Title: Antidepressants
1Antidepressants
- Chris Pelic M.D.
- Associate Dean for Students
- Medical University of South Carolina
2Objectives
- Learn the monamine theory of depression
- Understand how the various antidepressants work
(MAOIs, TCAs, SSRIs, SNRIs, etc) - Learn common side effects for antidepressant
medications - Understand basic pharmacodynamic and
pharmacokinetic properties of some of the more
common antidepressants
3History of Antidepressants
- Discovered by serendipity in 1950s
- Iproniazid - antitubercular drug
- First antidepressant observed to elevate mood and
stimulate activity in many patients - Monoamine oxidase inhibitor
- Multiple side effects off market
- Reserpine depletion of NE/SE
4History of Antidepressantscontinued
- 1957-58 - Imipramine TCA was tried to treat
schizophrenia (NOT EFFECTIVE) - Tried as antidepressant and effective
- Monoamine theory of depression
- (Serotonin/norepinephrine)
5History of Antidepressantscontinued
- Multiple TCAs and MAOIs marketed
- Search for meds with less SE began
- First SSRI, fluoxetine was released in 1987
- Multiple SSRIs developed
- Other norepinephrine/dopamine reuptake inhibitors
have been developed
6Who gets an antidepressant?
- People who are depressed
- People who are anxious (all anxiety d/o)
- People with chronic pain/sleep difficulty
- Prophylaxis for depression (post-partum)
- Other Bedwetting
7Types of antidepressants
- Selective Serotonin-Reuptake Inhibitors
- fluoxetine, sertraline, paroxetine, citalopram,
escitalopramfluvoxamine - Tricyclic Antidepressants
- amitriptyline, amoxapine, desimpramine, doxepin,
imipramine, maprotiline, nortriptyline,
protryptiline, trimipramine - Monoamine Oxidase Inhibitors
- phenelzine, tranylcypromine, seligiline
8Types of antidepressantscontinued
- Norepinephrine/dopamine reuptake inhibitor
- Bupropion
- Serotonin/norepinephrine (central antagonist)
- Mirtazapine
- Serotonin antagonist and reuptake inhibitor
- Trazodone, nefazodone
- Serotonin/norepinephrine/?dopamine reuptake
inhibitor - Venlafaxine, duloxetine
9 10Monoamine Oxidase Inhibitors
- Inhibits monoamine oxidase
- Increases synaptic concentatration of monoamines
Serotonin and Norepinephrine - Stop 2 weeks before starting another
antidepressant - Risk of serotonin syndrome when used with other
drugs - Tyramine Hypertensive crisis
- Most common SE hypotension.
- Most serious SE hypertensive crisis
- May be better for atypical depression
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14Monoamine Oxidase Inhibitorscontinued
- Tranylcypromine (Parnate) Irreversible MAO A
- Phenelzine (Nardil) - Irreversible MAO A
- Selegeline (EMSAM) comes in patch. Mainly MAOI
B but cross over to A. No diet restrictions at
low dose.
15Tricyclic AntidepressantsGeneral
- Serotonin/Norepinephrine reuptake inhibitors
- Effective but anticholinergic, antihistamine,
cardiac effects prominent - Lethal in overdose
- Used for sleep/pain/migraines/anxiety too
- 2 drugs have a TCA structure that are not
antidepressants - 1. cyclobenzaprine
- 2. carbamazepine
16Tricyclic AntidepressantsGeneral
- Can check level
- Paxil, Prozac can increase levels (2D6)
- Not generally first line tx now
- Tertiary amines have greater analgesic properties
than secondary amines - For anxiety start very low
17Tricyclic AntidepressantsTertiary Amines
- Amitriptyline (Elavil, Amitril, Endep)
- Clomipramine (Anafranil)
