Dobutamine Infusion Rate Calculation
For a 70-kg adult receiving dobutamine at 2 µg/kg/min using a 1 mg/mL (250 mg/250 mL) solution, set the syringe pump to 8.4 mL/hr.
Step-by-Step Calculation
Calculate the Required Dose in µg/min
- For a 70-kg patient at 2 µg/kg/min: 70 kg × 2 µg/kg/min = 140 µg/min 1
Convert to mg/min
- 140 µg/min ÷ 1000 = 0.14 mg/min 1
Convert to mg/hr
- 0.14 mg/min × 60 min/hr = 8.4 mg/hr 1
Calculate mL/hr Based on Concentration
- With a 1 mg/mL concentration: 8.4 mg/hr ÷ 1 mg/mL = 8.4 mL/hr 1
Clinical Context and Dosing Guidelines
Standard Dosing Range
Dobutamine infusion should be started at a low rate of 0.5-1.0 µg/kg/min and titrated at intervals of a few minutes based on the patient's response, including systemic blood pressure, urine flow, frequency of ectopic activity, heart rate, and measurements of cardiac output when possible 1
The optimal infusion rates typically range from 2-20 µg/kg/min, though rates slightly outside this range are sometimes necessary 1
The European Society of Cardiology recommends starting dobutamine at 2.5 µg/kg/min and doubling the dose every 15 minutes according to response, with dose titration usually limited by excessive tachycardia, arrhythmias, or ischemia 2
Hemodynamic Effects at 2 µg/kg/min
At this starting dose, dobutamine increases cardiac output by selectively augmenting stroke volume, with minimal effect on heart rate or systemic arterial pressure 3, 4
The drug produces a decrease in total peripheral vascular resistance that is mediated in part by reflex withdrawal of sympathetic tone to the vasculature 4
Pulmonary wedge pressure typically decreases, improving cardiac performance in patients with ventricular dysfunction 3
Solution Preparation and Stability
Standard Dilution Protocol
At the time of administration, dobutamine must be diluted in an IV container to at least a 50-mL solution using compatible diluents such as 5% Dextrose Injection, 0.9% Sodium Chloride Injection, or Lactated Ringer's Injection 1
The intravenous solution should be used within 24 hours of preparation 1
Concentrations of up to 5,000 µg/mL (5 mg/mL) have been administered to humans, with the final volume determined by the patient's fluid requirements 1
Visual Inspection Required
- Inspect the solution visually before administration and do not use if particulate matter or discoloration is present 1
Monitoring Parameters During Infusion
Essential Clinical Assessments
Monitor systemic blood pressure continuously, as dobutamine's hemodynamic profile includes minimal changes in mean arterial pressure (typically 93-98 mmHg range maintained) 3
Track heart rate, expecting only slight increases (approximately 7 beats/min elevation from baseline at therapeutic doses) 3
Assess urine output as a marker of improved organ perfusion 2
Monitor for frequency of ectopic activity and arrhythmias, which may limit dose escalation 2, 1
When possible, measure cardiac output, central venous pressure, and pulmonary capillary wedge pressure to guide titration 1
Common Pitfalls to Avoid
Calculation Errors
Anesthesiologists have significant difficulty calculating pediatric drug concentrations for continuous infusions, with only 15% providing all correct answers in one study, and incorrect calculations ranging from 50 times too low to 56 times too high 5
Use electronic infusion pumps rather than manual calculations whenever possible to minimize dosing errors 5
Double-check all weight-based calculations, as the mean time required for manual calculation is approximately 205 seconds, increasing the risk of errors under time pressure 5
Clinical Management Errors
Do not use dobutamine as primary treatment in conditions characterized by marked hypotension and shock, as it has less vasopressor activity than norepinephrine or dopamine 6
Avoid prolonged continuous infusions exceeding 72 hours, as tolerance to dobutamine develops with extended use 7
Do not mix dobutamine with sodium bisulfite and ethanol-containing agents or diluents 1
Recognize that dobutamine's mechanism involves complex interactions with β₁-, β₂-, and α₁-adrenoceptors, not just selective β₁-stimulation as previously thought 4