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Axial Low Back Pain: One Painful Area – Many Perceptions and Mechanisms

Axial low back pain can be considered as a syndrome with both nociceptive and neuropathic pain components (mixed-pain). Especially neuropathic pain comprises a therapeutic challenge in practical experience and may explain why pharmacotherapy in back pain is often disappointing for both the patient a...

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Autores principales: Förster, Matti, Mahn, Friederike, Gockel, Ulrich, Brosz, Mathias, Freynhagen, Rainer, Tölle, Thomas R., Baron, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699535/
https://www.ncbi.nlm.nih.gov/pubmed/23844179
http://dx.doi.org/10.1371/journal.pone.0068273
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author Förster, Matti
Mahn, Friederike
Gockel, Ulrich
Brosz, Mathias
Freynhagen, Rainer
Tölle, Thomas R.
Baron, Ralf
author_facet Förster, Matti
Mahn, Friederike
Gockel, Ulrich
Brosz, Mathias
Freynhagen, Rainer
Tölle, Thomas R.
Baron, Ralf
author_sort Förster, Matti
collection PubMed
description Axial low back pain can be considered as a syndrome with both nociceptive and neuropathic pain components (mixed-pain). Especially neuropathic pain comprises a therapeutic challenge in practical experience and may explain why pharmacotherapy in back pain is often disappointing for both the patient and the therapist. This survey uses epidemiological and clinical data on the symptomatology of 1083 patients with axial low back pain from a cross sectional survey (painDETECT). Objectives were (1) to estimate whether neuropathic pain contributes to axial low back pain and if so to what extent. (2) To detect subgroups of patients with typical sensory symptom profiles and to analyse their demographic data and co-morbidities. (3) To compare patients with and without prior intervertebral disc surgery (IVD). Neuropathic pain components could be detected in 12% of the entire cohort. Cluster analyses of these patients revealed five distinct subgroups of patients showing a characteristic sensory profile, i.e. a typical constellation and combination of symptoms. All subgroups occurred in relevant numbers and some showed distinct neuropathic characteristics while others showed nociceptive features. Post-IVD-surgery patients showed a tendency to score more “neuropathic” than patients without surgery (not statistically significant). Axial low back pain has a high prevalence of co-morbidities with implication on therapeutic aspects. From these data it can be concluded that sensory profiles based on descriptor severity may serve as a better predictor for therapy assessment than pain intensity or sole diagnosis alone. Standardized phenotyping of pain symptoms with easy tools may help to develop an individualized therapy leading to a higher success rate in pharmacotherapy of axial low back pain.
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spelling pubmed-36995352013-07-10 Axial Low Back Pain: One Painful Area – Many Perceptions and Mechanisms Förster, Matti Mahn, Friederike Gockel, Ulrich Brosz, Mathias Freynhagen, Rainer Tölle, Thomas R. Baron, Ralf PLoS One Research Article Axial low back pain can be considered as a syndrome with both nociceptive and neuropathic pain components (mixed-pain). Especially neuropathic pain comprises a therapeutic challenge in practical experience and may explain why pharmacotherapy in back pain is often disappointing for both the patient and the therapist. This survey uses epidemiological and clinical data on the symptomatology of 1083 patients with axial low back pain from a cross sectional survey (painDETECT). Objectives were (1) to estimate whether neuropathic pain contributes to axial low back pain and if so to what extent. (2) To detect subgroups of patients with typical sensory symptom profiles and to analyse their demographic data and co-morbidities. (3) To compare patients with and without prior intervertebral disc surgery (IVD). Neuropathic pain components could be detected in 12% of the entire cohort. Cluster analyses of these patients revealed five distinct subgroups of patients showing a characteristic sensory profile, i.e. a typical constellation and combination of symptoms. All subgroups occurred in relevant numbers and some showed distinct neuropathic characteristics while others showed nociceptive features. Post-IVD-surgery patients showed a tendency to score more “neuropathic” than patients without surgery (not statistically significant). Axial low back pain has a high prevalence of co-morbidities with implication on therapeutic aspects. From these data it can be concluded that sensory profiles based on descriptor severity may serve as a better predictor for therapy assessment than pain intensity or sole diagnosis alone. Standardized phenotyping of pain symptoms with easy tools may help to develop an individualized therapy leading to a higher success rate in pharmacotherapy of axial low back pain. Public Library of Science 2013-07-02 /pmc/articles/PMC3699535/ /pubmed/23844179 http://dx.doi.org/10.1371/journal.pone.0068273 Text en © 2013 Förster et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Förster, Matti
Mahn, Friederike
Gockel, Ulrich
Brosz, Mathias
Freynhagen, Rainer
Tölle, Thomas R.
Baron, Ralf
Axial Low Back Pain: One Painful Area – Many Perceptions and Mechanisms
title Axial Low Back Pain: One Painful Area – Many Perceptions and Mechanisms
title_full Axial Low Back Pain: One Painful Area – Many Perceptions and Mechanisms
title_fullStr Axial Low Back Pain: One Painful Area – Many Perceptions and Mechanisms
title_full_unstemmed Axial Low Back Pain: One Painful Area – Many Perceptions and Mechanisms
title_short Axial Low Back Pain: One Painful Area – Many Perceptions and Mechanisms
title_sort axial low back pain: one painful area – many perceptions and mechanisms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699535/
https://www.ncbi.nlm.nih.gov/pubmed/23844179
http://dx.doi.org/10.1371/journal.pone.0068273
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