Neurological Associates
Pain Management Center
Vero Beach, Florida
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H. Hooshmand, M. D. |
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DIPLOMATE AMERICAN BOARD OF PSYCHIATRY AND NEUROLOGY BOARD CERTIFIED IN ELECTROENCEPHOLOGRAPHY BOARD CERTIFIED IN ELECTROMYOGRAPHY BOARD CERTIFIED IN AMERICAN BOARD OF ELECTODIAGNOSTIC MEDICINE INTRACTABLE NEUROLOGY EPILEPSY, PAIN, MS An International Referral Center dedicated to Treatment, Education and Research |
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RSD PUZZLE #87
RSD AND CEREBRAL PALSY
Occasionally, the patients with Cerebral Palsy (CP) are afflicted by neuropathic pain, and
even by the full picture of RSD.
Cerebral Palsy is a nonspecific, generalized terminology referring to any injury before or
after birth, to any child, resulting in permanent and chronic disturbance of the central
nervous system (CNS) function.
The effect of pain on the CP is quite variable. Some patients show quite a high tolerance
to pain, whereas others have a low threshold for pain. Usually, the mild cases of cerebral
palsy are left undiagnosed. Usually such a child is categorized under a diagnoses such as
hyperactivity, ADHD, Clumsiness, or "slow learner".
In rear cases of CP, the patient manifest central sympathetic nervous system dysfunction
in the form of central pain and even disturbance of sympathetic dysfunction affecting the
entire one side of the body.
Usually, in such cases the patients is referred for evaluation of severe headaches, or
pain of an unknown cause. One of the earliest manifestations is attacks of severe pain
waking the patient up during late night sleep. The patient acts very sensitive to light
and noise, may show the manifestation of hypersensitivity of the skin to touch
(allodynia), and tendency for flexion and withdrawal of the involved extremities.
Thermography is quite diagnostic, in that it usually shows partial virtual sympathectomy
and paralysis of the sympathetic system involving one side of the body, manifested in the
form of hyperthermia and heat loss due to the partial inability of the sympathetic system
to preserve the body heat through vasoconstriction of the skin on the involved
extremities.
Such children, or the grownups who have been left undiagnosed, have an extremely low
threshold for pain, Their response to pain is quite emotional, and out of proportion to
the pain stimulus.
This is not because the child is spoiled or simply exaggerates the pain. This is because
of the fact that disturbance of the sympathetic system causes severe allodynia and
hyperpathia resulting in sensitivity to touch, or even to breathe. The patient has a
tendency to react paradoxically to muscle relaxants and tranquilizers such as Valium,
Xanax, etc. Instead of a calming effect, such medications stimulate the patient, causing
agitation and anxiety. This paradoxical phenomenon makes the treat treatment with
sympathetic nerve blocks extremely difficult.
In addition, the sympathetic nerve blocks are not usually helpful because the patient
already has
a paralyzed sympathetic system, rather than a simply hyperactive sympathetic system. If
the thermography shows increased temperature in the involved area, then there is no sense
in proceeding with sympathetic nerve blocks, because the sympathetic nerves are already
dysfunctional. This is one of the best examples of sympathetic dysfunction leading to RSD
without the accompanying sympathetic hyperactivity.
Treatment of choice for this condition is a combination of treatment with effective
analgesic antidepressants such as Desipramine, Trazodone, or Doxepin. The antidepressant
treatment should be combined with treatment with a specific anticonvulsant. The most
effective anticonvulsant for this condition is Tegretol. Tegretol, in non-generic brand
name form, is the most effective pain reliever for causalgic pain. In addition, Cai and
McCaslin (in European Journal of Pharmacology, 1992)[1] have reported that the combination
of Desipramine and Tegretol is quite effective in blocking NMDA receptors and relieving
the pain.
Obviously, as is the case with all neuropathic pains, and especially RSD, just prescribing
medication is not enough. The change of life habits is also very important. The proper
diet, which would avoid any use of chocolate, hot dogs, sausage, etc., and would encourage
the four F's diet (fresh fruit, fresh vegetables, fish
and fowl), as well as avoidance of extensive distressful exercise or extensive bed rest
are essential in the treatment of this sad condition. As mentioned above, the condition is
rare, and falls into the category of "Central Pain".
H. Hooshmand, M.D.
Reference
1. Cai Z, McCaslin PP: Amitriptyline, desipramine,
cyproheptadine and carbamazepine, in concentrations used therapeutically, reduce kainate-
and N-methyl-D- aspartate-induced intracellular Ca2+ levels in neuronal culture. Eur J Pharmacol 219:53-57 1992.
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Copyright © 1997-2006 H. Hooshmand, M.D. No part of this publication may be reproduced, transmitted, stored in a retrieval system other than this specific media, transcribed, or translated into any language without the expressed written permission from the author; H. Hooshmand, M.D. and Eric Phillips and CMNE. This material is for informational and education purposes. It is not meant to take the place of your physician. Before starting, changing, or stopping any treatments or medicines consult your physician.
Send e-mail to Eric Phillips: EricmP9512@aol.com with questions or comments about this media and content.
The material on the Neurological Associates Pain Management Center Homepage and all it's associated, linked or reference pages is for informational and education purposes. It is not meant to take the place of your physician. Before starting, changing, or stopping any treatments or medicines consult your physician. H. Hooshmand, M.D., Neurological Associates Pain Management Center and Associates will not be held liable for any damage or loss as a result of information provided on this page or associated documentation. Again, this WEB SITE is simply published as an information source and should not be used to treat or make judgments on RSD/CRPS. All associated material on this web site may not be copied, reproduced or quoted without expressed written permission from the owner; Copyright © 1999-2006 H. Hooshmand, M.D.
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This page was last updated on 3/11/2000.