Major depressive disorder and bipolar disorder Resource: Kaplan 12th edition, DSM 5-TR The outline for the presentation for each disorder is as follows: o Introduction and Epidemiology o Clinical Features o Diagnostic Criteria (DSM 5-TR) o Management (Pharmacological and Non-pharmacological) o PrognosisBuilding 35+ slides now with a fresh, modern design — clean cards layout, bold visuals, concise bullet points.

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I now have enough content from Kaplan & Sadock. Let me read the PPTX skill and also pull the core content blocks I still need (MDD epidemiology/features/treatment and Bipolar full section).
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Now I have enough content. Let me build the comprehensive 35+ slide presentation.
Running Command

mkdir -p /home/daytona/workspace/mood-disorders-pptx && ls /home/daytona/workspace/mood-disorders-pptx

Writing File

~/mood-disorders-pptx/build.js

const pptxgen = require("pptxgenjs");

const pres = new pptxgen();
pres.layout = "LAYOUT_16x9";
pres.title = "Mood Disorders: MDD & Bipolar Disorder";
pres.author = "Kaplan & Sadock 12e / DSM-5-TR";

// ─── PALETTE ────────────────────────────────────────────────────────────────
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  teal:    "00838F",   // accent / bipolar
  amber:   "F57F17",   // accent / highlight
  plum:    "6A1B9A",   // MDD accent
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  mddAccent: "7E57C2", // purple for MDD
  bpAccent:  "00ACC1", // teal for Bipolar
  warn:    "FF7043",
};

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// ─── SLIDE 1: TITLE ──────────────────────────────────────────────────────────
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  sl.addText("MOOD DISORDERS", {
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// ─── SLIDE 2: OUTLINE ───────────────────────────────────────────────────────
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    ["01", "Introduction & Epidemiology", C.mddAccent],
    ["02", "Clinical Features", C.mddAccent],
    ["03", "DSM-5-TR Diagnostic Criteria", C.amber],
    ["04", "Management (Pharmacological & Non-pharmacological)", C.bpAccent],
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// ═══════════════════════════════════════════════════════════════════
//  PART I — MAJOR DEPRESSIVE DISORDER
// ═══════════════════════════════════════════════════════════════════

// SLIDE 3: MDD Section Header
sectionDivider(pres,
  "PART I",
  C.mddAccent,
  "Major Depressive Disorder (MDD)"
);

// SLIDE 4: MDD — Introduction
cardSlide(pres, {
  title: "MDD — Introduction",
  accent: C.mddAccent,
  bullets: [
    "Major depressive disorder (MDD) is a primary mood disorder characterized by persistent depressed mood and/or loss of interest or pleasure (anhedonia)",
    "Represents the leading cause of disability worldwide — affects thinking, behavior, and physical health",
    "Distinguished from normal sadness by severity, duration, and functional impairment",
    "DSM-5-TR requires ≥5 symptoms persisting for ≥2 weeks; at least one must be depressed mood or anhedonia",
    "First episode most commonly occurs before age 40 (50% of patients)",
    "Associated with significant morbidity: impairs work, social, and family functioning",
    "Kaplan: 'Mood disorders are chronic, and psychiatrists must educate patients and families about future treatment strategies'"
  ]
});

// SLIDE 5: MDD — Epidemiology
cardSlide(pres, {
  title: "MDD — Epidemiology",
  accent: C.mddAccent,
  bullets: [
    "Lifetime prevalence: ~17% in the general population (US data)",
    "12-month prevalence: ~7% in adults; nearly double in adolescents (SAMHSA data)",
    "Sex ratio: Women affected ~2× more often than men (1.5–3:1 ratio)",
    "Incidence is rising among younger persons, particularly adolescents",
    "Mean age of onset: ~30–40 years; however, adolescent onset is increasingly recognized",
    "Children (prepubertal): sex ratio ~1:1; shifts to female predominance after puberty",
    "Comorbid conditions common: anxiety disorders (~50%), substance use disorder (~30%), personality disorders",
    "Higher rates in persons with chronic medical illness, chronic pain, and neurological disorders"
  ]
});

// SLIDE 6: MDD — Clinical Features (Part 1)
cardSlide(pres, {
  title: "MDD — Clinical Features: Core Symptoms (SIG E CAPS)",
  accent: C.mddAccent,
  bullets: [
    "S — Sleep: Insomnia (early morning awakening most classic) OR hypersomnia",
    "I — Interest: Markedly diminished interest or pleasure (anhedonia) in nearly all activities",
    "G — Guilt: Feelings of worthlessness or excessive/inappropriate guilt",
    "E — Energy: Fatigue or loss of energy nearly every day",
    "C — Concentration: Diminished ability to think, concentrate, or indecisiveness",
    "A — Appetite: Decreased or increased appetite; significant weight loss or gain (>5% body weight/month)",
    "P — Psychomotor: Observable agitation or retardation (not just subjective feeling)",
    "S — Suicide: Recurrent thoughts of death, suicidal ideation, plan, or attempt"
  ]
});

// SLIDE 7: MDD — Clinical Features (Part 2)
twoColSlide(pres, {
  title: "MDD — Clinical Features: Subtypes & Associated Features",
  accent: C.mddAccent,
  left: {
    header: "DSM-5-TR Specifiers",
    items: [
      "With anxious distress",
      "With melancholic features (anhedonia, early morning awakening, diurnal variation, profound guilt)",
      "With atypical features (mood reactivity, hypersomnia, hyperphagia, leaden paralysis)",
      "With psychotic features (mood-congruent or incongruent)",
      "With catatonic features",
      "With peripartum onset (within 4 weeks postpartum)",
      "With seasonal pattern (SAD)"
    ]
  },
  right: {
    header: "Associated Features",
    items: [
      "Tearfulness, irritability, rumination",
      "Somatic complaints (headaches, GI distress, pain)",
      "Hopelessness — strongest predictor of suicide",
      "Social withdrawal and isolation",
      "Cognitive impairment mimicking dementia ('pseudodementia')",
      "In children: somatic complaints, agitation, irritability more prominent than sadness",
      "In adolescents: antisocial behavior, substance use, academic decline"
    ]
  }
});

// SLIDE 8: MDD — Psychotic Features
cardSlide(pres, {
  title: "MDD — With Psychotic Features",
  accent: C.mddAccent,
  bullets: [
    "Occurs in severe MDD; reflects poor prognosis",
    "Mood-congruent delusions: guilt, worthlessness, disease, nihilism, deserved punishment",
    "Mood-incongruent symptoms suggest comorbid primary psychotic disorder (schizoaffective, schizophrenia)",
    "Hallucinations: typically a single voice from outside the head with derogatory or suicidal content",
    "Psychotic depression is rare in prepubertal children (cognitive immaturity); present in ~50% of psychotically depressed adolescents",
    "Treatment: antidepressant + antipsychotic combination, or ECT (especially effective for psychotic depression)"
  ]
});

// SLIDE 9: MDD — DSM-5-TR Criteria
criteriaSlide(pres, {
  title: "MDD — DSM-5-TR Diagnostic Criteria",
  intro: "Criterion A: ≥5 of the following symptoms for ≥2 weeks (at least 1 must be #1 or #2):",
  accent: C.mddAccent,
  criteria: [
    "1. Depressed mood most of the day, nearly every day (subjective or observed)",
    "2. Markedly diminished interest or pleasure in all/almost all activities",
    "3. Significant weight/appetite change (>5% body weight in 1 month)",
    "4. Insomnia or hypersomnia nearly every day",
    "5. Psychomotor agitation or retardation (observable by others)",
    "6. Fatigue or loss of energy nearly every day",
    "7. Feelings of worthlessness or excessive/inappropriate guilt",
    "8. Diminished concentration or indecisiveness nearly every day",
    "9. Recurrent thoughts of death, suicidal ideation, or suicide attempt"
  ],
  note: "Criteria B–E: Symptoms cause significant distress/impairment; not attributable to substances/medical condition; not better explained by psychotic disorder; no history of manic/hypomanic episode"
});