- Imipramine (Tofranil, Antipres)
- Trimipramine (Surmontil)
- Doxepin (Sinequan, Adapin)
18Tricyclic AntidepressantsSecondary amines
- Nortriptyline (Pamelor, Aventyl)
- Desipramine (Norpramin)
- Protriptyline (Vivactil)
- Less adverse effects (anticholinergic) than
tertiary amines - Some are metabolites are tertiary amines
19Amitriptyline
- Dosed qhs
- Serum Half Life 21 hours
- Frequently used for insomnia/pain/fibromyalgia
20Imipramine
- Dosed qhs
- Used for MDD, and enuresis (3rd line)
- Obtain serum levels in pediatric population
- Cases of sudden cardiac death in kids
- Not used much as full dose antidepressant
21Desipramine
- Primarily norepinephrine drug
- Used in past for ADHD (not first line)
- CLOMIPRAMINE
- Primarily serotonergic drug
- Used for mostly for OCD (not first line)
22 23SSRIs as a class
- 30-40 incidence of sexual dysfunction
- Can be sedating or activating
- Used for anxiety and depression
- Take a few weeks to work
- Thought to increase BDNF
- High doses needed for OCD
- First line for depression/anxiety
- Slower titration for anxiety
24Fluoxetine (SSRI) - PROZAC
- Usually prescribed in am
- Long half life days (has act. metabolite)
- Activating, minimal weight change
- Useful in pregnancy (CAT C), eating d/o
- Useful in anxiety d/o start low
- Comes in generic, liquid, weekly
- Potent P450 2D6 inhibitor (Inc TCA level)
- Indications MDD, OCD, Panic D/O Bulimia, PMDD
25Paroxetine (SSRI) - PAXIL
- Short half life (potential for flu-like
withdrawal) - Mild-modest weight gain
- May have more sexual dysfunction (Inhibits Nitric
O. Synthetase) - More potential for teratogenic effects
- Inhibits Cytochrome P450-2D6 (Inc. TCA levels)
- Indications MDD, social phobia, panic d/o, PTSD,
OCD, GAD
26Sertraline (SSRI) - ZOLOFT
- Often used in anxiety d/o (eg PTSD) and pregnancy
(cat C) - Minimal weight change, can have GI side effects
- Indications MDD, OCD, Panic d/o, Social Phobia,
PTSD, PMDD
27Fluvoxamine (SSRI) - LUVOX
- Not used clinically often but can be useful
alternative - Increases caffeine half life
- Indications OCD, GAD (CR)
28Citalopram (SSRI) - CELEXA
- Dosed in am often but can cause sedation
- Minimal weight change
- Used in medically sick or polypharmacy due to low
med-med interactions
29Escitalopram (SSRI) LEXAPRO
- Dosed in the am usually
- Also used for complex medical patients
- Newest SSRI, few med-med interactions
- S-Enantiomer of celexa (active med)
- In theory less SE than celexa (sedation
particularly if it was a problem) - Celexa 20mg10mg lexapro
- Indications MDD, GAD
30NRIs
- Not indicated for depression
- Maprotiline
- Reboxetine
31Bupropion (NDRI) - WELLBUTRIN
- Norepinephrine/dopamine reuptake inhibitor
- Dosed in am and mid afternoon
- May worsen anxiety
- No sexual dysfunction
- May suppress appetite or cause insomnia
- Dose dependent risk of seizures low at approved
doses - Contraindications seizure disorder, eating d/o
- Indications MDD, smoking cessation
- OFF LABEL ADHD
32Nefazodone (SARI)- SERZONE
- Serotonin antagonist and reuptake inhibitor
- Blocks Serotonin-1 Receptor (5-HT-1)
- 1. Anti-depressant effect
- Blocks 5-HT-2a Activity
- 1. Blocks 5-HT-2a inhibition of 5-HT-1
- 2. Blocks sexual dysfunction
- 3. Blocks Insomnia and anxiety effects
33Serzone nefazodone (SARI)
- Black box warning on death from acute liver
failure (one per 250,000) - May take off market. Name brand is off market.
