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Japanese Physicians’ Views on Drug Post-Marketing Surveillance

BACKGROUND: Registration trials leading to the approval of drugs are paramount in drug development. After approval, continuous efforts are necessary to ensure proper use of the approved drugs. In Japan, post-marketing surveillance (PMS) by drug companies is conducted in accordance with good post-mar...

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Autores principales: Maeda, Kazuki, Katashima, Rumi, Ishizawa, Keisuke, Yanagawa, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625816/
https://www.ncbi.nlm.nih.gov/pubmed/26566409
http://dx.doi.org/10.14740/jocmr2328w
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author Maeda, Kazuki
Katashima, Rumi
Ishizawa, Keisuke
Yanagawa, Hiroaki
author_facet Maeda, Kazuki
Katashima, Rumi
Ishizawa, Keisuke
Yanagawa, Hiroaki
author_sort Maeda, Kazuki
collection PubMed
description BACKGROUND: Registration trials leading to the approval of drugs are paramount in drug development. After approval, continuous efforts are necessary to ensure proper use of the approved drugs. In Japan, post-marketing surveillance (PMS) by drug companies is conducted in accordance with good post-marketing study practice (GPSP). Although the global standard for pharmacovigilance is incorporated into GPSP, attention has recently been focused on disassociating them. In this study, we examined physicians’ views on PMS with the aim of conducting PMS more effectively. METHODS: We retrospectively reviewed records between 2009 and 2013 from the institutional review board of Tokushima University Hospital, an academic hospital in rural Japan. The annual number of times PMS was performed was then determined. Next, we assessed physicians’ attitudes toward drug PMS, including ethical issues, in a cross-sectional study using a questionnaire designed for this study. Five- and two-point scales were used. The questionnaire was distributed in 2014 to 221 physicians listed as investigators in PMS contracts. RESULTS: Of the 221 physicians, 103 (46.6%) responded to the questionnaire. About 50% of the respondents had experience writing PMS reports. Many of the physicians considered PMS to be important but burdensome. Furthermore, from the viewpoint of research ethics, many physicians considered it improper within the present PMS framework to collect and provide data beyond the scope of routine clinical practice without obtaining informed consent in the case of extra blood sampling, provision of images, monitoring and controlled studies. CONCLUSIONS: Beyond practical factors such as workload, attention should be given to establishing an ethical infrastructure and globally harmonized system with regard to the Japanese PMS system. Given the limitations of this single-institution study, further research is needed to collect information for developing a suitable infrastructure.
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spelling pubmed-46258162015-11-12 Japanese Physicians’ Views on Drug Post-Marketing Surveillance Maeda, Kazuki Katashima, Rumi Ishizawa, Keisuke Yanagawa, Hiroaki J Clin Med Res Original Article BACKGROUND: Registration trials leading to the approval of drugs are paramount in drug development. After approval, continuous efforts are necessary to ensure proper use of the approved drugs. In Japan, post-marketing surveillance (PMS) by drug companies is conducted in accordance with good post-marketing study practice (GPSP). Although the global standard for pharmacovigilance is incorporated into GPSP, attention has recently been focused on disassociating them. In this study, we examined physicians’ views on PMS with the aim of conducting PMS more effectively. METHODS: We retrospectively reviewed records between 2009 and 2013 from the institutional review board of Tokushima University Hospital, an academic hospital in rural Japan. The annual number of times PMS was performed was then determined. Next, we assessed physicians’ attitudes toward drug PMS, including ethical issues, in a cross-sectional study using a questionnaire designed for this study. Five- and two-point scales were used. The questionnaire was distributed in 2014 to 221 physicians listed as investigators in PMS contracts. RESULTS: Of the 221 physicians, 103 (46.6%) responded to the questionnaire. About 50% of the respondents had experience writing PMS reports. Many of the physicians considered PMS to be important but burdensome. Furthermore, from the viewpoint of research ethics, many physicians considered it improper within the present PMS framework to collect and provide data beyond the scope of routine clinical practice without obtaining informed consent in the case of extra blood sampling, provision of images, monitoring and controlled studies. CONCLUSIONS: Beyond practical factors such as workload, attention should be given to establishing an ethical infrastructure and globally harmonized system with regard to the Japanese PMS system. Given the limitations of this single-institution study, further research is needed to collect information for developing a suitable infrastructure. Elmer Press 2015-12 2015-10-23 /pmc/articles/PMC4625816/ /pubmed/26566409 http://dx.doi.org/10.14740/jocmr2328w Text en Copyright 2015, Maeda et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Maeda, Kazuki
Katashima, Rumi
Ishizawa, Keisuke
Yanagawa, Hiroaki
Japanese Physicians’ Views on Drug Post-Marketing Surveillance
title Japanese Physicians’ Views on Drug Post-Marketing Surveillance
title_full Japanese Physicians’ Views on Drug Post-Marketing Surveillance
title_fullStr Japanese Physicians’ Views on Drug Post-Marketing Surveillance
title_full_unstemmed Japanese Physicians’ Views on Drug Post-Marketing Surveillance
title_short Japanese Physicians’ Views on Drug Post-Marketing Surveillance
title_sort japanese physicians’ views on drug post-marketing surveillance
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625816/
https://www.ncbi.nlm.nih.gov/pubmed/26566409
http://dx.doi.org/10.14740/jocmr2328w
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