ABSTRACT
Objective Determine the gentamicin pharmacokinetic and pharmacodynamic (PK/PD) profiles of once daily dosing (ODD) versus every 18-hour (q18h) regimens and to characterize the effect of antenatal steroid on gentamicin clearance (GentCL).
Study Design Retrospective cohort of preterm infants (≤34 weeks gestation; ≤7 days) who received gentamicin for >48 hours from January 2005 to June 2007. Serum gentamicin peak and trough concentrations were determined, and PK/PD profiles calculated using standard noncompartmental methods.
Result 122 (63%) infants received ODD and 73 (37%) received q18h regimen. Desired gentamicin peak (5 to 12 mcg/mL) and trough (<2 mcg/mL) concentrations were achieved in 80% (95%CI, 72-86) on ODD vs. 47% (95%CI, 36-58) on q18h (p<0.001). Target drug exposure (AUC >72 mcg/mL/hr) was achieved in 73% (89/122) of infants on ODD vs. 22% (16/73) on q18h (p < 0.001). GentCL was significantly lower in those who receive antenatal steroid (37+/-8 mL/kg/hr vs. 42+/-13 mL/kg/hr, p=0.04) but not affected by postnatal indomethacin treatment (p>0.86).
Conclusion PK/PD profile of gentamicin is improved by ODD in preterm infants. GentCl was significantly less in infants exposed to antenatal steroids but not in those treated with indomethacin.
Footnotes
CONFLICT OF INTEREST: The authors declare no conflict of interest.
FUNDING/ GRANTS: Pediatric Infectious Disease Society Fellowship Research Award 2006-08 (RPS & PJS); Department of Clinical Sciences (Master’s Program), UT Southwestern Medical Center Dallas (RPS); and Clinical Translational Research Center, UT Southwestern Medical Center Dallas – CTSA NIH UL1-RR024982 (PJS & RPS)