Comparison of in vitro and in vivo Toxicity of Bupivacaine in Musculoskeletal Applications

Introduction

Musculoskeletal surgeries rank amongst the most painful surgical interventions overall (1). The debilitating effects of postoperative pain include delayed mobilization and complications, such as pneumonia and decubitus, which in turn can lead to increased hospital stay and re-admissions (2). Pain resulting from musculoskeletal surgery is usually treated with multimodal pain regimens in which opioids often fulfill an important role. Opioids have, however, well-known side effects such as nausea, respiratory depression and drowsiness, and can lead to dependence and addiction. Of all patients enrolling in opioid-abuse treatment programs, almost half were first exposed to opioids through prescription from their physician (3, 4). Currently, an estimated two million American citizens are addicted to prescription pain killers, such as opioids (5). The risks of dependence and abuse are especially relevant for patients undergoing musculoskeletal surgery (6). Despite administration of opioids, poorly controlled postoperative pain is reported by 75% of patients (2). Therefore, the interest in alternative pain treatments not displaying the systemic side effects of current opioid-based regimes is increasing. The use of local anesthetics (LAs) has the potential to accelerate postoperative recovery and reduce opioid consumption in musculoskeletal surgery. To this end, bupivacaine is especially popular as it displays the longest duration of action of all LAs (up to 8 h) (7). In comparison, the effects of lidocaine last up to 2 h in soft tissue (8). Because of its extensive clinical use and the highest potency compared to other long-acting amino-amide LAs such as ropivacaine and levobupivacaine, this review focuses on bupivacaine (9). However, 8 h of analgesia is likely insufficient for postoperative pain control and therefore novel formulations aim to further extend the duration of action of LAs. In fact, bupivacaine is the main LA that has been incorporated in recent opioid-free inventions for postsurgical pain relief (10–14).

Recent studies have expressed concerns regarding the local toxic effects of bupivacaine infiltration when used for musculoskeletal applications. This review aims to assess (i) the in vitro, in vivo and clinical effects of bupivacaine on various musculoskeletal tissues, cell types and relevant environments (including cartilage, bone, muscle, nerves, intervertebral disc, and surgical wounds) and (ii) and the clinical translatability and real-world relevance of these effects. Furthermore, recent approaches and developments to decrease the toxic profile and increase the duration of action of bupivacaine are discussed. Studies providing data on in vitro, animal model or clinical local toxicity of bupivacaine were manually selected. References of selected papers were checked for relevant literature. In addition, separate searches were performed for studies comparing free bupivacaine with novel formulations of bupivacaine (e.g., liposomal bupivacaine). Articles published in languages other than English and case reports were excluded from review. Studies describing systemic toxicity following administration of bupivacaine were outside the scope of this review. This literature review did not require an ethical board approval because no patients or patient data were involved in the review, and only publicly available data was used.

Bupivacaine

After its discovery in 1957, bupivacaine (1-Butyl-N-(2,6-dimethylphenyl)-2-piperidinecarboxamide) (Figure 1) has become one of the most widely and frequently used LAs, and is listed as a World Health Organization Essential Drug (15, 16). Bupivacaine belongs to the class of amino-amide LAs, exerting their anesthetic action through binding to the intracellular portion of voltage-gated sodium channels, more specifically the alpha subunit. By inhibiting sodium influx into axons, depolarization and, therefore, pain signal transduction is inhibited (16). Examples of LA application in musculoskeletal surgery are local infiltration anesthesia (LIA) after total hip and total knee arthroplasty (THA and TKA, respectively). These local applications are associated with low rates of systemic toxicity and adverse effects, providing a favorable comparison with opioids (17–20). Besides therapeutic applications, LA infiltrations also serve as diagnostic tool in a variety of joint disorders, such as hip or shoulder osteoarthritis (21).

FIGURE 1

Figure 1. Bupivacaine structure formula.

The class of amino-amide LAs has been derived from amino-ester LAs, such as cocaine. All amino-amide LAs have a similar molecular structure, with an aromatic lipophilic portion linked with an amide-containing intermediate chain to an amine hydrophilic portion (22). Bupivacaine has the longest duration of action (up to 8 h) of all amino-amide LAs due to its butyl group attached to the tertiary amine. The lipophilic butyl group allows for easy membrane-crossing resulting in high anesthetic potency and prolonged duration of action. In plasma, 95% of bupivacaine is protein-bound, mainly to albumin. Bupivacaine is metabolized in the liver by conjugation with glucuronic acid and excreted renally (23). Elimination half-life is ~2.7 h in adults and 8.1 h in neonates (24). The recommended maximum doses are 2 mg/kg body weight or a maximum of 400 mg per day. The dose can be increased to 2.5 mg/kg body weight with addition of epinephrine, by virtue of decreased systemic uptake resulting from local vasoconstriction (25). The left-isomer-only formulation of bupivacaine, levobupivacaine, is commercially available separately and has been associated with decreased systemic toxicity, predominantly cardiotoxicity (9). In in vitro studies, the concentration of bupivacaine is often reported in mM3 or uM. To help comparison between studies presented in this review, it should be noted that a clinically used concentration of 0.5% Bupivacaine HCl solution equals a molarity of 15.4 mM. Bupivacaine HCl solutions are registered for use in spinal, epidural, regional, or local infiltrative anesthesia. In all cases the solution is administered by injection.

Effects of Bupivacaine on Skeletal Muscle

In musculoskeletal surgery, exposing osseous structure(s) often requires cutting through or releasing muscle tissue. Muscle recovery after surgery is of paramount importance, since it essential for wound healing, and facilitates quick mobilization and uneventful return to preoperative function.

It is known that LAs are myotoxic in vitro. Bupivacaine is reported to lead to 60–100% in vitro myocyte toxicity in concentrations >1 mM (i.e., in clinically used concentrations) (26). Previous studies have described histopathological changes at the injection site of LAs (27–30). Within min, hypercontraction of fiber bundles and myofibrils occurs. Within hours, a degenerative phase is observed, with disruption and condensation of myofilaments, lytic degeneration of the sarcoplasmic reticulum and mitochondria, and pathologic condensation of chromatin, which are signs of early necrosis and apoptosis. The sarcolemmal structure remains intact, potentially indicating that fiber degeneration occurs mainly intracellularly and does not affect the macroscopic structure of the muscle. This degenerative phase lasts for 24–48 h, after which phagocyte infiltration of the application site occurs. Debris is cleared without damage to basal laminae and satellite cells. As these cells remain largely intact, complete muscular regeneration can occur within 3–4 weeks.

