Noradrenaline

  • Description and indication for use

    Noradrenaline is a sympathomimetic agent that acts on adrenergic receptors. Its main effects include increased vascular resistance through vasoconstriction, increased heart rate and myocardial contractility.

    The main indications for use would be in the uncontrolled hypotensive neonate or to redirect blood flow more centrally in the peripherally vasodilated septic baby.

    Discussion with the NETS Consultant is mandatory if considering using Noradrenaline.  Ensure hypovolaemia is treated prior to commencement of Noradrenaline.

    Dose

    NB.  1 mg Noradrenaline Acid Tartrate = 0.5 mg Noradrenaline Base.

    Always prescribe doses in terms of base concentration to avoid confusion and check ampoule label carefully when administering.

    IV:

    Initially 0.05 – 0.5 micrograms/kg/min, titrate as required (usual max 1 – 2 microgram/kg/min).  NOTE: Doses greater than 500 nanogram/kg/min are rare and must be discussed with a consultant.

    Always given as a continuous infusion via central line.  Do not infuse through a peripheral vein due to risk of severe vasoconstrictive complications.  When administration is no longer necessary, gradually wean dose.  Do not stop abruptly.

    Reconstitution/Dilution

    Ampoule:

    Ampoule: Noradrenaline Base 2 mg/2 mL (labelled as Acid Tartrate Salt).

    IV Bolus

    Not recommended.

    IV Infusion

    0.05 micrograms/kg/min to a maximum 0.5 micrograms/kg/min.

    Add 0.3 mg/kg (300 micrograms/kg) to infusion solution (Glucose 5% or 10%) to a total volume of 50 mL (as shown in table below).

    How to make up Dose equivalent Dose range

    0.3 mg/kg in 50 mL

    (300 micrograms/kg in 50 mL)

    1 mL/hr = 0.1 micrograms/kg/min 0.05 to 0.5 micrograms/kg/min

    Route and method of administration

    Not to be given as IV bolus, IM or SC injection.

    Give centrally – never peripherally. Always given as a continuous infusion.

    Side effects

    Cardiac arrhythmias, tachycardia, bradycardia.

    Anxiety, headache.

    Respiratory difficulty.

    Extravasation necrosis at injection site.

    Anaphylaxis.

    Hypertension.

    Reduced renal blood flow – renal ischaemia.

    Hyperglycaemia.

    Contraindications

    Untreated hypovolaemic shock.

    Peripheral or mesenteric vascular thrombosis.

    Existing tachyarrhythmia.

    Asymmetric septal hypertrophy.

    Sulphite allergy.

    Drug interactions

    Monoamine oxidase inhibitors, Tricyclic antidepressants Prolonged hypertension can result.
    Halogenated anaesethetic agents Serious cardiac arrhythmias may occur with concomitant use.
    Digoxin Increased risk of arrhythmias.
    Beta blockers Risk of hypertension.
    Doxapram Risk of hypertension.

    Nursing responsibilities

    Administer via central line administration only.

    Monitor blood pressure and heart rate.

    Monitor peripheral perfusion.

    Monitor urine output.

    Do not administer bolus doses.

    Avoid interruption of infusion.

    Change infusion solution every 24 hours.

    Protect noradrenaline syringe from light. Cover syringe with foil.

    Compatibility information

    Important: Contact pharmacy for drugs not appearing in the table below.  Uncommon drugs have been omitted and may be incompatible.

      Compatible Incompatible
    Fluids Glucose 5% and 10%, Sodium Chloride 0.9%. Alkaline solutions, TPN.
    Drugs Amikacin Sulphate, Magnesium Sulphate, Meropenem, Ranitidine. Aminophylline, Insulin Neutral, Phenobarbitone Sodium, Phenytoin, Sodium Bicarbonate.
    Y-Site Adrenaline, Amiodarone, Calcium Salts, Dobutamine, Dopamine, Fentanyl Citrate, Frusemide, Glyceryl Trinitrate, Heparin Sodium, Hydrocortisone Sodium Succinate, Midazolam, Morphine Sulphate, Potassium Chloride, Vecuronium, Verapamil.  

    Notes:    Keep ampoules in manufacturers box until time of preparation

                   Do not subject ampoules or infusions to heat – decomposition rate increases.

    Extravasation     

    The antidote for extravasation ischaemia is Phentolamine. To prevent sloughing and necrosis of an area in which extravasation has occurred, immediately infiltrate 10 – 15 mL saline containing 5 – 10 mg Phentolamine.  Infiltrate liberally into the area with a needle and syringe.

Disclaimer:  This Drug information was designed for use by PIPER Neonatal. Whilst great care has been taken to check the information is accurate, it is possible that errors may have been missed. Furthermore, dosage schedules are continually being revised and new side effects recognised. For these reasons, the reader is strongly advised to consult the drug companies' printed information before administering any of the drugs recommended in this book.
Most drugs in this document are appropriate only for specialist use in hospitals.  A number of drugs should only be used in consultation with the appropriate Paediatric subspecialist. 

Note: The electronic version of this guideline is the version currently in use.  Any printed version cannot be assumed to be current. Printed copies of this document are valid for