Anterior Cruciate Ligament (ACL) injuries are common with nearly 400,000 reconstructions occurring yearly in the United States. They are more common in females and generally occur following non-contact pivoting injury.
The literature on postoperative pain management after ACL reconstruction has evolved greatly and has resulted in the development of several multimodal pain management strategies to reduce pain scores and also improve functional outcomes. Intraoperative peripheral nerve blocks (PNB) serve as the backbone of these strategies in ACL surgeries.1 Wound injections with local anesthetics are also commonly performed. There has also been significant conversation around intraarticular injections, with liposomal bupivacaine showing some recent promising results considering its long-activating and slowly dissolving form.
Several studies have pointed to opioid overuse in orthopedic surgery and specifically in ACL reconstructions. However, preoperative measures that can reduce opioid dependence in the post-operative period have been well demonstrated.2 It has been demonstrated that decreasing the strength of opioids given after surgery does not increase pain scores or subsequent opioid consumption.3 Thus, further study is needed in determining what, if any, role opioids play in the ideal multimodal pain management strategy after ACL reconstruction surgery.
Liposomal Bupivacaine serves as a promising adjunct to existing multimodal pain management therapies that can reduce dependency on opioids. The purpose of the present investigation, therefore, is to summarize the current state of opioid use after ACLR and to highlight the potential of LB to reduce postoperative opioid use in ACLR.
2. MATERIALS AND METHODS
This was an IRB-exempt scoping review. The scoping review checklist available at the Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews Checklist (RPSIMA-ScR) was followed strictly. The international prospective register of systematic reviews (PROSPERO) was contacted regarding our intention for this article and advised that scoping views do not require registration with PROSPERO.
2.2. Search Strategy
The literature search was performed using Medical Search Headings (MeSH) in Mendeley version 1.19.8. Articles published between January 1975 to December 2021 were Search fields were varied until no new articles were collected at which point the search was considered exhaustive.
2.3. Study Screening
All articles were screened by title and abstract. An initial decision to include a given article was made based on the relevance of the information within the abstract as determined by our inclusion/exclusion criteria (Table 1). This constructed a list of preliminarily included articles. These preliminarily included articles underwent classification as ‘Tier 1’, ‘Tier 2’, or ‘Tier 3’ articles. Tier 1 articles were defined as primary studies of level I clinical evidence that directly compared the use of liposomal bupivacaine in ACLR to a reasonable control with adherence to the remaining inclusion/exclusion criteria. Tier 2 articles were relevant articles that summarized the current state of pain control ACLR, the opioid epidemic ACLR, or the current standard of care regarding regional anesthesia in ACLR. Tier 3 articles were those that included relevant search terms but did not meet the above two criteria.
2.4. Study Selection
Articles from Tier 1 and Tier 2 then underwent a full-text screening process. This resulted in the elimination of many articles until 5 articles in Tier 1 and 18 articles in Tier 2. The results of the articles from Tier 2 are described qualitatively in Sections 3.1-3.4 and Section 3.6. The results of the Tier 1 articles are discussed in Section 3.5. Any question regarding the inclusion of an article was discussed by all authors until an agreement was reached. The bibliographies of these articles were also hand-searched to identify any missing articles.
3.1. Pathophysiology of Post-Surgical Pain in ACL Reconstructions
It is normal for patients to experience moderate pain after an ACLR. The current standard of care regarding postoperative pain control has evolved to include multimodal pain strategies that maximize pain control without affecting quadriceps function and rehabilitation.4 In this section, the pathophysiology of post-surgical pain in ACLR is described. This section provides the necessary basic science to understand the integration of liposomal bupivacaine into current multimodal pain strategies for ACLRs.
