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 | 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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News | Ventricular Assist Devices (VAD)

June 12, 2019 — In a letter sent to healthcare providers, the U.S. Food and Drug Administration (FDA) validates that ...

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News | Ventricular Assist Devices (VAD)

May 22, 2019 — Abiomed announced that the Impella CP with SmartAssist will be commercially available beginning at the 20 ...

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News | Cardiogenic Shock

May 20, 2019 – A newly released expert consensus statement proposes a classification schema for cardiogenic shock (CS) t ...

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Technology | Ventricular Assist Devices (VAD)

May 14, 2019 — The U.S. Food and Drug Administration (FDA) has approved the expansion of Abiomed’s Impella 5.0 and ...

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