Psychiatric Nursing + Neuro Flashcards
Alcohol Deterrent
Acamprosate
Used for alcohol abstinence management
PO
Interactions: Increase glucose, bilirubin, uric acid
Decreases Hgb/Hct and platelets
Side effects: Anxiety Dizziness Insomnia Chills Rhinitis Constipation N/V Depression Headache Tremors Drowsiness Anorexia Diarrhea
Adverse:
SI and Dyspnea
Intervention
Assess Mental status for depression, abnormal thoughts, suicidal thoughts
Obtain v/s
Evaluate therapeutic response
Education:
Notify prescriber of depression, abnormal/suicidal thoughts
Don’t engage in hazardous activities
Don’t drink alcohol
Aldehyde Dehydrogenase Inhibitor / Disulfiram
Used for alcoholism
Contraindications: Myocardial disease, Psychoses, Pregnancy
PO: 2 – 12 hours
Interactions: Severe unpleasant side effects when
taken with alcohol, or foods/ products containing alcohol such as mouthwash, cough medicine, cooking wine, vinegar.
Use with phenytoin can lead to phenytoin intoxication.
MoA: Disulfiram blocks the oxidation of alcohol. Blocks an enzyme that is involved in metabolizing alcohol intake. Disulfiram produces very unpleasant side effects when combined with alcohol in the body.
Side Effects: Flushing Sweating Increased thirst Swelling Rapid weight gain Nausea Severe vomiting Confusion Blurred vision Weakness Throbbing headache
Adverse Effects: Allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Severe abdominal pain Sudden vision loss Optic neuritis/Peripheral neuritis Hepatitis
Interventions:
Monitor liver function studies.
Assess for recent alcohol use. Do not administer for 12 hr
following alcohol ingestion.
If a severe disulfiram reaction occurs administer oxygen,
monitor ECG and serum potassium levels, and provide
supportive measures.
Monitor CBC and blood chemistry every 6 months during
therapy
Education:
Do NOT drink alcohol while taking this medication. Severe unpleasant side effects when taken with alcohol, or foods/ products containing alcohol such as mouthwash, cough medicine, cooking wine, vinegar.
Wear a medical alert tag or carry an ID card.
Used with behavior modification, psychotherapy, and counseling support.
Inform patient of purpose of disulfiram and the consequences of drinking alcohol during therapy.
Avoid driving and other activities requiring alertness
Anti Anxiety: Antihistamines - Hydroxyzine
Common use: Anxiety disorders, Pre and post op sedation, N/V
Contraindications: 1s trimester of pregnancy
PO/IM/ 15 to 60 mins
Interactions:
Increased CNS effect with use of barbiturates, opioids, analgesics, alcohol, sedative/hypnotics.
Increased anticholinergic effects with use of phenothiazines, antihistamines, antidepressants,
atropine, haloperidol, MAOIs
MoA: Depresses subcortical levels of CNS, including the limbic system.
Side Effects: Headache Dry mouth Dizziness Fatigue Increased appetite Nausea Diarrhea Weight gain
Adverse Effects:
Hypotension
Hives
Seizures
Nursing Interventions: Administer IM deep in large muscle using Z-track method to decrease pain, chance of necrosis. Do NOT give IV or SQ. Monitor for sedative effects. Monitor BP Assist with ambulation
Education: Avoid OTC medications. Avoid driving, activities that require alertness. Avoid alcohol, psychotropic medications. Do not discontinue quickly. Rise slowly.
Benzodiazepines - Diazepam (Valium), Lorazepam (Ativan), Alprazolam (Xanax), Triazolam (Halcion), Midazolam (Versed)
Common Uses: Anxiety disorders, Alcohol withdrawal Personality disorders Panic attacks Seizures Pre-op sedation
Contraindications: Narrow angle glaucoma Hypersensitivity Myasthenia gravis Sleep apnea
PO/iM/IV/RECTAL
Interactions:
Increase diazepam effect with amiodarone, cimetidine, verapamil, valproic acid.
Increase toxicity with barbiturates, SSRIs, cimetidine, CNS
depressants, valproic acid
MoA: Potentiates the actions of GABA, especially in the limbic system.