34Trazodone (SARI) - DESYREL
- Serotonin antagonist and reuptake inhibitor
(SARI) - No associated liver failure
- Used mostly for sleep and adjunct for depression
- Risk of priapism (1/6000)
35Venlafaxine (SNRI) - EFFEXOR
- Similar activity TCAs- SNRI
- Can cause serotonin withdrawal/short half life
- Serotonin/Norepinephrine reuptake Inhibitor
- Selective Serotonin Reuptake Inhibitor (lt150
mg/day) - Norepinephrine Reuptake Inhibitor (gt150 mg/day)
- Minimally inhibits dopamine uptake
- ? It can elevate diastolic BP)
- XR Indicated for MDD, GAD, Social Phobia, panic
d/o
36Duloxetine CYMBALTA
- SNRI
- Similar to venlafaxine with main difference that
has SNRI effects even at low dose - Associated with liver failure (rare)
- Has short half-life/potential for withdrawal
- Indicated for depression, fibromyalgia, and
diabetic neuropathy (higher dose often needed)
37Mirtazapine - REMERON
- Norepinephrine/serotonin antagonist
- Blocks Pre-synaptic alpha 2 adrenergic Receptors
- Enhances central noradrenergic activity
- Blocks post-synaptic 5-HT2, 5-HT3 Serotonin
Receptors - Enhances central Serotoninergic activity at
5-HT-1
38Remeron Mirtazapinecontinued
- Significant antihistamine activity
- Dose dependent effect
- Dose 15 mg antihistamine effects predominate
- Dose 45 mg Noradrenergic effects predominate
- Antihistamine Symptoms
- Weight gain
- Sedation
39Antidepressant Withdrawal
- Occurs with sudden antidepressant withdrawal
- Symptom onset occurs within 24 hours to 2-3 weeks
- Likely results from cholinergic overdrive
- Symptoms similar to Organophosphate Poisoning or
THE FLU - Most common with Paxil, effexor, cymbalta
- Not seen with Prozac (naturally tapers)
40Clinical Pearls
- Start with an SSRI, SNRI, or NDRI for depression
- Chose on basis of patient history, family
history, side effect profile, cost - Bupropion, trazodone, nefazodone, mirtazapine
no sexual dysfunction
41What you need to know Mood Stabilizers
- Chris Pelic M.D.
- Associate Dean for Students
- Medical University of South Carolina
42Objectives
- Learn definition of a mood stabilizer
- Understand the proposed mechanisms for the most
commonly used mood stabilizers (valproic acid,
lithium, carbamazepine) - Know the most common side effects of lithium,
valproic acid, and carbamazepine - Learn the medications used to treat dementia
(mechanism, side effects) - Learn the medications used for ADHD
43Mood Stabilizer????
- A mood stabilizer is a medication used in the
treatment of Bipolar Disorder to suppress swings
between mania and depression. - Some meds seem just antimanic drugs
- Can also treat cyclothymia, personality d/o mood
lability, aggression/impulsivity - Term developed with loose meaning
44History
- 1817 Lithium discovered by Johan Arvedson
- In 1890, Doctors Robert B. Cloud, Christopher
Columbus Garrett, and W. H. Whitehead established
the first hospital in America, the Lithia Springs
Sanitarium - Natural lithium water in treating alcoholism,
opium addiction, and compulsive behavior - Mania had not yet been identified as such
45History continued
- Dr Cloud Lithium Santiarium
46History continued
- Lithium Carbonate was discovered as treatment for
mania in 1948 by Australian Psychiatrist John F.
Cade working with rats - 1970, FDA approved Li
- 1970 first report Carbamazepine useful in mania
- Valproic acid soon folllowed
- Typical antipsychotic agents used in the hospital
setting - Newer anticonvulsants then began to be looked at
- Atypical agents used for acute mania, mixed
episodes, and maintenance
47Who Gets a Mood Stabilizer?
- People with BPAD I, II, and cyclothymia
- People with personality disorders
- People with unipolar depression (e.g lithium,
lamictal) - People with behavioral/anger/impulsive outbursts
(intermittent expl. d/o, MR, ODD, etc) - People with anxiety or in alcohol withdrawal
48 49Types of Mood Stabilizers
- Lithium indicated for acute mania and long term
control of BPAD - Depakote indicated for treatment of mania
- Tegretol XL indicated for BPAD
- Lamictal indicated for maintenance treatment of
BPAD - Topamax, Neurontin, Keppra, Trileptal also used
with little to no evidence - All atypical antipsychotics are indicated for
acute mania. Some have mixed episode indication
and others have maintenance indication.
50Types of Mood Stabilizerscontinued
- Benzodiazepines used but not indicated (effective
anti-manic agents usually in adjunct) - Typical antipsychotic agents used when atypical
agents and regular mood stabilizers cannot be
used
51Lithium
- Gold standard for treatment of Bipolar disorder
- Effective as antimanic and antidepressant
- Side effects often limit compliance tremor,
polydipsia, hypothyroidism hyperthyroidism,
weight gain, nausea/vomiting, cognitive
blunting, worsen psoriasis, hair loss, diarrhea,
renal problems
52Lithium
- Steady state reached in 5 days
- Therepeutic trough levels
- Maintenance Bipolar Disorder 0.6 to 1.2
meq/liter
53Lithium proposed mechanism
- i) Modulation of neurotransmitters by lithium
likely readjusts balances between excitatory and
inhibitory activities, and decreased
glutamatergic activity may contribute to
neuroprotection. - (ii) Lithium modulates glycogen synthase,
kinase-3beta, cyclic AMP-dependent kinase, and
protein kinase C, which may be critical for the
neural plasticity involved in mood recovery and
stabilization. - (iii) Lithium adjusts signaling activities
regulating second messengers, transcription
factors, and gene expression.