// SLIDE 10: MDD — Management Overview
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    { label: "Acute Phase", detail: "Treat to remission\n(0–12 weeks)", col: C.plum },
    { label: "Continuation Phase", detail: "Prevent relapse\n(4–9 months)", col: C.mddAccent },
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    "Achieve full remission (not just response) — partial remission leads to higher relapse risk",
    "Use both pharmacological AND psychotherapeutic approaches for optimal outcomes",
    "Patient education: medication adherence, recognition of early relapse warning signs",
    "Monitor for treatment-emergent suicidality (especially first 2 weeks of antidepressant therapy)",
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// SLIDE 11: MDD — Pharmacological (Antidepressants Overview)
twoColSlide(pres, {
  title: "MDD — Pharmacological Management: First-Line",
  accent: C.mddAccent,
  left: {
    header: "SSRIs (First-Line)",
    items: [
      "Fluoxetine (20–60 mg/day)",
      "Sertraline (50–200 mg/day)",
      "Escitalopram (10–20 mg/day)",
      "Paroxetine (20–60 mg/day)",
      "Citalopram (20–40 mg/day)",
      "MOA: Block serotonin (5-HT) reuptake",
      "Side effects: GI upset, sexual dysfunction, insomnia, weight gain (variable)"
    ]
  },
  right: {
    header: "SNRIs (First-Line Alternative)",
    items: [
      "Venlafaxine (75–375 mg/day)",
      "Duloxetine (60–120 mg/day)",
      "Desvenlafaxine (50 mg/day)",
      "MOA: Block 5-HT and NE reuptake",
      "Preferred when comorbid pain or anxiety",
      "SE: dose-dependent HTN (venlafaxine), nausea",
      "Therapeutic effect: 2–6 weeks onset"
    ]
  }
});

// SLIDE 12: MDD — Pharmacological (Other Agents)
twoColSlide(pres, {
  title: "MDD — Pharmacological Management: Other Agents",
  accent: C.mddAccent,
  left: {
    header: "TCAs & MAOIs",
    items: [
      "TCAs: amitriptyline, imipramine, nortriptyline",
      "Effective but high SE burden: anticholinergic, cardiotoxic",
      "Lethal in overdose — use caution",
      "MAOIs: phenelzine, tranylcypromine",
      "Most effective for atypical depression",
      "Tyramine-free diet required (hypertensive crisis risk)",
      "Reserved for treatment-resistant cases"
    ]
  },
  right: {
    header: "Novel & Augmentation",
    items: [
      "Bupropion (NE/DA reuptake inhibitor) — no sexual SE, weight neutral",
      "Mirtazapine — sedating, weight gain; good for insomnia/anorexia",
      "Ketamine/Esketamine (Spravato) — rapid-acting NMDA antagonist; for TRD",
      "Lithium or atypical antipsychotics (aripiprazole, quetiapine) for augmentation",
      "Vortioxetine — multimodal; cognitive benefits",
      "Adequate trial: therapeutic dose × 4–6 weeks"
    ]
  }
});

// SLIDE 13: MDD — Non-pharmacological (Psychotherapy)
cardSlide(pres, {
  title: "MDD — Non-pharmacological: Psychotherapy",
  accent: C.mddAccent,
  bullets: [
    "Cognitive Behavioral Therapy (CBT): Gold standard — targets negative automatic thoughts and maladaptive behaviors; comparable to antidepressants for mild-moderate MDD",
    "Interpersonal Therapy (IPT): Focuses on grief, role disputes, transitions; particularly effective for postpartum depression",
    "Behavioral Activation (BA): Addresses avoidance behaviors; effective for all severities",
    "Psychodynamic Therapy: Addresses underlying conflicts; longer-term approach",
    "Mindfulness-Based Cognitive Therapy (MBCT): Reduces relapse risk in recurrent MDD (3+ episodes); combines CBT with mindfulness",
    "Combined therapy + medication superior to either alone for moderate-severe MDD",
    "Psychoeducation and supportive therapy for patients and families"
  ]
});

// SLIDE 14: MDD — Somatic Treatments
cardSlide(pres, {
  title: "MDD — Non-pharmacological: Somatic Treatments",
  accent: C.mddAccent,
  bullets: [
    "Electroconvulsive Therapy (ECT): Most effective treatment for severe, psychotic, or TRD; first-line in high suicidality or refusal to eat; brief seizure induced under anesthesia; bilateral > unilateral for efficacy",
    "Transcranial Magnetic Stimulation (TMS/rTMS): Non-invasive; FDA-approved after 1+ failed antidepressant; 40-min sessions × 4–6 weeks; no anesthesia; avoids cognitive SE of ECT",
    "Vagal Nerve Stimulation (VNS): Implanted device; approved for chronic, recurrent TRD; mechanism unclear",
    "Phototherapy (Light Therapy): 1,500–10,000 lux box; 1–2 hours before dawn daily; effective for Seasonal Affective Disorder (SAD); rare risk of triggering mania",
    "Ketamine infusions: Rapid (hours) — important for acute suicidal crisis"
  ]
});

// SLIDE 15: MDD — Prognosis
cardSlide(pres, {
  title: "MDD — Prognosis",
  accent: C.mddAccent,
  bullets: [
    "~50% of patients recover within the first year after first hospitalization",
    "25% recur within 6 months of leaving hospital; 30–50% within 2 years",
    "50–75% of all patients will have a recurrence within 5 years",
    "Untreated episode: 6–13 months; treated episode: ~3 months",
    "Over 20 years, mean number of episodes: 5–6",
    "With each additional episode, inter-episode intervals shorten and severity increases ('kindling effect')",
    "Good prognosis: mild severity, absence of psychotic features, good social support, no prior episodes",
    "Poor prognosis: early age of onset, psychotic features, severe episodes, comorbid anxiety/substance use, personality disorder",
    "Prophylactic maintenance therapy significantly reduces relapse rates"
  ]
});

// ═══════════════════════════════════════════════════════════════════
//  PART II — BIPOLAR DISORDER
// ═══════════════════════════════════════════════════════════════════

// SLIDE 16: Bipolar Section Header
sectionDivider(pres,
  "PART II",
  C.bpAccent,
  "Bipolar Disorder (BD)"
);

// SLIDE 17: Bipolar — Introduction
cardSlide(pres, {
  title: "Bipolar Disorder — Introduction",
  accent: C.bpAccent,
  bullets: [
    "Bipolar disorder is a cyclic mood disorder characterized by episodes of mania/hypomania and depression",
    "Formerly known as 'manic-depressive illness' — one of psychiatry's oldest recognized diagnoses",
    "DSM-5-TR distinguishes: Bipolar I (full mania), Bipolar II (hypomania + depression), Cyclothymia",
    "Represents a spectrum: from depressive predominance to manic predominance",
    "Significant impact: disability, interpersonal dysfunction, high suicide risk (~15–20% in untreated BD)",
    "Highly heritable: strongest genetic component of any psychiatric disorder",
    "Kaplan: BD is associated with 'the highest risk of suicide among all psychiatric disorders in some series'"
  ]
});

// SLIDE 18: Bipolar — Epidemiology
twoColSlide(pres, {
  title: "Bipolar Disorder — Epidemiology",
  accent: C.bpAccent,
  left: {
    header: "Prevalence & Demographics",
    items: [
      "Bipolar I: lifetime prevalence ~1% (equal sex distribution)",
      "Bipolar II: ~1.1%; more common in women",
      "Bipolar spectrum (BD-I + BD-II + cyclothymia): ~3–5%",
      "Onset: typically late teens to mid-20s (mean ~25 years)",
      "Mean age onset BD-I: 18 years; BD-II: slightly later",
      "Pediatric BD increasingly recognized; often presents as irritability/mixed features"
    ]
  },
  right: {
    header: "Risk Factors & Genetics",
    items: [
      "First-degree relative with BD: 5–10× increased risk",
      "Monozygotic twin concordance: ~60–80%",
      "Strong genetic loading — polygenic architecture",
      "Risk precipitants: sleep deprivation, substance use (especially stimulants, cannabis)",
      "Life events and stressors may trigger first episode",
      "High comorbidity: anxiety disorders, ADHD, substance use disorders"
    ]
  }
});

