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A multilevel structural equation model for assessing a drug effect on a patient‐reported outcome measure in on‐demand medication data

We analyze data from a clinical trial investigating the effect of an on‐demand drug for women with low sexual desire. These data consist of a varying number of measurements/events across patients of when the drug was taken, including data on a patient‐reported outcome consisting of five items measur...

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Autores principales: Kessels, Rob, Moerbeek, Mirjam, Bloemers, Jos, van der Heijden, Peter G.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292391/
https://www.ncbi.nlm.nih.gov/pubmed/34270801
http://dx.doi.org/10.1002/bimj.202100046
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author Kessels, Rob
Moerbeek, Mirjam
Bloemers, Jos
van der Heijden, Peter G.M.
author_facet Kessels, Rob
Moerbeek, Mirjam
Bloemers, Jos
van der Heijden, Peter G.M.
author_sort Kessels, Rob
collection PubMed
description We analyze data from a clinical trial investigating the effect of an on‐demand drug for women with low sexual desire. These data consist of a varying number of measurements/events across patients of when the drug was taken, including data on a patient‐reported outcome consisting of five items measuring an unobserved construct (latent variable). Traditionally, these data are aggregated prior to analysis by composing one sum score per event and averaging this sum score over all observed events. In this paper, we explain the drawbacks of this aggregating approach. One drawback is that these averages have different standard errors because the variance of the underlying events differs between patients and because the number of events per patient differs. Another drawback is the implicit assumption that all items have equal weight in relation to the latent variable being measured. We propose a multilevel structural equation model, treating the events (level 1) as nested observations within patients (level 2), as alternative analysis method to overcome these drawbacks. The model we apply includes a factor model measuring a latent variable at the level of the event and at the level of the patient. Then, in the same model, the latent variables are regressed on covariates to assess the drug effect. We discuss the inferences obtained about the efficacy of the on‐demand drug using our proposed model. We further illustrate how to test for measurement invariance across grouping covariates and levels using the same model.
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spelling pubmed-92923912022-07-20 A multilevel structural equation model for assessing a drug effect on a patient‐reported outcome measure in on‐demand medication data Kessels, Rob Moerbeek, Mirjam Bloemers, Jos van der Heijden, Peter G.M. Biom J Study Design and Methodology We analyze data from a clinical trial investigating the effect of an on‐demand drug for women with low sexual desire. These data consist of a varying number of measurements/events across patients of when the drug was taken, including data on a patient‐reported outcome consisting of five items measuring an unobserved construct (latent variable). Traditionally, these data are aggregated prior to analysis by composing one sum score per event and averaging this sum score over all observed events. In this paper, we explain the drawbacks of this aggregating approach. One drawback is that these averages have different standard errors because the variance of the underlying events differs between patients and because the number of events per patient differs. Another drawback is the implicit assumption that all items have equal weight in relation to the latent variable being measured. We propose a multilevel structural equation model, treating the events (level 1) as nested observations within patients (level 2), as alternative analysis method to overcome these drawbacks. The model we apply includes a factor model measuring a latent variable at the level of the event and at the level of the patient. Then, in the same model, the latent variables are regressed on covariates to assess the drug effect. We discuss the inferences obtained about the efficacy of the on‐demand drug using our proposed model. We further illustrate how to test for measurement invariance across grouping covariates and levels using the same model. John Wiley and Sons Inc. 2021-07-16 2021-12 /pmc/articles/PMC9292391/ /pubmed/34270801 http://dx.doi.org/10.1002/bimj.202100046 Text en © 2021 The Authors. Biometrical Journal published by Wiley‐VCH GmbH. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Study Design and Methodology
Kessels, Rob
Moerbeek, Mirjam
Bloemers, Jos
van der Heijden, Peter G.M.
A multilevel structural equation model for assessing a drug effect on a patient‐reported outcome measure in on‐demand medication data
title A multilevel structural equation model for assessing a drug effect on a patient‐reported outcome measure in on‐demand medication data
title_full A multilevel structural equation model for assessing a drug effect on a patient‐reported outcome measure in on‐demand medication data
title_fullStr A multilevel structural equation model for assessing a drug effect on a patient‐reported outcome measure in on‐demand medication data
title_full_unstemmed A multilevel structural equation model for assessing a drug effect on a patient‐reported outcome measure in on‐demand medication data
title_short A multilevel structural equation model for assessing a drug effect on a patient‐reported outcome measure in on‐demand medication data
title_sort multilevel structural equation model for assessing a drug effect on a patient‐reported outcome measure in on‐demand medication data
topic Study Design and Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292391/
https://www.ncbi.nlm.nih.gov/pubmed/34270801
http://dx.doi.org/10.1002/bimj.202100046
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