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Responsiveness of five condition-specific and generic outcome assessment instruments for chronic pain

BACKGROUND: Changes of health and quality-of-life in chronic conditions are mostly small and require specific and sensitive instruments. The aim of this study was to determine and compare responsiveness, i.e. the sensitivity to change of five outcome instruments for effect measurement in chronic pai...

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Autores principales: Angst, Felix, Verra, Martin L, Lehmann, Susanne, Aeschlimann, André
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386498/
https://www.ncbi.nlm.nih.gov/pubmed/18439285
http://dx.doi.org/10.1186/1471-2288-8-26
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author Angst, Felix
Verra, Martin L
Lehmann, Susanne
Aeschlimann, André
author_facet Angst, Felix
Verra, Martin L
Lehmann, Susanne
Aeschlimann, André
author_sort Angst, Felix
collection PubMed
description BACKGROUND: Changes of health and quality-of-life in chronic conditions are mostly small and require specific and sensitive instruments. The aim of this study was to determine and compare responsiveness, i.e. the sensitivity to change of five outcome instruments for effect measurement in chronic pain. METHODS: In a prospective cohort study, 273 chronic pain patients were assessed on the Numeric Rating Scale (NRS) for pain, the Short Form 36 (SF-36), the Multidimensional Pain Inventory (MPI), the Hospital Anxiety and Depression Scale (HADS), and the Coping Strategies Questionnaire (CSQ). Responsiveness was quantified by effect size (ES) and standardized response mean (SRM) before and after a four week in-patient interdisciplinary pain program and compared by the modified Jacknife test. RESULTS: The MPI measured pain more responsively than the SF-36 (ES: 0.85 vs 0.72, p = 0.053; SRM: 0.72 vs 0.60, p = 0.027) and the pain NRS (ES: 0.85 vs 0.62, p < 0.001; SRM: 0.72 vs 0.57, p = 0.001). Similar results were found for the dimensions of role and social interference with pain. Comparison in function was limited due to divergent constructs. The responsiveness of the MPI and the SF-36 was equal for affective health but both were better than the HADS (e.g. MPI vs HADS depression: ES: 0.61 vs 0.43, p = 0.001; SF-36 vs HADS depression: ES: 0.54 vs 0.43, p = 0.004). In the "ability to control pain" coping dimension, the MPI was more responsive than the CSQ (ES: 0.46 vs 0.30, p = 0.011). CONCLUSION: The MPI was most responsive in all comparable domains followed by the SF-36. The pain-specific MPI and the generic SF-36 can be recommended for comprehensive and specific bio-psycho-social effect measurement of health and quality-of-life in chronic pain.
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spelling pubmed-23864982008-05-16 Responsiveness of five condition-specific and generic outcome assessment instruments for chronic pain Angst, Felix Verra, Martin L Lehmann, Susanne Aeschlimann, André BMC Med Res Methodol Research Article BACKGROUND: Changes of health and quality-of-life in chronic conditions are mostly small and require specific and sensitive instruments. The aim of this study was to determine and compare responsiveness, i.e. the sensitivity to change of five outcome instruments for effect measurement in chronic pain. METHODS: In a prospective cohort study, 273 chronic pain patients were assessed on the Numeric Rating Scale (NRS) for pain, the Short Form 36 (SF-36), the Multidimensional Pain Inventory (MPI), the Hospital Anxiety and Depression Scale (HADS), and the Coping Strategies Questionnaire (CSQ). Responsiveness was quantified by effect size (ES) and standardized response mean (SRM) before and after a four week in-patient interdisciplinary pain program and compared by the modified Jacknife test. RESULTS: The MPI measured pain more responsively than the SF-36 (ES: 0.85 vs 0.72, p = 0.053; SRM: 0.72 vs 0.60, p = 0.027) and the pain NRS (ES: 0.85 vs 0.62, p < 0.001; SRM: 0.72 vs 0.57, p = 0.001). Similar results were found for the dimensions of role and social interference with pain. Comparison in function was limited due to divergent constructs. The responsiveness of the MPI and the SF-36 was equal for affective health but both were better than the HADS (e.g. MPI vs HADS depression: ES: 0.61 vs 0.43, p = 0.001; SF-36 vs HADS depression: ES: 0.54 vs 0.43, p = 0.004). In the "ability to control pain" coping dimension, the MPI was more responsive than the CSQ (ES: 0.46 vs 0.30, p = 0.011). CONCLUSION: The MPI was most responsive in all comparable domains followed by the SF-36. The pain-specific MPI and the generic SF-36 can be recommended for comprehensive and specific bio-psycho-social effect measurement of health and quality-of-life in chronic pain. BioMed Central 2008-04-25 /pmc/articles/PMC2386498/ /pubmed/18439285 http://dx.doi.org/10.1186/1471-2288-8-26 Text en Copyright © 2008 Angst 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
Angst, Felix
Verra, Martin L
Lehmann, Susanne
Aeschlimann, André
Responsiveness of five condition-specific and generic outcome assessment instruments for chronic pain
title Responsiveness of five condition-specific and generic outcome assessment instruments for chronic pain
title_full Responsiveness of five condition-specific and generic outcome assessment instruments for chronic pain
title_fullStr Responsiveness of five condition-specific and generic outcome assessment instruments for chronic pain
title_full_unstemmed Responsiveness of five condition-specific and generic outcome assessment instruments for chronic pain
title_short Responsiveness of five condition-specific and generic outcome assessment instruments for chronic pain
title_sort responsiveness of five condition-specific and generic outcome assessment instruments for chronic pain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386498/
https://www.ncbi.nlm.nih.gov/pubmed/18439285
http://dx.doi.org/10.1186/1471-2288-8-26
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