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在评估活性植入物患者的MR安全性时,错误数据的频率和影响

Samuel J Fahrenholtz¹, Yuxiang Zhou¹, William F Sensakovic¹

¹Department of Radiology, Mayo Clinic, Phoenix, AZ, USA.

Current problems in diagnostic radiology

|October 9, 2024

概括

活性植入物磁共振 (MR) 安全性评估中的数据完整性问题发生在16%的病例中. 提供易于访问正确的设备手册显著改善了MRI成像安全的数据完整性.

科学领域:

医疗成像医学成像
生物医学工程生物医学工程
患者安全患者安全

背景情况:

活性植入物,带有电源的设备,在磁共振成像 (MR) 过程中构成风险.
机构需要强大的工作流程来对活跃植入物进行MR安全评估.
评估中的数据完整性较低,可能导致安全性评估不正确,患者风险增加.

研究的目的:

确定活性植入物的MR安全评估中数据完整性问题的发生率和原因.
评估提供对植入物供应商手册的访问在提高数据完整性的有效性.

主要方法:

采用了一项调查,收集2020年3月至2023年4月期间用于植入器械MR安全评估的信息数据.
749名患者的病历被MR安全专家审查.
一个链接到植入器供应商手册存储库的列表于2021年12月实施.

主要成果:

在16%的案例中发现了数据完整性问题,这可能会影响47%的MR安全评估或扫描.
错误或缺失的供应商手册是数据完整性损失的主要原因 (78%).
实施集中列表的供应商手册链接改善了数据完整性,到2022年8月,利率稳定.

结论:

数据完整性对于对活体植入物进行准确的MR安全评估至关重要.
提供直接访问最新的植入物供应商手册是缓解数据完整性问题的有效策略.
改进的数据完整性提高了MRI成像程序期间的患者安全.

关键词:

积极植入的医疗器械积极植入的医疗器械植入物植入物植入物磁共振成像技术磁共振成像技术质量改善质量改善安全的安全的安全的安全的安全.

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