Drug Guide
Reteplase
Classification
Therapeutic: Thrombolytic agent
Pharmacological: Recombinant tissue plasminogen activator (tPA)
FDA Approved Indications
- Acute myocardial infarction (MI)
Mechanism of Action
Reteplase catalyzes the conversion of plasminogen to plasmin, leading to the degradation of fibrin and dissolution of thrombi in blood vessels.
Dosage and Administration
Adult: 30 units IV bolus over 2 minutes, repeated in 30 minutes for a total dose of 60 units.
Pediatric: Not approved for pediatric use.
Geriatric: Use with caution in elderly patients, monitor closely.
Renal Impairment: No specific adjustment indicated.
Hepatic Impairment: No specific adjustment indicated.
Pharmacokinetics
Absorption: Administered intravenously, so absorption is immediate.
Distribution: Plasmatic, distributes rapidly with a large volume of distribution.
Metabolism: Metabolized by the liver and cleared via the reticuloendothelial system.
Excretion: Excreted mainly in urine as metabolites.
Half Life: Approximately 13-16 minutes.
Contraindications
- Active bleeding or bleeding diathesis
- History of intracranial hemorrhage
- Recent major surgery or trauma
- History of cerebrovascular accident (stroke) within 3 months
- Severe uncontrolled hypertension.
Precautions
- Use with caution in patients with recent surgery, trauma, or bleeding risk factors.
- Monitor for signs of bleeding.
- Ensure availability of blood products and ready access to neurosurgical consultation.
Adverse Reactions - Common
- Bleeding at site of injection (Common)
- Bleeding elsewhere (Common)
Adverse Reactions - Serious
- Intracranial hemorrhage (Rare but serious)
- Allergic reactions (Rare)
Drug-Drug Interactions
- Anticoagulants (e.g., heparin, warfarin)
- Antiplatelet agents (e.g., aspirin, clopidogrel)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Assess for contraindications, baseline neurological status, and signs of bleeding.
Diagnoses:
- Risk for bleeding
- Ineffective tissue perfusion related to bleeding complications.
Implementation: Administer as ordered, monitor vital signs and neurological status closely, check for signs of bleeding.
Evaluation: Monitor for resolution of symptoms of MI, effectiveness of thrombolysis, and adverse effects.
Patient/Family Teaching
- Report any signs of bleeding, unusual pain, or neurological changes immediately.
- Avoid invasive procedures unless directed by healthcare provider.
- Inform about the importance of follow-up care.
Special Considerations
Black Box Warnings:
- Serious bleeding complications, including intracranial hemorrhage.
- Use only in hospitals with facilities to manage bleeding complications.
Genetic Factors: None specified.
Lab Test Interference: May interfere with coagulation tests temporarily.
Overdose Management
Signs/Symptoms: Excessive bleeding, signs of internal or external hemorrhage.
Treatment: Discontinue drug, provide supportive care, administer blood products if necessary, and manage bleeding according to protocols.
Storage and Handling
Storage: Store refrigerated at 2-8°C, protect from light.
Stability: Stable until expiration date when properly stored.