Evaluation of a Workflow to Define Low Specific Absorption Rate MRI Protocols for Patients With Active Implantable Medical Devices

Author:

Martinez Jessica A.12ORCID,Moulin Kévin3,Yoo Bryan2,Shi Yu2,Kim Hyun J.2,Villablanca Pablo J.2,Ennis Daniel B.3

Affiliation:

1. Department of BioengineeringUniversity of California Los Angeles California USA

2. Department of Radiological SciencesUniversity of California Los Angeles California USA

3. Department of RadiologyStanford University Stanford California USA

Funder

Abbott Laboratories

Consejo Nacional de Ciencia y Tecnología

National Heart, Lung, and Blood Institute

University of California Institute for Mexico and the United States

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging

Reference26 articles.

1. Standards for medical devices in MRI: Present and future

2. IEC 60601‐2‐33:2010 | IEC Webstore. IEC 60601‐2‐33:2010+AMD1:2013+AMD2:2015 CSV: Medical electrical equipment ‐ particular requirementsfor the basic safety and essential performance of magnetic resonance equipment for medicaldiagnosis Edition 3.2. Accessed December 15 2019. Available from:https://webstore.iec.ch/publication/2647.

3. 14:00‐17:00 ISO/TS 10974:2018. In: ISO. Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device Tech. Specif. ISOTS10974 vol. second edition 2018. Accessed December 15 2019. Available from:http://www.iso.org/cms/render/live/en/sites/isoorg/contents/data/standard/06/50/65055.html.

4. Food and Drug Administration(2014) Establishing Safety and Compatibility of Passive Implants in the Magnetic Resonance (MR) Environment. 10.

5. ASTM International(2013) ASTM F2503‐13 Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment. Available from:https://doi-org.stanford.idm.oclc.org/10.1520/F2503-13.

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