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PROLOTHERAPY: A TREATMENT FOR FIBROMYALGIA
At
Caring Medical
we always search for underlying causes whenever possible in order to avoid
simply “suppressing” symptoms, and usually we will test for
hormones,
heavy metals, and allergy and sensitivities. Environmental chemicals such as
various fumes, colognes, tobacco smoke, and artificial sweeteners often show up
as possible causative factors on comprehensive ALCAT blood testing. Sometimes
patients may be sensitive to the effect of a chemical without it showing up on
ALCAT testing. One example is aspartame sensitivity which is a not uncommon
cause of fibromyalgia syndrome and other joint symptomatology. In fact, Dr H.J.
Roberts studied this connection in 551 patients and reported it in the Townsend
Letter for Doctors in 1991. About 10% of the total aspartame sensitive group had
joint symptoms that resolved when aspartame was discontinued, and recurred when
it was reintroduced. Females outnumbered males 3 to 1. Whether formal testing is
done or not, we believe that any patient with rheumatic complaints deserves a
trial elimination
diet that removes commonly eaten foods, including artificial
sweeteners. When the other factors I listed have been considered and ruled out
or concurrently treated, we believe that further treatment of musculoskeletal
sore spots (ligaments and
tendons) with
Prolotherapy will
bring very significant additional relief of symptoms. Muscle
trigger
points
often result from strain secondary to weak underlying ligaments around the
nearby joints.
Prolotherapy
addresses this underlying weakness. In a 1994 study
published by K. Dean Reeves,1 greater than 75% of even severe
fibromyalgia patients saw reduced pain and increased functional capability after
Prolotherapy. Since it is a relatively little known treatment, I will present
the case for Prolotherapy as concisely as I can.
The Case for
Prolotherapy:
What is Prolotherapy?
Why should I be treated
by Prolotherapy rather than traditional approaches? Traditional approaches to chronic pain and injuries are frequently ineffective and can be harmful:
1. Traditional diagnostic
tests such as X rays, and CT and
MRI
scans commonly reveal findings which are only occasionally the true cause of the
patient’s pain, and thus serve as an inaccurate basis for the recommendation of
surgery. In CT scans of the lower back in the general population, 35%
irrespective of age had abnormal findings even though they had no pain. This
figure is 50% of pain free individuals over 40. With MRI testing, nearly 100% of
those over 60 tested positive for some type of abnormality, with 36% showing
herniated disks, and all but one had degeneration or bulging of at least one
lumbar disk.3,4,5,6 This is the problem of false positives, and has
been clearly published in the 1994 New England Journal of Medicine article by
Maureen Jensen, MD, 7
2. Traditional diagnostic
tests cannot identify laxity or damage to ligaments, the most common source of
chronic pain. Therefore this type of testing will never result in the
recommendation of the most appropriate treatment…Prolotherapy. This is the
problem of false negative findings.8
3. Surgically removing
anatomical structures such as intervertebral disks, bone,
cartilage,
or
menisci
causes near-by structures to undergo chronic abnormal mechanical stress. This
often initiates or accelerates the degenerative arthritic processes. This
includes arthroscopic surgery, and
spinal fusion
operations. Oftentimes patients continue to experience the same pain post
surgically. Peer review of pain cases treated with surgery (Finneson) suggested
as many as 80% of them should never have been operated upon.
4. Undergoing any procedure
which does not address the true underlying cause of the pain or disability is
bound to produce unsatisfactory results. Laxity or overstretching of ligaments
is the number one true cause, and is the one factor that is never addressed in
the orthodox approaches.8
5. Although providing
temporary symptom relief, the use of oral
anti-inflammatory drugs
is counter-productive because such drugs stop the inflammatory processs, without
which the body is unable to heal the injury or irritation. It has been
adequately documented that chronic use of such medications accelerates the
arthritis
process in the affected joint.10,11,12,13,14,15,16,17,18,
19,20
6. Injection of
cortisone into
damaged or painful areas is also counterproductive. Although sometimes providing
very modest short term relief of pain, cortisone always blocks the healing
response and weakens local bone, tendon, and ligament tissue. For example,
complete rupture of the
Achilles
tendon
is a well known complication associated with cortisone injection of that tendon
when injected locally for the treatment of partial tears or
tendonitis.
7. Traditional approaches to
the physical examination of the chronic pain patient usually fail to identify
the true source of the pain. In most cases no effort is made to manually
identify specific painful structures such as ligaments, reproduce the patient’s
pain, or to correlate patient localization of pain with known ligament
referral patterns. This frequently results in ineffective treatments because they are
directed at the wrong diagnosis.8
Prolotherapy is an
effective and safe method of eradicating chronic pain:
2.
As a non-surgical
treatment modality, Prolotherapy is relatively inexpensive and requires minimal
to no downtime from usual activities of daily living. It also shares none of the
usual list of general potential complications associated with surgery.
3. Prolotherapy does not
disturb, remove or weaken existing non-pathologically-involved structures in the
painful region, nor does it ever accelerate the degenerative arthritic process.
4.
Prolotherapy is an
effective treatment for chronic pain because it is able to specifically and
permanently strengthen tissue and reverse
ligament laxity
and tendon strain, the number one causes of chronic joint and other
musculoskeletal disturbances.9 Beyond relieving pain, the ligament
tightening effect of Prolotherapy stabilizes the commonly seen hyper-mobility in
affected joints, thus literally slowing down or arresting the actual cause of
the degenerative arthritis process. It is this abnormal motion and friction,
relieved by Prolotherapy, that causes the wearing down of joint cartilage and
reactive bone spur formation that brings on the pain and progression of the
common form of
osteoarthritis.21,22,23,24,25
5. Prolotherapy
consistently produces very favorable clinical results. Patient outcomes reported
by numerous clinicians (see references) after the application of Prolotherapy to
the treatment of various conditions and joints suggests an approximate 80 to 90%
significant improvement rate.8,9
6. Prolotherapy
is safe when properly applied by a trained Prolotherapy doctor.
