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USE OF INTRATHECAL BACLOFEN THERAPY IN MANAGEMENT OF THE BRAIN INJURED PATIENT
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The brain is an amazing organ. Its remarkable and vast capacity allows
us to be the people that we are. Traumatic brain injury can cause
damage that interferes with our ability to function to our optimum
capacity. Spasticity can occur as a result of brain Injury. Spasticity is
a syndrome associated with an increase in the involuntary reflex activity
of muscles to stretch. The consequences of spasticity are numerous and
may include stiffness, spasms, contractures as well as pain. Spasticity
can negatively impact on quality of life factors such as mobility and
independence, hygiene, self-care and self-esteem, mood, sleep, and
sexual function. In general, goals of spasticity treatment are relief of
subjective discomfort, facilitation of patient care, improvement of
functional capacity and prevention of long-term consequences of
excessive and unevenly distributed muscle tone. Unfortunately, the
treatment of moderate to severe spasticity by medication, physical
therapy and local injections often provide less than satisfying or
gratifying results.
Baclofen is a medication that works directly in the areas of the brain and
spinal cord that are important in controlling muscle tone and spasticity.
Baclofen by mouth can be an effective treatment for spasticity. Oral
Baclofen, however, is often ineffective in treating severe spasticity,
because to achieve effective therapeutic concentrations to the spinal
cord, unacceptable systemic side effects are often produced. These side
effects can include lethargy, confusion, drowsiness and muscle
weakness. This medication can be delivered directly to the spinal cord
and brain by an implanted catheter. This technique has been shown not
only to be safe but to have dramatic clinical effectiveness. This
technique is called Intrathecal Baclofen Therapy.
Intrathecal Baclofen is much more effective than when given by mouth
because the medication is delivered directly into the cerebral spinal fluid
surrounding the spinal cord which is the intended site of action. The
effective doses intrathecally are only a fraction of those doses given orally. Intrathecal
Baclofen Therapy is a non-destructive end-reversal treatment that reduces spasticity
without impairing underlying voluntary movement. A test dose can be given by a
spinal tap to allow the patient and family to judge for themselves the remarkable
effectiveness and safety of this treatment before making a commitment to a permanent
implantation of a pump and catheter system that is required for a long-term commitment to
treatment. This delivery system is called the SynchroMed Infusion System.
The dosage given can be adjusted to meet the needs of each patient with minimal
side effects. In reducing spasticity at both upper and lower extremities, this
treatment can enhance mobility, independence, urinary management, as well as quality of
life, among tetraplegic and diplegic patient ITB therapy may reduce the incidence of
contractures and other painful and costly medical complications associated
with spasticity and immobility as well as to facilitate rehabilitation and reduce
physical, logistic and financial burdens of caregiving. Careful patient selection
optimizes the benefits of ITB therapy.
Goal setting is important to define reasonable and realistic expectations to
assess whether this treatment is appropriate for the persons affected with severe
spasticity. This treatment is not only appropriate for those ambulatory or wheelchair
bound that spasms and/or spasticity interfere with some function that has not responded
to other treatment attempts. Even if the person is home or bed-bound and
intellectually impaired, this treatment can be appropriate and utilized if the focused goal
is for hygiene or improved transferring, improved sleep or reduction of pain
related to the spasticity. Even in this instance with generalized severe spasticity, this
treatment can be effective.
The explicit criteria includes severe spasticity, clinical stability, age
greater than 4 and patient size sufficient to support the implanted device. The inclusion
criteria must include realistic treatment goals as well as motivation and commitment of
patients, families and caregivers. The few explicit contra-indications to this
treatment include active infection, allergy to oral Baclofen or pregnancy.
The treatment team will determine whether the indications for this therapy
are present without any exclusion criteria also being present. The team will also
consider clinical, functional, as well as psychosocial parameters that bear on a particular
patient’s suitability for this treatment. I have been involved in treatment of
spasticity by Intrathecal Baclofen therapy over the past several years and have found this
to be an extremely affective and rewarding treatment. I have also been impressed by
the first gains that patients have achieved as a result of this therapy. This
treatment is extremely safe with appropriate clinical expertise, allows individualized
fine-tuning of clinical response. The treatment is reversible and does not involve
destruction of neural tissue. This treatment offers a marked consistently superior clinical
response in the difficult spasticity management situation.
If you, a family member, or someone you take care of have spasticity that
interferes with function and have not been satisfied with the results of other
treatment options, additional information about the use of Intrathecal Baclofen Therapy should
be obtained. This information can be obtained directly from Medtronic, Inc.,
the world wide web @ southshoreneurologic.com or Contact someone who is involved with
or knowledgeable about this therapy.
Written by: Mark Gudesblatt, M.D.
SOUTH SHORE NEUROLOGIC ASSOCIATES, P.C.
Copyright © 1999, 2000, * SOUTH SHORE NEUROLOGIC ASSOCIATES, P.C.
