Anxiolytics Flashcards

1
Q

what are the types of anxiety disorders

A
  • generalized anxiety disorder
  • panic disorder
  • social anxiety disorder
  • other:
  • separation anxiety disorder
  • specific phobia
  • selective mutism
  • agoraphobia
  • substance/medication-induced anxiety disorder
  • anxiety disorder due to another medical consition
  • other specified anxiety disorder
  • unspecified anxiety disorder
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2
Q

what is the common link between MDD and anxiety disorders

A

5HT

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3
Q

what are the symptoms of generalized anxiety disorder

A
  • excessive anxiety or worry
  • muscle tension
  • restlessness
  • fatigue
  • impaired concentration
  • irritability
  • insomnia
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4
Q

what are the symptoms of panic disorder- recurrent attacks

A
  • shortness of breath
  • dizziness or faintness
  • palpitations
  • sweating
  • trembling or shaking
  • nausea
  • dizziness
  • paresthesias
  • hot flashes or chills
  • chest pain
  • feelings of choking
  • discomfort or fear
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5
Q

what are the symptoms of social anxiety disorders

A
  • fear or anxiety about social situations
  • concern regarding scrutiny from others
  • concern regarding humiliation embrrassment
  • fear of rejection
  • concern regarding offending others
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6
Q

what are the first line therapies for generalized anxiety disorder

A
  • SSRI and SNRI pregabalin
  • buspirone
  • BZD
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7
Q

what are the first line therapies for panic disorder

A

-SSRI and SNRI
- BZD

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8
Q

what are the first line therapies for social anxiety disorder

A
  • SSRI
  • BZD
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9
Q

BZD is for _____ use

A

short term

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10
Q

what are the side effects of SSRIs important to dentistry

A
  • increased risk for bleeding and bruising due to decreased platelet aggregation
  • bruxism
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11
Q

what are the drug interactions with SSRIs with opiod medications (codeine, hydrocodone, and oxycodone)

A
  • pharmacokinetic interaction
  • drugs that inhibit CYP450 2D6 prevent the metabolism of codeine; hydrocodone and oxycodone to an active medication
  • outcome: pain relieving effects are reduced
  • antidepressants: paroxetine and fluoxetine
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12
Q

what are the FDA approved uses for pregabalin and MOA

A
  • postherpetic neuralgia, neuropathic pain due to diabetic neuropathy and spinal cord injury, seizures, and fibromyalgia
  • considered first line agent in treatment for GAD (no FDA approval)
  • MOA: unknown
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13
Q

what are the side effects of pregabalin

A
  • dizziness, sedation, ataxia, blurred vision, and weight gain
  • no life threatening side effects
  • no oral side effects
  • safe in overdose
  • low risk for drug interactions
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14
Q

what are the uses for gabapentin and MOA

A
  • FDA uses: postherpetic neuralgia and seizures
  • used off label for anxiety both scheduled and prn
  • limited evidence for use in anxiety
  • MOA: unknown
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15
Q

what are the common side effects of gabapentin

A
  • dizziness, sedation and ataxia
  • no life threatening side effects
  • no oral side effects
  • safe in overdose
  • low risk for drug interactions
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16
Q

what is the MOA and use for buspirone (buspar)

A
  • MOA: 5HT1A partial agonist
  • uses: FDA approval for GAD (not recommended as first line therapy)
  • used as adjunctive therapy with an antidepressant for treatment refractory depression
17
Q

describe the safety, onset of action of buspirone

A
  • no abuse or withdrawal potential
  • safe in overdose situations
  • low risk for drug interactions
  • onset of action 4-6 weeks
18
Q

what are the side effects of buspirone

A
  • GI
  • sedation
  • insomnia
  • agitation
  • headache
  • weakness
  • dizziness
  • no serious side effects
  • no oral side effects
19
Q

what are the common uses on benzodiazepines in treatment of anxiety

A
  • panic attacks (acute treatment only- NOT panic disorder)
  • anxiety (short term tx only)
  • seizures
  • insomnia
  • muscle relaxant
  • acute alcohol withdrawal
  • acute mania
  • acute agitation
  • PRN before medical/dental procedure
20
Q

benzos work on what receptors

21
Q

what is the onset of action, duration of action and main use of midazolam (Versed)

A
  • rapid
  • ultrashort
  • anesthetic
22
Q

what is the onset of action, duration of action and main use of triazolam (Halcion)

A
  • rapid
  • ultrashort
  • hypnotic
23
Q

what is the onset of action, duration of action and main use of alprazolam (xanax)

A
  • rapid
  • short
  • anxiolytic
24
Q

how fast is ultra rapid

A

less than 15 mins

25
how fast is rapid onset
15 mins
26
what are the side effects of BZD
- common: - drowsiness - sedation - psychomotor impairment - blurred vision - ataxia - daytime sedation - impairment in memory and recall - less common: - disorientation - aggression - confusion - paradoxical excitation - no oral side effects
27
what are the characteristics of BZDs
- synergistic effect with other CNS depressants: alcohol, TCA, barbituates, pain medication (opioids, opiates) - CNS respiratory depression in overdose - risk for pharmacokinetic and pharmacodynamic drug interactions - tolerance develops to sedative/hypnotic effect - tolerance does not develop for other uses: anticonvulsant, anxiolytic, muscle relaxant
28
describe the abuse potential with BZDs
- all benzodiazepines have the potential for abuse - benzodiazepines with a quick onset of action are more likely to be abused (alprazolam and diazepam) - use with caution in patients with a history of substance abuse - use with extreme caution in combo with pain medications (opiods)
29
what are the uses for propranolol (inderal) and MOA
- FDA approved: HTN, angina pectoris, atria fibrillation, myocardial infarction, migraine prophylaxis, essential tremor, hypertrophic subaortic stenosis, pheochromocytoma - used off label for performance anxiety - MOA: nonselective beta adrenergic receptor blocking agent
30
what are the side effects for proranolol
- common: dizziness, weakness and fatigue - no life threatening side effects - no oral side effects - overdose- hypotension and bradycardia - high risk for drug interactions
31