Anxiety- Krysiak

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51 Terms

1
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What is anxiety?

  • just recognize

an emotional state caused by the perception of real or perceived danger that threatens the security of an individual—> can produce uncomfy feelings

<p>an emotional state caused by the perception of real or perceived danger that threatens the security of an individual—&gt; can produce uncomfy feelings</p>
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According to DSM-V what are the 5 classifications of anxiety?

  • generalized anxiety disorder (GAD)

  • panic disorder (± agoraphobia)

  • social anxiety disorder (SAD)

  • posttraumatic stress disorder (PTSD)

  • obsessive compulsive disorder (OCD)

<ul><li><p>generalized anxiety disorder (GAD)</p></li><li><p>panic disorder (± agoraphobia)</p></li><li><p>social anxiety disorder (SAD)</p></li><li><p>posttraumatic stress disorder (PTSD)</p></li><li><p>obsessive compulsive disorder (OCD)</p></li></ul><p></p>
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What are a characteristic features of ALL CLASSES of anxiety?

anxiety and avoidance behavior—> fear and worry

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Diagnosis of Generalized Anxiety Disorder (GAD):

  • persistent symptoms for most days for at least 6m

  • the anxiety is accompanied by at least 3 psychologic or physiologic symptoms:

    • restlessness or feeling on edge

    • fatigue

    • difficulty concentrating or mind going blank

    • irritability

    • muscle tension

    • sleep disturbances

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Symptoms of GAD:

knowt flashcard image

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Noradrenergic Model of Anxiety Pathophysiology:

Hypersensitivity of the autonomic nervous system—> where the locus ceruleus (LC) serves as an alarm system—> releases norepinephrine (NE) and stimulates sympathetic and parasympathetic nervous systems

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GABA Receptor Model of Anxiety Pathophysiology:

GABA, the major inhibitory neurotransmitter, has a strong regulatory or inhibitory effect on the 5-HT, NE, and DA systems. Benzodiazepines enhance the inhibitory effects of GABA.

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Serotonin Model of Anxiety Pathophysiology (lack evidence):

  • 5HT normally inhibitory

  • dysfunction at presynaptic auto receptors—> serotonin reuptake transporter site or postsynaptic receptors may play a role in anxiety

9
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GAD treatment is a combination of what 2 therapies?

psychotherapy + drug therapy

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Nonpharm for GAD?

  • psychoeducation

  • counseling/stress management

  • psychotherapy

    • CBT most effective

  • mediation

  • exercise

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WHAT ARE THE 1st line, 2nd line, and alternative drugs for GAD?

  • 1st line:

    • duloxetine

    • escitalopram

    • paroxetine

    • sertraline

    • venlafaxine XR

  • 2nd line:

    • benzos

    • buspirone

    • imipramine

    • pregabalin

  • Alternative:

    • Hydroxyzine

    • Quetiapine

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What is the adequate trial period for antianxiety response? Following an adequate trial and good response, treatment should be continued for at least how long?

  • adequate trial: 4-6w

  • following adequate trial, good response—> continue tx for 1 year

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If benzodiazepines are the most frequently prescribed medications for acute treatment of anxiety, why are they not 1st line tx for GAD?

  • good for acute anxiety, however not recommended for long-term use

  • benzos are also not for depressive symptoms and should not be used with substance abuse disorders

  • antidepressants however—> can be used for acute and chronic anxiety, as well as for depressive symptoms (duh the name)

  • overall: GAD is mostly a long term disorder hence why antidepressants are 1st line

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PRACTICE:

A 34 YO female is looking to start treatment for her ACUTE anxiety. She also has a history of depression. Would Duloxetine or Lorazepam be a better option for managing her anxiety? Why?

Duloxetine—> Why? Duloxetine is 1st line for acute anxiety and anxiety with depression but also Lorazepam is NOT recommended for depressive symptoms and may contribute to depression long term

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REVIEW:

MOA and names of benzodiazepines:

  • Potentiation of the inhibitory activity of GABA by binding to GABAA receptors

  • names:

    • Alprazolam

    • Chlordiazepoxide

    • Clonazepam

    • Clorazepate

    • Diazepam

    • Lorazepam

    • Oxazepam

16
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Which benzos are lipophilic? result?

Which are NOT lipophilic? result?

  • diazepam and clorazepate= rapidly absorbed and distributed

  • lorazepam and oxazepam= slower absorption and onset

17
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Benzos undergo what 2 primary metabolic processes?

hepatic oxidation (CYP3A4) and glucuronide conjugation

18
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Most benzos are converted into the metabolize DMDZ. What is the result of this conversion?

a. increases absorption

b. lengthens half-life

c. increased side effect risk

d. enhanced sedation

b.

