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Minimal clinically important difference on the Beck Depression Inventory - II according to the patient's perspective

BACKGROUND: The Beck Depression Inventory, 2nd edition (BDI-II) is widely used in research on depression. However, the minimal clinically important difference (MCID) is unknown. MCID can be estimated in several ways. Here we take a patient-centred approach, anchoring the change on the BDI-II to the...

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Autores principales: Button, K. S., Kounali, D., Thomas, L., Wiles, N. J., Peters, T. J., Welton, N. J., Ades, A. E., Lewis, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611356/
https://www.ncbi.nlm.nih.gov/pubmed/26165748
http://dx.doi.org/10.1017/S0033291715001270
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author Button, K. S.
Kounali, D.
Thomas, L.
Wiles, N. J.
Peters, T. J.
Welton, N. J.
Ades, A. E.
Lewis, G.
author_facet Button, K. S.
Kounali, D.
Thomas, L.
Wiles, N. J.
Peters, T. J.
Welton, N. J.
Ades, A. E.
Lewis, G.
author_sort Button, K. S.
collection PubMed
description BACKGROUND: The Beck Depression Inventory, 2nd edition (BDI-II) is widely used in research on depression. However, the minimal clinically important difference (MCID) is unknown. MCID can be estimated in several ways. Here we take a patient-centred approach, anchoring the change on the BDI-II to the patient's global report of improvement. METHOD: We used data collected (n = 1039) from three randomized controlled trials for the management of depression. Improvement on a ‘global rating of change’ question was compared with changes in BDI-II scores using general linear modelling to explore baseline dependency, assessing whether MCID is best measured in absolute terms (i.e. difference) or as percent reduction in scores from baseline (i.e. ratio), and receiver operator characteristics (ROC) to estimate MCID according to the optimal threshold above which individuals report feeling ‘better’. RESULTS: Improvement in BDI-II scores associated with reporting feeling ‘better’ depended on initial depression severity, and statistical modelling indicated that MCID is best measured on a ratio scale as a percentage reduction of score. We estimated a MCID of a 17.5% reduction in scores from baseline from ROC analyses. The corresponding estimate for individuals with longer duration depression who had not responded to antidepressants was higher at 32%. CONCLUSIONS: MCID on the BDI-II is dependent on baseline severity, is best measured on a ratio scale, and the MCID for treatment-resistant depression is larger than that for more typical depression. This has important implications for clinical trials and practice.
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spelling pubmed-46113562015-10-22 Minimal clinically important difference on the Beck Depression Inventory - II according to the patient's perspective Button, K. S. Kounali, D. Thomas, L. Wiles, N. J. Peters, T. J. Welton, N. J. Ades, A. E. Lewis, G. Psychol Med Original Articles BACKGROUND: The Beck Depression Inventory, 2nd edition (BDI-II) is widely used in research on depression. However, the minimal clinically important difference (MCID) is unknown. MCID can be estimated in several ways. Here we take a patient-centred approach, anchoring the change on the BDI-II to the patient's global report of improvement. METHOD: We used data collected (n = 1039) from three randomized controlled trials for the management of depression. Improvement on a ‘global rating of change’ question was compared with changes in BDI-II scores using general linear modelling to explore baseline dependency, assessing whether MCID is best measured in absolute terms (i.e. difference) or as percent reduction in scores from baseline (i.e. ratio), and receiver operator characteristics (ROC) to estimate MCID according to the optimal threshold above which individuals report feeling ‘better’. RESULTS: Improvement in BDI-II scores associated with reporting feeling ‘better’ depended on initial depression severity, and statistical modelling indicated that MCID is best measured on a ratio scale as a percentage reduction of score. We estimated a MCID of a 17.5% reduction in scores from baseline from ROC analyses. The corresponding estimate for individuals with longer duration depression who had not responded to antidepressants was higher at 32%. CONCLUSIONS: MCID on the BDI-II is dependent on baseline severity, is best measured on a ratio scale, and the MCID for treatment-resistant depression is larger than that for more typical depression. This has important implications for clinical trials and practice. Cambridge University Press 2015-11 2015-07-13 /pmc/articles/PMC4611356/ /pubmed/26165748 http://dx.doi.org/10.1017/S0033291715001270 Text en © Cambridge University Press 2015 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Button, K. S.
Kounali, D.
Thomas, L.
Wiles, N. J.
Peters, T. J.
Welton, N. J.
Ades, A. E.
Lewis, G.
Minimal clinically important difference on the Beck Depression Inventory - II according to the patient's perspective
title Minimal clinically important difference on the Beck Depression Inventory - II according to the patient's perspective
title_full Minimal clinically important difference on the Beck Depression Inventory - II according to the patient's perspective
title_fullStr Minimal clinically important difference on the Beck Depression Inventory - II according to the patient's perspective
title_full_unstemmed Minimal clinically important difference on the Beck Depression Inventory - II according to the patient's perspective
title_short Minimal clinically important difference on the Beck Depression Inventory - II according to the patient's perspective
title_sort minimal clinically important difference on the beck depression inventory - ii according to the patient's perspective
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611356/
https://www.ncbi.nlm.nih.gov/pubmed/26165748
http://dx.doi.org/10.1017/S0033291715001270
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