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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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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. |
format | Online Article Text |
id | pubmed-8485844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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