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Anticoagulant / IV Fluid

Heparin Sodium in 5% Dextrose Injection

Osmolarity: ≈ 285 mOsm/LTonicity: IsotonicpH: 3.5 – 7.5

Clinical Indications

Systemic anticoagulation in: venous thromboembolism (DVT/PE) treatment and prophylaxis; acute coronary syndrome (ACS) management; atrial fibrillation with embolic risk; extracorporeal circulation; disseminated intravascular coagulation (DIC). Heparin in D5W is the standard pre-mixed IV heparin formulation.

Dosing & Administration Rate

Weight-based dosing protocol (e.g., Raschke protocol): Loading dose 80 units/kg IV bolus, then initial infusion 18 units/kg/hr. Adjust by aPTT every 6 hrs until therapeutic (aPTT 60–100 sec or 1.5–2.5× baseline). Each institution should have an approved heparin nomogram.

Warnings & Precautions

Heparin-Induced Thrombocytopenia (HIT): monitor platelets every 2–3 days during the first 14 days. A platelet fall of >50% from baseline should prompt HIT workup and immediate heparin cessation. Bleeding is the primary adverse effect. Overdose antidote: protamine sulphate 1 mg per 100 units heparin. Contraindicated in active uncontrolled bleeding and severe thrombocytopenia.

Contraindications

Severe thrombocytopenia. History of HIT (Heparin-Induced Thrombocytopenia). Uncontrolled active bleeding. Suspected intracranial hemorrhage.

Pharmacology & Safety Profile

Mechanism of Action

Potentiates the action of antithrombin III, inactivating thrombin and preventing the conversion of fibrinogen to fibrin.

Adverse Reactions

Hemorrhage, HIT (immune-mediated), osteoporosis (with long-term use), alopecia, elevation of aminotransferases.

Compatibility Notes

Incompatible with many medications — dedicated IV line or lumen strongly recommended. Incompatible with: gentamicin, amikacin, ciprofloxacin (in same line), alteplase.

Electrolyte & Composition Profile

ComponentAmount / Concentration
Heparin Sodium (porcine)25,000 units / 500 mL (50 units/mL) or 12,500 units / 250 mL
Dextrose (Anhydrous)50 mg/mL (5%)
Water for Injectionq.s.
Caloric Density170 kcal/L (from dextrose)

Clinical Parameters

RouteIntravenous (continuous infusion)
Fluid CategoryCrystalloid Solution
Required MonitoringVital signs, fluid intake/output, baseline electrolytes
Administration SetupPeripheral or central venous access via infusion pump. Never bolus.
Pregnancy SafetyCategory C (FDA). Does not cross the placenta. Generally the anticoagulant of choice during pregnancy, but carries maternal bleeding risks.
StorageStore at room temperature 20–25°C. Protect from freezing.
Prescription Status Rx Only

Clinical Disclaimer: Data compiled from FDA DailyMed, Baxter/Fresenius prescribing information, and USP monographs. Always verify against the physical product label, your institution's IV protocols, and current pharmacist guidance before administration.

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