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. Author manuscript; available in PMC: 2022 Aug 1.
Published in final edited form as: Clin Perinatol. 2021 Aug;48(3):595–618. doi: 10.1016/j.clp.2021.05.009

Table 3:

Commonly used vasoactive medications and pulmonary vasodilators in PPHN

Name of drug Dose Site of action Hemodynamic effects
Epinephrine 0.02–0.3 microgm/kg/min β1 and β2 receptors Inotropic effects; Decrease SVR
0.3–1 microgm/kg/min α1 receptors Vasopressor effects; Increase SVR
Norepinephrine 0.1–1microgm/kg/min α1 and α2 receptors Vasopressor effects; Increase SVR
Milrinone 0.25–0.75
microgm/kg/min
Phosphodiesterase III inhibitor and effects at β1 & β2 receptors Inodilator effects; Lusitropic effects; Increase contractility; Decrease SVR
Dobutamine 5–20 microgm/kg/min β1 and β2 receptors, some effect on α receptors Inotropic effects; Decrease SVR; Increase cardiac output
Dopamine 1–4 microgm/kg/min Dopaminergic receptors 1 & 2 Renal and mesenteric dilatation
4–10 microgm/kg/min α receptors Inotropic effects
11–20 microgm/kg/min β receptors Vasopressor, increase SVR and increase PVR
Hydrocortisone 1–2.5 mg/kg; 4–6 hourly Uncertain - enhance sensitivity to catecholamines
Vasopressin 0.018–0.12 units/kg/hour Vasopressin 1 receptors Increase SVR; No inotropic effect
Pulmonary vasodiators
Inhaled nitric oxide 1–20 ppm Selective pulmonary vasodilator Decrease PVR
Sildenafil IV: load of 0.42 mg/kg for 3 hours followed by 1.6 mg/kg per day as a continuous maintenance infusion Phosphodiesterase (PDE) 5 inhibitor Pulmonary and systemic vasodilator; Decreases PVR, decreases SVR
Oral: 1–2 mg/kg every 6 hours
Synthetic prostacyclin (Iloprost) Aerosolized: 1–2.5 mg/kg every 2–4 hours Pulmonary vasodilator acting locally Decreases PVR
IV 0.5 to 3 ng/kg per minute and titrated to 1–10 ng/kg per minute Pulmonary and systemic vasodilator Decreases SVR and hypotension
Prostacyclicn I2 (PGI2) Inhaled prostaglandin I2 at a dose of 50 ng/kg per minute Pulmonary vasodilator acting locally Decreases SVR

SVR – systemic vascular resistance; PVR – pulmonary vascular resistance; α- alpha and β- beta receptors; IV - intravenous