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PS1!Psychiatry Toronto Notes 2023
Mood Episodes
DSM-5 DIAGNOSTIC CRITERIA FOR MAJOR DEPRESSIVE EPISODE
Reprintedwithpermission Itom the Diagnostic and Statistical Manual ol Mental Disorders.5th ed. 2013.American Psychiatric Association
A.>5of the following symptoms have been present during the same 2 wk period and represent a change
from previousfunctioning; at least one of the symptoms is either 1) depressed mood or 2) loss of
interest or pleasure (anhedonia)
Note: Do not include symptoms that are clearly attributable to another medical condition
• depressed mood most of the day, nearly every day, as indicated by either subjective report or
observation made by others
markedly diminished interest or pleasure in all, or almost all, activities most of the day, nearly
every day
significant and unintentional weight loss/weight gain,or decrease/increase in appetite nearly
every day
insomnia or hypersomnia nearly every day
• psychomotor agitation or retardation nearly every day
• fatigue or loss of energy nearly every day
feelings of worthlessness or excessive or inappropriate guilt (which may be delusional) nearly
every day (not merely self-reproach or guilt about being sick)
diminished ability to think or concentrate,or indecisiveness nearly every day
• recurrent thoughts of death (not just fear of dying), recurrent suicidal ideation without a specific
plan, or a suicide attempt or a specific plan for committing suicide
B.the symptoms cause clinically significant distress or impairment in social, occupational, or other
important areas of functioning
C.the episode is not attributable to the direct physiological effects of a substance or a GMC
Criteria for Depression (>5)
MSIGECAPS
Mood:depressed
Sleep:increased/decreased
Interest decreased
Guilt
Energy: decreased
Concentration:decreased
Appetite:increased/decreased
Psychomotor:agitation/retardation
Suicidal ideation
<§) DSM-5 CRITERIA FOR MANIC EPISODE
Reprinted withpermission from the Diagnostic and Statistical Manual of Mental Disorders.5th ed. 2013.American Psychiatric Association
A.a distinct period of abnormally and persistently elevated, expansive, or irritable mood and abnormally
persistently increased goal-directed activity or energy, lasting £1 wk and present most of the day,
nearly every day (or any duration if hospitalization is necessary)
B.during the period of mood disturbance and increased energy or activity,>3of the following
symptoms have persisted (4 if the mood isonly irritable) and have been present to a significant degree
and represent a noticeable change from usual behaviour
inflated self-esteem or grandiosity
* decreased need for sleep (e.g. feels rested after only 3 h of sleep)
more talkative than usual or pressure to keep talking
flight of ideas orsubjective experience that thoughts are racing
distractibility (i.e.attention too easily drawn to unimportant or irrelevant externalstimuli)
increase in goal-directed activity (eithersocially,at work or school, orsexually) or psychomotor
agitation
• excessive involvement in pleasurable activities that have a high potential for painful consequences
(e.g. engaging in unrestrained shopping sprees,sexual indiscretions, or foolish business
investments)
C.the mood disturbance issufficiently severe to cause marked impairment in social or occupational
functioning or to necessitate hospitalization to prevent harm to self or others,or there are psychotic
features
D.the episode is not attributable to the physiological effects of a substance or another medical condition
Note: A full manic episode that emerges during antidepressant treatment but persists at a fully
syndromal level beyond the physiological effect of that treatment issufficient evidence for a manic
episode, and therefore, a bipolar 1 diagnosis
Note:Criteria A-D constitute a manic episode. At least one lifetime manic episode is required for the
diagnosis of bipolar I disorder
Hypomanic Episode
•criterion A and B of a manic episode is met, but duration is £4 d
•episode associated with an unequivocal change in functioning that is uncharacteristic of the
individual when not symptomatic and observable by others
•episode is not severe enough to cause marked impairment in social or occupational functioning or to
necessitate hospitalization
•absence of psychotic features(if these are present the episode is, by definition, manic)
Mixed Features
•episode specifier in a manic, hypomanic,or depressive episode of bipolar I or II (BDl/Ii) that indicates
the presence of both depressive and manic symptoms concurrently, classified by the disorder and
primary mood episode (i.e. BD1, current episode manic, with mixed features)
•clinical importance due to increased suicide risk and appropriate treatment
•if found in patient diagnosed with major depression, there is a high index ofsuspicion for BD
•while meeting the full criteria for a \1DE, the patient has on most days 3 of criteria B for a manic
episode
•while meeting the full criteria for a manic/ hypomanic episode, the patient has on most days 23of
criteria A for a depressive episode (the following criterion A cannot count: psychomotor agitation,
insomnia, difficulties concentrating, or weight changes)
Criteria tor Mania (s3)
and GST PAID
Grandiosity
Sleep (decreased need)
Talkative
Pleasurable activities, Painful
consequences
Activity (increased)
Ideas (flight of)
Distractiblc
r n
u
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PS12 Psychiatry Toronto Notes 2023
Depressive Disorders
Anlideprtssauts for Depression in Physically
IIIPeople
Cochrane MSysl Per 2010XOOO/SO3
Purpose:lo determine the efficacy of
antidepressants in treating depression in people with
comorbid physical illness.