Advantages:
Does not produce life-threatening respiratory depression or coma if taken in excessive amounts.
Result is less physical dependence than the
barbiturates.
Disadvantages: Increased risk of falls with elderly
Side Effects: Drowsiness Dizziness Sedation Headache Depression Blurred vision Tinnitus Constipation Diarrhea Anorexia Nausea/Vomiting
Adverse: Retrograde amnesia Hypotension Tachycardia Neutropenia Respiratory depression
Intervention:
BP lying, sitting, standing.
Monitor CBC, AST, ALT, bilirubin, creatinine, LDH, alkaline phosphate.
Monitor degree of anxiety, mental status.
Education:
May take with food.
Do not use for everyday stress or for > 4 months unless directed by prescriber.
Avoid OTC medications.
Avoid driving, activities that require alertness. Rise slowly.
Avoid alcohol.
Anticonvulsant - Topiramate
Common uses: Seizures, Bipolar Disorder, Alcohol dependence, mania, bulimia
Contraindications: Metabolic acidosis, Pregnancy
PO
Interactions: Increased CNS depression with alcohol, CNS
depressants. Decreased level of oral contraceptives,
estrogen, digoxin, lithium.
MoA: May prevent seizure spread as opposed to an elevation of seizure threshold.
Side Effects: Dizziness Fatigue Insomnia Anxiety Memory loss Tremors Diplopia Anorexia Nausea Dyspepsia Weight loss
Adverse:
SI, Pancreatitis and Death
Interventions: Assess mental status, mood, behaviour. Monitor seizures. Assess renal and hepatic studies. Assist with ambulation. Seizure precautions.
Education:
Swallow whole. Do not break, crush, or chew.
Carry emergency ID.
Avoid driving, other activities that require alertness.
Notify prescriber of blurred vision, periorbital pain.
Maintain adequate fluid intake to prevent kidney stones.
May need to increase amount of food consumed since weight loss may occur
Antidepressant Agents: Monamine Oxidase Inhibitors (MAOIs) - Phenelzine (Nardil),
Tranylcypromine
(Parnate)
Common uses: Severe depression, Psychosis / PTSD, Dissociative disorders Bulimia, Panic disorders when other agents are ineffective.
PO - up to three weeks
Interactions:
High serotonin levels result in confusion, high BP, tremor, hyperactivity, coma, and death when taken with paroxetine, fluoxetine, amitriptyline, nortriptyline,bupropion; pain
medications like methadone, tramadol, and meperidine;
dextromethorphan, St. John’s Wort, cyclobenzaprine, and mirtazapine.
MoA:
Affects chemical messengers (neurotransmitters) used to communicate between brain cells. MAOIs work by effecting changes in the brain
chemistry. An enzyme called monoamine oxidase is involved in removing the neurotransmitters norepinephrine, serotonin and dopamine from the brain. MAOIs prevent this from happening, which makes more of these brain chemicals available to effect changes in both cells and circuits that have been impacted by depression.
Advantage:
Prescribed when client does not respond to other antidepressants.
Disadvantages: Hypertensive crisis can be triggered by
foods rich in tyramine.
Side Effects: Dizziness Constipation Diarrhea Tremors Diaphoresis Sexual dysfunction Weight gain
Adverse: Orthostatic hypotension Seizures Coma Tachycardia
Interventions: Monitor vital signs, reflexes, affect, orientation, UOP.
Obtain CBC, urinalysis, thyroid function tests, ECG, EEG.
Monitor for symptoms of hypertensive crisis (elevated BP and severe headache)
Education:
Avoid tyramine containing foods and beverages (pickled
foods, aged cheese, fermented alcohol, sour cream, figs, shrimp, bananas, chocolate or caffeinated drinks).
Do not take any other medications without checking with primary healthcare provider when taking a MAOI.
Agents: Selective Serotonin Reuptake Inhibitors (SSRIs) - Fluoxetine (Prozac), Paroxetine (Paxil), Escitalopram (Lexapro), Citalopram (Celexa), Sertraline HCL (Zoloft)
Common uses: Depression, Bi-polar disorder Eating disorders, OCD Panic attacks, Anxiety disorder PTSD / Phobia Dissociative disorder Premenstrual dysphoric disorder
Contraindications: Hypersensitivity MI Taking MAOIs Dehydration Breastfeeding
PO - 2 - 4 weeks Interactions: Increase effects of CNS and respiratory depression, and hypotensive effect with alcohol and CNS depressants. Increase effect of hypoglycemic.