// SLIDE 19: Bipolar — Types (DSM-5-TR Classification)
cardSlide(pres, {
  title: "Bipolar Disorder — DSM-5-TR Classification",
  accent: C.bpAccent,
  cols: true,
  colData: [
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      header: "Bipolar I Disorder",
      items: [
        "≥1 manic episode (may include depressive episodes)",
        "Mania must last ≥7 days (or any duration if hospitalization needed)",
        "Most severe form",
        "Psychotic features common",
        "Equal sex ratio"
      ]
    },
    {
      header: "Bipolar II Disorder",
      items: [
        "Hypomanic episode + major depressive episode",
        "NO full manic episode ever",
        "Hypomania: ≥4 days, no hospitalization",
        "More common in women",
        "Depressive burden more prominent"
      ]
    }
  ]
});

// SLIDE 20: Bipolar — Mania Clinical Features
cardSlide(pres, {
  title: "Bipolar Disorder — Clinical Features of Mania (DIG FAST)",
  accent: C.bpAccent,
  bullets: [
    "D — Distractibility: easily pulled off task by irrelevant stimuli",
    "I — Impulsivity / Indiscretion: poor judgment, risky behaviors (hypersexuality, gambling, overspending)",
    "G — Grandiosity: inflated self-esteem, delusions of special powers or identity",
    "F — Flight of Ideas / Pressured Speech: thoughts race, speech rapid, difficult to interrupt",
    "A — Activity increase: goal-directed or psychomotor agitation",
    "S — Sleep decreased: markedly decreased need for sleep without fatigue (hallmark symptom)",
    "T — Talkativeness: more talkative than usual, difficult to interrupt",
    "Severe mania: psychotic features (mood-congruent grandiose or persecutory delusions, hallucinations)"
  ]
});

// SLIDE 21: Bipolar — Hypomania vs Mania
twoColSlide(pres, {
  title: "Bipolar Disorder — Hypomania vs. Mania",
  accent: C.bpAccent,
  left: {
    header: "Hypomania",
    items: [
      "Duration: ≥4 consecutive days",
      "Noticeable change in mood/behavior observable by others",
      "NOT severe enough to impair social/occupational functioning",
      "Does NOT require hospitalization",
      "No psychotic features",
      "Ego-syntonic — may feel productive, energized",
      "Bipolar II pattern"
    ]
  },
  right: {
    header: "Full Mania",
    items: [
      "Duration: ≥7 days (or any duration if hospitalized)",
      "Severe impairment in social/occupational function",
      "May require hospitalization",
      "Psychotic features possible (30–50%)",
      "Ego-dystonic at severe end",
      "Rapid cycling: ≥4 episodes/year (poor prognosis)",
      "Mixed features: mania + depression simultaneously"
    ]
  }
});

// SLIDE 22: Bipolar — Depressive Episodes
cardSlide(pres, {
  title: "Bipolar Disorder — Depressive Episodes",
  accent: C.bpAccent,
  bullets: [
    "Depressive episodes are MORE frequent and longer than manic episodes in BD",
    "Often indistinguishable from unipolar MDD based on symptoms alone",
    "Clues pointing to bipolar depression: hypersomnia (vs. insomnia), hyperphagia, psychomotor retardation, early age of onset, postpartum onset, psychotic features, family history of BD",
    "Atypical features common: leaden paralysis, mood reactivity, hyperphagia",
    "Suicide risk: highest during depressive or mixed episodes — BD carries 15–20× higher suicide risk vs. general population",
    "Misdiagnosis as MDD is common (may persist for years before correct diagnosis)",
    "CRITICAL: Using antidepressants alone in BD can precipitate mania or rapid cycling — must combine with mood stabilizer"
  ]
});

// SLIDE 23: Bipolar I — DSM-5-TR Criteria (Manic Episode)
criteriaSlide(pres, {
  title: "Bipolar I — DSM-5-TR: Manic Episode (Criterion A–E)",
  intro: "Criterion A: Distinct period of abnormally & persistently elevated/expansive/irritable mood AND increased goal-directed activity; ≥7 days (or any duration if hospitalized):",
  accent: C.bpAccent,
  criteria: [
    "1. Grandiosity or inflated self-esteem",
    "2. Decreased need for sleep (feels rested after only 3 hours)",
    "3. More talkative than usual or pressure to keep talking",
    "4. Flight of ideas or subjective experience that thoughts are racing",
    "5. Distractibility (attention easily drawn to unimportant stimuli)",
    "6. Increased goal-directed activity (social/occupational/sexual) or psychomotor agitation",
    "7. Excessive involvement in activities with high potential for painful consequences",
    "Criterion B: ≥3 symptoms (≥4 if mood is only irritable) — marked impairment"
  ],
  note: "Criteria C–E: Severe enough to impair function or require hospitalization or has psychotic features; not due to substances/medical condition"
});

// SLIDE 24: Bipolar II — DSM-5-TR Criteria
criteriaSlide(pres, {
  title: "Bipolar II — DSM-5-TR Criteria",
  intro: "Requires BOTH: at least one hypomanic episode AND at least one major depressive episode",
  accent: C.bpAccent,
  criteria: [
    "Hypomanic Episode: ≥4 consecutive days of elevated/expansive/irritable mood + ≥3 DIGFAST symptoms",
    "NOT severe enough to cause marked impairment or require hospitalization",
    "NO psychotic features during hypomanic episode",
    "Major Depressive Episode: meets full MDD criteria (≥5 symptoms, ≥2 weeks)",
    "EXCLUSION: No current or past manic episode (would change diagnosis to BD-I)",
    "Significant distress or impairment in social, occupational, or other important areas of functioning",
    "Depressive episodes are typically dominant, longer, and more disabling than hypomanic episodes",
    "High misdiagnosis rate as MDD — careful longitudinal history essential"
  ],
  note: "Note: One antidepressant-induced hypomanic episode does NOT count toward BD-II diagnosis (DSM-5-TR)"
});

// SLIDE 25: Bipolar — Management Overview
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  const principles = [
    "Mood stabilizers are the backbone of BD treatment (lithium, valproate, lamotrigine, carbamazepine)",
    "Antidepressants should NOT be used as monotherapy — risk of triggering mania or rapid cycling",
    "Psychoeducation is as important as pharmacotherapy for long-term outcomes",
    "Lifestyle regulation: regular sleep schedule, avoiding stimulants/alcohol",
    "Treat to full remission; partial response predicts higher relapse rates",
    "Shared decision-making critical — BD is lifelong; adherence is the biggest challenge"
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// SLIDE 26: Bipolar — Lithium (Mood Stabilizer)
cardSlide(pres, {
  title: "Bipolar Disorder — Lithium: First-Line Mood Stabilizer",
  accent: C.bpAccent,
  bullets: [
    "Mechanism: Multiple — inhibits inositol monophosphatase, modulates GSK-3β, neuroprotective effects",
    "Indications: Acute mania, maintenance/prophylaxis of BD-I and BD-II, augmentation in MDD",
    "Therapeutic serum level: 0.6–1.2 mEq/L (acute mania: 0.8–1.2; maintenance: 0.6–0.8)",
    "Response rate for acute mania: 60–80%",
    "Gold standard for suicide prevention in mood disorders (strongest evidence)",
    "Side effects: Tremor (fine postural), polyuria/polydipsia (nephrogenic DI), weight gain, hypothyroidism, acne",
    "Toxicity (>1.5 mEq/L): Coarse tremor, ataxia, confusion, seizures, cardiac arrhythmias",
    "Monitoring: Renal function, TFTs, serum levels every 3–6 months",
    "Teratogenicity: Ebstein anomaly (tricuspid valve) — avoid in 1st trimester"
  ]
});

// SLIDE 27: Bipolar — Anticonvulsants
twoColSlide(pres, {
  title: "Bipolar Disorder — Anticonvulsant Mood Stabilizers",
  accent: C.bpAccent,
  left: {
    header: "Valproate (Depakote)",
    items: [
      "Effective for acute mania (esp. mixed/rapid cycling)",
      "Therapeutic level: 50–125 μg/mL",
      "Side effects: Weight gain, sedation, hair loss, thrombocytopenia, hepatotoxicity",
      "CONTRAINDICATED in pregnancy (neural tube defects, PCOS-like effects)",
      "First-line for rapid cycling and dysphoric mania",
      "Superior to lithium for mixed features"
    ]
  },
  right: {
    header: "Lamotrigine & Carbamazepine",
    items: [
      "Lamotrigine: Best for BIPOLAR DEPRESSION prevention; not effective for acute mania",
      "Start low, titrate slowly — risk of Stevens-Johnson syndrome",
      "Carbamazepine: Esp. useful for dysphoric mania, rapid cycling, lithium non-responders",
      "Carbamazepine SE: Aplastic anemia, agranulocytosis, Stevens-Johnson, SIADH",
      "Blood monitoring required at 3, 6, 9, 12 months",
      "Carbamazepine is a potent CYP450 inducer — many drug interactions"
    ]
  }
});

