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Bipolar disorder

SNOMED: 83225003992 wordsUpdated 03/03/2026
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Exam Tips

  • Mania requires at least 7 days (or any duration if hospitalisation/psychosis), hypomania at least 4 days with no psychosis or marked functional impairment.
  • In OSCE depression stations, actively screen for past hypomanic/manic episodes (overactivity, reduced need for sleep, disinhibition) to avoid missing bipolar disorder.
  • Do not diagnose bipolar disorder in primary care using questionnaires alone; diagnosis requires specialist assessment with collateral history.
  • For bipolar depression, avoid antidepressant monotherapy; use bipolar-specific regimens and monitor for switch into mania.
  • Lithium monitoring is a frequent UK exam topic: 12-hour levels plus renal, thyroid, calcium, and toxicity counselling.
  • Valproate teratogenicity and UK Pregnancy Prevention Programme requirements are high-yield safety points.

Definition

Bipolar disorder is a chronic episodic mood disorder characterised by pathological shifts between elevated mood states (hypomania or mania) and depression, with periods of partial or full remission between episodes. Mania involves at least 7 days of abnormally elevated, expansive, or irritable mood with increased activity and marked functional impairment and/or psychosis, while hypomania lasts at least 4 days without psychosis or severe functional collapse. Diagnosis and subtype classification (bipolar I vs bipolar II) require specialist mental health assessment in UK practice.

Pathophysiology

Bipolar disorder is best understood as a neurobiological illness with strong genetic loading (around 70% heritability) plus environmental triggers. Current models describe dysregulation across fronto-limbic networks (prefrontal cortex, amygdala, striatum), altered monoaminergic and glutamatergic signalling, circadian rhythm instability, HPA-axis stress dysregulation, and inflammatory/mitochondrial abnormalities that may contribute to episode recurrence and cognitive decline over time. Kindling/sensitisation concepts explain why repeated episodes can become more frequent with shorter euthymic intervals. Image reference: see standard psychiatry textbook diagrams of fronto-limbic circuitry and circadian clock dysregulation in bipolar disorder chapters.

Risk Factors

  • First-degree family history of bipolar disorder (substantially increased lifetime risk)
  • Adverse childhood experiences (trauma, abuse, neglect, early parental loss)
  • Cannabis or cocaine use
  • Postpartum period (postpartum psychosis can be first presentation)
  • Possible in utero infectious exposures (for example toxoplasma, CMV, HSV associations)
  • Prior depressive episodes with early onset and episodic pattern

Clinical Features

Symptoms

  • Episodic elevated or irritable mood with increased energy/activity
  • Reduced need for sleep (feels rested after very little sleep)
  • Racing thoughts, distractibility, and pressure of speech
  • Disinhibition, increased libido, impulsive spending/risk-taking
  • Depressive episodes: persistent low mood or anhedonia, low energy, hopelessness, suicidal ideation
  • Mixed features: coexisting depressive and manic symptoms within same period

Signs

  • Psychomotor agitation, overfamiliarity, and intrusive behaviour during mania/hypomania
  • Rapid, loud, difficult-to-interrupt speech; flight of ideas
  • Grandiose delusions or hallucinations in severe mania
  • Neglect of self-care, dehydration, exhaustion in prolonged episodes
  • Objective functional deterioration (work, finances, relationships, legal/social harm)
  • Possible psychomotor retardation or catatonic features in severe depressive phases

Investigations

Specialist psychiatric assessment (history + collateral):Establishes DSM/ICD episode pattern (mania/hypomania/depression/mixed), severity, psychosis, risk, and bipolar subtype
Risk assessment (suicide, self-harm, harm to others, safeguarding):May identify urgent need for crisis team input, hospital admission, or Mental Health Act assessment
Thyroid function tests:Usually normal in primary bipolar disorder; abnormality suggests thyroid-related mood disorder
FBC, U&Es, eGFR, LFTs, calcium, glucose/HbA1c, lipids, weight/BMI, blood pressure:Baseline before lithium/antipsychotics/valproate; helps detect comorbidity and treatment risk
ECG (when clinically indicated, especially antipsychotic use/cardiac risk):Screens for conduction/QT issues before or during antipsychotic treatment
Urine toxicology screen:May detect substance-induced mood symptoms (for example stimulants/cannabis)
Pregnancy test in people of childbearing potential before teratogenic drugs:Essential before valproate; informs safer prescribing choices

