Depression Flashcards

1
Q

Define stigmafree

A

we should treat patients without bias (or stigma)

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2
Q

Why is depression treatment so important?

A
  • common problem –> massive public health consequences
  • often undetected
  • CAN be treated
  • the generic meds we have are really effective and not expensive
  • we have the ability to greatly improve function and health in seniors with careful screening
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3
Q

In what patients are we most likely to see depression?

A

females; age of onset in 20s

its really common

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4
Q

Depression increases risk of:

A
  • DM
  • HTN
  • CVD
  • stroke morbidity/mortality
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5
Q

What is needed for a MINOR depression diagnosis?

A

Depressed mood and/or loss of interest or pleasure

AND

  • loss or change in appetite
  • significant wt gain
  • insomnia or hypersomnia
  • psychomotor agitation (anxious/restlessness) or retardation (slowing down of thoughts/ decr. in physical movement)
  • fatigue or loss of energy
  • feelings of worthlessness or excessive or inappropriate guilt
  • thoughts of death, suicide ideation with or without a specific plan, suicide attempt
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6
Q

What is required for a MAJOR depression diagnosis?

A

1+ major depressive episode
(it’s sx must be present every day for at least 2 weeks, be a change from baseline, and cause significant distress/impairment/functioning impairment)

AND

anhedonia (inability to feel pleasure) and/or depressed mood

AND

3 additional symptoms from DSM-V

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7
Q

What defines a major depressive episode?

A

1+ of these:

  • depressed mood most of the day, nearly every day (subjective report or observation made by others)
  • decr. interest/pleasure in all or most activities most of the day, almost every day (anhedonia)

others to make a total of 5:

  • significant wt gain or loss/ change in appetite
  • insomnia or hyperinsomnia
  • psychomotor agitation or retardation
  • fatigue or loss of energy
  • feelings of worthlessness or excessive/ inappropriate guilt
  • indecisiveness or diminished ability to think or concentrate
  • recurrent thoughts of death, suicidal ideation with or without a specific plan, suicide attempt

–> the sx must cause significant distress or impairment in social, occupational, or other important areas of functioning
(not due to a substance, a general medical condition, or bereavement)

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8
Q

What are the 9 diagnostic symptoms of MDD?

A

SIG E CAPS

  • sleep
  • interest
  • guilt
  • energy
  • concentration
  • appetite
  • psychomotor
  • suicide
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9
Q

What are some screening tools?

A
  • PHQ2
  • Ham-D (7+ points - normal)
  • Macarthur PHQ (<10 mild or minimal sx)
  • Geriatric Depression Scale (GDS)

–> should question the patient further if a + screen to indicate a more specific diagnostic criteria for one or more of the depressive disorders

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10
Q

What would a + PHQ-2 screen look like?

A

3+ score

over the past 2 weeks how often have you been bothered by any of the following problems?

  • little interest or pleasure in doing things
  • feeling down, depressed or hopeless
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11
Q

How is the GDS scoring broken down?

A
0-9 = normal
10-19 = mild depression
20 = severe
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12
Q

What is non-pharm tx for MDD?

A
  • psychotherapy (CBT or interpersonal psychotherapy (IPT))
  • electroconvulsive tx (ECT)
  • ECT + TMS (transmagnetic stimulation)
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13
Q

Which is more beneficial: psychotherapy or medication?

A

work about equally well!

psychotherapy is found to be useful in cognitive intact patients

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14
Q

How does CBT work?

A

help patients modify maladaptive cognitions, beliefs, assumptions, and behaviors that maintain depressive sx
(time limited: 10-12 sessions)

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15
Q

How does IPT work?

A

focus on goals related to relationships, role transitions, role conflicts, prolonged grief, and interpersonal deficits

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16
Q

How does ECT work?

A

anesthesia prevents muscle movements associated with tonic-clonic seizures

–> may be the ONLY effective tx for withdrawn SEVEREly depressed older pts (illness is severe, preventing oral intake); ECT may be more effective than medication in elderly in general

(time limited: 6-12 sessions over 2-5 wks)

SE:

  • anterograde/retrograde amnesia
  • post-ictal confusion (mental/physical exhaustion)
  • post-treatment muscle aches
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17
Q

SSRI MOA?

A

selectively inhibits reuptake of 5-HT at presynaptic neuronal membrane

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18
Q

SNRI MOA?