MoA: Serotonin is increased in nerve cells because of blockage from nerve fibers.
Side Effects: Insomnia Weight loss Sexual dysfunction Palpitations Headache Diaphoresis GI complaints
Adverse effects: Seizures Hyponatremia Dehydration Bleeding Suicidal ideation
Interventions:
Do NOT give with MAOIs. Wait 14 days after stopping MAOIs to administer.
Monitor liver functions.
Withdrawal should be gradual.
Education: Therapeutic effect may take several weeks. Do not discontinue abruptly. Use with caution when driving. Avoid alcohol, other CNS depressants.
Antidepressant Agents: Tricyclic Antidepressants - Amitryptyline (Elavil),
Nortriptyline (Pamelor),
Imipramine (Tofranil)
Common Uses: Depression Anxiety Panic disorder OCD Bulimia Depression related to alcohol and cocaine withdrawal. Chronic pain disorder. Tofranil – childhood enuresis
Contraindications:
Clients with suicidal ideations.
History of seizures
Chronic cardiac disease.
PO/ 45 minutes
Interactions: Alcohol, hypnotics, sedatives,
barbiturates potentiate central nervous system depression
when taken with tricyclic antidepressants.
Concurrent use of MAOIs with amitriptyline may lead to cardiovascular instability and toxic psychosis.
Antithyroid medications taken with amitriptyline may increase the risk of dysrhythmias.
MoA: Blocks the uptake of the neurotransmitters norepinephrine and serotonin in the brain.
Advantages: Effective and less expensive than SSRI’s and other drugs
Disadvantages: Overdose is generally lethal
Side Effects: Headache Dry mouth Sedation Impotence Urinary retention Photosensitivity
Adverse: Orthostatic Hypotension, dysrhythmias
Interventions:
Increase fluids, bulk in diet if constipation, urinary retention occur.
Administer with food, milk for GI symptoms.
Crush is client unable to swallow medication whole.
Administer at bedtime if over sedation occurs during day
Education:
Therapeutic effects may take 2-3 weeks.
Use caution when driving, performing activities that require alertness.
Avoid alcohol, other CNS depressants.
Wear sunscreen or large hat when outdoors.
Antipsychotic Agents: Phenothiazines -
Chlorpromazine
(Thorazine),
Fluphenazine
Common Uses: Psychotic disorders Schizophrenia Mania Paranoia Tourette’s syndrome
Contraindications: Hypersensitivity Subcortical brain damage Blood dyscrasias Renal or liver damage Coma
PO/IM/IV/Rectal
Interactions:
Kava kava may increase the risk and severity of dystonic
reactions when taken with phenothiazines.
Increase depressive effects when taken with alcohol or
other CNS depressants.
MoA:
Blocks norepinephrine, causing sedation and hypotensive effects early in treatment. Also blocks the actions of dopamine.
Side Effects: Anorexia Urinary retention Dry mouth Sedation Polyuria Dizziness Headache Nasal congestion
Adverse Effects: Orthostatic hypotension Hypertension Extrapyramidal reactions Seizures Leukopenia Agranulocytosis Tardive dyskinesia Neuroleptic malignant syndrome
Interventions:
Assess baseline vital signs. Monitor serum glucose level.
Assess mental status, cardiac, eye, and respiratory disorders.
Remain with client while medication is taken and swallowed.
Avoid skin contact with liquid concentrations to prevent contact
dermatitis.
Protect liquid from light. Dilute liquid with fruit juice.
Administer with food or milk to decrease gastric irritation.
Administer IM deep into muscle.
Observe for Extra Pyramidal Symptoms.
Education:
Encourage client to take the drug exactly as prescribed.
Medication may take 6 weeks or longer to achieve full
clinical effect. Advise to wear an ID bracelet.
Do not consume alcohol or other CNS depressants, such
as narcotics.
Do not abruptly discontinue the drug.
