This summer, doctors at UnityPoint Health performed the QCA's first leadless pacemaker procedure. Now, Dr. Helbert Acosta ...
The US Food and Drug Administration (FDA) is reminding healthcare providers about the risk of major complications if cardiac perforation occurs during leadless pacemaker implantation. Cardiac ...
With more self-contained models potentially on their way to patients, the FDA is taking steps to remind healthcare providers of certain risks posed by leadless pacemakers, including the possibility of ...
The Food and Drug Administration (FDA) has issued a recall of nearly 62,000 pacemakers that were distributed between April 2015 and February 2019 after it was discovered that moisture could get inside ...
Background: Patients over the age of 75 represent more than half the recipients of permanent pacemakers. It is not known if they have a different risk of complications than younger patients. Methods: ...
Please provide your email address to receive an email when new articles are posted on . Risk for mortality, stroke and permanent pacemaker implantation after transcatheter aortic valve replacement ...
If you have a pacemaker installed to regulate your heart’s rhythm, you may wonder when you can return to your regular workout routines. Anything that stretches or puts direct pressure on the chest and ...
Generally, pacemakers improve quality of life for individuals who have a condition causing bradycardia, or a slowed heart rate. However, because there is an electrical device implanted near your heart ...
You will get medicine before the procedure. This helps you relax and helps prevent pain. The doctor makes a cut in the skin just below your collarbone. The cut may be on either side of your chest. The ...
CHICAGO — Parkinson's sufferers who had electrodes implanted in their brains improved substantially more than those who took only medicine, according to the biggest test yet of deep brain stimulation.
Tatiana Schlossberg, John F Kennedy's granddaughter, has died An AI deepfake was final straw for a Washington state trooper.
The Food and Drug Administration (FDA) has issued a recall of nearly 62,000 pacemakers that were distributed between April 2015 and February 2019 after it was discovered that moisture could get inside ...
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