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Transformation of Rasch model logits for enhanced interpretability

BACKGROUND: The Rasch model allows for linear measurement based on ordinal item responses from rating scales commonly used to assess health outcomes. Such linear measures may be inconvenient since they are expressed as log-odds units (logits) that differ from scores that users may be familiar with....

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Autores principales: Ekstrand, Joakim, Westergren, Albert, Årestedt, Kristofer, Hellström, Amanda, Hagell, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9783398/
https://www.ncbi.nlm.nih.gov/pubmed/36564722
http://dx.doi.org/10.1186/s12874-022-01816-1
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author Ekstrand, Joakim
Westergren, Albert
Årestedt, Kristofer
Hellström, Amanda
Hagell, Peter
author_facet Ekstrand, Joakim
Westergren, Albert
Årestedt, Kristofer
Hellström, Amanda
Hagell, Peter
author_sort Ekstrand, Joakim
collection PubMed
description BACKGROUND: The Rasch model allows for linear measurement based on ordinal item responses from rating scales commonly used to assess health outcomes. Such linear measures may be inconvenient since they are expressed as log-odds units (logits) that differ from scores that users may be familiar with. It can therefore be desirable to transform logits into more user-friendly ranges that preserve their linear properties. In addition to user-defined ranges, three general transformations have been described in the literature: the least measurable difference (LMD), the standard error of measurement (SEM) and the least significant difference (LSD). The LMD represents the smallest possible meaningful unit, SEM relates the transformed scale values to measurement uncertainty (one unit on the transformed scale represents roughly one standard error), and LSD represents a lower bound for how coarse the transformed scale can be without loss of valid information. However, while logit transformations are relatively common in the health sciences, use of LMD, SEM and LSD transformations appear to be uncommon despite their potential role. METHODS: Logit transformations were empirically illustrated based on 1053 responses to the Epworth Sleepiness Scale. Logit measures were transformed according to the LMD, SEM and LSD, and into 0–10, 0-100, and the original raw score (0–24) ranges. These transformations were conducted using a freely available Excel tool, developed by the authors, that transforms logits into user-defined ranges along with the LMD, SEM and LSD transformations. RESULTS: Resulting LMD, SEM and LSD transformations ranged 0-34, 0-17 and 0-12, respectively. When considering these relative to the three user-defined ranges, it is seen that the 0-10 range is narrower than the LSD range (i.e., loss of valid information), and a 0-100 range gives the impression of better precision than there is, since it is considerably wider than the LMD range. However, the 0-24 transformation appears reasonable since it is wider than the LSD, but narrower than the LMD ranges. CONCLUSIONS: It is suggested that LMD, SEM and LSD transformations are valuable for benchmarking in deciding appropriate ranges when transforming logit measures. This process can be aided by the Excel tool presented and illustrated in this paper. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-022-01816-1.
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spelling pubmed-97833982022-12-24 Transformation of Rasch model logits for enhanced interpretability Ekstrand, Joakim Westergren, Albert Årestedt, Kristofer Hellström, Amanda Hagell, Peter BMC Med Res Methodol Research BACKGROUND: The Rasch model allows for linear measurement based on ordinal item responses from rating scales commonly used to assess health outcomes. Such linear measures may be inconvenient since they are expressed as log-odds units (logits) that differ from scores that users may be familiar with. It can therefore be desirable to transform logits into more user-friendly ranges that preserve their linear properties. In addition to user-defined ranges, three general transformations have been described in the literature: the least measurable difference (LMD), the standard error of measurement (SEM) and the least significant difference (LSD). The LMD represents the smallest possible meaningful unit, SEM relates the transformed scale values to measurement uncertainty (one unit on the transformed scale represents roughly one standard error), and LSD represents a lower bound for how coarse the transformed scale can be without loss of valid information. However, while logit transformations are relatively common in the health sciences, use of LMD, SEM and LSD transformations appear to be uncommon despite their potential role. METHODS: Logit transformations were empirically illustrated based on 1053 responses to the Epworth Sleepiness Scale. Logit measures were transformed according to the LMD, SEM and LSD, and into 0–10, 0-100, and the original raw score (0–24) ranges. These transformations were conducted using a freely available Excel tool, developed by the authors, that transforms logits into user-defined ranges along with the LMD, SEM and LSD transformations. RESULTS: Resulting LMD, SEM and LSD transformations ranged 0-34, 0-17 and 0-12, respectively. When considering these relative to the three user-defined ranges, it is seen that the 0-10 range is narrower than the LSD range (i.e., loss of valid information), and a 0-100 range gives the impression of better precision than there is, since it is considerably wider than the LMD range. However, the 0-24 transformation appears reasonable since it is wider than the LSD, but narrower than the LMD ranges. CONCLUSIONS: It is suggested that LMD, SEM and LSD transformations are valuable for benchmarking in deciding appropriate ranges when transforming logit measures. This process can be aided by the Excel tool presented and illustrated in this paper. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-022-01816-1. BioMed Central 2022-12-23 /pmc/articles/PMC9783398/ /pubmed/36564722 http://dx.doi.org/10.1186/s12874-022-01816-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ekstrand, Joakim
Westergren, Albert
Årestedt, Kristofer
Hellström, Amanda
Hagell, Peter
Transformation of Rasch model logits for enhanced interpretability
title Transformation of Rasch model logits for enhanced interpretability
title_full Transformation of Rasch model logits for enhanced interpretability
title_fullStr Transformation of Rasch model logits for enhanced interpretability
title_full_unstemmed Transformation of Rasch model logits for enhanced interpretability
title_short Transformation of Rasch model logits for enhanced interpretability
title_sort transformation of rasch model logits for enhanced interpretability
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9783398/
https://www.ncbi.nlm.nih.gov/pubmed/36564722
http://dx.doi.org/10.1186/s12874-022-01816-1
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