MOOD DISORDERS ASSESSMENT & MANAGEMENT
Dr Aparna Laddipeerla MBBS DPM Senior Psychiatry Registrar
Country Health SA
You should be familiar with:
• The clinical features of Mood Disorders: • Major Depressive Disorder
• Dysthymic Disorder
• Bipolar Disorders
• Cyclothymic Disorder
• Other disorders with affective features: • Schizoaffective Disorder
• Adjustment Disorders
• Mood Disorder due to General Medical Condition
• Mood Disorder due to Substances
• How to assess an affective presentation
• Treatment of Mood Disorders • Pharmacology of anti-depressants and mood stabilising agents
• ECT
• Psychotherapies
• Other supportive measures
Learning objectives
Framework
THEORY
• Epidemiology
• Etiology
• Clinical features
• Diagnosis DD
• Management
PRACTICE
• HPC
• PH
• FH
• PH
• MSE
• Unipolar vs. bipolar
• DSM-IV-TR
NB. Unipolar MDD may be an unstable diagnosis over time
Classifications
Unipolar Bipolar
DSM-IV-TR Major Depressive
Disorder
Dysthymic
Disorder
Bipolar I Disorder
Bipolar II Disorder
Bipolar Disorder NOS
Cyclothymic Disorder
(“bipolar spectrum”)
• Gender
Major Depressive Disorder F:M=2:1
Bipolar disorders (all) F:M=1:1
(Some subtype has gender preponderance)
• Age of onset
BDs <20 yrs
Dysthymic Disorder Childhood – adolescence
Recurrent MDD 30-35 yrs
Single episode MDD Mid-late adulthood
Epidemiology
Epidemiology
DEPRESSION
• Life time prevalence –20%
• Co-morbidity is the rule
• National Co morbidity survey and Epidemiological Catchment Area survey (ECA) -74% & 75% respectively with other lifetime diagnoses
• Risk –ECA study-Lifetime risk of suicide 7.9% , 19.5% with concurrent alcohol and drug misuse
• Risk of suicide 21times that of normal population
BIPOLAR DISORDER
• 65% co morbidity
• High SMR´s: 15–20 times
more likely to die by
suicide
• High rates of
cardiovascular disease
‘SKETCH ARTIST’ MISTAKE:
TOO LITTLE INFORMATION
CASE EXAMPLE:
XYZ is a 44 yr old Caucasian female, currently in a relationship with a 37 yr old man on Disability support pension, lives with her 9 yr old son, also has a 5 year old daughter who doesn’t live with her. She has been on unemployment benefits for the last 2 years. She is currently a voluntary in-patient on the ward. She gives a 2 year history of depressive symptoms.
Establish broad spectrum
• –neurosis, depression or psychosis
• Once domain breached establish diagnosis according to
DSM criteria.
• Follow up immediately with most important co morbidities
and differentials.
• Depression-bipolarity, anxiety, substance misuse and
personality dysfunction
• Psychosis- depression, mania, substance misuse or
schizophrenia
• Establish criteria for domains!!