Methods: Systematic review olICIs comparing
the efliucy of antidepressants vs. placebo in the
treatment of major depression,adpistment disorder,
and dystbyoia in adults with comorbid depression
and physical illness.Physical illnesswas defined as
any medical condition known to have a biological
underpinning where diagnosis is not purely symptom
based.
Results:fifty-one studies including 3003
participants were included in thisreview.Both
tricyclic antidepressants and selective serotonin
reuptake inhibitors were more effective than placebo
at treating depression m adultswith concunent
physical illness.Ory mouth and seual dysfunction
were more com man in patieatstreated with an
antidepressant.
MAJOR DEPRESSIVE DISORDER
DSM-5 DIAGNOSTIC CRITERIA FOR MAJOR DEPRESSIVE DISORDER (MDD)
Reprinted withpermission from the Diagnostic andStatistical Manual of Mental Disorders,5th ed.2013.AmericanPsychiatricAssociation
A.presence of a single MDE (vs. recurrent, which requires presence of two or more MDEs; to be
considered separate episodes, there must be an interval of at least 2 consecutive mo in which criteria
arc not met for a MDE)
B.the MDE is not better accounted for by schizoaffective disorder and is notsuperimposed on
schizophrenia,schizophreniform disorder, delusional disorder,or psychotic disorder NOS
C.there has never been a manic episode or a hypomanic episode
• note:
'
this exclusion does not apply ifall of the manic-like, or hypomanic-likc episodes are substance
or treatment-induced or are due to the direct physiological effects of another medical condition
• specifiers:with anxious distress, mixed features, melancholic features, atypical features,moodcongruent psychotic features,mood-incongruent psychotic features, catatonia, peripartum onset,
seasonal pattern
Epidemiology
• Canadian annual/lifetime prevalence:5%/ll%
• peak prevalence age 15-25 yr (M:F=l:2)
Etiology
• biological
genetic:65-75% MZ twins; 14-19% DZ twins, 2-4 fold increased risk in first-degree relatives
neurotransmitter dysfunction:decreased activity of 5-HT, NE, and DA at neuronalsynapse;
changes in GABA and glutamate; various changes detectable by fMRI
neuroendocrine dysfunction:abnormal HPA axis activity
neuroanatomy and neurophysiology:decreased hippocampal volume,increased size of ventricles;
decreased REM latency and slow-wave sleep; increased REM length
• immunologic: increased pro-inflammatory cytokines 1L-6 and TNI;
secondary to medical condition, medication,substance use disorder
• psychosocial
cognitive (i.e. distorted schemata. Beck’s cognitive triad: negative views of oneself, the world, and
the future)
environmental factors (i.e. job loss, bereavement, history of abuse or neglect, early life adversity)
comorbid psychiatric diagnoses(i.e. anxiety,substance use disorder, developmental disability,
dementia,eating disorders)
Risk Factors
• sex:E:M=2:1
• family history:depression, alcohol use disorder,suicide attempt or completion
• adverse childhood experiences:loss of parent before age 11, negative home environment (abuse,
neglect)
• personality: neuroticisni, insecure, dependent, obsessional
• recent stressors: illness, financial, legal,relational,academic
• lack of intimate,confiding relationships orsocial isolation
• low socioeconomic status
Clinically Significant Depressive Symptoms in the Elderly
• affects about 15% of community residents >65 ylo; up to 50% in nursing homes
• high suicide risk due to social isolation, chronic medical illness, and decreased independence
• suicide peak: males ages 80-90, females ages 50-65
• low mood or dysphoria may not be a reliable indicator of depression in those >70 y/o
• often present with somatic complaints (i.e. changesin weight,sleep, energy;chronic pain) or anxiety
symptoms
• may have prominent cognitive changes after onset of mood symptoms (dementia syndrome of
depression)
• see Table 3,PS26,for a comparison of delirium and dementia
Treatment
• lifestyle:increased aerobic exercise, mindfulness-based stress reduction,sleep hygiene
• biological:SSRIs, SNRls, other antidepressants, somatic therapies(see Pharmacotherapy; PS5I and
Somatic Therapies,PS60)
for MDE of moderate or greaterseverity, 1st line pharmacotherapy are used: most 2nd generation
antidepressants, with escitalopram, mirtazapine, sertraline, venlafaxine, agomelatine,and
dtalopram showing evidence for superiority
for non or partial response, optimize the dose,switch to antidepressant with superiority, or add
augmenting agent (i.e.aripiprazole, quetiapine,risperidone)
typical response to antidepressant treatment:physical symptoms improve at 2 wk, mood/
cognition by 4 wk;if no improvement after 4 wk at the highest tolerated therapeutic dosage, alter
regimen
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PS13 Psychiatry Toronto Notes 2023
ECT: currently fastest and most effective treatment for MDD.Consider in severe, psychotic,or
treatment-resistant cases
tTMS: 1st line treatment for MDD for patients who have failed at least I antidepressant treatment.
