Dopamine Starting Dose
The typical starting dose of dopamine is 5-10 mcg/kg/min for most patients requiring vasopressor support, with lower doses of 2-5 mcg/kg/min appropriate for patients who may respond to modest increases in cardiac contractility and renal perfusion. 1, 2, 3
Initial Dosing Strategy
For adults and pediatric patients:
- Start at 2-5 mcg/kg/min if the patient is likely to respond to modest increments in heart force and renal perfusion 3
- Start at 5-10 mcg/kg/min for more seriously ill patients or those with symptomatic bradycardia and hypotension 1, 2, 3
- In pediatric patients specifically, the dosing range is 2-20 mcg/kg/min, titrated to maintain adequate blood pressure 4, 2
Titration Protocol
After initiating therapy, increase gradually using 5-10 mcg/kg/min increments up to 20-50 mcg/kg/min as needed based on hemodynamic response 1, 3. The maximum recommended dose is 20 mcg/kg/min, as doses exceeding this may cause excessive vasoconstriction 5. If the target mean arterial pressure cannot be achieved at 20 mcg/kg/min, switch to norepinephrine or add a second-line agent rather than escalating dopamine further 5.
Dose-Dependent Effects
Understanding dopamine's pharmacology guides appropriate starting doses:
- <3 mcg/kg/min: Predominantly dopaminergic effects with renal vasodilation 1, 5
- 3-5 mcg/kg/min: Inotropic (β-adrenergic) effects predominate 1, 5
- >5-10 mcg/kg/min: Combined inotropic and vasopressor (α-adrenergic) effects with increasing vasoconstriction 1, 5
Critical Administration Requirements
Before starting dopamine:
- Ensure adequate fluid resuscitation (central venous pressure 10-15 cm H₂O or pulmonary wedge pressure 14-18 mm Hg) 3
- Use only an infusion pump, preferably volumetric—never rely on gravity drips 3
- Establish continuous hemodynamic monitoring including blood pressure, heart rate, and ECG 1, 2
- Place an arterial line as soon as practical for accurate blood pressure monitoring 2
- Infuse into a large vein (antecubital fossa preferred) to prevent extravasation and tissue necrosis 3
When Dopamine Is NOT the Right Choice
Do not use dopamine as first-line therapy for:
- Septic shock: Norepinephrine is the first-choice vasopressor with strong evidence (Grade 1B recommendation) 2, 5, 6, 7
- Cardiogenic shock: Norepinephrine is associated with lower mortality compared to dopamine 1, 6
- Renal protection: Low-dose dopamine (≤3 mcg/kg/min) for renal protection is strongly discouraged and provides no benefit (Grade 1A recommendation) 1, 5, 8
Dopamine is specifically indicated for:
- Hypotension with symptomatic bradycardia 1, 2
- Highly selected patients with low risk of tachyarrhythmias 2
- Post-cardiac arrest hypotension when bradycardia coexists 2
Common Pitfalls to Avoid
- Arrhythmia risk: Dopamine causes significantly more arrhythmic events (24.1%) compared to norepinephrine (12.4%) 6. Use caution in patients with heart rate >100 bpm 5
- Extravasation: Can cause severe tissue necrosis even at low doses. If extravasation occurs, immediately infiltrate the site with phentolamine 5-10 mg diluted in 10-15 mL saline 2, 3
- Alkaline incompatibility: Never add sodium bicarbonate or other alkalinizing substances, as dopamine is inactivated in alkaline solution 3
- Fluid overload: More than 50% of patients are satisfactorily maintained on doses <20 mcg/kg/min. If higher doses are needed, consider switching agents rather than continuing escalation 3
Monitoring During Therapy
Watch for signs requiring dose reduction or discontinuation: