• Dose adjustment Renal Impairment
  • Hepatic impairment
  • Maximum dose Not applicable Total cumulative dose
  • 1g VIAL
  • Fluid restriction
  • Monitoring Renal function, full blood count, hearing function and serum vancomycin concentrations. Target trough concentration
  • Measure trough vancomycin concentration immediately prior to 3rd dose with the exception of: 1.
  • Check concentration prior to the 4th dose after any change in dose or frequency.
  • Standard dose: 15 mg/kg/dose. Dosing interval as per table below




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    Standard dose: 15 mg/kg/dose. Dosing interval as per table below24


    Method

    Interval

    Corrected Gestational Age/Postmenstrual Age

    Postnatal Age

    < 30+0 weeks

    0─2 days

    18 hourly

    < 30+0 weeks

    3+ days

    12 hourly

    30+0─36+6 weeks

    0─14 days

    12 hourly

    30+0─36+6 weeks

    15+ days

    8 hourly

    37+0─44+6 weeks

    0─7 days

    12 hourly

    37+0─44+6 weeks

    8+ days

    8 hourly

    ≥ 45+0 weeks

    0+ days

    6 hourly


    Severe sepsis: Consider giving a loading dose of 20 mg/kg/dose in suspected severe sepsis including MRSA, bone infection, meningitis, endocarditis. However, data in neonates are limited.

    Dose adjustment


    Renal Impairment:

    • For infants with renal impairment, consider using an antibiotic without nephrotoxicity in consultation with an infectious diseases specialist.

    • If vancomycin is used, perform a trough level before the 2nd dose.

    • Adjust the dosage interval5, 21 to achieve a trough level 10─20 mg/L (higher trough level 15─20 mg/L in severe sepsis). Repeat trough level before the next dose after each dosage adjustment or before every 3rd dose for infants within the target range.

    Hepatic impairment: Not applicable.

    Therapeutic hypothermia: Measure trough concentration prior to 2nd dose.27

    ECMO: Current evidence is insufficient to recommend a specific dose adjustment.

    Maximum dose

    Not applicable

    Total cumulative dose

    Not applicable

    Route

    IV

    Preparation

    500mg VIAL

    Add 10 mL of water for injection to the 500 mg vial to make a 50 mg/mL solution



    FURTHER DILUTE

    Draw up 2 mL (100 mg of vancomycin) of the above solution and add 18 mL glucose 5% or sodium chloride 0.9% to make a final volume of 20 mL with a final concentration of 5 mg/mL.


    1g VIAL

    Add 20 mL of water for injection to the 1g vial to make a 50 mg/mL solution



    FURTHER DILUTE

    Draw up 2 mL (100 mg of vancomycin) of the above solution and add 18 mL glucose 5% or sodium chloride 0.9% to make a final volume of 20 mL with a final concentration of 5 mg/mL.


    Fluid restriction To prepare 10 mg/mL concentration
    Vancomycin can be diluted to 10 mg/mL solution, however this dilution increases the risk of infusion-related events (see adverse reactions).

    500mg VIAL

    Add 10 mL of water for injection to the 500 mg vial to make a 50 mg/mL solution

    Further Dilute

    Draw up 4 mL (200 mg of vancomycin) of the above solution and add 16 mL glucose 5% or sodium chloride 0.9% to make a final volume of 20 mL with a final concentration of 10 mg/mL.

    To prepare 10 mg/mL concentration

    1g VIAL

    Add 20 mL of water for injection to the 1g vial to make a 50 mg/mL solution

    Further Dilute

    Draw up 4 mL (200 mg of vancomycin) of the above solution and add 16 mL glucose 5% or sodium chloride 0.9% to make a final volume of 20 mL with a final concentration of 10 mg/mL.

    Administration

    IV infusion over ONE hour.

    Adequately flush the intravenous lines before and after administration of vancomycin.



    Monitoring

    Renal function, full blood count, hearing function and serum vancomycin concentrations.
    Target trough concentration 10─20 mg/L

    Aim for higher trough level of 15─20 mg/L in suspected severe sepsis e.g., MRSA, bone infection, meningitis, endocarditis.



    Measure trough vancomycin concentration immediately prior to 3rd dose with the exception of:

    1. <29+0 CGA weeks – before 2nd dose,

    2. therapeutic hypothermia – before 2nd dose and

    3. renal impairment – before 2nd dose, but refer to renal impairment section below.



    Check concentration prior to the 4th dose after any change in dose or frequency.

    Once target trough levels are reached, measure trough levels every 3 days prior to consecutive doses.

    More frequent monitoring may be required in renal impairment, infants receiving other nephrotoxic drugs or suspected severe sepsis.

    If a peak concentration is required to guide dosing, perform this 1 hour after completion of infusion, and target a peak concentration 20-40 mg/L. [22]



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    Standard dose: 15 mg/kg/dose. Dosing interval as per table below

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