Efficacy equivalent to medications (but not to ECT) with good safety and tolerability
phototherapy:especially ifseasonal component,shift work,sleep dysregulation
•psychological
individual therapy (CUT, interpersonal, behavioural activation, dynamic), group therapy, family
therapy
•social:vocational rehabilitation,socialskillstraining
•experimental: magnetic seizure therapy, deep brain stimulation, ketamine
Prognosis
•1 yr after diagnosis of MDD without treatment: 40% of individuals will still have symptoms that are
sufficiently severe to meet criteria for MDD, 20% will continue to have some symptoms that no longer
meet criteria for MDD, 40% will have no symptoms
PERSISTENT DEPRESSIVE DISORDER
Sec landmark Psychiatry Trials table
(or mote information on TRANSFORM-2,
which detailsthe use of esk etamine
nasalspray for patients with treatmentresistant depression.
DSM-5 DIAGNOSTIC CRITERIA FOR PERSISTENT DEPRESSIVE DISORDER
Note:in DSM-1V-TR this was referred to as Dysthymic Disorder
Reprinted withpermission from the Diagnostic and Statistical Manual of Men
A.depressed mood for most of the day, for more days than not, asindicated either by subjective account
or observation by others, for S2 yr
Note:In children and adolescents, mood can be irritable and duration must be at least 1 yr
B.presence, while depressed, of 2 of the following
poor appetite or overeating
insomnia or hypersomnia
low energy orfatigue
low self-esteem
poor concentration or difficulty making decisions
feelings of hopelessness
C.during the 2 yr period (1 yr for children or adolescents) of the disturbance,the person has never been
without the symptoms in criteria A and B for more than 2 mo at a time
D.criteria for a major depressive disorder may be continuously present for 2 yr
E.there has never been a manic episode or a hypomanic episode, and criteria have never been met for
cyclothymic disorder
F. the disturbance is not better explained by a persistent schizoaffective disorder, schizophrenia,
delusional disorder, or other specified or unspecified schizophrenia spectrum and other psychotic
disorder
G.the symptoms are not due to the direct physiological effects of a substance or another medical
condition
H.the symptoms cause clinically significant distress or impairment in social, occupational, or other
important areas of functioning
•specifiers:
with anxious distress, mixed features, melancholic features, atypical features, mood-congruent
psychotic features, mood-incongruent psychotic features, catatonia, peripartum onset,seasonal
pattern
partial remission,full remission
early onset (<21 y/o), late onset (>21 y/o)
with pure dysthymic syndrome (full criteria for MDE have not been met in at least preceding 2
yr), with persistent MDE (full criteria for MDE have been met throughout preceding 2 yr)
with intermittent MDEs,with current episode:full criteria for a MDE are currently met, but
there have been periods of at least 8 wk in at least the preceding 2 yr with symptoms below the
threshold for a full MDE
with intermittent MDEs, without current episode:full criteria for a MDE are not currently met,
but there has been one or more MDEs in at least the preceding 2 yr
specify current severity: mild, moderate,severe
tal Disorders,5th ed.2013.American Psychiatric Association
Epidemiology
•lifetime prevalence: 2-3%; M=F
Treatment
•psychological
traditionally, psychotherapy was the principal treatment for persistent depressive disorder;
recent evidence suggests some (but generally inferior) benefit for pharmacological treatment.
Combinations of the two may be most efficacious
n
L J
•biological
antidepressant therapy:SSRls (e.g.sertraline,escitalopram),
'
l
'
CAs (e.g. nortriptyline) +
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PS14 Psychiatry Toronto Notes 2023
Postpartum Mood Disorders
Selective Serotonin IteuptakeInhibitors in
Pregnancy and Infant Outcomes
PttdiitrChM Health 2011;16:S62 63
Canadian Paediatric Society|CPS) clinical practice
guideline recommendations:It is important tn treat
depression in pregnancy.There is noevidence that
SSHIS increase the risk of major matformations. there
Is conflicting tmdenct concerning the association of
paroxetine and cardiac malformations.SSRIs are not
contraindicated nhile breast-feeding.
Postpartum “Blues"
• transient period of mild depression, mood instability, anxiety, decreased concentration; considered
to be normal in response to fluctuating hormonal levels, the stress of childbirth, and the increased
responsibilities of motherhood
• occurs in 50-80% of mothers;begins 2-4 d postpartum, usually lasts 48 h, can last up to 10 d
• does not require psychotropic medication
• usually mild or absent:feelings of inadequacy, anhedonia, thoughts of harming baby,suicidal
thoughts
MAJOR DEPRESSIVE DISORDER WITH PERIPARTUM ONSET
(POSTPARTUM DEPRESSION)
Antidepressant Use in Pregnancy and the Disk of
Cardiac Defects
ItJM 2014 Jun19;370(25):2397-2407
Purpose: It is oncerUin whetherselective serotoninreuptake inhibitors (SSRIs) and other antidepressants
during pregnancy are associated mth increased risk
uf congenital cardiac defects.There areconcerns
about an association between paroxetine use and
right ventricular outflow tract obstruction, and
between sertraline use and ventricular septal defects.
Methods:Cohortstudy Including 949S04 women
enrolled in Medicaidfor a 7 yr period.The risk oT
major cardiacdelects among infants born to women
who took antidepressants during thelst trimester
wot compared with the fish among infants bom
to women rnhodid not useanbdtpreisonti.tn
unadjusted analysis was used, possible conTounders
were considered.
Results:Overall, the chance of infants not exposed
to antidepressants born with a cardiac defect was
72.3 per 10000 infants,and infantswith exposuro
was90.1 per 10000 infants, the relative risks of
any cardiacdefect w ilb the useof SSRIs were106
(95% Cl,0.93to1.22) in the fuly adjusted a na lysis
restricted towomen with depression.No significant
association wasfoond belwtrn the use ol paroxetine
and right reotricolir outflow trad obstruction (11.
1.07|or between the use of sertraine and ventricular
septal defects(PR,1.04).
Conclusions:No substantial increase in risk uf
cardiac malformations attributable to antidepressant
use during thelst trimester.
Clinical Features
• thisspecifier can apply to a MDE with onset during pregnancy or within 4 wk following delivery
• typically lasts 2-6 mo; residual symptoms can last up to I yr
• may present with psychosis (rare, 0.2% - more frequent with prior postpartum mood episodes and
postpartum mania)
• severe symptoms may include complete disinterest in baby,suicidal and infanticidal ideation
Epidemiology
• occurs in up to 3-6% of mothers, up to 50% risk of recurrence
Risk Factors
• previous history of a mood disorder (postpartum or otherwise),family history of mood disorder
• psychosocial factors:stressful life events, unemployment, marital conflict, lack of social support,
unwanted pregnancy, colicky orsick infant
Treatment
• psychotherapy (CBT or IPT)
• short-term safety of maternal SSRIs for breastfeeding infants established; long-term effects unknown
• if depression severe or psychotic symptoms present,consider ECT
Prognosis
• impact on child development; increased risk of cognitive delay, insecure attachment, behavioural
disorders
• treatment of mother improves outcome for child at 8 mo through increased mother-child interaction
Bipolar Disorders
BIPOLAR I/BIPOLAR II DISORDER
Definition
• Bipolar I Disorder
disorder in which at least one manic episode has occurred
if manic symptomslead to hospitalization, or if there are psychotic symptoms, the diagnosis is
bipolar I
• commonly accompanied by at least 1 MDE but not required for diagnosis
time spent in mood episodes:53% asymptomatic,32% depressed,9% cycling/mixed,6% hypo/
manic
• Bipolar II Disorder
disorder in which there is at least 1 MDE, 1 hypomanic episode, and no manic episodes
• while hvpomania isless severe than mania, bipolar 11 is not a “milder"
form of bipolar I
time spent in mood episodes:46% asymptomatic,50% depressed, 1% cycling/mixed, 2% hypo/
manic
• bipolar 11 is often missed due to the severity and chronicity of depressive episodes and low rates of
spontaneous reporting and recognition of hypomanic episodes
Classification
• classification of BD involves describing the disorder (1 or II) and the current or most recent mood
episode as either manic, hypomanic, or depressed
• specifiers; with anxious distress, hypo/manic/depressed with mixed features, rapid cycling,
melancholic features, atypical features, mood-congruent or -incongruent psychotic features,catatonia,
peripartum onset,seasonal pattern, rapid cycling (>4 mood episodes in 1 yr)
Bipolar It is quite often missed and many
patients are symptomatic for up to a
decade before accurate diagnosis and
treatment
Patients with bipolar disorder are at
higher risk for suicide when they switch
(tom mania to depression, especially as
they become aware of consequences
of their behaviour during the manic
episode
Lithium is among few agents with
proven efficacy in preventing suicide
attempts and completions LJ
+
Epidemiology
• lifetime prevalence: 1% BD 1, 1.1% BD II, 2.4% Subthreshold BD;M:F=1:1
• mean age of onset:25 yr, usually MDE first, manic episode 6-10 yr after; average age of first manic
episode: 32 yr
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PS15 Psychiatry Toronto Notes 2023
Risk Factors
• genetic: 60-65% of bipolar patients have family history of a major mood disorder, especially bipolar
disorder
• clinical features of MDE history favouring bipolar over unipolar diagnosis:early age of onset (<25 yr),
increased number of MDEs, psychotic symptoms, postpartum onset, anxiety disorders (especially
separation, panic), antidepressant failure due to early “poop out"or hypomanic symptoms, early
impulsivity and aggression, substance misuse,cyclothymic temperament,family history of bipolar
disorder
Monotherapy with antidepressants
should be avoided in patients with
bipolar depression as patients can
switch horn depression into mania
The 4 L's for Bipolar Depression
Lithium, lamotriginc. Lurasidonc.
SeroqueL
Treatment
• lifestyle:psychoeducation regarding cycling nature of illness, ensure regular check ins,develop early
warning system, “emergency plan” for manic episodes, promote stable routine (sleep,meals, exercise)
• biological:lithium, anticonvulsants, antipsychotics,ECT (if resistant); monotherapy with
antidepressants should be avoided
• mood stabilizers vary in their ability to treat (reduce symptoms acutely) orstabilize (prevent
relapse and recurrence) manic and depressive symptoms; multi-agent therapy is common
treating mania:lithium,divalproex, carbamazepine (2nd line), SGA,ECT (2nd line),
benzodiazepines (for acute agitation)
preventing mania:same as above but usually at lower dosages, minus ECT and benzodiazepines
treating depression:lithium,lurasidone, quetiapine, lamotrigine,antidepressants (2nd line,only
with mood stabilizer), ECT (2nd line)
preventing depression:same as above plus aripiprazole, divalproex (note: quetiapine is first line in
treating bipolar II depression)
mixed episode or rapid cycling:multi-agent therapy:lithium or divalproex + SGA (lurasidone,
aripiprazole)
• psychological:supportive psychotherapy, CBT, 1PT or interpersonal social rhythm therapy, family
therapy
• social: vocational rehabilitation,consider leave of absence from school/work, assess capacity to
manage finances, drug and EtOH cessation,sleep hygiene,social skills training, recruitment and
education of family members
A Randoumed Controlled Trialof Cognitive
Therapyfor Bipolar Disorder:focus onloug-Teim
Orange
J Clin Psychiatry 2006:67:277 86
Purpose: lo evaluate long term change with
cognitive therapy plus emotive techniqueslor the
treatment of bipolar disorder.
Methods: 3 - ded RCI including patents with DSM-IV
b poiar I or it disorder allocated to either a (mo trial
o!cognitive therapy (Cl) with emotive techniques
or treatment as usual.Both groups received mood
stobilirers. Main outcomes were relapse rates,
dysfunctional attitudes, psychosocialfuncliomag,
hopelessness,self-control, and medication
adherence.Patients were assessed by independent
raters htnded to treatmentgroup.
Results:At 6no.CT patientserepe rienced fewer
depressive symptoms and fewer dysfunctional
attitudes,
(here was a non sgr ficant (p-0.06) trend
to greater time to depressive relapse.At12mo followup,CT patents had lower Toung Mania Rating scores
and improved behavioural self -control. At IB mo.Cl
patients repotted letssoveiity ol illness.
Conclusions:Cl appearsto piovide benefitsin the12
mo after completion ol therapy.
Course and Prognosis
• high suicide rate ( 15% mortality from suicide), especially depressive episodes in mixed states
• bipolar I and II disorder are chronic conditions with a relapsing and remitting course featuring
alternating manic and depressive episodes;depressive symptoms tend to occur more frequently and
last longer than manic symptoms
• can achieve high level of functioning betsveen episodes
• may switch rapidly between depression and mania without any period of euthymia in between
• high recurrence rate for mania -90% will have a subsequent episode in the next 5 yr
• long term follow-up of bipolar 1 - 15% well, 45% well with relapses, 30% partial remission, 10%
chronically ill
Efficacy of Cognitive-Behavioural Therapy in
Patients withBipolar Disorder: A Meta-Analysis
dRandomited Controlled Trials
PLoS One 20U;12|5|:e01/6849
Purpose:lo determine the efficacy of cognitive
behavioural therapy (CBT)in the treatment of type I
and II bipolar disorder.
Methods:A systematic review and meta-arutyui of
RCIs of Cll in the trealmeof of adultswith bipolar
disorder.
Results:It nefeen RCIs includmg1284 patients with
type I or II BO weie included.C81 lowered the relapse
rate|pooUd 0R*0.506;95\ 0*
0.218 -0.921) end
improved depieisme symptoms|g
—0.494;95%
CI--0.963 to-D.026), mania seventy )
-0.581:95%
CM.127to-0.035), and psychosodal functioning
|g*
0.45J;95\0*
0.106-0.809). treater effects
weie seen with CBI treatment duration >90 mil.
Relapse rates were lower in people with type I bipolar
disorder.
CYCLOTHYMIA
Diagnosis
• presence of numerous periods of hypomanic and depressive symptoms(not meeting criteria for full
hypomanic episode or MDE) for 2 yr; never without symptoms for >2 mo
• have never met criteria for MDE, manic, or hypomanic episodes
• symptoms are not due to the direct physiological effects of a substance or GMC
• symptoms cause clinically significant distress or impairment in social, occupational,or other
important areas of functioning
Treatment
• similar to Bipolar I:mood stabilizer ± psychotherapy
Anxiety Disorders
Definition
• fear is a universal human experience which can serve as an adaptive mechanism to facilitate
appropriate reactions to external threat
• anxiety may be seen as pathological fear when:
fear is greatly out of proportion to risk/severity of threat
response continues beyond existence of threat (prolonged, excessive, etc.) or becomes generalized
to othersimilar or dissimilar situations
social or occupational functioning is impaired
r i
L J
+
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PS16 Psychiatry Toronto Notes 2023
•manifestations of anxiety are a result of the activation of the sympathetic nervous system and can be
described through:
physiology:main brain structure involved is the amygdala;neurotransmitters involved include
5-HT,cholecystokinin, epinephrine, norepinephrine,and DA
psychology:one’
sthoughts about a given situation orstimulus contribute to the feeling of fear and
perception of threat
• behaviour:anxiety can lead to avoidance which can perpetuate the fear/avoidance
• often comorbid with substance use and depression; more than 50°u have multiple anxiety
disorders
• when starting medication for anxiety:start low, go slow, aim high, and explain symptoms to
expect prior to initiation of therapy to prevent non-adherence due to side effects
• psychotherapy:individual or group CBT
Differential Diagnosis
Table 2. Differential Diagnosis of Anxiety Disorders
Post-Ml.arrhythmia,congestive heart failure,pulmonary embolus,mitral valve prolapse
Asthma.COPD.pneumonia
Hyperthyroidism,hypoglycemia,hyperadrenalism.hyperparathyroidism
Vitamin BUleficiency,folate deficiency,porphyria,hypoxemia.hypercalcemia
Neoplasm,vestibular dysfunction,encephalitis,trauma (contusion or hematoma).MS.temporal lobeepilepsy,migraine
Cerebral (meningitis,HIV.syphilis) or systemic
Gastritis,esophageal spasm
Substance-Induced Intoxication (caffeine,cannabis, amphetamines,cocaine,thyroid replacement,OTC for colds/decongestants, steroids),
withdrawal (benzodiazepines, alcohol)
Cardiovascular
Respiratory
Endocrine
Metabolic
Neurologic
Infectious
Gl
Medical Workup of Anxiety Disorder
• only proceed with medical workup as clinically indicated
• routine screening:vitals, physical exam, CBC, electrolytes,thyroid function test, glucose, EGG
• additionalscreening: extended electrolytes, vitamin Bi:, (5-HCG,folate, chest x-ray, any other tests as
per DDx in Table 2
Risk Factors for the Development of Anxiety Disorders
• biological
endocrine disorders (i.e. hyperthyroidism), respiratory conditions (i.e. asthma), CNS conditions
(Le.temporal lobe epilepsy),substances/medications(Le.excessive stimulant use), chronic
medical illness
personal or family history of anxiety or mood disorder
• XX>XY chromosomes
• psychological
