4.5 Article

Lumbar Spinal Stenosis with Degenerative Spondylolisthesis Treated with Decompression Alone. A Cohort of 346 Patients at a Large Spine Unit. Clinical Outcome, Complications and Subsequent Surgery

Journal

SPINE
Volume 47, Issue 6, Pages 470-475

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/BRS.0000000000004291

Keywords

clinical outcome; cohort study; complications; decompression alone; decompression with fusion; degenerative spondylolisthesis; lumbar degeneration; lumbar spinal stenosis; spine; subsequent surgery

Funding

  1. Uppsala institutional Avtal om Lakarutbildning och Forskning-ALF (Agreement concerning Cooperation on Medical Education and Research)
  2. Stockholm Spine Center

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This study investigates the clinical outcome, complications, and subsequent surgery rate of DA treatment for lumbar spinal stenosis (LSS) with disc protrusion (DS). The results demonstrate significant clinical improvement after a 2-year follow-up, with low rates of complications and subsequent surgeries.
Study Design. Cohort study. Objective. To study the clinical outcome, complications and subsequent surgery rate of DA for lumbar spinal stenosis (LSS) with DS. Summary of Background Data. There is still no consensus regarding the treatment approach for LSS with DS. Methods. We performed a retrospectively designed cohort study on prospectively collected data from a single high productive spine surgical center. Results from the Swedish Spine Registry and a local register for complications were used for the analyses. Patients with LSS and DS (>3 mm) who underwent DA during January 2012 to August 2017 were included. Patient reported outcome measures at baseline and 2 years after surgery were analyzed. Complications within 30 days of surgery and all subsequent surgery in the lumbar spine were registered. Results. We identified and included 346 patients with completed 2-year follow-up registration. At 2-year follow-up there was a significant improvement in all outcome measures. The global assessment success rate for back and leg pain was 68.3% and 67.6% respectively. Forty-one patients had at least 1 intra- or postoperative complication (11.9%). Nine patients (2.6%), underwent subsequent surgery within 2 years of the primary surgery whereof 2 underwent fusion. During the whole period of data collection, that is, as of June 2020, 28 patients had undergone subsequent surgery (8.1%) whereas 8 of them had had 2 surgeries. Fifteen patients underwent fusion. Conclusion. DA provides good clinical outcome at 2-year follow-up in patients with LSS and DS with low rate of intra- and postoperative complications and subsequent surgery. Our data supports the evidence that DA is effective and safe for LSS with DS.

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