AED failures may lead to cardiac arrest deaths

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AED failures may lead to cardiac arrest deaths

news-medical.net

More than 1,000 cardiac arrest deaths over 15 years are connected to the failure of automated external defibrillators (AEDs); battery failure accounted for almost one-quarter of the failures. The study was published online last week in Annals of Emergency Medicine.

View full resource at news-medical.net

Tags: Heart, Emergency, Advanced Life Support, Cardiopulmonary Resuscitation, Emergency Medicine, First Aid and Emergency, Mortality, Medicine

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Most Recently Shared on August 31, 2011 at 12:07 pm By:

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AED failures may lead to cardiac arrest deaths: More than 1,000 cardiac arrest deaths over 15 years are connecte... http://t.co/JOndGQM

8 months ago...

Cardiac Science Powerheart, CardioVive, CardioLife; GE Responder and Responder Pro; and Nihon-Kohden Automated External Defibrillators (AEDs): Class I Recall - Defective Component

fda.gov — “Unexpected component failure may lead to AEDs not delivering defibrillation therapy, causing serious adverse health consequences, including death.View full resource at fda.gov

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Most Recently Shared on March 3, 2012 at 12:11 am By:

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St. Marys teen's death inspires movement of heart-saving devices | jacksonville.com

jacksonville.com — “KINGSLAND — In a millisecond, two boys collided on a baseball field and 15-year-old Andrew Cohn's healthy heart was jerked into an abnormal rhythm.By the day's end, the St. Marys teenager had lost his life to sudden cardiac arrest.Just over a year since Andrew's May 15, 2010, death, his parents are leading an effort to build awareness about automated external defibrillators, or AEDs, the electronic devices that can shock hearts back into their normal rhythm. If an AED had been neaView full resource at jacksonville.com

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Most Recently Shared on July 28, 2011 at 6:16 am By:

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St. Marys teen's death inspires movement of heart-saving devices http://bit.ly/rtmBft

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Noninvasive monitoring of cardiac allograft vasculopathy with fast MR imaging

news-medical.net — “Cardiac allograft vasculopathy (CAV), also known as chronicle rejection, is a leading cause of graft (foreign heart) loss and death in patients who survive the first year after heart transplantation. The typical pathological change of CAV is gradually thickening of coronary wall in "foreign" heart due to continuous immunological reaction between donated heart and the host. In some cases, undetected CAV may silently cause graft failure with global myocardial ischemia without any documenView full resource at news-medical.net

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Noninvasive monitoring of cardiac allograft vasculopathy with fast MR imaging: Cardiac allograft vasculopathy (CAV... http://bit.ly/aZbZgm

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CPR without Mouth-To-Mouth Rescue Breathing May be Better for Many Victims of Cardiac Arrest

newswise.com — “A leading expert in cardiopulmonary resuscitation says two new studies from U.S. and European researchers support the case for dropping mouth-to-mouth, or rescue breathing by bystanders and using hands-only chest compressions during the life-saving practice, better known as CPR.View full resource at newswise.com

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Symposier - Certain Powerheart/CardioVive/CardioLife AED Recalled (FDA April 2010)

symposier.com — “Uploaded and Shared in Youtube by: LawsuitGuru In February, Cardiac Science Corporation initiated a recall of several models of automated external defibrillators because manufacturing problems may make them susceptible to failure. If that happens, they might not be able to deliver therapy during a resuscitation attempt, and that could lead to serious adverse health consequences or death. The company says this action affects more than 12,000 AEDs manufactured or serviced between October 19, 2009 View full resource at symposier.com

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Most Recently Shared on April 8, 2010 at 2:18 am By:

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Certain Powerheart/CardioVive/CardioLife AED Recalled (FDA April 2010). http://bit.ly/aBKciH

2 years ago...

Cardiac Science Notifies AED Customers of Voluntary Medical Device Recall

fda.gov — “Cardiac Science Corporation [NASDAQ: CSCX] is initiating a worldwide voluntary recall after determining that approximately 12,200 automated external defibrillators (AEDs) may not be able to deliver therapy during a resuscitation attempt, which may lead to serious adverse events or death. These AEDs were manufactured in a way that makes them potentially susceptible to failure under certain conditions. The FDA has been informed of this situation.View full resource at fda.gov

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Most Recently Shared on February 9, 2010 at 5:51 pm By:

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