Evidence map›Paper›PMID 20571461›Full record

ArticleThe Pediatric infectious disease journal2010

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

Susan M Abdel-Rahman, Gregory L Kearns, Santiago Topelberg, Richard F Jacobs, Goutam C Mistry, Anup Majumdar, Yang Xu, John A Wagner, Chester J Kitchen, Michelle Groff and 2 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in The Pediatric infectious disease journal, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Albumin and Other Plasma Proteins in Pediatric Patients: What, When, and How Much They Influence Antimicrobial Pharmacology.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Exploring the advancements of Australian OPAT.Therapeutic advances in infectious disease
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 2 countries.

Susan M Abdel-RahmanDivision of Pediatric Clinical Pharmacology and Medical Toxicology, The Children's Mercy Hospital, Kansas City, MO, USA.
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
Merck & Co., Inc., Rahway, NJ, USA (United States) · USArkansas Children's Hospital · USChildren's Mercy Hospital · USHospital Roberto del Rio · CLUniversity of Missouri–Kansas City · US

Funding

Pediatric Pharmacology Research UnitU10HD031323 · NICHD · CASE WESTERN RESERVE UNIVERSITY · PI BLUMER, JEFFREY L. · 2004 to 2009
$2.2M
NICHD NIH HHS 5U10HD031323-13NICHD NIH HHS U10 HD031323
6 · The paper itself

Abstract

backgroundErtapenem is a carbapenem antibiotic with broad spectrum activity and a pharmacokinetic profile that favors once-daily administration in adults.

objectivesThis investigation was designed to evaluate the dose-exposure profile of ertapenem in children from infancy through adolescence.

methodsEighty-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.

resultsErtapenem 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.

conclusionsChildren 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.

Indexed as

AdolescentAnti-Bacterial Agentsbeta-LactamsChildChild, PreschoolChromatography, High Pressure LiquidErtapenemFemaleHumansInfantMalePlasmaAnti-Bacterial Agentsbeta-LactamsErtapenem

Identifiers

PMID20571461
PMCPMC2991518
OpenAlexW2062212441

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.