Keyword Search:
text size: A | A | A
FDA OKs breathing device used by Christopher Reeve
   posted 12:53 pm Wed June 18, 2008 - CLEVELAND
NewsChannel 8 - FDA OKs breathing device used by Christopher Reeve
  NewsChannel 8 - Share FDA OKs breathing device used by Christopher Reeve  NewsChannel 8 - Print FDA OKs breathing device used by Christopher Reeve  NewsChannel 8 - Email FDA OKs breathing device used by Christopher Reeve  NewsChannel 8 - RSS Feeds  NewsChannel 8 - Send FDA OKs breathing device used by Christopher Reeve via Instant Messager
NewsChannel 8 - Share This Article
related stories:
Stay on top of breaking news! Sign up for NewsChannel 8 e-mail alerts.
Your Email:  
The Food and Drug Administration on Wednesday approved a medical device tested about five years ago on actor Christopher Reeve to help him breathe without a ventilator. The implantable device, called NeuRx DPS RA/4 Respiratory Stimulation System and developed by Synapse Biomedical Inc. of Oberlin, Ohio, electrically stimulates the muscles and nerves that run through the diaphragm. It allows some spinal cord injury patients to breathe for at least four hours a day without a mechanical ventilator. Reeve was paralyzed from the neck down in a horseback riding accident in 1995. The "Superman" star received the experimental device in 2003 and could breathe off a ventilator for about 15 minutes while using it. He died in 2004.

"While the NeuRx RA/4 does not cure paralysis of the diaphragm, allowing patients to be free from a mechanical ventilator for at least four hours a day may enhance their quality of life," said Dr. Daniel Schultz, director of the FDA's Center for Devices and Radiological Health.

NewsChannel 8 myTAKE - What's Your Opinion? Spinal cord injuries can affect the muscles of the chest and abdomen, including the diaphragm, which is a lower abdominal muscle essential for breathing.

Normally, a person inhales when the diaphragm contracts and the lungs expand with air and a person exhales when the diaphragm relaxes and the air flows back out of the lungs.

The stimulation device uses four electrodes implanted in the muscle of the diaphragm to stimulate contraction.

The FDA approved the distribution of the stimulation system under a Humanitarian Device Exemption, an approval process for medical devices intended to treat or diagnose conditions that affect fewer than 4,000 people per year.

Need Some Help Around The House? The Pro Knows
You need to be a registered member of
NewsChannel 8 to leave comments on news stories.
Not a member yet? Click Here to sign up.
Username or Email Address
Password
Please leave your comments below:
Messages that harass, abuse or threaten other members; have obscene or otherwise objectionable content; have spam, commercial or advertising content or inappropriate links may be removed and may result in the loss of your posting privileges. Please do not post any private information unless you want it to be available publicly. Never assume that you are completely anonymous and cannot be identified by your posts.


TM & © WJLA/NewsChannel 8, a division of Allbritton Communications Company
Please read our Privacy Policy. By using this site, you accept our Terms of Service.
Children's Television | EEO Reports | NewsChannel 8 adheres to the ICRA RATING SYSTEM