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Planning an MR Suite: What Can Be Done to Ensure MR Safety?

  • MRI Safety (M Bock, Section Editor)
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Abstract

In the past decades, various safety measures for magnetic resonance (MR) have been formulated by national and international standardization committees and professional non-standardization groups. These published standards and white papers on MR system safety include architectural installation and design guides for the MR suite, guidelines for MR safety experts, and MR marking practices for items used with MRI. Although the interests of the MR community are represented in documents pertaining to safety requirements for MR site planning, these documents show a lack of agreement among community members. For a comprehensive approach, the MR owner and MR user must consider all the current MR safety requirements regarding centralized MR suite planning, realization, performance of clinical or research services, and maintenance of the MR facility and must address the MR safety needs of all individuals as well as the MR procedural requirements of an MR suite.

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References

Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance

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Acknowledgments

Thanks to Hans Engels, Harald Kugel, and Michael Bock for their thorough review and advice.

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Correspondence to Gregor Schaefers.

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Conflict of Interest

Gregor Schaefers declares grants from Germany and EU, revenue from MR:comp MR safety seminar clients and MR:comp implant and medical device manufacturer clients, shareholder of and personal fees from MRI-STaR—Magnetic Resonance Institute for Safety, Technology and Research GmbH and MR:comp GmbH, personal fees and non-financial support from ESMRMB School of MRI, non-financial support from ISMRM and IPEM for invited talks, revenue and non-financial support from MagResource.eu/.com LLC MR implant safety online database, and MRI-Tec.com MR accessories ONE-STOP-SHOP. Convener of IEC TC62 SC62B WG45 for IEC 62570 “Marking medical devices and other items for safety in the magnetic resonance environment”, member of ASTM Subcommittee F04.15 on Material Test Methods, member of DIN Magnetic Resonance Processes for DIN 6876 “Operation of medical magnetic resonance systems”, member of IEC/ISO JWG for ISO/TS 10974 “Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device”. Björn Mierau declares no potential conflicts of interest.

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This article does not contain any studies with human or animal subjects performed by any of the authors.

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This article is part of the Topical Collection on MRI Safety.

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Schaefers, G., Mierau, B. Planning an MR Suite: What Can Be Done to Ensure MR Safety?. Curr Radiol Rep 4, 37 (2016). https://doi.org/10.1007/s40134-016-0154-z

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