日本宫城县和北海道地区药师药物不良反应发生率、影响因素及未报告原因

T. Obara, Hiroaki Yamaguchi, M. Satoh, Y. Iida, T. Sakai, Y. Aoki, Yuriko Murai, Masaki Matsuura, Mayumi Sato, T. Ohkubo, K. Iseki, N. Mano
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引用次数: 15

摘要

日本药剂师对药物不良反应(ADR)未报告的可能性知之甚少。本研究的目的是阐明日本宫城县和北海道地区药师未报告药品不良反应的患病率、决定因素和原因。在这项横断面、自我填写问卷的研究中,我们在2013年1月至3月的3个月内联系了宫城县医院药剂师协会或北海道医院药剂师协会的3164名药剂师。1795名被调查者中,年龄<30岁的占22.4%,≥50岁的占25.6%,女性占42.1%。77.6%的受访者没有个人不良反应报告史。多因素logistic回归分析显示,女性(优势比,1.52;95%置信区间,1.17-1.97),实践经验<10年(2.59,5-9年为1.39-4.82;<5年者(7.03,2.94 ~ 16.83)、在社区药房或药店工作(1.90,1.16 ~ 3.12)、工作场所药师人数<5人(2.01,1.48 ~ 2.75)、不了解ADR报告制度(5.93,4.23 ~ 8.33)与没有个人ADR报告史存在显著独立相关。未报告不良反应最常见的原因是“已知不良反应”(43.0%),其次是“药物与不良反应的关系不清楚”(38.0%)、“轻微不良反应”(29.0%)、“不知道如何报告”(17.4%)、“从未咨询过不良反应”(17.2%)。由于了解ADR报告系统与ADR报告密切相关,因此有必要在药剂师中更积极地推广ADR报告系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence, Determinants, and Reasons for the Non-Reporting of Adverse Drug Reactions by Pharmacists in the Miyagi and Hokkaido Regions of Japan
Little is known about the potential of adverse drug reaction (ADR) non-reporting by Japanese pharmacists. The aim of the present study was to clarify the prevalence, determinants, and reasons for ADR non-reporting by pharmacists in the Miyagi and Hokkaido regions of Japan. In this cross-sectional, self-administered questionnaire-based study, we contacted 3,164 pharmacists who belonged to the Miyagi Prefecture Hospital Pharmacists Association or the Hokkaido Society of Hospital Pharmacists during the 3-month period between January to March 2013. Of the 1,795 respondents 22.4% were <30 years of age, 25.6% were ≥ 50 years of age, and 42.1% were female. A total of 77.6% of the respondents did not have a personal history of ADR reporting. The multivariate logistic regression analysis showed that female sex (odds ratio, 1.52; 95% confidence interval, 1.17-1.97), having <10 years of practical experience (2.59, 1.39-4.82 for 5-9 years; 7.03, 2.94-16.83 for <5 years), working at a community pharmacy or drugstore (1.90, 1.16-3.12), having <5 pharmacists in the workplace (2.01, 1.48-2.75), and not understanding the ADR reporting system (5.93, 4.23-8.33) were significantly and independently associated with not having a personal history of ADR reporting. The most common reason for ADR non-reporting was “It was a well-known adverse drug reaction” (43.0%) followed by “Association between the drug and adverse reaction was not clear” (38.0%), “It was a minor adverse drug reaction” (29.0%), “Did not know how to make a report” (17.4%), and “Never been consulted about ADRs” (17.2%). As an understanding the ADR reporting system was strongly associated with ADR reporting, a more aggressive promotion of the ADR reporting system among pharmacists is warranted.
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