It is hypothesized that the myotoxic effects of bupivacaine are induced by calcium influx in muscle cells. This is supported by the finding that bupivacaine in concentrations >>1 mM leads to activation of the Ca-release channel-ryanodine receptor in the sarcoplasmic reticulum (27, 31). Interestingly, levobupivacaine has been shown to have stronger effects on Ca-uptake in muscle cells compared with racemic bupivacaine, theoretically potentiating its myotoxicity (31, 32). Another factor that might play a key role in myotoxicity is pH. Indeed, the free base form of LAs reaching the sarcoplasmic reticulum is thought to be responsible for myocyte injury. At higher pH (i.e., closer to and beyond the drug's pKa), the free base fraction increases, potentiating bupivacaine's capacity to damage muscle (33).

Bupivacaine displays considerable myotoxicity in vitro, leading to apoptosis and (myo-)necrosis (Figure 2) (34–36). Bupivacaine-induced myotoxicity is dose and time dependent (37), with the myotoxic effects being reversible within 3 weeks (38). Animal models have been established to study muscle damage using bupivacaine as an agent to induce myotoxicity (39). A recent systematic review summarized the in vivo myotoxicity of bupivacaine and its effect on muscle recovery. Myotoxicity was defined as the presence of (a combination of) muscle weakness or paralysis, or enzymatic changes indicative of muscle damage (e.g., elevated creatine phosphokinase serum levels). Muscle tissue recovery time was defined as regeneration of muscle fibers, normalization of myofibil diameters, and resolution of inflammation and was doubled after LA administration (up to 30 days, vs. normal regeneration time of 14 days) (26, 40). Full recovery to preoperative function was reported in 21 studies, partial recovery in 17 studies and minimal recovery in four studies (26). Notably, myotoxicity also occurred after administration of liposomal bupivacaine (26, 41). The authors remarked that myotoxicity was correlated with increased concentrations of and exposure time to bupivacaine. The occurrence of myotoxicity can be explained by the fact that liposomal bupivacaine uses relatively high bupivacaine concentrations and sustained release leads to increased exposure time.

FIGURE 2

Figure 2. Light microscopy images of LA-induced myotoxicity. (A) Skeletal muscle 2 days after 0.9% saline injection, showing connective tissue (CT) between normal muscle fibers (MC) (20× magnification, insert 40×). (B) Skeletal muscle 2 days after 0.5% bupivacaine injection, showing degenerative (DA) and inflammatory areas (IA) alternated with MC (20× magnification). (C) Skeletal muscle 2 days after 0.5% ropivacaine injection, also displaying DA and IA (20× magnification). (D) Skeletal muscle 2 days after 0.5% levobupivacaine injection, showing incidental IA and blood vessels (BV) between MC (20× magnification). Öz Gergin et al. Comparison of the Myotoxic Effects of Levobupivacaine, Bupivacaine, and Ropivacaine: An Electron Microscopic Study. Ultrastructural Pathology, May 2015. Reprinted by permission of the publisher (Taylor & Francis Ltd.) (34).

Clinically, effects of muscle damage appear negligible except in muscles of the eye, where temporary diplopia after local anesthesia has been reported (42). Continuous infusion of LAs after rotator cuff surgical repair did not lead to worse clinical outcomes. The authors concluded that myotoxicity may be reversible or is not severe enough to affect tissue healing and postoperative outcomes (43). In orthopedic surgery about 0.14% of patients experienced clinical symptoms of LA-induced myotoxicity, which included significant loss of muscle contraction force and tenderness of the operated extremity. Recovery times ranged from 4 days up to 1 year (26). However, clinical symptoms of muscle damage after LA infiltration are prone to be under-reported. Pain and dysfunction after injections administered for post-surgical analgesia can easily be attributed to- or masked by postsurgical pain (33). Furthermore, a variable degree of damage to muscle (and the associated elevated serum creatine phosphokinase levels) will be caused by muscle dissection during the surgical intervention, complicating isolation of myotoxicity induced specifically by bupivacaine.

Effects of Bupivacaine on Articular Cartilage

Bupivacaine ranks amongst the most chondrotoxic LAs (44). Levobupivacaine (the S-enantiomer of bupivacaine) induces similar chondrotoxicity when compared to racemic bupivacaine, with some studies also reporting increased in vitro chondrocyte mortality after 1 h of exposure to levobupivacaine, when compared to the racemic mixture (45, 46). The cytotoxicity of LAs might be due to lipophilicity rather than stereoisomers, possibly explaining these differences (47). The in vitro chondrotoxicity has been thoroughly reviewed and is dependent on exposure time, dose and concentration, and occurs at clinically used concentrations (44, 48–50). Interestingly, osteoarthritic joints appear more susceptible to LA-induced damage compared with joints with healthy cartilage. Management of osteoarthritis-associated pain with LA injections can, therefore, lead to increased cartilage damage, potentially resulting in more pain (48). Exposure of cultured chondrocytes to LAs in in vitro studies is often limited to 1 h (48). As the elimination half-life of bupivacaine is ~2.7 h, the limited in vitro exposure time could hamper translatability of laboratory findings to the clinic (24).

The chondrotoxic effects of bupivacaine solutions and liposomal bupivacaine were studied in a porcine model. The bupivacaine solution (0.5% w/v) was injected in the stifle joint, leading to significant chondrocyte death in vivo (33% non-viable cells), when assessing full-thickness cartilage biopsies with live/dead staining 1 week after administration (51). The use of liposomal bupivacaine formulation (1.3% w/v) resulted in a higher chondrocyte viability when compared to bupivacaine HCl (6.2% non-viable cells for liposomal bupivacaine vs. 33% non-viable cells for bupivacaine HCl) and was therefore considered safer for intra-articular use. However, histological changes regarding surface integrity, fibrillation and chondrocyte viability did not show significant differences between bupivacaine solutions and liposomal bupivacaine formulation 1 week after injection in a porcine model. The synovial membrane was not assessed (51).

