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Bipolar disorders are chronic, recurrent mood disorders marked by episodes of mania or hypomania, usually alternating with major depressive episodes. Onset is typically in late adolescence or early adulthood. Heritability is among the highest of all psychiatric disorders. Proposed mechanisms include dysregulated monoamine signaling, disrupted circadian rhythms, and abnormal intracellular signaling; sleep loss, stimulants, antidepressants, and stress can trigger episodes.
| Episode | Requirements |
|---|---|
| Manic | Abnormally elevated, expansive, or irritable mood AND increased activity or energy for ≥ 1 week (any duration if hospitalized), with ≥ 3 additional symptoms (4 if mood is only irritable); marked impairment, hospitalization, or psychotic features |
| Hypomanic | Same symptoms for ≥ 4 consecutive days; a clear change noticeable to others but no marked impairment, no hospitalization, no psychosis |
| Major depressive | Same criteria as in MDD (≥ 5 symptoms for ≥ 2 weeks) |
Manic symptoms (mnemonic DIG FAST): Distractibility; Impulsive, risky activity (spending sprees, sexual indiscretion, reckless driving); Grandiosity or inflated self-esteem; Flight of ideas or racing thoughts; increased goal-directed Activity or psychomotor agitation; decreased need for Sleep (feels rested after 3 hours); Talkativeness or pressured speech.
| Disorder | Definition |
|---|---|
| Bipolar I | At least one manic episode. Depressive episodes are common but not required |
| Bipolar II | At least one hypomanic episode and at least one major depressive episode; never a manic episode. Not a milder illness — depression is often long and disabling |
| Cyclothymic disorder | Numerous hypomanic and depressive symptoms for ≥ 2 years (1 year in youth) that never meet full episode criteria |
| Substance/medication-induced; due to another medical condition | E.g., corticosteroids, stimulants, hyperthyroidism |
A full manic episode that emerges during antidepressant treatment and persists beyond the drug's physiological effect counts toward bipolar I.
Specifiers: with mixed features, with rapid cycling (≥ 4 mood episodes in 12 months), with psychotic features, with anxious distress, with peripartum onset, with seasonal pattern.
Bipolar depression — same features as MDD, often with hypersomnia and psychomotor slowing; suicide risk is high, especially during depressive or mixed episodes and after discharge.
Assess: safety (suicide, violence, recklessness), nutrition and hydration, sleep, substance use, finances and relationships affected, medication adherence, family history, early warning signs of past relapses.
| Test / tool | Purpose |
|---|---|
| Mood Disorder Questionnaire; Young Mania Rating Scale | Screening; severity of mania |
| TSH, urine drug screen, CBC, metabolic panel | Medical or substance causes; baseline |
| Pre-lithium baseline | Creatinine and eGFR, urinalysis, electrolytes (sodium), TSH, calcium, weight/BMI; ECG if cardiac risk or older age; pregnancy test |
| Pre-valproate baseline | Liver function tests, CBC with platelets, weight, pregnancy test |
| Pre-carbamazepine baseline | CBC, liver tests, sodium; HLA-B*15:02 testing in people of Asian ancestry |
| Pre-antipsychotic baseline | Weight, BMI, glucose or HbA1c, lipids, BP |
Acute mania: lithium, valproate, or a second-generation antipsychotic (olanzapine, quetiapine, risperidone, aripiprazole, cariprazine), or haloperidol; severe cases may combine lithium or valproate with an antipsychotic. Benzodiazepines (e.g., lorazepam, clonazepam) are used short term as adjuncts for agitation and insomnia — not as mood stabilizers. Stop antidepressants during mania.
Bipolar depression: quetiapine, lurasidone, cariprazine, lumateperone, olanzapine-fluoxetine, lithium, or lamotrigine. Antidepressant monotherapy is avoided (risk of switching to mania or rapid cycling).
