TY - JOUR
T1 - Validation of the inflammatory bowel disease disability index in a population-based cohort
AU - International Programme to Develop New Indexes for Crohn's Disease (IPNIC) group
AU - Gower-Rousseau, Corinne
AU - Sarter, Hélène
AU - Savoye, Guillaume
AU - Tavernier, Noémie
AU - Fumery, Mathurin
AU - Sandborn, William J.
AU - Feagan, Brian G.
AU - Duhamel, Alain
AU - Guillon-Dellac, Nathalie
AU - Colombel, Jean Frédéric
AU - Peyrin-Biroulet, Laurent
AU - Reinisch, Walter
AU - Tilg, Herbert
AU - Kamm, Michael
AU - D'Haens, Geert
AU - Louis, Edouard
AU - Van Assche, Geert
AU - Feagan, Brian
AU - Irvine, E. Jan
AU - Michetti, Pierre
AU - Hibi, Toshifumi
AU - Schölmerich, Jürgen
AU - Schreiber, Stefan
AU - Munkholm, Pia
AU - Panes, Julian
AU - Alarcos, Cieza
AU - Cosnes, Jacques
AU - Lémann, Marc
AU - Lewin, Maïté
AU - Mary, Jean Yves
AU - Pariente, Benjamin
AU - Travis, Simon
AU - Chowers, Yehuda
AU - Danese, Silvio
AU - Vecchi, Maurizio
AU - Hommes, Daan W.
AU - Oresland, Tom
AU - Fletcher, Joel
AU - Loftus, Edward V.
AU - Sands, Bruce E.
N1 - Funding Information:
The authors wish to thank the interviewing practitioners who collected data: I. Rousseau, A Pétillon, B. Turck, V. Kail, C. Cunisse, S. Auzou, M. Leconte, C. Le Gallo, D. Rime. The authors thank all patients and all gastroenterologists who participated in this study and the European Charity Fondation Digestscience. The authors would also like to thank all the people who were actively involved in the qualitative study. EPIMAD is organised under an agreement between the Institut National de la Santé et de la Recherche Médicale (INSERM) and the Institut de Veille Sanitaire (InVS) and also received financial support from the François Aupetit Association, Lille, Amiens and Rouen University Hospitals. This study has been funded by "le Programme Hospitalier de Recherche Clinique Inter Regional" 2011 (Promoteur : CHRU Lille, Financement: Ministère de la Santé, France). AbbVie Company participated in developing the content for the IPNIC meetings, but was not involved in the development or review of this article with the authors. Editing services, including for the slides at the IPNIC meetings, were provided by Margaux-Orange, and financial support for these services was provided by AbbVie. The Health French Ministry grant registration number is 2011-A00877-34. CG-R has served as speaker for Abbvie France, Ferring International, Janssen International and MSD France. GS has served as speaker for MSD France, Ferring France, Abbvie France and Vifor France. MF has served as speaker for Abbvie France, Ferring France and MSD France. WJS has received consulting fees from Abbott, ActoGeniX NV, AGI Therapeutics, AlbaTherapeutics Corp, Albireo, Alfa Wasserman, Amgen, AM-Pharma BV, Anaphore, Astellas, Athersys, Atlantic Healthcare Ltd, Aptalis, BioBalance Corp, Boeh-ringer-Ingelheim, Bristol-Myers Squibb, Celgene, CelekPharmaceuticals, Cellerix SL, Cerimon Pharmaceuticals, ChemoCentryx, CoMentis, Cosmo Technologies, Coro-nado Biosciences, Cytokine Pharmasciences, Eagle Phar-maceuticals, EnGene, Eli Lilly, Enteromedics, ExagenDiagnostics, Ferring Pharmaceuticals, Flexio Thera-peutics, Funxional Therapeutics Ltd, Genzyme Corp, Gilead Sciences, Given Imaging, GlaxoSmithKline, HumanGenome Sciences, Ironwood Pharmaceuticals, KaloBiosPharmaceuticals, Lexicon Pharmaceuticals, Lycera Corp, Meda Pharmaceuticals, Merck Research Laboratories,Merck