Plj. Degraeuwe et al., USE OF TEICOPLANIN IN PRETERM NEONATES WITH STAPHYLOCOCCAL LATE-ONSETNEONATAL SEPSIS, Biology of the neonate, 73(5), 1998, pp. 287-294
Objective: To study the clinical pharmacology of teicoplanin in babies
admitted to a newborn intensive care unit, by monitoring serum levels
, efficacy and potential side effects. Methods: An open, nonrandomized
descriptive study was performed in the neonatal intensive and high ca
re unit of the University Hospital Maastricht, The Neterlands. Twenty-
three preterm neonates, gestational age ranging from 26 to 32 weeks (m
edian 28.4 weeks), postnatal age from 5 to 47 days, and birth weight f
rom 570 to 1,740 g, presenting with (suspected) late onset septicemia,
were studied. Of 21 culture-proven septicemias, 20 were caused by sta
phylococci. The teicoplanin loading dose was 15 mg/kg i.v., followed b
y a maintenance dose of 8 mg/kg every 24 h. Intravenous gentamicin was
also administered pending blood culture. Serum teicoplanin concentrat
ions were measured by fluorescence polarization immunoassay. Clinical
and microbiological cure/failure rates were determined and possible si
de effects were monitored. Results: The study of individual pharmacoki
netics during multiple-dose intravenous infusions was rendered impossi
ble by apparently inaccurate dosing. Peak (30 min after end of the inf
usion) and trough teicoplanin levels were stable throughout the study
and averaged 27.8 (interquartile range 23.7-32.9) and 12.3 (interquart
ile range 9.1-16.8) mg/l, respectively. The microbiological and clinic
al cure rates were 90% in gram-positive septicemia. There was no appar
ent toxicity. Conclusions: Inaccurate drug administration was a proble
m in this study, making a multidose pharmacokinetic study impossible.
It is possible that inaccurate drug administration and not current dos
age guidelines yielded trough levels below 10 mg/l in 57 (32%) of 176
instances. This pharmaceutical aspect clearly warrants further study.
However, microbiological and clinical cure rates were high in gram-pos
itive septicemias, No side effects attributable to teicoplanin therapy
were encountered.