Teach smoking cessation (Smoking increases metabolism of some antipsychotics).
Guide client to maintain good oral hygiene by frequent brushing and flossing of teeth.
Tardive Dyskinesia
Tardive dyskinesia is a side effect of antipsychotic medications. These drugs are used to treat schizophrenia and other mental health disorders.
TD causes stiff, jerky movements of your face and body that you can’t control. You might blink your eyes, stick out your tongue, or wave your arms without meaning to do so.
Symptoms Stick out your tongue without trying Blink your eyes fast Chew Smack or pucker your lips Puff out your cheeks Frown Grunt
It can also affect your arms, legs, fingers, and toes. That can cause you to:
Wiggle your fingers
Tap your feet
Flap your arms
Thrust out your pelvis
Sway from side to side
These movements can be fast or slow. You may find it hard to work and stay active.
Some psychiatric medications block a brain chemical called dopamine. It helps cells talk to each other and makes the muscles move smoothly. When you have too little of it, your movements can become jerky and out of control.
Includes: Chlorpromazine (Thorazine) Fluphenazine (Prolixin) Haloperidol (Haldol) Thioridazine (Mellaril) Trifluoperazine (Stelazine)
Extra-pyramidal reactions
Antipsychotic medications commonly produce extrapyramidal symptoms as side effects. The extrapyramidal symptoms include acute dyskinesias and dystonic reactions, tardive dyskinesia, Parkinsonism, akinesia, akathisia, and neuroleptic malignant syndrome.
Neuroleptic Malignant syndrome
Neuroleptic malignant syndrome (NMS) is a life-threatening idiosyncratic reaction to antipsychotic drugs characterized by fever, altered mental status, muscle rigidity, and autonomic dysfunction.
Mental status change is the initial symptom in 82 percent of patients [37]. It is not surprising, given the usual psychiatric comorbidity of the typical patient, that its significance is often underappreciated. This often takes the form of an agitated delirium with confusion rather than psychosis. Catatonic signs and mutism can be prominent. Evolution to profound encephalopathy with stupor and eventual coma is typical [16].
●Muscular rigidity is generalized and is often extreme. The increased tone can be demonstrated by moving the extremities and is characterized by “lead-pipe rigidity” or stable resistance through all ranges of movement. Superimposed tremor may lead to a ratcheting quality or a cogwheel phenomenon. Other motor abnormalities include tremor (seen in 45 to 92 percent), and less commonly, dystonia, opisthotonus, trismus, chorea, and other dyskinesias [3,5]. Patients can also have prominent sialorrhea, dysarthria, and dysphagia.
●Hyperthermia is a defining symptom according to many diagnostic criteria. Temperatures of more than 38°C are typical (87 percent), but even higher temperatures, greater than 40°C, are common (40 percent) [5]. Fever may be a less consistent symptom in patients with NMS associated with second-generation antipsychotic agents [38,39].
●Autonomic instability typically takes the form of tachycardia (in 88 percent), labile or high blood pressure (in 61 to 77 percent), and tachypnea (in 73 percent) [3,20]. Dysrhythmias may occur. Diaphoresis is often profuse.
Akinesia
loss or impairment of the power of voluntary movement.
Akathisia
is a movement disorder characterized by a feeling of inner restlessness and inability to stay still.
Atypical Antipsychotics -Risperidone (Risperdal),
Quetiapine (Seroquel),
Aripiprazole (Abilify)
Common uses: Psychotic disorders Schizophrenia Bipolar mania Paranoia Personality disorder
Contraindications:
Seizures disorders, suicidal ideation
PO/IM
Interactions: Use with other CNS depressants, alcohol will increase sedation. Use with other antipsychotics, lithium increase risk of EPS.
Advantages:
Less likely to cause extrapyramidal effects,
neuroleptic malignant syndrome and
tardive dyskinesia than the phenothiazines.
Side Effects: Sedation Drowsiness Headache Dry mouth Agitation Anxiety Appetite stimulation with weight gain
Adverse effects: Orthostatic hypotension Seizures Stroke Suicidal ideation Neuroleptic malignant syndrome
Interventions:
IM – give deeply into muscle mass.
Monitor for hoarding / not swallowing medication.
