Treatment effect modifiers for individuals with acute low back pain: secondary analysis of the TARGET trial

被引:4
作者
Beneciuk, Jason M. [1 ,2 ,12 ]
George, Steven Z. [3 ,4 ]
Patterson, Charity G. [5 ]
Smith, Clair N. [5 ]
Brennan, Gerard P. [6 ]
Wegener, Stephen T. [7 ]
Roseen, Eric J. [8 ,9 ,10 ]
Saper, Robert B. [11 ]
Delitto, Anthony [5 ]
机构
[1] Univ Florida, Coll Publ Hlth & Hlth Profess, Dept Phys Therapy, Gainesville, FL USA
[2] Brooks Rehabil, Clin Res Ctr, Jacksonville, FL USA
[3] Duke Univ, Dept Orthopaed Surg, Durham, NC USA
[4] Duke Univ, Duke Clin Res Inst, Durham, NC USA
[5] Univ Pittsburgh, Sch Hlth & Rehabil Sci, Dept Phys Therapy, Pittsburgh, PA USA
[6] Intermt Healthcare, Dept Rehabil Serv, Murray, UT USA
[7] Johns Hopkins Sch Med, Dept Phys Med & Rehabil, Baltimore, MD USA
[8] Boston Univ, Sch Med, Dept Family Med, Boston, MA USA
[9] Boston Med Ctr, Boston, MA USA
[10] MGH Inst Hlth Profess, Dept Rehabil Sci, Boston, MA USA
[11] Cleveland Clin Fdn, Dept Wellness & Prevent Med, Cleveland Hts, OH USA
[12] Univ Florida, Coll Publ Hlth & Hlth Profess, Dept Phys Therapy, POB 100154, Gainesville, FL 32610 USA
关键词
Treatment effect modifiers; Risk stratification; Psychologically informed physical therapy; Acute low back pain; START BACK; BEHAVIORAL INTERVENTIONS; CLINICAL-TRIALS; LEG PAIN; CARE; DISABILITY; THERAPY; IMPACT; MODERATORS; DIAGNOSIS;
D O I
10.1097/j.pain.0000000000002679
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Treatment effect modifiers identify patient characteristics associated with treatment responses. The purpose of this secondary analysis was to identify potential treatment effect modifiers for disability from the TARGET trial that compared usual care (control) with usual care + psychologically informed physical therapy (PIPT). The sample consisted of a STarT Back tool identified high-risk patients with acute low back pain that completed Oswestry Disability Index (ODI) data at index visit and 6 months later (n = 1250). Candidate treatment effect modifiers were identified a priori and informed by the literature. Linear mixed models tested for treatment effect modification through tests of statistical interaction. All statistical interactions (P <= 0.20) were stratified by modifier to inspect for specific effects (P <= 0.05). Smoking was identified as a potential effect modifier (treatment * smoking interaction, P = 0.08). In participants who were smokers, the effect of PIPT was (ODI = 5.5; 95% CI: 0.6-10.4; P = 0.03) compared with usual care. In participants who were nonsmokers, the effect of PIPT was (ODI = 1.5; 95% CI: -1.4 to 4.4; P = 0.31) compared with usual care. Pain medication was also identified as a potential effect modifier (treatment x pain medication interaction, P = 0.10). In participants prescribed >= 3 pain medications, the effect of PIPT was (ODI = 7.1; 95% CI: -0.1 to 14.2; P = 0.05) compared with usual care. The PIPT effect for participants prescribed no pain medication was (ODI = 3.5; 95% CI: -0.4 to 7.4; P = 0.08) and for participants prescribed 1 to 2 pain medications was (ODI = 0.6; 95% CI: -2.5 to 3.7; P = 0.70) when compared with usual care. These findings may be used for generating hypotheses and planning future clinical trials investigating the effectiveness of tailored application of PIPT.
引用
收藏
页码:171 / 179
页数:9
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