Calcium Gluconate

  • Description and indication for use

    Used in the treatment of hypocalcaemia (Ionised Calcium < 1.1 mmol/L) in:

    • Stable preterm infants only when Ionised Calcium < 0.8 mmol/L
    • Unstable preterm or term infants with:

            a.     Cardiovascular instability (hypotension, poor perfusion, metabolic acidosis, PPHN)

            b.     Encephalopathy and/or seizures

            c.     Exchange transfusion

    Symptoms of hypocalcaemia in neonates may include: muscle twitching, jitteriness, generalized seizures, and prolonged QT interval.1

    When treating hypocalcaemia, it should be ensured that hypomagnesaemia is also treated if present. Correction of hypomagnesaemia may also correct hypocalcaemia.

    Dose

    Symptomatic hypocalcaemia – acute treatment

    IV Bolus:

    0.11 mmol/kg of Calcium Ions = 0.5 mL/kg of 10% Calcium Gluconate solution. 

    Hypocalcaemia – Acute treatment

    IV Correction:

    0.44 mmol/kg of Calcium Ions = 2.0 mL/kg of 10% Calcium Gluconate solution.

    Hypocalcaemia – maintenance

    IV Infusion:

    1 mmol/kg/day of Calcium Ions = 4.5 mL/kg/day of 10% Calcium Gluconate solution.

    Exchange transfusion:

    Routinely, 0.22 – 0.44 mmol of Calcium Ions (1-2 ml of 10% Calcium Gluconate solution) is given at every 100 mL point of the exchange.

    It may be injected slowly, or added to a 10mL aliquot. Calcium may be added before 100 mL of exchange if infant appears symptomatic of hypocalcaemia.4

    Reconstitution/Dilution

    Available as: Calcium Gluconate 10%, 10 mL ampoules = 0.22 mmol Calcium Ions/mL.

    IV Bolus and Correction:      

    Dilute 1 to 5: Add 1 mL of Calcium Gluconate 10% to 4 mL of Glucose 5% or 10% to give a final volume of 5 mL = 0.044 mmol Calcium/mL.

    IV Infusion:

    Used for maintenance.

    Withdraw required dose and make up to ordered volume of infusion solution (Glucose 5 or 10%).

    Route and method of administration

    Do not give by IM injection.3

    Do not give intra-arterially.1

    IV Bolus:

    Give diluted solution slowly over 20 to 60 minutes.

    IV Correction:

    Give diluted solution over 6 hours using an infusion pump.

    IV Infusion:                 

    Continuous IV infusion using an infusion pump.

    Side effects

    Rapid administration may cause bradycardia or cardiac arrest.1

    Cutaneous necrosis and/or calcium deposition occurs with extravasation.1

    Bolus doses via UAC have been associated with intestinal bleeding and lower extremity tissue necrosis.1

    Nursing responsibilities

    Monitor for bradycardia and arrhythmias on ECG whilst giving bolus doses

    Observe IV infusion site closely for extravasation.

    Observe solution & complete length of infusion line for precipitation (haziness).

    Compatibility information3

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

      Compatible Incompatible
    Fluids

    Glucose 5%

    Sodium chloride 0.9%

    Glucose 10%.1

    PN, IL
    Drugs Amikacin, Aminophylline, Benzylpenicillin, Chloramphenicol, Frusemide, Heparin, Hydrocortisone, Magnesium Sulphate, Noradrenaline, Potassium Chloride, Tobramycin, Vancomycin, Verapamil. Amphotericin, Clindamycin1, Dobutamine, Digoxin, Flucloxacillin, Fluconazole, Indomethacin1, Phosphate, Sodium Bicarbonate.
    Y-Site Adrenaline, Ciprofloxacin, Dobutamine, Filgrastim, Heparin, Hydrocortisone, Meropenem, Potassium Chloride.  

             

    References:

    1.        Neofax 12th Ed. 1999 A Manual of Drugs Used in Neonatal Care, Young T, Mangum O.

    2.        Neonatal Pharmacopoeia 1st Ed. 1998, Pharmacy Department, The Royal Women's Hospital, Carlton 3053.

    3.        Australian Injectable Drugs Handbook, 2nd Ed., The Society of Hospital Pharmacists of Australia, 1999.

    4.        Royal Women’s Hospital Continuum of Care – 9W-04-2-076       .        

     

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