Abiomed Announces First Patient Enrolled In MINI-AMI FDA Study

Abiomed, Inc. has announced the first patient enrolled in MINI-AMI, an FDA prospective, randomized, controlled multi-center study to assess the role of 24-hours of direct unloading of the left ventricle with Impella(R) 2.5 support to reduce infarct size in patients with ST-elevation myocardial infarction without cardiogenic shock.

PREVENT Study Indicates Potential for Reduced Risk of Adverse Clinical Outcomes with Enhanced BIOTRONIK Pacemaker Algorithm

Biotronik PREVENT study indicates lower percent of right ventricular pacing (%VP) correlates with less risk of heart failure (HF) hospitalization, mortality and atrial fibrillation (AF)

Medtronic Reports Positive Results with CoreValve and Acquisition of Peak Surgical, Salient Surgical Technologies

Investigators reported that cardiac survival of patients, who were implanted with the 21F CoreValve system in 2005 and 2006, was 77.9 percent at two years and 68 percent at four years; in other Medtronic news, company announces completing the acquisition of Peak Surgical Inc. and Salient Surgical Technologies Inc.

Balloon pump use prior to PCI does not reduce infarct size in STEMI patients without shock

Intra-aortic balloon pump counterpulsation prior to PCI in patients with ST segment elevation MI does not reduce infarct size as measured by MRI, according to results from the Counterpulsation Reduces Infarct Size Acute Myocardial Infarction (CRISP AMI) trial.

MitraClip less effective than Mitral Valve Surgery: “Heart Team” approach recommended

The results of the first randomised controlled trial comparing percutaneous mitral valve repair against conventional mitral valve surgery suggests the short term advantages of the technique may be outweighed by inferior long term results compared with conventional surgery.

Cardiola Penetrates European Market with Its Muscular CounterPulsation (MCP)-based m.pulse® system

Cardiola AG announced today that it has placed its patented m.pulse® system in 10 hospitals located in Germany and Switzerland, on the heels of the system’s CE-Mark approval.

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