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FDA approval of brain aneurysm device gives Jefferson neurosurgeons another life-saving tool
Date:4/18/2011

eurosurgeons, who are among the busiest in the nation performing both open and endovascular procedures, to offer better treatment to other patients in this subset (about 10 percent of the 30,000 brain aneurysms cases in the United States per year) who wouldn't benefit from coils or traditional stents because of the size of their aneurysm.

"Numerous studies have shown that in certain types of surgery experience, the number of cases a surgeon and an institution perform has an impact on quality and patient outcomes," said Robert H. Rosenwasser, M.D., chairman of the Department of Neurological Surgery at Thomas Jefferson University. "Volume does matter, and it clearly matters for patient outcomes in neurosurgical cases for brain tumors, vascular and endovascular procedures, spinal surgery and for both surgical and medical treatment of stroke."

"JHN easily ranks in the top five for each of these treatments," he adds.

Dr. Gonzalez, who is one of the few people with experience with the device on the East Coast, used the PED on a Jefferson patient who had four aneurysms on her carotid and ophthalmic arteries. Open surgery wasn't an option because the patient was on blood thinners for Sickle Cell Anemia, so Dr. Gonzalez filed for paperwork with the FDA for "compassionate-use" of the device. The procedure was approved and performed with great successthe aneurysms have since completely disappeared.

"Because of our experience in endovascular treatments and with the device we are going to be proctors nationally as the PED is rolled out," Dr. Rosenwasser said.


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Contact: Steve Graff
stephen.graff@jefferson.edu
215-955-5291
Thomas Jefferson University
Source:Eurekalert

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