Maintenance: lithium (the long-standing first-line mood stabilizer and the drug with the best evidence for reducing suicide), valproate, lamotrigine (prevents depressive relapse; does not treat acute mania), or selected antipsychotics. ECT for severe, psychotic, or treatment-resistant episodes and in some pregnancies.
| Item | Details |
|---|---|
| Serum level | Commonly 0.6–1.2 mEq/L (mmol/L — same numeric value); acute mania often targeted at the upper part, maintenance often 0.6–1.0. Draw 12 hours after the last dose (trough), about 5 days after starting or any dose change, then every 3–6 months when stable |
| Ongoing monitoring | Kidney function, TSH, and calcium at least every 6 months; weight; sodium when ill |
| Common early effects | Nausea, diarrhea, fine hand tremor, polyuria and polydipsia, metallic taste, weight gain, fatigue |
| Long-term effects | Hypothyroidism, nephrogenic diabetes insipidus (AVP resistance), chronic kidney disease, hyperparathyroidism with hypercalcemia, acne or psoriasis flares, cardiac conduction changes |
| Toxicity (usually above 1.5 mEq/L; can occur at therapeutic levels in older adults) | Early: vomiting, diarrhea, coarse tremor, muscle weakness, drowsiness, ataxia, slurred speech. Severe (often above 2.0): confusion, hyperreflexia, myoclonus, seizures, dysrhythmias, oliguria, coma |
| Toxicity management | Hold lithium, notify prescriber, obtain level, electrolytes, creatinine, and ECG; IV isotonic fluids; activated charcoal does not bind lithium; whole-bowel irrigation may be used for sustained-release overdose; hemodialysis for severe toxicity. Older adults often need lower targets (about 0.4–0.8 mEq/L) |
| Interactions that raise levels | NSAIDs, thiazide diuretics, ACE inhibitors, ARBs, dehydration, low-sodium diet, heavy sweating, vomiting, diarrhea, fever |
| Pregnancy | Small increased risk of cardiac malformation (Ebstein anomaly); levels shift in pregnancy and fall sharply after delivery — close level monitoring and specialist planning; neonatal toxicity possible. Discuss breastfeeding with the prescriber |
Lamotrigine — serious rash (Stevens-Johnson syndrome/toxic epidermal necrolysis); slow titration; stop and report any rash. If lamotrigine has been stopped for about 5 days or more (≥ 5 half-lives), restart the titration schedule — do not resume the prior dose. Estrogen-containing contraceptives lower lamotrigine levels; rash risk is higher with valproate co-therapy (lamotrigine dose is halved).
Class warning: all antiseizure mood stabilizers (valproate, lamotrigine, carbamazepine) carry a warning for increased suicidal thoughts and behavior — monitor mood.
Carbamazepine — agranulocytosis and aplastic anemia, hyponatremia, SJS/TEN (HLA-B*15:02), enzyme induction (lowers hormonal contraceptive and other drug levels), teratogenic.
Second-generation antipsychotics — metabolic effects, EPS, sedation, orthostatic hypotension; boxed warning for older adults with dementia-related psychosis (see schizophrenia topic).
Psychosocial — psychoeducation, family-focused therapy, interpersonal and social rhythm therapy (regular sleep and daily routines), CBT, relapse-prevention planning.
Listed in priority order.
| Complication | What to watch for |
|---|---|
| Suicide | Depressive or mixed episodes, hopelessness, after discharge |
| Lithium toxicity | GI symptoms, coarse tremor, ataxia, confusion, seizures |
| Exhaustion, dehydration | Continuous activity, no food or sleep |
| Injury, violence, legal or financial harm | Impulsivity, grandiosity, irritability |
| Hepatotoxicity, pancreatitis (valproate) | Jaundice, abdominal pain, vomiting |
| SJS/TEN (lamotrigine, carbamazepine) | Rash, blisters, mucosal lesions, fever |
| Hypothyroidism, nephrogenic DI (lithium) | Fatigue, weight gain, large urine volumes |
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