I&O
Check bilirubin, CBC, weight, lipid profile, fasting glucose monthly.
BP lying, sitting, standing
Education
Rise slowly from lying or sitting position.
Avoid hot tubs, hot showers, hot tub baths as hypotension may
occur.
Avoid OTC medications unless approved by prescriber.
Avoid use with alcohol.
Heat stroke may occur in hot weather.
CNS Stimulants: ADHD/ADD Stimulants - Methylphenidate (Ritalin), Amphetamine (Adderall), Lisdexamfetamine (Vyvanse), Dexmethylphenidate (Focalin)
ADD/ ADHD
Contraindications: Heart problems Bipolar disorder Glaucoma Tourette’s Syndrome
PO/ 20 - 30 minutes
Interactions:
Taking MAO inhibitors with this medication may cause a serious (possibly fatal) drug interaction.
MoA: Blocking the dopamine transporter and norepinephrine transporter, leading to increased concentrations of dopamine and
norepinephrine within the synaptic cleft
Disadvantages: High abuse potential due to stimulant effects.
Sudden death has been reported in children
taking amphetamine with structural cardiac
abnormalities.
Side Effects: Headache Insomnia Dry mouth Blurred vision Anxiety Nervousness Weight loss Nausea/Vomiting Decreased Appetite
Adverse Effect: Hypertension Tachycardia Suicidal thoughts Sudden death in children with structural Cardiac abnormalities.
Interventions:
Monitor mental status and observe for changes in level of consciousness
and adverse effects such as persistent drowsiness, psychomotor agitation
or anxiety, dizziness, trembling or seizures.
Monitor vital signs.
Monitor gastrointestinal and nutritional status.
Monitor laboratory tests such as CBC, differential, and platelet count.
Monitor effectiveness of drug therapy. Monitor growth and development.
Monitor sleep–wake cycle
Education:
May be habit forming. Avoid drinking alcohol.
To prevent sleep problems, take this medicine in the morning.
Methylphenidate may impair thinking or reactions. Do not drive or do anything that requires alertness.
Instruct client to report any significant increase in motor behavior,
changes in sensorium, or feelings of dysphoria.
Take drug with meals to reduce GI upset and counteract anorexia; eat frequent, small nutrient-and calorie-dense snacks.
Weigh weekly and report significant losses over 1 lb. Report shortness of breath, profound fatigue, pallor, bleeding or excessive bruising (these are signs of blood
disorder).
CNS Stimulants: Anorexiants - Phentermine
Ionamin
Common Uses: Appetie suppressant, Obesity
Contraindication: Hypersensitivity Hypertension Glaucoma Heart disease
PO
Interactions: Taking MAO inhibitors with this medication may cause a serious (possibly fatal) drug interaction.
MoA: Reduces hunger perception, a cognitive process mediated through nuclei within the hypothalamus. Outside the brain, phentermine releases norepinephrine and epinephrine causing fat cells to break down stored fat as well.
Advantages: Indicated for treatment of obesity (BMI
>30) and for those overweight (BMI
27-30) who have comorbidities such as
hypertension, high cholesterol, diabetes
Side Effects: Anxiety Dizziness Insomnia Headache Dry mouth Nausea/Vomiting Diarrhea Constipation
Adverse: Hypertension Hallucinations Seizures Pulmonary hypertension Chest pain
Interventions:
Assess for tolerance to the anorectic effect of the drug. Withhold drug and report to physician when this occurs.
Lab tests: Periodic CBC with differential and blood glucose.
Monitor periodic cardiovascular status, including BP, exercise tolerance, peripheral edema.
Monitor weight at least 3 times/wk.
Education:
Take 1 or 2 hours after breakfast. Do not crush or chew.
Avoid drinking alcohol with Ionamin. May affect blood sugar of client with diabetes. Do not breast feed while taking this drug.
Report immediately any of the following: Shortness of breath, chest pains, dizziness or fainting, swelling of the extremities.
Tolerance to the appetite suppression effects of the drug usually develops in a few weeks. Notify physician, but do not increase the drug dose. Weigh self at least 3 times/week at the same time with the same amount of clothing.
