Cargando…
Primary Limited Lumbar Discectomy with an Annulus Closure Device: One-Year Clinical and Radiographic Results from a Prospective, Multi-Center Study
OBJECTIVE: Discectomy as a treatment for herniated lumbar discs results in outcomes after surgery that are not uniformly positive. Surgeons face the dilemma between limited nucleus removal which is associated with a higher risk of recurrence, or more aggressive nucleus removal which may lead to disc...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Spinal Neurosurgery Society
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430560/ https://www.ncbi.nlm.nih.gov/pubmed/25983843 http://dx.doi.org/10.14245/kjs.2012.9.4.340 |
_version_ | 1782371196533211136 |
---|---|
author | Lequin, Michiel B. Barth, Martin Thomė, Claudius Bouma, Gerrit J. |
author_facet | Lequin, Michiel B. Barth, Martin Thomė, Claudius Bouma, Gerrit J. |
author_sort | Lequin, Michiel B. |
collection | PubMed |
description | OBJECTIVE: Discectomy as a treatment for herniated lumbar discs results in outcomes after surgery that are not uniformly positive. Surgeons face the dilemma between limited nucleus removal which is associated with a higher risk of recurrence, or more aggressive nucleus removal which may lead to disc height loss and persistent back-pain. annulus closure devices may allow for the benefits of limited nucleus removal without the increased risk of recurrence. This is an interim report of an ongoing 24-month post-marketing study of the Barricaid® annulus closure device, consisting of a flexible polymer mesh that blocks the defect, held in place by a titanium bone anchor. METHODS: We prospectively enrolled 45 patients at four hospitals, and implanted the Barricaid® after a limited discectomy. annulus defect size and volume of removed nucleus were recorded. Reherniations were reported, pain and function were monitored and imaging was performed at regular intervals during 24 months of follow-up. RESULTS: At 12 months postsurgery, pain and function were significantly improved, comparing favorably to reported results from limited discectomy. Disc height has been well maintained. One reherniation has occurred (2.4%), which was associated with a misplaced device. No device fracture, subsidence or migration has been observed. CONCLUSION: The use of an annulus closure device may provide a reduction in reherniation rate for lumbar discectomy patients with large annulus defects who are at the greatest risk of recurrence. Using such a device should provide the surgeon increased confidence in minimizing nucleus removal, which, in turn, may preserve disc height and biomechanics, reducing degeneration and associated poor clinical outcomes in the long-term. A randomized multicenter study evaluating limited discectomy with and without the Barricaid® is currently underway, and will provide a higher level of evidence. |
format | Online Article Text |
id | pubmed-4430560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Spinal Neurosurgery Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-44305602015-05-15 Primary Limited Lumbar Discectomy with an Annulus Closure Device: One-Year Clinical and Radiographic Results from a Prospective, Multi-Center Study Lequin, Michiel B. Barth, Martin Thomė, Claudius Bouma, Gerrit J. Korean J Spine Clinical Article OBJECTIVE: Discectomy as a treatment for herniated lumbar discs results in outcomes after surgery that are not uniformly positive. Surgeons face the dilemma between limited nucleus removal which is associated with a higher risk of recurrence, or more aggressive nucleus removal which may lead to disc height loss and persistent back-pain. annulus closure devices may allow for the benefits of limited nucleus removal without the increased risk of recurrence. This is an interim report of an ongoing 24-month post-marketing study of the Barricaid® annulus closure device, consisting of a flexible polymer mesh that blocks the defect, held in place by a titanium bone anchor. METHODS: We prospectively enrolled 45 patients at four hospitals, and implanted the Barricaid® after a limited discectomy. annulus defect size and volume of removed nucleus were recorded. Reherniations were reported, pain and function were monitored and imaging was performed at regular intervals during 24 months of follow-up. RESULTS: At 12 months postsurgery, pain and function were significantly improved, comparing favorably to reported results from limited discectomy. Disc height has been well maintained. One reherniation has occurred (2.4%), which was associated with a misplaced device. No device fracture, subsidence or migration has been observed. CONCLUSION: The use of an annulus closure device may provide a reduction in reherniation rate for lumbar discectomy patients with large annulus defects who are at the greatest risk of recurrence. Using such a device should provide the surgeon increased confidence in minimizing nucleus removal, which, in turn, may preserve disc height and biomechanics, reducing degeneration and associated poor clinical outcomes in the long-term. A randomized multicenter study evaluating limited discectomy with and without the Barricaid® is currently underway, and will provide a higher level of evidence. The Korean Spinal Neurosurgery Society 2012-12 2012-12-31 /pmc/articles/PMC4430560/ /pubmed/25983843 http://dx.doi.org/10.14245/kjs.2012.9.4.340 Text en Copyright © 2012 The Korean Spinal Neurosurgery Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Article Lequin, Michiel B. Barth, Martin Thomė, Claudius Bouma, Gerrit J. Primary Limited Lumbar Discectomy with an Annulus Closure Device: One-Year Clinical and Radiographic Results from a Prospective, Multi-Center Study |
title | Primary Limited Lumbar Discectomy with an Annulus Closure Device: One-Year Clinical and Radiographic Results from a Prospective, Multi-Center Study |
title_full | Primary Limited Lumbar Discectomy with an Annulus Closure Device: One-Year Clinical and Radiographic Results from a Prospective, Multi-Center Study |
title_fullStr | Primary Limited Lumbar Discectomy with an Annulus Closure Device: One-Year Clinical and Radiographic Results from a Prospective, Multi-Center Study |
title_full_unstemmed | Primary Limited Lumbar Discectomy with an Annulus Closure Device: One-Year Clinical and Radiographic Results from a Prospective, Multi-Center Study |
title_short | Primary Limited Lumbar Discectomy with an Annulus Closure Device: One-Year Clinical and Radiographic Results from a Prospective, Multi-Center Study |
title_sort | primary limited lumbar discectomy with an annulus closure device: one-year clinical and radiographic results from a prospective, multi-center study |
topic | Clinical Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430560/ https://www.ncbi.nlm.nih.gov/pubmed/25983843 http://dx.doi.org/10.14245/kjs.2012.9.4.340 |
work_keys_str_mv | AT lequinmichielb primarylimitedlumbardiscectomywithanannulusclosuredeviceoneyearclinicalandradiographicresultsfromaprospectivemulticenterstudy AT barthmartin primarylimitedlumbardiscectomywithanannulusclosuredeviceoneyearclinicalandradiographicresultsfromaprospectivemulticenterstudy AT thomeclaudius primarylimitedlumbardiscectomywithanannulusclosuredeviceoneyearclinicalandradiographicresultsfromaprospectivemulticenterstudy AT boumagerritj primarylimitedlumbardiscectomywithanannulusclosuredeviceoneyearclinicalandradiographicresultsfromaprospectivemulticenterstudy |