Julianna Borbely and Ann Stewart, chapter editors John Hanlon and Andrea Mok, associate editors Caroline Collins, EBM editor Dr. Jodi Lofchy and Dr. Johanne Roberge, staff editors The Psychiatric Assessment History Mental Status Exam Summary of Axes Mini-Mental Status Exam (Folstein) Psychotic Disorders Differential Diagnosis of Psychosis Schizophrenia Mood Disorders Mood Episodes Depressive Disorders Bipolar Disorders Anxiety Disorders Panic Disorder Generalized Anxiety Disorder (GAD) Phobic Disorders Obsessive-Compulsive Disorder (OCD) Post-Traumatic Stress Disorder (PTSD) Eating Disorders Anorexia Nervosa Bulimia Nervosa Personality Disorders Pharmacotherapy Antipsychotics Antidepressants Mood Stabilizers Anxiolytics Electroconvulsive Therapy (ECT)
Diagnostic Criteria reprinted with permission from the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision. 2000 American Psychiatric Association.
Chief Complaint
in patients own words duration, previous history of disorder or treatment
Speech
rate (e.g. pressured, slowed), rhythm/fluency, volume, tone, articulation, quantity, spontaneity
Thought Process
coherence coherent, incoherent logic logic, illogical stream goal-directed circumstantiality speech that is indirect and delayed in reaching its goal; eventually comes back to the point tangentiality speech is oblique or irrelevant; does not come back to the original point loosening of associations illogical shifting between topics flight of ideas skipping verbally from one idea to another where the ideas are marginally connected word salad jumble of words lacking meaning or logical coherence perseveration repetition of phrases or words echolalia thought blocking sudden cessation of flow of thought and speech clang associations speech based on sound such as rhyming or punning
Thought Content
suicidal ideation/homicidal ideation low fleeting thoughts, no formulated plan, no intent intermediate more frequent ideation, well formulated plan, no active intent high persistent ideation and profound hopelessness/anger, well formulated plan and active intent, believes suicide/homicide is the only helpful option available obsession recurrent and persistent thought, impulse or image which is intrusive or inappropriate cannot be stopped by logic or reason causes marked anxiety and distress common themes: contamination, orderliness, sexual, pathological doubt/worry/guilt pre-occupations, ruminations (reflections/thoughts at length) overvalued ideas magical thinking ideas of reference (unusual/odd beliefs that are not of delusional proportions) delusion a fixed false belief that is out of keeping with a persons cultural or religious background and is firmly held despite incontrovertible proof to the contrary first rank symptoms: thought insertion/withdrawal/broadcasting; delusions of control belief that ones thoughts/actions are controlled by some external source
Perception
hallucination sensory perception in the absence of external stimuli that is similar in quality to a true perception; auditory (most common), visual, gustatory, olfactory, tactile illusion misperception of a real external stimulus depersonalization change in self-awareness such that the person feels unreal, detached from his or her body, and/or unable to feel emotion
Cognition
level of consciousness orientation: time, place, person memory: immediate, recent, remote intellectual functions attention, concentration, calculation, abstraction (proverb interpretation, similarities test), language, communication
Insight
patients ability to realize that he or she has a physical or mental illness and to understand its implications
Judgement
ability to understand relationships between facts and draw conclusions that determine ones action
Summary of Axes
Multiaxial Assessment Axis I Axis II Axis III Axis IV Axis V Formulation
a diagram outlining current issues and interrelations between an individual's biological, psychological, and social factors for each category: predisposing, precipitating, perpetuating, and protecting factors differential diagnosis of DSM-IV clinical disorders personality disorders; mental retardation general medical conditions that are potentially relevant to the understanding or management of the mental disorder psychosocial and environmental issues global assessment of functioning (GAF, 0 to 100) incorporating effects of Axes I to IV
Memory
immediate recall [3 points] ask patient to immediately repeat the following 3 words: honesty, tulip, black delayed recall [3 points] ask patient to recall the 3 words previously given, after approximately 5 minutes
Language Tests
comprehension (three stage command) [3 points] take this piece of paper in your left hand, fold it in half, and place it on the floor (Note: tell patient to take paper in non-dominant hand) reading [1 point] ask patient to read the words close your eyes on a piece of paper, and then to do what it says writing [1 point] ask patient to write any complete sentence repetition [1 point] repeat no ifs, ands, or buts naming [2 points] point to a watch and pen and ask patient to name them
Interpretation
total score out of 30, abnormal if < 24 needs further investigation gross screen for cognitive dysfunction: 20-24 mild; 10-19 moderate; < 10 severe other items not officially part of the Folstein include drawing a clock with the time showing 10 after 11; asking patient to name as many animals or words as possible beginning with the letter f in one minute; linking a series of numbers or letters in order; copying a diagram of alternating shapes (test for perseveration)
Source: Folstein MF, Folstein SE and McHugh PR (1975). Mini-Mental State: A practical method for grading the state of patients for the cllinician. Journal of Psychiatric Research. 12: 189-198.
