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Validity, Reliability, and Responsiveness of the Brief Pain Inventory in Inflammatory Bowel Disease
Background and Aims. No patient-reported outcome measures targeting pain have yet been validated for use in IBD patients. Consequently, the aim of this study was to test the psychometrical properties of the brief pain inventory (BPI) in an outpatient population with IBD. Methods. Participants were r...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930809/ https://www.ncbi.nlm.nih.gov/pubmed/27446848 http://dx.doi.org/10.1155/2016/5624261 |
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author | Jelsness-Jørgensen, Lars-Petter Moum, Bjørn Grimstad, Tore Jahnsen, Jørgen Opheim, Randi Prytz Berset, Ingrid Hovde, Øistein Torp, Roald Frigstad, Svein Oskar Huppertz-Hauss, Gert Bernklev, Tomm |
author_facet | Jelsness-Jørgensen, Lars-Petter Moum, Bjørn Grimstad, Tore Jahnsen, Jørgen Opheim, Randi Prytz Berset, Ingrid Hovde, Øistein Torp, Roald Frigstad, Svein Oskar Huppertz-Hauss, Gert Bernklev, Tomm |
author_sort | Jelsness-Jørgensen, Lars-Petter |
collection | PubMed |
description | Background and Aims. No patient-reported outcome measures targeting pain have yet been validated for use in IBD patients. Consequently, the aim of this study was to test the psychometrical properties of the brief pain inventory (BPI) in an outpatient population with IBD. Methods. Participants were recruited from nine hospitals in the southeastern and western parts of Norway. Clinical and sociodemographic data were collected, and participants completed the BPI, as well as the Short-Form 36 (SF-36). Results. In total, 410 patients were included. The BPI displayed high correlations with the bodily pain dimension of the SF-36, as well as moderate correlations with disease activity indices. The BPI also displayed excellent internal consistency (Cronbach's alpha value of 0.91, regardless of diagnosis) and good to excellent test-retest values (intraclass correlation coefficient (ICC) 0.84–0.90 and Kappa values > .70). In UC, calculation of responsiveness revealed that only BPI interference in patients reporting improvement reached the threshold of 0.2. In CD, Cohen's d ranged from 0.26 to 0.68. Conclusions. The BPI may serve as an important supplement in patient-reported outcome measurement in IBD. There is need to confirm responsiveness in future studies. Moreover, responsiveness should ideally be investigated using changes in objective markers of inflammation. |
format | Online Article Text |
id | pubmed-4930809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49308092016-07-13 Validity, Reliability, and Responsiveness of the Brief Pain Inventory in Inflammatory Bowel Disease Jelsness-Jørgensen, Lars-Petter Moum, Bjørn Grimstad, Tore Jahnsen, Jørgen Opheim, Randi Prytz Berset, Ingrid Hovde, Øistein Torp, Roald Frigstad, Svein Oskar Huppertz-Hauss, Gert Bernklev, Tomm Can J Gastroenterol Hepatol Research Article Background and Aims. No patient-reported outcome measures targeting pain have yet been validated for use in IBD patients. Consequently, the aim of this study was to test the psychometrical properties of the brief pain inventory (BPI) in an outpatient population with IBD. Methods. Participants were recruited from nine hospitals in the southeastern and western parts of Norway. Clinical and sociodemographic data were collected, and participants completed the BPI, as well as the Short-Form 36 (SF-36). Results. In total, 410 patients were included. The BPI displayed high correlations with the bodily pain dimension of the SF-36, as well as moderate correlations with disease activity indices. The BPI also displayed excellent internal consistency (Cronbach's alpha value of 0.91, regardless of diagnosis) and good to excellent test-retest values (intraclass correlation coefficient (ICC) 0.84–0.90 and Kappa values > .70). In UC, calculation of responsiveness revealed that only BPI interference in patients reporting improvement reached the threshold of 0.2. In CD, Cohen's d ranged from 0.26 to 0.68. Conclusions. The BPI may serve as an important supplement in patient-reported outcome measurement in IBD. There is need to confirm responsiveness in future studies. Moreover, responsiveness should ideally be investigated using changes in objective markers of inflammation. Hindawi Publishing Corporation 2016 2016-06-19 /pmc/articles/PMC4930809/ /pubmed/27446848 http://dx.doi.org/10.1155/2016/5624261 Text en Copyright © 2016 Lars-Petter Jelsness-Jørgensen et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Jelsness-Jørgensen, Lars-Petter Moum, Bjørn Grimstad, Tore Jahnsen, Jørgen Opheim, Randi Prytz Berset, Ingrid Hovde, Øistein Torp, Roald Frigstad, Svein Oskar Huppertz-Hauss, Gert Bernklev, Tomm Validity, Reliability, and Responsiveness of the Brief Pain Inventory in Inflammatory Bowel Disease |
title | Validity, Reliability, and Responsiveness of the Brief Pain Inventory in Inflammatory Bowel Disease |
title_full | Validity, Reliability, and Responsiveness of the Brief Pain Inventory in Inflammatory Bowel Disease |
title_fullStr | Validity, Reliability, and Responsiveness of the Brief Pain Inventory in Inflammatory Bowel Disease |
title_full_unstemmed | Validity, Reliability, and Responsiveness of the Brief Pain Inventory in Inflammatory Bowel Disease |
title_short | Validity, Reliability, and Responsiveness of the Brief Pain Inventory in Inflammatory Bowel Disease |
title_sort | validity, reliability, and responsiveness of the brief pain inventory in inflammatory bowel disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930809/ https://www.ncbi.nlm.nih.gov/pubmed/27446848 http://dx.doi.org/10.1155/2016/5624261 |
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