Pharmacokinetics and tolerability of single-dose daptomycin in young infants

Pediatr Infect Dis J. 2012 Sep;31(9):935-7. doi: 10.1097/INF.0b013e31825d2fa2.

Abstract

Background: Daptomycin is approved for the treatment of complicated skin and skin-structure infections and Staphylococcus aureus bacteremia. We sought to characterize daptomycin single-dose pharmacokinetics and tolerability in young infants.

Methods: Subjects < 120 days of age with suspected systemic infections were eligible for inclusion. Each subject was given a single 6 mg/kg intravenous dose of daptomycin. An average of 4 postdose concentrations per infant was obtained.

Results: Data from 20 infants are presented. Median gestational age at birth and postnatal age were 32 weeks (range: 23, 40) and 3 days (1, 85), respectively. The median area under the concentration curve at 24 hours, volume of distribution, total body clearance and half-life of daptomycin were 262.4 mg×h/L (166.7, 340.2), 0.21 L/kg (0.11, 0.34), 0.021 L/h/kg (0.016, 0.034) and 6.2 hours (3.7, 9.0), respectively. No adverse events related to daptomycin were observed, including changes in creatine phosphokinase concentrations.

Conclusions: Daptomycin clearance in young infants was similar to that in children 2-6 years of age and higher than that observed in adolescents and adults.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anti-Bacterial Agents / adverse effects*
  • Anti-Bacterial Agents / pharmacokinetics*
  • Bacteremia / drug therapy
  • Bacteremia / metabolism*
  • Daptomycin / adverse effects*
  • Daptomycin / pharmacokinetics*
  • Female
  • Humans
  • Infant, Newborn
  • Male
  • Prospective Studies
  • Staphylococcal Skin Infections / drug therapy
  • Staphylococcal Skin Infections / metabolism*

Substances

  • Anti-Bacterial Agents
  • Daptomycin