{
  "abstract": "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.",
  "authors": [
    {
      "affiliations": [
        "Anesthesiology Institute, Cleveland Clinic, Cleveland, Ohio, USA"
      ],
      "name": "Mariusz Ligocki"
    },
    {
      "affiliations": [
        "Anesthesiology and Perioperative Medicine, Mayo Clinic Minnesota, Rochester, Minnesota, USA"
      ],
      "name": "Anna Maria Ligocki"
    },
    {
      "affiliations": [
        "Orthopedic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA"
      ],
      "name": "Mark W Rodosky"
    },
    {
      "affiliations": [
        "Anesthesiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA"
      ],
      "name": "Jacques E Chelly"
    },
    {
      "affiliations": [
        "Anesthesiology, University of Pittsburgh Medical Center Health System, Pittsburgh, Pennsylvania, USA"
      ],
      "name": "Steven L Orebaugh"
    }
  ],
  "title": "Auricular neuromodulation after rotator cuff repair: insights from a pilot feasibility experience",
  "uid": "5c01b80a-14fe-540d-8750-2cae0bb3a00a"
}