IPD without bony decompression versus conventional surgical decompression for lumbar spinal stenosis: 2-year results of a double-blind randomized controlled trial

被引:35
作者
Moojen, Wouter A. [1 ,2 ]
Arts, Mark P. [2 ]
Jacobs, Wilco C. H. [1 ]
van Zwet, Erik W. [3 ]
van den Akker-van Marle, M. Elske [4 ]
Koes, Bart W. [5 ]
Vleggeert-Lankamp, Carmen L. A. M. [1 ]
Peul, Wilco C. [1 ,2 ]
机构
[1] Leiden Univ, Dept Neurosurg, Med Ctr, Leiden, Netherlands
[2] Med Ctr Haaglanden, Dept Neurosurg, The Hague, Netherlands
[3] Leiden Univ, Dept Med Stat, Med Ctr, NL-2300 RA Leiden, Netherlands
[4] Leiden Univ, Dept Med Decis Making, Med Ctr, Leiden, Netherlands
[5] Erasmus MC, Dept Gen Practice, Rotterdam, Netherlands
关键词
Lumbar spinal stenosis; Interspinous implants; Bony decompression; Randomized trial; LOW-BACK-PAIN; NEUROGENIC INTERMITTENT CLAUDICATION; SHUTTLE WALKING TEST; QUALITY-OF-LIFE; X-STOP; INTERSPINAL IMPLANT; DEGENERATIVE SPONDYLOLISTHESIS; NATURAL-HISTORY; OUTCOME MEASURE; HEALTH-STATUS;
D O I
10.1007/s00586-014-3748-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Interspinous process devices (IPDs) are implanted to treat patients with intermittent neurogenic claudication (INC) based on lumbar spinal stenosis. It is hypothesized that patients with lumbar spinal stenosis treated with IPD have a faster short-term recovery, an equal outcome after 2 years and less back pain compared with bony decompression. A randomized design with variable block sizes was used, with allocations stratified according to center. Allocations were stored in prepared opaque, coded and sealed envelopes, and patients and research nurses were blind throughout the follow-up. Five neurosurgical centers (including one academic and four secondary level care centers) included participants. 211 participants were referred to the Leiden-The Hague Spine Prognostic Study Group. 159 participants with INC based on lumbar spinal stenosis at one or two levels with an indication for surgery were randomized into two groups. Patients and research nurses were blinded for the allocated treatment throughout the study period. 80 participants received an IPD and 79 participants underwent spinal bony decompression. The primary outcome at long-term (2-year) follow-up was the score for the Zurich Claudication Questionnaire. Repeated measurement analyses were applied to compare outcomes over time. At two years, the success rate according to the Zurich Claudication Questionnaire for the IPD group [69 % (95 % CI 57-78 %)] did not show a significant difference compared with standard bony decompression [60 % (95 % CI 48-71 %) p value 0.2]. Reoperations, because of absence of recovery, were indicated and performed in 23 cases (33 %) of the IPD group versus 6 (8 %) patients of the bony decompression group (p < 0.01). Furthermore, long-term VAS back pain was significantly higher [36 mm on a 100 mm scale (95 % CI 24-48)] in the IPD group compared to the bony decompression group [28 mm (95 % CI 23-34) p value 0.04]. This double-blinded study could not confirm the advantage of IPD without bony decompression over conventional 'simple' decompression, two years after surgery. Moreover, in the IPD treatment arm, the reoperation rate was higher and back pain was even slightly more intense compared to the decompression treatment arm.
引用
收藏
页码:2295 / 2305
页数:11
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