Authors: Brian M. Ilfeld, M.D., M.S. et al
Anesthesiology 10 2018, Vol.129, 623-626.
“…use of liposomal bupivacaine was not associated with a change in billing patterns for opioids…[or] decreased use of naloxone or incidence of opioid-related… complications…”
TOTAL knee arthroplasty is among the most common and painful surgical procedures, with more than 700,000 performed annually in the United States alone. Infiltration of the surgical site with local anesthetic is frequently performed by surgeons to provide postoperative analgesia, although the duration of action is limited to that of the longest-acting local anesthetic available, bupivacaine. By encasing standard bupivacaine in liposomes, the duration of local anesthetic release may be prolonged as the liposomes break down and emit the active medication. In 2011, the first (and currently only) liposomal bupivacaine formulation was approved by the U.S. Food and Drug Administration for surgical wound infiltration (Exparel; Pacira Pharmaceuticals, Inc., USA). In the interim, multiple randomized, controlled clinical trials have been published and, while this type of study design has advantages such as determining effectiveness while minimizing confounding, it also has limitations including modest sample size and uncertain generalizability to daily practice.
It is therefore noteworthy that a retrospective cohort study of nearly 90,000 patients appears in this issue of Anesthesiology by Pichler et al., providing the largest, most nationally-representative view to date into the practice patterns of multiple hospitals and practitioners involving liposomal bupivacaine.1 The authors used the well-known national Premier database to sample patients who underwent total knee arthroplasty with a peripheral nerve block within the United States between 2013 and 2016. A number of significant insights are gleaned from this investigation, including a finding of no clinically meaningful difference in the amount billed for opioids between patients who either did or did not receive liposomal bupivacaine (when accounting for confounding variables). In other words, the use of liposomal bupivacaine was not associated with a change in billing patterns for opioids.
Importantly, the actual opioid consumption was not included in this database, which was designed primarily to capture billing practices in patients undergoing acute care. Unfortunately, the relationship between opioid prescription and consumption is uncertain. For example, bundled payments in which institutions and practitioners are compensated a set amount for performing a total knee arthroplasty may result in an “average” opioid dose being billed, regardless of actual consumption. Similarly, if intravenous patient-controlled analgesia is used, the total amount of opioid in the pump would most likely be billed regardless of the amount consumed. Therefore, we do not have adequate data from this study to definitely address a possible effect of liposomal bupivacaine on decreasing opioid consumption. Conversely, healthcare administrators and policymakers can deduce that the introduction of liposomal bupivacaine into practices has not decreased opioid charges to a clinically-meaningful degree within the healthcare system.
Highly relevant for both clinicians and policymakers is that the use of liposomal bupivacaine was not associated with a decreased use of naloxone or incidence of opioid-related respiratory, genitourinary, central nervous system, or gastrointestinal complications (after accounting for confounding variables). Similarly valuable is the finding that the use of liposomal bupivacaine failed to decrease hospitalization duration or total costs. One might question whether it is realistic to expect the introduction of a single dose of infiltrated liposomal bupivacaine into the surgical wound to decrease either hospitalization duration or costs, but this is precisely what multiple relatively small, retrospective studies—nearly all supported by the manufacturer—have reported for a multitude of surgical procedures, including total knee arthroplasty.2–5 In contrast, not one of nine randomized, controlled trials comparing joint infiltration/infusion of liposomal bupivacaine and unencapsulated local anesthetic that evaluated length of stay following total knee arthroplasty reported a significant difference.6–14
Pichler et al. could not determine which patients in their study had received unencapsulated bupivacaine infiltration, so they could not compare the effects of these two formulations. This does not, however, negate their findings of a lack of beneficial effect of liposome bupivacaine in their study, results that stand in stark contrast to smaller retrospective studies that reported decreased hospitalization duration and/or costs by switching from unencapsulated to liposomal bupivacaine or simply adding liposomal bupivacaine (alone or in combination with nonsteroidal antiinflammatory drugs and/or acetaminophen).2–5,15–18
A critical caveat is that Pichler et al. exclusively included in their analysis patients with a single-injection peripheral nerve block. Of 452,740 total patients within the database, only 88,817—fewer than 20%—received such a block (written personal communication, Stavros Memtsoudis, M.D., Ph.D., F.C.C.P., Hospital for Special Surgery, New York, New York, May 7, 2018). Therefore, their results may not be applicable to more than 80% of patients undergoing total knee arthroplasty nationwide. Although it is conceivable that patients not receiving a peripheral nerve block would benefit most from liposome bupivacaine, the preponderance of evidence from the 13 randomized, controlled trials published to date suggests that there are few, if any, benefits in switching from intraoperative infiltration with unencapsulated bupivacaine to liposomal bupivacaine.
In contrast to infiltration, early trials involving liposomal bupivacaine administered as part of a single-injection peripheral nerve block show promise to significantly extend analgesia and decrease opioid consumption and opioid-related side effects,19–22 as well as possibly shorten hospitalization duration and related costs.21 Importantly, the U.S. Food and Drug Administration has approved the use of liposomal bupivacaine specifically for transversus abdominis plane and interscalene blocks,20–22 although other anatomic locations remain off-label at the time of this writing.19,23 So, the route of administration does, unsurprisingly, appear to influence clinical effects: joint infiltration must be differentiated from use in a peripheral nerve block.
Pichler et al. accurately and responsibly state that, “because of the retrospective design, we can only determine associations and not causal relationships. Therefore, associations have to be interpreted taking into account plausibility [emphasis added].”1 As we noted previously, due to the limitations of the Premier database, which was designed to capture billing activity and not opioid consumption, no conclusions may be drawn from the present study regarding the clinical effectiveness of liposomal bupivacaine in decreasing opioid requirements. However, their other findings regarding a lack of change in hospitalization duration/costs and opioid-related complications with the addition of liposomal bupivacaine are more than plausible given the previously published data from multiple well-controlled, randomized clinical trials. In this respect, the investigation by Pichler et al. is important because it lends external validity to the findings of the majority of randomized trials.
Medicine is constantly evolving with ongoing research and the application of liposome bupivacaine for analgesia after total knee arthroplasty will certainly be no different. For example, recent industry funded studies theorize that liposome bupivacaine may be superior to plain bupivacaine for knee infiltration using a specific technique involving 94 to 103 separate needle passes/injections, a technique which likely deviates from common practice (based on nearly all other published reports).24,25 However, given the results of a large majority of published prospective clinical trials, and now a large retrospective cohort study, it seems incumbent on those proposing a switch to liposomal bupivacaine to provide high-quality data conclusively demonstrating results that justify the 100-fold increase in cost.12,26
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