• At least 5 of the following occurring nearly every day (except for #9) over at least 2 weeks, which are a change from previous functioning:
1) Depressed mood, most of the day*
2) Loss of interest or pleasure, most of the day*
3) Psychomotor agitation or retardation
4) or appetite, or significant weight loss or gain
5) Insomnia or hypersomnia
6) Loss of energy
7) concentration or indecisiveness
8) Feelings of worthlessness or excessive/inappropriate guilt
9) Recurrent thoughts of death or suicide
*One of the symptoms must be either (1) or (2)
• Symptoms cause clinically significant distress or functional impairment
• Excludes bereavement, substance, general medical condition and mixed episode
DSM-IV-TR criteria for MDD
• With Catatonic Features
• rare
• With Melancholic Features
• older people
• no pre-morbid personality traits
• marked weight loss, early morning wakening, psychomotor retardation/agitation, diurnal mood variation, anhedonia
• can present with delusions (psychotic depression)
• responds well to antidepressants and ECT
• responds less well to psychotherapies
• With Atypical Features
• With Postpartum Onset
MDE Subtypes
• Dysthymic Disorder • DSM-IV-TR criteria:
• Depressed mood plus at least 2 other symptoms Poor appetite or overeating Insomnia or hypersomnia Low energy or fatigue Poor concentration or indecisiveness Feelings of hopelessness Low self-esteem
• For most days over at least 2 years, during which no asymptomatic periods have exceeded 2 months
• Cyclothymic Disorder • DSM-IV-TR criteria:
• Fluctuating mood over at least 2 years, involving numerous periods of hypomanic and depressive symptoms, which do not meet the criteria for Manic Episode or Major Depressive Episode
• No asymptomatic periods have exceeded 2 months
Longitudinal diagnosis: Mood Disorders
- Dysthymic and Cyclothymic Disorders
• Individuals with mood disorders
• Risk of substance use disorders (especially alcohol)
• Risk of anxiety disorders (e.g. OCD, panic disorder, social anxiety disorder)
• Magnitude of risk:
• Bipolar disorders > MDD > general population
• Risk of mood disorders in those with • Substance use disorders
• Anxiety disorders
• Some personality disorders
• Medical co-morbitidy
Comorbidity
Depression
• Anxiety
• Bipolarity
• Substance misuse
• Personality disorder
Depression • How are you feeling in yourself / in your spirits. On a scale of 1-10 if 10 was really down
where would you put yourself. How long does it last for? (mood, clinical depression)
• Have you been tearful lately? (mood)
• When was the last time you smiled/cried? (mood)
• What are the kinds of things you normally enjoy doing. / how do you spend your day? (anhedonia)
• If TV, mowing the lawn etc -have you been enjoying these things as much as you’ve done in the past. (anhedonia)
• When was the last time you played….(anhedonia)
• What have your energy levels been like. / do your energy levels keep up with .e.g. physical work (anergia)
• What about your concentration/ how long can you read a book for/ do you find it difficult taking things in when watching TV or reading a book .Has that affected your work? (anergia)
• What are your plans for the future? /How do you see your future? (hopelessness)
• Is there anything hurting your conscience? Have you been blaming yourself lately? (guilt)
• Do you feel there is something wrong with functioning of your body? (hypochondriacal ideation)
• What about your confidence levels? (self esteem, self confidence)
• Do you think other people would be better off without you? (worthlessness)
ANY SUGGESTIONS/ INSIGHTS INTO ASKING
THESE QUESTIONS OR STARTING THIS
CONVERSATION?
-Listen to patients’ cues: use experience-near terms (down not ‘depressed’)
• CLUB 2 OR 3 CRITERIA:
NEGATIVE THOUGHTS (GUILT, HOPELESS, HELPLESS,
WORTHLESS) OR
PHYSICAL EFFECTS (PANIC ATTACKS, ENERGY, MEMORY,
CONCENTRATION, SLEEP, APPETITE CHANGES ETC.) OR
EMOTIONS (SAD, DIURNAL VARIATION, ANHEDONIA, CRYING)
OR
BEHAVIOURS (AVOIDANCE, SOCIAL ISOLATION, POOR
FUNCTIONING, DRINKING)
-Cognitive model (depression & mania)
-Psychosis: positive, negative, cognitive domains & mood
Anxiety: …
STRESSORS & PRECIPITANT(S)
What does the ‘precipitant’ tell us?
“Could you please tell me how you came about to being in hospital?”
Chronic histories- “I wonder what made you seek help now!” “Why now?”