A

Inhibit reuptake of 5-HT and NE

weakly inhibit dopamine reuptake

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19
Q

MAOi MOA?

A

competitively inhibit monoamine oxidase

there are differences within class of reversibility and activity against MAOa and MAOb

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20
Q

serotonin modulators MOA?

A

selective inhibition of 5-HT reuptake, 5-HT antagonist

trazadone, trazadone ER

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21
Q

dopamine-NE inhibitor MOA?

A

inhibit dopamine reuptake with some effect on NE

bupropion

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22
Q

NE and specific 5-HT antidepressants MOA?

A

block presynaptic central a2-adrenergic autoreceptors
–> incr. neurotransmission of NE and 5-HT

block post synaptic 5-HT2 and 5-HT3 receptors

(mirtazapine)

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23
Q

TCADs MOA?

A

inhibit reuptake of NE and 5-HT into presynaptic terminals

amitriptyline, nortriptyline, imipramine, desipramine

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24
Q

SSRI + partial agonist 5-HT1A MOA?

A

5-HT reuptake inhibitor with partial agonist activity at 5-HT1A

(vilazodone)

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25
Q

SSRI + antagonist at 5-HT1, -HT3 MOA?

A

5-HT reuptake inhibitor with inhibition of 5-HT1 and 5-HT3

vortioxetine

26
Q

When would we want to use SSRI?

A
  • anxiety (start low dose)
  • adolescents [fluoxetine, sertraline, and escitalopram]

[sertraline]
- CV disease

[fluoxetine]

  • psychomotor slowing
  • overweight/obese

[paroxetine]

  • underweight
  • insomnia
27
Q

Caution use with SSRI:

A
  • QTc prolongation or Torsades risk
  • pregnancy

[paroxetine] overweight/obese; elderly
[fluoxetine] agitation or insomnia

(QuinTin)

28
Q

When would we want to use SNRIs?

A
  • anxiety
  • chronic pain from fibromyalgia/neuropathy

[duloxetine]
- psychomotor slowing

29
Q

Caution use with SNRIs:

A

HTN
agitation
insomnia

(Hati)

30
Q

Indications for mirtazapine

A
  • agitation/insomnia
  • sexual dysfunction concern
  • underweight

u said

31
Q

Mirtazapine caution:

A
  • overweight/obese patients
  • hyperlipidemia

Alistair OH

32
Q

Indications for bupropion

A
  • sexual dysfunction concern
  • smokers
  • psychomotor slowing/fatigue
  • overweight/obese patients

SAM

33
Q

Bupropion caution:

A
  • seizure disorders
  • HTN
  • anxiety/insomnia

(SHAI)

34
Q

Indications for Vilazodone or Vortioxetine

A
  • sexual dysfunction concern
  • overweight/obese pts
  • cognitive dysfunction

Victor

35
Q

Vilazodone or Vorioxetine caution:

A

nausea

Nate

36
Q

What side effect could women on SSRI/SNRI experience?

women on TCAD?

A

SSRI/SNRI: problems with arousal

TCAD: problems with desire, lubrication, orgasm

37
Q

What side effect could men on SSRI/SNRI experience?

A

ED, desire, and orgasm

38
Q

Which agents are least likely to cause sexual side effects?

A
  • mirtazapine
  • bupropion
  • vortiolexetine
  • vilazodone
  • duloxetine
  • fluovoxamine
  • levomilnacipran (this is a 5-HT-NE reuptake inhibitor)
39
Q

What type of agent has a higher risk for antidepressant withdrawal syndrome?

A

short acting

(paroxetine, desvenlafaxine, venlafaxine)

–> fluoxetine has the lowest risk

40
Q

Why shouldn’t we prescribe concomitant tx of sympathomimetic amines + MAOis?

A

hypertensive crisis

  • incr. BP
  • stiff/sore neck
  • N/V
  • sweating
41
Q

Why shouldn’t we combine SSRI/SNRI + MAOis/multiple serotonergic drugs?

A

serotonin syndrome

the multiple serotonergic drugs includes cocaine!

42
Q

What are common sx of serotonin syndrome?

A
  • confusion
  • restlessness
  • fever
  • sweating
  • hyperreflexia
  • tachycardia
  • hyperthermia
  • diarrhea
  • shivering
43
Q

Of all of the depression medication classes discussed which should we avoid in the elderly?

A

TCADs!!!

