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This document serves as a consent form for patients undergoing MRI procedures, specifically those with permanent pacemakers or implantable cardioverter defibrillators. It outlines procedure details,
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How to fill out consent for magnetic resonance

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How to fill out Consent for Magnetic Resonance Imaging in a Patient with a Permanent Pacemaker and/or Implantable Cardioverter Defibrillator

01
Obtain the Consent for Magnetic Resonance Imaging form from the patient's medical records or the imaging facility.
02
Confirm the patient's identity and ensure the form is for the correct patient.
03
Explain the purpose of the MRI scan and the reasons why consent is necessary, particularly in relation to their pacemaker or ICD.
04
Discuss the potential risks and benefits of undergoing MRI with a permanent pacemaker or ICD.
05
Ensure the patient understands the procedure and answer any questions they may have.
06
Have the patient read the consent form thoroughly before signing.
07
Obtain the patient's signature on the consent form, indicating their understanding and agreement.
08
Sign the form as a witness after the patient has signed.
09
Submit the signed consent form to the relevant department or keep it in the patient's medical records.

Who needs Consent for Magnetic Resonance Imaging in a Patient with a Permanent Pacemaker and/or Implantable Cardioverter Defibrillator?

01
Patients with a permanent pacemaker and/or an implantable cardioverter defibrillator (ICD) who are being considered for a Magnetic Resonance Imaging (MRI) procedure.
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Both thoracic and non-thoracic MRIs have been performed safely on individuals with implantable loop monitors with no impact on device function, battery life, or patient-reported symptoms [53]. The loop monitor recording may falsely record arrhythmias that actually are from artifact during MR scanning.
Read more about who can and can't have an MRI scan. Once you have completed the questionnaire, you'll usually be asked to give your signed consent for the scan to go ahead. As the MRI scanner produces strong magnetic fields, it's important to remove any metal objects from your body.
Historically patients with a pacemaker were not able to get MRI scans due to the risk of damaging the device or surrounding tissue. Fortunately, due to evolving technology most new pacemakers and ICDs are now MRI compatible. Many individuals, however, have older devices that are deemed non-MR conditional.
Your implanted defibrillation system is listed on your current medical device ID card. You should keep this card with you at all times, and take it with you to the MRI facility. Before the scan, your defibrillator will be programmed to the MRI settings. These settings are necessary for you to receive an MRI scan.
If you need an MRI, having an implanted Medtronic heart monitor device won't stop you. † See patient manual for additional information. Neither security nor scanning will affect your heart monitor.
Conclusion. In patients with a PM or ICD, the benefit of MRI may far outweigh its risks if the indication has been established for the particular patient as an interdisciplinary decision and if the appropriate precautions are observed during scanning.
Both thoracic and non-thoracic MRIs have been performed safely on individuals with implantable loop monitors with no impact on device function, battery life, or patient-reported symptoms [53]. The loop monitor recording may falsely record arrhythmias that actually are from artifact during MR scanning.
Conclusions. We evaluated the safety of MRI, performed with the use of a prespecified safety protocol, in 1509 patients who had a legacy pacemaker or a legacy implantable cardioverter–defibrillator system. No long-term clinically significant adverse events were reported.

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Consent for Magnetic Resonance Imaging (MRI) in a patient with a permanent pacemaker and/or implantable cardioverter defibrillator (ICD) refers to the formal agreement obtained from the patient or their legal representative before conducting an MRI procedure. This consent acknowledges the patient's understanding of the possible risks associated with the MRI due to the presence of the pacemaker or ICD.
The healthcare provider or facility conducting the MRI is responsible for ensuring that the consent form is filled out and signed. This includes the radiologist, attending physician, or any authorized personnel involved in the patient's care.
To fill out the consent form, the healthcare provider must provide detailed information regarding the MRI procedure, potential risks and benefits, alternative imaging methods, and address any patient questions. The patient or their representative should then read, understand, and sign the document, indicating their agreement to proceed.
The purpose of the consent is to ensure that patients are informed about the specific risks and benefits of undergoing an MRI with an implanted device like a pacemaker or ICD, and to obtain their explicit permission to perform the procedure.
The consent form must report the patient's identity and medical history, details of the pacemaker or ICD, description of the MRI procedure, potential risks involved, possible alternatives, and a section for the patient's signature and date.
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