In another study, the long-term effects of bupivacaine during 48 h of continuous infusion were studied in a rabbit shoulder model (52). No macroscopic or radiological differences were observed between infused glenohumeral joints and controls after 3 months. Cartilage metabolism assessed with sulfate uptake increased after bupivacaine infusion, potentially indicating a regenerative response. No difference in cell density, percentage of live cells, macroscopic or radiographic changes were observed. Therefore, in the model used, articular cartilage has the potential to recover from chondrotoxic effects induced by bupivacaine. However, other animal studies conclude that chondrocyte homeostasis does not fully recover following intra-articular bupivacaine administration. Rats received a 0.5% bupivacaine injection into the stifle joint. The contralateral joint received 0.9% saline with the same volume. Cartilage was assessed histologically after 1, 4, 12 weeks, and 6 months. Bupivacaine did not lead to damage to the chondral surface, or superficial chondrocyte viability up to 12 weeks after injection. After 6 months, chondrocyte density had significantly decreased when compared with the control joint, despite cell viability remaining constant (53).

Clinically, chondrolysis following a single intra-articular LA administration has seldom been reported. This phenomenon is characterized by increasing pain and stiffness in the treated joint, with radiological signs of cartilage breakdown and reduced joint space width. A 2015 systematic review discussed reports of four clinical cases. The rate of chondrolysis when studying continuous infusion was considerably higher compared with single injections, and 97.7% (163 out of 167) of chondrolysis cases reported occurred after continuous infusion and the majority of cases occurred in the glenohumeral joint. It should be noted that in most studies adrenaline was co-administered with bupivacaine (54).

Effects of Bupivacaine on the Intervertebral Disc

Bupivacaine is a commonly used LA for both diagnosis and treatment of discogenic back pain. However, various in vitro studies have shown toxic effects of bupivacaine on intervertebral disc (IVD) cells. Bupivacaine appears to lead to both concentration- and exposure time-dependent necrosis and apoptosis of IVD cells, and decreased matrix synthesis (55–60).

As with osteoarthritic synovial joints, attempts to relieve pain from degenerative disc disease using LAs could lead to an increase of symptoms due to the cytotoxic effects of these LAs. Interestingly, these findings only partially correlate with data from in vivo and clinical studies. For instance, increased rates of apoptosis were observed seven days after bupivacaine (0.5%) injection into intervertebral discs of a rabbit model when compared to saline controls, which are in agreement with previous in vitro studies (61, 62). However, no significant differences in IVD degeneration as scored on MRI, histological scoring using safranin-O staining, or amount of viable IVD cells between saline and bupivacaine injection were observed after 6 and 12 months. The main cause of damage appeared to be insertion of the needle into the annulus fibrosus (61). When comparing bupivacaine-treated (discography or disc-block, both single injection) IVDs with control discs 5 years after treatment, no significant radiological differences were observed between groups regarding disc height, pain, disability scores or range of motion (63). Accelerated disc degeneration 10 years after discography has been reported, but this study did not specify the injection fluid used (64). Therefore, the observed degeneration following diagnostic or therapeutic disc injections appears to be induced mainly by damage caused by insertion of the needle and/or by the use of a contrast agent (61, 65). A potential explanation for the discrepancies between in vitro and in vivo or clinical observations might be cell proliferation reported in vivo after bupivacaine injection into the IVD, which is potentially associated with a regenerative response (66).

Effects of Bupivacaine on Bone Repair/Regeneration

Bone (re)generation and formation are essential processes in the recovery period following musculoskeletal interventions. Impaired bone healing can have severe clinical consequences, such as mal- or non-union of fractures or reduced osteointegration of implants. Lucchinetti et al. reported a dose-dependent reduction of mineralized matrix deposition by MSCs during LA exposure, with bupivacaine being the most inhibitory. At bupivacaine concentrations of 250 uM (=0.008%) no osteogenesis was observed in vitro (67). These findings are in contrast to studies in animal models assessing bone healing in the presence of bupivacaine. Fourteen and thirty-five days after hematoma infiltration with 0.25% bupivacaine following a closed diaphysis fracture in rat femora, no difference in callus composition, bone tensile strength, or histological appearance was observed between bupivacaine-treated and control groups (68, 69). Similar results were reported in dogs for 0.5% bupivacaine infiltration (70). Clinical studies describing effects of bupivacaine on bone healing is limited. Results of the few studies available seem to agree with findings from the animal studies mentioned. A retrospective cohort study assessing feasibility of hematoma block following femoral fracture in 35 children did not report delayed bone healing (71). The effect of liposomal bupivacaine (120 mg) on bone healing was assessed on X-ray images taken 4–6 weeks after bunionectomy. None of the 158 patients showed evidence of impaired bone healing. However, whether the surgery included any correction osteotomy was not specified. In the case of bunionectomy only, no bone fragments would have to fuse (72).

Effects of Bupivacaine on Wound Healing

Wound healing is an important regenerative process following surgery. Various drugs are known to be associated with delayed or disturbed wound healing (73). In an in vitro wound healing scratch assay, MSCs were cultured using medium supplemented with 20 ng/mL TNF-alpha and exposed to bupivacaine 100 uM (=0.00325%). Following 3 and 6 h of bupivacaine exposure, delayed migration of MSCs and delayed repopulation of the in vitro defect size compared with controls were observed (67). Population doubling time increased significantly from 40 to 93 h at these concentrations. At higher concentrations of bupivacaine, a decrease in cell count was observed. This phenomenon was accompanied by LDH release, a marker for cytotoxicity and increased membrane permeability (67).

However, in a rat model of wound healing, no differences regarding amount of collagen fibers, wound tensile strength, and inflammatory parameters were observed between the intervention and control group after 14 days, indicating that bupivacaine did not negatively affect wound healing (74). Similar studies have been performed in mice (75). After 3 days, no differences regarding wound surface, re-epithelialization, or neutrophil numbers were observed compared to controls in both the healthy and impaired healing groups. In contrast to results from the rat model, a non-significant trend toward decreased collagen accumulation in wounds following LA administration was found in mice. However, this study did not objectify wound tensile strength and used a shorter follow-up period (3 vs. 14 days) (74, 75).

Furthermore, results of clinical studies showed no significant differences in wound healing or scar formation in later phases when using liposome bupivacaine or conventional bupivacaine HCl. Overall, satisfactory wound healing in both interventional groups was reported across various surgical models (76). A randomized clinical trial reported no wound healing complications of bupivacaine infiltration compared to control group in human breast surgery (77).

Effects of Bupivacaine on Neural Tissue

The musculoskeletal system, especially the spinal column, is in close relationship with the central and peripheral nervous system. To obtain anesthesia during orthopedic interventions, administering regional or spinal blocks with bupivacaine are common in the perioperative pain management.

