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I am writing to share our experience integrating percutaneous auricular neuromodulation into the postoperative course following arthroscopic rotator cuff repair (RCR). Our intent was not to conduct a powered efficacy study, but to describe feasibility, tolerability, and general postoperative pain trajectories observed in a small group of patients who used the NSS-2 Bridge auricular neuromodulation device after surgery. We hope this experience may assist others considering similar implementation efforts and inform the design of future controlled trials.