Abstract:Following 1 hour of treatment, liposomal bupivacaine demonstrated the highest chondrocyte viability. Chondrocyte viability was inversely proportional to anesthetic concentration.
“…By virtue of the formulation, this product has a longer duration of analgesic effect compared to bupivacaine HCl [15,19]. Although not currently approved for IA administration, a recent report describing the effects of liposomal bupivacaine on bovine and porcine chondrocyte viability, is encouraging with respect to the safety of this drug for IA use [16,17]. In the presently described study, we report on the plasma pharmacokinetics and synovial fluid concentrations of liposomal bupivacaine as well as chondrotoxicity following IA administration to horses.…”
Section: Discussionmentioning
confidence: 97%
“…A secondary objective of this study was to assess the potential chondrotoxicity of liposomal bupivacaine following IA administration. Shaw and colleagues recently assessed the effects of liposomal bupivacaine on cell viability in cultured bovine chondrocytes. While decreased cell viability was noted in the chondrocytes incubated with bupivacaine HCl, no significant difference in cell count was found between cells treated with liposomal bupivacaine and 0.9% saline .…”
Section: Discussionmentioning
confidence: 99%
“…Liposomal bupivacaine formulations are not currently approved by the FDA for IA administration in any species, however, presumably slow release over time would lead to lower overall exposure to bupivacaine, compared to the HCl formulation at a given time. In an in vitro model, Shaw and colleagues reported no effects on chondrocyte viability, relative to control, following treatment of bovine chondrocytes with liposomal bupivacaine . In a subsequent study, the same group of investigators studied the effects of liposomal bupivacaine on porcine chondrocytes in vivo following IA administration .…”
Sustained concentrations of IA bupivacaine suggest viability of this medication as an intra-articular analgesic. Effects on equine chondrocytes need further study.
“…By virtue of the formulation, this product has a longer duration of analgesic effect compared to bupivacaine HCl [15,19]. Although not currently approved for IA administration, a recent report describing the effects of liposomal bupivacaine on bovine and porcine chondrocyte viability, is encouraging with respect to the safety of this drug for IA use [16,17]. In the presently described study, we report on the plasma pharmacokinetics and synovial fluid concentrations of liposomal bupivacaine as well as chondrotoxicity following IA administration to horses.…”
Section: Discussionmentioning
confidence: 97%
“…A secondary objective of this study was to assess the potential chondrotoxicity of liposomal bupivacaine following IA administration. Shaw and colleagues recently assessed the effects of liposomal bupivacaine on cell viability in cultured bovine chondrocytes. While decreased cell viability was noted in the chondrocytes incubated with bupivacaine HCl, no significant difference in cell count was found between cells treated with liposomal bupivacaine and 0.9% saline .…”
Section: Discussionmentioning
confidence: 99%
“…Liposomal bupivacaine formulations are not currently approved by the FDA for IA administration in any species, however, presumably slow release over time would lead to lower overall exposure to bupivacaine, compared to the HCl formulation at a given time. In an in vitro model, Shaw and colleagues reported no effects on chondrocyte viability, relative to control, following treatment of bovine chondrocytes with liposomal bupivacaine . In a subsequent study, the same group of investigators studied the effects of liposomal bupivacaine on porcine chondrocytes in vivo following IA administration .…”
Sustained concentrations of IA bupivacaine suggest viability of this medication as an intra-articular analgesic. Effects on equine chondrocytes need further study.
“…Other studies showed chondrotoxicty at higher concentrations of 0.75% [19]. Shaw compared rovicapaine with liposomal bupivacaine, demonstrating higher viability of chondrocytes in the liposomal group [16].…”
Section: Discussionmentioning
confidence: 94%
“…A novel formulation of liposomal bupivacaine has recently been introduced, but there is a paucity of data published regarding the safety of intra-articular liposomal bupivacaine. Shaw et al harvested bovine knee cartilage and isolated the chondrocytes in the medium prior to exposure to liposomal bupivacaine, bupivacaine, and ropivacaine [16]. eir results showed that after a 1-hour exposure to liposomal bupivacaine, chondrocyte viability was similar to the control.…”
Objective. The purpose of this study is to determine whether (1) liposomal bupivacaine is chondrotoxic; (2) the chondrotoxicity of liposomal bupivacaine differs from standard bupivacaine; and (3) chondrotoxic effects are time dependent. Materials and Methods. We obtained 72 10 mm articular cartilage plugs from 12 fresh bovine distal femoral knee joints and exposed them to either saline, 0.5% bupivacaine, or liposomal bupivacaine for either 30 or 90 minutes. Twenty-four hours after treatment, chondrocyte viability was measured with the use of a fluorescent live/dead assay. An ANOVA test of variance was performed followed by a Holm–Sidak test to make pairwise comparisons across conditions. Student’s t-test was used to compare means. Results. Percent viability of cells exposed to liposomal bupivacaine for 30 minutes was less versus saline control (53.9% ± 21.5% vs. 73.7 ± 18.4%, p=0.035), and this remained significant at 90 minutes (49.1% ± 20.3% vs. 67.2% ± 25.6%, p<0.001). Liposomal bupivacaine had less chondrotoxic effects when compared with bupivacaine after 90 minutes, with greater viability (49.1% ± 20.3% vs. 21.4% ± 14.0%, p=0.003). Chondrotoxicity was found to be time dependent within the bupivacaine group (percent viability at 30 min: 45.5 ± 18.2%, 90 min: 21.4 ± 14.0%, p=0.001); however, liposomal bupivacaine did not demonstrate a significant time-dependent chondrotoxic relationship (p=0.583). Conclusions. Bupivacaine and liposomal bupivacaine are both toxic to chondrocytes. Liposomal bupivacaine is less chondrotoxic than standard bupivacaine and does not demonstrate a time-dependent toxicity.
The authors provide a comprehensive summary of all randomized, controlled trials (n = 76) involving the clinical administration of liposomal bupivacaine (Exparel; Pacira Pharmaceuticals, USA) to control postoperative pain that are currently published. When infiltrated surgically and compared with unencapsulated bupivacaine or ropivacaine, only 11% of trials (4 of 36) reported a clinically relevant and statistically significant improvement in the primary outcome favoring liposomal bupivacaine. Ninety-two percent of trials (11 of 12) suggested a peripheral nerve block with unencapsulated bupivacaine provides superior analgesia to infiltrated liposomal bupivacaine. Results were mixed for the 16 trials comparing liposomal and unencapsulated bupivacaine, both within peripheral nerve blocks. Overall, of the trials deemed at high risk for bias, 84% (16 of 19) reported statistically significant differences for their primary outcome measure(s) compared with only 14% (4 of 28) of those with a low risk of bias. The preponderance of evidence fails to support the routine use of liposomal bupivacaine over standard local anesthetics.
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