Bupivacaine can lead to significant neuronal cell death in vitro. In experiment using human SH-SY5Y neuroblastoma cells, a concentration-dependent decrease in cell viability after exposure to various LAs was observed in 10 min. Bupivacaine had the highest toxic potency of all LAs included in the study. Cell death was primarily due to necrosis, but bupivacaine also led to apoptosis when concentration or exposure time increased (78). These results are in agreement with other reports (79).

In vivo, the effect of intraneural injection of both plain bupivacaine solution and liposomal bupivacaine was studied at clinically used concentrations in a porcine model. No persistent neurological deficits were observed 12 h after treatment. The sciatic nerve was excised 2 weeks after injection and assessed for histological nerve injury. Immune cell count, cytokine mRNA and axonal density did not differ significantly in both groups when compared to controls (80). In rabbits, bupivacaine led to moderate neurotoxicity (regarding CSF glutamate concentrations and vacuolation of the dorsal funiculus) of the spinal cord 1 week after intrathecal administration. However, the LA concentrations used in the study were higher than those used clinically (81).

From a clinical perspective, persisting neurological damage from LAs is rare, with risks of neurological injury after peripheral nerve blocks estimated to be around 0.04% (82). The risk of lasting damage is lower in central nerve blocks (i.e., spinal and epidural applications), with estimates between 1 and 4 in 100.000 cases (83). The incidence of anesthesia-related neurologic complications varies, however, both over time and between studies (83, 84). For example, neurological deficits have been reported in 3–5% of patients 2 weeks after undergoing a brachial plexus block. After 4 weeks, 0.4% of patients still experienced deficits (85). These numbers, apart from being at risk for publication bias, might overestimate the actual damage done by LAs, as injection pressure, needle trauma and patient positioning during surgery can also account for (persisting) neurological damage (83).

Recent Developments

To both extend duration of action and minimize toxicity, alternative formulations of bupivacaine have been developed. Examples are liposomal formulations and biodegradable polymer matrices, with liposome bupivacaine being the only formulation to have reached market approval presently (10–14). A hydrogel formulations of bupivacaine, liposome bupivacaine, and a conventional bupivacaine solution have been tested in vivo in direct comparison (14). Following plantar incision, rats were administered 0.1 mL near the sciatic nerve of either liposome bupivacaine (13.3 mg/mL), hydrogel matrix containing bupivacaine HCl (105 mg/mL), or the hydrogel matrix without any bupivacaine. An irritant rank score was calculated based on histological analysis, grading the presence of inflammatory cells, fibroblasts, neovascularization, fibrosis, necrosis, hemorrhage, and tissue ingrowth into the material. Mechanical pain sensitivity threshold was tested using Von Frey ligaments. Rats treated with the bupivacaine-containing hydrogel matrix tolerated higher mechanical forces on the injured paw compared to the liposomal bupivacaine group and the empty hydrogel matrix group. However, this group also displayed the highest irritant ranking scores after 5 (moderate score) and 42 (slight score) days. The empty hydrogel matrix also displayed moderate and slight irritant rank scores at 5 and 42 days, respectively, indicating local toxic effects of the matrix itself. It is pointed out that only the cumulative score was reported, preventing evaluation of specific local effects on inflammation, vascularization, necrosis and other factors. Furthermore, not only the concentration but also the cumulative dose of bupivacaine differed between the intervention and control group, hampering their comparability. No clinical trials of the hydrogel bupivacaine formulation are available yet. Liposomal bupivacaine formulations have been tested clinically; however, the analgesic advantages compared with plain bupivacaine solutions appear limited (86). In vivo, the myotoxic effects of liposomal bupivacaine (13.3 mg/mL bupivacaine HCl) were comparable to 5 mg/mL plain bupivacaine HCl solution after 5 days, and significantly less than a 13.3 mg/mL plain bupivacaine HCl solution. However, the degree of inflammation after 2 weeks was comparable between the 13.3 mg/mL bupivacaine HCl solution and liposomal bupivacaine (41).

Conclusions and Outlook

Bupivacaine is extensively used in (surgical) treatment of musculoskeletal diseases since its discovery in 1957. In bone regeneration, muscle repair, nerve damage, wound healing, and intervertebral disc damage, the in vitro effects of bupivacaine point toward an inhibitory effect, even at concentrations lower and exposure times shorter than those used clinically. Racemic mixtures of bupivacaine enantiomers and levobupivacaine lead to similar degrees of in vitro toxicity. However, in both animal and clinical studies, these effects are rarely reproduced and, if they are, appear largely reversible. In IVD, neural and muscle applications, the local toxic effects of bupivacaine displayed reversibility, albeit delayed compared to controls. Clinically observed adverse events following local toxicity of bupivacaine have seldom been reported. The local toxic effects of bupivacaine, when used as perioperative anesthetic, may have minimal impact compared to the extensive tissue damage and systemic response elicited by the surgery itself. Bupivacaine seems to induce chondrotoxicity in vitro and up to a certain extent also in in vivo and in clinical studies. Therefore, the use of bupivacaine in synovial joints might best be avoided. Recently developed liposomal and polymer matrix formulations of bupivacaine provide a longer duration of action, but with similar degrees of local toxicity. This leaves an unmet need for a LA-formulation that increases the duration of pain blockage without increasing local toxicity. As described in this review, the in vitro toxic effects of bupivacaine are rare in in vivo studies. Interestingly, if adverse effects are observed in vivo or clinically, they appear to be reversible. A possible explanation for the discrepancies observed between in vitro and in vivo data might be the models used to study in vitro toxicity of bupivacaine. Indeed, most of the in vitro tests are performed in two-dimensional cell cultures, which are not representative of the complex architecture and systemic absorption and metabolism of the human body. Furthermore, the inflammatory, high-perfusion, regenerative phase taking place after both bupivacaine injection and surgery is overlooked in vitro. In summary, this review revealed that current literature report low levels of bupivacaine local toxicity in clinically used concentrations for the majority of musculoskeletal applications.

