Psych meds Flashcards

1
Q

What is the most common med to treat anxiety?

A

Benzodiazepines (-am family; midazolam, alprazolam, dazepam)

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2
Q

MOA of benzodiazepines

A

acts on GABA to enhance effects on neurons

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3
Q

ADR of benzodiazepines

A

excessive sedation, significant hypotension with IV, amnesia, or paradoxical reactions (insomnia, etc)

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4
Q

antidote for benzodiazepine

A

flumazenil

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5
Q

therapeutic effects of benzodiazepine

A

CNS depression, sedation, muscle relaxation

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6
Q

what is the drug of choice for generalized anxiety?

A

buspirone

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7
Q

MOA of buspirone

A

act on serotonin to have anxiolytic effect without sedation; less dependency, can take daily

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8
Q

antihistamines for anxiety

A

may use as a mild tranquilizer

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9
Q

ADR of antihistamines

A

excessive drowsiness, dry mouth, secretions

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10
Q

what antihistamine is given for anxiolytic effect/ tranquilizer?

A

hydroxyzine (IM z track admin); use as take down drug in crisis

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11
Q

NE Reuptake Inhibitor use

A

ADHD main use; off-label for some anxiety disorders

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12
Q

NE Reuptake Inhibitor MOA

A

block uptake of NE resulting in more NE in the blood to increase energy and focus

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13
Q

NE Reuptake Inhibitor ADRs

A

nausea, dry mouth, insomnia, BP elevates

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14
Q

NE Reuptake Inhibitor specific drug for anxiety

A

atomoxetine

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15
Q

how long does it take for full effects of benzodiazepines?

A

1-2 weeks; longer if combo with antidepressants

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16
Q

Do’s and Don’ts of Anxiety

A

DO NOT… stop therapy abruptly, take with OTC cough/cold meds with CNS depressants, drink alcohol, drive heavy machinery

DO… teach pt to seek counseling and learn healthy coping skills

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17
Q

who is given mood stabilizer drugs?

A

bipolar pts and manic pts

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18
Q

MOA of mood stabilizers

A

alters level of neurotransmitters in brain to control manic behavior (exact MOA unknown); alter in sodium transport in nerve and muscle cells

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19
Q

what is the primary mood stabilizing drug?

A

lithium

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20
Q

ADR of lithium use

A

slowed reflexes/reaction time, lithium toxicity; long use can lead to hypothyroidism

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21
Q

what are the S&S of lithium toxicity?

A

polyuria, memory deficits, confusion, tremors, muscle weakness, CV collapse, coma

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22
Q

acute mania therapeutic level of lithium

A

1-1.5 mEq / L

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23
Q

long term maintenance therapeutic level of lithium

A

0.6-1.2 mEq / L

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24
Q

Factors affecting lithium levels

A

-Sodium deficiency (increase reabsorption and risk for lithium toxicity)
- Sodium excess (decrease reabsorption and risk for non-therapeutic levels)
- NSAIDs and diuretic use- increase levels
- Cannot give in single dose (low therapeutic index and short half life)
-Need good kidney function to take med

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25
Q

Misc mood stabilizers

A

valproates, carbamazepine, antipsychotics for severe mania episodes

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26
Q

valproates MOA

A

possible GABA elevation; does not need frequent monitoring, but higher incidence of suicides; may use in combo with lithium

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27
Q

valproate drugs

A

Divalproex sodium and Valproic acid

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28
Q

antipsychotic drugs for severe mania

A

Aripiprazole
Lurasidone - safer in pregnancy
Brexpiprazole
Symbyax (Combo of olanzapine (antipsychotic) and fluoxetine (antidepressant) ; Effective in improving bipolar disorder without increasing mania

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29
Q

Antidepressants Black Box Warning

A

suicidal thoughts and behaviors; increase risk in children, adolescents, and young adults

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30
Q

what are TCAs?

A

Tricyclic Antidepressants; 1st generation of 1950s

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31
Q

TCAs MOA

A

Corrects the imbalance of serotonin and NE; Blocks inactivation of NE and serotonin in the brain which increases levels of the neurotransmitters

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32
Q

TCA ADRs

A

orthostatic hypotension, arrhythmias, dry mouth, urinary retention, constipation, sedation, confusion, weight gain

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33
Q

TCA drugs

A

Amitriptyline - low dose for depression treatment, more used for pain
Imipramine - give to kids who wet the bed

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34
Q

what are MAOI’s?