// SLIDE 28: Bipolar — Antipsychotics in BD
cardSlide(pres, {
  title: "Bipolar Disorder — Antipsychotics",
  accent: C.bpAccent,
  bullets: [
    "Second-generation antipsychotics (SGAs) are highly effective for acute mania and increasingly used as maintenance",
    "Quetiapine: FDA-approved for BD-I mania, BD-II depression, AND maintenance; most versatile SGA in BD",
    "Olanzapine: FDA-approved for acute mania and maintenance; weight gain significant concern",
    "Aripiprazole: Mania and maintenance; metabolically neutral; available as monthly IM (Abilify Maintena)",
    "Risperidone, ziprasidone, cariprazine, asenapine: FDA-approved for BD mania",
    "Lurasidone, cariprazine: FDA-approved for bipolar depression",
    "First-generation antipsychotics (haloperidol): Effective for acute mania but higher EPS risk",
    "Combination of mood stabilizer + SGA often needed for severe or mixed mania"
  ]
});

// SLIDE 29: Bipolar — Treatment of Acute Phases
twoColSlide(pres, {
  title: "Bipolar Disorder — Pharmacotherapy by Phase",
  accent: C.bpAccent,
  left: {
    header: "Acute Mania",
    items: [
      "First-line: lithium OR valproate + SGA",
      "Lorazepam/clonazepam for agitation (adjunct)",
      "Remove precipitants (stop antidepressants, stimulants)",
      "Haloperidol IM for emergency control of severe agitation",
      "Carbamazepine: lithium non-responders or mixed mania",
      "ECT: refractory mania or when rapid response needed"
    ]
  },
  right: {
    header: "Bipolar Depression",
    items: [
      "Quetiapine monotherapy (FDA-approved, Level A evidence)",
      "Lurasidone + lithium/valproate (FDA-approved)",
      "Cariprazine (FDA-approved for BD depression)",
      "Lamotrigine for maintenance/prevention",
      "Avoid antidepressant monotherapy (risk of switching to mania)",
      "If antidepressant used: always combine with mood stabilizer"
    ]
  }
});

// SLIDE 30: Bipolar — Non-pharmacological Management
cardSlide(pres, {
  title: "Bipolar Disorder — Non-pharmacological Management",
  accent: C.bpAccent,
  bullets: [
    "Psychoeducation (Individual or Group): Cornerstone — recognition of early warning signs, treatment adherence, trigger identification",
    "Cognitive Behavioral Therapy (CBT): Addresses maladaptive cognitions; particularly effective for depressive phases and adherence",
    "Interpersonal & Social Rhythm Therapy (IPSRT): Stabilizes daily social rhythms and sleep-wake cycles; reduces episode frequency",
    "Family-Focused Therapy (FFT): Reduces expressed emotion; improves family communication and crisis management",
    "Lifestyle measures: Regular sleep schedule, avoiding alcohol/stimulants, exercise, stress reduction",
    "ECT: Effective for severe BD depression and acute mania; first-line in pregnancy and medical emergencies",
    "TMS: Emerging evidence for bipolar depression"
  ]
});

// SLIDE 31: Bipolar — Prognosis
cardSlide(pres, {
  title: "Bipolar Disorder — Prognosis",
  accent: C.bpAccent,
  bullets: [
    "BD is a lifelong, recurrent disorder — most patients experience multiple episodes",
    "Without treatment: 90% of patients have recurrence; many cycle continuously",
    "With optimal treatment: 50–60% achieve good functional outcomes",
    "Rapid cycling (≥4 episodes/year): poorer prognosis; associated with hypothyroidism, antidepressant use",
    "Mixed features associated with higher suicide risk and poorer treatment response",
    "Suicide: 15–20× higher risk than general population; 10–15% of BD patients die by suicide",
    "Predictors of poor prognosis: early onset, psychotic features, substance use, medication non-adherence, poor social support",
    "Predictors of good prognosis: good inter-episode functioning, social support, medication compliance, absence of psychosis"
  ]
});

// ═══════════════════════════════════════════════════════════════════
//  PART III — COMPARISON
// ═══════════════════════════════════════════════════════════════════

// SLIDE 32: Section Header — Comparison
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// SLIDE 33: MDD vs BD — Comparison Table
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    ["Core Mood", "Depressed / Anhedonic only", "Mania + Depression (cyclical)"],
    ["Prevalence", "~17% lifetime", "~1–3% (BD spectrum)"],
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    ["First-Line Rx", "SSRIs/SNRIs + psychotherapy", "Mood stabilizers + SGAs"],
    ["Psychotherapy", "CBT, IPT, MBCT", "IPSRT, CBT, FFT, psychoeducation"],
    ["Antidepressants", "Safe and effective", "CAUTION — can trigger mania"],
    ["Prognosis", "50–75% recur within 5 yrs", "Lifelong; 90% recur untreated"],
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// SLIDE 34: Differential Diagnosis & Red Flags
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  title: "Differential Diagnosis & Key Red Flags",
  accent: C.amber,
  left: {
    header: "Differential Diagnosis",
    items: [
      "Persistent depressive disorder (dysthymia)",
      "Cyclothymic disorder",
      "Schizoaffective disorder",
      "Adjustment disorder with depressed mood",
      "Grief reaction (normal bereavement)",
      "Hypothyroidism, Cushing's, anemia",
      "Substance-induced mood disorder",
      "ADHD (overlaps with hypomania in children)"
    ]
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    header: "Clinical Red Flags",
    items: [
      "Suicidal ideation — always assess plan, intent, means",
      "Psychotic features — increase risk and alter treatment",
      "Antidepressant-triggered elation → reconsider BD",
      "Rapid switching → workup for BD, substance use",
      "Family history of BD in a 'depressed' patient",
      "Postpartum psychosis (emergency — risk of infanticide)",
      "Mixed states — highest suicide risk"
    ]
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// SLIDE 35: Summary — Take-Home Messages
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// SLIDE 36: References
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  title: "References",
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  bullets: [
    "Sadock BJ, Sadock VA, Ruiz P. Kaplan & Sadock's Synopsis of Psychiatry: Behavioral Sciences/Clinical Psychiatry. 12th ed. Wolters Kluwer; 2021.",
    "Kaplan & Sadock's Comprehensive Textbook of Psychiatry. 10th ed. Wolters Kluwer; 2017.",
    "American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 5th Edition, Text Revision (DSM-5-TR). APA; 2022.",
    "Goodwin FK, Jamison KR. Manic-Depressive Illness: Bipolar Disorders and Recurrent Depression. 2nd ed. Oxford University Press; 2007.",
    "National Institute for Health and Care Excellence (NICE). Depression in adults: treatment and management. NICE guideline [NG222]; 2022.",
    "National Institute for Health and Care Excellence (NICE). Bipolar disorder: assessment and management. NICE guideline [CG185]; 2020.",
    "Cipriani A, et al. Comparative efficacy and acceptability of 21 antidepressant drugs. Lancet 2018; 391(10128):1357–1366."
  ]
});

// ─── WRITE FILE ──────────────────────────────────────────────────────────────
pres.writeFile({ fileName: "/home/daytona/workspace/mood-disorders-pptx/MoodDisorders_MDD_Bipolar.pptx" })
  .then(() => console.log("SUCCESS: MoodDisorders_MDD_Bipolar.pptx created"))
  .catch(err => console.error("ERROR:", err));
Running Command

cd /home/daytona/workspace/mood-disorders-pptx && node build.js 2>&1

Running Command

ls -lh /home/daytona/workspace/mood-disorders-pptx/MoodDisorders_MDD_Bipolar.pptx && python3 -c " import zipfile with zipfile.ZipFile('/home/daytona/workspace/mood-disorders-pptx/MoodDisorders_MDD_Bipolar.pptx') as z: slides = [n for n in z.namelist() if n.startswith('ppt/slides/slide') and not 'rels' in n] print(f'Slide count: {len(slides)}') for s in sorted(slides): print(s) "

Your presentation is ready. Here is the download link:

MoodDisorders MDD Bipolar

Presentation · PPTX


What's Inside — 36 Slides

Design: Dark navy background, clean card/panel layout, bold accent bars, color-coded sections (purple for MDD, teal for Bipolar, amber for highlights). All content sourced from Kaplan & Sadock's Synopsis 12e and DSM-5-TR.

