Electrical stimulation for spinal fusion
Introduction to electrical stimulation
The use of electrical stimulation to improve the effectiveness
of lumbar spinal fusion has grown significantly over the
past decade. As the number of scientific and clinical
studies validating the use of electrical stimulation to
enhance spine fusion has increased, there is a better
understanding among spine surgeons about how and when
to use specific electrical stimulation devices.
Electrical stimulation is sometimes used as an adjunctive
therapy to enhance the chances of obtaining a solid
spinal fusion. A solid fusion between two vertebrae
eliminates the motion at a painful motion segment, helping
reduce or eliminate the back pain associated with motion
at that spinal segment.
The earliest reported use of electrical stimulation
to improve the efficacy of spinal fusion was over 25
years ago. At that time, a study showed that adjunctive
electrical stimulation improved the fusion rate of a
diagnostically varied group of patients undergoing both
anterior and posterior spinal fusion.1
Bone growth stimulators are most typically employed
for patients who have a lower likelihood of obtaining
a solid spine fusion, such as for patients with the following
risk factors:
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Multi-level fusions
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Revision surgery (after a failed fusion)
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Smokers
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Diagnosis of Grade III or worse spondylolisthesis
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Other risk factors, such as obesity or diabetes
Electrical bone growth stimulation devices costing
between $3,000 and $5,000 have been shown to be cost
effective as they increase the percentage for success
of a solid fusion.
A 1996 study analyzed a large database of patients
and the costs incurred in caring for patients over a
two-year follow-up after a posterolateral spinal fusion
performed with and without pedicle screw instrumentation
and with and without direct current electrical stimulation.
Those patients having a fusion with and without pedicle
screw instrumentation but with internal bone stimulators
showed significant long term cost savings over those
patients fused without the use of internal bone stimulators.2
Before assessing the scientific and clinical efficacy
of these devices to aid spine fusion, it must be appreciated that not all
electrical stimulation devices work in the same manner,
and, all spinal fusions do not physiologically or biomechanically
heal in the same manner.
-
Anterior interbody spine fusions are revascularized
primarily through the vertebral bodies themselves
and the bone graft is under compressive forces.
Bone responds well to compression and this helps
stimulate a healing response.
-
Posterolateral spine fusions are revascularized
primarily from the surrounding muscle tissue. There
is little or no compressive force on the graft material.
The three most common types of bone growth stimulation
used as adjuncts to spinal fusion are: a surgically
implanted stimulator (Internal bone stimulator)
that delivers a direct current (DC) at the fusion site
and two different types of external stimulation (External
bone stimulators).
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Internal bone stimulatorsare implantable
devices that utilize direct current (DC) electrical
stimulation and are implanted at the time of the
spinal fusion.
-
External bone stimulatorsare external
devices worn outside the skin and are either worn
as a brace type stimulator or are attach to the
skin with pads. One common type of external device
utilizes pulsed electromagnetic fields (PEMF). The
newest type of non-invasive stimulation is a capacitive
coupling device (CC) that delivers a constant current
to the fusion site.
This article includes a review of both internal and
external bone stimulators, including how they work and
reviews of clinical studies about their efficacy in
enhancing spinal fusion.
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