A retrospective analysis of pain and opioid usage in head and neck free flap reconstruction

Author:

Towfighi Parhom1ORCID,Hill Alison1,Crossley Jason R.2,Walsh Amanda2,Leonard James A.2,Giurintano Jonathan P.2,Pierce Matthew L.2,Reilly Michael J.2

Affiliation:

1. Georgetown University School of Medicine Washington District of Columbia USA

2. Department of Otolaryngology—Head and Neck Surgery Medstar Georgetown Washington District of Columbia USA

Abstract

AbstractObjectivesInvestigate opioid usage and postoperative pain in patients undergoing head and neck free flap surgery.MethodsA retrospective review of 100 consecutive patients undergoing head and neck free flap reconstruction at two academic centers was performed. Data captured included demographics, postoperative inpatient pain, pain at postoperative visits, morphine equivalent doses (MEDs) administration, medication history, and comorbidities. Data were analyzed using regression models, χ2 tests, and student's t‐tests.ResultsSeventy‐three percent of patients were discharged with opioid medication, with over half (53.4%) continuing to take opioids at their second postoperative visit, and over one‐third (34.2%) continuing to take them around 4‐month postoperatively. One out of every five (20.3%) opioid‐naïve patients chronically took opioids postoperatively. There was a poor association between inpatient postoperative pain scores and daily MEDs administered (R2 = 0.13, 0.17, and 0.22 in postoperative Days 3, 5, and 7, respectively). Neither preoperative radiotherapy nor postoperative complications were associated with an increase in opioid usage.ConclusionsFor patients undergoing head and neck free flap operations, opioid medications are commonly used for postoperative analgesia. This practice may increase the chance an opioid‐naïve patient uses opioids chronically. We found a poor association between MEDs administered and patient‐reported pain scores, which suggests that standardized protocols aimed at optimizing analgesia while reducing opioid administration may be warranted.Level of Evidence: 3 (Retrospective cohort study).

Publisher

Wiley

Subject

Otorhinolaryngology,Surgery

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