Author Contributions

JS and J-JV conceptualized the review. JS performed the literature search and data analysis. SP and JM drafted and critically revised the work. All authors contributed to the article and approved the submitted version.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Gerbershagen HJ, Aduckathil S, van Wijck AJM, Peelen LM, Kalkman CJ, Meissner W. Pain intensity on the first day after surgery: a prospective cohort study comparing 179 surgical procedures. Anesthesiology. (2013) 118:934–44. doi: 10.1097/ALN.0b013e31828866b3

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Joshi GP, Ogunnaike BO. Consequences of inadequate postoperative pain relief and chronic persistent postoperative pain. Anesthesiol Clin North Am. (2005) 23:21–36. doi: 10.1016/j.atc.2004.11.013

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Cicero TJ, Ellis MS, Kasper ZA. Psychoactive substance use prior to the development of iatrogenic opioid abuse: a descriptive analysis of treatment-seeking opioid abusers. Addict Behav. (2017) 65:242–4. doi: 10.1016/j.addbeh.2016.08.024

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Madras BK. The surge of opioid use, addiction, and overdoses: responsibility and response of the US health care system. JAMA Psychiatry. (2017) 74:441–2. doi: 10.1001/jamapsychiatry.2017.0163

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Substance Abuse and Mental Health Services Administration, Rockville MD. Results from the 2012 National Survey on Drug Use and Health: Summary of National Findings. (2013) Available online at: https://www.samhsa.gov/data/sites/default/files/NSDUHresults2012/NSDUHresults2012.pdf. (accessed May 19, 2021).

Google Scholar

6. Volkow ND, McLellan TA, Cotto JH, Karithanom M, Weiss SRB. Characteristics of opioid prescriptions in 2009. JAMA. (2011) 305:1299–301. doi: 10.1001/jama.2011.401

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Accord Healthcare Limited. Bupivacaine 0.5%w/v Solution for Injection. (2015). Utrecht: Accord Healthcare Limited.

8. Becker DE, Reed KL. Local anesthetics: review of pharmacological considerations. Anesth Prog. (2012) 59:90–101. doi: 10.2344/0003-3006-59.2.90

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Casati A, Putzu M. Bupivacaine, levobupivacaine and ropivacaine: are they clinically different? Best Pract Res Clin Anaesthesiol. (2005) 19:247–68. doi: 10.1016/j.bpa.2004.12.003

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Chahar P, Cummings KC. Liposomal bupivacaine: a review of a new bupivacaine formulation. J Pain Res. (2012) 5:257–64. doi: 10.2147/JPR.S27894

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Cusack SL, Reginald P, Hemsen L, Umerah E. The pharmacokinetics and safety of an intraoperative bupivacaine-collagen implant (XaraColl^®) for postoperative analgesia in women following total abdominal hysterectomy. J Pain Res. (2013) 6:151–9. doi: 10.2147/JPR.S40976

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Viscusi E, Minkowitz H, Winkle P, Ramamoorthy S, Hu J, Singla N. HTX-011 reduced pain intensity and opioid consumption versus bupivacaine HCl in herniorrhaphy: results from the phase 3 EPOCH 2 study. Hernia. (2019) 23:1071–80. doi: 10.1007/s10029-019-02023-6

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Ellis D, Verity N, Lissin D, Wendicke-Lophaven K. Treatment of postoperative pain in shoulder surgery with SABER-Bupivacaine. J Pain. (2013) 14:S84. doi: 10.1016/j.jpain.2013.01.673

CrossRef Full Text | Google Scholar

14. Hutchins J, Taylor W. An evaluation of the analgesic effect of AnestaGel on mechanical allodynia in a rat model of postoperative incisional pain. J Pain Res. (2017) 10:2807–13. doi: 10.2147/JPR.S146759

PubMed Abstract | CrossRef Full Text | Google Scholar

15. World Health Organization. WHO Model List of Essential Medicines. 20th ed. (2017). p. 1. Available online at: https://apps.who.int/iris/bitstream/handle/10665/273826/EML-20-eng.pdf?ua=1 (accessed April 26, 2019).

Google Scholar

16. Shafiei FT, Lopez J. Bupivacaine. In: StatPearls. (2020). Available online at: http://www.ncbi.nlm.nih.gov/pubmed/30422478. (accessed November 19, 2020).

Google Scholar

17. Rubin DS, Matsumoto MM, Weinberg G, Roth S. Local anesthetic systemic toxicity in total joint arthroplasty: incidence and risk factors in the United States from the National Inpatient Sample 1998-2013. Reg Anesth Pain Med. (2018) 43:131–7. doi: 10.1097/AAP.0000000000000684

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Mörwald EE, Zubizarreta N, Cozowicz C, Poeran J, Memtsoudis SG. Incidence of local anesthetic systemic toxicity in orthopedic patients receiving peripheral nerve blocks. Reg Anesth Pain Med. (2017) 42:442–5. doi: 10.1097/AAP.0000000000000544

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Møiniche S, Mikkelsen S, Wetterslev J, Dahl JB. A systematic review of intra-articular local anesthesia for postoperative pain relief after arthroscopic knee surgery. Reg Anesth Pain Med. (1999) 24:430–7. doi: 10.1016/S1098-7339(99)90010-X

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Andersen L Ø, Kehlet H. Analgesic efficacy of local infiltration analgesia in hip and knee arthroplasty: a systematic review. Br J Anaesth. (2014) 113:360–74. doi: 10.1093/bja/aeu155

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Cardone DA, Tallia AF. Diagnostic and therapeutic injection of the hip and knee. Am Fam Physician. (2003) 67:2147–52.

PubMed Abstract | Google Scholar

22. Pfizer. Bupivacaine HCl injection, USP [Internet]. (2015). p. 1–14. Available online at: http://labeling.pfizer.com/ShowLabeling.aspx?id=4377 (accessed April 30, 2019).

23. National Institute of Health. Bupivacaine HCl Archived Drug Label - NIH [Internet]. (2006). Available online at: https://dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=1828 (accessed April 30, 2019).

24. bupivacaine hydrochloride (Bupivacaine Hydrochloride) injection, solution [Internet]. (2017). Available online at: https://dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=1828 (accessed December 20, 2017).

25. Williams DJ, Walker JD. A nomogram for calculating the maximum dose of local anaesthetic. Anaesthesia. (2014) 69:847–53. doi: 10.1111/anae.12679

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Hussain N, McCartney CJL, Neal JM, Chippor J, Banfield L, Abdallah FW. Local anaesthetic-induced myotoxicity in regional anaesthesia: a systematic review and empirical analysis. Br J Anaesth. (2018) 121:822–41. doi: 10.1016/j.bja.2018.05.076

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Zink W, Graf BM. Local anesthetic myotoxicity. Reg Anesth Pain Med. (2004) 29:333–40. doi: 10.1097/00115550-200407000-00007

CrossRef Full Text | Google Scholar

28. Hall-Craggs EC. Early ultrastructural changes in skeletal muscle exposed to the local anaesthetic bupivacaine (Marcaine). Br J Exp Pathol. (1980) 61:139–49.

