ADRSupport Community  

Go Back   ADRSupport Community > General Discussion > The Big File

The Big File All issues not easily categorized in the above forums are here. Comments on general health, diet, "getting comfortable," and more are here.


Reply
 
Thread Tools
  #1  
Old 10-16-2005, 03:08 PM
Harrison's Avatar
Harrison Harrison is offline
Administrator
 
Join Date: Oct 2004
Posts: 7,014
Default

The following information describes BCBS�s criteria for assessing the viability or �effectiveness� of a new technology relative to insurance coverage. A new member emailed me info on the BCBS medical advisory panel and noted that of the 19 experts, not one has orthopedic expertise. I think it�s helpful to post this here, as many people are still battling BCBS for ADR coverage. (Thanks for the reminder Charles!)

Technology Evaluation Center Criteria
The Blue Cross and Blue Shield Association uses the five criteria below to assess whether a technology improves health outcomes such as length of life, quality of life and functional ability.

1. The technology must have final approval from the appropriate governmental regulatory bodies.
� This criterion applies to drugs, biological products, devices and any other product or procedure that must have final approval to market from the U.S. Food and Drug Administration or any other federal governmental body with authority to regulate the technology.
� Any approval that is granted as an interim step in the U.S. Food and Drug Administration's or any other federal governmental body's regulatory process is not sufficient.
� The indications for which the technology is approved need not be the same as those which Blue Cross and Blue Shield Association's Technology Evaluation Center is evaluating.

2. The scientific evidence must permit conclusions concerning the effect of the technology on health outcomes.
� The evidence should consist of well-designed and well-conducted investigations published in peer-reviewed journals. The quality of the body of studies and the consistency of the results are considered in evaluating the evidence.
� The evidence should demonstrate that the technology can measure or alter the physiological changes related to a disease, injury, illness, or condition. In addition, there should be evidence or a convincing argument based on established medical facts that such measurement or alteration affects health outcomes.
� Opinions and evaluations by national medical associations, consensus panels, or other technology evaluation bodies are evaluated according to the scientific quality of the supporting evidence and rationale.

3. The technology must improve the net health outcome.
� The technology's beneficial effects on health outcomes should outweigh any harmful effects on health outcomes.

4. The technology must be as beneficial as any established alternatives.
� The technology should improve the net health outcome as much as, or more than, established alternatives.

5. The improvement must be attainable outside the investigational settings.
� When used under the usual conditions of medical practice, the technology should be reasonably expected to satisfy TEC criteria #3 and #4.

http://www.bcbs.com/tec/whatistec.html
__________________
"Harrison" - info (at) adrsupport.org
Fell on my ***winter 2003, Canceled fusion April 6 2004
Reborn June 25th, 2004, L5-S1 ADR Charite in Boston
Founder & moderator of ADRSupport - 2004
Founder Arthroplasty Patient Foundation a 501(c)(3) - 2006
Creator & producer, Why Am I Still Sick? - 2012
Donate www.arthropatient.org/about/donate
Reply With Quote
  #2  
Old 10-16-2005, 05:59 PM
sahuaro sahuaro is offline
Senior Member
 
Join Date: May 2005
Posts: 455
Default

What pops out is criterion #4, that the technology must be "as beneficial" as any established alternatives. My impression has been that insurance denials have been based on the claim that ADR is not more beneficial than fusion.
__________________
2001 MVA; C5-C6 disk extruded
ongoing physical therapy, exercise and massage
ESI's, oral prednisone, trigger point injections
foraminal and central stenosis C5/C6 and c6/C7
2007 EMG/nerve conduction shows pattern of chronic radiculopathy
January, 2008: Prestige ST Artificial Disk Replacement, C5/6
Reply With Quote
  #3  
Old 10-18-2005, 02:17 AM
ans ans is offline
Senior Member
 
Join Date: Mar 2005
Posts: 1,596
Default

Sounds like fancy mumbo-jumbo in keeping costs down.
__________________
Severe, extensive DDD, considered inoperable by Dr. Regan, Lauressen, & some guy at UCLA. Severe foraminal stenosis (guess they can't operate!) and some spinal cord compression that Lauryssen would fix if gets outta hand.
Reply With Quote
  #4  
Old 11-05-2005, 10:07 PM
Mariaa Mariaa is offline
Banned
 
Join Date: Nov 2004
Posts: 1,121
Default

The technology must improve the net health outcome.
� The technology's beneficial effects on health outcomes should outweigh any harmful effects on health outcomes.

4. The technology must be as beneficial as any established alternatives.
� The technology should improve the net health outcome as much as, or more than, established alternatives.

These two make me laugh.. one would only know the answer after having the surgery/using the medication, undergoing whatever procedure...
Reply With Quote
Reply

Bookmarks


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Blue Cross Blue Shield ADR Denial finally reversed ZorroSF Insurance Hell 17 01-30-2014 07:46 PM
Blue Cross Blue Shield {aka Blue Crap} chasswen Insurance Hell 16 06-06-2012 05:03 PM
Blue Cross Blue Shield ADR Coverage stuschulz Insurance Hell 10 09-24-2007 09:54 AM
Technology Evaluation Center Blue Cross Blue Shield Abbe Insurance Hell 2 07-03-2007 07:30 PM
Federal Blue Cross Blue Shield misty The Big File 6 04-04-2005 11:34 PM


All times are GMT -4. The time now is 08:15 AM.


© Copyright 2006-2023 ADRSupport.org All rights reserved.