Hemodynamic Support Devices

This hemodynamic support systems channel includes content on intra-aortic balloon pumps (IABP), percutaneous ventricular assist devices (pVAD) like the Impella or TandemHeart, extracorporeal membrane oxygenation (ECMO), and ventricular assist devices (VAD). This channel also includes use of these devices in support of patients in cardiogenic shock and advanced heart failure

News | Ventricular Assist Devices (VAD)

January 7, 2020 — Abbott announced U.S. Food and Drug Administration (FDA) approval of a new alternative surgical ...

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The Philips Lumify hand-held ultrasound technology is an important component of the mobile ECMO unit. Members of the ECMO team use Lumify for real-time visual guidance when inserting tubes in veins and arteries in a process called ECMO cannulation. #RSNA2019 #RSNA19 #POCUS
Feature | Ultrasound Imaging

November 26, 2019 — Physicians from the University of New Mexico (UNM) and local emergency responders recently treated a ...

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November 19, 2019 — Since Maquet/Datascope first recalled all of its  intra-aortic balloon pumps (IABP) due to reports ...

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News | Hemodynamic Support Devices

November 4, 2019 — Abbott is recalling its CentriMag Acute Circulatory Support System due to a calibration system error ...

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News | Hemodynamic Support Devices

October 28, 2019 — Nearly two years of real-world outcomes data on Abiomed’s Impella RP heart pump shows that when ...

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Videos | Hemodynamic Support Devices

Jeffrey J. Popma, M.D., director of interventional cardiology clinical services at Beth Israel Deaconess Medical Center ...

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Videos | Cardiogenic Shock

William O’Neill, M.D., medical director of the Center for Structural Heart Disease at Henry Ford Hospital, Detroit ...

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Technology | Ventricular Assist Devices (VAD)

September 27, 2019 — Abiomed’s newest heart pump, the Impella 5.5 with SmartAssist, has received U.S. Food and Drug ...

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Videos | Hemodynamic Support Devices

There was a 77 percent increase in survival in cardiogenic shock patients treated using a new protocol in the National ...

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News | Ventricular Assist Devices (VAD)

September 12, 2019 — CorWave announced successful completion of its first 60-day preclinical study to evaluate its ...

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Videos | Hemodynamic Support Devices

A discussion with William O'Neill, M.D., director of the structural heart program, Henry Ford Hospital, and Michele ...

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In July, the biggest news item was Datascope initiating a Class I recalled of its intra-aortic balloon pumps due to potential battery failure.  Most Popular Cardiology Technology Content in July 2019
Feature | Dave Fornell, Editor

August 2, 2019 — Here is the list of the most popular content on the Diagnostic and Interventional Cardiology (DAIC) mag ...

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Technology | Heart Failure

July 30, 2019 – Procyrion Inc. secured Breakthrough Device designation by the U.S. Food and Drug Administration (FDA) ...

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Datascope Recalls Intra-Aortic Balloon Pumps Due to Potential Battery Failure. FDA Class I recall includes the Cardiosave Hybrid, Cardiosave Rescue, CS300 and CS100/100i IABP.
Feature | Intra-Aortic Balloon Pumps (IABP)

July 24, 2019 — The U.S. Food and Drug Administration announced Maquet/Datascope is recalling all intra-aortic balloon ...

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