Risk Factors for the Development of Multisite Pain in Children

被引:12
作者
Kaplan, Chelsea M. [1 ,5 ]
Schrepf, Andrew [1 ]
Boehnke, Kevin F. [1 ]
He, Ying [1 ]
Smith, Tristin [1 ]
Williams, David A. [1 ]
Bergmans, Rachel [1 ]
Voepel-Lewis, Terri [1 ]
Hassett, Afton L. [1 ]
Harris, Richard E. [1 ,2 ,3 ]
Clauw, Daniel J. [1 ]
Beltz, Adriene M. [1 ,4 ]
Harte, Steven E. [1 ]
机构
[1] Michigan Med, Dept Anesthesiol, Ann Arbor, MI USA
[2] Univ Calif Irvine, Susan Samueli Integrat Hlth Inst, Sch Med, Irvine, CA USA
[3] Univ Calif Irvine, Sch Med, Dept Anesthesiol & Perioperat Care, Irvine, CA USA
[4] Univ Michigan, Dept Psychol, Ann Arbor, MI 48106 USA
[5] Univ Michigan, Chron Pain & Fatigue Res Ctr, Dept Anesthesiol, 24 Frank Lloyd Wright Dr,POB 385,Lobby M, Ann Arbor, MI 48106 USA
基金
美国国家卫生研究院;
关键词
multisite pain; children; risk factors; development; WIDESPREAD PAIN; PROGNOSTIC-FACTORS; ADOLESCENT RISK; CHILDHOOD; ONSET; SLEEP; FIBROMYALGIA; DISORDERS; PREDICT; EPIDEMIOLOGY;
D O I
10.1097/AJP.0000000000001148
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Objective: Chronic pain has economic costs on par with cardiovascular disease, diabetes, and cancer. Despite this impact on the health care system and increasing awareness of the relationship between pain and mortality, efforts to identify simple symptom-based risk factors for the development of pain, particularly in children, have fallen short. This is critically important as pain that manifests during childhood often persists into adulthood. To date, no longitudinal studies have examined symptoms in pain-free children that presage a new, multisite manifestation of pain in the future. We hypothesized that female sex, sleep problems, and heightened somatic symptoms complaints at baseline would be associated with the risk of developing new multisite pain 1 year later.Methods: Symptom assessments were completed by parents of youth (ages 9 to 10) enrolled in the Adolescent Brain Cognitive Development study. Multivariate logistic regression models focused on children who developed multisite pain 1 year later (n=331) and children who remained pain free (n=3335).Results: Female sex (odds ratio [OR]=1.35; 95% CI, 1.07, 1.71; P=0.01), elevated nonpainful somatic symptoms (OR=1.17; 95% CI, 1.06, 1.29; P<0.01), total sleep problems (OR=1.20; 95% CI, 1.07, 1.34; P<0.01), and attentional issues (OR=1.22; 95% CI, 1.10, 1.35; P<0.001) at baseline were associated with new multisite pain 1 year later. Baseline negative affect was not associated with new multisite pain.Discussion: Identifying symptom-based risk factors for multisite pain in children is critical for early prevention. Somatic awareness, sleep and attention problems represent actionable targets for early detection, treatment, and possible prevention of multisite pain in youth.
引用
收藏
页码:588 / 594
页数:7
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