
Advancements in mechanical circulatory support (MCS) devices for high-risk percutaneous coronary intervention (HR-PCI) have focused on achieving hemodynamic stability with minimal complications. The Impella device, a well-established transvalvular microaxial pump, is widely used and being actively investigated for supporting HR-PCI. Its use reduced all-cause mortality in patients with acute myocardial infarction-related cardiogenic shock, most of whom were treated with PCI, in the DanGer Shock trial. The cost was device-related complications, including more bleeding and limb ischemia in the Impella arm, emphasizing the need to develop safer mechanical circulatory support devices.
The Magenta Elevate is an innovative, expandable MCS device designed to address the limitations of traditional systems. It features a 9-Fr catheter-mounted microaxial pump that expands to 30-Fr within the left ventricle, providing high-output support. Delivered through a 10-Fr femoral introducer sheath, this device minimizes vascular trauma while offering flows up to 5.4 L/min. This expandable design allows for lower rotational speeds, potentially reducing hemolysis. In theory, this device is designed to provide adequate hemodynamic support with improved access-related safety profile and hemocompatibility.
The first-in-human study of the Magenta Elevate system, conducted by Schwammenthal et al., assessed its safety and efficacy in 14 patients undergoing HR-PCI, including interventions on unprotected left main coronary arteries. Device insertion, support, and removal were successful in all patients, although device malfunction in one required replacement with a new device. The device successfully maintained mean arterial pressure (MAP) and reduced left ventricular workload during a total of 20 prolonged left main balloon occlusions lasting an average of 39 +/- 16 seconds. MAP decreased by a median of only 7 mm Hg (7 mm Hg [13 to 2 mm Hg]; P < 0.001), while diastolic aortic pressure increased (7 mm Hg [4 to 10 mm Hg]; P < 0.0055), preserving myocardial perfusion. There were no hypotensive episodes and no need for vasoactive medications. There were no major device-related adverse events, and all patients survived to 30 days without significant complications.