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Effective dose 50 method as the minimal clinically important difference: Evidence from depression trials

OBJECTIVE: Previous research on the minimal clinically important difference (MCID) for depression and anxiety is based on population averages. The present study aimed to identify the MCID across the spectrum of baseline severity. STUDY DESIGN AND SETTINGS: The present analysis used secondary data fr...

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Autores principales: Bauer-Staeb, Clarissa, Kounali, Daphne-Zacharenia, Welton, Nicky J., Griffith, Emma, Wiles, Nicola J., Lewis, Glyn, Faraway, Julian J., Button, Katherine S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485844/
https://www.ncbi.nlm.nih.gov/pubmed/33892086
http://dx.doi.org/10.1016/j.jclinepi.2021.04.002
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author Bauer-Staeb, Clarissa
Kounali, Daphne-Zacharenia
Welton, Nicky J.
Griffith, Emma
Wiles, Nicola J.
Lewis, Glyn
Faraway, Julian J.
Button, Katherine S.
author_facet Bauer-Staeb, Clarissa
Kounali, Daphne-Zacharenia
Welton, Nicky J.
Griffith, Emma
Wiles, Nicola J.
Lewis, Glyn
Faraway, Julian J.
Button, Katherine S.
author_sort Bauer-Staeb, Clarissa
collection PubMed
description OBJECTIVE: Previous research on the minimal clinically important difference (MCID) for depression and anxiety is based on population averages. The present study aimed to identify the MCID across the spectrum of baseline severity. STUDY DESIGN AND SETTINGS: The present analysis used secondary data from 2 randomized controlled trials for depression (n = 1,122) to calibrate the Global Rating of Change with the PHQ–9 and GAD–7. The MCID was defined as a change in scores corresponding to a 50% probability of patients "feeling better", given their baseline severity, referred to as Effective Dose 50 (ED50). RESULTS: MCID estimates depended on baseline severity and ranged from no change for very mild up to 14 points (52%) on the PHQ–9 and up to 10 points (48%) on the GAD–7 for very high severity. The average MCID estimates were 3.7 points (23%) and 3.3 (28%) for the PHQ–9 and GAD–7 respectively. CONCLUSION: The ED50 method generates MCID estimates across the spectrum of baseline severity, offering greater precision but at the cost of greater complexity relative to population average estimates. This has important implications for evaluations of treatments and clinical practice where users can use these results to tailor the MCID to specific populations according to baseline severities.
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spelling pubmed-84858442021-10-06 Effective dose 50 method as the minimal clinically important difference: Evidence from depression trials Bauer-Staeb, Clarissa Kounali, Daphne-Zacharenia Welton, Nicky J. Griffith, Emma Wiles, Nicola J. Lewis, Glyn Faraway, Julian J. Button, Katherine S. J Clin Epidemiol Article OBJECTIVE: Previous research on the minimal clinically important difference (MCID) for depression and anxiety is based on population averages. The present study aimed to identify the MCID across the spectrum of baseline severity. STUDY DESIGN AND SETTINGS: The present analysis used secondary data from 2 randomized controlled trials for depression (n = 1,122) to calibrate the Global Rating of Change with the PHQ–9 and GAD–7. The MCID was defined as a change in scores corresponding to a 50% probability of patients "feeling better", given their baseline severity, referred to as Effective Dose 50 (ED50). RESULTS: MCID estimates depended on baseline severity and ranged from no change for very mild up to 14 points (52%) on the PHQ–9 and up to 10 points (48%) on the GAD–7 for very high severity. The average MCID estimates were 3.7 points (23%) and 3.3 (28%) for the PHQ–9 and GAD–7 respectively. CONCLUSION: The ED50 method generates MCID estimates across the spectrum of baseline severity, offering greater precision but at the cost of greater complexity relative to population average estimates. This has important implications for evaluations of treatments and clinical practice where users can use these results to tailor the MCID to specific populations according to baseline severities. Elsevier 2021-09 /pmc/articles/PMC8485844/ /pubmed/33892086 http://dx.doi.org/10.1016/j.jclinepi.2021.04.002 Text en © 2021 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bauer-Staeb, Clarissa
Kounali, Daphne-Zacharenia
Welton, Nicky J.
Griffith, Emma
Wiles, Nicola J.
Lewis, Glyn
Faraway, Julian J.
Button, Katherine S.
Effective dose 50 method as the minimal clinically important difference: Evidence from depression trials
title Effective dose 50 method as the minimal clinically important difference: Evidence from depression trials
title_full Effective dose 50 method as the minimal clinically important difference: Evidence from depression trials
title_fullStr Effective dose 50 method as the minimal clinically important difference: Evidence from depression trials
title_full_unstemmed Effective dose 50 method as the minimal clinically important difference: Evidence from depression trials
title_short Effective dose 50 method as the minimal clinically important difference: Evidence from depression trials
title_sort effective dose 50 method as the minimal clinically important difference: evidence from depression trials
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485844/
https://www.ncbi.nlm.nih.gov/pubmed/33892086
http://dx.doi.org/10.1016/j.jclinepi.2021.04.002
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