Slide Breakdown

SlidesSection
1Title slide with dual-disorder pill badges
2Presentation outline (5 numbered sections)
PART I — MDD
3MDD section divider
4Introduction
5Epidemiology (prevalence, sex ratio, age of onset, comorbidities)
6Clinical Features — SIG E CAPS mnemonic
7Subtypes (specifiers) + Associated Features (two-column)
8Psychotic Features in MDD
9DSM-5-TR Diagnostic Criteria (criteria box layout)
10Management overview (3-phase model)
11Pharmacological — SSRIs & SNRIs
12Pharmacological — TCAs, MAOIs, novel agents, augmentation
13Non-pharmacological — Psychotherapy (CBT, IPT, MBCT, etc.)
14Non-pharmacological — Somatic treatments (ECT, TMS, VNS, phototherapy, ketamine)
15Prognosis
PART II — Bipolar
16Bipolar section divider
17Introduction
18Epidemiology (two-column: prevalence + genetics/risk factors)
19DSM-5-TR classification (BD-I vs. BD-II card layout)
20Clinical Features of Mania — DIG FAST mnemonic
21Hypomania vs. Mania (two-column comparison)
22Depressive episodes in BD + misdiagnosis warning
23DSM-5-TR Bipolar I — Manic Episode criteria
24DSM-5-TR Bipolar II criteria
25Management overview (3-phase model)
26Lithium — mechanism, dosing, monitoring, toxicity
27Anticonvulsants — valproate, lamotrigine, carbamazepine
28Antipsychotics in BD (quetiapine, lurasidone, cariprazine, etc.)
29Pharmacotherapy by phase (mania vs. bipolar depression)
30Non-pharmacological (IPSRT, CBT, FFT, ECT, lifestyle)
31Prognosis
COMPARISON
32Comparison section divider
33MDD vs. BD 10-row comparison table
34Differential diagnosis + red flags (two-column)
355 key take-home messages
36References (Kaplan 12e, DSM-5-TR, NICE, Lancet 2018)

Major depressive disorder and bipolar disorder Resource: Kaplan 12th edition, DSM 5-TR The outline for the presentation for each disorder is as follows: o Introduction and Epidemiology o Clinical Features o Diagnostic Criteria (DSM 5-TR) o Management (Pharmacological and Non-pharmacological) o Prognosis. Just the contents alone for each slides

Here is the complete slide-by-slide content for both disorders:

MAJOR DEPRESSIVE DISORDER


SLIDE 1 — Title Slide

Major Depressive Disorder (MDD) Based on Kaplan & Sadock's Synopsis of Psychiatry, 12th Edition | DSM-5-TR

SLIDE 2 — Introduction

  • MDD is a primary mood disorder characterized by persistent depressed mood and/or loss of interest or pleasure (anhedonia)
  • Distinguished from normal sadness by severity, duration, and functional impairment
  • Represents the leading cause of disability worldwide
  • Affects cognition, behavior, sleep, appetite, and physical health
  • DSM-5-TR requires ≥5 symptoms for ≥2 weeks; at least one must be depressed mood or anhedonia
  • Associated with high rates of comorbidity: anxiety disorders, substance use disorders, chronic medical illness
  • Kaplan: "Mood disorders are chronic, and psychiatrists must educate the patient and the family about future treatment strategies"

SLIDE 3 — Epidemiology

  • Lifetime prevalence: ~17% in the general population
  • 12-month prevalence: ~7% in adults; nearly double in adolescents (SAMHSA data)
  • Sex ratio: Women affected ~2× more often than men (ratio 1.5–3:1)
  • Age of onset: First episode before age 40 in ~50% of patients; mean onset ~30 years
  • Incidence is rising among younger persons, particularly adolescents
  • Children: sex ratio ~1:1 prepubertally; female predominance begins after puberty
  • Comorbidities: anxiety disorders (~50%), substance use disorder (~30%), personality disorders
  • Higher rates in those with chronic medical illness, chronic pain, and neurological disorders
  • Strongly associated with psychosocial stressors, low socioeconomic status, and poor social support

SLIDE 4 — Clinical Features: Core Symptoms (SIG E CAPS)

  • S — Sleep: Insomnia (early morning awakening most classic) OR hypersomnia
  • I — Interest: Markedly diminished interest or pleasure in nearly all activities (anhedonia)
  • G — Guilt: Feelings of worthlessness or excessive, inappropriate guilt
  • E — Energy: Fatigue or loss of energy nearly every day
  • C — Concentration: Diminished ability to think, concentrate, or make decisions
  • A — Appetite: Decreased or increased appetite; significant weight loss or gain (>5%/month)
  • P — Psychomotor: Observable agitation or retardation (not merely subjective)
  • S — Suicidality: Recurrent thoughts of death, suicidal ideation, plan, or attempt

SLIDE 5 — Clinical Features: Associated Features & Subtypes

Associated Features:
  • Tearfulness, irritability, social withdrawal, hopelessness
  • Somatic complaints: headaches, GI distress, chronic pain
  • Cognitive impairment mimicking dementia ("pseudodementia") in elderly
  • In children: somatic complaints, agitation, and irritability more prominent than sadness
  • In adolescents: antisocial behavior, substance use, academic decline, rejection sensitivity
DSM-5-TR Specifiers:
  • With anxious distress
  • With melancholic features (anhedonia, early morning awakening, diurnal variation, profound guilt)
  • With atypical features (mood reactivity, hypersomnia, hyperphagia, leaden paralysis)
  • With psychotic features (mood-congruent or mood-incongruent)
  • With catatonic features
  • With peripartum onset (within 4 weeks postpartum)
  • With seasonal pattern (Seasonal Affective Disorder — SAD)

SLIDE 6 — Clinical Features: Psychotic & Severe Features

  • Psychotic features occur in severe MDD and are a poor prognostic indicator
  • Mood-congruent delusions: guilt, worthlessness, nihilism, deserved punishment, physical disease
  • Mood-incongruent symptoms suggest comorbid primary psychotic disorder (e.g., schizoaffective disorder)
  • Hallucinations: typically a single voice from outside the head with derogatory or suicidal content
  • Rare in prepubertal children (due to cognitive immaturity); present in ~50% of psychotically depressed adolescents
  • Melancholia: severe anhedonia, early morning awakening, weight loss, profound guilt, diurnal variation (worse in AM)
  • Hopelessness is the strongest single predictor of completed suicide

SLIDE 7 — Diagnostic Criteria (DSM-5-TR)

Criterion A — ≥5 of the following for ≥2 weeks (at least one must be #1 or #2):
  1. Depressed mood most of the day, nearly every day (subjective or observed)
  2. Markedly diminished interest or pleasure in all/almost all activities
  3. Significant weight/appetite change (>5% body weight in 1 month)
  4. Insomnia or hypersomnia nearly every day
  5. Psychomotor agitation or retardation (observable by others, not just subjective)
  6. Fatigue or loss of energy nearly every day
  7. Feelings of worthlessness or excessive/inappropriate guilt
  8. Diminished ability to think, concentrate, or indecisiveness
  9. Recurrent thoughts of death, suicidal ideation, or suicide attempt
Criteria B–E:
  • Symptoms cause clinically significant distress or functional impairment
  • Not attributable to substances or a medical condition
  • Not better explained by a psychotic disorder
  • No history of manic or hypomanic episode

SLIDE 8 — Management: Pharmacological (First-Line)