Psychotic Disorders
Definition
characterized by a significant impairment in reality testing delusions or hallucinations (with/without insight into their pathological nature) behaviour so disorganized that it is reasonable to infer that reality testing is disturbed
Schizophrenia
DSM-IV-TR Diagnostic Criteria for Schizophrenia
A. characteristic symptoms (active phase): 2 or more of the following, each present for a significant portion of time during a 1-month period (or less if successfully treated): delusions hallucinations disorganized speech (e.g. frequent derailment or incoherence) grossly disorganized or catatonic behaviour negative symptoms, i.e. affective flattening, alogia (inability to speak), or avolition (inability to initiate and persist in goal-directed activities) Note: only 1 A symptom is required if delusions are bizarre or hallucinations consist of a voice keeping a running commentary on the person's behaviour or thoughts, or 2 or more voices conversing with each other B. social/occupational dysfunction: ? 1 major areas of functioning (work, interpersonal relations, self-care) markedly below the level achieved prior to the onset of symptoms C. continuous signs of disturbance for at least 6 months, including at least 1 month of active phase symptoms; may include prodromal or residual phases D. schizoaffective and mood disorders excluded E. the disturbance is not due to the direct physiological effects of a substance or a general medical condition (GMC) F. if history of pervasive developmental disorder, additional diagnosis of schizophrenia is made only if prominent delusions or hallucinations are also present for at least 1 month
Subtypes
paranoid preoccupation with one or more delusions (typically persecutory or grandiose) or frequent auditory hallucinations relative preservation of cognitive functioning and affect; onset tends to be later in life; believed to have the best prognosis catatonic at least two of: motor immobility (catalepsy or stupor); excessive motor activity (purposeless, not influenced by external stimuli); extreme negativism (resistance to instructions/attempts to be moved) or mutism; peculiar voluntary movement (posturing, stereotyped movements, prominent mannerisms); echolalia (repeating words/phrases of anothers speech) or echopraxia (imitative repetition of anothers movements, gestures or posture) disorganized
disorganized speech and behaviour; flat or inappropriate affect poor premorbid personality, early and insidious onset, and continuous course without significant remissions undifferentiated symptoms of criteria A met, but does not fall into the 3 previous subtypes residual absence of prominent delusions, hallucinations, disorganized speech, grossly disorganized or catatonic behaviour continuing evidence of disturbance indicated by the presence of negative symptoms or two or more symptoms in criteria A present in attenuated form
Epidemiology
prevalence: 0.5%-1%; M:F = 1:1 mean age of onset: females ~27; males ~21
Etiology
multifactorial: disorder is a result of interaction between both biological and environmental factors genetic 50% concordance in monozygotic (MZ) twins; 40% if both parents have schizophrenia; 10% of dizygotic (DZ) twins, siblings, children affected neurochemistry dopamine hypothesis theory: excess activity in the mesolimbic dopamine pathway may mediate the positive symptoms of psychosis (i.e. delusions, hallucinations, disorganized speech and behaviour, and agitation) neuroanatomy decreased frontal lobe function, asymmetric temporal/limbic function, decreased basal ganglia function; subtle changes in thalamus, cortex, corpus callosum, and ventricles; cytoarchitectural abnormalities neuroendocrinology - abnormal growth hormone (GH), prolactin (PRL), cortisol, and adrenocorticotropic hormone (ACTH) indirect evidence of geographical variance, winter season of birth, and prenatal viral exposure neuropsychology: global defects seen in attention, language, and memory suggest lack of connectivity of neural networks
Pathophysiology
neurodegenerative theory natural history may be rapid or gradual decline in function and ability to communicate glutamate system may mediate progressive degeneration by excitotoxic mechanism which leads to production of free radicals neurodevelopmental theory abnormal development of the brain from prenatal life neurons fail to migrate correctly, make inappropriate connections, and break down in later life inappropriate apoptosis during neurodevelopment resulting in faulty connections between neurons
Management of Schizophrenia
pharmacological (see Pharmacotherapy, PS38) acute treatment and maintenance with antipsychotics anticonvulsants anxiolytics management of side effects psychosocial psychotherapy (individual, family, group): supportive, cognitive behavioural therapy (CBT) assertive community treatment (ACT) social skills training and employment programs housing (group home, boarding home, transitional home)
Course
the majority of individuals display some type of prodromal phase course is variable some individuals have exacerbations and remissions and others remain chronically ill; accurate prediction of the long term outcome is not possible early in the illness, negative symptoms may be prominent; positive symptoms appear
