Psychotherapeutic drugs ex 4 Flashcards

1
Q

positive symptoms

A

hallucinations
delusions
agitation
disordered speech
bizarre beahviors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

negative symptoms

A

social withdrawal
poor self-care
lack of motivation
poverty of speech
blunted affect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

cognitive symptoms

A

disordered thinking
lack of focus
learning disability
memory problems

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

first gen antipsychotics MOA

A

block several receptors in the CNS - dopamine, acetylcholine, histamine, norepinephrine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

first gen antipsychotics take how long?

A

2-4 weeks, several months for full effect
inhibits positive symptoms best

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

first gen antipsychotics classified by?

A

potency; low,med,high
contributes to severity of adverse effects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Acute Dystonia

A

adverse effect of FGA
occurs hours to days, spasms of tongue, face, neck, back muscles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Parkinsonism

A

occurs within 1 month looks like parkinson’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Akthisia

A

occurs within 2 months, pacing, restless, agitated, squirming

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Tardive Dyskinesia

A

occurs within months to years
involuntary twisting, movements of tongue and face, progresses to difficulty speaking swallowing down to body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Other FGA adverse effects

A

neuroleptic malignant syndrome: lead pipe, muscle rigidity, sudden very high fever, labile BP
anticholinergic effect
O hypotension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

FGA interactions

A

anticholinergic drugs
CNS depressants
Levodopa and direct dopamine receptro agonists

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Second Generation Antipsychotics (SGAs) MOA

A

block dopamine and serotonin receptors in CNS
takes 2-4 weeks, several months for full efect
$$$

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

SGA adverse effects

A

Metabolic effects: weight gain, diabetes, HDL
Neuroleptic Malignant syndrome
myocarditis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Goals of Therapy

A

suppress acute episode, prevent exacerbations, promote high quality of life and function

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

shared properties of antidepressants

A

initial response 1-3 weeks max 12 weeks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

4 antidepressants and protoype

A

SSRIS: fluoxetine
TCA: Imipramine
MAOIs: Phenelzine
Atypical: Buproprion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Selective Serotonin Reuptake Inhibitor (SSRIs) fluoxetine MOA

A

Prevent reuptake of serotonin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

(SSRIs) fluoxetine pharmacokinetics

A

PO 94% protein bound 9 day half life

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

(SSRIs) fluoxetine adverse effects

A

N/V
sexual dysfunction
weight gain
withdrawal
serotonin syndrom

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

(SSRIs) fluoxetine interactions

A

MAOIs - drugs that increase serotonin activation
TCAs and lithium
Antiplatelete and anticoagulants

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

(SSRIs) fluoxetine nursing considerations

A

dont stop abruptly,
suicide risk
serotonin syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

serotonin syndrome

A

altered mental status - agitation, confusion, disorientation
increases SNS activity - sweating, termoy, fever, incoordination

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Tricyclic Antidepressants (TCAs): amitriptyline (Elavil) MOA

A

prevent reuptake of NE and or seratonin
used for depression, insomnia, and pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
(TCAs): amitriptyline (Elavil) adverse effects
O hypoTN sedation anticholinergic effect sweating seizures hypomania
26
(TCAs): amitriptyline (Elavil) interactions
MAOIs (sever HTN) anticholinergics CNS depressants
27
(TCAs): amitriptyline (Elavil) nursing considerations
monitor BP night time dosing monitor for adverse side effects
28
MonoAmine Oxidase inhibitors (MAOIs) phenelzine MOA
irreversibly inhibits MAO and allows more uptake of NE and serotonin used for depression and OCD as last choice
29
(MAOIs) phenelzine adverse effects
CNS stimulation O HypotTN HTN crisis from dietary tyramine
30
atypical antidepressants: bupropion MOA
prevents reuptake of NE and Dopamine
31
atypical antidepressants: bupropion adverse effects
seizures, CNS stimulation
32
atypical antidepressants: bupropion benefits
weight loss increased libido
33
atypical antidepressants: bupropion interactions
some SSRIs MAOIs
34
mood stabilizer
lithium
35
lithium MOA
unclear
36
lithium pharmacokinetics
short half life, affected by Na levels
37
lithium toxicity
>1.5
38
lithium interactions
thiazide loop diuretics NSAIDS anticholinergics
39
lithium nursing consderations
give with food monitor ther range 0.6-1.0
40
sedatives and hypnotics examples
benzodiazepines, benzodiazepine like drugs, barbiturates
41
sedatives and hypnotics cause/use
some levels of CNS depression main use it control of anxiety - anxiolytics for anxiety - hypnotics for insomnia
42
benzodiazepines MOA
potentiate effects of GABA. inhibitory neurotransmitter
43
benzodiazepines uses
anxiety insomnia, muscle spasms, seizures, ETOH withdrawal, anesthesia induction
44
benzodiazepines pharmacokinetics
PO,IM, and IV well absorbed highly lipid soluble (crosses BBB) ' metabolized by liver
45
benzodiazepines expected/adverse effects
CNS depression : reduce anxiety, promote, sleep, muscle relaxation Cardiac: PO no effect, IV hypotension --> Cardiac arrest Respiratory: mild
46
benzodiazepines interactions
CNS depressants
47
benzodiazepines tolerance/dependance
cross tolerance for those who have tolerance to barbiturates, alcohol, and opioid potential for abuse withdrawal likely in long term use
48
benzodiazepines nursing considerations
fall risk BP residual sedation (no driving)' teratogenic dont mix with other CNS depressants
49
benzodiazepines acute toxicity rare in
oral overdose drowsiness, lethargy, confusion
50
benzodiazepines acute toxicity common in
IV overdose profound hypotension, cardiac and resp arrest life threatening!
51
antidote for benzodiazepines acute toxicity is
flumazenil (Romazicon) rapid IV over 15 seconds short T1/2 ~ frequent dosing reverses sedation, but not resp depression may cause seizures
52
common benzodiazepines
alprazolam (Xanax) clonazepam (Klonopin) Diazepam (Valium) Lorazepam (Ativan)
53
benzodiazepines-like drugs: zolpidem MOA
potentiates effects of GABA, an inhibitory neurotransmitter
54
benzodiazepines-like drugs: zolpidem use
insomnia (not anxiety)
55
benzodiazepines-like drugs: zolpidem adverse effects
daytime drowsiness dizziness sleep related behaviors (sleep walking/driving) no resp depression, but don't combine with CNS depressants long term use --> tolerance and dependence
56
Barbiturates: phenobarbital MOA
enhances and mimics action of GABA
57
Barbiturates: phenobarbital uses
seizure control and anesthesia (no longer used for insomnia)
58
Barbiturates: phenobarbital expected/adverse effects`
CNS depression: sedation --> anesthesia Cardiac: hypotension & bradycardia --> severe hypotension/arrest CYP P450 enzymes (inducer) tolerance/dependence teratogenic
59
Barbiturates phenobarbital toxicity s/sx
respiratory depression, coma, pinpoint pupils, hypotension, hypothermia no specific antidote
60
What is used to treat generalized anxiety disorder
SRIs SSRIs SNRis benzodiazepines (not first line) anxiolytic drug: Buspirone
61
anxiolytic:
buspirone
62
buspirone MOA
unclear bind to serotonin and some dopamine receptors
63
benefits of buspirone
no abuse potential no cross dependence with benzos therapeutic effect takes 1 week not a CNS depressant, just as effective
64
buspirone uses
anxiety control
65
buspirone pharmacokinetics
food delays absorption
66
adverse effects of buspirone
nausea dizziness sedation for some, excitement for others
67
buspirone interactions
grapefruit juice erythromycin ketoconazole