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Spinal Decompression
By Thomas A. Gionis, MD, JD, MBA,
MHA, FICS, FRCS, and Eric Groteke, DC, CCIC
Orthopedic Technology
Review, Vol. 5-6, Nov-Dec 2003.
The outcome of a clinical
study evaluating the effect of nonsurgical intervention on symptoms of
spine patients with herniated and degenerative disc disease is
presented.
This clinical outcomes
study was performed to evaluate the effect of spinal decompression on
symptoms and physical findings of patients with herniated and
degenerative disc disease. Results showed that 86% of the 219 patients
who completed the therapy reported immediate resolution of symptoms,
while 84% remained pain-free 90 days post-treatment. Physical
examination findings showed improvement in 92% of the 219 patients, and
remained intact in 89% of these patients 90 days after treatment. This
study shows that disc disease-the most common cause of back pain, which
costs the American health care system more than $50 billion annually-can
be cost-effectively treated using spinal decompression. The cost for
successful non-surgical therapy is less than a tenth of that for
surgery. These results show that biotechnological advances of spinal
decompression reveal promising results for the future of effective
management of patients with disc herniation and degenerative disc
diseases. Long-term outcome studies are needed to determine if
non-surgical treatment prevents later surgery, or merely delays it.
INTRODUCTION: ADVANCES IN
BIOTECHNOLOGY
With the recent advances
in biotechnology, spinal decompression has evolved into a cost-effective
nonsurgical treatment for herniated and degenerative spinal disc
disease, one of the major causes of back pain. This nonsurgical
treatment for herniated and degenerative spinal disc disease works on
the affected spinal segment by significantly reducing intradiscal
pressures.1 Chronic low back pain disability is the most expensive
benign condition that is medically treated in industrial countries. It
is also the number one cause of disability in persons under age 45.
After 45, it is the third leading cause of disability.2 Disc disease
costs the health care system more than $50 billion a year.
The intervertebral disc
is made up of sheets of fibers that form a fibrocartilaginous structure,
which encapsulates the inner mucopolysaccharide gel nucleus. The outer
wall and gel act hydrodynamically. The intrinsic pressure of the fluid
within the semirigid enclosed outer wall allows hydrodynamic activity,
making the intervertebral disc a mechanical structure.3 As a person
utilizes various normal ranges of motion, spinal discs deform as a
result of pressure changes within the disc.4 The disc deforms, causing
nuclear migration and elongation of annular fibers. Osteophytes develop
along the junction of vertebral bodies and discs, causing a disease
known as spondylosis. This disc narrows from the alteration of the
nucleus pulposus, which changes from a gelatinous consistency to a more
fibrous nature as the aging process continues. The disc space thins with
sclerosis of the cartilaginous end plates and new bone formation around
the periphery of the contiguous vertebral surfaces. The altered
mechanics place stress on the posterior diarthrodial joints, causing
them to lose their normal nuclear fulcrum for movement. With the loss of
disc space, the plane of articulation of the facet surface is no longer
congruous. This stress results in degenerative arthritis of the
articular surfaces.5
This is especially
important in occupational repetitive injuries, which make up a majority
of work-related injuries. When disc degeneration occurs, the layers of
the annulus can separate in places and form circumferential tears.
Several of these circumferential tears may unite and result in a radial
tear where the material may herniate to produce disc herniation or
prolapse. Even though a disc herniation may not occur, the annulus
produces weakening, circumferential bulging, and loss of intervertebral
disc height. As a result, discograms at this stage usually reveal
reduced interdiscal pressure.
The early changes that
have been identified in the nucleus pulposus and annulus fibrosis are
probably biomechanical and relate to aging. Any additional trauma on
these changes can speed up the process of degeneration. When there is a
discogenic injury, physical displacement occurs, as well as tissue edema
and muscle spasm, which increase the intradiscal pressures and restrict
fluid migration.6 Additionally, compression injuries causing an endplate
fracture can predispose the disc to degeneration in the future.
The alteration of normal
kinetics is the most prevalent cause of lower back pain and disc
disruption and thus it is vital to maintain homeostasis in and around
the spinal disc; Yong-Hing and Kirkaldy-Willis7 have correlated this
degeneration to clinical symptoms. The three clinical stages of spinal
degeneration include:
1. Stage of Dysfunction.
There is little pathology and symptoms are subtle or absent. The
diagnosis of Lumbalgia and rotatory strain are commonly used.
2. Stage of Instability.
Abnormal movement of the motion segment of instability exists and the
patient complains of moderate symptoms with objective findings.
Conservative care is used and sometimes surgery is indicated.
3. Stage of
Stabilization. The third phase where there are severe degenerative
changes of the disc and facets reduce motion with likely stenosis.
