消费者对澳大利亚药物不良反应报告的知识和经验:一项全国调查
Mohammed Gebre Dedefo1, Renly Lim2, Gizat M Kassie2
1Quality Use of Medicines and Pharmacy Research Centre, UniSA Clinical and Health Sciences, University of South Australia, Adelaide, Australia. mohammed_gebre.dedefo@mymail.unisa.edu.au.
European journal of clinical pharmacology
|July 12, 2024
概括
许多澳大利亚人知道报告药物不良反应 (ADRs),但缺乏对数字工具的认识. 需要增加报告和数字工具的使用,以提高患者安全.
科学领域:
- 药物监督 药物监督 药物监督
- 消费者健康行为
- 数字健康数字健康
背景情况:
- 药物不良反应 (ADRs) 是一个重要的公共卫生问题.
- 有效的报告系统对于监测药物安全至关重要.
- 消费者参与ADR报告对于药物监督至关重要.
研究的目的:
- 评估澳大利亚消费者对ADR报告的知识和经验.
- 确定报告或不报告ADR的原因.
- 探索使用数字工具进行ADR报告.
主要方法:
- 对澳大利亚成年人服用药物的横截面在线调查.
- 结构化问卷评估消费者特征,知识和报告实践.
- 描述性统计和奇平方/费舍尔精确测试用于数据分析.
主要成果:
- 58%的消费者知道他们可以向当局或医疗保健专业人员报告副作用.
- 75%的受访者报告经历了ADR,但只有36%的人报告了它.
- 39%的人没有报告ADR,因为他们认为它们不够严重; 58%的人不知道数字报告工具.
结论:
- 虽然人们对ADR报告道的认识存在,但仍然存在重大差距.
- 需要改善消费者对数字报告工具的教育.
- 提高ADR报告率,特别是通过数字平台,对于药物安全至关重要.
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