The device acts on the supraorbital nerve and supratrochlear nerve, the nerves that transmit migraine pain. The Food and Drug Administration (FDA) has cleared WAT Medical’s HeadaTerm 2 as an ...
Researchers at Thomas Jefferson University Hospital have shown that combining distal protection devices with the prophylactic use of the drug nicardipine can reduce the risk of complications following ...
February 17, 2011 — Dental patients should not take prophylactic antibiotics simply because they have pacemakers or implanted defibrillators, according to a new statement from the American Heart ...
The sponsor submitted a de novo cost analysis using a decision tree model that estimated the cost associated with the geko device compared with no mechanical prophylaxis. The model population was ...
Urokinase administration every 2 weeks significantly affects the rate of occlusive events in ports and tunneled catheters and of infectious events in external catheters compared with heparin ...
Of 500 physicians surveyed, 162 (32%) returned the survey. Characteristics of the respondents are displayed in Table I. The vast majority of physicians were male (87%) specializing in either ...
St. Jude Medical is issuing a “recall and correction” and warning physicians and patients that the batteries in certain brands of the company’s implantable cardioverter defibrillator (ICD) and cardiac ...
Feb. 27 (UPI) --Medtronic has recalled 48 implantable and cardiac resynchronization defibrillators that are failing to deliver the proper shock to pace a patient's heartbeat or revive a patient in ...
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