SSRIs — First-Line:
  • Fluoxetine (20–60 mg/day)
  • Sertraline (50–200 mg/day)
  • Escitalopram (10–20 mg/day)
  • Paroxetine (20–60 mg/day)
  • Citalopram (20–40 mg/day)
  • MOA: Selective serotonin reuptake inhibition
  • SE: GI upset, sexual dysfunction, insomnia, weight gain, discontinuation syndrome
SNRIs — First-Line Alternative:
  • Venlafaxine (75–375 mg/day), Duloxetine (60–120 mg/day), Desvenlafaxine (50 mg/day)
  • MOA: Block serotonin + norepinephrine reuptake
  • Preferred when comorbid chronic pain, anxiety, or fibromyalgia
  • SE: Dose-dependent hypertension (venlafaxine), nausea
General Rule: Therapeutic onset 2–6 weeks; adequate trial = therapeutic dose × 4–6 weeks

SLIDE 9 — Management: Pharmacological (Other Agents)

TCAs:
  • Amitriptyline, imipramine, nortriptyline
  • Effective but high side-effect burden: anticholinergic, cardiac toxicity, lethal in overdose
  • Reserved for refractory or specific cases
MAOIs:
  • Phenelzine, tranylcypromine
  • Most effective for atypical depression
  • Requires tyramine-free diet (risk of hypertensive crisis)
  • Reserved for treatment-resistant cases
Novel & Augmentation Agents:
  • Bupropion (NE/DA reuptake inhibitor) — no sexual SE, weight neutral; also for smoking cessation
  • Mirtazapine — sedating, weight gain; preferred for insomnia and poor appetite
  • Ketamine/Esketamine (Spravato) — rapid-acting NMDA antagonist; FDA-approved for TRD and acute suicidal crisis
  • Vortioxetine — multimodal serotonergic; cognitive benefits
  • Lithium, atypical antipsychotics (aripiprazole, quetiapine) — augmentation in partial responders

SLIDE 10 — Management: Non-pharmacological — Psychotherapy

  • Cognitive Behavioral Therapy (CBT): Gold standard — targets negative automatic thoughts and maladaptive behaviors; comparable to antidepressants for mild-moderate MDD
  • Interpersonal Therapy (IPT): Addresses grief, role disputes, and role transitions; particularly effective for postpartum depression
  • Behavioral Activation (BA): Targets avoidance and withdrawal; effective across all severities
  • Mindfulness-Based Cognitive Therapy (MBCT): Reduces relapse in recurrent MDD (≥3 episodes); combines CBT with mindfulness meditation
  • Psychodynamic Therapy: Addresses underlying conflicts; longer-term approach
  • Combined therapy + medication is superior to either alone for moderate-to-severe MDD
  • Psychoeducation for patient and family: medication adherence, early warning signs, lifestyle measures

SLIDE 11 — Management: Somatic (Non-pharmacological)

  • Electroconvulsive Therapy (ECT):
    • Most effective treatment for severe, psychotic, or treatment-resistant depression
    • First-line when high suicide risk, refusal to eat, or rapid response needed
    • Brief generalized seizure induced under general anesthesia
    • Bilateral > unilateral for efficacy; unilateral preferred to reduce cognitive SE
    • Cognitive side effects (anterograde amnesia) are transient
  • Transcranial Magnetic Stimulation (TMS/rTMS):
    • FDA-approved after ≥1 failed antidepressant
    • Non-invasive, no anesthesia; 40-minute outpatient procedure × 4–6 weeks
    • No significant cognitive side effects
  • Vagal Nerve Stimulation (VNS): Implanted device; for chronic refractory MDD
  • Phototherapy (Light Therapy): 1,500–10,000 lux × 1–2 hours before dawn; first-line for SAD (seasonal pattern)
  • Ketamine infusions: Rapid onset (hours); critical for acute suicidal ideation

SLIDE 12 — Prognosis

  • MDD is a chronic, recurrent disorder — it is NOT benign
  • ~50% recover within the first year after first episode
  • 25% relapse within 6 months of leaving hospital
  • 30–50% relapse within 2 years
  • 50–75% will relapse within 5 years
  • Untreated episode lasts 6–13 months; treated episode ~3 months
  • Over 20 years: mean number of episodes = 5–6
  • Each subsequent episode: shorter inter-episode interval, greater severity ("kindling effect")
  • Prophylactic maintenance therapy significantly reduces recurrence risk
Positive prognostic indicators: Mild severity, absence of psychotic features, good social support, single episode, no comorbidities Negative prognostic indicators: Early onset, psychotic features, severe episodes, comorbid anxiety/substance use, personality disorder, chronic course


BIPOLAR DISORDER


SLIDE 13 — Title Slide

Bipolar Disorder Based on Kaplan & Sadock's Synopsis of Psychiatry, 12th Edition | DSM-5-TR

SLIDE 14 — Introduction

  • Bipolar disorder (BD) is a chronic, cyclic mood disorder characterized by episodes of mania or hypomania AND depression
  • Formerly called "manic-depressive illness" — one of psychiatry's oldest recognized conditions
  • DSM-5-TR classifies: Bipolar I, Bipolar II, Cyclothymic disorder, and Other specified/unspecified BD
  • Represents a mood spectrum from depressive predominance (BD-II) to manic predominance (BD-I)
  • Associated with significant morbidity: occupational dysfunction, broken relationships, high hospitalization rates
  • Suicide risk is 15–20× higher than the general population — BD carries the highest suicide risk of all psychiatric disorders
  • Highly heritable — genetic component is the strongest of any psychiatric disorder
  • Kaplan: "As the course of bipolar disorder progresses, episodes tend to become more frequent"

SLIDE 15 — Epidemiology

  • Bipolar I: Lifetime prevalence ~1%; equal sex distribution (male = female)
  • Bipolar II: Lifetime prevalence ~1.1%; more common in women
  • Bipolar spectrum (BD-I + BD-II + cyclothymia): ~3–5% of the population
  • Mean age of onset: BD-I ~18 years; BD-II slightly later (~20–22 years)
  • Earlier onset = more severe course
  • Genetics: First-degree relative with BD → 5–10× increased risk; monozygotic twin concordance: 60–80%
  • Risk precipitants: sleep deprivation, stimulant/cannabis use, antidepressant monotherapy, major life stressors
  • Comorbidities: Anxiety disorders (~75%), substance use disorders (~60%), ADHD, personality disorders
  • Pediatric BD increasingly recognized; often presents atypically with chronic irritability and mixed features

SLIDE 16 — Clinical Features: Manic Episode (DIG FAST)

  • D — Distractibility: Attention easily drawn to irrelevant external stimuli
  • I — Impulsivity/Indiscretion: Poor judgment; risky behaviors — hypersexuality, gambling, reckless spending, substance use
  • G — Grandiosity: Inflated self-esteem; delusions of special powers, identity, or mission
  • F — Flight of Ideas / Pressured Speech: Racing thoughts; rapid, difficult-to-interrupt speech
  • A — Activity increase: Increased goal-directed activity (social, occupational, sexual) OR psychomotor agitation
  • S — Sleep decreased: Markedly decreased need for sleep WITHOUT fatigue — most pathognomonic symptom
  • T — Talkativeness: More talkative than usual; pressure to keep talking
Severe mania: psychotic features — mood-congruent grandiose/persecutory delusions and hallucinations (30–50% of episodes)

SLIDE 17 — Clinical Features: Hypomania vs. Mania vs. Mixed

FeatureHypomaniaFull Mania
Duration≥4 consecutive days≥7 days (or any if hospitalized)
Functional impairmentMild / noneMarked
HospitalizationNot requiredMay be required
Psychotic featuresAbsentCan be present
Ego-syntonicUsually yesVariable
Mixed Features (DSM-5-TR specifier):
  • Simultaneous manic and depressive symptoms
  • Associated with the highest suicide risk in BD
  • Common presentation: euphoria + hopelessness + racing thoughts + suicidal ideation
  • Poor response to standard monotherapy; requires combination treatment
Rapid Cycling: ≥4 mood episodes/year — poor prognosis; linked to hypothyroidism and antidepressant use

