Please provide your email address to receive an email when new articles are posted on . The FDA announced it has designated a recall of intra-aortic balloon pumps by Datascope/Getinge as class I, the ...
IABP systems are typically inserted within the multidisciplinary environment that is the cardiac catheterization laboratory. The specific role of the physiologist during IABP insertion is to ensure ...
Among the top stories in cardiology this week was an FDA recall of intra-aortic balloon pumps and a report that explained how icosapent ethyl improved outcomes in adults with elevated CV risk that are ...
DURHAM, N.C.—Inserting intra-aortic balloon pumps prior to angioplasty in patients with acute myocardial infarction (AMI) does not reduce the scope of heart muscle damage, a condition referred to as ...
Two deaths, one serious injury and more than 60 medical device reports have been linked to Maquet/Datascope’s intra-aortic balloon pumps in the past year, the FDA warned healthcare providers in a Nov.
Compared with standard medical care, early use of a temporary intra-aortic balloon pump (IABP) to support heart function in patients who were critically ill with cardiogenic shock caused by heart ...
"In short, it seems likely that the returned arterialized blood should be returned during diastole when the aortic valve is closed. This would probably offer less resistance to the ailing heart's ...
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