News Daily News HeartMate 3 Problem With Outflow Graft Twisting Called Class I Recall by FDA Todd Neale May 23, 2018
News Daily News LV Diastolic Dysfunction Linked With Higher Mortality Post-TAVR Yael L. Maxwell March 01, 2018
News Daily News Impella Heart Pumps Get Expanded Indication for Cardiogenic Shock in Setting of Cardiomyopathy Todd Neale February 13, 2018
News Daily News Ten Principles for Successful Treatment of HF With Reduced EF: New ACC Decision Pathway Michael O'Riordan January 02, 2018
News Daily News Year in Review: Physicians Pick the Biggest News of 2017, in Interventional Cardiology and Beyond Shelley Wood December 26, 2017
News Daily News Hemodynamics of First-Gen Sapien Valve Hold Up Well Over the Years: PARTNER Analysis Caitlin E. Cox September 29, 2017
News Daily News FDA Grants HeartWare LVAD a Destination Therapy Indication Todd Neale September 28, 2017
News Daily News New Guidelines for Cardiogenic Shock Push for Regionalized Care, More Research Shelley Wood September 21, 2017
News Daily News Pulmonary Artery Injury More Likely With Real-World Use of CardioMEMS, Analysis Suggests Todd Neale September 19, 2017
News Daily News Technique for Diluting the Blood During Primary PCI to Prevent Reperfusion Injury Seems Safe, Feasible Todd Neale July 04, 2017
News Daily News HeartMate II Left Ventricular Assist System Under Recall Due to Controller Exchange Problems Todd Neale May 24, 2017
News Daily News FDA Classifies Latest HeartWare VAD Recalls as Class I Michael O'Riordan October 24, 2016
News Daily News Según un Estudio Los Pacientes con Cardiomiopatía Isquémica se Benefician de Descargas Miocárdicas Michael O'Riordan October 17, 2016
News Daily News Ischemic Cardiomyopathy Patients Can Benefit From Myocardial Unloading, Study Suggests Michael O'Riordan October 17, 2016
News Daily News Increased Risk of In-Hospital Complications, Including Mortality, Among A-fib Patients Undergoing PCI Michael O'Riordan August 24, 2016
News Daily News FDA Warns of Class I Recall for HeartWare VAD Batteries Michael O'Riordan June 29, 2016
News Daily News FDA Issues Class I Recall for Intra-Aortic Balloon Catheter and Percutaneous Insertion Kits Michael O'Riordan March 18, 2016