• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

日本用于确认植入式医疗设备磁共振兼容性的基于网络的可搜索系统:一项初步研究。

A Web-based searchable system to confirm magnetic resonance compatibility of implantable medical devices in Japan: a preliminary study.

作者信息

Fujiwara Yasuhiro, Fujioka Hitoshi, Watanabe Tomoko, Sekiguchi Maiko, Murakami Ryuji

机构信息

Department of Medical Imaging, Faculty of Life Sciences, Kumamoto University, 4-24-1 Kuhonji, Chuo-ku, Kumamoto, 862-0976, Japan.

Medie Corporation Ltd, Tokyo, Japan.

出版信息

Radiol Phys Technol. 2017 Sep;10(3):340-348. doi: 10.1007/s12194-017-0409-2. Epub 2017 Jul 31.

DOI:10.1007/s12194-017-0409-2
PMID:28762005
Abstract

Confirmation of the magnetic resonance (MR) compatibility of implanted medical devices (IMDs) is mandatory before conducting magnetic resonance imaging (MRI) examinations. In Japan, few such confirmation methods are in use, and they are time-consuming. This study aimed to develop a Web-based searchable MR safety information system to confirm IMD compatibility and to evaluate the usefulness of the system. First, MR safety information for intravascular stents and stent grafts sold in Japan was gathered by interviewing 20 manufacturers. These IMDs were categorized based on the descriptions available on medical package inserts as: "MR Safe," "MR Conditional," "MR Unsafe," "Unknown," and "No Medical Package Insert Available". An MR safety information database for implants was created based on previously proposed item lists. Finally, a Web-based searchable system was developed using this database. A questionnaire was given to health-care personnel in Japan to evaluate the usefulness of this system. Seventy-nine datasets were collected using information provided by 12 manufacturers and by investigating the medical packaging of the IMDs. Although the datasets must be updated by collecting data from other manufacturers, this system facilitates the easy and rapid acquisition of MR safety information for IMDs, thereby improving the safety of MRI examinations.

摘要

在进行磁共振成像(MRI)检查之前,必须确认植入式医疗设备(IMD)的磁共振(MR)兼容性。在日本,很少有这样的确认方法在使用,而且它们耗时较长。本研究旨在开发一个基于网络的可搜索MR安全信息系统,以确认IMD的兼容性,并评估该系统的实用性。首先,通过采访20家制造商,收集了在日本销售的血管内支架和覆膜支架的MR安全信息。这些IMD根据医疗包装说明书上的描述被分类为:“MR安全”、“MR条件性安全”、“MR不安全”、“未知”和“无医疗包装说明书”。基于先前提出的项目清单创建了一个植入物MR安全信息数据库。最后,使用该数据库开发了一个基于网络的可搜索系统。向日本的医护人员发放了一份问卷,以评估该系统的实用性。通过12家制造商提供的信息以及调查IMD的医疗包装,收集了79个数据集。尽管必须通过收集其他制造商的数据来更新数据集,但该系统有助于轻松快速地获取IMD的MR安全信息,从而提高MRI检查的安全性。

相似文献

1
A Web-based searchable system to confirm magnetic resonance compatibility of implantable medical devices in Japan: a preliminary study.日本用于确认植入式医疗设备磁共振兼容性的基于网络的可搜索系统:一项初步研究。
Radiol Phys Technol. 2017 Sep;10(3):340-348. doi: 10.1007/s12194-017-0409-2. Epub 2017 Jul 31.
2
Development of a Searchable System to Confirm MR Imaging Safety Information for Implantable Medical Devices.开发一个可搜索的系统,以确认植入式医疗器械的磁共振成像安全信息。
Magn Reson Med Sci. 2019 Oct 15;18(4):286-292. doi: 10.2463/mrms.tn.2018-0100. Epub 2019 Feb 19.
3
[Survey on the Number and Percentage of MR Safety Labeling Changed for Implantable Medical Devices].[植入式医疗器械MR安全标识变更数量及百分比调查]
Nihon Hoshasen Gijutsu Gakkai Zasshi. 2024 Feb 20;80(2):188-198. doi: 10.6009/jjrt.2024-1424. Epub 2023 Dec 19.
4
[Development of an magnetic resonance imaging safety management system for metallic biomedical products using an magnetic resonance compatibility database and inquiry-based patient records].
Nihon Hoshasen Gijutsu Gakkai Zasshi. 2014 Dec;70(12):1413-9. doi: 10.6009/jjrt.2014_JSRT_70.12.1413.
5
New Insights into MR Safety for Implantable Medical Devices.植入医疗器械磁共振安全的新见解。
Magn Reson Med Sci. 2022 Mar 1;21(1):110-131. doi: 10.2463/mrms.rev.2021-0160. Epub 2022 Feb 25.
6
Magnetic resonance imaging compatibility and safety of the SOUNDTEC Direct System.SOUNDTEC Direct系统的磁共振成像兼容性与安全性
Laryngoscope. 2006 Aug;116(8):1321-33. doi: 10.1097/01.mlg.0000230479.39551.4a.
7
Testing methods for MR safety and compatibility of medical devices.医疗器械的磁共振安全性与兼容性测试方法。
Minim Invasive Ther Allied Technol. 2006;15(2):71-5. doi: 10.1080/13645700600640865.
8
MRI information for commonly used otologic implants: review and update.常用耳科植入物的 MRI 信息:综述与更新。
Otolaryngol Head Neck Surg. 2014 Apr;150(4):512-9. doi: 10.1177/0194599813518306. Epub 2014 Jan 7.
9
Virtual Humans for Implantable Device Safety Assessment in MRI: Mitigating Magnetic Resonance Imaging Hazards for Implanted Medical Devices.用于磁共振成像中植入式设备安全评估的虚拟人体:减轻植入式医疗设备的磁共振成像危害
IEEE Pulse. 2017 Jul-Aug;8(4):50-53. doi: 10.1109/MPUL.2017.2701258.
10
MR safety assessment of active implantable medical devices.有源植入式医疗器械的磁共振安全性评估。
Radiologe. 2019 Dec;59(Suppl 1):40-45. doi: 10.1007/s00117-019-0541-6.