and typically diminish with treatment; negative symptoms persist between episodes of positive symptoms in many individuals; negative symptoms may become steadily more prominent in some persons during the course of the illness over time, 1/3 improve, 1/3 remain the same, 1/3 worsen
Mood Disorders
Definitions
mood disorders are defined by the presence of episodes mood episodes represent a combination of symptoms comprising a predominant mood state, examples include: major depressive, manic, mixed, hypomanic types of mood disorders include: depressive (major depressive disorder, dysthymia) bipolar (bipolar I/II disorder, cyclothymia) secondary to general medical condition (GMC), substances, medications
Mood Episodes
DSM-IV-TR Criteria for Major Depressive Episode
A. five (or more) of the following symptoms have been present during the same 2-week period and represent a change from previous functioning; at least one of the symptoms is either 1) depressed mood or; 2) loss of interest or pleasure Note: Do not include symptoms that are clearly due to a general medical condition, or mood-incongruent delusions or hallucinations (1) depressed mood most of the day, nearly every day, as indicated by either subjective report or observation made by others (2) markedly diminished interest or pleasure in all, or almost all, activities most of the day, nearly every day (3) significant weight loss when not dieting or weight gain, or decrease or increase in appetite nearly every day (4) insomnia or hypersomnia nearly every day (5) psychomotor agitation or retardation nearly every day (6) fatigue or loss of energy nearly every day (7) feelings of worthlessness or excessive or inappropriate guilt (which may be delusional) nearly every day (not merely self-reproach or guilt about being sick) (8) diminished ability to think or concentrate, or indecisiveness, nearly every day (9) 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 do not meet criteria for a Mixed Episode (see below) C. the symptoms cause clinically significant distress or impairment in social, occupational, or other important areas of functioning D. the symptoms are not due to the direct physiological effects of a substance or a GMC E. the symptoms are not better accounted for by bereavement, i.e. after the loss of a loved one, the symptoms persist for longer than 2 months or are characterized by marked functional impairment, morbid preoccupation with worthlessness, suicidal ideation, psychotic symptoms, or psychomotor retardation
Mixed Episode
criteria met for both manic episode and MDE nearly every day for 1 week criteria D and E from manic episodes are met
Hypomanic Episode
criteria A of a manic episode is met, but duration is at least 4 days criteria B and E of manic episodes are met episode associated with an uncharacteristic decline in functioning that is observable by others change in function is NOT severe enough to cause marked impairment in social or occupational functioning or to necessitate hospitalization absence of psychotic features
Depressive Disorders
DSM-IV-TR Diagnostic Criteria for Major Depressive Disorder
A. presence of two or more MDE. Note: To be considered separate episodes there must be an interval of at least 2 consecutive months in which criteria of MDE are not met B. the MDE are not better accounted for by Schizoaffective Disorder and are not superimposed on a psychotic disorder C. there has never been a manic, hypomanic or mixed episode (This does not apply if these episodes occur secondary to a substance or GMC) D. history of one or more MDE E. absence of a previous manic, hypomanic, or mixed episode
Features
psychotic with hallucinations or delusions; these may be mood-congruent chronic lasting 2 years or more melancholic quality of mood is distinctly depressed, mood is worse in the morning, early morning awakening, marked weight loss, excessive guilt, psychomotor retardation atypical increased sleep, weight gain, leaden paralysis, rejection hypersensitivity postpartum (see Postpartum Mood Disorders, PS11) seasonal (pattern of onset at same time each year)
Epidemiology
prevalence: male 2-4%, female 5-9% (M:F = 1:2) mean age of onset: ~30 years
Etiology
biological genetic: 65-75% MZ twins; 14-19% DZ twins neurotransmitter dysfunction at level of synapse (decreased activity of serotonin, norepinephrine, dopamine) secondary to general medical condition (GMC) psychosocial psychodynamic (e.g. low self-esteem) cognitive (e.g. negative thinking) environmental factors (e.g. job loss, bereavement, history of abuse) co-morbid psychiatric diagnoses (substance abuse, mental retardation, dementia, eating disorder)
Risk Factors
sex: female > male age: onset in 25-50 year age group family history: depression, alcohol abuse, sociopathy childhood experiences: loss of parent before 11 years old, negative home environment (abuse, neglect) personality: insecure, dependent, obsessional recent stressors (illness, financial, legal) postpartum < 6 months lack of intimate, confiding relationships or social isolation
psychological individual therapy: psychodynamic, interpersonal, cognitive behavioural therapy family therapy group therapy social: vocational rehabilitation, social skills training
