数字技术在药物不良反应管理中的应用:图书统计学分析
Olena Litvinova1,2, Andy Wai Kan Yeung2,3, Fabian Peter Hammerle2,4
1Department of Management and Quality Assurance in Pharmacy, National University of Pharmacy of the Ministry of Health of Ukraine, 61002 Kharkiv, Ukraine.
Pharmaceuticals (Basel, Switzerland)
|March 28, 2024
概括
数字技术越来越多地用于预防药物不良反应,提高药物治疗的安全性. 这一趋势显示出全球越来越多的努力,特别是来自美国和中国,通过创新来提高药物安全.
科学领域:
- 药理学和制药科学 药理学和制药科学
- 医疗信息学 医疗信息学
- 图书统计学 图书统计学
背景情况:
- 药物不良反应 (ADRs) 带来了重大的临床和社会挑战.
- 有效管理ADR对于患者安全和医疗保健质量至关重要.
研究的目的:
- 为ADR预防进行数字技术的文献计量分析.
- 概述这些技术在改善药物治疗安全方面的应用.
主要方法:
- 使用科学网数据库对1991-2023年出版物的图书统计分析.
- 使用VOSviewer软件进行关键词可视化,以识别研究集群.
- 分析出版趋势和领先的国家/机构.
主要成果:
- 在ADR管理的数字技术出版物中观察到积极的趋势.
- 美国,中国,英国,印度和德国是主要贡献者 (72%的出版物).
- 确定了四个主要研究集群:临床前研究,临床试验,药物监测和减少患者生活质量的ADR.
结论:
- 数字工具,如分子设计,毒性建模和数据集成是临床前研究的关键.
- 机器学习和各种来源 (电子健康记录,社交媒体,设备) 的数据分析增强了临床试验和药物监管.
- 整合这些技术提供了协同效益,为利益相关者提供了有价值的信息,以提高药物安全性.
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