IntroductionWith the increasing incidence of total shoulder arthroplasty (TSA) being performed worldwide, there is a growing effort to reduce postoperative pain, the consumption of opioids (oral morphine equivalents [OMEs]), and subsequent in hospital length of stay. Although perioperative pain control regimens have been widely studied in patients undergoing TSA, patients continue to consume a significant quantity of opioids after surgery. In the era of an opioid epidemic, novel methods for the improvement of perioperative pain control is of utmost importance. The aim of this quality improvement initiative was to evaluate the effect of liposomal bupivacaine (LB) versus ropivacaine (RP) in interscalene peripheral nerve blockade (IPNB) in patients undergoing TSA. MethodsThis quality improvement initiative prospectively evaluated a consecutive group of patients undergoing TSA from June 2017 to September 2019. Patients were included if they underwent either an anatomic or reverse shoulder arthroplasty at a single institution by 1 of 2 fellowship trained surgeons. Patients were divided in to 2 temporal cohorts based on the US Food and Drug administration's approval of LB. Patients who received a RPIPNB were in the control group, while those who received a LBIPNB were in the treatment group. Outcome measures studied included average visual analog pain scores (VAS) at 24 and 48 hours in the hospital, OME's, and length of stay. ResultsA total of 114 patients underwent TSA and met the inclusion criteria to be included in the analysis: 58 received RPIPNB and 56 received LBIPNB. The cohorts did not demonstrate any statistically different attributes (eg, age, sex, dominance, smoking status, psychiatric disorders, diabetes, HTN, or ASA class). Difference in 24 hour and 48 hour VAS pain scores was significantly improved in the LBIPNB group as compared to the RPIPNB group (2.46 vs. 0.72, and 2.02 and −0.41, respectively P < .01). Difference in OME's and length of stay were not statistically significant. ConclusionDespite significantly improved pain scores at 24 hours and 48 hours, patients who received LBIPNB did not demonstrate a statistically significant improvement in LOS or quantity of OME's consumed. The discrepancy between subjective numeric pain scores and objective healthcare metrics is likely multifactorial, and brings to light the difficulty in determining the value of new pain regimens. In lieu of these findings, it is difficult to endorse or reject the use of LBIPNB in TSA. Without further studies demonstrating improved efficacy in reduction of opioid consumption and LOS, given the additional expense of the drug, its continued use remains uncertain. Level of EvidenceLevel III.