Zacks Investment Research | Jun 08, 2021 07:11AM ET
Abbott Laboratories (NYSE:ABT) MDT last week’s decision to discontinue the global distribution and sale of Medtronic’s competitive product HeartWare ventricular assist device (HVAD).
Abbott’s HearMate 3 thus is expected to meet the excess demand that has been created due to the sudden discontinuation of Medtronic’s HVAD.
In addition, Abbott is working with physicians and health systems to ensure supply of left ventricular assist devices (LVADs) as well as training and education for physicians offering Abbott's HeartMate 3 to patients.
Abbott is expected to strengthen its electrophysiology and heart failure business and expand its customer base globally with adequate capacity and supply to meet the growing demand.
Abbott’s HeartMate 3 heart pump is a small, implantable mechanical circulatory support device for patients with advanced heart failure in need of either short or long-term support awaiting a heart transplant or who are not eligible for heart transplantation.
In a recent study published in the Annals of Thoracic Surgery regarding the risk of adjusted and propensity matched patients supported with the HeartMate 3 demonstrated that actuarial survival rates were 87% at one year and 84% at two years.
Per Abbott’s management, life-savings results has been seen in patients treated with mechanical circulatory support devices and ensuring continued access to these devices is important for patients. Abbott is working to make sure that physicians have the support and training as they adopt HeartMate 3 to enhance outcomes for advanced heart failure patients.
Further, left ventricular assist devices (LVADs) remain a vital option for patients with advanced heart failure, either awaiting a heart transplant or not eligible for transplantation which can extend patients’ lives and restore quality of life. Abbott's HeartMate 3 heart pump is available to support physicians and patients globally in markets where the technology has been approved for use.
In May 2021, Abbott announced a new trial focused on improving treatment for people simultaneously suffering from both atrial fibrillation (AFib) and heart failure. Notably, the trial will make use of Abbott’s technology, including cardiac ablation and sensors to monitor for both pulmonary artery pressure and abnormal heartbeats. The first-of-its-kind trial intends to offer new insights into more effective treatment for patients with AFib and heart failure -- a complex combination that has historically presented significant challenges to physicians.
In April 2021, Abbott announced the receipt of CE Mark for TriClip Transcatheter Tricuspid Valve Repair System -- the first-of-its-kind minimally invasive tricuspid heart valve repair device to treat tricuspid (TR) regurgitation available in Europe. Notably, the clip-based therapy called TriClip G4 is a non-surgical heart valve repair system designed particularly to treat TR, or a leaky tricuspid valve.
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