CNS Stimulants - Caffeine
Common Uses: Migraine headache Tension headache Promotes alertness Alleviates fatigue In combination with pain medication.
Contraindications: History of cardiac disease or peptic ulcer disease Pregnancy
PO/Rectal/IV
Interactions:
Taking caffeine along with ephedrine might
cause heart problems. Caffeine might block the effects of adenosine,dipyridamole.
Ciprofloxacin, cimetidine, disulfiram, estrogen
decrease how quickly the body breaks down
caffeine. Caffeine decreases how quickly the body breaks down clozapine. Taking caffeine along with medications that slow clotting might increase the chances bleeding
MoA: Stimulates the CNS, especially the medullary respiratory center. Has a pronounced diuretic effect and is a myocardial stimulant. It can worsen peripheral vasoconstriction in those with hypertension and causes cerebral vasodilation, making it an effective treatment for
migraines and headaches.
Disadvantages: Caffeine combined with alcohol
appears to improve response time but does not reduce the errors in judgment caused by alcohol.
Side Effects:
Nervousness Insomnia
Irritability Flushing
Palpitations Headache
Adverse: Cardiac arrhythmias Hypertension Tachypnea Confusion Dehydration
Interventions:
For IV use: Assess respiratory status frequently.
Monitor for signs of necrotizing enterocolitis (abdominal
distension, vomiting, bloody stools, lethargy).
Monitor serum caffeine levels before and during therapy.
Monitor serum glucose levels.
Education:
Instruct on correct technique for administration. Measure oral dose accurately with a 1-mL syringe.
Advise to consult health care professional immediately if signs of necrotizing enterocolitis occur.
Necrotizing
Enterocolitis
Necrotizing enterocolitis (NEC) is a devastating disease that affects mostly the intestine of premature infants. The wall of the intestine is invaded by bacteria, which cause local infection and inflammation that can ultimately destroy the wall of the bowel (intestine).
CNS Depressants - Barbiturates - Phenobarbital
(Luminal), Secobarbital
(Seconal), Pentobarbital
(Nembutal)
Common Uses: Anesthesia induction. Short-term anesthesia Seizures Short-term use of insomnia
Contraindication: Pregnancy Hypersensitivity Depression Suicidal tendency Liver disease Respiratory disease
PO/IM/IV Interactions: Increased CNS depression with alcohol, narcotics, sedativehypnotics. Decreased effectiveness of beta-adrenergic blockers, clozapine, corticosteroids, digitoxin, doxycycline, estrogens, oral contraceptives, quinidine, theophyllines, voriconazole, or warfarin
MoA: Acts on GABAA receptors, increasing synaptic inhibition. This has the effect of elevating seizure threshold. Phenobarbital may also
inhibit calcium channels, resulting in a decrease in excitatory transmitter release. The sedative-hypnotic effects of phenobarbital are likely the result of its effect on the polysynaptic midbrain reticular formation, which controls CNS arousal.
Disadvantages: Loading dose may be required. Cautious use in elderly, associated with increased risk of falls
Side Effects: Drowsiness Lethargy Dizziness Headache Hangover effect Interferes with REM sleep
Adverse Effects: Respiratory depression Mental depression Hepatic toxicity Renal toxicity
Interventions:
Monitor vital signs. Ensure patient safety. Perform neuro-checks regularly.
Keep resuscitative equipment accessible.
Monitor response to and effectiveness of drug therapy.
Monitor for signs of hepatic or renal toxicity.
Monitor laboratory blood tests and urinalysis: CBC with differential,
electrolytes, BUN, PT, PTT, liver enzymes.
Education:
Do not drive or perform unsafe tasks.
Do not drink alcohol or use medicines that may cause
drowsiness
Hormonal birth control may not work as well.
To prevent pregnancy, use an extra form of birth control
Gabapentin
Seizures Peripheral neuropathy Migraine prophylaxis Vasomotor symptoms in women with breast cancer or postmenopausal women
PO/ 1-3 hours
Interactions:
CNS depression with alcohol, sedatives, antihistamines.
Increase gabapentin levels with morphine.
Decrease gabapentin levels with antacids, cimetidine.
MoA: Acts on the peripheral nerves and CNS by inhibiting spontaneous neuronal firing. May increase seizure threshold.
