Arch. Dis. Child. Fetal Neonatal Ed.. Published Online First: 1 May 2008. doi:10.1136/adc.2007.128280
Original articles |
Continuous-infusion vancomycin therapy for preterm neonates with suspected or documented infections:a new dosage schedule
1 Montpellier University Hospital, neonatology, France
2 Montpellier University Hospital, département d'information médicale, France
* To whom correspondence should be addressed. E-mail: jc-picaud{at}chu-montpellier.fr.
Accepted 23 April 2008
Abstract
Background: Intermittent infusion of vancomycin is widely used to treat late-onset sepsis in neonates. On the other hand, the continuous infusion of vancomycin could improve bactericidal efficacy since its action is time-dependent.
Objective: To evaluate a simplified dosage schedule for continuous-infusion vancomycin therapy. Methods: Prospective study in premature neonates (<34 weeks) with suspected coagulase negative staphylococci (CoNS) sepsis. Before antibiotics at time zero (T0), serum creatinine was measured and blood cultures were collected. Vancomycin dosage began with 25 or 15 mg/kg/d (period 1) and 30 or 20 mg/kg/d (period 2) depending on whether serum creatinine was below or above 90 µmol/L. Two days after beginning treatment (first timepoint: T1), serum vancomycin was measured and second blood cultures were collected.
Results: Between June 2002 and December 2005, 145 neonates were evaluated. At birth, median body weight was 920 ([Q25, Q75]: [500, 1160]) g and gestational age was 28 [26, 29] weeks. At T1, serum vancomycin was within the required range in 74.5% of neonates (108/145). Serum vancomycin levels were higher in period 2 than in period 1 (20 mg/L versus 13 mg/L, p<0.05). At T0, 55% (80/145) of blood cultures were positive for CoNS, but 71% (57/80) were negative at T1. Four days after beginning treatment, 92% of subjects had recovered without removing the central venous catheter.
Conclusion: Using this simplified dosage schedule, bactericidal efficacy was maintained and most subjects had serum vancomycin concentrations within the therapeutic range.
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Arch. Dis. Child. Fetal Neonatal Ed. 2008 93: F399.[Extract] [Full Text] [PDF]
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