Seron, Millenium Pharmaceuticals, Nisshin Kyorin Pharmaceuticals, Novo Nordisk, NPS Pharmaceuticals, Optimer Pharmaceuticals, Orexigen Therapeutics, PDL Biopharma, Pfizer, Procter and Gamble, Prometheus Laboratories, ProtAb Ltd, Purgenesis Technologies, Relypsa, Roche, Salient Pharmaceuticals, Salix Pharmaceuticals, Santarus, Schering Plough, Shire Pharmaceu-ticals, Sigmoid Pharma Ltd, Sirtris Pharmaceuticals, SLAPharma UK Ltd, Targacept, Teva Pharmaceuticals, Therakos, Tillotts Pharma AG, TxCell SA, UCB Pharma, ViametPharmaceuticals, Vascular Biogenics Ltd, Warner ChilcottUK Ltd, and Wyeth; WJS received research grants from Abbott, Bristol-Myers Squibb, Genentech, GlaxoSmithKline, Janssen, Milennium Pharmaceuticals, Novartis, Pfizer, Procter and Gamble, Shire Pharmaceuticals, and UCB Pharma; WJS received payments for lectures/speakers bureaux from Abbott, Bristol-Myers Squibb, and Janssen; and holds stock/stock optionsin Enteromedics. BGF has served as consultant for Abbott/AbbVie, Actogenix, Akros, Albireo Pharma, Amgen, Astra Zeneca, Avaxia Biologics, Avir Pharma, Axcan, Baxter Healthcare Corp., Biogen Idec, Boehringer-Ingelheim, Bristol-Myers Squibb, Calypso Biotech, Celgene, Elan/Biogen, EnGene, Ferring Pharma, Roche/Genentech, GiCare Pharma, Gilead, Given Imaging, GSK, Ironwood Pharma, Janssen Biotech (Centocor), JnJ/Janssen, Kyowa Kakko Kirin, Lexicon, Lilly, Lycera BioTech, Merck, Millennium, Nektar, Novonordisk, Pfizer, Prometheus Therapeutics and Diagnostics, Protagonist, Receptos, Salix Pharma, Serono, Shire, Sigmoid Pharma, Synergy Pharma, Takeda, Teva Pharma, TiGenix, Tillotts, UCB Pharma, Vertex Pharma, VHsquared, Warner-Chilcott, Wyeth, Zealand, Zyngenia. BGF received Research and Grant from Abbott/AbbVie, Amgen, Astra Zeneca, Bristol-Myers Squibb (BMS), Janssen Biotech (Centocor), JnJ/Janssen, Roche/Genentech, Millennium, Pfizer, Receptos, Santarus, Sanofi, Tillotts, UCB Pharma. BGF is speaker's bureau for Abbott/AbbVie, JnJ/Janssen, Takeda, Warner-Chilcott, UCB Pharma. BGF is Member or/and Scientific Advisory Board for Abbott/AbbVie, Amgen, Astra Zeneca, Avaxia Biologics, Bristol-Myers Squibb, Celgene, Centocor, Elan/Biogen, Ferring, JnJ/Janssen, Merck, Novartis, Novonordisk, Pfizer, Prometheus Laboratories, Protagonist, Salix Pharma, Takeda, Teva, TiGenix, Tillotts Pharma AG, UCB Pharma. Brian G Feagan is Board of Directors for Officer - Robarts Clinical Trials. JFC has served as consultant or advisory board member for Abbvie, ABScience, Amgen, Bristol Meyers Squibb, Celltrion, Danone, Ferring, Genentech, Giuliani SPA, Given Imaging, Janssen, Immune Pharmaceuticals, Medimmune, Merck and Co., Millenium Pharmaceuticals, Neovacs, Nutrition Science Partners, Pfizer, Prometheus Laboratories, Protagonist, Receptos, Sanofi, Schering Plough Corporation, Second Genome, Shire, Takeda, Teva Pharmaceuticals, Tigenix, UCB Pharma, Vertex, Dr August Wolff GmbH and Co. J-FC has served as speaker for Abbvie, Ferring, Janssen, Merck and Co., Nutrition Science Partners, Takeda. LP-B has served as consultant for Merck, Abbvie, Janssen, Genentech, Mitsubishi, Ferring, Norgine, Tillots, Vifor, Therakos, Pharmacosmos, Pilège, BMS, UCB-pharma, Hospira, Celltrion, Takeda, Biogaran, Boerhinger-Ingelheim, Lilly, Pfizer, HAC-Pharma, Index Pharmaceuticals. LP-B has served as speaker Lecture fees from Merck, Abbvie, Takeda, Janssen, Ferring, Norgine, Tillots, Vifor, Therakos, Mitsubishi, HAC-pharma.
