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Arch Dis Child Fetal Neonatal Ed doi:10.1136/adc.2007.128280

Continuous-infusion vancomycin therapy for preterm neonates with suspected or documented infections:a new dosage schedule

  1. PLAN Odile (o-plan{at}chu-montpellier.fr)
  1. Montpellier University Hospital, neonatology, France
    1. CAMBONIE Gilles (g-cambonie{at}chu-montpellier.fr)
    1. Montpellier University Hospital, neonatology, France
      1. MEYER Pierre (pagmeyer{at}yahoo.fr)
      1. Montpellier University Hospital, neonatology, France
        1. BARBOTTE Eric (e-barbotte{at}chu-montpellier.fr)
        1. Montpellier University Hospital, département d'information médicale, France
          1. MILESI Christophe (c-milesi{at}chu-montpellier.fr)
          1. Montpellier University Hospital, neonatology, France
            1. PIDOUX Odile (o-pidoux{at}chu-montpellier.fr)
            1. Montpellier University Hospital, neonatology, France
              1. BADR Maliha (m-badr{at}chu-montpellier.fr)
              1. Montpellier University Hospital, neonatology, France
                1. PICAUD Jean-Charles (jc-picaud{at}chu-montpellier.fr)
                1. Montpellier University Hospital, neonatology, France
                  • Published Online First 1 May 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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