical wound or the joint. Recently, there have been concerns that the use of such devices may be associated with chondrotoxicity and even cases of chondrolysis in the shoulder. An experimental model is presented that investigates potential chondrotoxic effects of a continuous intra-articular infusion of bupivacaine in the rabbit shoulder.
We divided 30 rabbits into 3 groups that received continuous infusions of either saline solution, bupivacaine, or bupivacaine with epinephrine into the glenohumeral joint over a period of 48 hours. Animals were killed after 1 week, and osteochondral and synovial samples from the glenohumeral joint underwent analyses with confocal microscopy for live/dead cell assay, metabolic sulfate uptake assessment, and conventional histologic analysis.
Infusion of bupivacaine with epinephrine and without epinephrine decreased sulfate uptake by 56% (P = .009) and 50% (P = .02), respectively, when compared with saline solution; cell viability decreased by 20% (P = .08) and 32% (P = .02), respectively. Histologic analysis yielded significantly worse scores for bupivacaine infusion with epinephrine (P = .004) and without epinephrine (P = .02). The results for bupivacaine with or without epinephrine were not significantly different.
Continuous intra-articular infusion of bupivacaine with and without epinephrine led to significant histopathologic and metabolic changes in articular cartilage.
Bupivacaine showed profound chondrotoxic effects in an experimental model that closely followed the current clinical application of postoperative pain pumps. The results caution against the use of such devices in applications for smaller joints with minimal clearance or dilution as a result of hematoma, where continuous exposure of cartilage to bupivacaine is expected.
术后镇痛泵越来越多地用于向手术伤口或关节持续输注局部麻醉剂。最近,人们担心使用此类装置可能与软骨毒性有关,甚至会导致肩部出现软骨溶解病例。本文介绍了一个实验模型,该模型研究了布比卡因持续关节内输注对兔肩部的潜在软骨毒性作用。
我们将30只兔子分为3组,在48小时内分别向其盂肱关节持续输注生理盐水、布比卡因或含肾上腺素的布比卡因。1周后处死动物,对取自盂肱关节的骨软骨和滑膜样本进行共聚焦显微镜分析,以进行活/死细胞检测、代谢性硫酸盐摄取评估和常规组织学分析。
与生理盐水相比,含肾上腺素和不含肾上腺素的布比卡因输注分别使硫酸盐摄取降低了56%(P = 0.009)和50%(P = 0.02);细胞活力分别降低了20%(P = 0.08)和32%(P = 0.02)。组织学分析显示,含肾上腺素的布比卡因输注(P = 0.004)和不含肾上腺素的布比卡因输注(P = 0.02)的评分明显更差。含或不含肾上腺素的布比卡因的结果无显著差异。
含或不含肾上腺素的布比卡因持续关节内输注均导致关节软骨出现明显的组织病理学和代谢变化。
在一个紧密遵循术后镇痛泵当前临床应用的实验模型中,布比卡因显示出显著的软骨毒性作用。由于血肿导致间隙或稀释最小的较小关节应用此类装置时,预计软骨会持续暴露于布比卡因,这些结果提醒人们对此要谨慎使用。