The predictive value of sympathetic block for the success of spinal cord stimulation

被引:22
作者
Hord, ED
Cohen, SP
Cosgrove, GR
Ahmed, SU
Vallejo, R
Chang, YC
Stojanovic, MP
机构
[1] Massachusetts Gen Hosp, MGH Pain Ctr, Intervent Pain Program, Dept Anesthesia, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, MGH Pain Ctr, Intervent Pain Program, Dept Crit Care & Neurol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Uniformed Serv Univ Hlth Sci, Walter Reed Army Med Ctr, Pain Management Ctr, Dept Anesthesia, Washington, DC USA
[5] Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
[6] Massachusetts Gen Hosp, MGH Pain Ctr, Dept Crit Care, Boston, MA 02114 USA
[7] Massachusetts Gen Hosp, Med Practices Evaluat Ctr, Boston, MA 02114 USA
关键词
causalgia; complex regional region pain syndrome; reflex sympathetic dystrophy; spinal cord stimulation; sympathetic block;
D O I
10.1227/01.NEU.0000080061.26321.8D
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: The purpose of this study was to assess the predictive value of response to sympathetic blockade (SB) on the success rate of spinal cord stimulation (SCS) in patients with complex regional pain syndrome. Methods: We performed a retrospective study on 23 patients with complex regional pain syndrome who underwent both SB and subsequent SCS trials in the past 3 years at the Massachusetts General Hospital Pain Center, Boston, MA, and Walter Reed Army Medical Center, Washington, DC. Fifteen of these patients underwent permanent placement of an SCS device, and pain relief at 1- and 9-month follow up was recorded. Results: Among the 23 patients included in the study, those having transient pain relief with SB were more likely to have a positive SCS trial: all 13 with positive SB had good pain relief during the trial, compared with only 3 of the 10 with negative SB (100% versus 30%, p < 0.001). Among the 10 patients with negative SB, 7 noted poor pain relief during the trial despite adequate coverage, and they did not undergo placement of a permanent device. Among the patients who underwent permanent placement of the SCS device, those who received good pain relief with SB were more likely to have greater than 50% pain relief at 1 month follow-up (100% versus 33%, p = 0.029) and 9-month follow-up (87.5% versus 33.3%, P = 0.15). Conclusion: We conclude that patients with good response to SB before SCS are more likely to have a positive response during their SCS trial and long-term pain relief after placement of permanent SCS device.
引用
收藏
页码:626 / 632
页数:7
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