Prognosis
one year after diagnosis of a MDE without treatment, 40% of individuals still have symptoms that are sufficiently severe to meet criteria for a full MDE, 20% continue to have some symptoms that no longer meet criteria for a MDE, 40% have no mood disorder
Epidemiology
point prevalence: 3%, life prevalence 6%; M:F = 1:2-3
Treatment
psychological treatment principle treatment for dysthymia individual, group, and family therapy medical treatment out patient antidepressant therapy (SSRIs/SNRIs)
Bipolar Disorders
BIPOLAR I / BIPOLAR II DISORDER Definition
Bipolar I Disorder disorder in which at least one manic or mixed episode has occurred commonly accompanied by at least 1 MDE but not required for diagnosis Bipolar II Disorder disorder in which there is at least 1 MDE and at least 1 hypomanic episode no past manic or mixed episode
Epidemiology
prevalence: 0.6-0.9%; M:F = 1:1 age of onset: teens to 20s
Risk Factors
slight increase in upper socioeconomic groups 60-65% of bipolar patients have family history of major mood disorders
Classification
classification of bipolar disorder involves describing the current or most recent mood episode as either manic, hypomanic, mixed or depressed the current or most recent episode can be further classified as without psychotic features, with psychotic features, with catatonic features, with postpartum onset, with seasonal pattern, with rapid cycling
Treatment
biological: mood stabilizers, anticonvulsants, antipsychotics, antidepressants, ECT psychological: supportive and psychodynamic psychotherapy, cognitive or behavioural therapy social: vocational rehabilitation, leave of absence from school/work, drug and EtOH cessation, substitute decision maker for finances, sleep hygiene, social skills training, education for family members
CYCLOTHYMIA Diagnosis
presence of numerous periods of hypomanic and depressive symptoms (not meeting criteria for MDE) for at least 2 years; never without symptoms for > 2 months no MDE, manic or mixed episodes; no evidence of psychosis not due to GMC/substance use symptoms cause clinically significant distress or impairment in social, occupational, or other important areas of functioning
Treatment
anticonvulsants psychotherapy
Anxiety Disorders
Definition
anxiety is a universal human characteristic involving tension, apprehension, or even terror, which serves as an adaptive mechanism to warn about an external threat by activating the sympathetic nervous system (fight or flight) manifestations of anxiety can be described along a continuum of physiology, psychology, and behaviour physiology main brain structure involved is the amygdala; neurotransmitters involved include serotonin, cholecystokinin, epinephrine, norepinephrine, dopamine psychology ones perception of a given situation is distorted which causes
one to believe it is threatening in some way behaviour once feeling threatened, one responds by escaping or facing the situation, thereby causing a disruption in daily functioning anxiety becomes pathological when fear is greatly out-of-proportion to risk/severity of threat response continues beyond existence of threat or becomes generalized to other similar/dissimilar situations social or occupational functioning is impaired
Differential Diagnosis
endocrine: hyper- or hypothyroidism, pheochromocytoma, hypoglycemia, hyperadrenalism, hyperparathyroidism CVS: congestive heart failure, pulmonary embolus, arrhythmia, mitral valve prolapse respiratory: asthma, pneumonia, hyperventilation metabolic: vitamin B12 deficiency, porphyria neurologic: neoplasm, vestibular dysfunction, encephalitis differentiate from substance-induced anxiety disorder: drugs of abuse (caffeine, amphetamine, cocaine), medications (benzodiazepine withdrawal), toxins (EtOH withdrawal)
Panic Disorder
DSM-IV-TR Diagnostic Criteria for Panic Disorder without Agoraphobia
A. Both (1) and (2): (1) recurrent unexpected Panic Attacks A discrete period of intense fear or discomfort, in which four (or more) of the following symptoms develop abruptly and reach a peak within 10 minutes: palpitations, pounding heart, or accelerated heart rate sweating trembling or shaking sensations of shortness of breath or smothering feeling of choking chest pain or discomfort nausea or abdominal distress feeling dizzy, unsteady, lightheaded, or faint derealization (feelings of unreality) or depersonalization (being detached from oneself) fear of losing control or going crazy fear of dying paresthesias (numbness or tingling sensations), chills or hot flushes (2) at least one of the attacks has been followed by 1 month (or more) of one (or more) of the following: (a) persistent concern about having additional attacks
(b) worry about the implications of the attack or its consequences (e.g. losing control, having a heart attack, "going crazy") (c) a significant change in behavior related to the attacks B. absence of Agoraphobia C. the Panic Attacks are not due to the direct physiological effects of a substance or a GMC D. the Panic Attacks are not better accounted for by another mental disorder, such as Social Phobia, Specific Phobia, Obsessive-Compulsive Disorder, Post-traumatic Stress Disorder, Separation Anxiety Disorder