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Benzodiazepine ADRs:

  • biggest complication: abuse, dependence, tolerance

  • CNS: drowsy, sedation, psychomotor impairment, disorientation, depression, confusion, irritability, impairment of memory and recall

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Benzos have a risk of tolerance to some side effects but not others.

What side effects does tolerance develop in?

What side effects do NOT develop a tolerance?

  • tolerance: sedative, muscle relaxant, and anticonvulsant effects

  • no tolerance: anxiolytic or antipanic effects

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WHAT IS THE RECOMMENDED DURATION FOR BENZOS?

only 2-4 weeks for acute anxiety

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Why is Buspirone (Buspar) considered second-line?

  • inconsistent efficacy for long term use

  • delayed onset

  • lack of efficacy for concurrent depressive or anxiety disorders

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Unlike Benzos, Buspirone is effective for what symptoms of anxiety?

Buspirone effective for PSYCHIC symptoms of anxiety (Worry, rumination, apprehension)

Helpful tip: I think of it like this— buspirone treats the "mind" of anxiety (thoughts), while benzos treat the "body" (physical symptoms)

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Answer the following about Buspirone:

  • dosing of Buspirone is __-__ times a day. Affect on adherence?

  • drug interactions?

  • when will we see a therapeutic benefit?

  • 2-3 times a day—> negatively affects adherence

  • D/I: CYP3A4 INHIBITORS INCREASE LEVELS, MAOI

    • ex: rifampin can lower levels of buspar x10

    • with an MAOI, buspar can cause hypertensive crisis

  • full benefit might not be seen for 4-6 weeks

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For monitoring outcomes of GAD:

  • initially patients should be monitored every __ weeks

  • initial pharm therapy with an _____ will not lead to remission

  • following an adequate trial/good response, tx should be continued for at least __ year(s)

  • initially patients should be monitored every 2 weeks

  • initial pharm therapy with an SSRI will not lead to remission

  • following an adequate trial/good response, tx should be continued for at least 1 year(s)

26
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What is Panic Disorder (PD)?

  • Begins as unexpected panic attacks involving intense, terrifying fear of life-threatening danger

  • followed by persistent concern about future attacks, worry about the consequences, or behavioral changes related to the attacks

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About 70% of pts. with panic disorder develop Agoraphobia.

What is Agoraphobia?

  • anxiety about being in places or situations where escape might be difficult or where help might not be available in the event of a panic attack

  • as a result—> pts. may avoid specific situations in which they fear a panic attack may occur

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Diagnosis of Panic Disorder (PD):

  • a discrete period of intense fear or discomfort in which ≥4 of the following symptoms develop and reach a peak within 10 minutes:

    • Palpitations/ increased HR

    • sweating

    • trembling/shaking

    • shortness of breath/ sensations

    • feeling of choking

    • chest pain/discomfort

    • nausea

    • dizziness/faint

    • derealization/depersonalization

    • fear of losing control

    • fear of dying

    • paresthesias

    • chills/hot flushes.

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PD symptoms usually lasts between ___-___ with peak intensity of symptoms within the first 10 minutes.

20-30

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PD treatment uses what kinds of therapies?

single or combo pharm therapy + psychotherapy OR psychotherapy followed by pharmacotherapy

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Nonpharm for PD?

  • SAME AS GAD!!!!!!!!!!!

  • psychoeducation

  • counseling/stress management

  • psychotherapy

    • CBT most effective

  • mediation

  • exercise

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WHAT ARE THE 1st LINE, 2nd LINE, and LAST LINE DRUGS FOR PD?

  • 1st line

    • SSRIs (fluoxetine, sertraline, paroxetine approved)

    • SNRIs (Venlafaxine XR approved)

  • 2nd line

    • Benzos (Clonazepam and Alprazolam approved)

    • TCAs (Clomipramine, imipramine not approved)

  • LAST LINE

    • MAOIs

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At the start of therapy for PD, SSRIs can cause _________ syndrome.

activation syndrome (increased anxiety, jitters, shakes, agitation)

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Phases of therapy for PD:

  • acute phase is __-__ months

  • alter therapy if no response after ___-___ weeks at max dose

  • pts. who respond to pharm therapy should continue at full dose for a least ___ year (s)

  • acute phase is 1-3 months

  • alter therapy if no response after 6-8 weeks at max dose

  • pts. who respond to pharm therapy should continue at full dose for a least 1 year

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What is Social Anxiety Disorder (SAD):

  • characterized by intense, irrational, and persistent fear of being negativity evaluated or scrutinized in at least one social or performance situation

  • exposure to feared circumstance usually provokes a panic attack

  • the person recognizes that the fear is excessive/unreasonable

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Social Anxiety Disorder (SAD) and Panic Disorder (PD) are difficult to differentiate sometimes. What is the difference between these two?

