Drug Guide
Tirofiban Hydrochloride
Classification
Therapeutic: Antiplatelet agent, Glycoprotein IIb/IIIa inhibitor
Pharmacological: Integrin receptor antagonist
FDA Approved Indications
- Reduction of thrombotic cardiovascular events in patients with unstable angina undergoing percutaneous coronary intervention (PCI).
Mechanism of Action
Tirofiban is a non-peptide antagonist of the glycoprotein IIb/IIIa receptor on platelets, inhibiting fibrinogen binding and platelet aggregation, thereby preventing thrombus formation.
Dosage and Administration
Adult: Administer an initial bolus of 25 mcg/kg over 3 minutes, followed by a continuous infusion of 0.15 mcg/kg/min. Adjust based on bleeding risk and clinical response.
Pediatric: Not recommended; data insufficient.
Geriatric: Use with caution; consider renal function. Adjust dosage as necessary.
Renal Impairment: Reduce infusion rate in patients with moderate to severe renal impairment due to decreased clearance.
Hepatic Impairment: No specific adjustment recommended.
Pharmacokinetics
Absorption: Administered intravenously; bioavailability is 100%.
Distribution: Volume of distribution approximately 21 liters; minimal protein binding.
Metabolism: Metabolized minimally; primarily cleared unchanged.
Excretion: Renal excretion of unchanged drug; important for dose adjustment.
Half Life: Approximately 2 hours.
Contraindications
- Active internal bleeding
- History of hemorrhagic stroke
- Recent major surgery or trauma
- Severe uncontrolled hypertension
Precautions
- Use caution in patients with bleeding disorders or recent surgical procedures.
- Monitor closely for signs of bleeding.
- Use with caution in elderly patients.
Adverse Reactions - Common
- Bleeding (including minor bleeding) (Common)
- Hypotension (Common)
- Headache (Common)
Adverse Reactions - Serious
- Major bleeding (Uncommon but serious)
- Thrombocytopenia (Rare)
Drug-Drug Interactions
- Other anticoagulants (e.g., heparin, warfarin)
- Other antiplatelet agents
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor bleeding signs, blood pressure, and platelet count regularly.
Diagnoses:
- Risk for bleeding related to antiplatelet therapy
- Impaired tissue perfusion due to bleeding
Implementation: Administer as prescribed, ensure proper infusion techniques, and monitor patient closely.
Evaluation: Assess for bleeding complications and efficacy of therapy.
Patient/Family Teaching
- Report any unusual bleeding or bruising immediately.
- Avoid activities that increase bleeding risk.
- Inform healthcare providers of all medications being taken.
Special Considerations
Black Box Warnings:
- Significant risk of bleeding; use only as indicated.
Genetic Factors: No specific genetic considerations.
Lab Test Interference: May cause false-positive results in urine bilirubin tests.
Overdose Management
Signs/Symptoms: Excessive bleeding, hypotension, bleeding at surgical sites.
Treatment: Discontinue drug immediately, provide supportive care, and administer platelet transfusions if needed.
Storage and Handling
Storage: Store at room temperature (20-25°C); protect from light.
Stability: Stable for the duration specified on the package when stored properly.