Epidemiology
prevalence: 1.5-5% (one of the top five most common reasons to see a family doctor); M:F = 1:2-3 onset: average late 20s, familial pattern
Treatment
supportive psychotherapy, relaxation techniques (visualization, box-breathing), cognitive behavioural therapy (correct distorted thinking, desensitization/exposure therapy) pharmacotherapy benzodiazepines (short term, low dose, regular schedule, long half-life, no PRN) SSRIs/SNRI (start low, go slow, aim high since anxiety patients are very sensitive other antidepressants (serzone, trazodone, remeron, MAOIs); avoid wellbutrin
Prognosis
6-10 years post-treatment: 30% well, 40-50% improved, 20-30% no change or worse clinical course: chronic, but episodic with psychosocial stressors
Epidemiology
1-year prevalence: 3-8%; M:F = 1:2; if considering only those receiving inpatient treatment, ratio is 1:1 most commonly presents in early adulthood (termed "overanxious disorder of childhood" in children)
Treatment
psychotherapy, relaxation, and CBT caffeine and EtOH avoidance, sleep hygiene pharmacotherapy: benzodiazepines (short term, low dose, regular schedule, long half-life, no PRN) buspirone (TID dosing) others: SSRIs/SNRI, TCAs, beta blockers combinations of above
Prognosis
chronically anxious adults become less so with age depends on pre-morbid personality functioning, stability of relationships, work, and severity of environmental stress difficult to treat
Phobic Disorders
Specific Phobia
definition: marked and persistent fear that is excessive or unreasonable, cued by presence or anticipation of a specific object or situation 1year prevalence 9%, lifetime prevalence 12-16%; M:F ratio variable depending on nature of specific phobia types: animal/insect, environment (heights, storms), blood/injection/injury, situational (airplane, closed spaces), other (loud noise, clowns)
Social Phobia
definition: marked and persistent fear of social or performance situations in which person is exposed to unfamiliar people or to possible scrutiny by others; person fears
he/she will act in a way that may be humiliating or embarrassing (e.g. public speaking, initiating or maintaining conversation, dating, eating in public) 6-month prevalence = 2-3% lifetime prevalence may be as high as 13-16%; M:F = 1:1 in clinical setting, but M<F in community
Treatment
exposure therapy/desensitization, insight-oriented psychotherapy pharmacotherapy beta blockers or benzodiazepines in acute situations (i.e. public speaking) SSRIs, MAOIs; no TCAs behavioural therapy is more efficacious than medication
Prognosis
chronic
Epidemiology
lifetime prevalence rates 2-3%; M=F MZ twins = 75%, DZ = 32% rate of OCD in first-degree relatives is higher than in the general population
Treatment
CBT desensitization, flooding, thought stopping, implosion therapy, aversive conditioning pharmacotherapy clomipramine, SSRIs (higher doses and longer treatment needed, i.e. up to 8-12 weeks) atypical and typical antipsychotics pimozide, haloperidol
Prognosis
tends to be refractory and chronic
Epidemiology
lifetime prevalence: 1-3% mens trauma is most commonly combat experience; womens trauma is usually physical or sexual assault
Complications
substance abuse, relationship difficulties, depression, impaired social and occupational functioning, Axis II disorders
Treatment
CBT systematic desensitization, relaxation techniques, thought stopping pharmacotherapy
SSRIs benzodiazepines (for acute anxiety) 1st line adjunct atypicals (quetiapine, olanzapine, risperidone)
Suicide
Epidemiology
attempted:complete = 120:1 M:F = 3:1 for completed; 1:4 for attempts
Risk Factors
epidemiologic factors age: increases after age 14; 2nd cause of death for ages 15-24; highest rates in persons > 65 years sex: male race/ethnic background: white or native Canadians on reserves marital status: widowed/divorced living situation: lives alone; no children < 18 years old in the household other: stressful life events; access to firearms psychiatric disorders mood disorders (15% lifetime risk in depression; higher in bipolar) anxiety disorders (especially panic disorder) schizophrenia (10-15% risk) substance abuse (especially EtOH 15% lifetime risk) eating disorders (5% lifetime risk) adjustment disorder conduct disorder personality disorders (borderline, antisocial) past history prior suicide attempt family history of suicide attempt
Clinical Presentation
symptoms associated with suicide hopelessness anhedonia insomnia severe anxiety impaired concentration psychomotor agitation panic attacks
Approach
assessment of suicidal ideation Onset of suicidal thoughts? Stressors precipitating suicidal thoughts? Frequency of suicidal thoughts? Feelings of being a burden? Or that life isn't worth living? What makes them feel better (e.g. contact with family, use of substances)? What makes them feel worse (e.g. being alone)? How much control over suicidal ideas do they have? Can they suppress them or call someone for help? What keeps them alive? Stops them from killing themselves (e.g. family, religious beliefs)? assessment of lethality Is there a plan to end their life? Do they own a gun, have access to firearms or potentially harmful medications? Have they imagined their funeral, and how people will react to their death? Have they "practiced" the suicide? (e.g. put the gun to head or held medications in hand)? Have they changed their will or life insurance policy or given away possessions? if an attempt was made: Planned or impulsive attempt? Triggers for attempt (stressors)? Lethality of attempt? Chance of discovery? Reaction to being saved? MSE may reveal psychiatric disorder (e.g. depression), perception disturbance (e.g. command hallucination), poor insight and judgement
