ETIOLOGY
- Typically, a primary psychiatric disorder, with genetic association
- May be secondary to medical disorder (e.g., drug toxicity, endocrine, neurologic process)
- Particularly likely to be secondary if
- 1st episode
- patient >40 yr
- atypical or mixed presentation
- abnormal sensorium
DIAGNOSIS
SIGNS AND SYMPTOMS
History
- Psychiatric history:
- Recent symptoms of mania (often collateral sources critical): Elevated, expansive, or irritable mood; increased energy and activity; decreased need for sleep; irresponsibility, disregard for negative consequences of actions; talkativeness; distractibility; fast thoughts; grandiosity, overconfidence
- Past mania or depression
- Noncompliance with mood stabilizer
- Recent initiation or discontinuation of antidepressant
- Recent substance abuse
- Bipolar family history
- Medical history:
- Endocrine, metabolic, or neurologic disorders
- Current or recent medications
Physical-Exam
- Appearance:
- Hyperactive, if not agitated
- Talkative, often with loud, rapid, or “pressured” speech
- Affect:
- Irritable, argumentative, often multiple recent arguments or fights
- Less commonly euphoric or expansive
- Often labile with depressed or tearful intervals (may confound diagnosis)
- Patient likely to describe mood as tense, irritable, or depressed rather than euphoric
- Neurovegetative:
- Increased energy, engaged in multiple goal-directed activities many hours per day
- Racing thoughts
- Decreased sleep
- Thought process:
- Rapid, distractible, may be incoherent, delirious
- Thought content:
- Psychosis possible, either mood congruent (e.g., delusions of grandeur or power) or mood incongruent (may be indistinguishable from other psychotic disorders)
- Judgment:
- Inflated self-esteem, perhaps to grandiose or psychotic extent
- Uncharacteristic, irresponsible behavior, such as financial or sexual indiscretions, with inability to recognize negative consequences of actions.
- Substance abuse is frequent during mania.
- Sensorium:
- Typically normal
- Confusion or delirium possible
ESSENTIAL WORKUP
- Physical and neurologic exam; vital signs
- Mania may present as delirium and need workup of full differential diagnosis of delirium.
DIAGNOSIS TESTS & NTERPRETATION
Lab
- Toxicology screen (urine or serum)
- Blood alcohol level
- Electrolytes
- Blood glucose
- CBC
- TSH
- Lithium, carbamazepine, valproate serum levels, if relevant
- Other tests as suggested by history or physical exam
Imaging
CT head only with suspicion of neurologic etiology
DIFFERENTIAL DIAGNOSIS
- Primary mania of bipolar or schizoaffective disorder
- Psychosis
- Agitated depression
- Personality disorders:
- Borderline
- Narcissistic
- Antisocial
- Attention deficit disorder
- Conduct or intermittent explosive disorders
- Organic brain syndrome
- Intoxication or withdrawal from alcohol or sedative hypnotics
- Intoxication with cocaine, amphetamines, phencyclidine, or other sympathomimetics
- Accidental or deliberate toxic overdose
- Treatment with antidepressants or electroshock therapy in susceptible individuals
- Recent discontinuation of antidepressant medication
- Corticosteroid or thyroid hormones
- Anticholinergics
- Treatment of Parkinson disease
- Cyclobenzaprine (Flexeril)
- Endocrine or metabolic disorders (particularly thyroid disease)
- Encephalitis
- Meningitis
- Postictal states
- MS
- Postcerebrovascular accident
- CNS tumors
- CNS vasculitis
- General paresis
TREATMENT
INITIAL STABILIZATION/THERAPY
- High violence potential:
- Quiet environment
- Prompt evaluation
- Nonconfrontational manner
- Adequate security backup
- Physical restraint and sedation, as needed
- For cooperative, but agitated patient:
- PO neuroleptics (e.g., haloperidol, consider olanzapine or chlorpromazine as alternate) or PO benzodiazepines (e.g., lorazepam)
- For uncooperative agitated patient:
- Synergistic combination of IM, IV, or PO haloperidol and lorazepam widely used (some authorities favor monotherapy with benzodiazepine or neuroleptic):
- Benztropine for prevention of acute dystonic reaction to haloperidol is not usually required when concurrent benzodiazepine is given.
- Consider lorazepam, olanzapine, ziprasidone, or chlorpromazine IM as alternative.
