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# Norepinephrine
## Overview
Norepinephrine is a potent catecholamine acting primarily as an alpha-1 adrenergic agonist (vasoconstriction) with moderate beta-1 adrenergic activity (inotropic effect). It is the first-line vasopressor for septic and vasodilatory shock.
## Primary Indications
* Acute hypotensive states (e.g., septic shock, cardiogenic shock).
* Cardiac arrest (less common, usually second-line).
## Adult Dosing
* **Initial:** 0.05–0.1 mcg/kg/min continuous IV infusion.
* **Titration:** Titrate to achieve target Mean Arterial Pressure (MAP), typically ≥65 mmHg.
* **Maintenance:** 0.01–3 mcg/kg/min.
* **Maximum:** No established federal limit; limited by systemic vasoconstriction, tissue ischemia, and refractory tachyarrhythmias. Infusions at >1 mcg/kg/min often necessitate the addition of a second agent (e.g., vasopressin).
## Pediatric Dosing
* **Initial:** 0.05–0.1 mcg/kg/min continuous IV infusion.
* **Titration:** Titrate by 0.05–0.1 mcg/kg/min every 5–15 minutes based on hemodynamic response.
* **Maintenance/Range:** 0.05–2 mcg/kg/min.
* *Note: Dosing is highly dependent on institutional protocols and local pediatric intensive care guidelines.*
## Dose Adjustments
* **Renal/Hepatic:** No specific dose adjustment defined; however, cautious titration is required as patients with organ failure may exhibit altered pharmacodynamics.
* **Volume Status:** Efficacy is significantly reduced in hypovolemic patients; ensure adequate fluid resuscitation prior to or concurrent with initiation.
## Contraindications
* Hypersensitivity to norepinephrine or bisulfites.
* Hypovolemia (without concomitant fluid replacement).
* Mesenteric or peripheral vascular thrombosis (due to risk of increasing ischemia).
## Adverse Effects
* **Cardiovascular:** Hypertension, bradycardia (reflex), tachyarrhythmias, myocardial ischemia.
* **Dermatologic:** Extravasation can cause severe tissue necrosis and sloughing (treat with phentolamine infiltration if local protocol permits).
* **Peripheral:** Digital ischemia, limb gangrene.
* **Metabolic:** Hyperglycemia, metabolic acidosis.
## Key Drug Interactions
* **MAO Inhibitors / TCAs:** May cause severe, prolonged hypertension.
* **Beta-Blockers:** May trigger unopposed alpha-mediated vasoconstriction, leading to severe hypertension and reflex bradycardia.
* **Anesthetics (Halogenated):** Increased risk of ventricular arrhythmias.
## Monitoring
* **Hemodynamics:** Continuous invasive arterial pressure monitoring is preferred.
* **Cardiac:** Continuous ECG monitoring for arrhythmias.
* **Access Site:** Assess infusion site frequently for signs of extravasation (pallor, coldness).
* **End-Organ Perfusion:** Urine output, serum lactate, and peripheral perfusion (capillary refill, extremity warmth).
## Clinical Pearls
* **Central Line:** Must be administered via a large-bore central venous catheter (CVC) whenever possible to minimize risk of extravasation necrosis.
* **Weaning:** Wean slowly to avoid abrupt hemodynamic collapse.
* **Compatibility:** Highly acidic; check Y-site compatibility as it is incompatible with many common drugs (e.g., sodium bicarbonate, insulin).
* **Concentration:** Standardize concentrations (e.g., 4mg/250mL or 8mg/250mL) per institutional policy to reduce medication errors.
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*Disclaimer: This information is for educational purposes only. Clinical practice varies by institution. Always verify specific dosing, safety protocols, and drug compatibility via current hospital-approved formulary references and recent prescribing information.*