报告医疗器械不良影响的障碍:文献综述
Sukhpreet Kaur1, Ayush Gandhi1, Sahibjot Kaur Sandhu2
1Dasmesh College of Pharmacy, Faridkot, Punjab, India.
Naunyn-Schmiedeberg's archives of pharmacology
|September 11, 2024
概括
报告医疗器械的不良事件对于医疗保健安全至关重要. 主要障碍包括缺乏意识,资源和组织问题,需要改进报告系统和更广泛的专业参与.
科学领域:
- 医疗器械安全 医疗器械安全
- 改善医疗保健质量 改善医疗保健质量
- 药物监督 药物监督 药物监督
背景情况:
- 医疗器械是必不可少的,但存在风险,包括死亡率和发病率.
- 印度的物质警计划是为了监测这些风险而建立的.
- 目前医疗器械不良事件报告率仍然非常低.
研究的目的:
- 识别阻碍医疗器械不良事件报告的障碍.
- 提出克服这些报告障碍的策略.
- 通过改进设备监控,提高医疗保健的整体安全性和标准.
主要方法:
- 进行了对相关文献的系统审查.
- 31篇论文根据预先定义的纳入标准进行了选择.
- 分析的重点是确定影响报告的个人和组织因素.
主要成果:
- 个人层面的障碍包括缺乏意识,负面态度和资源不足.
- 组织障碍包括层次结构,时间限制,缺乏激励措施和行业反应不佳.
- 低报告率是一个持续的挑战,尽管现有计划.
结论:
- 改善医疗器械不良事件报告需要解决意识,资源和态度障碍.
- 组织变革至关重要,包括更容易获得报告系统和激励措施.
- 让所有医疗保健专业人员 (医生,护士,药剂师,技术人员) 参与全面监测是必不可少的.
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