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A modified score to identify and discriminate neuropathic pain: a study on the German version of the neuropathic pain symptom inventory (NPSI)

BACKGROUND: Neuropathic pain must be correctly diagnosed for optimal treatment. The questionnaire named Neuropathic Pain Symptom Inventory (NPSI) was developed in its original French version to evaluate the different symptoms of neuropathic pain. We hypothesized that the NPSI might also be used to d...

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Autores principales: Sommer, Claudia, Richter, Helmut, Rogausch, Jan P, Frettlöh, Jule, Lungenhausen, Margitta, Maier, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180265/
https://www.ncbi.nlm.nih.gov/pubmed/21861889
http://dx.doi.org/10.1186/1471-2377-11-104
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author Sommer, Claudia
Richter, Helmut
Rogausch, Jan P
Frettlöh, Jule
Lungenhausen, Margitta
Maier, Christoph
author_facet Sommer, Claudia
Richter, Helmut
Rogausch, Jan P
Frettlöh, Jule
Lungenhausen, Margitta
Maier, Christoph
author_sort Sommer, Claudia
collection PubMed
description BACKGROUND: Neuropathic pain must be correctly diagnosed for optimal treatment. The questionnaire named Neuropathic Pain Symptom Inventory (NPSI) was developed in its original French version to evaluate the different symptoms of neuropathic pain. We hypothesized that the NPSI might also be used to differentiate neuropathic from non-neuropathic pain. METHODS: We translated the NPSI into German using a standard forward-backward translation and administered it in a case-control design to patients with neuropathic (n = 68) and non-neuropathic pain (headache and osteoarthritis, n = 169) to validate it and to analyze its discriminant properties, its sensitivity to change, and to detect neuropathic pain subgroups with distinct profiles. RESULTS: Using a sum score (the NPSI-G score), we found sensitivity to change (r between 0.37 and 0.5 for pain items of the graded chronic pain scale) and could distinguish between neuropathic and other pain on a group basis, but not for individual patients. Post hoc development of a discriminant score with optimized diagnostic properties to distinguish neuropathic pain from non-neuropathic pain resulted in an instrument with high sensitivity (91%) and acceptable specificity (70%). We detected six different pain profiles in the patient group with neuropathic pain; three profiles were found to be distinct. CONCLUSIONS: The NPSI-G potentially combines the properties of a diagnostic tool and an instrument to identify subtypes of neuropathic pain.
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spelling pubmed-31802652011-09-27 A modified score to identify and discriminate neuropathic pain: a study on the German version of the neuropathic pain symptom inventory (NPSI) Sommer, Claudia Richter, Helmut Rogausch, Jan P Frettlöh, Jule Lungenhausen, Margitta Maier, Christoph BMC Neurol Research Article BACKGROUND: Neuropathic pain must be correctly diagnosed for optimal treatment. The questionnaire named Neuropathic Pain Symptom Inventory (NPSI) was developed in its original French version to evaluate the different symptoms of neuropathic pain. We hypothesized that the NPSI might also be used to differentiate neuropathic from non-neuropathic pain. METHODS: We translated the NPSI into German using a standard forward-backward translation and administered it in a case-control design to patients with neuropathic (n = 68) and non-neuropathic pain (headache and osteoarthritis, n = 169) to validate it and to analyze its discriminant properties, its sensitivity to change, and to detect neuropathic pain subgroups with distinct profiles. RESULTS: Using a sum score (the NPSI-G score), we found sensitivity to change (r between 0.37 and 0.5 for pain items of the graded chronic pain scale) and could distinguish between neuropathic and other pain on a group basis, but not for individual patients. Post hoc development of a discriminant score with optimized diagnostic properties to distinguish neuropathic pain from non-neuropathic pain resulted in an instrument with high sensitivity (91%) and acceptable specificity (70%). We detected six different pain profiles in the patient group with neuropathic pain; three profiles were found to be distinct. CONCLUSIONS: The NPSI-G potentially combines the properties of a diagnostic tool and an instrument to identify subtypes of neuropathic pain. BioMed Central 2011-08-23 /pmc/articles/PMC3180265/ /pubmed/21861889 http://dx.doi.org/10.1186/1471-2377-11-104 Text en Copyright ©2011 Sommer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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 cited.
spellingShingle Research Article
Sommer, Claudia
Richter, Helmut
Rogausch, Jan P
Frettlöh, Jule
Lungenhausen, Margitta
Maier, Christoph
A modified score to identify and discriminate neuropathic pain: a study on the German version of the neuropathic pain symptom inventory (NPSI)
title A modified score to identify and discriminate neuropathic pain: a study on the German version of the neuropathic pain symptom inventory (NPSI)
title_full A modified score to identify and discriminate neuropathic pain: a study on the German version of the neuropathic pain symptom inventory (NPSI)
title_fullStr A modified score to identify and discriminate neuropathic pain: a study on the German version of the neuropathic pain symptom inventory (NPSI)
title_full_unstemmed A modified score to identify and discriminate neuropathic pain: a study on the German version of the neuropathic pain symptom inventory (NPSI)
title_short A modified score to identify and discriminate neuropathic pain: a study on the German version of the neuropathic pain symptom inventory (NPSI)
title_sort modified score to identify and discriminate neuropathic pain: a study on the german version of the neuropathic pain symptom inventory (npsi)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180265/
https://www.ncbi.nlm.nih.gov/pubmed/21861889
http://dx.doi.org/10.1186/1471-2377-11-104
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