Chronic widespread pain after motor vehicle collision typically occurs through immediate development and nonrecovery: results of an emergency department-based cohort study

被引:31
|
作者
Hu, JunMei [1 ,2 ]
Bortsov, Andrey V. [1 ,2 ]
Ballina, Lauren [1 ,2 ]
Orrey, Danielle C. [1 ,2 ]
Swor, Robert A. [3 ]
Peak, David [4 ]
Jones, Jeffrey [5 ]
Rathlev, Niels [6 ]
Lee, David C. [7 ]
Domeier, Robert [8 ]
Hendry, Phyllis [9 ]
Parry, Blair A. [4 ]
McLean, Samuel A. [1 ,2 ,10 ]
机构
[1] Univ N Carolina, TRYUMPH Res Program, Chapel Hill, NC USA
[2] Univ N Carolina, Anesthesiol, Chapel Hill, NC USA
[3] William Beaumont Hosp, Emergency Med, Royal Oak, MI 48072 USA
[4] Massachusetts Gen Hosp, Emergency Med, Boston, MA 02114 USA
[5] Spectrum Hlth Syst, Emergency Med, Grand Rapids, MI USA
[6] Baystate Med Ctr, Emergency Med, Springfield, MA USA
[7] N Shore Univ Hosp, Emergency Med, Manhasset, NY USA
[8] St Joseph Mercy Hlth Syst, Emergency Med, Ypsilanti, MI USA
[9] Univ Florida, Emergency Med, Jacksonville, FL USA
[10] Univ N Carolina, Emergency Med, Chapel Hill, NC USA
基金
美国国家卫生研究院;
关键词
Motor vehicle collision; Chronic widespread pain; Pain trajectory; WHIPLASH-ASSOCIATED DISORDERS; PERITRAUMATIC DISTRESS INVENTORY; 2000-2010; TASK-FORCE; MUSCULOSKELETAL PAIN; RISK-FACTORS; NECK PAIN; FOLLOW-UP; SEXUAL ASSAULT; NEW-ONSET; STRESS;
D O I
10.1097/j.pain.0000000000000388
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
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.
引用
收藏
页码:438 / 444
页数:7
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