PubMed Abstract | Google Scholar

29. Nonaka I, Takagi A, Ishiura S, Nakase H, Sugita H. Pathophysiology of muscle fiber necrosis induced by bupivacaine hydrochloride (Marcaine). Acta Neuropathol. (1983) 60:167–74. doi: 10.1007/BF00691863

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Horiguchi T, Shibata M-A, Ito Y, Eid NAS, Abe M, Otsuki Y. Macrophage apoptosis in rat skeletal muscle treated with bupivacaine hydrochloride: possible role of MCP-1. Muscle Nerve. (2002) 26:79–86. doi: 10.1002/mus.10162

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Zink W, Graf BM, Sinner B, Martin E, Fink RHA, Kunst G. Differential effects of bupivacaine on intracellular Ca2+ regulation: potential mechanisms of its myotoxicity. Anesthesiology. (2002) 97:710–6. doi: 10.1097/00000542-200209000-00026

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Zink W, Missler G, Sinner B, Martin E, Fink RHA, Graf BM. Differential effects of bupivacaine and ropivacaine enantiomers on intracellular Ca2+ regulation in murine skeletal muscle fibers. Anesthesiology. (2005) 102:793–8. doi: 10.1097/00000542-200504000-00015

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Hogan Q, Dotson R, Erickson S, Kettler R, Hogan K. Local anesthetic myotoxicity: a case and review. Anesthesiology. (1994) 80:942–7. doi: 10.1097/00000542-199404000-00029

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Öz Gergin Ö, Yildiz K, Bayram A, Sencar L, Coşkun G, Yay A, et al. Comparison of the myotoxic effects of levobupivacaine, bupivacaine, and ropivacaine: an electron microscopic study. Ultrastruct Pathol. (2015) 39:169–76. doi: 10.3109/01913123.2015.1014610

PubMed Abstract | CrossRef Full Text

35. Zink W, Seif C, Bohl JRE, Hacke N, Braun PM, Sinner B, et al. The acute myotoxic effects of bupivacaine and ropivacaine after continuous peripheral nerve blockades. Anesth Analg. (2003) 97:1173–9, table of contents. doi: 10.1213/01.ANE.0000080610.14265.C8

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Irwin W, Fontaine E, Agnolucci L, Penzo D, Betto R, Bortolotto S, et al. Bupivacaine myotoxicity is mediated by mitochondria. J Biol Chem. (2002) 277:12221–7. doi: 10.1074/jbc.M108938200

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Hofmann P, Metterlein T, Bollwein G, Gruber M, Plank C, Graf BM, et al. The myotoxic effect of bupivacaine and ropivacaine on myotubes in primary mouse cell culture and an immortalized cell line. Anesth Analg. (2013) 117:634–40. doi: 10.1213/ANE.0b013e31829e4197

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Yildiz K, Efesoy SN, Ozdamar S, Yay A, Bicer C, Aksu R, et al. Myotoxic effects of levobupivacaine, bupivacaine and ropivacaine in a rat model. Clin Invest Med. (2011) 34:E273. doi: 10.25011/cim.v34i5.15670

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Plant DR, Colarossi FE, Lynch GS. Notexin causes greater myotoxic damage and slower functional repair in mouse skeletal muscles than bupivacaine. Muscle Nerve. (2006) 34:577–85. doi: 10.1002/mus.20616

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Zhao P, Hoffman EP. Musculin isoforms and repression of MyoD in muscle regeneration. Biochem Biophys Res Commun. (2006) 342:835–42. doi: 10.1016/j.bbrc.2006.01.188

PubMed Abstract | CrossRef Full Text | Google Scholar

41. McAlvin JB, Padera RF, Shankarappa SA, Reznor G, Kwon AH, Chiang HH, et al. Multivesicular liposomal bupivacaine at the sciatic nerve. Biomaterials. (2014) 35:4557–64. doi: 10.1016/j.biomaterials.2014.02.015

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Jehan FS, Hagan JC, Whittaker TJ, Subramanian M. Diplopia and ptosis following injection of local anesthesia without hyaluronidase. J Cataract Refract Surg. (2001) 27:1876–9. doi: 10.1016/S0886-3350(01)01099-9

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Rhee S-M, Chung NY, Jeong HJ, Oh JH. Subacromial local anesthetics do not interfere with rotator cuff healing after arthroscopic repair. Am J Sports Med. (2018) 46:1097–105. doi: 10.1177/0363546517753827

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Jayaram P, Kennedy DJ, Yeh P, Dragoo J. Chondrotoxic effects of local anesthetics on human knee articular cartilage: a systematic review. PM R. (2018) 11:379–400. doi: 10.1002/pmrj.12007

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Gungor I, Yilmaz A, Ozturk AM, Ergun MA, Menevse S, Kaya K. Bupivacaine and levobupivacaine induce apoptosis in rat chondrocyte cell cultures at ultra-low doses. Eur J Orthop Surg Traumatol. (2014) 24:291–5. doi: 10.1007/s00590-013-1202-5

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Cobo-Molinos J, Poncela-Garcia M, Marchal-Corrales JA, Delgado-Martinez AD. Effect of levobupivacaine on articular chondrocytes: an in-vitro investigation. Eur J Anaesthesiol. (2014) 31:635–9. doi: 10.1097/EJA.0000000000000115

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Werdehausen R, Braun S, Fazeli S, Hermanns H, Hollmann MW, Bauer I, et al. Lipophilicity but not stereospecificity is a major determinant of local anaesthetic-induced cytotoxicity in human T-lymphoma cells. Eur J Anaesthesiol. (2012) 29:35–41. doi: 10.1097/EJA.0b013e32834cd6c4

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Kreuz PC, Steinwachs M, Angele P. Single-dose local anesthetics exhibit a type-, dose-, and time-dependent chondrotoxic effect on chondrocytes and cartilage: a systematic review of the current literature. Knee Surg Sports Traumatol Arthrosc. (2018) 26:819–30. doi: 10.1007/s00167-017-4470-5