Management
see SAD PERSONS scale do not leave patient alone; remove potentially dangerous objects from room patients with a plan, access to lethal means, recent social stressors, and symptoms suggestive of a psychiatric disorder should be hospitalized immediately if patients refuses to be hospitalized, complete form for involuntary admission depression: if severe, hospitalize; otherwise outpatient treatment with good supports and SSRIs/SNRIs alcohol related: usually resolves with abstinence for a few days; if not, suspect depression personality disorders: crisis intervention/confrontation schizophrenia/psychotic: hospitalization parasuicides/self-mutilation: long term psychotherapy with brief crisis intervention when necessary
Eating Disorders
Epidemiology
anorexia nervosa (AN) - 1% of adolescent and young adult females; onset 13-20 years old bulimia nervosa (BN) - 2-4% of adolescent and young adult females; onset 16-18 years old F:M = 10:1; mortality 5-10%
Etiology
commonly multifactorial - psychological, sociological and biological associations individual: perfectionism, lack of control in other life areas, history of sexual abuse personality: obsessive-compulsive, histrionic, schizoid/schizotypal familial: maintenance of equilibrium in dysfunctional family cultural factors: prevalent in industrialized societies, idealization of thinness in the media genetic factors: AN: 6% prevalence in siblings, with one study of twin pairs finding concordance in 9 of 12 monozygotic pairs versus concordance in 1 of 14 dizygotic pairs BN: higher familial incidence of affective disorders than the general population
Risk Factors
physical factors: obesity, chronic medical illness (e.g. diabetes mellitus) psychological factors: individuals who by career choice are expected to be thin, family history (mood disorders, eating disorders, substance abuse), history of sexual abuse, homosexual men, competitive athletes, concurrent associated mental illness (depression, OCD, anxiety disorder (especially panic and agoraphobia), substance abuse (BN))
Specify Type
Restricting Type: during the current episode of Anorexia Nervosa, the person has not regularly engaged in binge-eating or purging behavior (i.e. self-induced vomiting or the misuse of laxatives, diuretics, or enemas) Binge-Eating/Purging Type: during the current episode of Anorexia Nervosa, the person has regularly engaged in binge-eating or purging behavior (i.e. self-induced vomiting or the misuse of laxatives, diuretics, or enemas)
Other Features
deteriorating mood (irritable, anxious, extremeness of sensitivity, sadness) isolation (e.g. free time devoted to studying, social circle sacrificed)
trouble concentrating due to repetitive, intrusive, irresolvable and anxiety provoking thoughts about food and weight malnutrition poor sleep
Management
criteria for admission vary among hospitals admit to hospital if: < 65% of standard body weight, hypovolemia requiring intravenous fluid, abnormal serum chemistries or if actively suicidal agree on target body weight on admission and reassure this weight will not be surpassed psychotherapy (individual/group/family) addressing food and body perception, coping mechanisms, health effects monitor for complications (see Table 6)
Prognosis
early intervention much more effective with treatment, 70% resume a weight of at least 85% of expected levels and about 50% resume normal menstrual function eating peculiarities and associated psychiatric symptoms are common and persistent long-term mortality - 10% to 20% of patients hospitalized will die in next 10 to 30 years, secondary to severe and chronic starvation, metabolic or cardiac catastrophies, with a significant proportion committing suicide
Specify Type
Purging Type: during the current episode of Bulimia Nervosa, the person has regularly engaged in self-induced vomiting or the misuse of laxatives, diuretics, or enemas Nonpurging Type: during the current episode of Bulimia Nervosa, the person has used other inappropriate compensatory behaviors, such as fasting or excessive exercise, but has not regularly engaged in self-induced vomiting or the misuse of laxatives, diuretics, or enemas
Other Features
fatiguability and muscle weakness due to repetitive vomiting and fluid/electrolyte imbalance tooth decay swollen appearance around angle of jaw and puffiness of eye sockets due to fluid retention reddened knuckles, Russells sign (knuckle callus) trouble concentrating weight fluctuation (rhythmic pattern) over time
Management