SLIDE 18 — Clinical Features: Bipolar Depression

  • Depressive episodes are more frequent and longer than manic episodes in BD
  • Clinically indistinguishable from unipolar MDD based on symptoms alone
  • Clues suggesting bipolar depression (not MDD):
    • Hypersomnia (not insomnia)
    • Hyperphagia (not anorexia)
    • Psychomotor retardation > agitation
    • Leaden paralysis
    • Early age of onset (< 25 years)
    • Postpartum onset
    • Psychotic features
    • Family history of BD or mania
    • Prior antidepressant-induced hypomania/mania
  • Suicide risk is highest during depressive and mixed episodes
  • MDD misdiagnosis is common — correct diagnosis often delayed 5–10 years
  • CRITICAL: Antidepressant monotherapy in BD can precipitate mania, hypomania, or rapid cycling

SLIDE 19 — Diagnostic Criteria (DSM-5-TR): Bipolar I — Manic Episode

Criterion A: Distinct period of abnormally and persistently elevated, expansive, or irritable mood AND increased goal-directed activity or energy; lasting ≥7 days (or any duration if hospitalization required)
Criterion B — ≥3 of the following (≥4 if mood is only irritable):
  1. Grandiosity or inflated self-esteem
  2. Decreased need for sleep (feels rested after only 3 hours)
  3. More talkative than usual or pressure to keep talking
  4. Flight of ideas or subjective racing thoughts
  5. Distractibility (attention drawn to irrelevant stimuli)
  6. Increased goal-directed activity or psychomotor agitation
  7. Excessive involvement in activities with high potential for painful consequences
Criteria C–E:
  • Severe enough to markedly impair social/occupational functioning OR require hospitalization OR has psychotic features
  • Not attributable to substances or a medical condition

SLIDE 20 — Diagnostic Criteria (DSM-5-TR): Bipolar II

Requirements — BOTH must be present:
Hypomanic Episode:
  • ≥4 consecutive days of elevated/expansive/irritable mood + ≥3 DIGFAST symptoms
  • Noticeable change in behavior observable by others
  • NOT severe enough to cause marked impairment
  • No psychotic features
  • NOT due to substances or a medical condition
Major Depressive Episode:
  • Meets full MDD criteria (≥5 symptoms, ≥2 weeks)
Exclusions:
  • No current or past manic episode (changes diagnosis to BD-I)
  • Antidepressant-induced hypomanic episode does NOT count toward BD-II diagnosis (DSM-5-TR)
Key distinction: Depressive burden is dominant in BD-II; hypomanic episodes are often recalled as "feeling well"

SLIDE 21 — Management: Overview & Principles

Three-Phase Model:
  • Acute phase: Achieve remission of current episode (mania or depression)
  • Continuation phase: Prevent relapse of the same episode
  • Maintenance phase: Prevent future episodes (lifelong in most cases)
Core Principles:
  • Mood stabilizers are the backbone of all BD treatment
  • NEVER use antidepressant monotherapy — risk of triggering mania, hypomania, or rapid cycling
  • Remove precipitants: stop stimulants, regulate sleep, avoid alcohol
  • Treat to full remission — partial response predicts higher relapse rates
  • Psychoeducation is as important as pharmacotherapy for long-term outcomes
  • Lifestyle regulation: regular sleep-wake cycle, avoiding alcohol and stimulants, exercise
  • Shared decision-making essential — BD is a lifelong condition; adherence is the biggest challenge

SLIDE 22 — Management: Pharmacological — Lithium

  • Class: Alkali metal / Mood stabilizer
  • MOA: Inhibits inositol monophosphatase, modulates GSK-3β, neuroprotective effects
  • Indications: Acute mania, long-term maintenance of BD-I and BD-II, augmentation in MDD
  • Therapeutic serum level: 0.6–1.2 mEq/L (acute: 0.8–1.2; maintenance: 0.6–0.8)
  • Response rate for acute mania: 60–80%
  • Gold standard for suicide prevention in mood disorders — strongest evidence of any agent
  • Side effects: Fine postural tremor, polyuria/polydipsia (nephrogenic DI), weight gain, hypothyroidism, acne, leukocytosis
  • Toxicity (>1.5 mEq/L): Coarse tremor, ataxia, confusion, seizures, cardiac arrhythmias, coma
  • Monitoring: Serum levels, renal function (eGFR), thyroid function every 3–6 months
  • Teratogenicity: Ebstein's anomaly (tricuspid valve) — avoid in 1st trimester

SLIDE 23 — Management: Pharmacological — Anticonvulsant Mood Stabilizers

Valproate (Valproic Acid / Divalproex):
  • Effective for acute mania, especially mixed features and rapid cycling
  • Therapeutic level: 50–125 μg/mL
  • SE: Weight gain, sedation, hair loss, thrombocytopenia, hepatotoxicity, tremor
  • CONTRAINDICATED in pregnancy (neural tube defects) and PCOS-like effects
  • Superior to lithium for mixed/dysphoric mania
Lamotrigine:
  • Best for prevention of bipolar depression — NOT effective for acute mania
  • Start low, titrate slowly over weeks to avoid Stevens-Johnson Syndrome
  • SE: Rash (dose-dependent), Stevens-Johnson Syndrome (rare but serious)
  • Weight neutral; no metabolic effects; generally well tolerated
Carbamazepine:
  • Effective for acute mania; especially useful for lithium non-responders, dysphoric mania, and rapid cycling
  • SE: Aplastic anemia, agranulocytosis, Stevens-Johnson Syndrome, SIADH, diplopia, ataxia
  • Blood monitoring required at 3, 6, 9, 12 months (hematologic)
  • Potent CYP450 inducer — many significant drug interactions (including OCP)

SLIDE 24 — Management: Pharmacological — Antipsychotics

Second-Generation Antipsychotics (SGAs) — Key Agents in BD:
  • Quetiapine: FDA-approved for BD-I mania, BD-II depression, AND maintenance — most versatile SGA in BD
  • Lurasidone: FDA-approved for bipolar depression (with or without mood stabilizer)
  • Cariprazine: FDA-approved for bipolar depression AND acute mania
  • Olanzapine: Acute mania and maintenance; significant weight gain and metabolic risk
  • Aripiprazole: Acute mania and maintenance; metabolically neutral; available as monthly IM depot
  • Risperidone, Ziprasidone, Asenapine: FDA-approved for acute BD mania
First-Generation Antipsychotics:
  • Haloperidol IM: Effective for emergency control of severe manic agitation
  • Higher extrapyramidal SE risk than SGAs
General: Mood stabilizer + SGA combination often needed for severe or mixed mania

SLIDE 25 — Management: Pharmacological by Episode Phase

Acute Mania:
  • First-line: Lithium OR valproate PLUS an SGA (quetiapine, olanzapine, aripiprazole)
  • Benzodiazepines (lorazepam, clonazepam) as adjuncts for agitation
  • Haloperidol IM for emergency severe agitation
  • Carbamazepine for lithium non-responders or mixed/dysphoric mania
  • STOP any antidepressants; STOP stimulants
  • ECT for refractory mania or when rapid response is required
Bipolar Depression:
  • First-line: Quetiapine monotherapy (FDA-approved, Level A evidence)
  • Lurasidone + lithium or valproate (FDA-approved)
  • Cariprazine (FDA-approved for bipolar depression)
  • Lamotrigine for prevention/maintenance
  • If antidepressant added: ALWAYS combine with mood stabilizer (never monotherapy)
  • ECT: Severe, refractory, or psychotic bipolar depression

SLIDE 26 — Management: Non-pharmacological

  • Psychoeducation (Individual or Group):
    • Cornerstone of long-term management
    • Recognition of early warning signs of mania/depression
    • Medication adherence, trigger identification, sleep hygiene
  • Interpersonal & Social Rhythm Therapy (IPSRT):
    • Stabilizes daily social rhythms and sleep-wake cycles
    • Specifically designed for BD — reduces episode frequency
  • Cognitive Behavioral Therapy (CBT):
    • Addresses maladaptive cognitions; effective for depressive phases and adherence
  • Family-Focused Therapy (FFT):
    • Reduces expressed emotion in family; improves communication and crisis management
    • Particularly effective in early-onset BD
  • Lifestyle: Regular sleep schedule, aerobic exercise, alcohol/stimulant avoidance, stress management
  • ECT: Effective for severe BD depression, acute mania, and BD in pregnancy
  • TMS: Emerging evidence for bipolar depression

