What is the dopamine infusion rate in drops per minute for a 50kg female?

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Dopamine Infusion Rate Calculation for a 50kg Female

For a 50kg female, dopamine infusion rates should be calculated using the "rule of 6" method: multiply 0.6 × 50kg = 30mg dopamine diluted to 100mL saline, where 1mL/hour delivers 0.1 mcg/kg/min, and drops per minute equals mL/hour when using a microdrop apparatus (60 drops/mL). 1

Standard Preparation Methods

Rule of 6 Method (Preferred for Pediatric/Lower Weight Patients)

  • Calculation: 0.6 × 50kg = 30mg dopamine in 100mL saline 1
  • Concentration: 300 mcg/mL
  • Conversion: 1 mL/hour = 0.1 mcg/kg/min = 1 drop/minute (with microdrop set) 1

Standard Adult Concentration

  • Alternative preparation: 400mg dopamine in 500mL D5W yields 800 mcg/mL 2
  • For this concentration in a 50kg patient:
    • 2 mcg/kg/min = 100 mcg/min = 7.5 mL/hour = 7.5 drops/minute (microdrop)
    • 5 mcg/kg/min = 250 mcg/min = 18.75 mL/hour = 19 drops/minute (microdrop)
    • 10 mcg/kg/min = 500 mcg/min = 37.5 mL/hour = 38 drops/minute (microdrop)
    • 20 mcg/kg/min = 1000 mcg/min = 75 mL/hour = 75 drops/minute (microdrop) 2

Dosing Guidelines by Clinical Indication

Initial Dosing

  • Start at 2-5 mcg/kg/min for most patients requiring modest increases in cardiac output and renal perfusion 3, 1, 2
  • Using Rule of 6 preparation: 20-50 drops/minute 1
  • Using 800 mcg/mL preparation: 7.5-19 drops/minute 2

Dose-Dependent Effects

  • 2-3 mcg/kg/min: Dopaminergic receptor stimulation (renal/mesenteric vasodilation) with limited diuretic effect 3, 1
  • 3-5 mcg/kg/min: β-adrenergic effects predominate (increased cardiac contractility and output) 3, 1
  • 5-10 mcg/kg/min: Mixed β-adrenergic and increasing α-adrenergic effects 3, 1
  • >10 mcg/kg/min: Progressive α-adrenergic stimulation with peripheral vasoconstriction 3, 1

Titration Strategy

  • Increase in 5-10 mcg/kg/min increments up to 20-50 mcg/kg/min as needed for blood pressure support 2
  • Maximum recommended: 20 mcg/kg/min; doses >20 mcg/kg/min risk excessive vasoconstriction 1
  • More than 50% of patients respond adequately to <20 mcg/kg/min 2

Critical Safety Measures

Administration Requirements

  • Use only volumetric infusion pump—gravity drip with mechanical clamps is inadequate 2
  • Infuse into large vein (antecubital fossa preferred) to prevent extravasation necrosis 2
  • Continuous hemodynamic monitoring including blood pressure, heart rate, and ECG is mandatory 3, 1
  • Arterial line placement recommended for doses approaching upper range 1

Extravasation Management

  • If extravasation occurs: Inject phentolamine 0.1-0.2 mg/kg (up to 10mg) diluted in 10mL saline intradermally at the site 1
  • Watch continuously for signs of infiltration as tissue necrosis can occur 2

Important Contraindications and Cautions

  • Avoid in tachycardia >100 bpm—both dopamine and dobutamine should be used cautiously 3
  • Consider alternative vasopressors (norepinephrine) if inadequate response at 20 mcg/kg/min or if excessive tachycardia develops 1
  • Protect solution from light using foil covering to prevent drug breakdown 1
  • Do NOT add sodium bicarbonate—dopamine is inactivated in alkaline solutions 2

Discontinuation

  • Gradually taper by decreasing dose in 2 mcg/kg/min increments while optimizing oral therapy 3
  • Expand blood volume with IV fluids during weaning to prevent marked hypotension 2

Clinical Pearls

Time to steady state: Expect 70-125 minutes to reach 90% of plateau concentration depending on infusion rate, due to redistribution kinetics 4

Diuretic effect: At 2 mcg/kg/min, expect increased urine output (mean increase from 0.29 to 1.04 mL/kg/hr) with peak effect at approximately 7 hours, though this effect is drug-dependent and reversible 5

Pharmacodynamic variability: Individual patient response shows significant variability; plasma levels correlate with infusion rates but hemodynamic effects require individualized titration based on clinical response rather than fixed dosing 6

References

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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