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High Rate of Head Injuries in Iraq Soldiers Portends Potential Wave of Epilepsy

September 14th, 2009

Tony Coelho is having déjà vu. The former congressman and author of the Americans with Disabilities Act recalls a commencement address he gave a quarter-century ago, in the wake of the Vietnam war, in which he warned of the potential for seizure disorders in returning troops who had suffered head injuries and called for more research on the link between traumatic brain injury (TBI) and epilepsy. Today, as he watches the storm build amid reports of alarmingly high TBI rates among soldiers returning from Iraq – and the military’s apparent inability to care for them properly – Coelho is struck by the parallels. “Here I am, 25 years later, talking about the same thing,” says Coelho, who has epilepsy as a result of a head injury and is the immediate past chair of the Epilepsy Foundation. “What have we learned?

Growing Chorus of Concern

Coelho is not alone in his concern for the long-term effects of the head injuries that have become the signature injury of the Iraq conflict. A chorus of concern is rising among veterans’ advocates and medical experts across the USA who understand the heightened risk America’s returning war heroes have for a range of posttraumatic europsychological problems. Epilepsy is prominent among them.

The risk is very real, even if the precise numbers are impossible to predict. Trauma to the brain, whether mild or severe, is a clearly defined risk factor for epilepsy. Studies suggest that about 20 to 25 percent of individuals with “closed-head” brain injuries will go on to develop what is termed post-traumatic epilepsy (PTE). PTE accounts for 5 percent of epilepsy overall. The only study that has investigated the prevalence of PTE in the military, reported in 1985, found that as many as 50 percent of Vietnam veterans who had suffered penetrating brain injuries during combat developed seizure disorders months or years later.

Penetrating injuries – when a foreign object or piece of fractured skull enters the brain – are the most severe form of TBI. They are relatively uncommon in civilians and are distinct from the types of head injuries most commonly seen in U.S. troops serving in Iraq. There, most head trauma seems to be a result of the “shock wave” of high pressure that reverberates out from the point of an explosion. Improvised Explosive Devices, or IED’s, have notoriously become the weapon of choice against U.S. troops; the Department of Veterans Affairs (VA) estimates that IED’s account for two-thirds of combat injuries. These “blast injuries” can – and apparently often do – cause brain trauma, even in the absence of obvious wounds.

There is little hard data on the incidence of blast-related head injuries among U.S. soldiers in Iraq, at least that is available to the public. 2003 data from the Walter Reed Army Medical Center found evidence of brain injury in 61 percent of returning soldiers who had been exposed to blasts, according to the Defense and Veterans Brain Injury Center, a partnership between the VA and the Department of Defense (DoD).

No one knows how many of those troops with brain injuries will eventually develop epilepsy.

But with an estimated 1.4 million troops who have served or are currently serving in Iraq, even the most conservative statistics portend a looming crisis of post-TBI neurologic problems that will haunt these soldier heroes, and society at large, for generations to come.

Preventing PTE: New Priority?

The specter of a coming wave of combat-related TBI has refocused attention on the critical need to better predict whom among the head-injured are likely to develop epilepsy, and how to prevent it. It also underscores how little we yet know about preventing epilepsy.

“For many years – even decades – epilepsy research has been focused primarily on the seizures themselves: what they are, how they are generated in the brain, how they spread and what drugs might control them,” says Marc Dichter, M.D., Ph.D., professor of neurology and pharmacology at the University of Pennsylvania. “Basically, we’ve been waiting for epilepsy to happen and then seeing if we can treat it.”

This approach is in stark contrast, Dichter says, to how we as a society deal with other public health problems, such as cancer or heart disease, where we identify risk factors and try to prevent disease from occurring.

“Why aren’t we paying attention to the development of epilepsy, as we do for every other medical disease?” he asks.