引用本文的文献

1
Torque property of titanium alloy cerebral aneurysm clips in a magnetic resonance scanner.钛合金颅内动脉瘤夹在磁共振扫描仪中的扭矩性能。
J Mater Sci Mater Med. 2019 Dec 14;31(1):6. doi: 10.1007/s10856-019-6329-4.
2
Development of a Searchable System to Confirm MR Imaging Safety Information for Implantable Medical Devices.开发一个可搜索的系统,以确认植入式医疗器械的磁共振成像安全信息。
Magn Reson Med Sci. 2019 Oct 15;18(4):286-292. doi: 10.2463/mrms.tn.2018-0100. Epub 2019 Feb 19.

本文引用的文献

1
Response to Standardized MR Terminology and Reporting of Implants and Devices as Recommended by the American College of Radiology Subcommittee on MR Safety.对美国放射学会磁共振安全小组委员会推荐的植入物和设备标准化磁共振术语及报告的回应。
Radiology. 2016 Jun;279(3):906-9. doi: 10.1148/radiol.2015151108. Epub 2015 Nov 23.
2
[Development of an magnetic resonance imaging safety management system for metallic biomedical products using an magnetic resonance compatibility database and inquiry-based patient records].
Nihon Hoshasen Gijutsu Gakkai Zasshi. 2014 Dec;70(12):1413-9. doi: 10.6009/jjrt.2014_JSRT_70.12.1413.
3
MRI-conditional pacemakers: current perspectives.MRI条件性起搏器:当前观点
Med Devices (Auckl). 2014 May 7;7:115-24. doi: 10.2147/MDER.S44063. eCollection 2014.
4
ACR guidance document on MR safe practices: 2013.ACR 磁共振安全实践指南:2013 年版。
J Magn Reson Imaging. 2013 Mar;37(3):501-30. doi: 10.1002/jmri.24011. Epub 2013 Jan 23.
5
[Collection of information regarding implants, internal and external metallic objects for MRI examinations].[关于用于MRI检查的植入物、体内和体外金属物体的信息收集]
Nihon Hoshasen Gijutsu Gakkai Zasshi. 2011;67(10):1314-9. doi: 10.6009/jjrt.67.1314.
6
[An investigative report concerning safety and management in the magnetic resonance environment: there are more accidents than expected].[关于磁共振环境中安全与管理的调查报告:事故比预期更多]
Nihon Hoshasen Gijutsu Gakkai Zasshi. 2011;67(8):895-904. doi: 10.6009/jjrt.67.895.
7
MR labeling information for implants and devices: explanation of terminology.植入物和器械的磁共振标记信息:术语解释
Radiology. 2009 Oct;253(1):26-30. doi: 10.1148/radiol.2531091030.
8
Safety of magnetic resonance imaging in patients with cardiovascular devices: an American Heart Association scientific statement from the Committee on Diagnostic and Interventional Cardiac Catheterization, Council on Clinical Cardiology, and the Council on Cardiovascular Radiology and Intervention: endorsed by the American College of Cardiology Foundation, the North American Society for Cardiac Imaging, and the Society for Cardiovascular Magnetic Resonance.心血管装置患者的磁共振成像安全性:美国心脏协会诊断与介入心脏导管插入术委员会、临床心脏病学理事会以及心血管放射学与介入理事会的科学声明:得到美国心脏病学会基金会、北美心脏成像学会和心血管磁共振学会认可
Circulation. 2007 Dec 11;116(24):2878-91. doi: 10.1161/CIRCULATIONAHA.107.187256. Epub 2007 Nov 19.
9
MR procedures: biologic effects, safety, and patient care.磁共振成像检查:生物学效应、安全性及患者护理
Radiology. 2004 Sep;232(3):635-52. doi: 10.1148/radiol.2323030830. Epub 2004 Jul 29.
10
Pre-MRI procedure screening: recommendations and safety considerations for biomedical implants and devices.MRI检查前程序筛查:生物医学植入物和设备的建议及安全注意事项
J Magn Reson Imaging. 2000 Jul;12(1):92-106. doi: 10.1002/1522-2586(200007)12:1<92::aid-jmri11>3.0.co;2-7.