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Relationship between New Osteoporotic Vertebral Fracture and Instrumented Lumbar Arthrodesis

STUDY DESIGN: Retrospective study. PURPOSE: To evaluate the relationship between a new osteoporotic vertebral fracture and instrumented lumbar arthrodesis. OVERVIEW OF LITERATURE: In contrast to the growing recognition of the importance of adjacent segment disease after lumbar arthrodesis, relativel...

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Autores principales: Kim, Bung-Hak, Choi, Dong-Hyuk, Jeon, Seong-Hun, Choi, Yong-Soo
Formato: Texto
Lenguaje:English
Publicado: Korean Society of Spine Surgery 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996631/
https://www.ncbi.nlm.nih.gov/pubmed/21165309
http://dx.doi.org/10.4184/asj.2010.4.2.77
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author Kim, Bung-Hak
Choi, Dong-Hyuk
Jeon, Seong-Hun
Choi, Yong-Soo
author_facet Kim, Bung-Hak
Choi, Dong-Hyuk
Jeon, Seong-Hun
Choi, Yong-Soo
author_sort Kim, Bung-Hak
collection PubMed
description STUDY DESIGN: Retrospective study. PURPOSE: To evaluate the relationship between a new osteoporotic vertebral fracture and instrumented lumbar arthrodesis. OVERVIEW OF LITERATURE: In contrast to the growing recognition of the importance of adjacent segment disease after lumbar arthrodesis, relatively little attention has been paid to the relationship between osteoporotic vertebral fractures and instrumented lumbar arthrodesis. METHODS: Twenty five patients with a thoracolumbar vertebral fracture following instrumented arthrodesis for degenerative lumbar disorders (study group) were investigated. The influence of instrumented lumbar arthrodesis was examined by comparing the bone mineral density (BMD) of the femoral neck in the study group with that of 28 patients (control group) who had sustained a simple osteoporotic vertebral fracture. The fracture after instrumented arthrodesis was diagnosed at a mean 47 months (range, 7 to 100 months) after the surgery. RESULTS: There was a relatively better BMD in the study group, 0.67 ± 0.12 g/cm(2) compared to the control group, 0.60 ± 0.13 g/cm(2) (p = 0.013). The level of back pain improved from a mean of 7.5 ± 1.0 at the time of the fracture to a mean of 4.9 ± 2.0 at 1 year after the fracture (p = 0.001). However, 12 (48%) patients complained of severe back pain 1 year after the fracture. There was negative correlation between the BMD of the femoral neck and back pain at the last follow up (r = - 0.455, p = 0.022). CONCLUSIONS: Osteoporotic vertebral fractures after instrumented arthrodesis contribute to the aggravation of back pain and the final outcome of degenerative lumbar disorders. Therefore, it is important to examine the possibility of new osteoporotic vertebral fractures for new-onset back pain after lumbar instrumented arthrodesis.
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spelling pubmed-29966312010-12-16 Relationship between New Osteoporotic Vertebral Fracture and Instrumented Lumbar Arthrodesis Kim, Bung-Hak Choi, Dong-Hyuk Jeon, Seong-Hun Choi, Yong-Soo Asian Spine J Clinical Study STUDY DESIGN: Retrospective study. PURPOSE: To evaluate the relationship between a new osteoporotic vertebral fracture and instrumented lumbar arthrodesis. OVERVIEW OF LITERATURE: In contrast to the growing recognition of the importance of adjacent segment disease after lumbar arthrodesis, relatively little attention has been paid to the relationship between osteoporotic vertebral fractures and instrumented lumbar arthrodesis. METHODS: Twenty five patients with a thoracolumbar vertebral fracture following instrumented arthrodesis for degenerative lumbar disorders (study group) were investigated. The influence of instrumented lumbar arthrodesis was examined by comparing the bone mineral density (BMD) of the femoral neck in the study group with that of 28 patients (control group) who had sustained a simple osteoporotic vertebral fracture. The fracture after instrumented arthrodesis was diagnosed at a mean 47 months (range, 7 to 100 months) after the surgery. RESULTS: There was a relatively better BMD in the study group, 0.67 ± 0.12 g/cm(2) compared to the control group, 0.60 ± 0.13 g/cm(2) (p = 0.013). The level of back pain improved from a mean of 7.5 ± 1.0 at the time of the fracture to a mean of 4.9 ± 2.0 at 1 year after the fracture (p = 0.001). However, 12 (48%) patients complained of severe back pain 1 year after the fracture. There was negative correlation between the BMD of the femoral neck and back pain at the last follow up (r = - 0.455, p = 0.022). CONCLUSIONS: Osteoporotic vertebral fractures after instrumented arthrodesis contribute to the aggravation of back pain and the final outcome of degenerative lumbar disorders. Therefore, it is important to examine the possibility of new osteoporotic vertebral fractures for new-onset back pain after lumbar instrumented arthrodesis. Korean Society of Spine Surgery 2010-12 2010-11-24 /pmc/articles/PMC2996631/ /pubmed/21165309 http://dx.doi.org/10.4184/asj.2010.4.2.77 Text en Copyright © 2010 by Korean Society of Spine Surgery 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 Study
Kim, Bung-Hak
Choi, Dong-Hyuk
Jeon, Seong-Hun
Choi, Yong-Soo
Relationship between New Osteoporotic Vertebral Fracture and Instrumented Lumbar Arthrodesis
title Relationship between New Osteoporotic Vertebral Fracture and Instrumented Lumbar Arthrodesis
title_full Relationship between New Osteoporotic Vertebral Fracture and Instrumented Lumbar Arthrodesis
title_fullStr Relationship between New Osteoporotic Vertebral Fracture and Instrumented Lumbar Arthrodesis
title_full_unstemmed Relationship between New Osteoporotic Vertebral Fracture and Instrumented Lumbar Arthrodesis
title_short Relationship between New Osteoporotic Vertebral Fracture and Instrumented Lumbar Arthrodesis
title_sort relationship between new osteoporotic vertebral fracture and instrumented lumbar arthrodesis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996631/
https://www.ncbi.nlm.nih.gov/pubmed/21165309
http://dx.doi.org/10.4184/asj.2010.4.2.77
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