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DEFINITIONS psychotropic drugs I: Chemical agents that affect the brain and nerv
ous system, alter the feelings, emotions and consciousness in various ways. Neur
otransmitters: Chemicals that allow transmission of electrical impulses from one
neuron to another across the synapse.
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DEFINITIONS III Neuroleptic malignant syndrome: rare, but potentially lethal, tr
eatment with antipsychotic drugs. Symptoms include severe muscle rigidity, hyper
thermia, hypertension, tachycardia, diaphoresis, and increased creatine. Electro
convulsive therapy (ECT): induction of a tonic-clonic seizure (generalized) by a
pplying an electric current to the brain.
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Extrapyramidal system DEFINITIONS II: Routes of motor neurons from the brain to
areas of the spinal cord, this system has complex relay and connections to areas
of the cerebral cortex, cerebellum, brainstem and thalamus. The extrapyramidal
system helps maintain balance and muscle tone.
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I FUNDAMENTAL CONCEPTS
Psychotropic medications are not used to cure mental illness, only relieve the p
hysical and behavioral symptoms. Biological therapies can induce healing by prod
ucing changes in cellular functions of the CNS. Such changes make the emergence
of new behaviors.
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FUNDAMENTAL CONCEPTS II
Some neurotransmitters, and their relationship to mental disorders are:
n
Dopamine: Excessive dopaminergic activity is associated with schizophrenia. Sero
tonin and norepinephrine: causal factors of depression and mania. Currently it i
s believed that mood disorders are the result of different chemicals such as neu
rotransmitters and hormones.
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n
BASIC CONCEPTS III
n
Gamma-aminobutyric acid (GABA): the creation of a inhibitory effect on anxiety.
Acetylcholine: it is postulated that the cognitive deficits of Alzheimer's disea
se are due to a reduction of acetylcholine. Monoamine oxidase: enzyme responsibl
e for the destruction of some neurotransmitters
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n
n
FUNDAMENTAL CONCEPTS IV
Some depressed individuals improve with ECT, having failed other forms of treatm
ent. Classification of major psychotropic drugs: 1 .- 2 .- Antidepressants Antip
sychotics antimanic 3 .- 4 .- 5 .- Benzodiazepine Sedative-hypnotics
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MAIN psychotropic drugs
Antipsychotic drugs
Initial treatment may require parenteral doses. According recedes conduct disord
er is changed to oral tablets or concentrated preparations. The doses are calcul
ated according to the needs of each individual. To achieve symptomatic changes,
it is essential guideline doses carefully.
The divided doses are changed to single doses, primarily administered at bedtime
to maximize the sedative properties of these drugs.
To achieve sustained improvements, most clients need maintenance dose.
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GENERAL II
In elderly clients recommended low-dose treatment. Adverse side effects and are
more common in elderly clients, which is due to their lower renal and hepatic fu
nction and to their smaller muscle mass compared with fat tissue. Its half-life
in serum is about 24 hours. The drug accumulates in fatty tissue. After stopping
the medication, fat is releasing the drug, so side effects may persist.
High therapeutic index and can be administered at high doses with minimal risk.
These drugs are not addictive and do not produce euphoria. Not recommended durin
g pregnancy.
SIDE EFFECTS I
Antipsychotics:
s d. e. f. s i. j. k. l. m.
Type cardiovascular: Hypotension. Orthostatic hypotension, tachycardia. Antichol
inergic Type: urinary retention and hesitancy. Constipation Blurred vision. Nasa
l congestion. Dry mouth
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SIDE EFFECTS II
1. b.
c.
Extrapyramidal: Seudoparkinsonismo (mask facies, stooped, rigid posture, shuffli
ng gait, drooling, tremors, movement of "counting money"). Acute dystonic reacti
on (contractions of the tongue, face, neck and back; opisthotonos, where the who
le body arches so tetanus, and oculogyric crisis, in which the eyes are facing u
p).
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SIDE EFFECTS II
b.
Acaticia (restlessness and excessive walking).
d.
Tardive dyskinesia (writhing movements and remove the tongue, puffs, pops and li
cking. Spastic distortion may also occur on the face and choreic or athetoid mov
ements of the limbs) irreversible symptom.
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SIDE EFFECTS III
1. b. c.
d. e.
f.
Other side effects: sedation. Skin disorders (hives or contact dermatitis). Phot
osensitivity endocrine disorders (moderate increase in breast and galactorrhea i
n women, gynecomastia in males, altered sex drive, loss of libido in both sexes
and possibly amenorrhea in females). Weight gain.
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SIDE EFFECTS IV
1. b. c.
d.
