• FURTHER DILUTE
  • Must have adequate maintenance fluids to prevent hypoglycaemia




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    Must have adequate maintenance fluids to prevent hypoglycaemia.

    Infusion strength

    Prescribed amount

    1 mL/kg/hour = 0.2 unit/kg/hour

    10 units insulin and make up to 50 mL

    Draw up 0.5 mL (50 units of insulin) and add 9.5 mL sodium chloride 0.9%, glucose 5% or glucose 10% to make a final volume of 10 mL with a concentration of 5 units/mL.

    FURTHER DILUTE: Draw up 2 mL (10 units of insulin) of solution and dilute with glucose 5%, glucose 10% or sodium chloride 0.9% to make a final volume of 50 mL with a concentration/dose rate of 1 mL/kg/hour = 0.2 units/kg/hour.
    Cardiac arrest due to hyperkalaemia

    Infusion strength

    Prescribed amount

    1 mL/kg/hour = 0.2 units/kg/hour

    10 units insulin and make up to 50 mL

    Mix 25 g (50 mL of glucose 50%) glucose and 10 units regular insulin and give 1 mL/kg (0.2 units/kg of insulin) IV over 15 to 30 minutes. Glucose:insulin ratio = 2.5 g:1 unit.

    Administration


    Intravenous:

    Insulin is adsorbed to the plastic of intravenous bags, syringes and tubing which reduces the delivery of insulin.[1, 2] To saturate binding to plastic, infuse 20 mL of insulin solution through plastic tubing prior to infusion. Insulin concentrations ≤ 0.05 units/mL are not reliably delivered even after preconditioning and flushing [2].

    Infuse with maintenance fluids.

    Do not include in maintenance fluid requirements.

    Insulin binds to the filter. Do not filter infusion.


    Monitoring


    Blood glucose must be closely monitored to detect either hypo/hyperglycaemia.

    Recommend blood glucose every 20 minutes for the first hour, every 30 minutes for the second hour and every 2 to 4 hours thereafter. Increase frequency of monitoring during weaning.

    Recommend check potassium within 30–60 minutes of commencing glucose/insulin infusion. Serum potassium should be closely monitored to monitor response to treatment and avoid hypokalaemia.


    Contraindications


    Hypersensitivity to human insulin or any component of the formulation.

    During episodes of hypoglycaemia.



    Precautions

    Possible adverse effects include hypersensitivity, hypoglycaemia, hyperglycaemia and hypokalaemia.

    Use with caution in cardiac disease, hepatic impairment, renal impairment.



    Drug Interactions

    The following may reduce insulin requirements: Octreotide, beta-adrenergic blocking agents, angiotensin converting enzyme inhibitors, salicylates, anabolic steroids, alpha-adrenergic blocking agents, quinine, quinidine and sulfonamides.

    The following may increase insulin requirements: Thiazides, furosemide, ethacrynic acid, glucocorticoids, thyroid hormones, sympathomimetics, growth hormone, diazoxide.

    Sympathomimetics have a potassium lowering effect.


    Adverse Reactions


    Insulin/glucose infusion is associated with a high rate of hyperglycaemia and hypoglycaemia during infusion and hypoglycaemia during weaning (insulin has a longer half-life than glucose).

    Hypokalaemia if infusion continued.

    Hypertonic solution – potential for extravasation.


    Compatibility

    Glucose 5%, glucose 10%, glucose 50%, sodium chloride 0.9%, lactated Ringer's injection


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    Must have adequate maintenance fluids to prevent hypoglycaemia

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