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The Doctor Will See You At The Next Window; Drive-Through Pandemic Exercise Was First In Nation
A couple of months ago, Stanford Hospital had a preview of what a real pandemic might look like: hundreds of people, fearing they might be sick with the H1N1 virus, showed up at the emergency department looking for help. Hospital officials scrambled fast, converting some space over night into an infection-controlled triage area.
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Depression Medications May Reduce Male Fertility
As many as half of all men taking the antidepressant medication paroxetine (trade names Seroxat, Paxil) may have increased sperm DNA fragmentation -- a predictor of compromised fertility. Research led by NewYork-Presbyterian Hospital/Weill Cornell Medical Center also found that the changes are reversible with normal levels of sperm returning after discontinuation of the drug.
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IKARIA(R) To In-License BioLineRx's BL-1040
Ikaria Holdings, Inc. and BioLineRx Ltd. (TASE: BLRX) announced that Ikaria has entered into an agreement to obtain a worldwide exclusive license to BioLineRx"s BL-1040, a potential breakthrough treatment for preventing pathological cardiac remodeling following acute myocardial infarction (AMI).
Endocrinology

Lives May Be Saved By Osteoporosis Drug's Strengthening Of The Immune System

An osteoporosis drug proven to save lives after hip fractures may do so by strengthening the body"s immune system, according to geriatrics researchers at Duke University Medical Center. In 2007, Duke researchers reported a 28 percent reduction in death among patients who received zoledronic acid (Reclast) within 90 days of surgery for a hip fracture. Zoledronic acid is a yearly intravenous injection of bisphosphonate that inhibits the progression of bone loss. The researchers also reported that the 2,111 people who participated in the study were 35 percent less likely to suffer another fracture. "The findings marked the first time an osteoporosis medication was shown to have an effect on mortality, but they didn"t tell us why the mortality rate was lower," says Cathleen Colon-Emeric, MD, an associate professor of medicine at Duke. "People assumed it was due to a reduction in secondary fractures. We wanted to know if that was the reason or were other conditions being affected by the medication." In the current study, now online in the Journal of Bone and Mineral Research, Colon-Emeric and her colleagues report that the reduction in additional broken bones accounts for only eight percent of the mortality benefit. "Even after adjusting for secondary fractures and other risk factors, we found the risk of mortality was still 23 percent lower in the zoledronic acid-treated participants. That suggests the drug must work in other ways." The link between osteoporosis and an increased risk of death has been observed for some time. Up to 25 percent of the 345,000 Americans hospitalized annually with hip fractures die within a year of their fracture. Typically, most patients die from cardiovascular problems like heart attacks, arrhythmias and strokes, infections such as pneumonia, and cancer. "People who received the drug experienced common complications at the same rate as those who didn"t," says Colon-Emeric. But the people in the zoledronic acid group were better able to survive these events. "In particular, people with certain cardiac problems such as arrhythmias and pneumonias were much less likely to die from those conditions." Patients who lived in a nursing home before their broken hip, or who had high levels of cognitive impairment did not receive a mortality benefit from the drug. It still remains unclear what role zoledronic acid plays. "We know it affects the immune system and inflammation, and both of those are important in fighting infection and cardiovascular disease," Colon-Emeric says. "It may be that the drug is changing the body"s ability to fight off and recover from those illnesses." That idea will require confirmation in new studies. Other investigators participating in this study include: Kenneth W. Lyles, MD and Carl F. Pieper, DrPH, Duke University Medical Center; Steven Boonen, MD, PhD, Katholieke Universiteit Leuven, Belgium; Pierre Delmas, MD, PhD, Claude Bernard University, Lyon, France; Jay Magaziner, PhD, University of Maryland; Peter Mesenbrink, PhD, of Novartis Pharmceuticals, NJ; and Erik F. Eriksen, MD, DMsc, Novartis Pharma AG, Switzerland. This study was funded in part by Novartis Pharmaceuticals. Drs. Colon-Emeric, Lyles, Magaziner, Pieper and Boonen are consultants for Novartis. Debbe Geiger Duke University Medical Center


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