Publisher Copyright:
© 2017, BMJ Publishing Group. All rights reserved.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Background: IBDs are chronic destructive disorders that negatively affect the functional status of patients. Recently, the Inflammatory Bowel Disease Disability Index (IBD-DI) was developed according to standard WHO processes. The aims of the current study were to validate the IBD-DI in an independent patient cohort, to develop an index-specific scoring system and to describe the disability status of a well-defined population-based cohort of French patients with IBD. Methods: From February 2012 to March 2014, the IBD-DI questionnaire was administered to a random sample of adult patients with an established diagnosis of IBD issued from a French population-based registry. The IBD-DI consists of 28 items that evaluate the four domains of body functions, activity participation, body structures and environmental factors. Validation included item reduction and data structure, construct validity, internal consistency, interobserver and intraobserver reliability evaluations. Results: 150 patients with Crohn's disease (CD) and 50 patients with UC completed the IBD-DI validation phase. The intraclass correlation coefficient for interobserver reliability was 0.91 and 0.54 for intraobserver reliability. Cronbach's α of internal consistency was 0.86. IBD-DI scores varied from 0 to 100 with a mean of 35.3 (Q1=19.6; Q3=51.8). IBD-DI scores were highly correlated with Inflammatory Bowel Disease Questionnaire (-0.82; p<0.001) and SF-36 (-0.61; p<0.05) scores. Female gender (p<0.001), clinical disease activity (p<0.0001) and disease duration (p=0.02) were associated with higher IBD-DI scores. Conclusions: The IBD-DI has been validated for use in clinical trials and epidemiological studies. The IBD-DI showed high internal consistency, interobserver reliability and construct validity, and a moderate intraobserver reliability. It comprises 14 questions and ranges from 0 to 100. The mean IBD-DI score was 35.3 and was associated with gender, clinical disease activity and disease duration. Further research is needed to confirm the structural validity and to assess the responsiveness of IBD-DI. Trial registration number: 2011-A00877-34.
AB - Background: IBDs are chronic destructive disorders that negatively affect the functional status of patients. Recently, the Inflammatory Bowel Disease Disability Index (IBD-DI) was developed according to standard WHO processes. The aims of the current study were to validate the IBD-DI in an independent patient cohort, to develop an index-specific scoring system and to describe the disability status of a well-defined population-based cohort of French patients with IBD. Methods: From February 2012 to March 2014, the IBD-DI questionnaire was administered to a random sample of adult patients with an established diagnosis of IBD issued from a French population-based registry. The IBD-DI consists of 28 items that evaluate the four domains of body functions, activity participation, body structures and environmental factors. Validation included item reduction and data structure, construct validity, internal consistency, interobserver and intraobserver reliability evaluations. Results: 150 patients with Crohn's disease (CD) and 50 patients with UC completed the IBD-DI validation phase. The intraclass correlation coefficient for interobserver reliability was 0.91 and 0.54 for intraobserver reliability. Cronbach's α of internal consistency was 0.86. IBD-DI scores varied from 0 to 100 with a mean of 35.3 (Q1=19.6; Q3=51.8). IBD-DI scores were highly correlated with Inflammatory Bowel Disease Questionnaire (-0.82; p<0.001) and SF-36 (-0.61; p<0.05) scores. Female gender (p<0.001), clinical disease activity (p<0.0001) and disease duration (p=0.02) were associated with higher IBD-DI scores. Conclusions: The IBD-DI has been validated for use in clinical trials and epidemiological studies. The IBD-DI showed high internal consistency, interobserver reliability and construct validity, and a moderate intraobserver reliability. It comprises 14 questions and ranges from 0 to 100. The mean IBD-DI score was 35.3 and was associated with gender, clinical disease activity and disease duration. Further research is needed to confirm the structural validity and to assess the responsiveness of IBD-DI. Trial registration number: 2011-A00877-34.
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U2 - 10.1136/gutjnl-2015-310151
DO - 10.1136/gutjnl-2015-310151
M3 - Article
C2 - 26646934
AN - SCOPUS:84954290045
SN - 0017-5749
VL - 66
SP - 588
EP - 596
JO - Gut
JF - Gut
IS - 4
ER -