Spinal decompression has
been shown to decompress the disc space, and in the clinical picture of
low back pain is distinguishable from conventional spinal traction.8,9
According to the literature, traditional traction has proven to be less
effective and biomechanically inadequate to produce optimal therapeutic
results.8-11 In fact, one study by Mangion et al concluded that any
benefit derived from continuous traction devices was due to enforced
immobilization rather than actual traction.10 In another study, Weber
compared patients treated with traction to a control group that had
simulated traction and demonstrated no significant differences.11
Research confirms that traditional traction does not produce spinal
decompression. Instead, decompression, that is, unloading due to
distraction and positioning of the intervertebral discs and facet joints
of the lumbar spine, has been proven an effective treatment for
herniated and degenerative disc disease, by producing and sustaining
negative intradiscal pressure in the disc space. In agreement with
Nachemon's findings and Yong-Hing and Kirkaldy-Willis,1 spinal
decompression treatment for low back pain intervenes in the natural
history of spinal degeneration.7,12 Matthews13 used epidurography to
study patients thought to have lumbar disc protrusion. With applied
forces of 120 pounds x 20 minutes, he was able to demonstrate that the
contrast material was drawn into the disc spaces by osmotic changes.
Goldfish14 speculates that the degenerated disc may benefit by lowering
intradiscal pressure, affecting the nutritional state of the nucleus
pulposus. Ramos and Martin8 showed by precisely directed distraction
forces, intradiscal pressure could dramatically drop into a negative
range. A study by Onel et al15 reported the positive effects of
distraction on the disc with contour changes by computed tomography
imaging. High intradiscal pressures associated with both herniated and
degenerated discs interfere with the restoration of homeostasis and
repair of injured tissue.
Biotechnological advances
have fostered the design of Food and Drug Administration-approved
ergonomic devices that decompress the intervertebral discs. The
biomechanics of these decompression/reduction machines work by
decompression at the specific disc level that is diagnosed from finding
on a comprehensive physical examination and the appropriate diagnostic
imaging studies. The angle of decompression to the affected level causes
a negative pressure intradiscally that creates an osmotic pressure
gradient for nutrients, water, and blood to flow into the degenerated
and/or herniated disc thereby allowing the phases of healing to take
place.
This clinical outcomes
study, which was performed to evaluate the effect of spinal
decompression on symptoms of patients with herniated and degenerative
disc disease, showed that 86% of the 219 patients who completed therapy
reported immediate resolution of symptoms, and 84% of those remained
pain-free 90 days post-treatment. Physical examination findings revealed
improvement in 92% of the 219 patients who completed the therapy.
METHODS
The study group included
229 people, randomly chosen from 500 patients who had symptoms
associated with herniated and degenerative disc disease that had been
ongoing for at least 4 weeks. Inclusion criteria included pain due to
herniated and bulging lumbar discs that is more than 4 weeks old, or
persistent pain from degenerated discs not responding to 4 weeks of
conservative therapy. All patients had to be available for 4 weeks of
treatment protocol, be at least 18 years of age, and have an MRI within
6 months. Those patients who had previous back surgery were excluded. Of
note, 73 of the patients had experienced one to three epidural
injections prior to this episode of back pain and 22 of those patients
had epidurals for their current condition. Measurements were taken
before the treatments began and again at week two, four, six, and 90
days post treatment. At each testing point a questionnaire and physical
examination were performed without prior documentation present in order
to avoid bias. Testing included the Oswetry questionnaire, which was
utilized to quantify information related to measurement of symptoms and
functional status. Ten categories of questions about everyday activities
were asked prior to the first session and again after treatment and 30
days following the last treatment.
Testing also consisted of
a modified physical examination, including evaluation of reflexes
(normal, sluggish, or absent), gait evaluation, the presence of kyphosis,
and a straight leg raising test (radiating pain into the lower back and
leg was categorized when raising the leg over 30 degrees or less is
considered positive, but if pain remained isolated in the lower back, it
was considered negative). Lumbar range of motion was measured with an
ergonometer. Limitations ranging from normal to over 15 degrees in
flexion and over 10 degrees in rotation and extension were positive
findings. The investigator used pinprick and soft touch to determine the
presence of gross sensory deficit in the lower extremities.
Of the 229 patients
selected, only 10 patients did not complete the treatment protocol.
Reasons for noncompletion included transportation issues, family
emergencies, scheduling conflicts, lack of motivation, and transient
discomfort. The patient protocol provided for 20 treatments of spinal
decompression over a 6-week course of therapy. Each session consisted of
a 45-minute treatment on the equipment followed by 15 minutes of ice and
interferential frequency therapy to consolidate the lumbar paravertebral
muscles. The patient regimen included 2 weeks of daily spinal
decompression treatment (5 days per week), followed by three sessions
per week for 2 weeks, concluding with two sessions per week for the
remaining 2 weeks of therapy.
