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Volume 132, Issue 1, Pages 179-188 (November 2007)


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

Krishna KumaraCorresponding Author Informationemail addressemail address, Rod S. Taylorb, Line Jacquesc, Sam Eldabed, Mario Meglioe, Joan Moletf, Simon Thomsong, Jim O’Callaghanh, Elon Eisenbergi, Germain Milbouwj, Eric Buchserk, Gianpaolo Fortinil, Jonathan Richardsonm, Richard B. Northn

Received 28 November 2006; received in revised form 29 July 2007; accepted 30 July 2007. published online 10 September 2007.

Abstract 

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 1 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 (p0.05 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.

a Department of Neurosurgery, Regina General Hospital, 1440 14th Avenue, Regina, Sask., Canada S4P OW5

b Peninsula Medical School, University of Exeter, UK

c Department of Neurosurgery, Montreal Neurological Institute and Hospital, Montreal, Canada

d Department of Pain and Anaesthesia, James Cook University Hospital, Middlesbrough, UK

e Department of Functional Neurosurgery, Gemelli Catholic University Hospital, Rome, Italy

f Department of Neurosurgery, Santa Creu i Sant Pau Hospital, Barcelona, Spain

g Pain Clinic, Basildon and Thurrock University Hospitals, Basildon, UK

h Pain Clinic, Axxon Pain Medicine, Brisbane, Australia

i Pain Relief Unit, Rambam Medical Center, Haifa, Israel

j Neurosurgery, Namur Regional Hospital, Namur, Belgium

k Pain Clinic, Morges Hospital, Morges, Switzerland

l Pain Clinic, Varese Regional Hospital and Macchi Foundation, Varese, Italy

m Department of Pain and Anesthesia, Bradford Hospitals, Bradford, UK

n Department of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD, USA

Corresponding Author InformationCorresponding author. Tel.: +1 306 781 6154; fax: +1 306 781 6153.

PII: S0304-3959(07)00432-0

doi:10.1016/j.pain.2007.07.028


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