• current stress,early childhood adversity or trauma, early parental loss, parental factors
Panic Disorder
DSM-5 DIAGNOSTIC CRITERIA FOR PANIC DISORDER
Reprintedwithpermission from the Diagnostic and Statistical Manual of Mental Disorders.Sth ed.2013.American PsychiatricAssociation
A.recurrent unexpected panic attacks; a panic attack is an abrupt surge of intense fear or intense
discomfort that reaches a peak within minutes, and during which time four (or more) of the following
symptoms occur
palpitations, pounding heart, or accelerated heart rate
sweating
trembling orshaking
sensations ofshortness of breath orsmothering
feelings of choking
• chest pain or discomfort
• nausea or abdominal distress
• feeling dizzy, unsteady,light-headed,or faint
• chills or heat sensations
paresthesias (numbness or tingling sensations)
• derealization (feelings of unreality) or depersonalization (being detached from oneself)
• fear of losing control or "
going crazy”
• fear of dying
B. at least one of the attacks has been followed by 1 mo (or more) of one or both of the following:
persistent concern or worry about additional panic attacks or their consequences
« a significant maladaptive change in behaviour related to the attacks
C.the disturbance is not attributable to the physiological effects of a substance or another medical
condition
D.the disturbance is not better explained by another mental disorder
Situational trigger Panic attack
t ]
Mentally
associated with
situation
Increased anxiety
and generalization
to other situations
Figure 2. Mechanism of panic
attacks
<§>
Criteria for Panic Attack (>4)
STUDENTS FEAR the 3 Cs
Sweating
Trembling/shaking
Unsteadiness,dizziness
Depersonalization.Derealization
Excessive heart rate,palpitations
Nausea 'abdominal distress
Tingling numbness
Shortness of breath
Fear of dying,losing control,going
crazy
3 Cs:Chest pain,Chills
'
hot flashes.
Choking
i.j
+
Duration typically 5-10 min
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PS17 Psychiatry Toronto Notes 2023
Epidemiology
• lifetime prevalence:5% (one of the top five most common reasons to see a family physician); M:l
'
=l:2-
3
• onset:average early-mid 20s, familial pattern
• comorbidities: depression, agoraphobia, medical comorbidity
Treatment
• pharmacological and psychological treatment together can be very effective
• psychological
CBT:exposure (graduated exposure to unpleasant sensations of arousal associated with a panic
attack for experiential disconfirmation of their fears), cognitive restructuring (addressing
underlying beliefs regarding the panic attacks),relaxation techniques (visualization, boxbreathing), psychoeducation
• pharmacological (first line agents)
• SSKIs:fluoxetine, citalopram, escitalopram, paroxetine,sertraline, fluvoxamine
SNR!: venlafaxine extended release
• with SSKI/SNKls,start with low doses and titrate up as tolerated
• anxiety disorders often require treatment at higher doses for a longer period of time than
depression (full response may take up to 12 wk)
treat for up to 1 yr aftersymptoms resolve to avoid relapse
explain expected adverse effects prior to initiation of therapy to prevent non-adherence
other antidepressants:(mirtazapine,TCAs)
benzodiazepines considered 2nd line (short-term,lowest effective dose, helpful while titrating
antidepressant)
Panic Attack vs. Panic Disorder
. Panic disorder requires recurrent
unexpected panic attacks + fear of
another panic attack
. Panic attacks can occur in the
context of many different disorders
Starting Medication for Anxiety
Start low. go slow, aim high, and explain
symptoms to expect prior to initiation of
therapy to prevent non-adherence due
to side effects
Prognosis
• 85% can achieve good results, 10-20% continue with significant symptoms. Longer term, 65% achieve
remission
• clinical course: chronic, but episodic with psychosocial stressors
Agoraphobia
DSM-5 DIAGNOSTIC CRITERIA FOR AGORAPHOBIA
Reprinted with permission from the Diagnostic and Statistical Manual ol Mental Disorders, 5th cd. 2013.American Psychiatric Association
A. marked fear or anxiety about two (or more) of the following five situations:
• using public transportation
being in open spaces
being in enclosed places
standing in line or being in a crowd
being outside of the home alone
B. the individual fears or avoids these situations because of thoughts that escape might be difficult or
help might not be available in the event of developing panic-like symptoms or other incapacitating
or embarrassing symptoms
C. the agoraphobic situations almost always provoke fear or anxiety
D. the agoraphobic situations are actively avoided, require the presence of a companion,or are
endured with intense fear or anxiety
L. the fear or anxiety is out of proportion to the actual danger posed by the agoraphobic situations and