Risk factors Sociodemographic factors
Life stressors
Sociodemographic factors
• Largely weak correlation • Marital status
• Separation/divorce: Bipolar > MDD > Dysthymia
• Socioeconomic status • Lower SES: MDD and BD
• Geography • Distance from the Equator
• Distal from the Equator: Depression
• Proximity to the Equator: Mania
• Western > Far Eastern countries
• Urbanicity • Urban residence > Rural
residence
• Season • Spring & Autumn: Depression
• Summer: Mania
• Diet • Folate
• Omega-3-fatty-acids
• Western diet > Traditional diet
• Physical activity • with MDD
• Adiposity • with MDD
Life stressors
• Life stressors
• Stressors are not all the same in pertinence
• Less consistent association with bipolar disorder and melancholic/psychotic MDD cf non-melancholic/non-psychotic MDD
• Association with number of episodes (“kindling”)
• For non-melancholic/non-psychotic MDD:
• Cumulative stress (series, chronic) more important than acute stressors
• Early life adversities: E.g. Poor parental relationship, prolonged separation from parent, intrafamilial sexual abuse
• Early parental death (before adolescence)
• For bipolar disorder:
• Disruption in biorhythm
• Negative and positive “stress”
• Social support
• Social isolation: MDD
RISK ISSUES CASE EXAMPLE:
XYZ is a 44 yr old Caucasian female, currently in a relationship with a 37 yr old man on Disability support pension, lives with her 9 yr old son, also has a 5 year old daughter who doesn’t live with her. She has been on unemployment benefits for the last 2 years. She is currently a voluntary in-patient on the ward. She gives a 2 year history of depressive symptoms.
Suicidal ideation
• Sometimes when people get depressed they may find life not
worth living? Have you felt like this ….?
• What thoughts have crossed your mind? (ideation)
• How long have you been thinking about this? (intent/ideation)
• What have you planned? (plans)
• Have you made arrangements for after your death e.g. made a
will or written a note? (intent)
• How close have you come to actually carrying out your plan?(
take patient through) (intent)
• What stopped you/stops you? (protective factors)
• Is there anything to live for at all? Mention friends , family
(protective factors)
Suicidal Attempt
• Go through detail of attempt
• Alcohol
• Seriousness
• Impulsivity-How long had you been planning this?
• Did you make any arrangements for your death e.g. note,
will , finances
• How do you feel now that you have survived?
• Do you really want to die/ have you actually imagined
yourself dead?
• Do you currently have any thoughts of suicide?
BIPOLAR DISORDER
DSM-IV-TR criteria for mania: Distinct period of abnormally & persistently elevated,
expansive or irritable mood, lasting at least 1 week (or if
hospitalised)
Plus 3 of (4 if mood is only irritable): 1) Inflated self-esteem or grandiosity
2) Decreased need for sleep
3) More talkative or pressure to keep talking
4) Flight of ideas or racing thoughts
5) Distractibility
6) Increase in goal-directed activity or psychomotor agitation
7) Excessive involvement in activities that have a high potential for
painful consequences
Severity: cause marked functional impairment, necessitate
hospitalisation, or if psychotic
Exclusion: direct physiological effects of a substance or general
medical condition
• A less severe form of mania
• DSM-IV-TR criteria is the same as Manic Episode, except:
• Duration: at least 4 days (rather than 1 week)
• No psychotic symptoms
• No hospitalisation
• Not severe enough to cause marked impairment in functioning
• Criticism
• Duration is too long
• Recognised brief hypomanic episodes (1-2 days) are common among those
with bipolar disorders
• Subthreshold symptoms still clinically and functionally significant
Hypomanic Episode
• Concurrent presence of both depressive & manic symptoms
• DSM-IV-TR criteria:
• Concurrent fulfilment of criteria for Major Depressive Episode and Manic Episode for at least 1 week
• In broader terms, subthreshold “mixed states” refer to “non-pure” depressive or manic states
• Intrusion of manic features in depression
or
• Intrusion of depressive features in mania
• Mixed Episode and subthreshold mixed states signal bipolarity
Mixed Episode
• History of a single MDE or recurrent MDEs
= Major Depressive Disorder
• History of a single or recurrent Manic or Mixed Episode(s)
+/- MDE(s)
= Bipolar I Disorder
• History of both MDE(s) + Hypomanic Episode(s)
= Bipolar II Disorder
• Schizophrenia + any mood episode
= Schizoaffective Disorder (MDD or Bipolar types)
Longitudinal diagnosis: Mood Disorders
AKISKAL
