Inotropes and vasopressors are used critically ill patients with shock or severe hypotension in order to restore perfusion and maintain blood pressure.
| Category | Function | Examples |
|---|---|---|
| Vasopressors | Increase systemic vascular resistance (SVR) by vasoconstriction | Noradrenaline, adrenaline, phenylephrine, vasopressin, and dopamine |
| Inotropes | Increase cardiac contractility and cardiac output (CO) | Dobutamine and milrinone |
Individual drugs
| Drug | Description | Adverse effects |
|---|---|---|
| Noradrenaline | First-line vasopressor for septic shock. Has mixed α1 > β1 activity | Arrhythmia, bradycardia, and tissue necrosis if extravasation occurs |
| Adrenaline | Used in anaphylaxis and refractory shock. Has strong α and β effects | Tachycardia, anxiety, and pulmonary oedema |
| Phenylephrine | Pure α1 agonist that causes vasoconstriction only | Reduced cardiac output and peripheral ischaemia |
| Dopamine | Has a dose-dependent effect. At low dose it causes vasodilation, at moderate dose it causes β stimulation, and at high dose it casues α stimulation. | Tachycardia, arrhythmias, and tissue necrosis. |
| Dobutamine | A strong inotrope thaat is used in cardiogenic shock, HFrEF, and cardiac stress testing. It is mainly a β1 agonist | Arrhythmias, hypokalaemia, and increaed myocarial oxygen demand |
| Vasopressin | Acts on V1 receptors to cause vasoconstriction, and on V2 receptors for an antidiuretic effect | Hyponatremia, mesenteric ischaemia, and coronary vasoconstriction |
- Mechanism of action
- α1 receptors → vasoconstriction → ↑ SVR
- β1 receptors → ↑ heart rate and contractility
- β2 receptors → vasodilation
- V1 receptors → vasoconstriction
- V2 receptors → antidiuretic effect
- Indications
- Septic shock
- Neurogenic shock
- Cardiogenic shock
- Contraindications
- Hyperesensitivity reactions
- Tachyarrhythmias
- Pheochromocytoma
- Dobutamine is contraindicated in hypertrophic obstructive cardiomyopathy
- MAOi use increases the risk of vasopressor toxicity