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Psychotropic Drugs
Psychotropic Drugs
Antipsychotic Drugs
A. The term extrapyramidal disease refers to a motor disorder often associated with pathologic dysfunction
in the basal ganglia. Antiparkinson drugs block the extrapyramidal symptoms.
1. Clinical symptoms of the disease include abnormal involuntary movement, change in tone of the
skeletal muscles, and a reduction of automatic associated movements
2. Reversible extrapyramidal reactions may follow the use of certain drugs - the most common are
the phenothiazine derivatives.
B. Antiparkinson drugs act on the extrapyramidal system to reduce disturbing symptoms experienced from
antipsychotic medications.
1. They are usually given in conjunction with antipsychotic
drugs
2. The most common drugs are anticholinergics: Artane, Cogentin, Kemadrin, and Akineton.
3. Side effects are dizziness, gastrointestinal disturbance, headaches, urinary hesitancy, and memory
impairment
C. Benadryl, an antihistamine is often given in place of Artane or Cogentin,because it does not cause as many
untoward side effects as the other antiparkinson drugs.
D. Other drugs occasionally ordered in this category are Amantadine,
benzodiazepines, propranolol, clonidine, nifedipine (Procardia), verapamil, and dantrolene (Dantrium)
used for treating neuroleptic malignant syndrome.
Antianxiety Drugs
A. Drugs induce sedation, relax muscles, and inhibit convulsions; major use toreduce anxiety
B. Demand is great for relief from anxiety and they are safer than sedative-hypnotics
C. Potentiate drug abuse. Greatest harm occurs when combined with alcohol
D. Prescribed for neuroses, psychosomatic disorders, but do not modify
psychotic behaviors.
E. Drugs from two major classes.
1. Benzodiazepines: safer and more common (Librium, Valium, Ativan, restoril, Centrax, Serax, and
Xanax - being tested for use in depression, panic, and obsessive-compulsive disorders)
2. Nonbenzodiazepines: Vistaril, Buspar
E. Side effects.
1. Drowsiness (avoid driving or working around equipment)
2. Blurred vision, constipation, dermatitis, mental confusion, anorexia, polyuria, menstrual
irregularities, and edema
3. Habituation and increased tolerance
4. Pancytopenia, thrombocytopenia, and agranulocytopenia
5. Withdrawal symptoms occur with prolonged use (6+ months) and high doses
Antidepressant Drugs
A. Tricyclics, one of the most commonly used antidepressants; includes Elavil, Norpramin, Tofranil, Aventyl,
Vivactil, and Pamelor.
1. Blocks uptake of norepinephrine and serotonin
2. A lag period of 1 to 6 weeks between starting the medication and experiencing symptom relief
exists
3. Anticholinergic effect - produces antagonism of the parasympathetic system
4. Side effects:
a. Anticholinergic effects: dry mouth, blurred vision,
constipation, postural hypotension
b. CNS effects: tremor, agitation, angry states, mania, seizures
c. Cardiovascular effects: palpitations. Exerts a quinidine like
effect on the heart, so assess any client with a history of
myocardial infarction
d. Alterations in sexual functioning
e. Orthostatic hypotension
f. Sedation
g. Weight gain
h. Most side effects appear in first 1 to 2 weeks and diminish over a period of a few weeks or
months.
5. If client is switched from a tricyclic drug to MAOI, a period of 1 to 3 weeks must elapse between
drugs.
6. Blood levels assay provide therapeutic levels of tricyclic antidepressants
E. Serotonin
1. Relatively free of side effects
2. Useful in treatment of severely depressed and melancholic
clients
3. Some clients experience heightened anxiety, nausea, vomiting, and dizziness
4. Some clients experience abnormal ejaculation, and male impotence
F. Selective Serotonin reuptake inhibitors (SSRIs)
1. Examples are Prozac, Zoloft, Paxil, and Luvox
2. Exhibit less side effects than other antidepressant drugs
a. Anticholinergic side effects such as dry mouth, constipationare fewer
b. Side effects observed are nausea, the most common,
anxiety or nervousness, insomnia, drowsiness, and
headache
3. Normal dietary intake of sodium with adequate fluids to prevent dehydration is necessary
4. Diuretics will increase absorption of lithium leading to toxic
effects
5. Serum levels measured 2 to 3 times weekly (12 hours after last doe) in beginning of therapy; for
long-term maintenance therapy, every 2 to 3 months.
G. Drug concentration and side effects
1. Therapeutic range of serum levels is 0.6 to 1.2 mEq/L; for acute manic state, 1.0 to 1.5 mEq/L
2. Side effects occur at upper ranges, usually above 1.5 mEq/L
3. Gastrointestinal disturbances, metallic taste in mouth, muscle weakness, fatigue, thirst, polyuria,
and fine hand tremors are common side effects
4. Hypothyroidism is a long-term side effect of lithium therapy
H. Lithium toxicity
1. Appears when blood levels exceed 1.5 to 2.0 mEq/L.
2. Central nervous system is the chief target
3. Initial symptoms include nausea, vomiting, drowsiness, tremors, slurred speech, blurred vision,
muscle twitching, oliguria
4. If drug is continued, coma, convulsions, and death may result
5. Treatment for toxicity: gastric lavage, correction of fluid balance, administration of Mannitol to
increase urine excretion