54Lithium Before starting
- Check BMP, TFTS, EPT, /- EKG
- Tell pt to maintain current salt intake
- See if pt is on meds that can impair renal
excretion diuretics, ACE inhibitors, NSAIDS
55Lithium Maintenance
- Once pt is on therapeutic dose.
- Check BMP, Li trough level, TFTs 2x/year if no
problems - Reassess pts other meds (NSAIDS)
- Most patients develop polydipsia with chronic use
- Can cause Epsteins Heart Anomaly
56Renal Toxicity of Lithium
- 10-20 pts on li for gt10 years have morphological
kidney changes - Chronic lithium ingestion has been associated
with several different forms of renal injury - Nephrogenic DI is the most common
- Renal tubular acidosis
- Nephrotic syndrome
- Chronic interstitial nephritis
57Lithium - Overdose
- Symptoms slurred speech, incoordination,
tremor, weakness, increased thirst, increased
urine output, rash, diarrhea, vomiting, low blood
pressure, rare abnormal rhythms, drowsiness,
coma, seizures, stupor
58Hemodialysis
- Lithium is the most dialyzable toxin known, due
to its low molecular weight, negligible protein
binding, and volume of distribution similar to
that of water
59Depakote - (Divalproex Na and Valproic Acid)
- Anticonvulsant
- Effective anti-manic medication
- Considered a first line treatment
- Comes in generic (valproic acid), liquid, IV
form, regular release, DR, and ER - Side effects weight gain, headaches, somnolence,
GI upset hair loss, rash, dizziness, rare
hepatotoxicity, rare pancreatitis, rare
thrombocytopenia
60Depakote (Divalproex Na)
- Steady state reached in 3 days
61Depakote (Divalproex Na) proposed mechanism
- Increases or potentiates GABA in the brain
(inhibitory NT) - Puts brakes on the brain
- Seems effective as antimanic and anticonvulsant
62Depakote (Divalproex Na) Before Starting
- Check LFTs, CBC prior to starting
- Do not use in liver disease
- Good choice if patient also has migraines or
seizures
63Depakote - Maintainance
- At stable level clinically, check LFTs, CBC,
trough level 1-2/year (unless otherwise
indicated) - Can use higher doses in acute phase
- Watch for drug interactions
- Can cause neural tube defects - 5
- ? Polycystic ovary disease
64Tegretol - Carbamazepine
- Carbamazepine is used to treat certain types of
seizures in the treatment of epilepsy - Relieves facial nerve pain
- Used for alcohol withdrawal, mood stabilizer
- Like other tricyclic compounds, carbamazepine has
a moderate anticholinergic action which is
responsible for some of its adverse effects
65Tegretol - Carbamazepine
- Reaches steady state in 4-5 days
- Will increase metabolism of itself over time so
you may need increased doses later in tx.
66Tegretol - Carbamazepine
- Common side effects dizziness or
lightheadedness, dry, walking, drowsiness or
fatigue, double vision, nausea or vomiting,
clumsiness, delay in urinating - Less Common Side Effects of carmbamezpine
aplastic anemia, hepatitis, rash
67Tegretol - Carbamazepine proposed mechanism
- Mechanism unknown
- Believed to be serotonergic and block voltage
sensitive Na channels - Modulates high voltage Ca channels
- Reduces polysynaptic responses
68Neurontin - gabapentin
- Adjunctive anticonvulsant
- Mechanism of Action Structurally related to
GABA, but does not bind to GABA sight - Side Effects Mild sedation
- Uses ?Good anti-anxiety effects, alcohol
withdrawal, neuropathic pain - Evidence does not seem to support use as mood
stabilizer - Expensive placebo??