Management

Lifestyle Modifications

  • Psychoeducation for patient and family (early warning signs, relapse prevention plan, adherence)
  • Regular sleep-wake routine and circadian stabilisation; avoid sleep deprivation
  • Avoid alcohol and recreational drugs (especially cannabis/cocaine)
  • Structured daily routine, stress management, and support for employment/finances/relationships
  • Crisis planning including who to contact if mania, psychosis, or suicidality escalates

Pharmacological Treatment

Acute mania/hypomania (first-line antipsychotic options)

  • Olanzapine 10 mg once daily initially; usual range 5-20 mg/day
  • Quetiapine (immediate release) titrated from 100 mg day 1 to 400 mg day 4; usual 400-800 mg/day in divided doses
  • Risperidone 2 mg once daily initially; usual range 1-6 mg/day
  • Haloperidol 2-10 mg/day in divided doses (dose individualised to response and adverse effects)

Choose based on prior response, side-effect profile, and comorbidity. If inadequate response, switch antipsychotic; if still inadequate, consider adding lithium. Monitor for EPS, metabolic effects, sedation, prolactin effects, and QT prolongation.

Mood stabiliser (acute mania adjunct and long-term relapse prevention)

  • Lithium carbonate modified-release usually 400 mg at night initially (200 mg in older/frail adults), then titrate to 12-hour plasma level target (commonly 0.6-0.8 mmol/L maintenance; often 0.8-1.0 mmol/L in acute treatment if tolerated)

Key safety: narrow therapeutic index; toxicity risk rises with dehydration, AKI, NSAIDs, ACE inhibitors, and thiazide diuretics. Monitor lithium level, renal function, thyroid function, calcium, and weight regularly; counsel on fluid/salt consistency and toxicity symptoms (tremor, diarrhoea, ataxia, confusion).

Bipolar depression

  • Fluoxetine 20 mg once daily combined with olanzapine (for example olanzapine 5-20 mg/day)
  • Quetiapine for bipolar depression: 50 mg day 1, 100 mg day 2, 200 mg day 3, 300 mg day 4; usual target 300 mg at night
  • Lamotrigine titration: 25 mg once daily for 2 weeks, then 50 mg once daily for 2 weeks, then increase toward usual 200 mg/day maintenance (adjust with interacting drugs)

Avoid antidepressant monotherapy in bipolar depression due to switching risk into mania/hypomania. Lamotrigine requires slow titration to reduce serious rash risk (including SJS/TEN); stop urgently if rash with systemic features develops.

Valproate-containing regimens (selected adults only)

  • Sodium valproate (or semisodium valproate) often started at 750 mg/day in divided doses, or about 20 mg/kg/day, then adjusted to response/tolerability

Major UK warning: contraindicated in pregnancy unless strict Pregnancy Prevention Programme requirements are met; avoid in women/girls of childbearing potential unless no effective alternative. Monitor LFTs, FBC/platelets, and pancreatitis/hepatotoxicity symptoms.

Surgical / Interventional

  • Electroconvulsive therapy (ECT) can be considered for severe or treatment-resistant bipolar depression/mania, especially with psychosis, catatonia, or urgent high-risk clinical states

Complications

  • High lifetime risk of suicidal ideation, suicide attempt, and completed suicide
  • Deliberate self-harm and accidental injury (including road traffic accidents during disinhibited states)
  • Financial, occupational, legal, and relationship breakdown due to impulsive/risky behaviour
  • Sexual risk-taking, STI exposure, and unplanned pregnancy
  • Substance and alcohol misuse, gambling-related harms, exploitation vulnerability
  • Physical multimorbidity (cardiovascular disease, obesity, type 2 diabetes, dyslipidaemia, CKD, respiratory disease)
  • Functional and cognitive decline with recurrent episodes

Prognosis

Bipolar disorder is lifelong with a relapsing-remitting course and substantial inter-individual variability. Relapse is common (about 50% within 1 year after an episode and around 75% within 4 years), particularly with poor adherence, incomplete recovery, substance misuse, and sleep disruption. Long-term outcomes improve with early specialist care, sustained pharmacological treatment, psychoeducation, and close monitoring for suicide risk and cardiometabolic disease.

Sources & References

💊BNF Drug References(17)

NICE Guidelines(1)

📖Textbook References(1)

  • Guyton and Hall Textbook of Medical Physiology (John E. Hall, Michael E. Hall) (Z-Library).pdf(pp. 751)[context]

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