Spinal disc replacement with the CHARITÉ Artificial Disc
Introduction to artificial discs
In October 2004 the CHARITÉ™ Artificial Disc was the
first disc approved for disc replacement use in the general population
of back pain patients in the U.S. There is a great deal of interest
in the medical community and among back pain patients regarding
the potential of artificial discs for lumbar disc replacement. But
despite all the publicity, it’s important to remember that
artificial discs are not a miracle cure. Like any medical treatment
for low back pain, lumbar artificial disc replacement surgery has
both good potential and some considerable risks. Given that artificial
discs are still a relatively new technology and procedure, disc
replacement surgery also has a number of unknown risks.
To date, ongoing low back pain from degenerative low back conditions
that does not get better with non-surgical care has been treated
with some type of lumbar spinal fusion surgery. It is important
to note that modern spinal fusion techniques and technologies
have dramatically improved the outcomes of fusion surgery in recent
years. When spine fusion surgery is done for the right indications
by an experienced spine surgeon, it is generally a very reliable
surgery.
However, spine fusion does change the mechanics of the segment
of the low back that is fused. One major intended benefit of artificial
disc replacement (ADR) surgery over spine fusion is that it does
not change the biomechanics of the lower spine, allowing the spine
to maintain its normal range of motion and thereby reducing or
eliminating the risk of degeneration in adjacent segments of the
spine.
The CHARITÉ Artificial Disc (DePuy Spine, Inc., a Johnson
and Johnson company), is composed of two metallic endplates and
a polyethylene core that moves between them. During the surgery,
the patient’s degenerated disc is removed and a pair of
endplates made of cobalt chromium are inserted in the space between
the vertebrae and attached to the vertebrae above and below the
disc. A polyethylene material is then inserted between the plates
to create a disc-like structure that mimics the normal disc by
providing both a normal level of separation between the vertebrae
and allowing the usual range of motion and flexibility for that
segment of the spine.
While this article reviews the CHARITÉ disc prosthesis
(see Figure 1),there are several other artificial discs that have
been developed and are currently in clinical trials in the U.S.
or are in the process of development.
The CHARITÉ Artificial Disc was approved for use in the
U.S. in October 2004, but variations of the CHARITÉ disc
replacement technology have long been in use in other countries
and the CHARITÉ Artificial Disc replacement procedure is
now available in more than 30 countries. Prior to approval for
use in the U.S., approximately 95% of all procedures for the CHARITÉ
Artificial Disc device were done in the United Kingdom, France,
Germany, and the Netherlands.
Theoretical advantages of the CHARITÉ Artificial Disc
The CHARITÉ disc implant is designed to mimic the functionality
of the patient’s own intervertebral disc (see Figure 2).
The prosthesis is intended to maintain the normal movement between
the vertebral bodies and prevent them from collapsing (and thereby
irritating or damaging the nerve root) by maintaining the disc
space height between the bones.
One of the main theoretical advantages of artificial discs (vs.
spine fusion surgery) is to preserve the mobility of the patient’s
adjacent discs and delay the onset of arthritic changes adjacent
to a fused level. The procedure can be a substitute for spinal
fusion, which eliminates the motion from a painful motion segment
by fusing the vertebrae together. Spinal fusion does tend to place
increased stress on the adjacent vertebral segments.
Theoretical disadvantages of the CHARITÉ Artificial Disc
Since artificial hips and knees were introduced in the 1960’s,
doctors have explored the idea of prosthetic replacements for
damaged or degenerated intervertebral discs. The disc is a very
complicated joint, so the engineering challenge to partially or
fully replace a disc is considerable. Also, because disc injury
is a common cause of back pain in younger adults (age 30 to 50),
an artificial disc needs to be designed to last for decades. The
demands on a lumbar artificial disc will be very great and may
not outlast the lifetime of the patient - meaning patients may
need revision surgery. And because of the nearby vascular structures
and scar tissue from the original surgery, revision procedures
for a lumbar artificial disc can be very dangerous.
The outcome of any treatment, especially surgery, relies on the
accurate or precise diagnosis of the source of pain. There are
also psychological, physical, and social factors involved in the
successful treatment of chronic pain. Collectively, these are
known as surgical indications. Diagnostic procedures, spine imaging,
surgical indications, and surgical techniques have been refined
over the years so that experienced spinal practitioners can reliably
and predictably achieve excellent clinical outcomes with modern
spinal fusion surgery. Because it is a new technology, the indications,
as well as the type of disc replacement implants, are quite specific.
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