Thursday, September 20, 2012

Wheelchair suppliers say crack down on Medicare fraud goes too far; insurer applauds effort

By Associated Press, Published: September 19

WASHINGTON — Wheelchair suppliers raised concerns Wednesday about a new government program that requires Medicare contractors to sign off before power wheelchairs can be delivered to elderly and disabled consumers.

Federal health officials countered that the changes are needed because nearly 80 percent of the power wheelchair claims submitted to Medicare don’t meet program requirements. That error rate represents more than $492 million in improper payments annually.

The new program began on Sept. 1 and requires providers in seven states to get confirmation from a government contractor that Medicare will pay for the device before they deliver it.
Michael Clark, general counsel for the SCOOTER Store, says the pilot project goes too far and every claim his business has submitted under the new program has been denied.

GOP members of the Senate Special Aging Committee called the hearing to learn how the pilot project was working. Sen. Bob Corker, R-Tenn., said that television commercials promoting wheelchairs give him the impression that the companies would figure out some way for the government to foot the bill if customers would only inquire.

“I think most Americans have seen these advertisements on TV and probably question what the federal government is doing. I certainly do.”

Clark told Corker that only 13 percent of those who seek a power wheelchair end up getting one. He said the idea that the company is simply trying to sell as many chairs as it can regardless of merit was incorrect.

The cost for the devices ranges from $1,500 for scooters to $3,600 for more complex power wheelchairs over the course of the rental period.

Under Medicare rules, power wheelchairs are covered only when patients need them for daily activities within the home and when canes, walkers or manual wheelchairs are considered as insufficient assistance.

Medicare will only pay after a physician meets with patients face-to-face and prescribes the wheelchair. A supplier recommends the type of wheelchair needed and also submits a claim to Medicare. Under the demonstration project, a doctor or supplier will submit a prior authorization request along with all relevant documents supporting Medicare coverage. The contractor then decides whether a request has met the requirements for coverage.

Medicare officials said such prior authorization is routinely required in the private sector. It does not add paperwork, but simply requires that documents be submitted earlier in the review process.
Stephen Peake, a medical director at Blue Cross Blue Shield of Tennessee, applauded the Centers for Medicare and Medicaid Services for the new program and that he would welcome it being used in Tennessee. He said if the program’s results mirror those with his company then it will result in significant savings for taxpayers.

Copyright 2012 The Associated Press. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.

http://www.washingtonpost.com/politics/health_care/wheelchair-suppliers-say-effort-to-crack-down-on-medicare-fraud-goes-too-far/2012/09/19/032ee93a-02ab-11e2-9132-f2750cd65f97_story.html
 

Tuesday, September 18, 2012

A Brain Implant that Thinks


From: Technology Review - 09/13/2012
By: Susan Young

Researchers have used a neural implant to recapture a lost decision-making process in monkeys-demonstrating that a neural prosthetic can recover cognitive function in a primate brain. The results suggest that neural implants could one day be used to recover specific brain functions in patients with brain injuries or localized brain disease.

Read the entire article at:


 
Links:

Facilitation and restoration of cognitive function in primate prefrontal cortex by a neuroprosthesis that utilizes minicolumn-specific neural iring
http://iopscience.iop.org/1741-2552/9/5/056012

Brain Chip Helps Quadriplegics Move Robotic Arms with Their Thoughts http://www.technologyreview.com/news/427939/brain-chip-helps-quadriplegics-move-robotic-arms/

 Brain Pacemakers
http://www.technologyreview.com/featured-story/401160/brain-pacemakers/


Samuel A. Deadwyler, PhD
http://www.wakehealth.edu/Faculty/Deadwyler-Samuel-A.htm?LangType=1033

How technology is helping people with speech impairments to talk

 

New technology is allowing people such as Alan Martin, who has cerebral palsy, the chance to communicate properly for the first time
 
 
 
Alan Martin joking with Jon Henley
The world at his fingertips: Alan Martin shares a joke with Jon Henley. Photograph: Christopher Thomond for the Guardian
 
I am sitting staring at a computer screen. So far so banal, except that this screen features a red dot that, by some technological magic, tracks the movement of my eyes: I can place it where I want on the screen just by looking. The bottom of the screen portrays a keyboard, although I could, if I chose, select other screens made up of various vocabulary, grammar and expression-based menus, which, for experienced users, would doubtless speed things up.

