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Optimising assessment of dark adaptation data using time to event analysis
In age-related macular degeneration (AMD) research, dark adaptation has been found to be a promising functional measurement. In more severe cases of AMD, dark adaptation cannot always be recorded within a maximum allowed time for the test (~ 20–30 min). These data are recorded either as censored dat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050245/ https://www.ncbi.nlm.nih.gov/pubmed/33859209 http://dx.doi.org/10.1038/s41598-021-86193-3 |
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author | Higgins, Bethany E. Montesano, Giovanni Binns, Alison M. Crabb, David P. |
author_facet | Higgins, Bethany E. Montesano, Giovanni Binns, Alison M. Crabb, David P. |
author_sort | Higgins, Bethany E. |
collection | PubMed |
description | In age-related macular degeneration (AMD) research, dark adaptation has been found to be a promising functional measurement. In more severe cases of AMD, dark adaptation cannot always be recorded within a maximum allowed time for the test (~ 20–30 min). These data are recorded either as censored data-points (data capped at the maximum test time) or as an estimated recovery time based on the trend observed from the data recorded within the maximum recording time. Therefore, dark adaptation data can have unusual attributes that may not be handled by standard statistical techniques. Here we show time-to-event analysis is a more powerful method for analysis of rod-intercept time data in measuring dark adaptation. For example, at 80% power (at α = 0.05) sample sizes were estimated to be 20 and 61 with uncapped (uncensored) and capped (censored) data using a standard t-test; these values improved to 12 and 38 when using the proposed time-to-event analysis. Our method can accommodate both skewed data and censored data points and offers the advantage of significantly reducing sample sizes when planning studies where this functional test is an outcome measure. The latter is important because designing trials and studies more efficiently equates to newer treatments likely being examined more efficiently. |
format | Online Article Text |
id | pubmed-8050245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80502452021-04-16 Optimising assessment of dark adaptation data using time to event analysis Higgins, Bethany E. Montesano, Giovanni Binns, Alison M. Crabb, David P. Sci Rep Article In age-related macular degeneration (AMD) research, dark adaptation has been found to be a promising functional measurement. In more severe cases of AMD, dark adaptation cannot always be recorded within a maximum allowed time for the test (~ 20–30 min). These data are recorded either as censored data-points (data capped at the maximum test time) or as an estimated recovery time based on the trend observed from the data recorded within the maximum recording time. Therefore, dark adaptation data can have unusual attributes that may not be handled by standard statistical techniques. Here we show time-to-event analysis is a more powerful method for analysis of rod-intercept time data in measuring dark adaptation. For example, at 80% power (at α = 0.05) sample sizes were estimated to be 20 and 61 with uncapped (uncensored) and capped (censored) data using a standard t-test; these values improved to 12 and 38 when using the proposed time-to-event analysis. Our method can accommodate both skewed data and censored data points and offers the advantage of significantly reducing sample sizes when planning studies where this functional test is an outcome measure. The latter is important because designing trials and studies more efficiently equates to newer treatments likely being examined more efficiently. Nature Publishing Group UK 2021-04-15 /pmc/articles/PMC8050245/ /pubmed/33859209 http://dx.doi.org/10.1038/s41598-021-86193-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Higgins, Bethany E. Montesano, Giovanni Binns, Alison M. Crabb, David P. Optimising assessment of dark adaptation data using time to event analysis |
title | Optimising assessment of dark adaptation data using time to event analysis |
title_full | Optimising assessment of dark adaptation data using time to event analysis |
title_fullStr | Optimising assessment of dark adaptation data using time to event analysis |
title_full_unstemmed | Optimising assessment of dark adaptation data using time to event analysis |
title_short | Optimising assessment of dark adaptation data using time to event analysis |
title_sort | optimising assessment of dark adaptation data using time to event analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050245/ https://www.ncbi.nlm.nih.gov/pubmed/33859209 http://dx.doi.org/10.1038/s41598-021-86193-3 |
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