EMBARGOED FOR RELEASE ON APRIL 28, 9:30 A.M. CST
CHICAGO (April 28, 2008) - Currently, the most common form of surgery for
treating cervical degenerative disc disease is an anterior cervical discectomy
and fusion (ACDF). More than 200,000 cervical procedures are performed each
year in the United States to relieve compression on the spinal cord or nerve
roots. Spinal fusion surgery creates a solid union between two or more vertebrae
to help strengthen the spine and alleviate chronic neck pain. There are several
types of spinal fusion surgery, as well as varied instrumentation used to secure
the fusion.
The solid union created between the vertebrae stops the movement between
the bones . While this treatment is effective in helping to reduce pain from
motion and nerve root inflammation, the limited mobility of the neck may lead
to the herniation of other discs over time.
In July 2007, the PRESTIGE ® cervical disc, a product of Medtronic, became
the first and only artificial disc to date approved by the Food and Drug Administration
(FDA) for use in the cervical spine. The PRESTIGE cervical disc underwent an
FDA-approved multicenter clinical trial in the United States, concluding in
2005.
The PRESTIGE cervical disc is indicated for spinal arthroplasty in skeletally
mature patients with degenerative disc disease at one level from C3 to C7,
for intractable radiculopathy and/or myelopathy. This is a stainless-steel
device with a ball-in-trough design, held in place with bone screws.
While cervical artificial discs have been shown to preserve motion at the
operated segment in most patients, their effectiveness in reducing the rate
symptomatic adjacent disc problems has not been established; and a lthough
this technology is promising, the long-term safety and effectiveness of implanted
metal alloys is unknown. Not all patients with symptomatic degenerative cervical
disc disease are candidates, and as with all surgeries, there are related risks.
Researchers recently analyzed data on 541 patients who received either the
PRESTIGE cervical disc or fusion. The results of this study, The Economic
Impact of the Prestige® Cervical Disc System: Results from a Randomized
Clinical Trial , will be presented by Vincent C. Traynelis, MD, (the University
of Iowa), 9:45 to 9:59 a.m. on Tuesday, April 29, 2008, during the 76th Annual
Meeting of the American Association of Neurological Surgeons in Chicago. Co-authors
are Joseph Menzin, PhD (primary author), Bin Zhang, MD, Lisa M. Lines, BS (Boston
Health Economics, Inc), Peter J. Neumann, ScD ( Tufts Medical Center), and
David W. Polly Jr., MD (the University of Minnesota).
Direct costs in 2006 US dollars, were defined as the sum of the costs of
the initial surgery, secondary procedures, and medical devices. Based on the
human capital approach, work productivity was estimated by multiplying the
average daily wage by days of work after surgery. Net benefit was calculated
as the gains in work productivity minus incremental medical costs. The following
results were noted:
- Overall, from a societal perspective, the net benefit of arthroplasty
versus fusion was $5,988 at 2 years postsurgery.
- The total direct cost per patient was $380 higher for arthroplasty patients
than for fusion patients.
- The mean initial procedure cost for the arthroplasty group was $947
higher than for the fusion group.
- Because of fewer secondary procedures, the mean secondary procedure
cost for arthroplasty patients was $567 lower than for fusion patients.
- Arthroplasty patients returned to work following surgery an average
of 38 days sooner than fusion patients, yielding a gain in work productivity
of $6,368.
Arthroplasty patients had fewer secondary procedures and returned to work
earlier thanfusion patients. “From a societal perspective, the economic
benefits associated with these outcomes may offset the increased device costs
associated with arthroplasty therapy,” stated Dr. Tryanelis.
Founded in 1931 as the Harvey Cushing Society, the American Association of
Neurological Surgeons (AANS) is a scientific and educational association with
more than 7,200 members worldwide. The AANS is dedicated to advancing the specialty
of neurological surgery in order to provide the highest quality of neurosurgical
care to the public. All active members of the AANS are certified by the American
Board of Neurological Surgery, the Royal College of Physicians and Surgeons
(Neurosurgery) of Canada or the Mexican Council of Neurological Surgery, AC.
Neurological surgery is the medical specialty concerned with the prevention,
diagnosis, treatment and rehabilitation of disorders that affect the entire
nervous system, including the spinal column, spinal cord, brain and peripheral
nerves.
Boston Health Economics, Inc. (BHE) is an independent research firm located in Waltham, Massachusetts . BHE was responsible for leading the economic evaluation for this clinical trial.
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Media Representatives: If you would like to cover
the meeting or interview a neurosurgeon - either on-site or via telephone -
please contact the AANS Communications Department at (847) 378-0517 or call
the Annual Meeting Press Room beginning Monday, April 28, at (312) 949-3205.