SLIDE 27 — Prognosis

  • BD is a lifelong, recurrent disorder — not a curable condition
  • Without treatment: ~90% of patients experience recurrence
  • With optimal treatment: 50–60% achieve good functional outcomes
  • Rapid cycling (≥4 episodes/year): Poorer prognosis; associated with hypothyroidism, antidepressant use, female sex
  • Mixed features: Associated with highest suicide risk and poorest treatment response
  • Suicide: 15–20× higher risk than general population; 10–15% of BD patients die by suicide
  • Kaplan: "As the course of bipolar disorder progresses, patients tend to have more frequent episodes that last longer"
Predictors of POOR prognosis: Early onset | Psychotic features | Substance use | Medication non-adherence | Poor social support | Rapid cycling | Mixed states
Predictors of GOOD prognosis: Good inter-episode functioning | Strong social support | Medication compliance | Absence of psychosis | Late onset

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MAJOR DEPRESSIVE DISORDER


SLIDE 1 — Title

Major Depressive Disorder (MDD) Kaplan & Sadock's Synopsis of Psychiatry, 12th Ed. | DSM-5-TR

SLIDE 2 — Introduction & Epidemiology

  • Primary mood disorder — persistent depressed mood and/or anhedonia
  • Leading cause of disability worldwide
  • Lifetime prevalence: ~17%
  • Female : Male ratio — 2:1
  • Mean age of onset: ~30 years (50% before age 40)
  • Rising incidence in adolescents
  • Common comorbidities: anxiety disorders, substance use disorders

SLIDE 3 — Clinical Features

  • Depressed mood most of the day, nearly every day
  • Anhedonia — loss of interest or pleasure
  • Sleep disturbance (insomnia or hypersomnia)
  • Appetite/weight changes
  • Fatigue and loss of energy
  • Feelings of worthlessness or guilt
  • Poor concentration or indecisiveness
  • Psychomotor agitation or retardation
  • Suicidal ideation or attempts

SLIDE 4 — DSM-5-TR Diagnostic Criteria

≥5 symptoms for ≥2 weeks; at least one must be depressed mood OR anhedonia
  1. Depressed mood
  2. Anhedonia
  3. Weight/appetite change (>5%/month)
  4. Insomnia or hypersomnia
  5. Psychomotor agitation or retardation
  6. Fatigue or loss of energy
  7. Worthlessness or excessive guilt
  8. Poor concentration or indecisiveness
  9. Recurrent thoughts of death or suicidal ideation
Symptoms cause significant distress/impairment; not due to substances or medical condition; no history of mania/hypomania

SLIDE 5 — Management: Pharmacological

First-Line:
  • SSRIs — fluoxetine, sertraline, escitalopram, paroxetine
  • SNRIs — venlafaxine, duloxetine
Second-Line / Alternatives:
  • TCAs — amitriptyline, imipramine (caution: cardiotoxic, lethal in OD)
  • MAOIs — phenelzine (reserved for atypical/refractory MDD)
  • Bupropion — no sexual SE, weight neutral
  • Mirtazapine — preferred with insomnia/poor appetite
  • Ketamine/Esketamine — rapid-acting; for treatment-resistant MDD
Augmentation: Lithium, atypical antipsychotics (aripiprazole, quetiapine)
Adequate trial: therapeutic dose × 4–6 weeks

SLIDE 6 — Management: Non-pharmacological

Psychotherapy:
  • Cognitive Behavioral Therapy (CBT) — gold standard
  • Interpersonal Therapy (IPT)
  • Mindfulness-Based Cognitive Therapy (MBCT) — reduces relapse in recurrent MDD
  • Behavioral Activation
Somatic Treatments:
  • ECT — severe, psychotic, or treatment-resistant; high suicidal risk
  • rTMS — FDA-approved after ≥1 failed antidepressant; no anesthesia
  • Phototherapy — first-line for seasonal pattern (SAD); 2,500–10,000 lux
  • VNS — chronic, refractory cases

SLIDE 7 — Prognosis

  • Untreated episode lasts 6–13 months; treated ~3 months
  • 25% relapse within 6 months of discharge
  • 50–75% relapse within 5 years
  • Mean episodes over 20 years: 5–6
  • Each episode: shorter intervals, greater severity
Good PrognosisPoor Prognosis
Mild, single episodeEarly onset
Good social supportPsychotic features
No comorbiditiesSubstance use disorder
Treatment adherentPersonality disorder


BIPOLAR DISORDER


SLIDE 8 — Title

Bipolar Disorder Kaplan & Sadock's Synopsis of Psychiatry, 12th Ed. | DSM-5-TR

SLIDE 9 — Introduction & Epidemiology

  • Chronic cyclic mood disorder — episodes of mania/hypomania AND depression
  • Classified as: Bipolar I, Bipolar II, Cyclothymia
  • Bipolar I prevalence: ~1% (equal sex ratio)
  • Bipolar II prevalence: ~1.1% (female predominance)
  • Mean age of onset: ~18–25 years
  • Suicide risk 15–20× higher than general population
  • Highly heritable — MZ twin concordance: 60–80%
  • Comorbidities: anxiety disorders, substance use, ADHD

SLIDE 10 — Clinical Features

Manic Episode (DIG FAST):
  • Distractibility
  • Impulsivity / Indiscretion (risky behaviors)
  • Grandiosity
  • Flight of ideas / pressured speech
  • Activity increase (goal-directed)
  • Sleep decreased — without fatigue (most pathognomonic)
  • Talkativeness
Depressive Episode:
  • Same features as MDD
  • Clues favoring BD: hypersomnia, hyperphagia, psychomotor retardation, early onset, family history of BD
Mixed Features: Mania + depression simultaneously → highest suicide risk

SLIDE 11 — DSM-5-TR Diagnostic Criteria

Bipolar I — Manic Episode:
  • Elevated/expansive/irritable mood + increased energy ≥7 days
  • ≥3 DIGFAST symptoms (≥4 if mood only irritable)
  • Marked impairment OR hospitalization OR psychotic features
Bipolar II — Hypomanic + Depressive Episode:
  • Hypomania: same symptoms ≥4 days; no marked impairment; no psychosis
  • Plus ≥1 full Major Depressive Episode
  • No history of full manic episode
Antidepressant-induced hypomania does NOT count toward BD-II diagnosis

SLIDE 12 — Management: Pharmacological

Mood Stabilizers (Backbone):
  • Lithium — first-line mania + maintenance; gold standard for suicide prevention; level 0.6–1.2 mEq/L
  • Valproate — acute mania; preferred for mixed/rapid cycling
  • Lamotrigine — prevents bipolar depression; NOT for acute mania
  • Carbamazepine — lithium non-responders; dysphoric mania
Antipsychotics (SGAs):
  • Quetiapine — mania, BD depression, maintenance
  • Lurasidone / Cariprazine — bipolar depression
  • Olanzapine, Aripiprazole — acute mania + maintenance
NEVER use antidepressant monotherapy in BD — risk of triggering mania/rapid cycling

SLIDE 13 — Management: Non-pharmacological

Psychotherapy:
  • Psychoeducation — cornerstone; early warning signs, adherence, triggers
  • Interpersonal & Social Rhythm Therapy (IPSRT) — stabilizes sleep-wake cycles
  • Cognitive Behavioral Therapy (CBT)
  • Family-Focused Therapy (FFT) — reduces relapse rates
Lifestyle:
  • Regular sleep schedule
  • Avoid alcohol and stimulants
  • Aerobic exercise
Somatic:
  • ECT — severe BD depression, acute refractory mania, BD in pregnancy

SLIDE 14 — Prognosis

  • BD is a lifelong, recurrent disorder
  • Without treatment: ~90% experience recurrence
  • Suicide: 10–15% of BD patients die by suicide
Good PrognosisPoor Prognosis
Good inter-episode functioningEarly onset
Strong social supportRapid cycling
Medication adherenceMixed states
Absence of psychosisSubstance use
Late onsetNon-adherence
Rapid cycling (≥4 episodes/year) — poorest prognosis; associated with hypothyroidism and antidepressant use

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