Week 9 - Anxiety Disorders Flashcards

(27 cards)

1
Q

When does anxiety become a disorder?

A

When feelings of tension and anxiety persist for most days for 6 months or more

There is not a proportional threat or stressor

Excessive fear and anxiety

Behavioural disturbances

Physical symptoms

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2
Q

What are the different types of anxiety disorders?

A

Generalised anxiety disorder

Panic disorder

Social anxiety disorder

Specific phobia

Separation anxiety disorder

Selective mutism

Agoraphobia

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3
Q

What are some treatments for anxiety disorders?

A

Psychotherapy
CBT
Medications
Healthy lifestyle

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4
Q

What are some medications for anxiety disorders?

A

Anti-depressants (SSRI and SNRI)

Benzodiazepines

Beta-blockers

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5
Q

What are some risks associated with anxiety?

A

Higher risk of depression, alcohol or other drug dependence

High risk of co-morbidity with other anxiety disorders

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6
Q

What neurotransmitter systems are targeted by anxiety drug treatments?

A

Serotonin

Noradrenaline

GABA

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7
Q

What are the disadvantages of benzodiazepines?

A

Withdrawal syndrome is frequently mistaken by patients as indicating that the anxiety for which the drug was originally started has returned

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8
Q

How do benzodiazepines assist with anxiety disorders?

A

Reduces somatic and psychological symptoms of anxiety in panic disorder, generalised anxiety disorder and for high potency benzodiazepines, social anxiety disorder

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9
Q

Why are barbiturates and benzodiazepines commonly mistaken for one another?

A

They are both in the same drug classification

They act similarly when it comes to how they affect the human body

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10
Q

What is the composition of barbituates?

A

Varies as it is an umbrella term for sedative-hypnotics that affect the CNS

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11
Q

What are the forms of barbituates?

A

Overwhelmingly were and are capsules or pills

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12
Q

What are the effects of barbiturates?

A

Sedative

Anxiety reduction

Hypnotic

Anti-conlulsant

Anesthetic

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13
Q

What are the disadvantages of barbiturates?

A

Highly addictive

Extremely dangerous if mismanaged

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14
Q

How is physiological and psychological dependence different for barbiturates and benzodiazepines?

A

Barbs:
High physiological and psychological dependence

Benzos:
Less physiological and psychological dependence

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15
Q

Can you use both barbiturates and benzodiazepines long term?

A

No

Barbs:
Long term use avoided due to toxicity

Benzo:
Long term use relatively safe

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16
Q

How does sleep differ for those taking barbiturates and benzodiazepines?

A

Barbs:
Sleep induced by it causes hangover effect after waking up

Benzo:
Sleep induced by it is just like natural sleep and is refreshing to wake up

17
Q

How is the GABA CI channel affected by barbiturates and benzodiazepines?

A

Barbs:
Increase duration of GABA CI channel opening

Benzo:
Increase frequency of GABA CI channel opening

18
Q

How does respiratory depression differ for barbiturates and benzodiazepines?

A

Barbs:
High respiratory depression

Benzo:
Manageable respiratory depression

19
Q

How do beta blockers treat anxiety?

A

manages physical symptoms

20
Q

Is there evidence of a dose-response relationship between anti-depressants and anxiety?

A

Little evidence

Many patients will respond to standard doses

21
Q

Why should clinicians avoid rapid dose escalation for patients with anxiety?

A

Anxiety is generally slower to respond to treatment than depression

22
Q

How long does it take for SSRIs and SNRIs to have an anxiolytic effect?

23
Q

How long does buspirone take to have anxiolytic effects?

24
Q

How does buspirone interact with the presynaptic and post synaptic receptors?

A

Buspirone is a full agnost at presynaptic 5HT1A receptors

Buspirone is a partial agonist at postsynaptic 5HT1A receptors

25
What are the serotonin pathways for SSRs and SNRIs?
Distribution of serotonin and raphe nuclei through context and into the cerebellum
26
What is the fear center model?
Threat > Sensory system > Fear circuit > fear responses (Defensive behaviour, physiological responses)
27
What is the two-system model?
Threat > sensory system cognitive circuit > fear ((Defensive survival circuit)) > Defensive responses