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Covers EMI fundamentals, device responses such as oversensing, device reset, and reversion, and general clinician guidance to discuss with patients. 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It does not apply to patients with leadless transcatheter cardiac devices or implantable cardiac monitors.","Answer",{"name":115,"@type":110,"acceptedAnswer":116},"What device responses to EMI are described?",{"text":117,"@type":113},"The manual describes common responses including oversensing, device reset, and reversion.",{"name":119,"@type":110,"acceptedAnswer":120},"How does the manual structure guidance on medical procedures and EMI risk?",{"text":121,"@type":113},"It provides warnings and precautions for procedures and equipment, lists medical procedures considered acceptable, and includes technical guidance for using a Medtronic Model 9466 patient magnet, plus patient precautions organized by distance restrictions and special environments.","https://schema.org",{"og:url":83,"og:type":124,"og:title":65,"og:site_name":95,"og:description":67},"article",{"robots":126,"canonical":83},"index,follow",{"doc_id":128,"site_id":62},640678,1793107011,{"code":4,"msg":5,"data":131},{"doc_id":128,"user_id":132,"nickname":92,"user_avatar":133,"doc_module":4,"category_id":34,"category_name":35,"doc_title":65,"doc_description":67,"doc_content":134,"file_id":135,"file_url":136,"file_type":137,"file_size":138,"view_count":24,"is_deleted":4,"is_public":8,"is_downloadable":8,"audit_status":8,"page_count":139,"language":140,"language_code":63,"site_id":62,"html_lang":63,"table_of_contents":141,"faqs":142,"seo_title":143,"seo_description":67,"update_tm":144,"read_time":145,"preview_page_count":4},962094248839,"https://ap-avatar.wpscdn.com/davatar_994ba38a5ba835b3df7d355c54d3ed8d","Medical Procedure and EMI Warnings, Precautions, and Guidance  \nfor implanted pacemakers and defibrillators  \nManual for Health Care Professionals  \nMedtronic, Medtronic with rising man logo, and Medtronic logo are trademarks of Medtronic. Third-party trademarks (“TM*”) belong to their respective owners. The following list includes trademarks or registered trademarks of a Medtronic entity in the United States and/orin other countries.  \nAdapta™, EnPulse™, Kappa™, MVP™, Relia™, Sensia™, SureScan™, Versa™  \nContents  \n1 Introduction ......................................................................... 3  \n2 Overview of electromagnetic interference (EMI) .......................................... 4  \n2.1 Types of EMI ........................................................................... 4  \n2.2 Applicable standards for safety and electromagnetic compatibility ................................ 5  \n3 Device responses to EMI .............................................................. 5  \n3.1 Oversensing ........................................................................... 6  \n3.2 Device reset ............................................................................ 6  \n3.3 Reversion .............................................................................. 6  \n4 General guidelines for patients in the presence of EMI ..................................... 6  \n5 Perioperative management of patients with implanted pacemakers or ICDs ................... 7  \n6 Warnings and precautions for medical procedures and equipment .......................... 7  \n6.1 Medical procedures and equipment that require warnings, precautions, and guidance for health care professionals .............................................................................. 7  \n6.2 Medical procedures and devices that are acceptable for patients with implanted pacemakers and ICDs .................................................................................... 19  \n6.3 How to initiate asynchronous pacing in a Medtronic pacemaker with a Medtronic Model 9466 patient magnet .................................................................................. 19  \n6.4 How to suspend tachyarrhythmia detection and therapies in a Medtronic ICD with a Medtronic Model 9466  \npatient magnet ............................................................................ 20  \n6.5 Medtronic Model 9466 patient magnet ..................................................... 21  \n7 Warnings, precautions, and guidance for EMI for patients with an implanted pacemaker or ICD ................................................................................. 22  \n7.1 Items with no distance restriction from an implanted pacemaker or ICD .......................... 22  \n7.2 Items with a 15 cm (6 in) distance restriction from an implanted pacemaker or ICD ................. 23  \n7.3 Items with a 30 cm (12 in) distance restriction from an implanted pacemaker or ICD ................ 25  \n7.4 Items with a 60 cm (24 in) distance restriction from an implanted pacemaker or ICD ................ 26  \n7.5 Items with low potential for EMI at extended distances from an implanted pacemaker or ICD ......... 27  \n7.6 Items and environments with special considerations for EMI for patients with implanted pacemakers and ICDs .................................................................................... 27  \n7.7 Non-EMI environments with special consideration for patients with implanted pacemakers and ICDs .................................................................................... 28  \n1 Introduction  \nThis manual is for physicians and other health care professionals who treat patients who have the following Medtronic implanted cardiac devices:  \n• Pacemakers, including cardiac resynchronization therapy pacemakers (CRT-P)  \n• Cardioverter defibrillators (ICD), including cardiac resynchronization therapy defibrillators (CRT-D)  \nNote: The warnings, precautions, and guidance in this m","cbCaiqtr2bfVq7sG","https://ap.wps.com/l/cbCaiqtr2bfVq7sG","pdf",290156,32,"English","# Introduction\n# Overview of electromagnetic interference (EMI)\n## Types of EMI\n## Applicable standards for safety and electromagnetic compatibility\n# Device responses to EMI\n## Oversensing\n## Device reset\n## Reversion\n# General guidelines for patients in the presence of EMI\n# Perioperative management of patients with implanted pacemakers or ICDs\n# Warnings and precautions for medical procedures and equipment\n## Medical procedures and equipment requiring warnings\n## Acceptable procedures and devices\n## Initiating asynchronous pacing with a patient magnet\n## Suspending ICD tachyarrhythmia detection with a patient magnet\n## Medtronic Model 9466 patient magnet\n# Warnings, precautions, and guidance for EMI for patients\n## Distance restrictions (no restriction, 15 cm, 30 cm, 60 cm)\n## Items with special considerations and special environments\n## Non-EMI environments with special consideration","[{\"question\":\"Which implanted cardiac devices does the manual apply to?\",\"answer\":\"It applies to Medtronic implanted pacemakers (including CRT-P) and ICDs (including CRT-D). It does not apply to patients with leadless transcatheter cardiac devices or implantable cardiac monitors.\"},{\"question\":\"What device responses to EMI are described?\",\"answer\":\"The manual describes common responses including oversensing, device reset, and reversion.\"},{\"question\":\"How does the manual structure guidance on medical procedures and EMI risk?\",\"answer\":\"It provides warnings and precautions for procedures and equipment, lists medical procedures considered acceptable, and includes technical guidance for using a Medtronic Model 9466 patient magnet, plus patient precautions organized by distance restrictions and special environments.\"}]","Medical Procedure and EMI Warnings, Precautions, and Guidance - Manual for Health Care Professionals - Implanted Pacemakers and Defibrillators | PDF",1792710268,81]