Drug Guide
Heparin Calcium
Classification
Therapeutic: Anticoagulant, Antithrombotic
Pharmacological: Indirect Thrombin Inhibitor
FDA Approved Indications
- Prevention and treatment of thromboembolic disorders, such as deep vein thrombosis, pulmonary embolism, myocardial infarction, and disseminated intravascular coagulation
Mechanism of Action
Heparin enhances the activity of antithrombin III, which inhibits thrombin and factor Xa, leading to decreased blood clot formation.
Dosage and Administration
Adult: Dosage varies based on condition; often an initial intravenous bolus of 5,000 units followed by continuous infusion titrated to activated partial thromboplastin time (aPTT) levels.
Pediatric: Dosing similar to adults, but requires careful monitoring; specific pediatric protocols should be followed.
Geriatric: Start at lower doses due to increased bleeding risk; monitor closely.
Renal Impairment: Adjust dosage with caution; heparin itself is not mainly eliminated by renal pathway.
Hepatic Impairment: No specific adjustment needed, but monitor for bleeding.
Pharmacokinetics
Absorption: Not absorbed orally; administered parenterally (IV or subcutaneous)
Distribution: Widely distributed in the extravascular space, does not cross the blood-brain barrier or placenta significantly
Metabolism: Metabolized by the reticuloendothelial system, primarily in the liver
Excretion: Cleared via the reticuloendothelial system; minimal renal clearance
Half Life: Approx. 1 to 2 hours after IV administration
Contraindications
- Active major bleeding, severe thrombocytopenia (e.g., Heparin-Induced Thrombocytopenia, HIT), hypersensitivity to heparin or azure II dye
Precautions
- History of HIT, bleeding disorders, recent surgeries, uncontrolled hypertension, during lumbar puncture or spinal anesthesia due to bleeding risk
Adverse Reactions - Common
- Bleeding (Common)
- Heparin-Induced Thrombocytopenia (HIT) (Uncommon but serious)
- Elevated liver enzymes (Less common)
Adverse Reactions - Serious
- Bleeding leading to hemorrhage (Serious, requires immediate attention)
- HIT with thrombosis (Serious, can be life-threatening)
- Osteoporosis with long-term use (Rare)
Drug-Drug Interactions
- Other anticoagulants (e.g., warfarin, aspirin), antiplatelet agents, thrombolytics
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for signs of bleeding, baseline aPTT, platelet counts, signs of HIT, neurological status, and extremity checks for thrombosis.
Diagnoses:
- Risk for bleeding,
Implementation: Administer parenterally as prescribed, monitor coagulation parameters, watch for allergic reactions, ensure proper infusion techniques.
Evaluation: Effective anticoagulation confirmed by therapeutic aPTT levels, no bleeding complications, normal platelet counts.
Patient/Family Teaching
- Report any signs of bleeding (unusual bruising, hematuria, blood in stool), or symptoms of thrombosis.
- Inform about the importance of regular blood tests to monitor therapy.
- Advise on avoiding injury and activities that may cause bleeding.
Special Considerations
Black Box Warnings:
- Spinal/epidural hematoma risk with neuraxial anesthesia or puncture procedures.
Genetic Factors: Heparin resistance in some individuals, particularly with antithrombin deficiency.
Lab Test Interference: Can artificially elevate aPTT and interfere with certain coagulation tests.
Overdose Management
Signs/Symptoms: Uncontrolled bleeding, bruising, petechiae, hematuria, gastrointestinal bleeding.
Treatment: Discontinue heparin immediately, administer protamine sulfate (1 mg for every 100 units of heparin within the last 2-2.5 hours), supportive measures as needed.
Storage and Handling
Storage: Store at room temperature, protected from light, and moisture.
Stability: Stable until expiration date when stored properly.