Pharmacological risks following stroke.To the Editor: The physical therapist's examination of a patient who has had a stroke requires identification of the effects of medications being taken for the symptoms of the stroke and for other conditions. I applaud Joann Gallichio for writing "Pharmacologic Management of Spasticity spasticity /spas·tic·i·ty/ (spas-tis´i-te) the state of being spastic; see spastic (2). spas·tic·i·ty n. 1. A spastic state or condition. 2. Spastic paralysis. Following Stroke" in the October 2004 issue, because this article is a valuable resource to the physical therapist examining a patient who has had a stroke. Physical therapists should recognize the risk for an adverse response with the use of the drugs described in this report. For example, the author reported that diazepam diazepam /di·az·e·pam/ (di-az´e-pam) a benzodiazepine used as an antianxiety agent, sedative, antipanic agent, antitremor agent, skeletal muscle relaxant, anticonvulsant, and in the management of alcohol withdrawal symptoms. (Valium *) may "reduce motor coordination and impair intellect, attention, and memory" (p 974) and that oral baclofen (Lioresal ([dagger])) may cause "drowsiness, confusion, headache, and lethargy" (p 976). Those responses alone may be sufficient to adversely affect an individual's functional abilities following stroke. However, these medications carry additional risks for our patients. Using an animal model for stroke, Schallert et al (1) demonstrated that medicating with diazepam (a benzodiazepine benzodiazepine (bĕn'zōdīăz`əpēn'), any of a class of drugs prescribed for their tranquilizing, antianxiety, sedative, and muscle-relaxing effects. Benzodiazepines are also prescribed for epilepsy and alcohol withdrawal. ) increased the symptoms of hemiplegia hemiplegia /hemi·ple·gia/ (-ple´jah) paralysis of one side of the body.hemiple´gic alternate hemiplegia paralysis of one side of the face and the opposite side of the body. . The administration of diazepam during the acute phase (first 22 days) following a unilateral brain injury blocked the recovery of sensory ability in rats, and rats that were allowed to recover that ability developed a transient reinstatement of the deficit when medicated medicated /med·i·cat·ed/ (med´i-kat?id) imbued with a medicinal substance. medicated contains a medicinal substance. with diazepam) This response appears to have clinical importance, because patients recovering from a stroke who use drugs from the benzodiazepine class have been reported to have a poorer recovery of sensorimotor sensorimotor /sen·so·ri·mo·tor/ (sen?sor-e-mo´ter) both sensory and motor. sen·so·ri·mo·tor adj. Of, relating to, or combining the functions of the sensory and motor activities. (2) and upper-extremity (3) function. Goldstein (4-7) has documented the risks accompanying the use of diazepam and certain other medications by individuals who have had a stroke, and a review of that information is beyond the scope of this letter. However, physical therapists should note that there are medications that risk a detrimental effect on functional outcome following stroke. Goldstein summarized his recommendations about these medications as "the use of a [beta]-adrenergic receptor antagonist is preferable to either an [[alpha].sub.1]- or [[alpha].sub.2]-adrenergic receptor antagonist in the treatment of hypertension following stroke. Thiazide diuretics should be used cautiously. Haloperidol haloperidol /hal·o·peri·dol/ (hal?o-per´i-dol) an antipsychotic agent of the butyrophenone group with antiemetic, hypotensive, and hypothermic actions; used especially in the management of psychoses and to control vocal utterances and and other dopamine receptor antagonists Dopamine receptor antagonists (DAs) The older class of antipsychotic medications, also called neuroleptics. These primarily block the site on nerve cells that normally receive the brain chemical dopamine. Mentioned in: Schizophrenia should not be used unless absolutely necessary.... Benzodiazepines Benzodiazepines Definition Benzodiazepines are medicines that help relieve nervousness, tension, and other symptoms by slowing the central nervous system. Purpose Benzodiazepines are a type of antianxiety drugs. should generally be avoided." (6(q55)) Physical therapists who are managing the care of a patient who has had a stroke must recognize that diazepam (and some other medications) has the potential to adversely affect outcomes such as functional abilities. Therefore, analysis of medication effects should be included in the evaluation of the examination data for a patient who has had a stroke, and collaboration with the prescribing physician may be necessary for risk reduction. Jim Smith, PT, MA jsmith@nvcc.commnet.edu * Roche Pharmaceuticals, Roche Products Inc, Manati, Puerto Rico 00674. ([dagger]) Manufactured by Novartis Pharma AG, Basel, Switzerland, for Medtronic Inc, 710 Medtronic Pkwy NE, Minneapolis, MN 55432-5604. References (1) Schallert T, Hernandez TD, Barth TM. Recovery of function after brain damage: severe and chronic disruption by diazepam. Brain Res. 1986;379:104-111. (2) Goldstein LB, Matchar DB, Morgenlander JC, Davis JN. Drugs influence the recovery of function after stroke. Stroke. 1990;21:179. (3) Goldstein LB. Common drugs may influence motor recovery at]m stroke. Neurology. 1994;44 (suppl 2):A289. (4) Goldstein LB. Common drugs may influence motor recovery after stroke. Neurology. 1995;45:865-871. (5) Goldstein LB. Effects of amphetamines Amphetamines Sympathomimetic amines; sometimes called speed; synthetic chemicals that stimulate the central nervous system. Mentioned in: Weight Loss Drugs amphetamines and small related molecules on recovery after stroke in animals and man. Neuropharmacology neuropharmacology /neu·ro·phar·ma·col·o·gy/ (-fahr?mah-kol´ah-je) the scientific study of the effects of drugs on the nervous system. neu·ro·phar·ma·col·o·gy n. . 2000;39:852-859. (6) Goldstein LB. Influence of common drugs and related factors on stroke outcome. Curr Opin Neurol. 1997; 10:52-57. (7) Goldstein LB. Potential effects of common drugs on stroke recovery. Arch Neurol. 1998;55:454-456. |
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