Pacemakers Receive CE Mark with Options for MRI
By MedImaging International staff writers Posted on 10 Nov 2014 |
A range of pacemakers have received CE marking approval, and they are the first to enable patients to undergo full-body magnetic resonance imaging (MRI) scans in both 1.5 Tesla and 3.0 Tesla systems.
When implanted with the Ingevity leads, Accolade pacemakers enable patients to receive full-body MRI scans. Moreover, Boston Scientific’s (Marlborough, MA, USA) ImageReady technology offers the most flexible MRI options, allowing higher energy scan sequences, and featuring a programmable MRI timer designed to improve patient workflow.
The first Accolade device implant was performed by a group coordinated by Prof. Francesco Romeo, director of the cardiology department of Fondazione Policlinico Tor Vergata (Rome, Italy), and president-elect of Italian Society of Cardiology (SIC). “Thanks to the Accolade pacemaker family, I can offer my patients the best pacing therapies while giving them unparalleled access to imaging,” said Prof. Romeo. “Additionally, the full suite of diagnostics and the excellent longevity of the device mean that I should be able to utilize the device for my patients undergoing MRI scans in the future—many years from now.”
In addition to the CE marking approval and introduction of the Accolade pacemaker family, Boston Scientific received CE Marking approval for the Visionist and Valitude cardiac resynchronization therapy pacemakers (CRT-Ps) with quadripolar pacing technology. When combined with the Acuity X4 pacing leads, these systems offer many options to reach and pace the target location in the left ventricle, potentially improving the patient response to CRT therapy. Dr. Stuart Harris, clinical director of the Essex Cardiothoracic Center (Basildon, UK), performed the first implant of the Visionist X4 system.
“We have prioritized investments and now have the first and only subcutaneous ICD, the smallest ICD [cardioverter defibrillator], and the longest-lasting pacemaker, ICD and CRT devices in the world,” said Joe Fitzgerald, executive vice president and president, rhythm management. “Now, with the Accolade pacemaker family, we also offer the most flexible MRI-conditional pacemaker system, along with advanced diagnostics that assist physicians in detecting atrial arrhythmias. We believe that the provision of automatic daily monitoring and advanced diagnostics to our pacemaker devices will help physicians identify atrial fibrillation sooner, enabling them to initiate patient anti-coagulation therapy to reduce the risk of stroke.”
Boston Scientific is also actively pursuing MRI compatibility for their line of existing ICDs, cardiac resynchronization therapy defibrillators (CRT-Ds), including the Autogen, Dynagen, Inogen, and Origen CRT-Ds, and lead technologies such as the Ingevity, Reliance, and Acuity leads.
The Accolade, Visionist, Valitude, Autogen, Origen, Ingevity, and Acuity X4 devices are not yet available for sale in the United States.
Related Links:
Boston Scientific
When implanted with the Ingevity leads, Accolade pacemakers enable patients to receive full-body MRI scans. Moreover, Boston Scientific’s (Marlborough, MA, USA) ImageReady technology offers the most flexible MRI options, allowing higher energy scan sequences, and featuring a programmable MRI timer designed to improve patient workflow.
The first Accolade device implant was performed by a group coordinated by Prof. Francesco Romeo, director of the cardiology department of Fondazione Policlinico Tor Vergata (Rome, Italy), and president-elect of Italian Society of Cardiology (SIC). “Thanks to the Accolade pacemaker family, I can offer my patients the best pacing therapies while giving them unparalleled access to imaging,” said Prof. Romeo. “Additionally, the full suite of diagnostics and the excellent longevity of the device mean that I should be able to utilize the device for my patients undergoing MRI scans in the future—many years from now.”
In addition to the CE marking approval and introduction of the Accolade pacemaker family, Boston Scientific received CE Marking approval for the Visionist and Valitude cardiac resynchronization therapy pacemakers (CRT-Ps) with quadripolar pacing technology. When combined with the Acuity X4 pacing leads, these systems offer many options to reach and pace the target location in the left ventricle, potentially improving the patient response to CRT therapy. Dr. Stuart Harris, clinical director of the Essex Cardiothoracic Center (Basildon, UK), performed the first implant of the Visionist X4 system.
“We have prioritized investments and now have the first and only subcutaneous ICD, the smallest ICD [cardioverter defibrillator], and the longest-lasting pacemaker, ICD and CRT devices in the world,” said Joe Fitzgerald, executive vice president and president, rhythm management. “Now, with the Accolade pacemaker family, we also offer the most flexible MRI-conditional pacemaker system, along with advanced diagnostics that assist physicians in detecting atrial arrhythmias. We believe that the provision of automatic daily monitoring and advanced diagnostics to our pacemaker devices will help physicians identify atrial fibrillation sooner, enabling them to initiate patient anti-coagulation therapy to reduce the risk of stroke.”
Boston Scientific is also actively pursuing MRI compatibility for their line of existing ICDs, cardiac resynchronization therapy defibrillators (CRT-Ds), including the Autogen, Dynagen, Inogen, and Origen CRT-Ds, and lead technologies such as the Ingevity, Reliance, and Acuity leads.
The Accolade, Visionist, Valitude, Autogen, Origen, Ingevity, and Acuity X4 devices are not yet available for sale in the United States.
Related Links:
Boston Scientific
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