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Clinical experiences with a PEEK-based dynamic instrumentation device in lumbar spinal surgery: 2 years and no more
BACKGROUND: Dynamic spine implants were developed to prevent adjacent segment degeneration (ASD) and adjacent segment disease (ASDi). Purpose of this study was to investigate the clinical and radiological outcomes of “topping off” devices following lumbar spinal fusion procedure using a PEEK-based d...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085718/ https://www.ncbi.nlm.nih.gov/pubmed/30092790 http://dx.doi.org/10.1186/s13018-018-0905-z |
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author | Oikonomidis, Stavros Ashqar, Ghazi Kaulhausen, Thomas Herren, Christian Siewe, Jan Sobottke, Rolf |
author_facet | Oikonomidis, Stavros Ashqar, Ghazi Kaulhausen, Thomas Herren, Christian Siewe, Jan Sobottke, Rolf |
author_sort | Oikonomidis, Stavros |
collection | PubMed |
description | BACKGROUND: Dynamic spine implants were developed to prevent adjacent segment degeneration (ASD) and adjacent segment disease (ASDi). Purpose of this study was to investigate the clinical and radiological outcomes of “topping off” devices following lumbar spinal fusion procedure using a PEEK-based dynamic rod system. Moreover, this study focused on the hypothesis that “topping off” devices can prevent ASD. METHODS: This prospective nonrandomized study included patients with indication for single-level lumbar fusion and radiological signs of ASD without instability. The exclusion criteria were previous lumbar spine surgery and no sign of disc degeneration in the adjacent segment according to magnetic resonance imaging. All patients were treated with single-level lumbar interbody fusion and dynamic stabilization of the cranial adjacent segment. Patients underwent a clinical examination and radiographs preoperatively and at 1 and 2 years after surgery. Analyses were performed on clinical data collected with the German Spine Registry using the core outcome measure index (COMI) and visual analogue scale (VAS) scores for back and leg pain. RESULTS: A total of 22 patients (6 male and 16 female) with an average age of 57.6 years were included in the study; 20 patients completed the follow-up (FU). The average COMI score was 9.0 preoperatively, 4.2 at the 1-year FU, and 4.7 at the 2-year FU. The average preoperative VAS scores for back and leg pain were 7.7 and 7.1, respectively. At the 1-year FU, the scores were 4.25 for back pain and 2.2 for leg pain, and at the 2-year FU, the scores were 4.7 for back pain and 2.3 for leg pain. At FU, failure of the dynamic topping off implant material was verified in four cases, and ASD of the segment cranial to the topping off was confirmed in three cases. CONCLUSIONS: These results demonstrate significant improvements in clinical outcomes and pain reduction after lumbar spinal fusion with topping off at 2 years after surgery. However, the implant failed due to the high rate of implant failure and the development of ASD in the segment cranial to the dynamic stabilized segment. |
format | Online Article Text |
id | pubmed-6085718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60857182018-08-16 Clinical experiences with a PEEK-based dynamic instrumentation device in lumbar spinal surgery: 2 years and no more Oikonomidis, Stavros Ashqar, Ghazi Kaulhausen, Thomas Herren, Christian Siewe, Jan Sobottke, Rolf J Orthop Surg Res Research Article BACKGROUND: Dynamic spine implants were developed to prevent adjacent segment degeneration (ASD) and adjacent segment disease (ASDi). Purpose of this study was to investigate the clinical and radiological outcomes of “topping off” devices following lumbar spinal fusion procedure using a PEEK-based dynamic rod system. Moreover, this study focused on the hypothesis that “topping off” devices can prevent ASD. METHODS: This prospective nonrandomized study included patients with indication for single-level lumbar fusion and radiological signs of ASD without instability. The exclusion criteria were previous lumbar spine surgery and no sign of disc degeneration in the adjacent segment according to magnetic resonance imaging. All patients were treated with single-level lumbar interbody fusion and dynamic stabilization of the cranial adjacent segment. Patients underwent a clinical examination and radiographs preoperatively and at 1 and 2 years after surgery. Analyses were performed on clinical data collected with the German Spine Registry using the core outcome measure index (COMI) and visual analogue scale (VAS) scores for back and leg pain. RESULTS: A total of 22 patients (6 male and 16 female) with an average age of 57.6 years were included in the study; 20 patients completed the follow-up (FU). The average COMI score was 9.0 preoperatively, 4.2 at the 1-year FU, and 4.7 at the 2-year FU. The average preoperative VAS scores for back and leg pain were 7.7 and 7.1, respectively. At the 1-year FU, the scores were 4.25 for back pain and 2.2 for leg pain, and at the 2-year FU, the scores were 4.7 for back pain and 2.3 for leg pain. At FU, failure of the dynamic topping off implant material was verified in four cases, and ASD of the segment cranial to the topping off was confirmed in three cases. CONCLUSIONS: These results demonstrate significant improvements in clinical outcomes and pain reduction after lumbar spinal fusion with topping off at 2 years after surgery. However, the implant failed due to the high rate of implant failure and the development of ASD in the segment cranial to the dynamic stabilized segment. BioMed Central 2018-08-09 /pmc/articles/PMC6085718/ /pubmed/30092790 http://dx.doi.org/10.1186/s13018-018-0905-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Oikonomidis, Stavros Ashqar, Ghazi Kaulhausen, Thomas Herren, Christian Siewe, Jan Sobottke, Rolf Clinical experiences with a PEEK-based dynamic instrumentation device in lumbar spinal surgery: 2 years and no more |
title | Clinical experiences with a PEEK-based dynamic instrumentation device in lumbar spinal surgery: 2 years and no more |
title_full | Clinical experiences with a PEEK-based dynamic instrumentation device in lumbar spinal surgery: 2 years and no more |
title_fullStr | Clinical experiences with a PEEK-based dynamic instrumentation device in lumbar spinal surgery: 2 years and no more |
title_full_unstemmed | Clinical experiences with a PEEK-based dynamic instrumentation device in lumbar spinal surgery: 2 years and no more |
title_short | Clinical experiences with a PEEK-based dynamic instrumentation device in lumbar spinal surgery: 2 years and no more |
title_sort | clinical experiences with a peek-based dynamic instrumentation device in lumbar spinal surgery: 2 years and no more |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085718/ https://www.ncbi.nlm.nih.gov/pubmed/30092790 http://dx.doi.org/10.1186/s13018-018-0905-z |
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