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Clinical Pathway

Bipolar Disorder — Lithium Monitoring

Levels, routine bloods, toxicity triggers & shared care

Field: Mental HealthCode: MH-02BUpdated: June 2026Reference: RANZCP CPG / Aust Prescr 2020
Lithium is the GP's core share-care responsibility. Check the level 12 hours after the last dose, every time — regular monitoring is what keeps a uniquely effective drug safe.

Therapeutic levels

  • Maintenance: 0.6–0.8 mmol/L — the target range to maximise relapse prevention.
  • Acute mania: up to 0.6–1.0 mmol/L as tolerated, then back to the maintenance range once stable.
  • Depression augmentation: 0.4–0.8 mmol/L when lithium is added to an antidepressant for treatment-resistant depression.
  • Toxicity: symptoms commonly emerge above 1.5 mmol/L — the level alone doesn't reliably predict toxicity, so always correlate with the clinical picture.

Monitoring schedule

  • Early maintenance: baseline, then 7, 14 and 28 days after starting or any dose change.
  • Once stable: 3, 6 and 12 months, then annually if levels and renal/thyroid function stay stable.
  • Recheck sooner: any change in presentation, an abnormal result, a new interacting medicine, or intercurrent illness.

Routine bloods (6-12 monthly)

  • Renal: lithium level, electrolytes, urea, creatinine and eGFR — lithium can cause nephrogenic diabetes insipidus and, rarely, chronic kidney disease.
  • Thyroid & parathyroid: TSH and calcium — both hypothyroidism and hyperparathyroidism are recognised long-term effects.
  • Cardiometabolic: FBC, glucose, lipids, weight/BMI and a baseline ECG, repeated periodically.
Toxicity triggers. Dehydration, febrile illness, vomiting or diarrhoea (volume loss raises the level); NSAIDs (regular use more than occasional — reduces renal lithium clearance); ACE inhibitors or angiotensin receptor blockers (both can significantly raise the level); thiazide diuretics especially — consider amiloride instead if a diuretic is needed; any new or stopped interacting medicine, or major surgery — recheck around the time of the change.

Safety

  • Always measure the level 12 hours after the last dose — an early or late sample makes the result uninterpretable.
  • Recheck the level after starting or stopping an NSAID, ACE inhibitor, ARB or diuretic, and during any acute illness with vomiting, diarrhoea or reduced fluid intake.
  • Don't rely on the level alone to exclude toxicity — symptoms can occur at normal or therapeutic concentrations, especially in older patients.

Red flags / refer

  • Symptoms of toxicity (coarse tremor, ataxia, confusion, vomiting) → same-day medical assessment; measure the level urgently and consider hospital referral.
  • Declining renal function or a thyroid/parathyroid abnormality on long-term lithium → nephrology or endocrinology review alongside continued psychiatric care.
  • Planning pregnancy, or pregnant, while on lithium or valproate → specialist preconception review before any dose change.

MH-02B v1.0 · Reviewed Jun 2026 · Review Jun 2027

For health-professional use. Framework: RANZCP Mood Disorders CPG (2020); lithium interactions, Aust Prescr 2020;43:91-3. Companion sheet: MH-02A Recognition & Treatment.