Levosimendan (ICU — Calcium Sensitiser)
Brand names: Simdax
Levosimendan is an intravenous calcium-sensitising inodilator used in intensive care for short-term management of acute decompensated or low-output heart failure when conventional therapy is insufficient.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
It increases myocardial contractility by sensitising cardiac troponin C to calcium without raising intracellular calcium, and opens vascular ATP-sensitive potassium channels to produce systemic and coronary vasodilatation; an active metabolite prolongs its haemodynamic effect for days.
Prescribing in practice
- It commonly causes hypotension and tachyarrhythmias, so blood pressure and the cardiac rhythm must be monitored continuously and significant hypovolaemia corrected before starting.
- Effects persist well beyond the infusion because of its long-acting active metabolite, so haemodynamic monitoring should continue after the infusion ends.
- Use with caution in significant renal or hepatic impairment and in patients with hypokalaemia, which should be corrected beforehand.
Monitoring
Monitor continuous ECG, blood pressure, serum potassium and haemodynamic response throughout and for a period after the infusion.
Counselling the patient
- This is a heart-support drug given as a drip in critical care to help a weakened heart pump more effectively.
- Its benefit can last for several days after the drip finishes.
- Low blood pressure and a fast or irregular heartbeat are recognised effects that the team will watch for closely.
Evidence & guidelines
Randomised trials including SURVIVE and LIDO informed its haemodynamic profile; it improves haemodynamics in acute heart failure though a clear mortality benefit has not been established.
Reference: REVIVE II Trial (2006); SURVIVE Trial (JAMA 2007); ESC Acute Heart Failure Guidelines 2021; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.