Bipolar Illness (Mania) • Have you ever had the opposite of depression when you have been extremely
happy, over the top , doing things out of character for 2 weeks or more.? (mood)
• If yes clarify again how long does it last for (DD borderline construct)
• Had you/ have you taken on any new activities? (increased goal directed activity)
• What's your sleep been like. Do you feel like you can work all day without needing rest/ do you feel like you don’t need much sleep ? (decreased need for sleep)
• How do you see yourself in comparison to others./ do you consider yourself special in any way? (grandiosity)
• Do you think god has a special purpose for you here? (grandiosity/ delusions)
• Do you find your thoughts racing? (increased psycho(motor) activity)
• Have your friends commented on the way you talk/ too fast? (pressure of speech)
• Have you done any things that may be out of character for you like spending excessive amounts of money, promiscuity ? (reckless behaviour)
• Also ask for depressive symptoms to establish a mixed episode
RISKS Harm to self/ others/ dependents
Past History
• Previous admissions –diagnosis
• Trigger
• Medications/ Psychotherapy
• Leading Q’s- Carbamazepine, Lithium, Valproate
ECT , injections (Depots)
• Self harm
Medical
• Have you had any significant medical illnesses such
as…………diabetes, high blood pressure, seizures/ a
significant head injury
• Diabetes, HT-vascular hypothesis
• Head injury and epilepsy ( composite neuropsychiatric
hypothesis)
• Investigations & treatment
ANY OTHER MEDICAL HISTORY
FOR MOOD DISORDERS
If there is: eg. my patient in the exam had an anaphylactic reaction/ allergy (CL
rotation)
ANY OTHER MEDICAL HISTORY
FOR MOOD DISORDERS
• Temporal correlation
• Medications
• Current state & prognosis
• Stress
Family History
• Is there anyone in your family that has a significant mental
health problem/issue / nervous breakdown such as
parents, uncles, cousins, grandparents….depression,
bipolar /manic depression, schizophrenia
• Has anyone in your family tried to take their own life
(suicide)?
• What about problems with drugs, or alcohol or violence?
• USE OF GENOGRAM
Family history
• Stronger family history in bipolar disorders and early onset MDD
• For 1st degree relatives:
• Risk of BD with BD proband: 7x general population
• Risk of MDD with MDD proband: 2-3x general population
• Cross-over risk:
• BP probands: risk of MDD (MDD>BD)
• UP probands: Minimally risk of BD
• Twin concordance:
• BD: MZ 40% DZ 10%
• MDD: MZ 30% DZ 20%
• Overlap between bipolar disorder and schizophrenia
Genetic
Counselling
Patients frequently ask
clinicians two questions:
1) Are mood disorders
genetic?
2) What is the risk to
my children or
grandchildren?
Genetic Counselling
• Yes, mood disorders are genetic.
• The risk to children and grandchildren is the more difficult question -The family data
indicate that if one parent has a mood disorder, then a child will have a risk for mood
disorder of b/w 10- 25%. If both parents are affected, then this risk roughly doubles
(50%).
• Greater risk :
1. more members affected
2. affected family members are first-degree relatives
3. family history of bipolar disorder (+specifically, a much greater risk for bipolar
disorder)
4. presence of more severe illness
Future Directions
• Though much is understood about the familiality and heritability of mood
disorders, the identification of specific genes has been challenging.
• Studies to date have reproducibly identified a number of genes, although
these genes together explain only a small portion of the genetic variance.
• It remains unclear how many genes are involved and how the illness is
transmitted.
PERSONAL HISTORY
CASE EXAMPLE: XYZ is a 44 yr old Caucasian female, currently in a relationship with a 37 yr old man on Disability support pension, lives with her 9 yr old son, also has a 5 year old daughter who doesn’t live with her. She has been on unemployment benefits for the last 2 years. She is currently a voluntary in-patient on the ward. She gives a 2 year history of depressive symptoms.
Background of 3 previous significant depressive episodes, post natal depression, significant self-harm episode and treatment with ECT, several antidepressants, lithium and psychological treatment and strong family history
Domains
• Birth & development- “Did mom have PND?”
• Childhood- Nurturing, discipline, home atmosphere, Temperament
• Trauma- major developmental disruption, identification, scapegoating.
• Adolescence-
• Education- “How did you get along with?” “Were you bullied? Did you bully
others?”