69Trileptal - Oxcarbazepine
- Carbamazepine (anticonvulsant) with an oxygen
stuck on it - Mechanism of Action Blocks voltage sensitive Na
channels, Modulates high voltage Ca channels - Most common side effects (occurring in at least
5 of patients in clinical studies) were
dizziness, somnolence, double vision, fatigue,
nausea, vomiting, incoordination, abnormal
vision, abdominal pain, tremor, indigestion, and
abnormal gait. - Watch for hyponatremia,
70Lamictal - Lamotrigine
- Phenyltriazine class (an anticonvulsant)
- Mechanism inhibit voltage sensitive Na channels
stabilizing membranes modulating release of
excitatory amino acids - Good particularly for BPAD-depression/maintenance
- Potential for serious rash (Stevens-Johnson
Syndrome 0.3-0.8)
71Topamax- Topiramate
- Anticonvulsant
- Mechanism of Action State dependent Na channel
action, Enhances GABA, Antagonizes the glutamate
reception - Side Effects 10 memory cognitive problems,
weight loss 1/3 - Not indicated yet as mood stabilizer
72Benzodiazepines
- Not indicated but useful to slow down the manic
patient - Most frequently used are ativan, klonopin
73Stimulants
- Christopher Pelic M.D.
- Associate Dean for Students
- Medical University of South Carolina
74Stimulants ADHD/Narcolepsy
- ADHD- inattention or hyperactivity with onset
before age 7 that is seen in 2 or more settings - Narcolepsy REM sleep attacks, Cataplexy,
hypnogogic/hypnopompic hallucinations - Obstructive sleep apnea
75ADHD Treatments (medication options)
- Established Treatments
- Psychostimulants (1st line)
- Atomoxetine (1st line)
- Bupropion (2nd line)
- TCAs (2nd- 3rd line)
- Probable Efficacy
- Modafinil
- Alpha-2 agonists
76Stimulants
- Increase dopamine and norepinephrine release
- Stimulate certain areas of the brain to focus
better - FDA classifies a substance as psychostimulant
if nucleus accumbens is activated - In use for behavioral disorders in children
since 1930s - Many studies to document safety and efficacy
- 70-85 response rate
- do not use this to confirm diagnosis!
77Stimulants
- Special consideration
- Motor tics
- Problems with growth/insomnia
- Anxiety d/o (children w/ co-morbid anxiety may
improve on MPH, according to MTA study) - Seizure d/o
- Children under 6 years old may be safely treated,
starting with methylphenidate, once all
psychosocial treatments have been implemented
78Methylphenidate Formulations
79Amphetamine Formulations
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81Match the formulation with the needs of the
patient and family
- Have to know when youth needs the
psychostimulant (e.g., early in AM for school
only, or including homework, peer activities,
week-ends) - Parent and teen sometimes have definite
preferences for one or another, and so do HMOs - Train parents to observe efficacy and side
effects through the day and into the evening
82Serious side effects of psychostimulants
- Sudden cardiac death
- Anecdotal, but not irrelevant
- Cases thus far have been primarily in patients
with pre-existing cardiac conduction defects - Ask about history of sudden tachycardia,
fainting, and family history of sudden cardiac
death prior to initiating - 30 cases of psychosis or formal hallucinations
discontinue the medication - Growth Suppression (MTA 2004) effects are likely
to be made up in late teens or by drug holidays
especially at risk, those with nausea and vomiting
83Modafinil - PROVIGIL
- Used mostly for narcolepsy/sleep apnea
- Main mechanism unknown
- Modafinil, like other stimulants, increases the
release of monoamines but also elevates
hypothalamichistamine levels - Activates glutamatergic circuits while inhibiting
GABAergic neurotransmission
84ADHD Treatments (other medication options)
- Atomoxetine
- Potent norepinephrine (NE) reuptake inhibitor
- highly selective
- inhibits presynaptic NE transporter
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86ADHD
- Clonidine is used as an adjunct
- Bupropion is used off label for ADHD
87Dementia Medications
- Christopher Pelic M.D.
- Associate Dean for Students
- Medical University of South Carolina
88Memory loss Alzheimers
- Loss of cholinergic, serotonergic, and glutamate
neurons - Plaques, tangles, tau, amyloid
- Progressive memory loss
- Medications are used to try and slow the
progression (they do not prevent, cure, or stop
the disease)
89Donepezil (Aricept)
- Acetylcholine esterase inhibitor
- Inhibits the break down of acetylcholine
- Used in mild to moderate dementia
- Side effects nausea, headache, vomiting,
appetite suppression - OTHER inhibitors tacrine (liver toxicity),
rivastigmine, galantamine
90Memantine (Namenda)
- NMDA antagonist
- Side effects dizziness, headache, constipation