"Predicting at-risk opioid use three months after ed visit for trauma: " by Brittany E. Punches, Uwe Stolz et al.
 

Authors

Brittany E. Punches, The Ohio State University
Uwe Stolz, University of Cincinnati College of Medicine
Caroline E. Freiermuth, University of Cincinnati College of Medicine
Rachel M. Ancona, Washington University School of Medicine in St. Louis
Samuel A. McLean, UNC School of Medicine
Stacey L. House, Washington University School of Medicine in St. Louis
Francesca L. Beaudoin, The Warren Alpert Medical School
Xinming An, UNC School of Medicine
Jennifer S. Stevens, Emory University School of Medicine
Donglin Zeng, UNC Gillings School of Global Public Health
Thomas C. Neylan, University of California, San Francisco
Gari D. Clifford, Emory University School of Medicine
Tanja Jovanovic, Wayne State University School of Medicine
Sarah D. Linnstaedt, UNC School of Medicine
Laura T. Germine, McLean Hospital
Kenneth A. Bollen, College of Arts & Sciences
Scott L. Rauch, McLean Hospital
John P. Haran, University of Massachusetts Chan Medical School
Alan B. Storrow, Vanderbilt University Medical Center
Christopher Lewandowski, Henry Ford Health System
Paul I. Musey, Indiana University School of Medicine
Phyllis L. Hendry, University of Florida College of Medicine
Sophia Sheikh, University of Florida College of Medicine
Christopher W. Jones, Cooper Medical School of Rowan University
Michael C. Kurz, Heersink School of Medicine
Nina T. Gentile, Lewis Katz School of Medicine
Meghan E. McGrath, Boston Medical Center
Lauren A. Hudak, Emory University School of Medicine
Jose L. Pascual, University of Pennsylvania
Mark J. Seamon, University of Pennsylvania Perelman School of Medicine
Erica Harris, Einstein Healthcare Network
Anna M. Chang, Jefferson University Hospitals

Document Type

Article

Abstract

Objective Whether short-term, low-potency opioid prescriptions for acute pain lead to future at-risk opioid use remains controversial and inadequately characterized. Our objective was to measure the association between emergency department (ED) opioid analgesic exposure after a physical, trauma-related event and subsequent opioid use. We hypothesized ED opioid analgesic exposure is associated with subsequent at-risk opioid use. Methods Participants were enrolled in AURORA, a prospective cohort study of adult patients in 29 U. S., urban EDs receiving care for a traumatic event. Exclusion criteria were hospital admission, persons reporting any non-medical opioid use (e.g., opioids without prescription or taking more than prescribed for euphoria) in the 30 days before enrollment, and missing or incomplete data regarding opioid exposure or pain. We used multivariable logistic regression to assess the relationship between ED opioid exposure and at-risk opioid use, defined as any self-reported non-medical opioid use after initial ED encounter or prescription opioid use at 3-months. Results Of 1441 subjects completing 3-month follow-up, 872 participants were included for analysis. At-risk opioid use occurred within 3 months in 33/620 (5.3%, CI: 3.7,7.4) participants without ED opioid analgesic exposure; 4/16 (25.0%, CI: 8.3, 52.6) with ED opioid prescription only; 17/146 (11.6%, CI: 7.1, 18.3) with ED opioid administration only; 12/90 (13.3%, CI: 7.4, 22.5) with both. Controlling for clinical factors, adjusted odds ratios (aORs) for at-risk opioid use after ED opioid exposure were: ED prescription only: 4.9 (95% CI 1.4, 17.4); ED administration for analgesia only: 2.0 (CI 1.0, 3.8); both: 2.8 (CI 1.2, 6.5). Conclusions ED opioids were associated with subsequent at-risk opioid use within three months in a geographically diverse cohort of adult trauma patients. This supports need for prospective studies focused on the long-term consequences of ED opioid analgesic exposure to estimate individual risk and guide therapeutic decision-making.

Publication Date

9-1-2022

Volume

17

First Page

National Science Foundation

DOI

10.1371/journal.pone.0273378

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Repository URL

https://irl.umsl.edu/psychology-faculty/123