• Occupation- “How long have you been?” “How do you get along?”
• Relationships-
• “What did you like about her/ him?” “What led to the break-up?”
• “How many children do you have?”
• Sexual history
Personality
• Life/ PMP- “How would you describe yourself? How
would others describe you? How do you cope with stress?
What are your ambitions/ goals?”
• You get major clues from how people cope or appraise
illness, forensic history, relationship and work history.
Forensic history
• Have you ever been in trouble with the police? yes-
• Have you ever been charged or convicted? Ask for
charges
• Have you ever been in jail?-period
• If no-have you ever been violent towards others?
MENTAL STATE EXAMINATION
MSE (http://aitlvideo.uc.edu/aitl/MSE/MSEkm.swf)
• A) Paint a picture of the person in front
of you= Personal description(novelist
like) +general – apparent age, physical
stigmata, attire, hygiene, eye contact,
attitude
• B) Psychomotor activity (examiner’s
description of amount of motor and
cognitive activity by the pt- excessive &
non productive or visible slowing of
thoughts, speech & movements)
• C) Speech is examiner’s description of
pt’s ability to articulate thoughts. (RATE;
AMOUNT; PRAGMATICS-inflection,
reciprocal flow, articulation); Thought
form/ process/ content (delusions/
overvalued ideas/ obsessions/
ruminations/ suicidal or homicidal
ideation)
• A) CHARACTER, INTENSITY, RANGE;
REACTIVITY; APPROPRIATENESS;
MOBILITY; difficulty initiating, sustaining
or terminating emotional response. Give
examples.
• P) Mental process by which sensory
stimuli are brought to awareness.
Hallucinations/ illusions/
depersonalisation/ derealisation/
agnosia/ synaesthesia.
• C) Cognition- AOCM
• I) Recognition of having a mental illness
and the degree of personal awareness
and understanding of the illness.
• J) How does all the mental state you
have presented impact on decision
making regarding action. Clearly key
ones = suicide, risk to others and ability
to self care. Again don’t make global
statements without discussion – not
adequate to say “ judgement is
impaired” without saying why and how;
Social j. (subtle manifestations of
behaviour that are harmful to the patient
and are contrary to acceptable
behaviour in the culture, whether the
patient understands the likely outcome
of personal behaviour and is influenced
by that understanding.) Test j.
• R) Attitude towards the examiner and
the countertransference.
Marjorie
Insight
• What in your opinion is the issue/causing this distress?
• What do you think would help you?
• Do you think medication/talking therapy would help you?
DIAGNOSIS AXIS I- V
Consider 2 components:
• Cross-sectional clinical picture Does the picture fit with a mood syndrome (that is pathological)?
A mood episode i.e. major depressive, manic, hypomanic, mixed
Others e.g. Adjustment Disorders, Mood Disorder due to a GMC, Substance-Induced Mood Disorder
• Longitudinal clinical picture History of only MDE(s) = MDD
History of both MDE(s) and Hypomanic Episode(s) = Bipolar II Disorder
History of at least one Manic or Mixed episode = Bipolar I Disorder
Schizophrenia + any mood episode = Schizoaffective Disorder (MDD or Bipolar types)
Chronic low-grade depression = Dysthymic Disorder
Chronic low-grade bipolarity = Cyclothymic Disorder
*The combination of dysthymia and MDD is often called “double depression”
Diagnosis: Summary
Ms XYZ is a … who presents with a h/o…. (Crises or Axis I) associated with …
(risks). This is in the context of …stressor (grief/ re-traumatisation/ rejection).
Predisposing factors (PH,FH, PH) to XYZ’s mental illness include
Perpetuating factors (axis II/ III) include
Precipitating factors (axis II/ III/ IV) for the current exacerbation include
Protective factors
Formulation 4 Ps
Cultural
Bio Psycho Social
PREDISPOSING
PERPETUATING
PRECIPITATING
Biological
• Genetic predisposition
• Neurodevelopmental hypothesis (schizophrenia)
• Drugs and alcohol (schizophrenia)
• Head injury
• Epilepsy
• Other medical conditions
• Drugs causing psychiatric conditions
Psychological- Psychodynamic
• Response to Loss/Anger Turned Inward: LOSS
• Narcissistic vulnerability (from early loss or experiences with parents perceived as traumatically unempathic, frustrating, or rejecting): FAILURE
• Insecure attachments : RELATIONSHIP BREAKUPS
• Freud described mania as a fusion of the ego with its superego; defense mechanism of denial
• Mania could be considered a defensive reaction to depression.