Because this is painstaking. I look at a letter, and the red dot sits on it. I continue staring, and the dot blinks, twice. The letter then pops up at the top of the screen. I move on to the next letter (or, more often, the backspace).

It gets easier: there's predictive text, like on a mobile phone, so I stare at the word I want, which gets added to my sentence. Eventually, the phrase is complete. I stare at it and it blinks. "What an amazing machine," says a cool, synthesised voice. "Rather let down by its user."

This is eye-gaze technology, at the leading edge of a fast-evolving and – for those who need it – vital field known as augmentative and alternative communication (AAC), plus the closely related assistive technology (AT). Without it, we would have been denied access to the remarkable mind of Professor Stephen Hawking (not to mention his starring role at the Paralympics opening ceremony). Nor would the locked-in syndrome sufferer Tony Nicklinson have been able to express so memorably – using eye-gaze – his despair at being refused the right to an assisted suicide. Hawking, with characteristic elegance, summarises its value: "Even more important than the freedom of speech is the freedom to speak."

Most of us know nothing about it. Worse, says Anna Reeves of the ACE Centre, a national charity that provides independent AAC assessments, advice and training, "a lot of people who need it have real trouble getting it. The funding's a mess. It falls between education and health, and most local authorities don't have specific budgets for it."

Yet AAC can be life-changing. Alan Martin, who developed cerebral palsy as an infant, was 31 before friends clubbed together to buy his first communication aid. "Before that," he explains in one of several pre-recorded messages he can activate on his current machine, "I relied on facial expressions and gestures. It was very frustrating."

Jovial and instantly engaging, Martin now runs his own company, Mouse on the Move, providing inclusive dance workshops for people with disabilities. To talk, and teach, he uses a wheelchair-mounted portable computer. He has reasonable control of his right arm, so uses a finger to press symbols on the screen that open up successive folders of images, words and frequently used phrases. He can also send emails and – an exciting new addition – text messages through a mobile phone connected to his computer. The whole system, Reeves says, cost around £8,000, and is in the middle of a spectrum of more than 100 different kinds of communication aids. ("Rubbish," says Martin succinctly, when asked what he thought of his first device.)

At one end are simple picture books and communication boards from which users select letters, words, phrases, pictures or symbols to communicate their message. Simple electronic devices contain digitised speech messages pre-recorded by a family member or carer and activated by a big button. More sophisticated boards hold up to 32 symbols and attached messages.

But helpful as these devices are, they are limited to pre-set messages. Computer-generated speech lets users say what they want to say. A portable machine called the Lightwriter has existed since the 1970s, allowing people who can type to display messages on a screen and also speak synthetically. More recently, says Reeves, "we've seen some great apps being developed for iPads and the like. If they work for you, they're brilliant. Especially for kids, because they're cool."

One, Proloquo2Go, even features a couple of authentic British children's voices, as well as "sad" and "happy" versions of the same voice; until recently synthesised speech robbed users of accent, emotion and intonation. Alan, who was born on Merseyside and is a huge Liverpool fan, would love to be able to speak scouse.

At the top end are the systems used by Martin, Nicklinson and Hawking: fully functioning computers, controlled in any number of ingenious ways. Hawking now uses a muscle in his cheek; another system moves the mouse through minuscule lip movement. These systems are capable of emailing, texting and even opening doors, turning on lights and operating the telly.

There are, Reeves says, perhaps 260,000 people in Britain using AAC equipment, about 10% of them using this kind of hi-tech aid. Their conditions range from serious physical and learning disabilities through sensory impairment to autism, motor neurone disease, stroke and, commonly, cerebral palsy. "There are also many who are undiagnosed, who simply present to us with an inability to communicate," she says. "It's far more common than people think."

Formed this summer by the merger of two separate charities to develop what would be, astonishingly, Britain's first national AAC/AT service, the ACE Centre holds open information days, carries out in-depth needs assessments on individuals, and advises and trains children and adults with AAC needs as well as teachers and carers.

But it doesn't have the money to provide actual aids for any longer than a short test period. Reeves wants to see a proper, secure, nationwide provision model that would ensure everyone in the country who needs communication aids gets them, preferably on long-term loan. "At the moment," she says, "we feel a bit like ladies in a sweet shop. We say: 'Look, this is all the lovely stuff available. Now fund it.' Which is wrong: communication is not a privilege, it's a fundamental right."