On the first day of
treatment, the applied pressure was measured as one half of the person's
body weight minus 10 pounds, followed on the second day with one half of
the person's body weight. The pressure placed for the remainder of the
18 sessions was equivalent to one half of the patient's body weight plus
an additional 10 pounds. The angle of treatment was set according to
manufacturer's protocol after identifying a specific lumbar disc
correlated with MRI findings. A session would begin with the patient
being fitted with a customized lower and upper harness to fit their
specific body frame. The patient would step onto a platform located at
the base of the equipment, which simultaneously calculated body weight
and determined proper treatment pressure. The patient was then lowered
into the supine position, where the investigator would align the split
of table with the top of the patient's iliac crest. A pneumatic air pump
was used to automatically increase lordosis of the lumbar spine for
patient comfort. The patient's chest harness was attached and tightened
to the table. An automatic shoulder support system tightened and affixed
the patient's upper body. A knee pillow was placed to maintain slight
flexion of the knees. With use of the previously calculated treatment
pressures, spinal decompression was then applied. After treatment, the
patient received 15 minutes of interferential frequency (80 to 120 Hz)
therapy and cold packs to consolidate paravertebral muscles.
During the initial 2
weeks of treatment, the patients were instructed to wear lumbar support
belts and limit activities, and were placed on light duty at work. In
addition, they were prescribed a nonsteroidal, to be taken 1 hour before
therapy and at bedtime during the first 2 weeks of treatment. After the
second week of treatment, medication was decreased and moderate activity
was permitted.
Data was collected from
219 patients treated during this clinical study. Study demographics
consisted of 79 female and 140 male patients. The patients treated
ranged from 24 to 74 years of age (see Table 1). The average weight of
the females was 146 pounds and the average weight of the men was 195
pounds. According to the Oswestry Pain Scale, patients reported their
symptoms ranging from no pain (0) to severe pain (5).
RESULTS
According to the
self-rated Oswestry Pain Scale, treatment was successful in 86% of the
219 patients included in this study. Treatment success was defined by a
reduction in pain to 0 or 1 on the pain scale. The perception of pain
was none 0 to occasional 1 without any further need for medication or
treatment in 188 patients. These patients reported complete resolution
of pain, lumbar range of motion was normalized, and there was recovery
of any sensory or motor loss. The remaining 31 patients reported
significant pain and disability, despite some improvement in their
overall pain and disability score.
In this study, only
patients diagnosed with herniated and degenerative discs with at least a
4-week onset were eligible. Each patient's diagnosis was confirmed by
MRI findings. All selected patients reported 3 to 5 on the pain scale
with radiating neuritis into the lower extremities. By the second week
of treatment, 77% of patients had a greater than 50% resolution of low
back pain. Subsequent orthopedic examinations demonstrated that an
increase in spinal range of motion directly correlated with an
improvement in straight leg raises and reflex response. Table 2 shows a
summary of the subjective findings obtained during this study by
category and total results post treatment. After 90 days, only five
patients (2%) were found to have relapsed from the initial treatment
program.
Ninety-two percent of
patients with abnormal physical findings improved post-treatment. Ninety
days later only 3% of these patients had abnormal findings. Table 3
summarizes the percentage of patients that showed improvement in
physician examination findings testing both motor and sensory system
function after treatment. Gait improved in 96% of the individuals who
started with an abnormal gait, while 96% of those with sluggish reflexes
normalized. Sensory perception improved in 93% of the patients, motor
limitation diminished in 86%, 89% had a normal straight leg raise test
who initially tested abnormal, and 90% showed improvement in their
spinal range of motion.
SUMMARY
In conclusion,
nonsurgical spinal decompression provides a method for physicians to
properly apply and direct the decompressive force necessary to
effectively treat discogenic disease. With the biotechnological advances
of spinal decompression, symptoms were restored by subjective report in
86% of patients previously thought to be surgical candidates and
mechanical function was restored in 92% using objective data. Ninety
days after treatment only 2% reported pain and 3% relapsed, by physical
examination exhibiting motor limitations and decreased spinal range of
motion. Our results indicate that in treating 219 patients with MRI-documented
disc herniation and degenerative disc diseases, treatment was successful
as defined by: pain reduction; reduction in use of pain medications;
normalization of range of motion, reflex, and gait; and recovery of
sensory or motor loss. Biotechnological advances of spinal decompression
indeed reveal promising results for the future of effective management
of patients with disc herniation and degenerative disc diseases. The
cost for successful nonsurgical therapy is less than a tenth of that for
surgery. Long-term outcome studies are needed to determine if
nonsurgical treatment prevents later surgery or merely delays it.
Thomas A. Gionis, MD, JD,
MBA, MHA, FICS, FRCS, is chairman of the American Board of Healthcare
Law and Medicine, Chicago; a diplomate professor of surgery, American
Academy of Neurological and Orthopaedic Surgeons; and a fellow of the
International College of Surgeons and the Royal College of Surgeons.
Eric Groteke, DC, CCIC,
is a chiropractor and is certified in manipulation under anesthesia. He
is also a chiropractic insurance consultant, a certified independent
chiropractic examiner, and a certified chiropractic insurance
consultant. Groteke maintains chiropractic centers in northeastern
Pennsylvania, in Stroudsburg, Scranton, and Wilkes-Barre.
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