The U.S. Food and Drug Administration (FDA) has approved Portola Pharmaceuticals' Andexxa, the first antidote indicated for patients treated with rivaroxaban (Xarelto) and apixaban (Eliquis), when reversal of anticoagulation is needed due to life-threatening or uncontrolled bleeding.
Stereotaxis and Acutus Medical announced a strategic collaboration to integrate the Stereotaxis Niobe Magnetic Navigation System and the Acutus Medical AcQMap High Resolution Imaging and Mapping System. The goal of the collaboration is to improve patient care and the physician experience in electrophysiology.
In March, I made a day trip to New York City to receive the 2017 Jesse H. Neal Award for Best Use of Social Media. The ...
Cardiac PET/CT represents a major advancement in cardiovascular diagnostics, offering significant clinical and ...
Balancing high quality care with efficiency — and avoiding unnecessary procedures — is a priority for any hospital ...
May 4, 2018 — Transcatheter valve technology has been advancing very quickly and the links to aggregated content from ...
May 3, 2018 — The U.S. Food and Drug Administration (FDA) recently announced the availability of a draft guidance for ...
SPONSORED CONTENT — Studycast is a comprehensive imaging workflow system that allows healthcare professionals to work ...
May 3, 2018 — APN Health LLC announced its Navik 3D mapping system is commercially released and in clinical use. The ...
May 3, 2018 — The U.S. Food and Drug Administration (FDA) has granted market clearance for the Abbott Advisor HD Grid ...
May 3, 2018 — The U.S. Food and Drug Administration (FDA) has expanded the indication for the Medtronic In.Pact Admiral ...
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
May 2, 2018 — Conavi Medical Inc. has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its ...
Select adult patients born with a single functioning ventricle, and who have undergone a surgical operation called the ‘Fontan procedure’ during childhood, are being enrolled in a new global-first clinical trial. The trial, led by a multi-disciplinary team of heart and lung physicians, will examine the effects of a portable, non-invasive medical device never before tested on patients with this cardiac condition.
May 2, 2018 – The Board of Directors of the Radiological Society of North America (RSNA) announced that Charles E. Kahn ...
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
This is a 360 degree view inside the back of the Northwestern Medicine Central DuPage Hospital Mobile Stroke Unit ...
James K. Min, M.D., FSCCT, has been selected for a five-year term as the new editor-in-chief of the Journal of Cardiovascular Computed Tomography (JCCT). He in turn has named Todd C. Villines, M.D., FSCCT, as executive editor along with Gudrun Feuchtner, M.D.
Cerebrovascular imaging analysis company iSchemaView received final clearance from the U.S. Food and Drug Administration (FDA) for Rapid CTA, the company’s 3-D imaging solution for computed tomography angiography. Rapid CTA is the newest addition to iSchemaView’s neuroimaging platform — including Rapid CTP and Rapid MRI — which is designed to provide physicians with fast, fully-automated and easy-to-interpret imaging that facilitates clinical decision making around cerebrovascular disease, such as stroke.
May 07, 2018
