Drug Guide

Generic Name

Desirudin

Brand Names Iprivask

Classification

Therapeutic: Anticoagulant

Pharmacological: Direct Thrombin Inhibitor

FDA Approved Indications

Mechanism of Action

Desirudin is a recombinant analog of hirudin that directly inhibits thrombin, preventing fibrin formation and clot development.

Dosage and Administration

Adult: It is typically administered as a subcutaneous injection once daily. The dosage depends on the patient's weight and clinical condition. For prophylaxis, a common dose is 15 mg subcutaneously 6 hours after surgery, then 15 mg every 12 hours.

Pediatric: Not approved for use in pediatric patients; safety and efficacy not established.

Geriatric: Dose adjustments may be necessary based on renal function; careful monitoring is advised.

Renal Impairment: Dose adjustment is required in patients with renal impairment; specific guidelines recommend reducing dose or extending dosing interval based on creatinine clearance.

Hepatic Impairment: No specific adjustments recommended; caution advised. Liver function should be monitored.

Pharmacokinetics

Absorption: Rapid absorption following subcutaneous administration.

Distribution: Widely distributed; volume of distribution approximately 0.1-0.2 L/kg.

Metabolism: Metabolized primarily by proteolytic cleavage, with no significant hepatic metabolism.

Excretion: Excreted mainly by the kidneys.

Half Life: Approximately 4-6 hours.

Contraindications

Precautions

Adverse Reactions - Common

Adverse Reactions - Serious

Drug-Drug Interactions

Drug-Food Interactions

Drug-Herb Interactions

Nursing Implications

Assessment: Monitor for signs of bleeding, including sudden drops in hemoglobin, hematocrit, blood pressure drops, and bleeding at puncture sites.

Diagnoses:

  • Risk for bleeding related to anticoagulant therapy.

Implementation: Administer subcutaneously as prescribed; ensure proper injection techniques.

Evaluation: Assess for bleeding complications regularly. Adjust dose based on renal function and clinical response.

Patient/Family Teaching

Special Considerations

Black Box Warnings:

Genetic Factors: No specific genetic considerations known.

Lab Test Interference: May interfere with coagulation assays; INR is not used to monitor effect.

Overdose Management

Signs/Symptoms: Excessive bleeding, hematoma formation.

Treatment: Discontinue drug immediately. Supportive measures include applying pressure to bleeding sites, transfusions if necessary. No specific antidote available; recovery depends on renal clearance.

Storage and Handling

Storage: Store in a refrigerator at 2°C to 8°C. Protect from freezing and light.

Stability: Stable until expiration date if stored properly.

This guide is for educational purposes only and is not intended for clinical use.