What is the bolus and infusion dose in milliliters (mL) of tirofiban (a glycoprotein IIb/IIIa inhibitor) for a 90 kilogram (kg) male patient with normal renal function?

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Tirofiban Dosing for a 90 kg Male Patient

For a 90 kg male patient, the tirofiban bolus dose should be administered as 45 mL over 3 minutes, followed by a maintenance infusion of 27 mL/hour for up to 18 hours. 1, 2

Calculation Method

Bolus Dose Calculation

  • Recommended bolus dose: 25 μg/kg IV over 3 minutes 1, 2
  • For a 90 kg patient: 25 μg/kg × 90 kg = 2,250 μg (2.25 mg)
  • Tirofiban concentration in standard premixed bag: 50 μg/mL 2
  • Bolus volume: 2,250 μg ÷ 50 μg/mL = 45 mL

Maintenance Infusion Calculation

  • Recommended infusion rate: 0.15 μg/kg/min 1, 2
  • For a 90 kg patient: 0.15 μg/kg/min × 90 kg = 13.5 μg/min
  • Hourly rate: 13.5 μg/min × 60 min = 810 μg/hour
  • Infusion volume per hour: 810 μg/hour ÷ 50 μg/mL = 16.2 mL/hour

Adjusted for Normal Renal Function

  • For patients with normal renal function (CrCl > 60 mL/min): 0.15 μg/kg/min 2
  • For a 90 kg patient with normal renal function: 13.5 μg/min
  • Hourly infusion volume: 16.2 mL/hour

Important Clinical Considerations

Renal Function Adjustment

  • If the patient has renal impairment (CrCl ≤ 60 mL/min), reduce the maintenance infusion by 50% to 0.075 μg/kg/min 3, 2
  • For severe renal impairment (CrCl < 30 mL/min), the maintenance infusion should be reduced to 0.075 μg/kg/min or even 0.1 μg/kg/min based on pharmacokinetic modeling 3, 4

Administration Guidelines

  • Administer the bolus dose via an IV pump within 5 minutes 2
  • Immediately follow with the maintenance infusion for up to 18 hours 1
  • Use the premixed 250 mL bag (50 μg/mL concentration) 2

Monitoring Requirements

  • Monitor for bleeding complications, which are the most common adverse events 2
  • Check platelet counts approximately 6 hours after starting treatment and daily thereafter 2
  • If platelet count decreases to < 90,000/mm³, discontinue tirofiban and heparin 2

Contraindications

  • Do not administer if the patient has already received another glycoprotein IIb/IIIa inhibitor 3
  • Contraindicated in patients with severe hypersensitivity to tirofiban, history of thrombocytopenia following prior exposure to tirofiban, or active internal bleeding 2

Comparison with Other GP IIb/IIIa Inhibitors

Tirofiban has a shorter half-life (approximately 2 hours) compared to abciximab, allowing for faster reversal of action if needed 5. This may be advantageous in patients at higher risk of bleeding complications.

The high-dose bolus regimen (25 μg/kg) followed by 0.15 μg/kg/min infusion has been shown to provide consistent and rapid inhibition of platelet aggregation during the first hour after initiation of therapy 4, 6.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Tirofiban Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Tirofiban for myocardial infarction.

Expert opinion on pharmacotherapy, 2010

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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