criteria for admission: significant electrolyte abnormalities biological (see Table 6) treatment of starvation effects, SSRIs psychological develop trusting relationship with therapist to explore personal etiology and triggers reality-oriented feedback, cognitive behavioural therapy, family therapy recognition of health risks social challenge destructive societal views of women use of hospital environment to provide external patterning for normative eating behaviour
Prognosis
few recover without recurrence good prognostic factors: onset before age 15, achieving a healthy weight within 2 years of treatment poor prognostic factors: later age of onset, previous hospitalizations, individual and familial disturbance
Pharmacotherapy
Antipsychotics
antipsychotics and neuroleptics are terms used interchangeably indications: schizophrenia and other psychotic disorders, mood disorders with psychosis, violent behaviour, autism, Tourettes, somatoform disorders, dementia, OCD onset: immediate calming effect and decrease in agitation; thought disorder responds in 2-4 weeks mechanism of action typical - blocks D2 receptors (dopamine); treats only positive symptoms (hallucinations, delusions) atypical - blocks D2 and/or D1, 5-HT receptors (dopamine + serotonin); treats both positive and negative symptoms (flat affect, anhedonia, avolition) specific typical and atypical antipsychotics vary in terms of binding to adrenergic, 5-HT, cholinergic and histaminergic sites leading to different side effect profiles
ATYPICAL ANTIPSYCHOTICS
fewer EPS than typicals often effective for treating symptoms refractory to conventional antipsychotics Risperidone, Olanzapine, Quetiapine are the first line atypical antipsychotics no significant difference in efficacy, speed of response and stability of remission between first line atypicals disadvantages: expensive, lack of injectable forms
Clozapine
blocks a spectrum of receptors, including D1-D4, 5-HT2, 5-HT3, muscarinic, histaminergic indications treatment-resistat schizophrenia (i.e. other antipsychotics not effective) severe EPS limiting use of other agents advantages clozapine does not worsen tardive symptoms; it may actually treat them about 50% of patients benefit, especially paranoid patients and those with onset after 20 years old disadvantages: side effects: drowsiness/sedation (39%), hypersalivation (31%), tachycardia (25%), dizziness (19%), headache (7%), fever (5%), significant weight gain (4%), nausea/vomiting (3-5%), seizure (3%), agranulocytosis (1-2%), extrapyramidal, NMS weekly blood counts for at least 1 month, then q 2 weeks, due to risk of agranulocytosis
do not use with drugs which may cause bone marrow suppression due to risk of agranulocytosis
Risperidone
blocks 5-HT2, D2 and adrenergic indications psychosis negative symptoms intolerance to side effects of typical antipsychotics advantages: low incidence of EPS and lower doses (< 8) disadvantages side effects: insomnia (26%), agitation (22%), EPS (17%), headache (14%), anxiety (12%), rhinitis (10%), constipation (7%), nausea/vomiting (5-6%), dizziness (4%), sedation (3%), hypersalivation (2%), weight gain, impairment of ejaculation/orgasm, increased prolactin levels benefit limited to a narrow dose range: 4-8 mg/day only quick dissolve formulation will soon be available
Olanzapine
blocks 5-HT2,3,6, D1-D4, muscarinic, adrenergic, histaminergic indications psychosis intolerance to side effects of typical antipsychotics advantages overall efficacy is superior to haloperidol; well tolerated; comparable efficacy to risperdone quick dissolve formulation (ZydisTM) increasingly used in ER setting and for better compliance incidence of EPS and tardive dyskinesias (TD) much less than traditional neuroleptics disadvantages side effects: mild sedation (29%), insomnia (12%), dizziness (11%), dry mouth (9%), fever (6%), weight gain (5%), minimal anticholinergic, sexual dysfunction, early AST and ALT elevation in some individuals, restlessness weight gain associated with an increased risk of diabetes mellitus and hyperlipidemia
Quetiapine
blocks 5HT2A, D1-D2, adrenergic, and histaminergic receptors advantages associated with less weight gain as compared with clozapine and olanzapine disadvantages questionable effectiveness in treating both positive and negative symptoms, dose needs to be pushed (> 600mg/day) in order for drug to have any effect side effects: headache (19%), sedation (18%), dizziness (10%), constipation (9%), dry mouth (7%), hypotension (7%), tachycardia (7%), weight gain (2%) most sedating of the first line atypicals
Ziprasidone
5-HT2A and moderate D2 antagonism; moderately potent adrenergic and histaminergic blocker in process of gaining approval in Canada; difficulty with approval due to prolongation of Q-T interval dosing recommendations not yet known; range of efficacy expected to be between 40-80 mg/day, IM injection also available side effects: sedation (14%), nausea (10%), constipation (9%), dyspepsia (8%), dizziness (8%), akathisia (8%), asthenia (5%), EPS (5%), diarrhea (5%), tachycardia (2%)
LONG-ACTING PREPARATIONS
antipsychotics formulated in oil for deep IM injection received on an outpatient basis weekly or bimonthly