Psychological theories: Cognitive
• Cognitive
• The cognitive model is based on the recognition that an individual's
idiosyncratic perception of events affects his or her emotions and
behaviors.
• Triad of Affect, Behaviour, Cognition
• Negative cognitive schemata negative automatic thoughts
(cognitive distortions) depressed mood and behaviours
• Cognitive triad of negativity toward self, environment & future
• Foundation of CBT
Aaron Beck
Cognitive Model: Bipolar Illness
• Based on Diathesis stress model
• Patients with bipolar disorder also have an inherent
underlying biological vulnerability for instability of
circadian rhythms and motivational system controlling
reward and approach
Interpersonal therapy
• In simplest terms, interpersonal theory as applied to IPT can be understood as a link between mood and events
• For all people, upsetting external events evoke a sad or demoralized mood: In lay terms, they are “depressing.” For biologically or environmentally predisposed individuals, however, a sufficiently disturbing life event can trigger an episode of major depression
• 4 domains: grief, role transition, role disputes, interpersonal deficits
SOCIO-CULTURAL
Causes of poor mental health in
Aboriginal people • Intergenerational transmission of trauma through
psychodynamic, sociocultural and genetic mechanisms (Kellerman ,2001)
• Grief, loss and trauma resulting from high mortality rates, loss of land and culture and continuing impact of political policies that result in sociocultural dislocation
• Unresolved identity issues has been identified as source of stressor when people had not dealt with or felt they had lost or were uncertain about their aboriginal identity. (Swan P and Raphael B, 1995)
• Poor access to mental health services underpinned by cultural disparities
DIFFERENTIAL DIAGNOSIS
• Adjustment Disorders • An Adjustment Disorder is a psychological response to an identifiable
stressor that results in clinically significant symptoms. • DSM-IV-TR criteria:
• Clinically significant emotional or behavioural symptoms in response to an identifiable stressor(s), occurring within 3 months of its (their) onset & not persisting beyond 6 months upon its (their) termination.
• Clinical significance is defined as either marked distress in excess of what one would generally expect relative to the stressor(s), or significant impairment in social or occupational functioning.
• Symptoms do not represent bereavement or meet the criteria for another Axis I disorder.
• Mood Disorders due to Substances
• Mood Disorders due to a General Medical Condition
Other disorders with mood features
Depression vs. Grief
• Grief • Response to loss, threatened or actual
• Kübler-Ross’ stages of anticipatory grief (1969) • Denial, Anger, Bargaining, Depression, Acceptance
Not chronological or “stage-wise” progression
Not necessarily experience these
• Wide variations from person to person • Influenced by many factors:
• Personality, coping style, resilience
• Past experience of losses & traumas
• Nature & quality of relationship with lost object
• Available supports
• Culture
• Spiritual beliefs
• Duration varies, can be ongoing
Depression vs. Grief
Grief Depression
Symptoms occur in waves Low mood is persistent
Reactivity preserved Symptoms are pervasive
Yearning/longing a prominent
part of the affect
Apathy among range of
affects
Preserved hedonic capacity Anhedonic
Preserved self-esteem Worthlessness
Able to look forward to the
future
Hopelessness
MANAGEMENT OF MOOD DISORDERS
SHORT TERM
LONG TERM
RISK ASSESSMENT Static v/s dynamic
Acute v/s chronic
Intent Plan Means
• HIGH
• CHRONIC
• LOW
• CHRONIC
• HIGH
• ACUTE
• LOW
• ACUTE
CHRONIC
ACUTE
LOW HIGH
RANZCP GUIDELINES