For futher information visit: ace-centre.org.uk, communicationmatters.org.uk

Wednesday, September 12, 2012

ALS Service Locator for the iPad/iPhone

By Centers For Disease Control and Prevention

Description

This CDC iPad application, brought to you by the National Amyotrophic Lateral Sclerosis (ALS) Registry, has been designed as a way for users to easily access the closest ALS service providers nearest the user’s ZIP code. The application allows a user to pick a particular type of ALS facility (Clinics, ALS Association (ALSA) Chapters or Muscular Dystrophy Association (MDA) Offices), enter a valid ZIP code and perform a search. Alternatively, a user can use the geolocation feature to find their current location and use the returned ZIP code to perform a search. The results will return a map and table of the five closest ALS facilities nearest the provided ZIP code. The results are ordered from A – E, whereas A is the closest facility and E is the farthest facility. The tabular information contains the facility’s name, affiliation, address, phone and the approximate distance from the provided ZIP code. The map is fully interactive and allows the user to pan and zoom into the facilities location. The user can touch a facility point to get information on that particular facility.



 

iPad Screenshot 1
iPad Screenshot 2
iPad Screenshot 3
iPad Screenshot 4
iPad Screenshot 5


ALSSvcLocator
View In iTunes
  • Free
  • Category: Health & Fitness
  • Released: 05 September 2012
  • Version: 2.2
  • Size: 25.6 MB
  • Languages: English, Chinese, Czech, Dutch, French, German, Italian, Japanese, Korean, Polish, Portuguese, Russian, Spanish, Swedish, Turkish
  • Developer: Centers for Disease Control and Prevention
Requirements: Compatible with iPad. Requires iOS 4.0 or later.

Customer Ratings

We have not received enough ratings to display an average for the current version of this application.

More iPad Apps by Centers For Disease Control and Prevention

Tuesday, September 11, 2012

Giving everyone a voice: Researchers aim to improve alternative communication devices

Four University of Wisconsin-Milwaukee researchers will be exploring the issues and challenges faced by those using synthesized speech. The researchers bring different perspectives to the project, which is funded by a $200,000 Center for 21st Century Studies Interdisciplinary Challenge Award. Shelley Lund is an associate professor of communication sciences and disorders; Patricia Mayes is an associate professor of English with training in linguistics; Heather Warren-Crow is an assistant professor of art theory and practice in the Peck School of the Arts; and Yi Hu is an assistant professor of electrical engineering and computer science. Augmentative and Alternative Communication (AAC) technologies, developed in the 1970s and early 1980s, allow an individual to type what they want to say into a voice synthesizer, press a button and turn their typed words into spoken words.

Read more at: http://phys.org/news/2012-09-voice-aim-alternative-devices.html#jCp

Monday, September 10, 2012

28th Annual International CSUN Technology & Persons with Disabilities Conference

The Center on Disabilities at California State University, Northridge is pleased to announce that the Call for Papers for the 28th Annual International Technology and Persons with Disabilities Conference opens next week.

The Call for Papers will open on Tuesday, September 4, 2012 and will close on Friday, October 12, 2012.

Please Note: The Call for Papers will be open for 6 weeks to provide presenters ample time to prepare and submit proposals by the deadline. We would greatly appreciate your cooperation by adhering to this timeline. This will allow our Program Committee to review submissions continuously throughout the Call for Papers and acceptance notifications can be sent out on the same basis. Your support of this request will help us prepare once again for this year’s early event dates. Additionally, if the Program Committee receives submissions on a timely basis it would not only alleviate the workload of reviewing last-minute submissions, but would benefit speakers as they would receive notifications sooner and could begin coordinating their arrangements for travel and registration.

Visit http://www.csunconference.org for more information about the Call for Papers and the 2013 CSUN Conference. We strongly encourage you to review the information carefully as several updates to the submission procedures have been enacted.

One of the most important updates includes announcing that this year we will be launching our on-line Journal. This information and more is contained in the Call for Papers Procedures and Instructions. Your cooperation in reading, reviewing and adhering to the policies of the Procedures and Instructions would be greatly appreciated and is necessary to ensure that you understand and agree to the submission process and the online journal guidelines.

Other important information includes:

Please remember that labs are not available for General Session presentations.

All sessions will be open and available on a first-come/first-save basis as the feedback from your 2012 conference experience indicated that this option was preferred over the former “save a seat” procedure.

Exhibit Hall News! The Exhibit Hall will open on Wednesday, February 27 at 12:00 pm!

Exhibit Hours will be announced and posted on the website soon so please visit the conference site for information.