Dichter is leading a DoD-funded pilot study in civilians to determine if the anti-seizure drug topiramate (Topamax®)might decrease the risk of post-traumatic epilepsy if given within 12 hours or so of a head injury. Recruitment for the trial is just beginning.

Health and led by Pavel Klein, M.D., a neurologist with Washington Hospital Center in Washington D.C., is further along. The study is designed to evaluate the safety and tolerability of levetiracetam (Keppra®) in people who have suffered a head injury. (Keppra is approved as add-on therapy for partial seizures in adults.) Klein says about 50 adults and children with TBI had been enrolled as of late April, with an eventual goal of 90. If Keppra is found to be safe for use in this population – and so far Klein says it appears to be – the goal is to initiate a much larger study to investigate the drug’s efficacy in preventing PTE.

At least three well-designed clinical studies have previously investigated other anti-seizure medications for preventing injury-induced epilepsy. All have failed to show a benefit. The trials are exceedingly difficult to do, say Dichter and Klein, because they are labor intensive, costly, and take a long time to recruit enough subjects to have meaningful statistical power. Yet it’s critical that they be done. “If you don’t study the question, you’ll never get an answer,” says Dichter.

“Epilepsy is a chronic condition, and a proportion of people will develop refractory epilepsy, which requires life-long, extensive medical treatment and management,” says Klein. “It’s a complicated recovery, in many ways. Prevention is better than treatment.”

‘Strike While the Iron is Hot’

Coelho is particularly concerned that troops who develop seizures long after their active duty is finished may be denied disability benefits. “It has been a huge fight to get the VA and DoD to understand that epilepsy can be a delayed effect of war trauma,” he says.

Still, he points out, the current situation, dire though it is, presents an opportunity to act.

“Congress right now is very conscious of the need to take care of our military men and women,” Coelho says. “It is critically important that we take advantage of the heightened sensitivity to this situation to uncover the facts, identify the problems and go to Congress to get the appropriate funding to get the job done right. We need to strike while the iron is hot.”


Scientists find way to stop epilepsy in mice

August 19th, 2009

TUESDAY, Aug. 4 (HealthDay News) — Blocking a gene defect prevents epilepsy from being passed from adult mice to their offspring, a finding that may help in efforts to develop new treatments for people with epilepsy, British researchers say.

The study proves that a faulty version of a gene called ATP1A3 causes epileptic seizures in mice, said lead researcher Dr. Steve Clapcote, of the Faculty of Biological Sciences at University of Leeds, and colleagues.

“ATP1A3 makes an enzyme called a sodium-potassium pump that regulates levels of sodium and potassium in the brain’s nerve cells. An imbalance of sodium and potassium levels has long been suspected to lead to epileptic seizures, but our study is the first to show beyond any doubt that a defect in this gene is responsible,” Clapcote said in a university news release.

He and his team studied a special strain of mice with an inherited form of severe epilepsy and found that the mice had a defective ATP1A3 gene. When these mice were bred with mice that had an extra copy of the normal ATP1A3 gene, the additional normal gene counteracted the defective gene and the offspring didn’t have epilepsy.

“Our study has identified a new way in which epilepsy can be caused and prevented in mice, and therefore it may provide clues to potential causes, therapies and preventive measures in human epilepsy,” Clapcote said.

The study appears in this week’s online edition of the Proceedings of the National Academy of Sciences.

“Our results are very promising, but there’s a long way to go before this research could yield new antiepileptic therapies. However, the human ATP1A3 gene matches the mouse version of the gene by more than 99 percent, so we’ve already started to screen DNA samples from epilepsy patients to investigate whether ATP1A3 gene defects are involved in the human condition,” Clapcote said.

More information

The American Academy of Family Physicians has more about epilepsy.

 

– Robert Preidt

SOURCE: University of Leeds, news release, Aug. 3, 2009

Copyright © 2009 ScoutNews, LLC. All rights reserved.