Initial Clinical Assessment
CLARIFICATION & CONFIRMATION OF DIAGNOSIS
• Anti-depressants
• SSRI (Selective Serotonin Reuptake Inhibitor)
• sertraline, citalopram, escitalopram, fluoxetine, paroxetine, fluvoxamine
• SNRI (Serotonin Noradrenaline Reuptake Inhibitor)
• venlafaxine, desvenlafaxine, duloxetine
• NaSSA (Noradrenergic and Specific Serotonergic Antidepressant)
• mirtazapine, mianserin
• NARI (Noradrenaline Reuptake Inhibitor)
• reboxetine
• TCA (Tricyclic Antidepressant)
• MAOI (Monoamine Oxidase Inhibitor)
• tranylcypromine
• RIMA (Reversible Inhibitor of Monoamine Oxidase A)
• Moclobemide
• Agomelatine
• Mood stabilising agents
• Lithium
• Mood stabilising anti-convulsants (Na valproate, carbamazepine, lamotrigine)
• Atypical antipsychotics
Pharmacotherapy
DEPRESSION
Summary of STAR*D guidelines
• Number of patients that participated in medication trials
was 4 times that of Psychotherapy
• In primary switch any option is reasonable and no
statistical difference between different classes
• Cognitive therapy did as well as medication switching and
augmentation
• Overall 70% remission after 4 levels
• Not applicable for Psychotic depression
Treatment resistant depression
• Greater than or equal to 2 adequate monotherapy trials with antidepressants of 2 different classes fail to elicit a therapeutic response (APA DSM 2003)
• Prevalence :10-30% (Joffe,1996)
• Misdiagnosis
• Non-Compliance
• Inadequate duration, dose
• Psychosocial factors
• Medical condition –e.g. Hypothyroidism
• Drugs-B-Blockers, Methyldopa
Psychotic Depression
• First line –TCA +antipsychotic
• ECT is effective treatment
• 2 metaanalyses (Spiker,1985 & Parker,1992): 80%
response rate to ECT
• 80% response rate to combination antidepressant and
antipsychotic
• 33% to antipsychotic alone
• 25% to antidepressant alone
ECT
• Unilateral placement associated with less severe cognitive deficits
• Case by case basis
• Standard practice: D’Eliaposition (Non-Dominant unilateral ECT)
• If no response after 4-6 sessions consider Bilateral
• Stimulus dosing –titration method /fixed dose
• RUL-2.5-3 times seizure threshold
• BL-1.5 times seizure threshold
• Other types: Bifrontal , Right frontotemporal and left frontal
• EEG characteristics for response : short recruitment phase , high amplitude slow
waves, morphological regularity, bilateral synchronicity , post seizure suppression
• Inadequate seizures –<20-30sec EEG evidence
• Procedure
• General anaesthetic (pre-anaesthetic work up required)
• Frequency usually 3 times per week at the start, can be reduced as
clinically indicated
• Maintenance ECT can be an option
ECT - 2
ECT - 3
• First session: “Titration” (determine seizure threshold)
• Paralysed (minimal motor activity)
• Adequacy of seizure as determined by EEG tracing
• Minimum duration: 20 seconds
• Response judged on clinical basis
• Total number of treatments depend on response & tolerability
• Contraindication • Raised intracranial pressure
• Relative contraindications:
• Recent CVA
• Cerebral aneurysm or vascular malformations
• Unstable cardiovascular condition
• High anaesthetic risk
• Risks & adverse effects • General anaesthetic
• Post-ictal confusion
• Memory loss (anterograde & retrograde)
• Headache, aches and pains
• Chipped tooth, skin burns
ECT - 4
• Consent
• Informed consent from patient
or
• Guardianship Board consent
*Note: Detention is inadequate to give involuntary ECT
ECT - 5
BIPOLAR DISORDER
RANZCP- Treatment of manic episode
Texas Implementation of Medication Algorithm -Bipolar
I Disorder (Suppes, 2005 )
TIMA guidelines –Maintenance
Treatment: Hypomania/Mania
TIMA Guidelines –Maintenance Treatment +
Most Recent Episode Depression
Long term
THANK YOU Questions?