Prospective Cohort Analysis of DRG Stimulation for Failed Back Surgery Syndrome Pain Following Lumbar Discectomy

被引:25
作者
Kallewaard, Jan Willem [1 ]
Nijhuis, Harold [2 ]
Huygen, Frank [3 ]
Wille, Frank [4 ,5 ]
Zuidema, Xander [4 ,5 ]
van de Minkelis, Johan [6 ]
Raza, Adil [7 ]
机构
[1] Rijnstate Ziekenhuis, Velp, Netherlands
[2] St Antonius Hosp, Nieuwegein, Netherlands
[3] Erasmus Univ, Rotterdam, Netherlands
[4] Diakonessenhuis Utrecht, Zeist, Netherlands
[5] Acad Med Ctr Amsterdam, Amsterdam, Netherlands
[6] Elisabeth Tweesteden Ziekenhuis, Tilburg, Netherlands
[7] Abbott Labs, Plano, TX USA
关键词
failed back surgery syndrome; dorsal root ganglia; stimulation; neuromodulation; spinal cord stimulation; back; pain; neuropathic; SPINAL-CORD STIMULATION; DORSAL-ROOT GANGLION; CONVENTIONAL MEDICAL-MANAGEMENT; NEUROPATHIC PAIN; MULTICENTER; RELIEF; TRIAL; SAFETY;
D O I
10.1111/papr.12734
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Introduction Surgical lumbar discectomy is a commonly performed routine spinal procedure that is usually undertaken to alleviate lumbar radicular symptoms caused by a herniated intervertebral disc. Surgical lumbar discectomy can also lead to chronic postsurgical leg and/or back pain (failed back surgery syndrome [FBSS]), a condition that can be refractory to conventional medical management. Early clinical results on the use of dorsal root ganglion (DRG) stimulation for FBSS have supported the use of this treatment alternative. Methods A multicenter, single-arm, observational cohort study enrolled patients who had chronic pain following surgical lumbar discectomy, had failed conservative treatments, and reported pain intensity of at least 6 out of 10 in the primary region of pain. Data were collected on pain, quality of life, disability, and mood at baseline and through 12 months. Results Thirteen patients underwent a trial of DRG stimulation; 11 (84.6%; 95% confidence interval = 57.8% to 95.7%) had good outcomes and underwent permanent device placement. Pain was reduced from a score of 8.64 (+/- 0.92) at baseline to 2.40 (+/- 2.38; n = 9) after 12 months of treatment, a 72.05% average reduction (P < 0.001). Similar improvements were observed across the secondary clinical measures, and safety data were in line with published rates. Discussion These results suggest that DRG stimulation induces pain relief in subjects diagnosed with FBSS. These reductions in pain were also associated with improvements in quality of life and disability. Additional prospective studies are warranted to further investigate this potential application of DRG stimulation, as well as to optimize patient selection, lead placement, and programming strategies.
引用
收藏
页码:204 / 210
页数:7
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