ED TREATMENT/PROCEDURES
- Outpatient management:
- Neuroleptics for symptomatic treatment, on temporary or continuing basis
- Agents for sleep
- Discontinuation of antidepressant if related to present hypomania or mania
- Initiation or restart of mood-stabilizer therapy:
- Action of mood-stabilizing agents requires days or weeks, even after full serum level attained.
- Inpatient management:
- Sedation or initiation of mood stabilizer in consultation with admitting psychiatrist
MEDICATION
- Acute agitation:
- Lorazepam: 2 mg PO/IM (lower dose in mild agitation or in frail or elderly); may repeat q30min, generally not to exceed 12 mg/24h
- Haloperidol: 5 mg PO (lower dose in mild agitation or in frail or elderly); may repeat q30min, generally not to exceed 20 mg/24h
- Synergistic combination of haloperidol, 5 mg IM/IV/PO + lorazepam 1–2 mg IM/IV/PO, repeat q30min, as required (doses may be smaller in elderly or frail patients)
- Olanzapine 10 mg IM, ziprasidone 10 mg IM, aripiprazole 9.75 mg IM or chlorpromazine 50 mg IM may be useful parenteral alternatives, perhaps at a lower dose in frail or elderly (avoid chlorpromazine in hypotension; ziprasidone may have more QT prolonging effect than other neuroleptics but the clinical relevance of such effect at this dose is unclear).
- Typical outpatient medications:
- Aripiprazole: 5–20 mg PO QD
- Benztropine: 1 mg PO BID
- Carbamazepine: 400–2,000 mg/d (often in div. doses or in sustained-release dose forms)
- Clonazepam: 0.5–2 mg PO QHS or 0.5–2 mg PO BID
- Haloperidol: 0.5–5 mg PO BID
- Lamotrigine: 25–200 mg/d in 1 or 2 div. doses (typically up to 100 mg/d in patients taking valproate, up to 500 mg/d in patients taking carbamazepine or certain other cytochrome inducers, but not valproate)
ALERT
- Lamotrigine must be started by a gradual dose escalation schedule specified by manufacturer to avoid increased risk of severe dermatologic reactions; if resumed after discontinuation for more than 5 half-lives (about 5 days), the gradual dose escalation schedule must be used again (half-life is shorter with certain antiepileptics, OCPs, rifampin; see prescribing literature).
- Lithium: 600–3,000 mg/d (often in div. doses or in sustained-release dose forms; in acute mania, initiate at 300 mg PO TID)
- Olanzapine: 1.25–30 mg/d, QHS or in div. doses
- Perphenazine: 4–32 mg/d PO QHS or in div. doses
- Quetiapine: 50–400 mg PO QHS or 100–400 PO BID; quetiapine XR PO 50–800 mg QHS
- Risperidone: 0.5–6 mg/d PO QHS or in div. doses
- Valproate (e.g., Depakote): 750–3,000 mg/d (often in div. doses; in acute mania, initiate at 250 mg PO TID)
Pregnancy Considerations
The safety of psychotropic medications in pregnancy is a complex issue: Lithium, valproate, and carbamazepine are Pregnancy Category D and pose particular risks, highest in early pregnancy.
FOLLOW-UP
DISPOSITION
Admission Criteria
- Involuntary hospitalization is required by danger to self:
- Suicidal risk, especially if mixed or labile mood or psychotic
- Unsafe behaviors due to impaired judgment
- Medically unstable
- Hospitalization diagnostically required
- Involuntary hospitalization also required by:
- Risk of behaviors dangerous to others
- Inability to care for self (unable to obtain basic needs, such as food, clothing, or shelter)
Discharge Criteria
- Patients with mild symptoms may be discharged on medications noted above if:
- necessary supports to ensure safety are in place.
- patient is compliant with treatment plan.
- consultation with outpatient psychiatrist is available within 1–3 days.
- Some patients who are not legally committable may refuse treatment; explain availability of future treatment to patient and any involved friends or family.
PEARLS AND PITFALLS
- Manic patients are more likely to appear dysphoric or irritable, rather than “happy.”
- Patients presenting with depression should be asked about features suggesting mania and hypomania; 70% of bipolar patients have previously been misdiagnosed.
- Individuals with bipolar disorder are at high risk for addiction, further complicating treatment.
- Prompt recognition of the earliest signs of mania may allow prevention of a full episode.
- Bipolar disorder in children frequently manifests as behavioral disinhibition or irritability.