There is extensive innervation variation among patients with regard to the neurovascular anatomy of the knee joint. In general, the infrapatellar branch of the saphenous nerve originates at the knee joint and provides sensory innervation to the skin surrounding the patella and medial to the knee. Branching of the femoral nerve distal to the vastus medialis exits the adductor canal and supplies the knee with both motor and sensory innervation. Together, these nerves form a plexus that gives rise to the anterior and posterior genicular nerves.4
The types of nerves within the knee joint have been studied extensively and research in animal models has shown that up to eighty percent of afferent fibers in the knee are nociceptive.4 These free nerve endings mediate pain via many mechanisms such as neuropeptides activating sensory receptors on the nerve fibers, ion channel activation, and mechanoreceptor activation.4
Neuropeptides are released and elevated during injury and inflammation, and cause nociceptor sensitization which is perceived as a painful stimulus. Prominent neuropeptide and pain mediators released during ACLR are prostaglandins, glycosamines, chondroitin sulfate, immunocytes, substance P, vasoactive intestinal peptide, and calcitonin gene-related peptide.4
Ion channels, such as voltage-gated sodium channels, can also mediate pain as they can exist on nociceptors. Activation of ion channels via chronic inflammation gene upregulation or shear stress can lead to increased pain propagation.4 Mechanoreceptors can also play a role in pain sensation. Many myelinated mechanoreceptors located on the ACL are activated during both injury and surgery via postural changes, deformations of the ligament, and tension.4 The degree of initial joint inflammation is also implicated in long-term outcomes regarding pain with ACLR.5 Injury leads to local blood vessel dilation with increased vascular endothelial permeability to plasma proteins. This leads to an increased fluid flow to the interstitium, causing increased articular pressure that can affect the afferent nerve fibers mediating pain.4 The nerve anatomy and pathophysiology of post-surgical pain in ACLR are important when discussing the appropriate analgesic care.
3.2. The Opioid Epidemic
3.2.1. Opioid Epidemic in Orthopedic Surgery
In the 1990s, pain became classified as the “fifth patient vital sign,” and the reduction of pain became a staple of inpatient care. This resulted in a significant rise in the prescription of opioids.6 Due to the concern for litigation for undertreatment of pain and the expansion of the indications for the use of opioids to non-cancer-related pain, physicians across all specialties began prescribing opioids by more than 200%. Currently, the pharmaceutical industry in the United States has far outpaced many other nations in opioid prescription. This has had disastrous consequences on both the economy6 and drug addiction7 in the nation.
A 2006 study conducted by the National Survey on Drug Use and Health found that of those abusing opioids more than 90% came from a legitimate physician’s prescription. However, opioid overprescription is not isolated to any one subspecialty. Orthopedic surgeons prescribe nearly 7.7% of all opioid prescriptions,8 which is arguable a disproportionately small fraction considering the intimate relationship of pain management with the field. Part of the issue stems from the fact that only a minority of patients are counseled regarding the safe disposal of unused opioid medications.8 Patient education programs have been associated with lower rates of opioid use at 6 weeks post-operatively, and prescriber education is a useful tool for persuading physicians to prescribe dosages that are more in line with patients’ needs.8
3.2.2. Opioid Epidemic in ACL Surgery
ACL reconstruction is an example of a common operation with great potential to reduce the number of opioid prescriptions in orthopedic surgery. An estimated 48% of the opioid pills that are prescribed to ACL reconstruction patients are utilized for pain directly related to the procedure. It is reasonable to conclude that more than half of the prescribed could be reduced.9 It has also been shown that the strength of oxycodone (from 7.5 mg to 5.0 mg Percocet) did not increase pain scores or opioid consumption in patients undergoing ACLR.3 Two other studies that utilized a multimodal analgesia approach after ACL reconstruction found that they have the potential to reduce opioid prescriptions.2,10
An interesting case study around this conversation is that of the Ohio government. In August 2017, the government of Ohio imposed a limitation that reduced opioid prescription following ACL reconstruction surgery by more than 34%. A retrospective cohort study, comparing a group of patients undergoing ACLR before and after the limitations, demonstrated that there was no significant difference in pain-related complications, opioid demand, office calls, emergency department visits, unplanned readmissions, or subsequent surgery between the two groups.7 Thus, there may have been significant overprescribing of narcotic pain medication before the 2017 limitations. This study reasonably advocates that there is room for growth regarding cutting back on opioids in the postoperative period for ACLRs. These numbers are important for orthopedic surgeons and anesthesiologists alike to consider as we develop further multimodal pain strategies for ligament reconstruction surgeries.
