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Superior outcomes of decompression with an interlaminar dynamic device versus decompression alone in patients with lumbar spinal stenosis and back pain: a cross registry study

Röder, C. ; Baumgärtner, B. ; Berlemann, U. ; Aghayev, E.

In: European Spine Journal, 2015, vol. 24, no. 10, p. 2228-2235

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    Title
    • Superior outcomes of decompression with an interlaminar dynamic device versus decompression alone in patients with lumbar spinal stenosis and back pain: a cross registry study
    Author
    • Röder, C.. Institute for Evaluative Research in Medicine, University of Bern, Stauffacherstrasse 78, 3012, Bern, Switzerland
    • Baumgärtner, B.. Department of Orthopedic Surgery, Luzerner Kantonsspital, Spitalstrasse 16, 6000, Lucerne, Switzerland
    • Berlemann, U.. The Spine Center, Bahnhofstrasse 3, 3600, Thun, Switzerland
    • Aghayev, E.. Institute for Evaluative Research in Medicine, University of Bern, Stauffacherstrasse 78, 3012, Bern, Switzerland
    Document Type
    • Postprint
    OAI-PMH Identifier
    • oai:doc.rero.ch:333112
    Summary
    Introduction: Surgical decompression for lumbar spinal stenosis (LSS) has been associated with poorer outcomes in patients with pronounced low back pain (LBP) as compared to patients with predominant leg pain. This cross registry study assessed potential benefits of the interlaminar coflex® device as an add-on to bony decompression alone. Methods: Patients with lumbar decompression plus coflex® (SWISSspine registry) were compared with decompressed controls (Spine Tango registry). Inclusion criteria were LSS and a preoperative back pain level of ≥5 points. 1:1 propensity score-based matching was performed. Outcome measures were back and leg pain relief, COMI score improvement, patient satisfaction, complication, and revision rates. Results: 50 matched pairs without residual significant differences but age were created. At the 7-9months follow-up interval the coflex® group had higher back (p=0.014) and leg pain relief (p<0.001) and COMI score improvement (p=0.029) than the decompression group. Patient satisfaction was 90% in both groups. No revision was documented in the coflex® and one in the decompression group (2.0%). Discussion: In the short-term, lumbar decompression with coflex® compared with decompression alone in patients with LSS and pronounced LBP at baseline is a safe and effective treatment option that appears beneficial regarding clinical and functional outcomes. However, residual confounding of non-measured covariables may have partially influenced our findings. Also, despite careful inclusion and exclusion of cases the cross registry approach introduces a potential for selection bias that we could not totally controlfor and that makes additional studies necessary.