Lfm. Beenen et al., Pharmacokinetics of intraventricularly administered teicoplanin in Staphylococci ventriculitis, PHARM WORLD, 22(4), 2000, pp. 127-129
Following craniotomy for a medulloblastoma in the posterior cranial fossa,
a 6-year old girl developed a ventriculitis with coagulase negative staphyl
ococci associated with the use of a ventriculostomy. Treatment with intrave
nous (iv) and intraventricular (ivt) vancomycin resulted in negative cultur
es of the cerebrospinal fluid, but had to be stopped because of a severe al
lergic skin reaction. Teicoplanin was administered iv (240 mg once daily) a
nd ivt (10 mg once daily), resulting in high teicoplanin CSF levels that we
re used to model the pharmacokinetics of ivt teicoplanin in this patient. N
o signs of recurrent infection or adverse events occurred. It is concluded
that a pharmacokinetic model can be derived from this case that can be used
as prior to guide teicoplanin intraventricular therapy in other patients.