3.3. Risk Factors for Post-Operative Opioid Overuse in ACL Reconstruction Surgeries
Several risk factors have been highlighted regarding increased postoperative opioid usage after ACLR (Figure 1) including preoperative opioid use, increasing age, American Society of Anesthesiology (ASA) score of 3 or more, other activity at the time of injury, repaired meniscal injury, cartilage repair, chronic pulmonary disease, and substance abuse.11 A 2017 cohort study found that up to 35% of patients undergoing ACLR are filling opioid pain prescriptions pre-operatively. The same study also found that preoperative opioid use was a strong predictor of postoperative opioid demand.12 Preoperative opioid use for more than one month also leads to a longer hospital stay and lower patient-reported outcomes.12 Anthony et al. found that individuals filling preoperative opioid prescriptions were 7.54 and 6.42 times more likely to be filling ACLR postoperative opioid prescriptions at 9 and 12 months, respectively.12 Patients under the age of 25 and older than the age of 50 have also been shown to be at an increased risk of filling opioid prescriptions postoperatively.12,13 Studies have shown women to be more likely than men to fill prescriptions, and that race is an unimportant factor in predicting future opioid use.
3.4. Current Standard of Care for Pain Control in ACL Surgeries
3.4.1. Peripheral Nerve Blocks
Though the femoral nerve block (FNB) was priorly popular in ACLR, the effects that femoral nerve blocks have on ACL considering denervation of the quadriceps muscle have become well known to the orthopedic community. Thus, there has been a dramatic shift towards the ACB in recent years. Multiple studies suggest that between the ACB and the FNB, there is no statistically significant difference in post-operative pain.14,15 Further patients receiving an ACB have a significantly shorter time to straight leg raise and a reported greater satisfaction with pain control.
Though the saphenous nerve (adductor canal) nerve block is the most utilized, considering the recent literature does shed light on other nerve block options. These are discussed below.
A recent systematic review highlights the efficacy of the femoral-sciatic nerve block.16 They found multiple studies that demonstrated that a femoral nerve block significantly decreases postoperative VAS scores as compared to a saline injection, and the addition of a sciatic nerve block to an FNB (femoral nerve block) lowered both NRS scores and analgesic consumption.16 Though the sciatic nerve block is not widely prevalent in ACLR, it does represent a potential addition to the realm of multimodal pain control in ACLRs.17
The obturator nerve has also been described as an alternative. It has been shown that the FOS (femoral-obturator-sciatic) block has a higher success rate than the PLPS (posterior lumbar plexus-sciatic) block, less postoperative pain scores, and decreased opioid consumption in patients undergoing ACLR.18
A study evaluating the pain management of pediatric (ages 12-17) ACL reconstruction patients compared the FNB, combined femoral + sciatic block, and IA injection of bupivacaine. Patients in the combined femoral and sciatic block group had significantly better pain scores than the other two groups, significantly fewer opioid prescriptions filled and significantly fewer morphine equivalents among those who did receive opioids.19 This study not only highlights that postoperative pain control in the pediatric patient may be significantly different and require unique multimodal pain strategies, but also that standard bupivacaine may have its limitations.
3.4.2. Local anesthesia
A recent randomized control trial demonstrates the potential that local anesthesia alone can have in post-operative pain control and opioid use. Kurosaka et al. 2018 demonstrated that a group receiving a periarticular 44 mL solution of 7.5 mg/mL ropivacaine, 10 mg/mL of morphine hydrochloride hydrate, 40 mg of methylprednisolone, 20 mg/mL of ketoprofen, and 1 mg/mL of epinephrine to a group receiving an FNB. They demonstrated that the periarticular injection group demonstrated significantly lower VAS scores and opioid consumption with no difference in the complication rate as compared to the FNB group. Though it may be overzealous to interpret these results as evidence to abandon nerve blocks altogether, they certainly highlight the potential that local, periarticular analgesia has in ACLR.
Intraarticular injections of anesthetic certainly make the orthopedic community nervous considering the well-known chondrotoxic effects of local anesthetics within the joint. However, the recent systematic review does find several studies that utilize limited, low-concentration bupivacaine intraarticularly. Many studies in their review do clearly specify low-concentration and low-volume use and Secrist et al. did find that continuous infusion catheters do indeed cause chondrotoxicity.
Morphine and bupivacaine have been shown to significantly decrease VAS scores and analgesic consumption as compared to isolated bupivacaine, morphine, or saline (saline was also inferior to both bupivacaine alone and morphine alone). Intraarticular morphine injection has been shown to be superior to intraarticular methadone injection (significantly decreased VAS scores and analgesic consumption) but inferior to tenoxicam injection (more patients requiring pethidine in the morphine group). Regarding means of administering analgesic: preoperative and postoperative bupivacaine infiltrations and IA injection were demonstrated to be superior to IA bupivacaine injection; and periarticular or periarticular/IA injection of a “cocktail of drugs” (ropivacaine, morphine, ketorolac, and cefuroxime) proved to be superior to IA injection of the same drugs (significantly decreased VAS scores in the first 24 hours).16 The studies studying the role of liposomal bupivacaine in ACLRs have not been summarized to date and this is done so in Section 3.5.