The 2013 CSUN Conference will be held February 25-March 2 at the Manchester Grand Hyatt Hotel in San Diego, California.


Regards,
Sandy Plotin
Managing Director
Center on Disabilities
conference@csun.edu
818-677-2578
SAVE THE DATES!
Call for Papers: September 4-October 12, 2012
Conference: February 25-March 2, 2013

St. Ambrose (Iowa) professor's technology helps disabled

WATERLOO, Iowa (AP) — One person's trash is another's treasure.

The old saying is most commonly used when describing a fun thrift store find or a roadside freebie. For Dylan Huntbach, one man's trash is his lifeline to independence.

Huntbach, 20, was paralyzed from the neck down when he dove from the shore and struck the bottom of the Cedar River in early July. He was airlifted to University of Iowa Hospitals and Clinics and just recently returned to the Cedar Valley for intensive rehabilitation at Covenant Medical Center.

It was there that Huntbach met Katie Jo Wedeking, an occupational therapist and St. Ambrose University graduate. At St. Ambrose, Wedeking worked closely with Professor Jon Turnquist, an assistive technology professional.

At Covenant, she took that knowledge about assistive technology and put it to work for Huntbach.

Wedeking recently installed what is known as an environmental control unit in Huntbach's rehab room. The unit allows Huntbach to turn on his radio and his television, and to control the volume and channels. He can turn a lamp and a fan off and on and call his nurses at their station. He can even call his friends on the phone.

And when he leaves the hospital in just a few short weeks, Wedeking will install a similar system in his home at no cost to the family.

"This is my demonstration model, but I didn't want Dylan to have to wait," Wedeking said.

Similar units purchased through assistive technology companies would cost the family between $7,000 and $20,000. Huntbach said he used one of those units in Iowa City.

"It means more independence. I don't have to rely on someone to turn my TV or my radio on. I can just do it in the night or whenever," he said.

Huntbach's parents, Kim and Dave, said the device also has put their minds at ease.

"When he got his voice he could yell, but before he got his voice he could turn his TV up or his radio up and they would hear that," Dave Huntbach said.

Dylan uses a simple sip and puff switch to activate the computer program and make his choices. Others can activate the program using a tilt of their head, the tap of a finger, the pressure of their wrist, the flick of their big toe or even the blink of their eye.

"It is truly individualized for each person's ability and needs," Wedeking said.

Turnquist uses discarded computers, flatscreen monitors and other electronics to build the device for a fraction of the cost of the commercial options. The university covers the costs he does incur.
The only difference in the programs is the size of the unit. Commercial units are full computers housed inside small boxes that can attach to a chair or bed. People using Turnquist's program must have space for the computer in the room where they want the control.

Glen Henry, the former University of Northern Iowa swim coach who has been paralyzed from the chest down for more than eight years, said he had never heard of an ECU until Wedeking mentioned it during a therapy session. Now, he can't imagine life without it.

"Those are all outstanding assets I didn't possess prior to meeting up with Katie Jo," Henry said. "What it means to me is I have a lot more freedom to do some of the things I could not do before without assistance. I had to ask somebody to turn it on. Turn it off. Turn it up. Turn it down. Whistle and yell through the window for my wife on the other side of the house. I've explored and discovered there is some independence that has really come about because of this."

His wife, Karen, called the ECU "monumental" for the couple.

Turnquist, who also has a background in computer programming, started developing the program for the ECUs more than a decade ago in part because he was encountering patients he just couldn't help as an occupational therapist. His units, which are usually powered by computers up to a decade old, are now in hospitals and homes across the Midwest and even the world.

"All of these assistive technologies mean independence for the individual and also a decreased effort for the caregiver. Now they can get a break, too," Turnquist said. "Then, the patient starts feeling a lot better, not so helpless and hopeless."

And Huntbach is ready to start testing out some of that new assistive and adaptive technology. Next on his list of activities to tackle: the Xbox. The Microsoft Kinect's voice-activated feature already allows him to control his own movie selection, but he's got his sights set on playing video games again.

"That would be an example of the extremes you can take things with assistive technology and the things we have the capability of doing with adaptations," Wedeking said. "The things I have seen Jon Turnquist do with assistive technology is unbelievable. That he could potentially open up an Xbox remote and wire the connectors to adaptor remotes so that someone would be able to manipulate it to play their Xbox games, there is not a doubt in my mind that he can figure it out or direct one of his students to figure it out."
___
Information from: Waterloo-Cedar Falls Courier, http://www.wcfcourier.com