44
Q

How do we switch from one SSRI (except fluoxetine) to another?

A
  1. stop SSRI & start new SSRI at low dose (may taper off the first if a high dose)
  2. stop SSRI & start new agent within the same dose range
  3. Cross taper: taper and stop SSRI before starting new agent at low dose)
45
Q

What are some pharmacodynamic SSRI/SNRI drug interactions?

A
  • additive sedation
  • additive anti-cholinergic effects
  • increased seizure risk
  • 5-HT syndrome - MAOis & linezolid
  • Tramadol

(triptans are ok with SSRIs)

46
Q

What are pharmacokinetic SSRI/SNRI drug interactions?

A
  • CYP2C
  • CYP3A4

[fluoxetine],[paroxetine]: CYP2D6

47
Q

What when combined with MAOIs would result in hypertensive crisis?

A
  • pseudoephedrine
  • phenylephrine
  • ephedrine
  • phenylpropanolamine
  • aged cheese & wine (tyramine containing foods)
48
Q

What when combined with MAOIs would result in serotonin syndrome?

A
  • SSRI
  • TCADs
  • methadone
  • tramadol
  • meperidine
  • DM
  • St. Johns wort :/
  • cyclobenzaprine
  • mirtazapine
49
Q

What should we check before we dive into treatment decisions?

A
  • suicidality/intent to harm others
  • psychosis
  • minimal verbal interaction
  • severely restricted food intake
  • manic sx (…different tx needed!)
50
Q

When do we want to reassess?

A

4-6 wks or sooner for tolerance and efficacy

  • watch for suicide risk & med adherence!
51
Q

General treatment choices (assume progression to next step due to no remission)

A
  1. SSRI, bupropion, SNRI, or mirtazapine (reassess 4-6 wks)
  2. maximize dose of 1st agent
  3. Either:
    - combine SSRI + bupropion
    - augment with buspirone
    - switch to another 1st line agent
  4. Cycle through the different choices from step 3
  5. if all fail, either:
    - augment with triiodothyronine
    - TCA (2nd line drug) :(
    - combine venlafaxine + mirtazapine
    - refer to psychiatrist
52
Q

When should we use a second generation antipsychotic (SGA)?

A
  • depression with psychotic features
  • augmentation strategy with SSRI/SNRI
  • resistance to tx after trials with 1st and 2nd line agents
  • equivocal efficacy
  • consider referral to psychiatry
53
Q

When would we d/c tx?

A

decr. risk of polypharmacy and drug interactions after a minimum of 6 months (usually 6-12 mo)

(some patients need long-term tx, and that’s okay –> keep them on)

54
Q

Why should SSRIs be tapered off?

A

we want to avoid “discontinuation syndrome”

  • flu-like symptoms
  • insomnia
  • nausea
  • imbalance
  • sensory disturbances
  • hyperarousal

(these sx are usually mild, lasting 1-2 weeks. they will quickly stop if med re-instituted)

55
Q

Which agents are best in pregnancy?

How do we feel about breast feeding and treating depression?

A

fluoxetine, citalopram, and TCAD have the best hx of safety data

benefits > risks
(let’s treat them!)

56
Q

Geriatric Population key points:

A
  • under recognized and under treated
  • generally more sensitive to meds, so be careful
  • SSRI > TCADs
  • depression often leads to suicide in older adults (men!)
57
Q

Pediatric population key points:

A

used if:

  • severe or psychotic depression
  • failed psychotherapy
  • chronic/recurrent depression

SSRIs (initial choice)

CAUTION: incr. risk of suicidality in children & young adults

58
Q

Indications for Esketamine Nasal Spray

A
  • post-partum depression

- treatment resistant depression

59
Q

What are the 6 possible specifiers for depressive disorder?

A

with:

  • anxious distress
  • mixed features
  • melancholic features
  • atypical features
  • psychotic features
  • seasonal pattern

(these specifiers are used when characteristics of depressive disorders are not fully met, but distress or impairment is still seen)

60
Q

Antidepressant tx side effects (often not thought about)

A
  • hyponatremia (serum Na < 125 mEq/L)
  • bleeding
  • incr. risk of falls & fractures
  • inr. QTc intervals
61
Q

Key points regarding dosing:

A
  • start low, go slow, but don’t stop (“stall”) before at a therapeutic dose
  • give it time to take effect
  • when d/c taper to avoid withdrawal sx