Serious side effects but rare: Agranulocytosis. Cholestatic jaundice (fever, nau
sea, abdominal pain and jaundice). Neuroleptic malignant syndrome
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SIDE EFFECTS V atypical antipsychotics:
s
Agranulocytosis: incidence of 1 to 2% in clients treated with clozapine. Idem se
izures that typical antipsychotics: sedation, orthostatic hypotension, constipat
ion, effects on the SEP, neuroleptic malignant syndrome).
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5. s
Antidepressant drugs
TRICICLOS Monoamine Oxidase Inhibitors (MAOIs) NO INHIBITORS TRICICLOS ser
otonin reuptake inhibitors (SSRIs)
Antidepressant drugs
generic name brand name class daily maintenance dose Frequently 50-100 mg 50-150
mg 75-200 mg 75-100 mg 15-45 mg 75-150 mg 75-300 mg 150-225 mg
Tricyclic antidepressants (TCA)
Imipramine Amitriptyline Desipramine Nortriptyline Protriptyline Doxepin Clomipr
amine Maprotiline
Tofranil-Martimil Tryptizol, paxtibi - Ludiomil Sinequan Anafranil
Monoamine oxidase inhibitors (MAOIs)
Toranilcipromina isocarboxazid phenelzine
Parnate - Nardelzine
10-30 mg 10-30 mg 15-90 mg
31
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Antidepressant drugs
No tricyclic Trazodone Venlafaxine bupropion (bupropion) Fluoxetine Paroxetine S
ertraline Dobupal, vandral Deprax - Prozac, Adolf Besitrán Frosinor, Seroxat 150
-375 mg 150-400 mg 200-450 mg 50-200 mg 20-40 mg 20-50 mg
Inhibitors of serotonin reuptake inhibitors (SSRIs), second-generation antidepre
ssants
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INDICATIONS
1.
Used in the treatment of depressive disorders, they can positively change the de
gree of withdrawal, the level of activity and vegetative signs of depression.
those of the
3.
Use in the treatment of anxiety disorders, enuresis and childhood hyperactivity,
and chronic pain.
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MECHANISM OF ACTION
2.
It depends on the type of antidepressant Tricyclic antidepressants (TCA): Increa
se the levels of neurotransmitters by blocking reuptake of norepinephrine and se
rotonin at the level of the presynaptic neuron.
4.
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MECHANISM OF ACTION
2.
Monoamine oxidase inhibitors (MAOIs) inhibit monoamine oxidase, which is the enz
yme responsible for metabolizing the neurotransmitters. Atypical antidepressants
or selective inhibitors of serotonin reuptake inhibitors (SSRIs) act selectivel
y on the neurotransmitter serotonin by blocking its reuptake at the presynaptic
cell.
4.
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GENERAL I
1.
The TCAs are potentially lethal if taken in quantities of 10 to 30 times the rec
ommended daily dose. The client may not respond to antidepressants until after t
he three weeks of the first dose. Clients with severe depression and who have de
lusions or other psychotic symptoms, they may need the administration of an anti
psychotic with an antidepressant.
3.
5.
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GENERAL II
1.
Before TCAs were the drugs of choice for the treatment of nonpsychotic unipolar
depression. Currently, the drug of choice might be an SSRI. MAOIs are effective
antidepressants can be helpful to some clients who do not respond to TCAs and SS
RIs or who can not tolerate them. In clients who take antidepressants should be
monitored the emergence of suicidal ideation, and that the drugs increase levels
of energy consumption and its ability to carry out such plans.
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3.
5.
I CONTRAINDICATIONS AND PRECAUTIONS
2.
ATC: pre-existing cardiovascular disease. Background convulsionews. Narrow angle
glaucoma. Prostatic hypertrophy. Pregnancy and lactation.
ATC:
Anticholinergic effects. Cardiovascular effects. Sedation. Photosensitivity. Oth
er uncommon:
Decreased seizure threshold. Decreased or increased libido and erectile dysfunct
ion ejaculation.
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SIDE EFFECTS II
1. b. c.
d.
e.
MAOI: They may cause diarrhea, abdominal pain, restlessness, insomnia and dizzin
ess. The worst are the hypertensive crisis, appear to consume foods with tyramin
e or with drugs that increase noradrenergic activity. Symptoms of hypertensive c
risis include generalized headache, nausea, vomiting, pallor, chills, stiff neck
, muscle twitching, palpitations and chest pain.Treatment: slow administration
of phentolamine mesylate, hydration and electrolyte balance restoration.
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SIDE EFFECTS III
1. b. c.
SSRIs: Similar to the ATC. Customers treated with SSRIs have a lower incidence o
f anticholinergic side effects and have less cardiotoxicity.
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Antimanic drugs
LITHIUM CARBONATE LITHIUM CITRATE
INDICATIONS I
1.