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Piper SL, Kramer JD, Kim HT, Feeley BT. Effects of local anesthetics on articular cartilage. Am J Sports Med. (2011) 39:2245–53. doi: 10.1177/0363546511402780

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Baker JF, Mulhall KJ. Local anaesthetics and chondrotoxicty: what is the evidence? Knee Surg Sports Traumatol Arthrosc. (2012) 20:2294–301. doi: 10.1007/s00167-011-1804-6

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Shaw KA, Moreland C, Jacobs J, Hire JM, Topolski R, Hoyt N, et al. Improved chondrotoxic profile of liposomal bupivacaine compared with standard bupivacaine after intra-articular infiltration in a porcine model. Am J Sports Med. (2018) 46:66–71. doi: 10.1177/0363546517732558

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Gomoll AH, Yanke AB, Kang RW, Chubinskaya S, Williams JM, Bach BR, et al. Long-term effects of bupivacaine on cartilage in a rabbit shoulder model. Am J Sports Med. (2009) 37:72–7. doi: 10.1177/0363546508323748

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Chu CR, Coyle CH, Chu CT, Szczodry M, Seshadri V, Karpie JC, et al. In vivo effects of single intra-articular injection of 0.5% bupivacaine on articular cartilage. J Bone Joint Surg Am. (2010) 92:599–608. doi: 10.2106/JBJS.I.00425

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Gulihar A, Robati S, Twaij H, Salih A, Taylor GJS. Articular cartilage and local anaesthetic: a systematic review of the current literature. J Orthop. (2015) 12(Suppl. 2):S200–10. doi: 10.1016/j.jor.2015.10.005

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Lee H, Sowa G, Vo N, Vadala G, O'Connell S, Studer R, et al. Effect of bupivacaine on intervertebral disc cell viability. Spine J. (2010) 10:159–66. doi: 10.1016/j.spinee.2009.08.445

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Quero L, Klawitter M, Nerlich AG, Leonardi M, Boos N, Wuertz K. Bupivacaine–the deadly friend of intervertebral disc cells? Spine J. (2011) 11:46–53. doi: 10.1016/j.spinee.2010.11.001

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Wang D, Vo N V, Sowa GA, Hartman RA, Ngo K, Choe SR, et al. Bupivacaine decreases cell viability and matrix protein synthesis in an intervertebral disc organ model system. Spine J. (2011) 11:139–46. doi: 10.1016/j.spinee.2010.11.017

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Cai X-Y, Xiong L-M, Yang S-H, Shao Z-W, Xie M, Gao F, et al. Comparison of toxicity effects of ropivacaine, bupivacaine, and lidocaine on rabbit intervertebral disc cells in vitro. Spine J. (2014) 14:483–90. doi: 10.1016/j.spinee.2013.06.041

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Chee A V, Ren J, Lenart BA, Chen E-Y, Zhang Y, An HS. Cytotoxicity of local anesthetics and non-ionic contrast agents on bovine intervertebral disc cells cultured in a three-dimensional culture system. Spine J. (2014) 14:491–8. doi: 10.1016/j.spinee.2013.06.095

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Cai X-Y, Xia Y, Yang S-H, Liu X-Z, Shao Z-W, Liu Y-L, et al. Ropivacaine- and bupivacaine-induced death of rabbit annulus fibrosus cells in vitro: involvement of the mitochondrial apoptotic pathway. Osteoarthr Cartil. (2015) 23:1763–75. doi: 10.1016/j.joca.2015.05.013

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Iwasaki K, Sudo H, Yamada K, Higashi H, Ohnishi T, Tsujimoto T, et al. Effects of single injection of local anesthetic agents on intervertebral disc degeneration: ex vivo and long-term in vivo experimental study. PLoS ONE. (2014) 9:e109851. doi: 10.1371/journal.pone.0109851

PubMed Abstract | CrossRef Full Text | Google Scholar

62. Iwasaki K, Sudo H, Yamada K, Ito M, Iwasaki N. Cytotoxic effects of the radiocontrast agent iotrolan and anesthetic agents bupivacaine and lidocaine in three-dimensional cultures of human intervertebral disc nucleus pulposus cells: identification of the apoptotic pathways. PLoS ONE. (2014) 9:e92442. doi: 10.1371/journal.pone.0092442

PubMed Abstract | CrossRef Full Text | Google Scholar

63. Ohtori S, Inoue G, Orita S, Eguchi Y, Ochiai N, Kishida S, et al. No acceleration of intervertebral disc degeneration after a single injection of bupivacaine in young age group with follow-up of 5 years. Asian Spine J. (2013) 7:212–7. doi: 10.4184/asj.2013.7.3.212

PubMed Abstract | CrossRef Full Text | Google Scholar

64. Carragee EJ, Don AS, Hurwitz EL, Cuellar JM, Carrino JA, Carrino J, et al. 2009 ISSLS prize winner: does discography cause accelerated progression of degeneration changes in the lumbar disc: a ten-year matched cohort study. Spine. (2009) 34:2338–45. doi: 10.1097/BRS.0b013e3181ab5432

PubMed Abstract | CrossRef Full Text | Google Scholar

65. Gruber HE, Rhyne AL, Hansen KJ, Phillips RC, Hoelscher GL, Ingram JA, et al. Deleterious effects of discography radiocontrast solution on human annulus cell in vitro: changes in cell viability, proliferation, and apoptosis in exposed cells. Spine J. (2012) 12:329–35. doi: 10.1016/j.spinee.2012.02.003

PubMed Abstract | CrossRef Full Text | Google Scholar

66. Strube P, Pfitzner BM, Streitparth F, Hartwig T, Putzier M. In vivo effects of bupivacaine and gadobutrol on the intervertebral disc following discoblock and discography: a histological analysis. Eur Radiol. (2017) 27:149–56. doi: 10.1007/s00330-016-4358-7

PubMed Abstract | CrossRef Full Text | Google Scholar

67. Lucchinetti E, Awad AE, Rahman M, Feng J, Lou PH, Zhang L, et al. Antiproliferative effects of local anesthetics on mesenchymal stem cells: potential implications for tumor spreading and wound healing. Anesthesiology. (2012) 116:841–56. doi: 10.1097/ALN.0b013e31824babfe

PubMed Abstract | CrossRef Full Text | Google Scholar

68. Henry BJ, Kenison M, McVay C, Rolfe R, Graham S, Rasty J, et al. The effect of local hematoma blocks on early fracture healing. Orthopedics. (2002) 25:1259–62. doi: 10.3928/0147-7447-20021101-17