to the sociocultural context
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'
.the fear, anxiety, or avoidance is persistent, typically lasting S6 mo
G. the fear, anxiety, or avoidance causes clinically significant distress or impairment in social,
occupational, or other important areas of functioning
H. if another medical condition is present,the fear,anxiety, or avoidance is clearly excessive
I. the fear, anxiety,or avoidance is not better explained by the symptoms of another mental disorder
and are not related exclusively to obsessions, perceived defects or flaws in physical appearance,
reminders of traumatic events,or fear ofseparation
Note: agoraphobia is diagnosed irrespective of the presence of panic disorder.If an individual'
s
presentation meets criteria for panic disorder and agoraphobia, both diagnosesshould be assigned
Treatment
• as per specific panic disorder
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PS18 Psychiatry Toronto Notes 2023
Generalized Anxiety Disorder
DSM-5 DIAGNOSTIC CRITERIA FOR GENERALIZED ANXIETY DISORDER
Reprinted with permission from the Diagnostic and Statistical Manual of Mental Disorders, Sth ed. 2013. American PsychiatricAssociation
A.excessive anxiety and worry (apprehensive expectation), occurring more days than not for at least 6
mo, about a number of events or activities (such as work or school performance)
B.the individual finds it difficult to control the worry
C.the anxiety and worry are associated with three (or more) of the following six symptoms(svith at least
some symptoms having been present for more days than not for the past 6 mo)
1.restlessness orfeeling keyed up or on edge
2.being easily fatigued
3. difficulty concentrating or mind going blank
4. irritability
5. muscle tension
6.sleep disturbance (difficulty falling orstaying asleep,or restless, unsatisfying sleep)
D.the anxiety,worry,or physicalsymptoms cause clinically significant distress or impairment in social,
occupational, or other important areas of functioning
E.the disturbance is not attributable to the physiological effects of a substance or another medical
condition
l
:
. the disturbance is not better explained by another mental disorder
Epidemiology
• I yr prevalence: 1-4%, lifetime prevalence 6%; M:l =l:2
8% of all who seek primary care treatment (WHO)
• in primary care: 70% initially present with physical symptoms as main concern
• bimodal age of onset: before 20 or middle adulthood
Source:Depression and other common mental disorders:Global health estimates.Geneva:World Health Organization. 2017.
Criteria for GAD (>3)
C-FIRST
Concentration issues
Fatigue
Irritability
Restlessness
Sleep disturbance
Tension (muscle)
Treatment
• lifestyle:avoid caffeine and EtOH,sleep hygiene
• psychological:CBT (cognitive restructuring), muscle relaxation techniques, mindfulness
• biological
1st line:SSRIs (escitalopram,sertraline, paroxetine),SNRls (venlafaxine XR, duloxetine),
pregabalin
benzodiazepines considered 2nd line (short-term, lowest effective dose, helpful while titrating
antidepressant)
• (1-blockers not recommended
Prognosis
• good with treatment
• depends on pre-morbid personality functioning,stability of relationships, work, and severity of
environmental stress
Social Anxiety
• definition:marked and persistent (>6 mo) fear ofsocial or performance situations in which one is
exposed to unfamiliar people or to possible scrutiny by others. They fear that they will be negatively
evaluated in a way that may be humiliating, embarrassing,or lead to rejection (e.g.public speaking,
initiating or maintaining conversation,dating, eating in public)
• situations are avoided or endured with intense anxiety and causes significant distress or impairment
in functioning
• lifetime prevalence 8-12%;M:F ratio approximately equal
Phobic Disorders
Specific Phobias
• definition: marked and persistent (>6 mo) fear that is excessive or unreasonable, cued by presence or
anticipation of a specific object or situation
• lifetime prevalence 10-13%; M:l
;
ratio variable
• types: animal/inscct, environment (e.g. heights,storms), blood/injection/injury,situational (e.g.
airplane, closed spaces), other (e.g. loud noise,clowns), multiple fears
Diagnostic Criteria for Phobic Disorders
• marked fear/anxiety about a specific object/situation
• exposure to stimulus almost invariably provokes an immediate fear/anxiety response; may present as
a panic attack
• phobic object/situation is actively avoided or endured with intense anxiety.
• fear/anxiety out of proportion to actual danger/sociocultural context and persistent (lasting 6 mo or
more)
• person recognizes fear as excessive or unreasonable
• significant impact on daily routine, occupational/social functioning, and/or marked distress
LJ
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