Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Friday, August 27, 2021

FDA approves stroke rehabilitation system

 

 Really? You mean you haven't been doing this for survivors for 9 years already?

FDA approves stroke rehabilitation system

The FDA approved the Vivistim System, a drug-free rehabilitation system using vagus nerve stimulation for treating moderate and severe upper extremity mobility loss caused by chronic ischemic stroke.

“People who have lost mobility in their hands and arms due to ischemic stroke are often limited in their treatment options for regaining motor function,” Christopher M. Loftus, MD, acting director of the FDA’s Center for Devices and Radiological Health’s office of neurological and physical medicine devices, said in a press release. “Today’s approval of the Vivistim Paired VNS System offers the first stroke rehabilitation option using vagus nerve stimulation.”

MicroTransponder’s Vivistim Paired VNS System (Vivistim System) used in conjunction with rehabilitation therapy helps improve motor function in the hands and arms following ischemic stroke, according to the release. The system uses an implanted pulse generator to electrically stimulate the vagus nerve, which connects the brain and abdomen. The system can be used in clinical settings and at home.

The FDA granted approval based on a clinical study of 108 patients in the U.S. and the U.K., which found patients treated with the Vivistim System had more improved mobility than patients in the control group.

“Used alongside rehabilitative exercise, this device may offer benefit to those who have lost function in their upper limbs due to ischemic stroke,” Loftus said in the release.

 

2 comments:

  1. Dean,
    The underlying clinical trial was completed December 2014.
    https://clinicaltrials.gov/ct2/show/NCT01669161

    This is from the actual company:
    https://microtransponder.com/en-gb/stroke/physicians/clinical-experience

    Here is a story by FDA
    https://www.fda.gov/news-events/press-announcements/fda-approves-first-its-kind-stroke-rehabilitation-system

    The FDA story has this in it as how it got approved so fast:
    https://www.fda.gov/medical-devices/how-study-and-market-your-device/breakthrough-devices-program

    FDA idea of "fast" took 7 years. What a joke!


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  2. Dean, After sending comment yesterday. I found the following clinical trial that was just done from 2017-21 and was getting all the new press and appears to be a follow-up on the 2014 clinical trial. Sorry about that.
    Pivotal Study of VNS During Rehab After Stroke (VNS-REHAB) (VNS-REHAB)
    https://clinicaltrials.gov/ct2/show/NCT03131960

    ReplyDelete