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  1. Shanti, R., Sam, I.C., Hany Ariffin
    JUMMEC, 2009;12(1):35-38.
    MyJurnal
    Following craniotomy for an atypical rhabdoid tumour of the posterior cranial fossa, a fourteen-month-old boy developed a ventriculitis with methicillin resistant Staphylococcus epidermidis (MRSE) which is associated with the use of a ventriculoperitoneal shunt. Treatment with intravenous vancomycin resulted in a severe allergic skin reaction. Substitution with intravenous teicoplanin resulted in negative blood culture and MRSE ventriculitis was successfully eradicated with concomitant use of intraventricular teicoplanin. No signs of recurrent infection or adverse events occurred. Intraventricular teicoplanin is safe and effective for the treatment of staphylococcal neurosurgical shunt infections.
  2. Choong, Yi Fong, Chaw, Su Hlaing, Aye, Aye Mya Min, Chee, Geap Tay, Lai, Choo Ong, Hany Ariffin
    Neurology Asia, 2015;20(3):275-281.
    MyJurnal
    Background & Objective: Posterior reversible encephalopathy syndrome (PRES) is associated with
    immunosuppressive agents used in children with haemato-oncological diseases. There are no reports
    to date from the South Asia and South East Asia region. We report a Malaysian tertiary centre case
    series of children with haemato-oncological disease who developed PRES. Methods: Retrospective
    study of children seen with haemato-oncology diseases seen at the University Malaya Medical Centre
    Kuala Lumpur who developed PRES from 2011 – 2013. Clinical details were obtained from medical
    records and brain neuroimaging was reviewed. Results: Five patients met the inclusion criteria. All
    5 patients had significant hypertension acutely or subacutely prior to neurology presentation. Four
    presented with acute seizures and the remainder 1 presented with encephalopathy.Three patients
    were on chemotherapy, 1 had renal impairment and 1 had prior immunosupression for bone marrow
    transplantation. A full recovery was seen in 4 patients and 1 patient had mild residual quadriplegia.
    Conclusion: Our case series expands the clinico-radiological spectrum of PRES in children with
    underlying haemato-oncological disorders. It is the first to show that prior cyclosporin intake as long
    as 2 months is a potential risk factor for PRES. Clinicians need to be vigilant for development of
    PRES and closely monitor the blood pressure in these children who are receiving or recently had
    immunosuppressive drugs and present with acute neurological symptoms.
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