A

Monoamine Oxidase Inhibitors

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35
Q

MOAI’s mechanism?

A

Blocks monoamine oxidase, an enzyme that inactivates catecholamines to increase NE levels

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36
Q

MAOI drugs

A

Tranylcypromine
Phenelzine

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37
Q

MAOI ADRs

A

anorexia, orthostatic hypotension, dizziness, insomnia

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38
Q

severe drug to food interaction of MAOI’s?

A

Hypertensive crisis = MAOIs taken with tyramine containing foods (aged/smoked meats, cheese, and red wine)

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39
Q

what are SSRIs?

A

Selective Serotonin Reuptake Inhibitors

40
Q

What are SSRIs highly bound to? what does it indicate?

A

albumin; low albumin = more effect of drug

41
Q

SSRI MOA?

A

Block uptake of serotonin back into synaptic cells —> more free serotonin for activity

42
Q

what is the advantage of SSRIs over TCA?

A

not as many anticholinergic or antiadrenergic effects

43
Q

SSRIs ADRs

A

CNS stimulation, N/V/D, weight loss initially then weight gain as therapy progresses; skin rash

44
Q

SSRI drugs

A

Fluoxetine
Paroxetine
Sertraline
Trazodone (serotonin antagonist) - not SSRIs but the same effects achieved

45
Q

what are SNRI?

A

Serotonin/NE Reuptake Inhibitor

46
Q

MOA of SNRI

A

Results in more serotonin, NE, and dopamine

47
Q

ADR of SNRI

A

nausea, dry mouth, increase BP, tiredness, low libido, and ED

48
Q

SNRI drugs

A

Venlafaxine- off label use for ADHD
Desvenlafaxine
Duloxetine - clinically trialed for pain management for fibromyalgia and musculoskeletal pain

49
Q

Misc antidepressants

A

bupropion, mirtazapine

50
Q

bupropion

A

Weakly inhibits reuptake of dopamine, NE, and serotonin; used in smoking cessation

51
Q

mirtazapine

A

Noradrenergic and specific serotonergic antidepressant; Strongly blocks alpha 2 receptors to result in increase release of NE and serotonin; antihistamine effects

ADRs = increase sedation (can be sleep aid), weight gain

52
Q

how long before desired effects achieved for antidepressants?

53
Q

what is important to determine before starting MAOI therapy? why?

A

a good drug history; antidepressants cannot be taken within 2 weeks of MAOI therapy

54
Q

pt teaching with MAOI

A

dietary precautions, many drug to drug interactions

55
Q

other nursing considerations

A

Monitor VS, suicide precautions (BBW) (provide safety measures)

Risk of suicide is highest when patient begins to get energy again

Do not abruptly discontinue → withdrawal symptoms

Encourage counseling

56
Q

what is serotonin syndrome?

A

Hyperactivity of serotonin resulting from drug to drug interactions or high levels of one serotonin increasing drug

57
Q

S&S of serotonin syndrome

A

agitation, hyperreflexia, fever, diaphoresis, tachycardia, seizures (may cause death)

58
Q

what can antipsychotic meds be used for?

A

acute psychoses and schizophrenia; may also be used as take down drug in pts with acute aggression and agitation

59
Q

positive symptoms

A

irrational behavior, out of touch with reality, delusional, hallucinating, repetitive and uncontrollable movements, loose association, communication impairment

60
Q

negative symptoms

A

social and emotional withdrawal, poor judgement, poor self care, avolition, flat affect, apathy

61
Q

general MOA of antipsychotics

A

primarily block neurotransmitters, mainly dopamine and serotonin, varying degrees of anticholinergic and alpha antagonistic effects

62
Q

general ADRs of antipsychotics

A

dry mouth, constipation, tachycardia (anticholinergic effects); hypotension, drowsiness, seizures, bone marrow depression and EPS, TD, some pts may experience NMS

63
Q

Black Box Warning on Antipsychotic meds

A

dementia related psychosis; increase risk of death in elderly with dementia due to CV events (stroke)

64
Q

what is EPS?

