Spinal cord stimulation versus conventional medical management for neuropathic pain: A multicentre randomised controlled trial in patients with failed back surgery syndrome

被引:791
作者
Kumar, Krishna
Taylor, Rod S.
Jacques, Line
Eldabe, Sam
Meglio, Mario
Molet, Joan
Thomson, Simon
O'Callaghan, Jim
Eisenberg, Elon
Milbouw, Germain
Buchser, Eric
Fortim, Gianpaolo
Richardson, Jonathan
North, Richard B.
机构
[1] Regina Gen Hosp, Dept Neurosurg, Regina, SK S4P OW5, Canada
[2] Univ Exeter, Peninsula Med Sch, Exeter EX4 4QJ, Devon, England
[3] Montreal Neurol Hosp & Inst, Dept Neurosurg, Montreal, PQ, Canada
[4] James Cook Univ N Queensland, Dept Pain Anaesthesia, Middlesbrough, Cleveland, England
[5] Gemelli Catholic Univ Hosp, Dept Funct Neurosurg, Rome, Italy
[6] Santa Creu St Pau Hosp, Dept Neurosurg, Barcelona, Spain
[7] Basildon & Thurrock Univ Hosp, Pain Clin, Basildon, England
[8] Axxon Pain Med, Pain Clin, Brisbane, Qld, Australia
[9] Rambam Med Ctr, Pain Relief Unit, Haifa, Israel
[10] Namur Reg Hosp, Namur, Belgium
[11] Morges Hosp, Pain Clin, Morges, Switzerland
[12] Varese Reg Hosp, Macchi Fdn, Pain Clin, Varese, Italy
[13] Bradford Hosp, Dept Pain & Anesthesia, Bradford, W Yorkshire, England
[14] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21205 USA
关键词
D O I
10.1016/j.pain.2007.07.028
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Patients with neuropathic pain secondary to failed back surgery syndrome (FBSS) typically experience persistent pain, disability, and reduced quality of life. We hypothesised that spinal cord stimulation (SCS) is an effective therapy in addition to conventional medical management (CMM) in this patient population. We randomised 100 FBSS patients with predominant leg pain of neuropathic radicular origin to receive spinal cord stimulation plus conventional medical management (SCS group) or conventional medical management alone (CMM group) for at least 6 months. The primary outcome was the proportion of patients achieving 50% or more pain relief in the legs. Secondary outcomes were improvement in back and leg pain, health-related quality of life, functional capacity, use of pain medication and non-drug pain treatment, level of patient satisfaction, and incidence of complications and adverse effects. Crossover after the 6-months visit was permitted, and all patients were followed up to I year. In the intention-to-treat analysis at 6 months, 24 SCS patients (48%) and 4 CMM patients (9%) (p < 0.001) achieved the primary outcome. Compared with the CMM group, the SCS group experienced improved leg and back pain relief, quality of life, and functional capacity, as well as greater treatment satisfaction (p <= 0.05 for all comparisons). Between 6 and 12 months, 5 SCS patients crossed to CMM, and 32 CMM patients crossed to SCS. At 12 months, 27 SCS patients (32%) had experienced device-related complications. In selected patients with FBSS, SCS provides better pain relief and improves health-related quality of life and functional capacity compared with CMM alone. (C) 2007 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:179 / 188
页数:10
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