3.5. Use of Liposomal Bupivacaine in ACL Surgeries
Liposomal bupivacaine (LB) has demonstrated great potential in the recent literature in reducing post-operative pain scores in orthopedic surgery and sports medicine. Our literature search revealed four articles articles of level I clinical evidence that studied the role of liposomal bupivacaine in decreasing postoperative opioid use in ACLR (see Table 2). Liposomal bupivacaine combines bupivacaine with a multivesicular-based lipid delivery platform, specifically designed to provide a slow release of the anesthetic agent.20 As a long-acting non-opioid analgesic, it has many properties that make it ideal in arthroscopic surgery. Periarticular injection of liposomal bupivacaine following ACL reconstruction remains an exciting area of research: one randomized control trial demonstrated that though patients had increased pain in the acute postoperative period when treated with liposomal bupivacaine after this period was over, the same patients had adequate pain control, better sleep quality, and fewer numbers of calls to the physician related to rebound pain when compared to FNB.20 Another randomized control trial found that a group treated with liposomal bupivacaine reported diffusely better pain management and lower opioid consumption.21 A final randomized control trial showed that the number of opioid pills prescribed postoperatively was significantly lower in a group receiving liposomal bupivacaine as a local analgesic than in the control group.22
3.6. Other Measures
In addition to a nerve block, non-opioid adjuvant medication preoperatively shows some promise for potential integration into multimodal pain strategies. Though pre-operative gabapentin has demonstrated decreased pain scores and opioid use post-operatively following ACLRs,23 there is mixed evidence regarding its use with concurrent nerve blocks.24 However, a recent systematic review of randomized controlled trials did find that oral gabapentin did reduce opioid consumption. Postoperative zolpidem was also found to decrease opioid consumption.16
Pregabalin, a γ-aminobutyric acid analog, is another analgesic that has been considered an addition to post-operative pain analgesia. Though pregabalin has been proven efficacious for pain management in various types of surgeries, its role in ACL reconstruction has only recently been studied. One randomized control study determined that in patients undergoing ACL reconstruction, perioperative pregabalin administration was shown to greatly reduce postoperative pain without additional use of postoperative opioids and IV-PCA.25 Another study compared the use of pregabalin to an adductor nerve block, finding that preoperative pregabalin reduced postoperative opioid consumption to the same degree as the adductor nerve block.26 A final study determined that prolonged administration of pregabalin 7 days before and after ACL reconstruction decreased the need for supplemental analgesics.27 Thus, pregabalin may also represent a potential addition to future multimodal pain strategies in ACLRs.
Opioids may be overprescribed after ACLR in the United States. It is unclear whether or not opioid use significantly lowers pain scores or improves function after ACLR. The role of opioid medications in ACLR should continue to decrease over time. The existing clinical evidence in favor of liposomal bupivacaine is strong; however, significant barriers exist particularly the high cost. Liposomal bupivacaine is a powerful tool that can reduce post-operative opioid consumption in ACLR. As more evidence emerges for the use of periarticular liposomal bupivacaine, multimodal pain strategies that utilize its use liposomal bupivacaine may emerge carving the way for decreased opioid prescription after ACLR. However, further work including further comparisons to similar periarticular concoctions and efforts to decrease the costs of liposomal bupivacaine are required.
Study concept and design: N. V.; I. U.; O.V.; Acquisition of data: N. V.; I. U.; O.V.; Analysis and Interpretation of data: N. V.; O.N.; M.N.; H.T.; I.U.; O.V.; Drafting of the Manuscript N. V.; O.N.; M.N.; H.T.; I.U.; O.V.; critical revision of the manuscript for important intellectual content: N. V.; O.N.; M.N.; H.T.; I.U.; O.V.; A.K.; Statistical Analysis: none; Administrative, technical, and material support N. V.; I. U.; A.K.; O.V.; Study supervision: N. V.; I. U.; A.K.; O.V.;
We have no disclosures or potential conflicts of interest.
We did not receive any funding for the production of this manuscript.