Seizures, not epilepsy itself, may raise birth risks

August 19th, 2009

MONDAY, Aug. 10 (HealthDay News) — Epileptic seizures during pregnancy increase the likelihood of premature and small babies, says a new study. Taiwanese researchers compared children born to 1,016 women with epilepsy with those born to 8,128 women without epilepsy. During pregnancy, 503 of the women with epilepsy had seizures and 513 did not. Those who had seizures while pregnant were 36 percent more likely than women who did not have epilepsy to have had a baby that weighed less than 5.5 pounds (considered low birth weight), 63 percent more likely to deliver prematurely (before 37 weeks) and 37 percent more likely to have a baby who was small for gestational age. In another comparison, women with epilepsy who had seizures during pregnancy were 34 percent more likely to have a baby who was small for gestational age than were women with epilepsy who did not have seizures while pregnant. The study is in the August issue of Archives of Neurology. Some earlier studies suggested a link between epilepsy and adverse pregnancy outcomes, but others found no connection. The findings of the new study “suggest that it is the seizures themselves that seem to contribute greatly to the increased risk of infants being delivered preterm, of low birth weight and small for gestational age,” wrote Yi-Hua Chen, of Tai Pei Medical University in Taiwan, and colleagues. “For women who remained seizure-free throughout pregnancy, null or mild risk was identified, compared with unaffected women.” Epileptic seizures can affect pregnancy outcomes in a number of ways. Seizures can cause trauma that ruptures fetal membranes, increasing the risk for infection and early delivery. Or seizures can cause contractions in the uterus that cause tension and acute injury. The researchers emphasized the need for intervention strategies, such as helping women control seizures for a period of time before pregnancy, assisting them in sleeping better, providing education about the risks of seizures while pregnant and teaching them how to cope with stress.

More information The Epilepsy Foundation has more about women and epilepsy. — Robert Preidt SOURCE: JAMA/Archives journals, news release, Aug. 10, 2009 Copyright © 2009 ScoutNews, LLC. All rights reserved.


Are you getting the right RX?

July 28th, 2009

gmavideo

By ELISABETH LEAMY and VANESSA WEBER of Good Morning America on ABC
Imagine going to the pharmacy to fill your prescription only to learn later that the drug your doctor prescribed is not the one you received. The prescription was switched without your knowledge or permission.

Pharmacies could be switching your drugs without your knowledge.

Not just switched to a generic version of the prescribed drug, but to a different drug altogether…

Click on the image to view the video.


Software tool helps web developers identify seizure causing content

July 22nd, 2009

July 22, 2009

by Sandra Knisely

In 1997, an episode of the popular Pokemon cartoon gained worldwide attention when more than 800 Japanese children with photosensitive seizure conditions were admitted to the hospital after viewing the cartoon or the subsequent news coverage of it.

Researchers from the UW-Madison Trace Center have released a software tool that could prevent similar incidences of media-triggered seizures in children who are browsing the Internet or using computer programs.

The software, called the Photosensitive Epilepsy Analysis Tool (PEAT), allows Web developers to evaluate their site content and determine whether the content presents a danger to people with photosensitive epilepsy.

PEAT is the first tool developed for evaluating Web-based content, and a beta version is available for free download from the Trace Center, a pioneer center that designs mainstream information technology accessible to people with disabilities.

Gregg Vanderheiden, a UW-Madison professor of industrial and systems engineering and biomedical engineering, directs the Trace Center.

“As Web content becomes more dynamic and Web pages begin to resemble television, it is important that we not start inadvertently triggering seizures in people with photosensitive seizure disorders,” he says. “PEAT can help prevent that.”

Approximately one in 4,000 people are diagnosed with photosensitive epilepsy and are subject to seizures triggered by certain types of flashing in Web, computer or television content. The condition usually begins before age 20 and is most common between ages 7 and 19. Seizures are most likely to occur when children or teenagers with the condition view content where large areas of a screen flash rapidly and flicker on and off repeatedly.

