News Room
August 16, 2006 - Volume 8
PRESS RELEASE
from the Texas Back Institute
FDA
APPROVES PRODISC-L FOR TREATMENT OF LOW BACK PAIN
Texas Back Institute Served as one of the
Lead Investigators on New Motion Preserving Device which Offers
Alternative to Spinal Fusion Surgery
PLANO, TEXAS
– August 16, 2006
- Texas Back Institute’s Center for Spine Arthroplasty announced
today that the U.S. Food and Drug Administration (FDA) has
approved the Synthes’ ProDisc-L device, an artificial disc used
to replace damaged or worn out discs in order to treat severe
low back pain. Since Texas Back Institute (TBI) surgeon, Jack E.
Zigler, M.D., performed the first ProDisc-L implant in the U.S.
in October 2001, TBI has led the way in research during the
ongoing process of the device’s approval. More ProDisc-L
devices were implanted at TBI than at any other center in the
U.S. during the pivotal trial on single-level lumbar disc
disease.
Developed by
a French spine surgeon, the Synthes’ ProDisc-L total disc
replacement has more than 15 years of clinical follow-up in
Europe. Texas Back Institute served as the highest enrolling
site among the 19 centers in the U.S. that conducted
FDA-approval trials of the device, comparing its clinical
effectiveness and safety to 360○ fusion at any of the
lowest three lumbar disc levels.
“We are
thrilled to have been one of the lead investigators in the
ProDisc-L study,” said Zigler, principal investigator of the
ProDisc-L at Texas Back Institute. “The ProDisc-L is an
extraordinary device and we are excited about this FDA approval,
which will make it available to our patients in the U.S.
This will give our patients another surgical alternative to
fusion.”
Between each
of the vertebrae in the spine is a spongy disc. The discs,
collagen rings surrounding a gel/fluid-filled nucleus, act as
shock absorbers, ensuring vertebrae are properly separated and
cushioned, and that the spine remains flexible.
“Damage to
discs can be caused by injury or just by aging,” said Zigler.
“Worn discs may cause pain between vertebrae once they lose
their cushioning effect, or may place pressure on nerves,
causing muscle spasm and intense leg and back pain.”
The ProDisc-L
is only the second artificial disc replacement device approved
in the U.S.
“The
ProDisc-L is comprised of two metal plates that press into the
surrounding vertebrae, and hold a polyethylene dome in place,”
said Ralph F. Rashbaum, M.D., co-founder of Texas Back Institute
and a ProDisc-L investigator. “After being implanted, the
ProDisc-L device is designed to perform and move like the body’s
own spinal disc, helping to maintain the position of the disc
space while allowing for the flexibility to bend and twist.”
Lower back
pain due to the degeneration of discs affects almost every
American at some point in their lifetime. Each year,
approximately 200,000 Americans undergo lumber spinal fusion,
the most common surgical treatment for low back pain from
degenerative disc disease. In spinal fusion surgery, the damaged
spinal disc is removed and vertebrae are joined together using
bone grafts. Often metal screws and rods are used as well to
improve fusion rates so that motion can no longer occur in that
area of the spine.
Although
fusions relieve back pain, they may significantly limit range of
motion and place extra stress on discs above and below the
fusion site. Fusions usually require patients to wear a back
brace for several months and require an extended period of
rehabilitation, whereas ProDisc-L implant patients require only
a short period of soft bracing and a quicker return to normal
function. About 20 percent of fusion patients require additional
surgery for an adjacent disc problem within ten to fifteen
years.
“Our patients
are showing significant improvements in recovery with ProDisc,”
said Barton Sachs, M.D., MBA with Texas Back Institute.
“Almost all of our ProDisc-L patients are up and walking the
afternoon of surgery, usually with little pain.” Patients
are typically hospitalized for one to two days after surgery.
Clinical trials comparing artificial disc replacement to spinal
fusion surgery show that ProDisc-L recipients maintained or
improved their range of motion, experienced pain relief sooner,
had a quicker recovery and were more satisfied with the
procedure than the fusion patients. They spent less time in
surgery and left the hospital, on average, one day sooner than
patients who had fusions. At two-year follow-up, the
ProDisc-L patients were more satisfied with their outcomes than
the fusion control patients. No significant differences in
complications were found.
Two surgeons work together in a standard artificial disc
implantation procedure. A general surgeon approaches the spine
through an incision in the abdomen and carefully moves blood
vessels and internal organs out of the way to provide access to
the spine. A spine surgeon then removes the damaged disc to
create a space between two vertebrae for the implantation of the
artificial disc, which is done using fluoroscopic guidance.
Generally, the procedure takes about 60 to 90 minutes for a
single level.
“I feel great after my surgery,” said Paul Deasy, a host with
the television shopping network HSN and a ProDisc-L patient.
“I am very pleased with the outcome. I have my life back
and can move forward with all of the things I enjoy.”
Before the FDA approval of the ProDisc-L, the CHARITÉ implant
was the only artificial disc approved for the lumbar spine,
which was available to patients in the U.S. through the Texas
Back Institute’s Center for Spine Arthroplasty. The center
also participated in the two-level ProDisc-L FDA study (which is
not yet completed), and is currently conducting FDA
investigational trials for Synthes’ ProDisc-C, which is designed
as an artificial cervical disc to treat neck pain. In addition,
there are four additional artificial disc devices under FDA
investigation at the TBI Center for Spine Arthroplasty at this
time.
Artificial
disc replacement is not for everyone. As with any surgery, there
are possible complications that can occur. Spine surgery
for low back pain should not be considered unless at least 6
months of nonoperative treatment have been tried without
success. If you feel that you might be a candidate for
artificial disc replacement, call Texas Back Institute at
1-888-783-1937 to make an appointment with one of our doctors.
“If it is even possible, I am even more
thrilled now with my results than I was following my surgery.
I have been playing basketball competitively with players at
least 15 years younger than I since 8 weeks after the
surgery--and doing very well,” said Deasy. “I have also
been lifting weights with my 16 year old son and will soon be in
the best shape of my life since my Junior year in college thanks
to the Texas Back Institute. The only reason I haven't
attempted golf yet is that Dr. Zigler recommended waiting 6
months before trying that particular activity. I could not
be happier. This is truly a miracle of modern
science.”
Texas Back Institute
Texas Back Institute (TBI) is one of the
largest freestanding spine specialty clinics in the United
States. The Institute, based in Plano, Texas, was established in
1978 and provides comprehensive medical care for individuals
with back and neck pain. TBI is a back care leader specializing
in spinal arthroplasty minimally invasive spine surgery, spinal
deformation and spinal oncology care. As an academic health care
organization, TBI has trained hundreds of physicians, scientists
and allied health professionals. Its research institution
employs state-of-the-art technology and research to treat
patients and is involved in the most clinical trials of
artificial discs. TBI’s professional staff includes
board-certified spine surgeons, general surgeons, internists,
chiropractors, physiatrists, pain specialists, exercise
physiologists and a team of physical and occupational
therapists. Texas Back Institute’s main office is located in
Plano, with offices in Denton, Fort Worth, Greenville, Garland,
Midland, Trophy Club, TX and Phoenix, AZ. For more information,
visit
www.texasback.com.
MEDIA CONTACT
For more information, contact Meredith Falke, (214) 891-7795
meredith_falke@richards.com
Consumer phone number: 1-800-247-BACK
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