Dr. Gustav
Hemwall treated
over 10,000 patients with more than four million injections without a single
episode of paralysis, death, permanent nerve injury, or
infection.8
7. Considering
the number of treatments usually required (3 to 8),
prolotherapy treatments cost
only a small fraction of surgery.
Summary:
Myofascial pain syndrome
and fibromyalgia syndrome have no definite assigned “cause” at this time in
modern medicine. However, as we look at our clinical experience and open our
eyes to the threats that may come from environmental toxins, allergies, and
consider the impact of hormonal and nutritional balance, as well as the reality
that ligament laxity is probably the most common cause of chronic
musculoskeletal pain, we reach one inescapable conclusion. Fibromyalgia patients
can be greatly helped! References 1Reeves, K. “Treatment of consecutive severe fibromyalgia patients with Prolotherapy.” The Journal of Orthopaedic Medicine. 1994; 16:84-89. 2Babcock, P. et al. Webster’s Third New International Dictionary. Springfield, MA: G.&C. Merriam Co., 1971, p. 1815. 3Boden, S. “abnormal magnetic-resonance scans of the lumbar spine in asymptomatic subjects.” The Journal of Bone and Joint Surgery. 1990; 72A:403-408. 4Jensen, M. “Magnetic resonance imaging of the lumbar spine in people without back pain.” The New England Journal of Medicine. 1994; 331:69-73. 5Boden, S. “Abnormal magnetic-resonance scans of the lumbar spine in asymptomatic subjects.” The Journal of Bone and Joint Surgery, 1990; 72A”403-408. 6Jensen, M. “Magnetic resonance imaging of the lumbar spine in people without back pain.” The New England Journal of Medicine. 1994; 331:69-73. 7Wiesel, S. “A study of computer-related assisted tomography 1. The incidence of positive CAT scans in an asymptomatic group of patients.” Spine. 1984; 9:549-551. 8Hackett, G. Ligament and tendon Relaxation Treated by Prolotherapy. Third Edition. Springfield, IL: Charles C. Thomas Publisher, 1958, p. 5. 9Klein, R. “Proliferant injections for low back pain: histologic changes of injected ligaments and objective measures of lumbar spine mobility before and after treatment.” Journal of Neurology, Orthopedic Medicine and Surgery. 1989; 10:141-144. 10Mishra, D. “Anti-inflammatory medication after muscle injury: A treatment resulting in short-term improvement but subsequent loss of muscle function.” Journal of Bone & Joint Surgery. 1995; 77A:1510-1519. 11Brandt, K. “Should osteoarthritis be treated with nonsteroidal anti-inflammatory drugs?” Rheumatic Disease Clinics of North America. 1993; 19:697-712. 12Brandt, K. “The effects of salicylates and other nonsteroidal anti-inflammatory drugs on articular cartilage.” American Journal of Medicine. 1984; 77:65-69. 13Obeid, G. “Effect of ibuprofen on the healing and remodeling of bone and articular cartilage in the rabbit temporomandibular joint.” Journal of Oral and Maxillofacial Surgeons. 1992; pp. 843-850. 14Dupont, M. “The efficacy of anti-inflammatory medication in the treatment of the acutely sprained ankle.” The American Journal of Sports Medicine. 1987; 15:41-45. 15Newman, N. “Acetabular bone destruction related to nonsteroidal anti-inflammatory drugs.” The Lancet. 1985; July 6:11-13. 16Serup, J. and Oveson, J. “Salicylate arthropathy: accelerated coxarthrosis during long-term treatment with acetyl salicylic acid.” Praxis. 1981; 70:359. 17Ronningen, H. and Langeland, N. “Indomethacin treatment in osteoarthritis of the hip joint.” Acta Orthopedica Scandanavia. 1979; 50:169-174. 18Newman, N. “Acetabular bone destruction related to nonsteroidal anti-inflammatory drugs.” The Lancet. 1985; July 6:11-13. 19Serup, J. and Ovesen, J. “Salicylate arthropathy: accelerated coxarthrosis during long-term treatment with acetyl salicylic acid.” Praxis. 1981; 70:359. 20Ronningen, H. and Langeland, N. “Indomethacin treatment in osteoarthritis of the hip joint.” Acta Orthopedica Scandanavia. 1979; 50:169-174. 21Dorman, T. “Treatment for spinal pain arising in ligaments using Prolotherapy: A retrospective study.” Journal of Orthopaedic Medicine. 1991; 13(1):13-19. 22Ongley, M. and Dorman, T., et al. “Ligament instability of knees: A new approach to treatment.” Manual Medicine. 1988; 3:152-154. 23Klein, R. “A randomized double-blind trial of dextrose-glycerine-phenol injections for chronic, low back pain.” Journal of Spinal Disorders. 1993; 6:23-33. 24Ongley, M. “A New Approach to the Treatment of Chronic Low Back Pain.” Lancet. 1987; 2:143-146. |
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Prolotherapy is a medical
technique. As with any medical technique, results will vary among
individuals.
Prolotherapy may not work for you and as with all medical
procedures there are risks involved. These risks should be discussed with a qualified
health care professional prior to any treatment.
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