PEAT allows developers to capture on video a Web browser or application window and all of the actions that occur in the window. Developers then can analyze the video for seizure risk. Developers can also use PEAT to determine if Web content meets the new Web Content Accessibility Guidelines 2.0.

PEAT is the result of six years of collaboration between the Trace Center and professor Graham Harding from Cambridge Research Systems. The National Institute on Disability and Rehabilitation Research, which is part of the U.S. Department of Education, funded the development of PEAT.

source: University of Wisconsin http://www.news.wisc.edu/16917


Catastrophic Epilepsy caused by defect in one gene

July 15th, 2009

WEDNESDAY, July 8 (HealthDay News) — A mutation in a single gene causes catastrophic epilepsy, U.S. scientists say. And that finding, they say, could lead to treatments or a cure for the disorder. Read more


Epilepsy Phenome/Genome Project

July 10th, 2009

The Epilepsy Phenome/Genome Project is a research study sponsored by the National Institute of Neurological Disorders and Stroke designed to answer the following questions: 

  • Why do some families have several people with epilepsy?
  • How can we predict the best anti-seizure drug to use?
  • What causes epilepsy? 

To learn more about this study, visit  www.epgp.org


Dog can seize the day in family emergency.

July 10th, 2009

Dogs always have been known as man’s best friend, but when it comes to seizure-response dogs for those with epilepsy, these special canines become invaluable protectors. The Walker family in north suburban Grayslake — mom Candace and children Colin, 11, Carson, 9, and Cailean, 5 — know this all too well. They own a golden retriever seizure-response dog, Donut. The 4-year-old Donut helps Colin, who has Dravet syndrome a progressive childhood disorder characterized by epilepsy. Read more…


Effectiveness of the first AED in the Treatment of Pediatric Epilepsy

July 10th, 2009

Most previous studies on the effectiveness of the first antiepileptic drug have dealt with adults. The present retrospective study of 520 patients was designed to investigate the interaction among efficacy, tolerability, and overall effectiveness of the first antiepileptic drug in children with newly diagnosed epilepsy. A total of 344 patients became seizure-free with the first prescribed antiepileptic drug. A lower proportion of patients with symptomatic epilepsy (60.3%) or cryptogenic epilepsy (61.5%) became seizure-free, compared with patients with idiopathic epilepsy (73.8%), and more patients with symptomatic or cryptogenic epilepsy changed their treatments owing to intolerable side effects. Most patients (95.6%) received sodium valproate (n = 234), topiramate (n = 143), or carbamazepine (n = 120). The majority of seizure-free patients required only a moderate daily dose. Patients who took carbamazepine (16.7%) or topiramate (11.9%) had a higher incidence of adverse events, necessitating a change of treatment, compared with patients treated with valproate (4.3%), and fewer of them became seizure-free. Overall, 66.2% of the patients became seizure-free with the first-ever antiepileptic drug, and most of them at a moderate dose. Moreover, tolerability was as important as efficacy in determining overall effectiveness.

Department of Neurology, Beijing Children’s Hospital, The Capital Medical University, Beijing, China

 Department of Pediatrics, Chinese PLA General Hospital, Beijing, China

Communications should be addressed to: Dr. Zou; Department of Pediatrics; Chinese PLA General Hospital; 100853 Beijing, China 100045.

1 Both authors contributed equally to this work.

PII: S0887-8994(09)00050-2

doi:10.1016/j.pediatrneurol.2009.01.010


Easing the Seizures and Stigma of Epilepsy

June 22nd, 2009

:: Epilepsy affects millions of families worldwide; half of all epilepsy patients are children.

:: Some 30 percent of patients, many of them children, have intractable seizures that cannot be controlled by existing treatments. 

:: Follow the link below to read the story of a young girl and her battle with epilepsy.

http://health.nytimes.com/ref/health/healthguide/esn-epilepsy-ess.html