Should be used cautiously with the elderly
Side Effects: Drowsiness Dizziness Fatigue Confusion Anxiety Rhinitis Constipation
Adverse Effects: Increased frequency of partial seizures Leukopenia Depression Leukopenia Thrombocytopenia
Interventions: Monitor seizure activity. Monitor mental status. Seizure precautions Increase fluids, bulk in diet for constipation
Education: Do not crush or chew caps. Take at least 2 hours from antacids. May take without regard to meals. Carry ID Avoid driving and other activities requiring alertness.
Phenytoin
Seizures Status epilepticus Unlabeled: migraines, paroxysmal atrial tachycardia, ventricular tachycardia
Contraindications: Pregnancy Hypersensitivity Bradycardia Heart block Stokes-Adams syndrome
PO/IV
Interactions: Increase phenytoin effect with benzodiazepines, cimetidine, tricyclics, salicylates, alcohol. Decrease phenytoin effects with antacids, barbiturates, rifampin.
Side Effects: Gingival hyperplasia Dizziness Insomnia Paresthesias Depression Nystagmus Blurred vision Anorexia Weight loss Nausea/vomiting
Adverse Effects: Aplastic anemia Agranulocytosis Pancytopenia Hepatitis Suicidal tendency Bradycardia Ventricular fibrillation Cardiac arrest Stevens-Johnson Syndrome Blue-Glove syndrome
Interventions:
IV administration should not exceed 50 mg/min in adults. Administer slow IVP.
Monitor phenytoin level.
Monitor seizure activity.
Monitor EKG, BP, respiratory function during IV infusion.
Education:
Take with meals to decrease side effects.
Take antacids two hours before or after phenytoin.
Urine may turn pink
Oral hygiene
Avoid hazardous activities.
Carry ID
Chloral Hydrate
Common uses: Short term treatment of insomnia Sedation Alcohol withdrawal
Contraindications:
Hepatic failure
Renal failure
PO/ 10 - 20 minutes interactions: Side effects of barbiturates may be increased. Use with loop diuretics may cause tachycardia and blood pressure changes. Anticoagulants side effects may increase.
Advantages: Does not interfere with REM sleep
Side Effects:
Drowsiness Hangover effect
Nausea/Vomiting Flatulence
Diarrhea Confusion
Adverse Effects: Cardiac arrhythmias Sudden death Difficulty breathing Chest pain
Interventions:
May dilute syrup in water or other oral liquid (eg, fruit juice or ginger
ale) to minimize gastric irritation.
Administer capsules after meals (when used as sedative).
Education:
If stomach upset occurs, take with food.
Swallow chloral hydrate whole.
Take chloral hydrate with a full glass of water or other.
Do not take 2 doses at once.
Chloral hydrate may cause drowsiness or dizziness. Do not
drive, operate machinery, or do anything else that could be
dangerous.
Avoid drinking alcohol or taking other medications that cause
drowsiness while taking chloral hydrate.
Eszopiclone, Zolpidem
Insomnia
Contraindications: Hypersensitivity to benzodiazapine, Respiratory depression
PO/ 10 minutes Interactions: Decrease CNS function with alcohol, CNS depressants, anticonvulsants. Food decreases absorption.
MoA: The precise mechanism of action of eszopiclone as a hypnotic is unknown, but its effect is believed to result from its interaction with GABA-receptor complexes at binding domains located close to benzodiazepine receptors.
Zolpidem interacts with a GABA-BZ receptor complex and shares †fsome of the pharmacological properties of the benzodiazepines.
Side Effects: Headache Nervousness Anxiety Drowsiness Hot flashes Irritability Nausea / vomiting Erectile dysfunction
Adverse Effects: Tachycardia Depression Hypotension Sleep driving (Zolpidem)
Interventions: Assess vital signs. Check for signs of respiratory depression. Use bed alarm for older clients. Observe for side effects.
Education:
Teach nonpharmacologic ways to induce sleep – warm bath,
listening to music, drinking warm fluids, avoiding caffeine.
Avoid alcohol, antidepressants, antipsychotics, and narcotic
drugs.
Take 15-30 minutes before bedtime.