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Visually assessed severity of lumbar spinal canal stenosis is paradoxically associated with leg pain and objective walking ability

BACKGROUND: Lumbar spinal stenosis (LSS) is the common term used to describe patients with symptoms related to the anatomical reduction of the lumbar spinal canal size. However, some subjects may have a markedly narrowed canal without any symptoms. This raises the question of what is the actual role...

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Autores principales: Kuittinen, Pekka, Sipola, Petri, Saari, Tapani, Aalto, Timo Juhani, Sinikallio, Sanna, Savolainen, Sakari, Kröger, Heikki, Turunen, Veli, Leinonen, Ville, Airaksinen, Olavi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203914/
https://www.ncbi.nlm.nih.gov/pubmed/25319184
http://dx.doi.org/10.1186/1471-2474-15-348
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author Kuittinen, Pekka
Sipola, Petri
Saari, Tapani
Aalto, Timo Juhani
Sinikallio, Sanna
Savolainen, Sakari
Kröger, Heikki
Turunen, Veli
Leinonen, Ville
Airaksinen, Olavi
author_facet Kuittinen, Pekka
Sipola, Petri
Saari, Tapani
Aalto, Timo Juhani
Sinikallio, Sanna
Savolainen, Sakari
Kröger, Heikki
Turunen, Veli
Leinonen, Ville
Airaksinen, Olavi
author_sort Kuittinen, Pekka
collection PubMed
description BACKGROUND: Lumbar spinal stenosis (LSS) is the common term used to describe patients with symptoms related to the anatomical reduction of the lumbar spinal canal size. However, some subjects may have a markedly narrowed canal without any symptoms. This raises the question of what is the actual role of central canal stenosis in symptomatic patients. The purpose of this study was to compare radiological evaluations of LSS, both visually and quantitatively, with the clinical findings of patients with LSS. METHODS: Eighty patients [mean age 63 (11) years, 44% male], with symptoms severe enough to indicate LSS surgery, were included in this prospective single-center study. Lumbar magnetic resonance imaging was performed and one experienced neuroradiologist classified patients into three groups: 0 = normal or mild stenosis, 1 = moderate stenosis, and 2 = severe stenosis. In addition, the same observer measured the minimal dural sac area level by level from the inferior aspect of L1 to the inferior aspect of S1. The association between radiological and clinical findings were tested with Oswestry Disability Index, overall visual analog pain scale, specific low back pain, specific leg pain, Beck Depression Inventory, and walking distance on treadmill exercise test. RESULTS: In the visual classification of the central spinal canal, leg pain was significantly higher and walking distance achieved was shorter among patients with moderate central stenosis than in patients with severe central stenosis (7.33 (2.29) vs 5.80 (2.72); P = 0.008 and 421 (431) m vs 646 (436) m; P = 0.021, respectively). Patients with severe stenosis at only one level also achieved shorter walking distance than patients with severe stenosis of at least two levels. No correlation between visually or quantitatively assessed stenosis and other clinical findings was found. CONCLUSIONS: There is no straightforward association between the stenosis of dural sac and patient symptoms or functional capacity. These findings indicated that dural sac stenosis is not the single key element in the pathophysiology of LSS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2474-15-348) contains supplementary material, which is available to authorized users.
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spelling pubmed-42039142014-10-22 Visually assessed severity of lumbar spinal canal stenosis is paradoxically associated with leg pain and objective walking ability Kuittinen, Pekka Sipola, Petri Saari, Tapani Aalto, Timo Juhani Sinikallio, Sanna Savolainen, Sakari Kröger, Heikki Turunen, Veli Leinonen, Ville Airaksinen, Olavi BMC Musculoskelet Disord Research Article BACKGROUND: Lumbar spinal stenosis (LSS) is the common term used to describe patients with symptoms related to the anatomical reduction of the lumbar spinal canal size. However, some subjects may have a markedly narrowed canal without any symptoms. This raises the question of what is the actual role of central canal stenosis in symptomatic patients. The purpose of this study was to compare radiological evaluations of LSS, both visually and quantitatively, with the clinical findings of patients with LSS. METHODS: Eighty patients [mean age 63 (11) years, 44% male], with symptoms severe enough to indicate LSS surgery, were included in this prospective single-center study. Lumbar magnetic resonance imaging was performed and one experienced neuroradiologist classified patients into three groups: 0 = normal or mild stenosis, 1 = moderate stenosis, and 2 = severe stenosis. In addition, the same observer measured the minimal dural sac area level by level from the inferior aspect of L1 to the inferior aspect of S1. The association between radiological and clinical findings were tested with Oswestry Disability Index, overall visual analog pain scale, specific low back pain, specific leg pain, Beck Depression Inventory, and walking distance on treadmill exercise test. RESULTS: In the visual classification of the central spinal canal, leg pain was significantly higher and walking distance achieved was shorter among patients with moderate central stenosis than in patients with severe central stenosis (7.33 (2.29) vs 5.80 (2.72); P = 0.008 and 421 (431) m vs 646 (436) m; P = 0.021, respectively). Patients with severe stenosis at only one level also achieved shorter walking distance than patients with severe stenosis of at least two levels. No correlation between visually or quantitatively assessed stenosis and other clinical findings was found. CONCLUSIONS: There is no straightforward association between the stenosis of dural sac and patient symptoms or functional capacity. These findings indicated that dural sac stenosis is not the single key element in the pathophysiology of LSS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2474-15-348) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-16 /pmc/articles/PMC4203914/ /pubmed/25319184 http://dx.doi.org/10.1186/1471-2474-15-348 Text en © Kuittinen et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Kuittinen, Pekka
Sipola, Petri
Saari, Tapani
Aalto, Timo Juhani
Sinikallio, Sanna
Savolainen, Sakari
Kröger, Heikki
Turunen, Veli
Leinonen, Ville
Airaksinen, Olavi
Visually assessed severity of lumbar spinal canal stenosis is paradoxically associated with leg pain and objective walking ability
title Visually assessed severity of lumbar spinal canal stenosis is paradoxically associated with leg pain and objective walking ability
title_full Visually assessed severity of lumbar spinal canal stenosis is paradoxically associated with leg pain and objective walking ability
title_fullStr Visually assessed severity of lumbar spinal canal stenosis is paradoxically associated with leg pain and objective walking ability
title_full_unstemmed Visually assessed severity of lumbar spinal canal stenosis is paradoxically associated with leg pain and objective walking ability
title_short Visually assessed severity of lumbar spinal canal stenosis is paradoxically associated with leg pain and objective walking ability
title_sort visually assessed severity of lumbar spinal canal stenosis is paradoxically associated with leg pain and objective walking ability
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203914/
https://www.ncbi.nlm.nih.gov/pubmed/25319184
http://dx.doi.org/10.1186/1471-2474-15-348
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