Heparin Unfractionated (UFH)
Class:
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Actions:
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Facilitates antithrombin in inactivating thrombin and clotting factor Xa
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Indications:
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Unstable angina (UA) and non-ST segment elevation MI (NSTEMI)
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Adjunct to fibrinolytic therapy
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Pulmonary embolism
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evolving thrombotic stroke (CVA)
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Deep vein thrombosis
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Extracorporaeal circulation associated with hemodialysis or ECMO during cardiac surgery
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Disseminated intravascular coagulation (DIC)
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Pharmacokinetics:
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Onset: 20 – 60 minutes (SQ)
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Peak: immediately (IV)
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Half-Life: 1.5 hours
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Duration: 2 – 6 hours (IV); 8 – 12 hours (SQ)
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Adverse Effects:
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Spontaneous bleeding
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Transient thrombocytopenia
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Hypersensitivity (chills, fever, urticaria, hives, pruritis, bronchospasms, anaphylaxis)
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Osteoporosis, hypoaldosteronism, hyperkalemia (long-term use)
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Injection site reactions
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Contraindications:
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Thrombocytopenia (Platelet count < 100,000)
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Uncontrolled bleeding
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Recent intracranial, intraspinal, or eye surgery
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Lumbar puncture or regional anesthesia
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History of hypersensitivity
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Bleeding tendencies like hemophilia
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Severe hypertension
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Continuous tube drainage from stomach or intestines
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Active tuberculosis
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Ascorbic acid deficiency
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Advanced kidney or liver or pancreatic disease
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Cautious use in alcoholism, menstruation, indwelling catheters
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Caution with pregnancy (Category C) especially 3rd trimester & postpartum
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Dosages & Routes:
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Intravenous: bolus 60 units/kg (maximum bolus 4,000 units for ACS; 5,000 units otherwise)
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Intravenous Infusion: 12 units/kg/hour (around 1,000 units/hour)
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Subcutaneous: 1st dose: 10,000 – 20,000 units; subsequent doses: 8,000 – 20,000 units every 8 – 12 hours
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Nursing Implications:
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Drug Interactions: 1) Aspirin, NSAIDS, oral anticoagulants, and anti-platelet drugs may increase the risk of bleeding; 2) feverfew, ginkgo, ginger, and valerian may increase the risk of bleeding; 3) Nitroglycerin may decrease the anticoagulant effect of heparin; 4) Protamine sulfate is an antagonist to heparin.
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Drug Incompatibilities: Do not mix IV line with any other medications. There is a long list of incompatibilities.
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Protamine sulfate is the antidote for overly anticoagulated dose of heparin. (1 gm protamine inactivates 100 units heparin).
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Heparin drip should be continuous. Do not interrupt a heparin drip for any other drug or IV therapy. Short half-life: If infusion is turned off, therapeutic effect can be lost.
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Only routes of administration are IV or SQ (does not absorb PO; IM causes hematoma)
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Risk of bleeding increases. Screen patients for contraindications.
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To reduce risk of hemorrhage, dosage must be monitored closely and adjusted according to aPTT levels.
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Monitor with activated partial thromboplastin time (aPTT) which normally is around 40 seconds.
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Therapeutic goal for aPTT is 1.5 – 2 Ï normal level = 60 – 80 seconds).
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Draw blood for aPTT 30 minutes before SQ or intermittent doses of heparin.
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Does not cross placental barrier during pregnancy or pass into breast milk during lactation.
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Monitor injection sites for signs of hematoma.
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Apply direct pressure to venipuncture sites for longer durations (e.g., 3 minutes).
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Low molecular weight heparin (e.g., enoxaparin) is preferred for unstable angina and NSTEMI over unfractionated heparin.
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References:
American Heart Association. (2006). Handbook of Emergency Cardiac Care (p. 55). Salem, MA: AHA.
American Heart Association. (2005). 2005 AHA guidelines for cardiopulmonary resuscitation and emergency cardiac care: Stabilization of the patient with acute coronary syndromes. Circulation, 112(24 Supple.), IV 89-110.
Lehne, R.A. (2010). Pharmacology for nursing care (7th ed., pp. 594-618). St. Louis: Saunders Elsevier.
Wilson, B.A., Shannon, M.T., Shields, K.M., & Stang, C.L. (2007). Prentice Hall Nurse's Drug Guide 2007 (pp. 793-796). Upper Saddle River, NJ: Pearson Prentice Hall.
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