一个框架,开发用于扫描医疗植入物和设备在MRI中的患者的通用植入物安全程序
Jonathan P Ashmore1, Sarah J Prescott2,3, John McLean4,5,6
1Department of Medical Physics and Bioengineering, NHS Highland, Inverness, IV2 3UJ, United Kingdom.
The British journal of radiology
|November 13, 2024
概括
新的MRI安全程序简化了植入体患者的扫描. 这些指导方针减少了延迟,因为它允许在没有制造商确认的情况下对低风险设备进行风险效益评估.
科学领域:
- 医疗成像医学成像
- 放射学 放射学是一门学科.
- 生物医学工程 生物医学工程
背景情况:
- 目前英国的指导方针强制要求制造商就植入式医疗器械的MRI安全性进行咨询.
- 这个过程往往耗时,导致MRI延迟和取消.
- 挑战包括不明的植入物和过时的制造商安全数据.
研究的目的:
- 为了建立MRI的通用植入安全程序.
- 定义一种管理低风险植入物患者的过程.
- 为了使基于证据的风险-收益决策能够在没有特定制造商验证的情况下进行扫描.
主要方法:
- 由一个多专业工作组制定最佳实践建议.
- 纳入地方批准的,基于证据的风险/收益决策的范围.
- 专注于管理某些类型的植入物,扫描风险较低的患者.
主要成果:
- 建议简化对植入植入体患者的MRI安全性的方法.
- 减少对低风险设备的个人制造商确认的依赖.
- 通过减轻程序延迟,促进及时的MRI扫描.
结论:
- 一般的植入物安全程序可以优化MRI工作流程.
- 这些程序支持患者扫描的知情,局部决策.
- 这些建议旨在改善患者护理和获得MRI服务的机会.
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