General Psychiatry Depression Flashcards
Two Types of Depressive Disorders
1) Major Depressive Disorder
2) Dysthymic Disorder
Bipolar Disorders
1) Bipolar 1
2) Bipolar 2
3) Cyclothymic Disorder
Clinical Features of MDD
- decrease in interest in usual activities
- Decreased ability to think/concentrate
- Recurrent thoughts of suicide
- appetite changes
- sleep disturbances
- changes in energy levels
- feelings of guilt, helplessness, or worthlessness
Psychotherapy
- interpersonal psychotherapy and cognitive-behavioral therapy
- good for preventing relapse
Pharmacotherapy
may lead to a more rapid response, but increased risk of relapse
Selection of Rx
Rx interaction, family hx
Onset
4-6 weeks
Adequate trial
give enough time for optimal dosing
Response and Remission
defined as 50% reduction
Efficacy
-drugs are shown to do better in clinical trials
-Clinical trials have not shown that mixed action drugs work better than single action drugs
But, clinicians are seeing results in patients by using mixed action drugs
Drug interactions
CYP2D6 and CYP3A4
CYP 450 Enzyme 2D6 interaction antidepresant Med (2)
Fluoxetine, paraoxitine
5 Main Classes of anti-depressant Medications
1) TCAs
2) Monoamine Oxidase Inhibitors
3) Selective Serotonin Reuptake Inhibitors
4) Selective Serotonin Norepinephrine reuptake Inhibitors
5) Miscellaneous
TCAs: history, MOA
-first ones
-severe toxicity
MOA: block the reuptake of serotonin (5-HT) and norepinephrine (NE).
-have receptor effects including: alpha adrenergic blocking effects, antihistamine effects, anticholinergic effects, and effects on cardiac conduction
TCAs that cause high degree of Orthostatic Hypotension and Cariotoxicity
1) Imipramine
2) Amitriptyline
4 TCAs
1) Imipramine
2) Amitriptyline
3) Desipramine
4) Nortriptyline
What are the two major risks of TCAs
orthostatic hypotension- fall risk pts.
- cardiac pts.
- seizure pts.
How should TCA pts. have their dose if you want them taken off them
gradually tappered off
Monoamine Oxidase Inhibitors Rxs
- phenelzine (Nardel)
- Isocarboxazid (marplan)
- tranlcypromine (Parnate)
- selegline [parkinsons] (Eldepryl)
What foods and drugs must MAOI pts. avoid and why?
They must avoid foods hihg in tyramine- aged cheese, cause potential hypertensive crisis
-avoid antihistamines
How do you switch a patient taking MAOI to another antidepressant?
-wait 2 weeks after antidepressant is discontinued before starting MAOI- it is irreversibly binding so you need to wait to make new receptors
Exception: fluoxetine should be removed for 5-6 week
patch form of MAO Selegiline is called
Emsam
SSRI Rx names
Fluoxetine, sertraline, paroxetine, citalopram, and escitalopram
SSRI MOA
selectively inhibit the reuptake of 5-HT into the presynaptic neuron
Adverse effects of SSRIs
insomnia, reslessness, GI, agitation, anxiety, panic
Drug types that SSRIs interact with
MAOIs, dextromethorphan, meperidine
Serotonin Syndrome
careful with SSRIS
-as confusion, hypomania, restlessness, myoclonus, hyperreflexia, diaphoresis, shivering, tremor, diarrhea, and incoordination.
Treatment for Serotonin Syndrome
Discontinue offending agent, supportive measures
Is there a difference in efficacy among SSRIs?
No. But patients who don’t respond well to one may respond better to another
SSRI withdrawl syndrome
-make sure to tapper them
Escitalopram
-is the active ingredient in citalopram, only need hald as much escitalopram
SNRI Rxs
Venlafaxine, Desvenlafaxine, Duloxetine
MOA of SNRI
balanced NE and 5HT reuptake inhibitor
-at low doses 5HT effect is more prominant
Duloxetine (Cymbalta)
SNRI
- also indicated for for diabetic peripheral neuropathy
- CYP2D6 interactions
- liver toxicity- monitor BP
What happens as you increase SNRI dose?
NE becomes more pronounced, increased BP is likely
For severly depressed pts. is venlafaxine more effective than SSRIs?
Yes