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Antidepressants

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Title: Antidepressants


1
Antidepressants
  • Chris Pelic M.D.
  • Associate Dean for Students
  • Medical University of South Carolina

2
Objectives
  • 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

3
History 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

4
History of Antidepressantscontinued
  • 1957-58 - Imipramine TCA was tried to treat
    schizophrenia (NOT EFFECTIVE)
  • Tried as antidepressant and effective
  • Monoamine theory of depression
  • (Serotonin/norepinephrine)

5
History 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

6
Who 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

7
Types 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

8
Types 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
  • THE MEDS.

10
Monoamine 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

11
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12
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2
13
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14
Monoamine 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.

15
Tricyclic 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

16
Tricyclic 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

17
Tricyclic AntidepressantsTertiary Amines
  • Amitriptyline (Elavil, Amitril, Endep)
  • Clomipramine (Anafranil)
  • Imipramine (Tofranil, Antipres)
  • Trimipramine (Surmontil)
  • Doxepin (Sinequan, Adapin)

18
Tricyclic AntidepressantsSecondary amines
  • Nortriptyline (Pamelor, Aventyl)
  • Desipramine (Norpramin)
  • Protriptyline (Vivactil)
  • Less adverse effects (anticholinergic) than
    tertiary amines
  • Some are metabolites are tertiary amines

19
Amitriptyline
  • Dosed qhs
  • Serum Half Life 21 hours
  • Frequently used for insomnia/pain/fibromyalgia

20
Imipramine
  • 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

21
Desipramine
  • Primarily norepinephrine drug
  • Used in past for ADHD (not first line)
  • CLOMIPRAMINE
  • Primarily serotonergic drug
  • Used for mostly for OCD (not first line)

22
  • THE SSRIs

23
SSRIs 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

24
Fluoxetine (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

25
Paroxetine (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

26
Sertraline (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

27
Fluvoxamine (SSRI) - LUVOX
  • Not used clinically often but can be useful
    alternative
  • Increases caffeine half life
  • Indications OCD, GAD (CR)

28
Citalopram (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

29
Escitalopram (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

30
NRIs
  • Not indicated for depression
  • Maprotiline
  • Reboxetine

31
Bupropion (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

32
Nefazodone (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

33
Serzone nefazodone (SARI)
  • Black box warning on death from acute liver
    failure (one per 250,000)
  • May take off market. Name brand is off market.

34
Trazodone (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)

35
Venlafaxine (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

36
Duloxetine 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)

37
Mirtazapine - 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

38
Remeron Mirtazapinecontinued
  • Significant antihistamine activity
  • Dose dependent effect
  • Dose 15 mg antihistamine effects predominate
  • Dose 45 mg Noradrenergic effects predominate
  • Antihistamine Symptoms
  • Weight gain
  • Sedation

39
Antidepressant 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)

40
Clinical 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

41
What you need to know Mood Stabilizers
  • Chris Pelic M.D.
  • Associate Dean for Students
  • Medical University of South Carolina

42
Objectives
  • 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

43
Mood 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

44
History
  • 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

45
History continued
  • Dr Cloud Lithium Santiarium

46
History 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

47
Who 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
  • The Meds

49
Types 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.

50
Types 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

51
Lithium
  • 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

52
Lithium
  • Steady state reached in 5 days
  • Therepeutic trough levels
  • Maintenance Bipolar Disorder 0.6 to 1.2
    meq/liter

53
Lithium 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.

54
Lithium 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

55
Lithium 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

56
Renal 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

57
Lithium - 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

58
Hemodialysis
  • 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

59
Depakote - (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

60
Depakote (Divalproex Na)
  • Steady state reached in 3 days

61
Depakote (Divalproex Na) proposed mechanism
  • Increases or potentiates GABA in the brain
    (inhibitory NT)
  • Puts brakes on the brain
  • Seems effective as antimanic and anticonvulsant

62
Depakote (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

63
Depakote - 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

64
Tegretol - 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

65
Tegretol - Carbamazepine
  • Reaches steady state in 4-5 days
  • Will increase metabolism of itself over time so
    you may need increased doses later in tx.

66
Tegretol - 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

67
Tegretol - Carbamazepine proposed mechanism
  • Mechanism unknown
  • Believed to be serotonergic and block voltage
    sensitive Na channels
  • Modulates high voltage Ca channels
  • Reduces polysynaptic responses

68
Neurontin - 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??

69
Trileptal - 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,

70
Lamictal - 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)

71
Topamax- 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

72
Benzodiazepines
  • Not indicated but useful to slow down the manic
    patient
  • Most frequently used are ativan, klonopin

73
Stimulants
  • Christopher Pelic M.D.
  • Associate Dean for Students
  • Medical University of South Carolina

74
Stimulants 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

75
ADHD Treatments (medication options)
  • Established Treatments
  • Psychostimulants (1st line)
  • Atomoxetine (1st line)
  • Bupropion (2nd line)
  • TCAs (2nd- 3rd line)
  • Probable Efficacy
  • Modafinil
  • Alpha-2 agonists

76
Stimulants
  • 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!

77
Stimulants
  • 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

78
Methylphenidate Formulations
79
Amphetamine Formulations
80
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81
Match 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

82
Serious 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

83
Modafinil - 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

84
ADHD Treatments (other medication options)
  • Atomoxetine
  • Potent norepinephrine (NE) reuptake inhibitor
  • highly selective
  • inhibits presynaptic NE transporter

85
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86
ADHD
  • Clonidine is used as an adjunct
  • Bupropion is used off label for ADHD

87
Dementia Medications
  • Christopher Pelic M.D.
  • Associate Dean for Students
  • Medical University of South Carolina

88
Memory 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)

89
Donepezil (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

90
Memantine (Namenda)
  • NMDA antagonist
  • Side effects dizziness, headache, constipation
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