Spinal cord stimulation for failed back surgery syndrome: Outcomes in a workers' compensation setting

被引:79
作者
Turner, Judith A. [1 ]
Hollingworth, William [2 ,3 ]
Comstock, Bryan A.
Deyo, Richard A. [4 ,5 ]
机构
[1] Univ Washington, Sch Med, Dept Rehabil Med, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA
[2] Univ Bristol, Dept Social Med, Bristol, Avon, England
[3] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[4] Oregon Hlth & Sci Univ, Dept Internal Med, Portland, OR 97201 USA
[5] Oregon Hlth & Sci Univ, Dept Family Med, Portland, OR 97201 USA
基金
美国国家卫生研究院;
关键词
Spinal cord stimulation; Failed back surgery syndrome; Workers' compensation; Effectiveness; Prospective controlled study; Pragmatic study; LUMBAR DISC HERNIATION; CLINICAL-TRIALS; NEUROPATHIC PAIN; IMMPACT RECOMMENDATIONS; DISABILITY; ASSOCIATION; PREDICTORS;
D O I
10.1016/j.pain.2009.08.014
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Questions remain concerning effectiveness and risks of spinal cord stimulation (SCS) for chronic back and leg pain after spine surgery ("failed back surgery syndrome" [FBSS]). This prospective, population-based controlled cohort study evaluated outcomes of workers' compensation recipients with FBSS who received at least a trial of SCS (SCS group, n = 51) versus those who (1) were evaluated at a multidisciplinary pain clinic and did not receive SCS (Pain Clinic, n = 39) or (2) received neither SCS nor pain clinic evaluation (Usual Care, n = 68). Patients completed measures of pain, function, medication use, and work status at baseline and 6, 12, and 24 months later. We also examined work time loss compensation over 24 months. Few (<10%) patients in any group achieved success at any follow-up on the composite primary outcome encompassing less than daily opioid use and improvement in leg pain and function. At 6 months, the SCS group showed modestly greater improvement in leg pain and function, but with higher rates of daily opioid use. These differences disappeared by 12 months. Patients who received a permanent spinal cord stimulator did not differ from patients who received some pain clinic treatment on the primary outcome at any follow-up (<10% successful in each group at each follow-up) and 19% had them removed within 18 months. Both trial and permanent SCS were associated with adverse events. In sum, we found no evidence for greater effectiveness of SCS versus alternative treatments in this patient population after 6 months. (C) 2009 International Association for the Study of Pain. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:14 / 25
页数:12
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