Medtronic receives CE mark for its Pacing System
Medtronic Inc. has received CE (Conformité Européenne) Mark for the first-ever MR-Conditional pacemaker system, the EnRhythm MRI TM SureScan TM pacemaker and CapSureFix MRI TM SureScan TM pacing leads (Model 5086MRI). The new system was designed, tested and approved for use with magnetic resonance imaging (MRI) under specified scanning conditions, and is now commercially available in select European countries. Patients receiving the EnRhythm MRI SureScan Pacing System will for the first time be able to undergo MRI scans under certain conditions, representing a major milestone in the evolution of implantable cardiac devices.


The US federal government will continue to cover the scanning procedure to detect heart disease, despite having misgivings over whether such coverage is justified or not. The payments would be left up to the local insurance carriers who have been covering these tests so far. Dr. Barry Straube, CMO for the Centers for Medicare and Medicaid Services, said that more evidence is needed before the policy can be reversed.
According to a Dutch study, the often-used MRI scans to detect breast cancer frequently scare women unnecessarily. Five out of six scans were found to be incorrect, although the women concerned were going for mastectomies only after careful analysis. Published in the 
Using the newly designed 3-D ultrasound technology, Duke University bioengineers can compensate for the thickness and unevenness of the skull to see in real-time the arteries within the brain that most often clog up and cause strokes. The researchers believe that these advances will ultimately improve the treatment of stroke patients by enabling emergency medical technicians (EMT) to quickly scan the heads of potential stroke victims while in the ambulance or allowing physicians to easily monitor in real time the patients’ response to therapy at the bedside.
According to the authors of an article released on April 18, 2008, in