Mortara Instrument Inc. began its worldwide release of its latest resting electrocardiograph (ECG), the ELI 280. The new system combines advanced ECG processing with an intuitive interface, enabling clinicians optimized efficiency in their acquisition of routine diagnostic ECGs.
With Schiller's medilog electrocardiogram (ECG) Holter recorders and the new Fire of Life software, the heart rate variability (HRV) is analyzed and displayed in a new way to help judge the function of the autonomic nervous system.
Cardea Associates announced the launch of its new electrocardiographic (ECG) device, CardeaScreen. Specifically in-tune with normal conditions for the athletic heart, CardeaScreen is designed for use during pre-participation exams (PPE) for sports participants age 14 and older. This U.S. Food and Drug Administration (FDA)-cleared device helps physicians identify abnormal cardiac conditions that could lead to sudden cardiac arrest — at a much lower cost than other ECG systems currently on the market.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
Laboratory Corporation of America Holdings (LabCorp) announced it has launched its clinical next generation sequencing assay, GeneSeq: Cardio for genetic causes of familial cardiac disease.
The Society of Cardiovascular Computed Tomography (SCCT) has released a list of five interventions whose appropriateness physicians and patients should discuss as part of Choosing Wisely. The list includes:
The Society of Nuclear Medicine and Molecular Imaging (SNMMI) released a list of specific tests that are commonly ordered—but not always necessary — in nuclear medicine and molecular imaging as part of the Choosing Wisely campaign, an initiative of the ABIM Foundation. The list identifies five targeted, evidence-based recommendations that can support conversations between patients and physicians about what care is really necessary and appropriate.
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
February 26, 2013 — TeraMedica debuted the Evercore Connext Mobile at the 2013 HIMSS conference, bringing groundbreaking, seamless point-of-care data capture and archiving to an iPad or iPhone. At the touch of a button, Evercore Connext Mobile acquires photos, videos, sound files, notes and more with the highest level of security. Data is automatically archived directly to the hospital’s Evercore VNA as an integral part of the patient record for viewing through an electronic medical record (EMR) and the integrated TeraMedica Univision viewer.
The TIMS Medical division of Foresight Imaging released the TIMS version 3.0 platform to provide high resolution digital video formats in fluoroscopy and endoscopy.
Medtronic Inc. announced it received U.S. Food and Drug Administration (FDA) approval to conduct an early feasibility study using the Medtronic Native Outflow Tract Transcatheter Pulmonary Valve (TPV). This approval represents the first-ever FDA approval of an investigational device exemption (IDE) following the new draft FDA guidance for early feasibility studies.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
The U.S. Food and Drug Administration (FDA) has approved the 34 and 38 mm lengths of the Medtronic Resolute Integrity drug-eluting stent in diameters of 3, 3.5 and 4 mm with an indication for patients with diabetes.
New research at Saint Louis University shows physicians do not talk to patients about the psychosocial impact and long-term risks of implanting cardioverter defibrillators (ICDs) to treat irregular heart rhythms, leaving them misinformed about how the device may affect quality of life.
Taking a leadership role in addressing inefficient practices and improving care, the American Society of Echocardiography (ASE) has released a list of five interventions whose appropriateness physicians and patients should discuss as part of Choosing Wisely.
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
The White House’s recent approval of the Physician Payment Sunshine Act mandates transparency within physician-industry relationships. Data recording begins Aug. 1, 2013, so it is necessary for physicians and administrators to understand the implications of this section of the Affordable Care Act.
The American Heart Association (AHA) is focusing its advocacy efforts across the Midwest on the use of pulse oximetry screening (pulse ox) to detect congenital heart defects in newborns.
The U.S. Food and Drug Administration (FDA) granted final approval for the Biotronik Lumax 740 DX system. The device is a first-in-class implantable cardiac defibrillator (ICD) that utilizes a single lead with atrial sensing capabilities.