  • the RATIONALE behind the fear

    • fear of anxiety symptoms= PD

    • fear or embarrassment from social interaction= SAD

37
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How does SAD present?

  • fear of being ____________-

  • ex’s of feared situations?

  • physical symptoms?

  • what are the 2 types?

knowt flashcard image

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What types of treatments are utilized in SAD?

CBT + pharmacotherapy

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WHAT IS THE 1st LINE, 2nd LINE, and ALTERNATIVES for SAD?

  • 1st LINE

    • SSRIs (Paroxetine and Sertraline approved, Fluvoxamine not approved)

    • Venlafaxine XR

  • 2nd LINE

    • Benzos (Clonazepam, Citalopram)

  • Alternatives

    • gabapentin

    • b-blockers (propranolol, atenolol)

40
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During acute phase of tx for SAD, the patient should be seen on a _________ basis while drug dosage is being titrated.

a. weekly

b. biweekly

c. monthly

d. bimonthly

a.

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What is Post-Traumatic Stress Disorder (PTSD)?

Exposure to a traumatic event involving threatened death, serious injury, or harm, with a response of intense fear, helplessness, or horror.

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How is PTSD diagnosed?

  • sorry in advance, this is so long :(

  • A. The person has been exposed to a traumatic event in which both of the following have been present:

    • The person experienced, witnessed, or was confronted with an event that involved actual or threatened death or serious injury, or a threat to the physical integrity of self or others

    • The person’s response involved intense fear, helplessness or horror

  • B. The traumatic event is persistently re-experienced in ≥ 1 of the following ways:

    • Recurrent and intrusive images, thoughts, perceptions or distressing dreams of the event

    • Acting or feeling as if the traumatic event were recurring

    • Intense psychological distress at exposure to internal or external cues that symbolize or resemble an aspect of the traumatic event

    • Physiologic reactivity upon exposure to internal or external cues that symbolize or resemble an aspect of the traumatic event

  • C. Persistent avoidance of stimuli associated with the trauma and numbing of general responsiveness as indicated by ≥ 3 of the following:

    • Efforts to avoid thoughts, feelings, or conversations associated with the trauma

    • Efforts to avoid activities, places, or people that arose recollections of the trauma

    • Inability to recall an important aspect of trauma

    • Markedly diminished interest or participation in significant activities

    • Feeling of detachment or estrangement from others

    • Restricted range of affect (e.g. unable to have loving feelings)

    • Sense of foreshortened future (e.g. does not expect to have a career)

  • D. Persistent symptoms of increased arousal (not present before the trauma) indicated by at ≥ 2 of the following: difficulty falling asleep, irritability or outbursts of anger, difficulty concentrating, hypervigilance, exaggerated startle response

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When is pharmacotherapy utilized for PTSD?

if symptoms persist for 3-4 weeks and is causing impairment—> pharmacotherapy ± psychotherapy

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Nonpharm for PTSD?

  • psychotherapy—> CBT (extremely beneficial)

  • exposure therapy—> involves confronting trauma cues, best for pts. with mild symptoms or refuse meds

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WHAT IS THE 1st LINE, 2nd LINE, and ALTERNATIVES for PTSD?

  • 1st LINE

    • SSRIs (Sertraline and paroxetine FDA approved)

    • Venlafaxine XR

  • 2nd LINE

    • TCAs

  • Alternatives

    • Mirtazapine

    • Nefazodone

    • Phenelzine

    • Anticonvulsants

    • atypical antipsychotics (risperidone, olanzapine, quetiapine)

    • adrenergic inhibitors (prazosin, clonidine)

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WHAT CLASS OF MEDICATIONS SHOULD NOT BE USED IN PTSD?

BENZOS

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To be diagnosed with OCD a person has to have what?

obsessions, compulsions, or both

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Define obsessions:

Define compulsions:

(recognize the differences between them)

  • obsession: recurrent persistent ideas, thoughts, impulses or images that are experienced as intrusive and inappropriate and produces marked anxiety

    • the person attempts to ignore/suppress the thoughts, impulses, images with something else (like a compulsion)

  • compulsion: repetitive behaviors or mental acts that the person feels driven to perform in response to an obsession

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In OCD, the obsessions or compulsions take more than ___ hour(s) a day.

1

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What should be offered to every patient with OCD?

CBT —> it is the TREATMENT OF CHOICE in adolescents and adults with mild OCD

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Pharmacotherapy for OCD

Fluoxetine, Fluvoxamine, Paroxetine, Sertraline, Clomipramine