Interspinous Process Decompression With The Superion® Spacer For Lumbar Spinal Stenosis: Real-World Experience From A Device Registry

被引:10
作者
Tekmyster, Gene [1 ]
Sayed, Dawood [2 ]
Cairns, Kevin D. [3 ]
Raso, Louis J. [4 ]
Kim, Christopher [5 ]
Block, Jon E. [6 ]
机构
[1] Orthopaed & Sports Med Ctr, Trumbull, CT 06611 USA
[2] Univ Kansas Hlth Syst, Ctr Neuromodulat, Kansas City, KS 66103 USA
[3] Florida Spine Specialists, Ft Lauderdale, FL 33308 USA
[4] Jupiter Intervent Pain Management, Jupiter, FL 33477 USA
[5] Ctr Pain Relief, Charleston, WV 25304 USA
[6] Independent Clin Consultant, San Francisco, CA 94115 USA
关键词
Superion (R); interspinous spacer; lumbar spinal stenosis; neurogenic claudication; decompression;
D O I
10.2147/MDER.S220431
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Background: Interspinous process decompression (IPD) with stand-alone spacers has demonstrated excellent long-term clinical benefit for patients with lumbar spinal stenosis (LSS). Methods: IPD used the Superion (R) Indirect Decompression System (Vertiflex, Carlsbad, CA, USA). Perioperative and clinical data were captured via a registry for patients treated with IPD for LSS with intermittent neurogenic claudication. Three-hundred sixteen physicians at 86 clinical sites in the US participated. Patient data were captured from in-person interviews and a phone survey. Outcomes included intraoperative blood loss, procedural time, leg and back pain severity (100 mm VAS), patient satisfaction and treatment approval at 3 weeks, 6 and 12 months. Results: The mean age of registry patients was 73.0 +/- 9.1 years of which 54% were female. Mean leg pain severity decreased from 76.6 +/- 22.4 mm preoperatively to 30.4 +/- 34.6 mm at 12 months, reflecting an overall 60% improvement. Corresponding responder rates were 64% (484 of 751), 72% (1,097 of 1,523) and 75% (317 of 423) at 3 weeks, 6 and 12 months, respectively. Back pain severity improved from 76.8 +/- 22.2 mm preoperatively to 39.9 +/- 32.3 mm at 12 months (48% improvement); 12-month responder rate of 67% (297 of 441). For patient satisfaction at 3 weeks, 6 and 12 months, 89%, 80%, and 80% were satisfied or somewhat satisfied with their treatment and 90%, 75%, and 75% would definitely or probably undergo the same treatment again. In the phone survey, the rate of revision was 3.6% (51 of 1,426). Conclusion: These registry findings support the clinical adoption of minimally invasive IPD in patients with neurogenic claudication associated with LSS.
引用
收藏
页码:423 / 427
页数:5
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