indications: individuals with schizophrenia or other chronic psychoses who relapse because of noncompliance available preparations (all high potency typical antipsychotics) dosing: start at low dosages, and then titrate every 2 to 4 weeks to maximize safety and minimize side effects should be exposed to oral form prior to first injection side effects: risk of EPS, parkinsonism, increased risk of neuroleptic malignant syndrome Figure 4. Treatment Algorithm for Schizophrenia
CNS
Endocrine
exhaustion poor nutrition external heat load sex: male age: young adults clinical presentation: fever, autonomic reactivity, rigidity, mental status changes (usually occur first) develops over 24-72 hours labs: increased CPK, leukocytosis, myoglobinuria treatment: discontinue drug, hydration, cooling blankets, dantrolene (hydantoin derivative-used as a muscle relaxant), bromocriptine (DA agonist) mortality: 5%
Antidepressants
onset of effect neurovegetative symptoms 1-3 weeks emotional/cognitive symptoms 2-6 weeks may use mild stimulant (e.g. methylphenidate) for severe neurovegetative symptoms; briefly and taper down as antidepressant effect increases taper TCAs slowly (over weeks-months) because they can cause withdrawal reactions MAOIs and SSRIs can be tapered over 1 week
Serotonin Syndrome
rare but potentially life-threatening adverse reaction to SSRIs, especially when switching from an SSRI to an MAOI thought to be due to over-stimulation of the serotonergic system involves restlessness, confusion, and lethargy but can progress to myoclonus, hyperthermia, rigor and hypertonicity treatment: discontinue medication and administer emergency medical care as needed
Mood Stabilizers
before initiating get baseline: CBC, ECG (if patient > 45 years old or cardiovascular risk), urinalysis, BUN, Cr, lytes, TSH before initiating lithium: screen for pregnancy, thyroid disease, seizure disorder, neurological, renal, cardiovascular diseases use lithium or valproic acid first ( an antipsychotic) use carbamazepine in non-responders and rapid cycling can combine lithium and carbamazepine or valproic acid safely in lithium non-responders olanzapine may be used as a mood stabilizer, in conjunction with other mood stabilizers
side effects: fever (10%), nausea/vomiting (8%), sedation (8%), hostility (8%), dizziness (2.5%), increased cycling Lamotrigine (Lamictal): indications: treatment of dysphoric mania, mixed episodes and rapid cycling BAD mechanism: may inhibit 5-HT3 receptors and potentiate DA activity side effects: CNS: dizziness (38%), headache (29%), ataxia (22%), nausea (19%), somnolence (14%), fever (6%), anxiety (4%) Skin: rash (10%), Stevens-Johnson syndrome
Anxiolytics
indications: short term treatment of transient forms of anxiety disorders, insomnia, alcohol withdrawal (especially delirium tremens), barbiturate withdrawal, organic brain syndrome (agitation in dementia), EPS and akathisia due to antipsychotics, seizure disorders, musculoskeletal disorders relative contraindications: major depression (except as an adjunct to other treatment), history of drug/alcohol abuse, pregnancy, breast feeding mechanism of action: benzodiazepines: potentiate binding of GABA to its receptors; results in decreased neuronal activity buspirone: partial agonist of 5-HT type IA receptors
Benzodiazepines
should be used for limited periods (weeks-months) to avoid dependence all benzodiazepines are sedating have similar efficacy, so choice depends on half-life, metabolites and route of administration, OD or BID taper slowly over weeks-months because they can cause withdrawal reactions low dose withdrawal: tachycardia, hypertension, panic, insomnia, anxiety, impaired memory and concentration, perceptual disturbances high dose withdrawal: hyperpyrexia, seizures, psychosis, death avoid alcohol because of potentiation of CNS depression; caution with drinking and use of other machinery side effects: CNS: drowsiness (23%), cognitive impairment, reduced motor coordination (3%), memory impairment physical dependence, tolerance develops
Withdrawal (see Table 3 in Substance Abuse section) similar, but less severe, to alcohol withdrawal; can be fatal commonly used drug in overdose overdose is rarely fatal in combination with alcohol, other CNS depressants, or TCAs is more dangerous and may cause death Buspirone (Buspar)
primary use: generalized anxiety disorder (GAD) non-sedating and not prone to abuse; therefore, may be preferred over benzodiazepines does not interact with or show cross tolerance to other sedating drugs (e.g. alcohol, barbiturates, benzodiazepines) does not alter seizure threshold, interact with EtOH, act as a muscle relaxant onset of action: 2 weeks side effects: dizziness (12%), drowsiness (10%), nausea (8%), headache (6%), nervousness (5%), extrapyramidal
Drug
clonazepam (Rivotril)
T1/2 (hours)
18-50
Appropriate use
Akathisia, generalized anxiety seizure prevention,
diazepam (Valium)
2-40
30-100
panic disorder Generalized anxiety, seizure prevention, muscle relaxant Sleep, anxiety, alcohol withdrawal Sleep Panic disorder, sublingual available for very rapid action, high dependency rate Sleep, generalized anxiety, akathisia Sleep, generalized anxiety Sleep Shortest t1/2, rapid sleep, but rebound insomnia Generalized anxiety Sleep
lorazepam (Ativan) oxazepam (Serax) temazepam (Restoril) triazolam (Halcion) Azapirones buspirone (Buspar) zopiclone (Imovane)