Literature DB >> 20571461

Pharmacokinetics and tolerability of single-dose intravenous ertapenem in infants, children, and adolescents.

Susan M Abdel-Rahman1, Gregory L Kearns, Santiago Topelberg, Richard F Jacobs, Goutam C Mistry, Anup Majumdar, Yang Xu, John A Wagner, Chester J Kitchen, Michelle Groff, Gary Herman, Jeffrey L Blumer.   

Abstract

BACKGROUND: Ertapenem is a carbapenem antibiotic with broad spectrum activity and a pharmacokinetic profile that favors once-daily administration in adults.
OBJECTIVES: This investigation was designed to evaluate the dose-exposure profile of ertapenem in children from infancy through adolescence.
METHODS: Eighty-four children (3 months-16 years) requiring antibiotic therapy were enrolled in this multicenter trial. Children received a single intravenous dose of ertapenem at 15, 20, or 40 mg/kg followed by repeated blood sampling for 24 hours. Free and total plasma ertapenem concentrations were quantitated by high-performance liquid chromatography, and the pharmacokinetics were determined using a model-independent approach.
RESULTS: Ertapenem exposure increased proportionally with increasing dose; however, achievable concentrations were influenced by age. Children older than 12 years attained higher dose-normalized concentrations at the end of the infusion (concentration at the end of the infusion [Ceoi]: 8.7 ± 1.9 mg/L per mg/kg dose) and total body exposure (area under the curve area under the plasma concentration-time curve [AUC]0-∞: 34.7 ± 14.7 mg hr/L per mg/kg dose) as compared with children 2 to 12 years (Ceoi: 6.9 ± 2.4 mg/L per mg/kg dose, AUC0-∞: 18.4 ± 8.0 mg hr/L per mg/kg dose) and children younger than 2 years (Ceoi: 6.1 ± 2.2 mg/L per mg/kg dose, AUC0-∞: 17.0 ± 5.4 mg hr/L per mg/kg dose). These findings were accounted for by age-dependent changes in ertapenem clearance and distribution volume. In 3 children adverse events (nausea, n = 2; injection site reaction, n = 1) were considered related to study drug administration.
CONCLUSIONS: Children younger than 12 years require dosing more frequently than once daily to achieve optimal efficacy when treating organisms with a minimum inhibitory concentration near the susceptibility breakpoint.

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Year:  2010        PMID: 20571461      PMCID: PMC2991518          DOI: 10.1097/INF.0b013e3181e82608

Source DB:  PubMed          Journal:  Pediatr Infect Dis J        ISSN: 0891-3668            Impact factor:   2.129


  19 in total

1.  In-vitro antimicrobial activity of a carbapenem, MK-0826 (L-749,345) and provisional interpretive criteria for disc tests.

Authors:  P C Fuchs; A L Barry; S D Brown
Journal:  J Antimicrob Chemother       Date:  1999-05       Impact factor: 5.790

2.  A study evaluating the efficacy, safety, and tolerability of ertapenem versus ceftriaxone for the treatment of community-acquired pneumonia in adults.

Authors:  Guillermo Ortiz-Ruiz; Jose Caballero-Lopez; Ian R Friedland; Gail L Woods; Alexandra Carides
Journal:  Clin Infect Dis       Date:  2002-03-18       Impact factor: 9.079

3.  Comparative in vitro activities of carbapenem L-749,345 and other antimicrobials against multiresistant gram-negative clinical pathogens.

Authors:  G Jacoby; P Han; J Tran
Journal:  Antimicrob Agents Chemother       Date:  1997-08       Impact factor: 5.191

4.  Pharmacodynamic profile of ertapenem against Klebsiella pneumoniae and Escherichia coli in a murine thigh model.

Authors:  Dana Maglio; Mary Anne Banevicius; Christina Sutherland; Chinedum Babalola; Charles H Nightingale; David P Nicolau
Journal:  Antimicrob Agents Chemother       Date:  2005-01       Impact factor: 5.191

5.  Activity of ertapenem (MK-0826) versus Enterobacteriaceae with potent beta-lactamases.

Authors:  D M Livermore; K J Oakton; M W Carter; M Warner
Journal:  Antimicrob Agents Chemother       Date:  2001-10       Impact factor: 5.191

6.  In vitro pharmacodynamic studies of L-749,345 in comparison with imipenem and ceftriaxone against gram-positive and gram-negative bacteria.

Authors:  I Odenholt; E Löwdin; O Cars
Journal:  Antimicrob Agents Chemother       Date:  1998-09       Impact factor: 5.191

7.  Ertapenem once daily versus piperacillin-tazobactam 4 times per day for treatment of complicated skin and skin-structure infections in adults: results of a prospective, randomized, double-blind multicenter study.

Authors:  Donald R Graham; Christopher Lucasti; Osvaldo Malafaia; Ronald L Nichols; Paul Holtom; Nora Quintero Perez; Andrea McAdams; Gail L Woods; T Paulette Ceesay; Richard Gesser
Journal:  Clin Infect Dis       Date:  2002-05-09       Impact factor: 9.079

Review 8.  Ertapenem: a Group 1 carbapenem with distinct antibacterial and pharmacological properties.

Authors:  Milton L Hammond
Journal:  J Antimicrob Chemother       Date:  2004-06       Impact factor: 5.790

9.  Treatment of complicated urinary tract infection in adults: combined analysis of two randomized, double-blind, multicentre trials comparing ertapenem and ceftriaxone followed by appropriate oral therapy.

Authors:  Wilbur G Wells; Gail L Woods; Qi Jiang; Richard M Gesser
Journal:  J Antimicrob Chemother       Date:  2004-06       Impact factor: 5.790

10.  Pharmacodynamic assessment of ertapenem (MK-0826) against Streptococcus pneumoniae in a murine neutropenic thigh infection model.

Authors:  Dawei Xuan; Maryanne Banevicius; Blair Capitano; Myo-Kyoung Kim; Charles Nightingale; David Nicolau
Journal:  Antimicrob Agents Chemother       Date:  2002-09       Impact factor: 5.191

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  1 in total

1.  Quantification and validation of ertapenem using a liquid chromatography-tandem mass spectrometry method.

Authors:  S P van Rijn; A M A Wessels; B Greijdanus; D J Touw; J W C Alffenaar
Journal:  Antimicrob Agents Chemother       Date:  2014-04-14       Impact factor: 5.191

  1 in total

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