Medication | Receptor site action | Clinical relevance |
---|---|---|
Phenylephrine (10 mcg/min–200 mcg/min) | Pure α1 receptor agonist | Increases systemic vascular resistance (SVR), potential to increase pulmonary vascular resistance |
Norepinephrine (0.02 mcg/kg/min–0.3 mcg/kg/min Or (1–20 mcg/min) | α1, β1 receptor agonist | Increases in SVR may have some effect on contractility and HR |
Epinephrine (0.02 mcg/kg/min–0.3 mcg/kg/min) Or (1–20 mcg/min) | α1, β1, β2 receptor agonist | Increases SVR, increases HR, increases contractility |
Dobutamine (0.5 mcg/kg/min–20 mcg/kg/min) | β1, β2 receptor agonist | Increases HR, increases contractility, may lead to hypotension in some patients |
Dopamine (0.5 mcg/kg/min–10 mcg/kg/min) | δ1, α1, β1, β2 agonist | Increases SVR, Increased HR, Increased contractility |
Isoproterenol (2–10 mcg/min) | β1, β2 agonist | Increases HR, increases contractility |
Milrinone (0.1 mcg/kg/min–0.5 mcg/kg/min) | Phosphodiesterase III inhibitor | Increases contractility and decreases pulmonary vascular resistance (PVR), may lead to hypotension |
Vasopressin (0.02 U/min–0.04 U/min) | V1 receptor agonist | Increases SVR through splanchnic vessels, no effect on pulmonary vasculature can counteract Milrinone-induced decreases in SVR, no effect on HR |
Inhaled Nitric Oxide (1–20 PPM) | Activates soluble guanylate cyclase | Decreases PVR |
Inhaled Epoprostenol (0.01–0.1 mcg/kg/min) | Synthetic prostacyclin | Decreases PVR |