A

extrapyramidal symptoms; inability to sit still, involuntary muscle movements, tremors, drooling, stiff muscle, and facial movements

65
Q

treatment for EPS

A

diphenhydramine or benztropine

66
Q

what is TD

A

tardive dyskinesia; protrusion of tongue, slow rhythmic involuntary movements mainly of facial muscles (usually irreversible)

67
Q

treatment of TD

A

deutrabenazine and valbenazine

68
Q

what is NMS

A

neuroleptic malignant syndrome; a rare, potentially fatal, complication within hours of treatment with antipsychotics or occur years later

69
Q

symptoms of NMS

A

LEAD-PIPE MUSCLE RIGIDITY, severe temp elevation, dysrhythmias, seizures, may lead to death

70
Q

treatment of NMS

A

dantrolene

71
Q

what do typical antipsychotics treat?

A

only positive symptoms

72
Q

what is the main class of typical antipsychotics?

A

phenothiazine/phenothiazine-like

73
Q

main drugs of phenothiazine class

A

chlorpromazine; common for takedown of acutely psychotic pt or irrational acting pt

piperazine

piperidine

74
Q

main drug of phenothiazine-like class

A

haloperidol; common use for long term therapy in schizophrenia

75
Q

ADRs of haloperidol

A

high EPS effects; potentially fatal arrhythmias (must be on ECG monitor if med is IV)

76
Q

what are atypical antipsychotics?

A

treats both positive and negative symptoms; less EPS and NMS risk; preferred drug class

77
Q

MOA of 2nd generation antipsychotics (atypical)

A

block dopamine and serotonin receptors

78
Q

ADR of atypicals

A

little to no EPS, may result in diabetes, lipid problems, dysrhythmias

79
Q

first med started in atypicals/ what is the prodrug?

80
Q

clozapine

A

drug of last resort

Risk Evaluation Mitigation Strategy (REMS) requires additional documentation and consents due to risks of drug

81
Q

ADRs of clozapine

A

serious bone marrow depression, necessitating WBC evaluation every 1-2 weeks; can lead to serious infection risk if pt develops agranulocytosis

82
Q

when would we stop clozapine permanently?

A

if WBC drops below 2000

83
Q

common 1st line treatment for atypical antipsychotics

A

aripiprazole (monthly injections), brexpiprazole

ziprasidone IM for take down

quetiapine for bipolar and psychotic disorders (highly abused)

asenapine sublingual for clients who are difficult to give meds to

84
Q

nursing considerations for antipsychotics

A

monitor VS, behaviors, EPS status

safety precautions (meds cause drowsiness, impaired coordination)

pt teaching = need for concurrent blood work, do not abruptly stop meds, life long therapy

caution with antipsychotics and elderly pts due to increase risk for stroke

85
Q

medications for alcohol abuse/treatment

A

disulfiram and naltrexone

86
Q

disulfiram MOA

A

inhibit aldehyde dehydrogenase (accumulation of acetaldehyde); cause severe vomiting if taken with alcohol; always withdraw from alcohol first then treat with this drug

87
Q

naltrexone MOA

A

opiate antagonist that decreases craving for alcohol; given for maintenance drug after patient goes through withdrawals

88
Q

medications for nicotine abuse

A

varenicline (smoke for first 7 days then stop on 8th day; no go for public transport operators due to insomnia)

bupropion

89
Q

medication for opiate abuse

A

methadone- prevent withdrawal syndrome

buprenorphine- may use with or without naloxone

90
Q

examples of observed behaviors with abuse

A

preference in assignment , absenteeism, behavior on the job

91
Q

preference in assignment with alcohol abuse

A

often prefer less demanding areas and/or more independent role

92
Q

preference in assignment with drug abuse

A

often prefer high-volume drug use areas with lack of supervision

93
Q

absentee in alcohol abuse

A

frequent call-ins, tardiness, following scheduled days off

94
Q

absentee in drug abuse

A

workaholic, volunteer for extra shifts

95
Q

behavior on job with alcohol abuse

A

arrive late and leaves early; frequent breaks and trips to lounge, declines offer to join peers on breaks, inconsistent and erratic performance

96
Q

behavior on job with drug abuse

A

arrive early and stay later; frequent breaks and trips to lounge, declines offer to join peers on breaks, inconsistent and erratic performance