Artificial disc for cervical disc replacement (Research
article)
An artificial cervical disc is a device inserted between
two cervical vertebrae after an intervertebral disc
has been surgically removed in the process of decompressing
the spinal cord or a nerve root. The intent of the
device is to preserve motion at the disc space. It
is an alternative to the use of bone grafts, plates
and screws in pursuit of a fusion following such a
disc removal, which necessarily eliminates motion at
the operated disc space in the neck.
Cervical disc replacement surgery would most typically
be done for patients with cervical disc herniations
that have not responded to non-surgical treatment options
and are significantly affecting the individuals' quality
of life and ability to function.
An artificial disc surgery may be done instead of
an anterior cervical discectomy and fusion. The
theoretical advantages of the artificial cervical disc
over a fusion include:
-
Maintaining normal neck motion
-
Reducing degeneration of adjacent segments of
the cervical spine
-
Eliminating the need for a bone graft
-
Early postoperative neck motion
-
Faster return to normal activity
Postoperative neck braces are not required for
disc replacement operations.
There are currently a number of artificial disc technologies
undergoing clinical trials in the US to evaluate their
safety and effectiveness. Various cervical artificial
discs are in use outside the United States, with the
oldest prototype device dating back to the early 1990s
in England.
Artificial cervical disc background
Many people
may experience neck, shoulder, and/or arm pain in their
lifetime due to disc abnormalities in the neck. These
complaints can be signs of disc herniations or disc
degeneration, and/or arthritis of the neck.
The cervical spine (neck) is composed of vertebral
bodies (the boney building blocks of the spine) and
intervertebral discs, which act as combination universal
joints and shock absorbers between the vertebrae. With
time, the discs can become worn out and cause pain
and/or other symptoms, a condition typically referred
to as degenerative disc disease, a subgroup
of which will include cervical disc herniations. This
means the disc becomes compressed, frayed, and/or herniates
into the adjacent spinal canal where it can press on
nerves or the spinal cord.
Most patients with these types of symptoms do not
need surgery. They typically can improve with
conservative (non-surgical) treatment, which may include
anti-inflammatory medications, physical therapy, or
cold/heat therapy. Over 90% of patients will
experience pain relief with these modalities within
four to six weeks.
Anterior cervical discectomy and fusion
If
a person continues to have significant neck pain and/or
radicular arm pain (meaning that the pain is "shooting" down
from the neck into the arm) after a trial of conservative
treatment, then he or she may be a candidate for cervical
spine surgery. An anterior discectomy and
fusion is the most common operation for treating
patients with symptoms related to a degenerative or
herniated disc in the neck.
This procedure consists of removing the problem disc
entirely and replacing it with a piece of bone taken
either from the patient’s hip or a human cadaver.
A metal plate with screws and/or a cervical collar
may also be used to help hold the bone in place and
to allow this segment of the neck to fuse together.
The purpose of an anterior cervical discectomy and
fusion surgery is twofold:
-
To remove the offending agent—either the herniated
disc or the osteophytes that are compressing the
nerves and/or spinal cord.
-
To eliminate motion by inducing a fusion at the
disc space where the disc has been removed, aided
by the use of bone grafts and possibly plates/screws,
etc. and thereby creating stability and/or
eliminating pain associated with the motion.
This type of surgery typically improves the pain in
over 90% of people with one-level disease. However,
there are potential complications in using bone grafts
in pursuit of a fusion. Harvest of one's own
bone may be associated with both acute and potentially
long-term pain from the donor site. Any type
of bone graft may fail to heal, resulting in a so-called
'non-union', which may require another fusion operation.
Sterile bank bone (cadaver bone) is more convenient
and not associated with donor site complications, but
it tends to heal a lesser percentage of the time. Studies
have also shown that by fusing a segment of the spine,
the levels of the spine above and below the fused area
are now forced to absorb more load since there is no
longer any intervening motion shock absorption. These
adjacent levels will then wear out and become symptomatic
in more than 25% of these patients within ten years,
meaning possibly more surgery. This is called
adjacent-segment degeneration.
The development of artificial cervical discs is intended
to accomplish the same objectives as the traditional
decompression and fusion surgery in terms of providing
pain relief and stability, but with fewer drawbacks.
For example, the cervical artificial disc does not
include the potential complications involved with using
bone graft (e.g. 'non-unions') and theoretically
should lessen the risk of developing adjacent-segment
disc degeneration or disease.
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