Caffeine Citrate

  • Description and indication for use

    Caffeine is a trimethylxanthine that can be used for the prevention or treatment of apnoea of prematurity or apnoeas associated with respiratory infection or anaesthesia. Caffeine can also be used to aid extubation of ventilated babies.

    The pharmacological actions of caffeine in apnoea include stimulation of the medullary respiratory center, increased sensitivity to carbon dioxide, and enhanced diaphragmatic contractility.

    Dose

    Doses expressed as caffeine citrate (NB: 20 mg caffeine citrate = 10 mg caffeine base).

    IV/Oral:    

    Loading dose:          20 mg/kg caffeine citrate

    Maintenance dose:   5 mg/kg/dose caffeine citrate once daily*

    Maintenance dose can be increased by 5 mg/kg/dose every 24 hours to a maximum of 20 mg/kg/dose if apnoeas persist, unless side effects develop.1

    * Maintenance dose should commence at least 24 hours after loading dose.     

    Reconstitution/Dilution

    IV ampoules = 20 mg/mL (caffeine citrate).

    For IV use:

    Can be given undiluted.

    Route and method of administration

    IV:

    Infuse slowly over 30 minutes.#

    # Doses less than/equal to 5 mg/kg caffeine citrate may be infused over 10 minutes.

    Side effects

    Nausea, vomiting, gastric irritation.

    Agitation, irritability, restlessness.

    Hypo/hyperglycaemia.

    Tachycardia.

    Diuresis.

    Severe – necrotising enterocolitis.

    Overdose – arrhythmias, seizures.

    Special precautions

    Contraindications

    Hypersensitivity to caffeine or citrate.

    Precautions

    Seizure disorders.

    Renal and/or hepatic impairment.

    Gastro-oesophageal disease – relaxation of lower oesophageal sphincter may lead to gastro-oesophageal reflux.

    Compatible solutions/medications

    Sodium chloride 0.9%.

    Glucose 5% and 10%.

    Morphine sulphate.

    Incompatibilities

    Incompatible with TPN.

    Discoloured or cloudy solutions for injection should NOT be used.

    Contact Pharmacy if further information is required.

    Drug interactions

    Inhibitors or inducers for the Cytochrome P450 1A2 enzyme

    Inhibitors include

    amiodarone, erythromycin, fluoroquinolone antibiotics.

    Inducers include

    carbamazepine, omeprazole, phenobarbitone, phenytoin, rifampicin.

    Nursing responsibilities

    Therapeutic drug monitoring is not routinely required.

    Observe for signs of toxicity, including signs of necrotising enterocolitis (see Side Effects).

    The IV solution is usually clear and colourless – inspect for signs of discolouration, cloudiness, turbidity or particular matter prior to use. DO NOT use unless solution is clear and colourless.

    References:

    1.    Steer PS et al. High dose caffeine citrate for extubation of preterm infants: a randomised controlled trial.  ADC Fetal Neo Ed 2004 Nov; 89(6): F499-500. PMID: PMC1721801
    2.    RCH Paediatric Pharmacopoeia, 13th ed. 2002.
    3.    RWH Neonatal Pharmacopoeia, 2nd ed. 2005.
    4.    Natarajan G, Lulic-Botica M, Aranda JV.  Clinical Pharmacology of Caffeine in the Newborn. NeoReviews.May 2007, Vol. 8 No.5.
    5.    Lawrence Trissel, Handbook on Injectable Drugs, 17th ed. 2013.
    6.    Caffeine Citrate Sterile Injection Product Information ( http://www.tga.gov.au/pdf/auspar/auspar-cafnea.pdf- accessed 03/10/2013).

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