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Journal Article

Citation

Hu J, Bortsov AV, Ballina L, Orrey DC, Swor RA, Peak D, Jones J, Rathlev N, Lee DC, Domeier RM, Hendry P, Parry BA, McLean SA. Pain 2016; 157(2): 438-444.

Affiliation

TRYUMPH Research Program, University of North Carolina, Chapel Hill, NC, USAbAnesthesiology, University of North Carolina, Chapel Hill, NC, USAcEmergency Medicine, William Beaumont Hospital, Royal Oak, MI, USAdEmergency Medicine, Massachusetts General Hospital, Boston, MA, USAeEmergency Medicine, Spectrum Health System, Grand Rapids, MI, USAfEmergency Medicine, Baystate Medical Center, Springfield, MA, USAgEmergency Medicine, North Shore University Hospital, Manhasset, NY, USAhEmergency Medicine, Saint Joseph Mercy Health System, Ypsilanti, MI, USAiEmergency Medicine, University of Florida, Jacksonville, FL, USAjEmergency Medicine, University of North Carolina, Chapel Hill, NC, USA.

Copyright

(Copyright © 2016, Lippincott, Williams and Wilkins)

DOI

10.1097/j.pain.0000000000000388

PMID

26808013

Abstract

Motor vehicle collision (MVC) can trigger chronic widespread pain (CWP) development in vulnerable individuals. Whether such CWP typically develops through the evolution of pain from regional to widespread or through the early development of widespread pain with nonrecovery is currently unknown. We evaluated the trajectory of CWP development (American College of Rheumatology criteria) among 948 European-American individuals who presented to the emergency department (ED) for care in the early aftermath of MVC. Pain extent was assessed in the ED and 6 weeks, 6 months, and 1 year after MVC on 100%, 91%, 89%, and 91% of participants, respectively. Individuals who reported prior CWP at the time of ED evaluation (n = 53) were excluded. Trajectory modeling identified a 2-group solution as optimal, with the Bayes Factor value (138) indicating strong model selection. Linear solution plots supported a nonrecovery model. Although the number of body regions with pain in the non-CWP group steadily declined, the number of body regions with pain in the CWP trajectory group (192/895, 22%) remained relatively constant over time. These data support the hypothesis that individuals who develop CWP after MVC develop widespread pain in the early aftermath of MVC, which does not remit.


Language: en

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