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Standardized method to assess medicines’ acceptability: focus on paediatric population
OBJECTIVES: The purpose of this article was to present an original standardized tool assessing the medicine's acceptability whichever their characteristics and the patient features. METHODS: An acceptability map was built with objective measures from medicine use assessments collected in real‐l...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396311/ https://www.ncbi.nlm.nih.gov/pubmed/27109018 http://dx.doi.org/10.1111/jphp.12547 |
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author | Ruiz, Fabrice Vallet, Thibault Pensé‐Lhéritier, Anne‐Marie Aoussat, Ameziane |
author_facet | Ruiz, Fabrice Vallet, Thibault Pensé‐Lhéritier, Anne‐Marie Aoussat, Ameziane |
author_sort | Ruiz, Fabrice |
collection | PubMed |
description | OBJECTIVES: The purpose of this article was to present an original standardized tool assessing the medicine's acceptability whichever their characteristics and the patient features. METHODS: An acceptability map was built with objective measures from medicine use assessments collected in real‐life conditions. Multiple correspondence analysis (MCA) was used for the mapping process. Hierarchical classification on the principal components (HCPC) of the MCA was performed for the clustering process corresponding to distinct acceptability profiles. KEY FINDINGS: The results presented here focus on 234 evaluations issued from the paediatric population and gathered in four clusters: ‘well‐accepted’ (50%), ‘accepted’ (19%), ‘poorly accepted’ (25%) and ‘not accepted’ medicines (6%). The first one was characterized by a dose fully taken, in a short time, with a patient's positive reaction; the second by a longer administration time, a neutral reaction and the use of methods to achieve administration (reward, divided dose). Differentiation between the two last clusters was, respectively, originated by a required dose partially taken or not taken. CONCLUSIONS: The acceptability profile of each medicine can be evaluated with the map position of the related patient's assessments barycentre. This tool should satisfy expectations in terms of methods for appropriate acceptability evaluation and standardized comparison among medicines. |
format | Online Article Text |
id | pubmed-5396311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53963112017-04-25 Standardized method to assess medicines’ acceptability: focus on paediatric population Ruiz, Fabrice Vallet, Thibault Pensé‐Lhéritier, Anne‐Marie Aoussat, Ameziane J Pharm Pharmacol Research Papers OBJECTIVES: The purpose of this article was to present an original standardized tool assessing the medicine's acceptability whichever their characteristics and the patient features. METHODS: An acceptability map was built with objective measures from medicine use assessments collected in real‐life conditions. Multiple correspondence analysis (MCA) was used for the mapping process. Hierarchical classification on the principal components (HCPC) of the MCA was performed for the clustering process corresponding to distinct acceptability profiles. KEY FINDINGS: The results presented here focus on 234 evaluations issued from the paediatric population and gathered in four clusters: ‘well‐accepted’ (50%), ‘accepted’ (19%), ‘poorly accepted’ (25%) and ‘not accepted’ medicines (6%). The first one was characterized by a dose fully taken, in a short time, with a patient's positive reaction; the second by a longer administration time, a neutral reaction and the use of methods to achieve administration (reward, divided dose). Differentiation between the two last clusters was, respectively, originated by a required dose partially taken or not taken. CONCLUSIONS: The acceptability profile of each medicine can be evaluated with the map position of the related patient's assessments barycentre. This tool should satisfy expectations in terms of methods for appropriate acceptability evaluation and standardized comparison among medicines. John Wiley and Sons Inc. 2016-04-25 2017-04 /pmc/articles/PMC5396311/ /pubmed/27109018 http://dx.doi.org/10.1111/jphp.12547 Text en © 2016 The Authors. Journal of Pharmacy and Pharmacology published by John Wiley & Sons Ltd on behalf of Royal Pharmaceutical Society This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Papers Ruiz, Fabrice Vallet, Thibault Pensé‐Lhéritier, Anne‐Marie Aoussat, Ameziane Standardized method to assess medicines’ acceptability: focus on paediatric population |
title | Standardized method to assess medicines’ acceptability: focus on paediatric population |
title_full | Standardized method to assess medicines’ acceptability: focus on paediatric population |
title_fullStr | Standardized method to assess medicines’ acceptability: focus on paediatric population |
title_full_unstemmed | Standardized method to assess medicines’ acceptability: focus on paediatric population |
title_short | Standardized method to assess medicines’ acceptability: focus on paediatric population |
title_sort | standardized method to assess medicines’ acceptability: focus on paediatric population |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396311/ https://www.ncbi.nlm.nih.gov/pubmed/27109018 http://dx.doi.org/10.1111/jphp.12547 |
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