PubMed Abstract | CrossRef Full Text | Google Scholar

69. Huss MK, Felt SA, Pacharinsak C. Influence of pain and analgesia on orthopedic and wound-healing models in rats and mice. Comp Med. (2019) 69:535–45. doi: 10.30802/AALAS-CM-19-000013

PubMed Abstract | CrossRef Full Text | Google Scholar

70. Dimopoulou I, Anagnostou TL, Prassinos NN, Savvas I, Patsikas M. Effect of intrafragmentary bupivacaine (haematoma block) on analgesic requirements in dogs undergoing fracture repair. Vet Anaesth Analg. (2017) 44:1189–97. doi: 10.1016/j.vaa.2017.01.005

PubMed Abstract | CrossRef Full Text | Google Scholar

71. Herrera JA, Wall EJ, Foad SL. Hematoma block reduces narcotic pain medication after femoral elastic nailing in children. J Pediatr Orthop. (2004) 24:254–6. doi: 10.1097/00004694-200405000-00003

PubMed Abstract | CrossRef Full Text | Google Scholar

72. Golf M, Daniels SE, Onel E. A phase 3, randomized, placebo-controlled trial of DepoFoam® bupivacaine (extended-release bupivacaine local analgesic) in bunionectomy. Adv Ther. (2011) 28:776–88. doi: 10.1007/s12325-011-0052-y

PubMed Abstract | CrossRef Full Text | Google Scholar

73. Guo S, Dipietro LA. Factors affecting wound healing. J Dent Res. (2010) 89:219–29. doi: 10.1177/0022034509359125

PubMed Abstract | CrossRef Full Text | Google Scholar

74. Abrão J, Fernandes CR, White PF, Shimano AC, Okubo R, Lima GB, et al. Effect of local anaesthetic infiltration with bupivacaine and ropivacaine on wound healing: a placebo-controlled study. Int Wound J. (2014) 11:379–85. doi: 10.1111/j.1742-481X.2012.01101.x

PubMed Abstract | CrossRef Full Text | Google Scholar

75. Waite A, Gilliver SC, Masterson GR, Hardman MJ, Ashcroft GS. Clinically relevant doses of lidocaine and bupivacaine do not impair cutaneous wound healing in mice. Br J Anaesth. (2010) 104:768–73. doi: 10.1093/bja/aeq093

PubMed Abstract | CrossRef Full Text | Google Scholar

76. Baxter R, Bramlett K, Onel E, Daniels S. Impact of local administration of liposome bupivacaine for postsurgical analgesia on wound healing: a review of data from ten prospective, controlled clinical studies. Clin Ther. (2013) 35:312–20.e5. doi: 10.1016/j.clinthera.2013.02.005

PubMed Abstract | CrossRef Full Text | Google Scholar

77. Campbell I, Cavanagh S, Creighton J, French R, Banerjee S, Kerr E, et al. To infiltrate or not? Acute effects of local anaesthetic in breast surgery. ANZ J Surg. (2015) 85:353–7. doi: 10.1111/ans.12541

PubMed Abstract | CrossRef Full Text | Google Scholar

78. Perez-Castro R, Patel S, Garavito-Aguilar Z V, Rosenberg A, Recio-Pinto E, Zhang J, et al. Cytotoxicity of local anesthetics in human neuronal cells. Anesth Analg. (2009) 108:997–1007. doi: 10.1213/ane.0b013e31819385e1

PubMed Abstract | CrossRef Full Text | Google Scholar

79. Malet A, Faure M-O, Deletage N, Pereira B, Haas J, Lambert G. The comparative cytotoxic effects of different local anesthetics on a human neuroblastoma cell line. Anesth Analg. (2015) 120:589–96. doi: 10.1213/ANE.0000000000000562

PubMed Abstract | CrossRef Full Text | Google Scholar

80. Damjanovska M, Cvetko E, Kuroda MM, Seliskar A, Plavec T, Mis K, et al. Neurotoxicity of intraneural injection of bupivacaine liposome injectable suspension versus bupivacaine hydrochloride in a porcine model. Vet Anaesth Analg. (2019) 46:236–45. doi: 10.1016/j.vaa.2018.09.044

PubMed Abstract | CrossRef Full Text | Google Scholar

81. Yamashita A, Matsumoto M, Matsumoto S, Itoh M, Kawai K, Sakabe T. A comparison of the neurotoxic effects on the spinal cord of tetracaine, lidocaine, bupivacaine, and ropivacaine administered intrathecally in rabbits. Anesth Analg. (2003) 97:512–9. doi: 10.1213/01.ANE.0000068885.78816.5B

PubMed Abstract | CrossRef Full Text | Google Scholar

82. Barrington MJ, Watts SA, Gledhill SR, Thomas RD, Said SA, Snyder GL, et al. Preliminary results of the Australasian Regional Anaesthesia Collaboration: a prospective audit of more than 7000 peripheral nerve and plexus blocks for neurologic and other complications. Reg Anesth Pain Med. (2009) 34:534–41. doi: 10.1097/AAP.0b013e3181ae72e8

PubMed Abstract | CrossRef Full Text | Google Scholar

83. Brull R, McCartney CJL, Chan VWS, El-Beheiry H. Neurological complications after regional anesthesia: contemporary estimates of risk. Anesth Analg. (2007) 104:965–74. doi: 10.1213/01.ane.0000258740.17193.ec

PubMed Abstract | CrossRef Full Text | Google Scholar

84. Verlinde M, Hollmann MW, Stevens MF, Hermanns H, Werdehausen R, Lirk P. Local anesthetic-induced neurotoxicity. Int J Mol Sci. (2016) 17:339. doi: 10.3390/ijms17030339

PubMed Abstract | CrossRef Full Text | Google Scholar

85. Urban MK, Urquhart B. Evaluation of brachial plexus anesthesia for upper extremity surgery. Reg Anesth. (1994) 19:175–82.

PubMed Abstract | Google Scholar

86. Kendall MC, Castro Alves LJ, De Oliveira G. Liposome bupivacaine compared to plain local anesthetics to reduce postsurgical pain: an updated meta-analysis of randomized controlled trials. Pain Res Treat. (2018) 2018:5710169. doi: 10.1155/2018/5710169

PubMed Abstract | CrossRef Full Text | Google Scholar