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News Daily News

Year in Review: Tirzepatide, Finerenone, and Digitoxin Score Big in Heart Failure

Michael O'Riordan

December 30, 2025

News Daily News

FDA Panel Declines to Endorse Ventura Interatrial Shunt for HFrEF

Todd Neale

December 05, 2025

News Daily News

Lower Risk of Mortality for Shock Patients Transferred to Expert Centers

Caitlin E. Cox

March 17, 2025

News Daily News

Even on Tafamidis, ATTR-CM Patients Face High Mortality Over Time

Michael O'Riordan

February 13, 2025

News Daily News

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

Todd Neale

June 28, 2024

News Daily News

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

L.A. McKeown

May 15, 2024

News Daily News

TAVI Outcomes Linked to LV Recovery in Patients With Severe Dysfunction

Michael O'Riordan

May 06, 2024

News Daily News

Real-world MitraClip Impact in Secondary MR: Reassuring for Some, Not All

Michael O'Riordan

September 18, 2023

News Daily News

FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

Caitlin E. Cox

July 27, 2023

News Daily News

Takotsubo Trigger Type Matters, With Physical Shocks Linked to Worse Outcomes

Shelley Wood

July 19, 2023

News Daily News

Journal Series Explores How Eroding Abortion Access Impacts the HF Community

Todd Neale

June 15, 2023

News Daily News

Poor Outcomes in HF Patients With Moderate Aortic Stenosis: Observational Data

Michael O'Riordan

March 29, 2023

News Daily News

For Some, Hopes for a Heart Grow Dim as LVAD-Only Centers Spread

Michael O'Riordan

January 30, 2023

News Daily News

FDA Advisors Recommend Against Approval of Omecamtiv Mecarbil

Michael O'Riordan

December 14, 2022

News Daily News

Cardiogenic Shock Outcomes Markedly Worse in De Novo HF Patients

Caitlin E. Cox

December 09, 2022

News Daily News

Concerning or Reassuring? Long After COVID-19, CMR Still Yields Clues

Michael O'Riordan

October 03, 2022

News Daily News

Medtronic Recalls Batteries in Some HeartWare VAD Systems

L.A. McKeown

June 23, 2022

News Daily News

Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

L.A. McKeown

April 29, 2022

News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Shelley Wood

March 01, 2021

News Daily News

Don’t Overlook COVID-19’s Cardiovascular Footprint, Say NYC Physicians

Caitlin E. Cox

April 09, 2020

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Year in Review: Tirzepatide, Finerenone, and Digitoxin Score Big in Heart Failure

FDA Panel Declines to Endorse Ventura Interatrial Shunt for HFrEF

Lower Risk of Mortality for Shock Patients Transferred to Expert Centers

Even on Tafamidis, ATTR-CM Patients Face High Mortality Over Time

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

TAVI Outcomes Linked to LV Recovery in Patients With Severe Dysfunction

Real-world MitraClip Impact in Secondary MR: Reassuring for Some, Not All

FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

Takotsubo Trigger Type Matters, With Physical Shocks Linked to Worse Outcomes

Journal Series Explores How Eroding Abortion Access Impacts the HF Community

Poor Outcomes in HF Patients With Moderate Aortic Stenosis: Observational Data

For Some, Hopes for a Heart Grow Dim as LVAD-Only Centers Spread

FDA Advisors Recommend Against Approval of Omecamtiv Mecarbil

Cardiogenic Shock Outcomes Markedly Worse in De Novo HF Patients

Concerning or Reassuring? Long After COVID-19, CMR Still Yields Clues

Medtronic Recalls Batteries in Some HeartWare VAD Systems

Medtronic’s HeartWare HVAD Recalled for Pump Weld Defect

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Don’t Overlook COVID-19’s Cardiovascular Footprint, Say NYC Physicians

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