Minim Invasive Neurosurg 2010; 53(4): 179-183
DOI: 10.1055/s-0030-1263108
Original Article

© Georg Thieme Verlag KG Stuttgart · New York

Clinical Outcomes and Quality of Life 1 Year after Open Microsurgical Decompression or Implantation of an Interspinous Stand-Alone Spacer

R. Sobottke1 , M. Röllinghoff1 , J. Siewe1 , U. Schlegel1 , A. Yagdiran1 , M. Spangenberg1 , R. Lesch1 , P. Eysel1 , T. Koy1
  • 1Department of Orthopaedic and Trauma Surgery, University of Cologne, Cologne, Germany
Further Information

Publication History

Publication Date:
03 December 2010 (online)

Abstract

Background: Interspinous stand-alone implants are inserted without open decompression to treat symptomatic lumbar spinal stenosis (LSS). The insertion procedure is technically simple, low-risk, and quick. However, the question remains whether the resulting clinical outcomes compare with those of microsurgical decompression, the gold standard.

Material and Methods: This prospective, comparative study included all patients (n=36) with neurogenic intermittent claudication (NIC) secondary to LSS with symptoms improving in forward flexion treated operatively with either interspinous stand-alone spacer insertion (Aperius®; Medtronic, Tolochenaz, Switzerland) (group1) or microsurgical bilateral operative decompression (group 2) between February 2007 and November 2008. Data (patient data, operative data, COMI, SF-36 PCS and MCS, ODI, and walking tolerance) were collected preoperatively as well as at 6 weeks, at 3, 6, and 9 months, and at one year follow-up (FU). All patients had complete FU over 1 year.

Results: Compared to preoperative measurements, surgery led to improvements of all parameters in the entire collective as well as both individual groups. There were no statistically relevant differences between the 2 groups over the entire course of FU. However, improvements in the ODI and SF-36 MCS were not significant in group 1, in contrast to those of group 2. Also, although in group 1 the improvements in leg pain (VAS leg) were still significant (p<0.05) at 6 months, this was no longer the case at 1 year FU. In group 1 at 1 year FU an increase in leg pain was observed, while in group 2 minimal improvements continued. Walking tolerance was significantly improved at all FU times compared to preoperatively, regardless of group (p<0.01). At no time there was a significant difference between the groups. In group 1, admission and operative times were shorter and blood loss decreased. The complication rate was 0% in group 1 and 20% in group 2, however reoperation was required by 27.3% of group 1 patients and 0% of group 2.

Conclusion: Implantation of an interspinous stand-alone spacer yields clinical success comparable to open decompression, at least within the first year of FU. The 1-year conversion rate of 27.3% is, however, decidedly too high.

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Correspondence

R. SobottkeMD 

Department of Orthopaedic

and Trauma Surgery

University of Cologne

Joseph-Stelzmann-Straße 9

50939 Cologne

Germany

Phone: +49/221/478 4616

Fax: +49/221/478 86731

Email: rolf.sobottke@uk-koeln.de

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