Why the study?
Many patients with cardiac electrotherapy devices have indications for MRI, but CIEDs were long considered a contraindication and require specific procedures and precautions to perform imaging safely.
This expert consensus statement provides guidelines for safely performing MRI in patients with cardiac implantable electronic devices, a procedure previously considered contraindicated.
The year 2023 marks 60 years since the first pacemaker was implanted in Poland. The number of implantable cardiac electrotherapy devices (CIEDs), including pacemakers, cardioverter-defibrillators, and resynchronization therapy systems, has been systematically increasing in the subsequent decades. It is estimated that nearly 500,000 Poles have an implanted cardiac electrotherapy device, making optimal diagnostic imaging with the use of magnetic resonance imaging (MRI) a clinically and epidemiologically important issue. MRI has become a gold diagnostic standard in many disease states. In this situation, it is believed that 50-70% of patients who have a cardiac electrotherapy device may have indications for an MRI examination later in life. For many years, an implanted cardiac electrotherapy device was considered a definite contraindication to MRI. However, MRI has become possible in most patients with CIED if certain procedures and precautions are followed. In these guidelines, we describe the basic rules that should be followed in order to perform a safe MRI examination in patients with different CIEDs. Despite all the risks and organizational factors described in the text, it seems that for many MRI departments, MRI in patients with CIEDs is achievable and should be implemented immediately. A second important issue is the need for dedicated financial support for these procedures from public health insurance.
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Marczak et al. (2024) conducted a review in Implanted cardiac electrotherapy devices (CIEDs). Magnetic resonance imaging (MRI) was evaluated. Magnetic resonance imaging can be safely performed in most patients with cardiac implantable electronic devices if specific safety procedures and device programming protocols are followed.
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