Midazolam

  • Description and indication for use

    Midazolam is a short-acting benzodiazepine.  It is able to induce sedation, hypnosis, amnesia and anaesthesia, depending on the dose administered, the route of administration and the presence of other medication.  It also has anti-convulsant and muscle relaxant properties. 

    It is used as a short-acting sedative agent.

    Dose

    For induction of anaesthesia (intubated babies only):

    IV:

    0.15 to 0.3 mg/kg/dose.

    As a sedative/amnesic (intubated babies only):

    IV Infusion:

    0.5 to 2 microgram/kg/minute.

    Non-intubated babies:  Discuss with consultant 

    (*Can be given intranasal 0.2 to 0.3 mg/kg/dose using 5 mg/mL injectable form - Check with consultant prior to administration).

    If analgesia is required, and narcotics given concurrently, the dose may need to be lowered.

    Reconstitution/Dilution

    Ampoule = 5 mg in 1 mL.

    IV:

    STAT Dose - Medical Staff to be present for administration.

    Withdraw 0.2 mL of 5 mg/mL solution and add to 0.8 mL of water for injection in a second 1 mL syringe = 1 mg/mL.

    Withdraw required dose and discard remaining solution.

    IV Infusion:

    Withdraw required dose and make up to ordered fluid volume for infusion.

    Suitable infusion fluids include Sodium Chloride 0.9% and Glucose 5% and 10%.

    Usual order for infusion will be as follows:

    Drug How to make up Dose equivalent Dose range
    Midazolam 3.0 mg/kg in 50 mL glucose 10% 1 mL/hr  = 1 microgram/kg/min 0.5 to 2 micrograms/kg/min

    Route and method of administration

    IV:

    Given over at least 5 minutes.

    Note: Bolus doses are not recommended.

    IV Infusion:

    Infuse via syringe pump at prescribed rate.

    Side effects

    Respiratory arrest.

    Hypoventilation.

    Hypotension may occur if an opiate e.g. morphine or fentanyl is being used concurrently.

    Seizures, agitation or involuntary movements, including myoclonus, are usually due to improper dosing, rapid administration or in infants with underlying CNS abnormalities.

    Nasal administration may be uncomfortable because of a burning sensation.

    NOTE: Flumazenil can be used for reversal of overdose symptoms.

    Special precautions

    CAUTION in infants with renal or hepatic dysfunction - dosage adjustment may be required.

    Compatibilities

    Glucose 5% and 10%.

    Sodium Chloride 0.9%.

    Terminal injection site compatibility (if administered as an infusion):

    Dobutamine, Dopamine, Adrenaline, Morphine, Potassium Chloride, Insulin.

    Incompatibilities

    Ampicillin, Ceftazidime, Dexamethasone, Frusemide, Hydrocortisone, Sodium Bicarbonate.

    Midazolam must not be mixed together with: Pentobarbital, Ranitidine or Phenobarbitone.

    Administer alone or contact Pharmacy if further information is required.

    Drug interactions

    Cimetidine May reduce clearance of Midazolam and therefore increase effects and possibly lead to toxicity.
    Fentanyl and other opiates May have an additive effective when used with Midazolam, causing more pronounced sedation and possibly worsening respiratory depression.
    Theophylline May reduce the effectiveness of Midazolam.

    Nursing responsibilities

    Monitor heart rate and respiratory rate.

    Observe chest movement.

    Apply pulse oximeter.

    Apply transcutaneous CO2 monitor (if requested by doctor).

    Monitor BP.

    Change syringe every 24 hours and IV tubing every 3 days (as per RCH IV Line protocol).

    FLUMAZENIL should be available for reversal of overdose symptoms.

    Check that rate of infusion ordered corresponds with dose required (micrograms/kg/m).

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