Lithium carbonate and lithium citrate are used primarily antimanic agents:
Acute mania. Episodes of hypomania. Long-term prophylaxis of bipolar disorders.
Effective in preventing recurrent manic episodes.
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INDICATIONS II
1.
It is used experimentally to treat other psychiatric disorders that appear in mo
od disorders, such as:
Alcoholism. Drug Abuse. Premenstrual syndrome. Pathological sexual behaviors and
phobias.
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MECHANISM OF ACTION
1. 2.
3.
4.
The exact mechanism of action is not well known. Interferes with the metabolism
of norepinephrine, dopamine and serotonin. Electrolyte balance affect the brain
and alter sodium transport in nerve cells and muscle. Experts believe that lithi
um corrects an abnormality of ion exchange.
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GENERAL I
2.
Lithium is a natural salt found in the minerals, sea water, plants and animals.
Be absorbed rapidly after oral administration. Compete with sodium reabsorption
in renal proximal tubule.
4.
6.
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GENERAL I
2.
It has a success rate of 70-80% in the treatment of bipolar disorder. Lithium en
hances the effects of antidepressants and is effective in the resolution and pre
vention of recurrent major depression
4.
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GENERAL II
2.
Antipsychotics can be used with lithium in acute manic episodes to treat behavio
ral and psychotic manifestations. The onset of lithium therapy is usually 300 mg
three times a day for several days, increasing the dose until reaching a stable
level.
4.
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GENERAL II
•
During stabilization, regularly measured serum levels of lithium to identify the
therapeutic level. After resolution of symptoms, decrease the lithium to achiev
e the maintenance dose. Check blood levels every 2 or 3 months.
•
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GENERAL III
1.
s h.
Before initiating treatment with lithium, make the client a medical history and
complete physical examination, with the following information: Renal function: c
reatinine 24 hours. Blood urea nitrogen (BUN). Electrolyte levels. Personal or f
amily history of kidney disease or diabetes mellitus. Use of diuretics or analge
sics. Thyroid function: Evaluation of thyroid function and hematological tests.
Personal or family history of thyroid disease
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IV GENERAL
1.
The following are other anticonvulsant drugs that are used as antimanic: carbama
zepine (Tegretol), valproic acid (Depakine), clonazepam. Used when lithium is in
effective or not tolerated. They can also be used in combination with lithium. B
ecause anticonvulsant drugs, can not be stopped sharply, because it can trigger
an epileptic state.
c. d.
f.
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CONTRAINDICATIONS AND PRECAUTIONS
1.
2.
3.
Lithium has a narrow therapeutic window, the therapeutic dose is only slightly l
ower than toxic. Dehydration or sodium depletion may precipitate lithium toxicit
y. Administered with caution in clients:
Elderly or debilitated. Kidney or thyroid disease. With seizure disorder. Take m
edications incompatible
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POTENTIAL DRUG INTERACTIONS LITHIUM
DRUG EFFECT Antidepressants Antipsychotics Neurotoxicity with lithium manic rela
pse
Aminophylline or theophylline decreased serum levels of lithium sodium bicarbona
te or sodium chloride Diuretics Tetracycline, streptomycin, or NSAIDs. Muscle re
laxants and anesthetics. Increases lithium reabsorption by the kidney, triggerin
g poisoning Increased serum lithium levels Extension neuromuscular blockade with
succinylcholine and pancuronium. Suspend lithium from 48 to 72 hours prior to a
dministration of these agents and to resume oral feeding after surgery.Walter P
SYCHOPHARMACOLOGY 55 EU
G. Cortes
SIDE EFFECTS I
2.
Nausea, abdominal discomfort, diarrhea, loose stools (mild and temporary). Tremo
rs (fine to coarse). Sed. Weight gain.
or
4.
6.
8.
PSYCHOPHARMACOLOGY 56 EU Walter Cortes
SIDE EFFECTS I
2.
Temporary muscle weakness).
and
fatigue
(Benign
and
4.
Hair loss (temporary). Polyuria (benign but progress to diabetes insipidus). pos
sibility
6.
8.
Lithium intoxication (serum lithium levels higher than 2.0 mEq / L).
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SIDE EFFECTS II
Mild intoxication (serum level approx. 1.5 mEq / L): Slight apathy, lethargy, de
creased concentration, muscle weakness, mild ataxia, coarse tremor of hands, sli
ght muscle contractions. Moderate intoxication (serum level between 1.5 and 2.5
mEq / L): severe diarrhea, nausea, vomiting, mild to moderate ataxia, incoordina
tion, slurred speech, tinnitus, blurred vision, muscle twitching frank, ataxia,
tremors, irregular.
END OF SUBMISSION
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