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Sensory evaluation of edoxaban orally disintegrating tablets: an open-label interventional study (secondary publication)

BACKGROUND: This study involved a sensory evaluation of edoxaban orally disintegrating (OD) tablets in patients with nonvalvular atrial fibrillation who had been receiving the existing edoxaban film-coated tablets before the study. METHODS: Edoxaban OD tablets 30 or 60 mg were prescribed for patient...

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Autores principales: Yamashita, Takeshi, Hagii, Joji, Morishima, Yoshiyuki, Akasaka, Takaaki, Matsumoto, Takuyuki, Kimura, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376672/
https://www.ncbi.nlm.nih.gov/pubmed/30814914
http://dx.doi.org/10.1186/s12959-019-0192-x
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author Yamashita, Takeshi
Hagii, Joji
Morishima, Yoshiyuki
Akasaka, Takaaki
Matsumoto, Takuyuki
Kimura, Tetsuya
author_facet Yamashita, Takeshi
Hagii, Joji
Morishima, Yoshiyuki
Akasaka, Takaaki
Matsumoto, Takuyuki
Kimura, Tetsuya
author_sort Yamashita, Takeshi
collection PubMed
description BACKGROUND: This study involved a sensory evaluation of edoxaban orally disintegrating (OD) tablets in patients with nonvalvular atrial fibrillation who had been receiving the existing edoxaban film-coated tablets before the study. METHODS: Edoxaban OD tablets 30 or 60 mg were prescribed for patients who had been receiving the existing 30- or 60-mg edoxaban film-coated tablets before the study. Each dose group was randomized into groups taking the tablets with or without water. After ingestion of the edoxaban OD tablet, each patient was asked to complete a sensory evaluation questionnaire (12 items). RESULTS: In the evaluation of satisfaction with edoxaban OD tablets, 52.8% of the patients perceived “no difference” from the existing edoxaban film-coated tablets and 34.9% indicated that they were more satisfied with the OD tablets, thus demonstrating a relatively high degree of satisfaction. When asked about convenience and reliability in using edoxaban OD tablets, about half of the patients perceived “no difference” from the existing edoxaban film-coated tablets and the remaining half indicated preference for the OD tablets. Responses about taste, flavor, ease of ingestion, and motivation to continue taking edoxaban indicated the overall acceptance of the OD tablets. Recognition of edoxaban OD tablets was rated as “easy” by about half of the patients and “difficult” by the remaining half. Among all patients, 49.5% preferred a change to edoxaban OD tablets. The degree of satisfaction with taste, flavor, and ease of ingestion, as well as overall satisfaction, tended to be greater when the OD tablets were taken with rather than without water, and the percentage of patients who preferred a change was higher in the group taking the OD tablets with water. CONCLUSIONS: This study indicated that the degree of satisfaction with taste, flavor, ease of ingestion, and convenience, as well as overall satisfaction, in addition to motivation to continue drug intake and sense of confidence were greater for OD tablets than for the existing edoxaban film-coated tablets. Edoxaban OD tablet is a promising formulation for inducing greater patient adherence to medication and therefore ensures better treatment response. TRIAL REGISTRATION: UMIN-CTR UMIN000028788, registered 23-Aug-2017. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12959-019-0192-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-63766722019-02-27 Sensory evaluation of edoxaban orally disintegrating tablets: an open-label interventional study (secondary publication) Yamashita, Takeshi Hagii, Joji Morishima, Yoshiyuki Akasaka, Takaaki Matsumoto, Takuyuki Kimura, Tetsuya Thromb J Research BACKGROUND: This study involved a sensory evaluation of edoxaban orally disintegrating (OD) tablets in patients with nonvalvular atrial fibrillation who had been receiving the existing edoxaban film-coated tablets before the study. METHODS: Edoxaban OD tablets 30 or 60 mg were prescribed for patients who had been receiving the existing 30- or 60-mg edoxaban film-coated tablets before the study. Each dose group was randomized into groups taking the tablets with or without water. After ingestion of the edoxaban OD tablet, each patient was asked to complete a sensory evaluation questionnaire (12 items). RESULTS: In the evaluation of satisfaction with edoxaban OD tablets, 52.8% of the patients perceived “no difference” from the existing edoxaban film-coated tablets and 34.9% indicated that they were more satisfied with the OD tablets, thus demonstrating a relatively high degree of satisfaction. When asked about convenience and reliability in using edoxaban OD tablets, about half of the patients perceived “no difference” from the existing edoxaban film-coated tablets and the remaining half indicated preference for the OD tablets. Responses about taste, flavor, ease of ingestion, and motivation to continue taking edoxaban indicated the overall acceptance of the OD tablets. Recognition of edoxaban OD tablets was rated as “easy” by about half of the patients and “difficult” by the remaining half. Among all patients, 49.5% preferred a change to edoxaban OD tablets. The degree of satisfaction with taste, flavor, and ease of ingestion, as well as overall satisfaction, tended to be greater when the OD tablets were taken with rather than without water, and the percentage of patients who preferred a change was higher in the group taking the OD tablets with water. CONCLUSIONS: This study indicated that the degree of satisfaction with taste, flavor, ease of ingestion, and convenience, as well as overall satisfaction, in addition to motivation to continue drug intake and sense of confidence were greater for OD tablets than for the existing edoxaban film-coated tablets. Edoxaban OD tablet is a promising formulation for inducing greater patient adherence to medication and therefore ensures better treatment response. TRIAL REGISTRATION: UMIN-CTR UMIN000028788, registered 23-Aug-2017. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12959-019-0192-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-15 /pmc/articles/PMC6376672/ /pubmed/30814914 http://dx.doi.org/10.1186/s12959-019-0192-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Yamashita, Takeshi
Hagii, Joji
Morishima, Yoshiyuki
Akasaka, Takaaki
Matsumoto, Takuyuki
Kimura, Tetsuya
Sensory evaluation of edoxaban orally disintegrating tablets: an open-label interventional study (secondary publication)
title Sensory evaluation of edoxaban orally disintegrating tablets: an open-label interventional study (secondary publication)
title_full Sensory evaluation of edoxaban orally disintegrating tablets: an open-label interventional study (secondary publication)
title_fullStr Sensory evaluation of edoxaban orally disintegrating tablets: an open-label interventional study (secondary publication)
title_full_unstemmed Sensory evaluation of edoxaban orally disintegrating tablets: an open-label interventional study (secondary publication)
title_short Sensory evaluation of edoxaban orally disintegrating tablets: an open-label interventional study (secondary publication)
title_sort sensory evaluation of edoxaban orally disintegrating tablets: an open-label interventional study (secondary publication)
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376672/
https://www.ncbi.nlm.nih.gov/pubmed/30814914
http://dx.doi.org/10.1186/s12959-019-0192-x
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