Evidence map›Paper›PMID 33521971›Full record

ReviewClinical pharmacology and therapeutics2021

Variation in Target Attainment of Beta-Lactam Antibiotic Dosing Between International Pediatric Formularies.

Silke Gastine, Yingfen Hsia, Michelle Clements, Charlotte I S Barker, Julia Bielicki, Christine Hartmann, Mike Sharland, Joseph F Standing

Open access · hybridAbstract readReview
In one paragraph

Review in Clinical pharmacology and therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
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

8 authors at 5 institutions in 3 countries.

Silke GastineInfection, Immunity and Inflammation Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
Yingfen HsiaSchool of Pharmacy, Queen's University Belfast, Belfast, UK.
Michelle ClementsMRC Clinical Trials Unit, University College London, London, UK.
Charlotte I S BarkerDepartment of Medical & Molecular Genetics, King's College London, London, UK.
Julia BielickiPaediatric Infectious Diseases Research Group, Institute for Infection and Immunity, St George's University of London, London, UK.
Christine HartmannSchool of Pharmacy, Queen's University Belfast, Belfast, UK.
Mike SharlandPaediatric Infectious Diseases Research Group, Institute for Infection and Immunity, St George's University of London, London, UK.
Joseph F StandingInfection, Immunity and Inflammation Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
University College London · GBQueen's University Belfast · GBKing's College London · GBSt George's, University of London · GBUniversity Children’s Hospital Basel · CH

Funding

Department of HealthMedical Research Council MC_UU_00004/05Medical Research Council MC_UU_12023/22Medical Research Council MR/M008665/1
6 · The paper itself

Abstract

As antimicrobial susceptibility of common bacterial pathogens decreases, ensuring optimal dosing may preserve the use of older antibiotics in order to limit the spread of resistance to newer agents. Beta-lactams represent the most widely prescribed antibiotic class, yet most were licensed prior to legislation changes mandating their study in children. As a result, significant heterogeneity persists in the pediatric doses used globally, along with quality of evidence used to inform dosing. This review summarizes dosing recommendations from the major pediatric reference sources and tries to answer the questions: Does beta-lactam dose heterogeneity matter? Does it impact pharmacodynamic target attainment? For three important severe clinical infections-pneumonia, sepsis, and meningitis-pharmacokinetic models were identified for common for beta-lactam antibiotics. Real-world demographics were derived from three multicenter point prevalence surveys. Simulation results were compared with minimum inhibitory concentration distributions to inform appropriateness of recommended doses in targeted and empiric treatment. While cephalosporin dosing regimens are largely adequate for target attainment, they also pose the most risk of neurotoxicity. Our review highlights aminopenicillin, piperacillin, and meropenem doses as potentially requiring review/optimization in order to preserve the use of these agents in future.

Indexed as

AdolescentAnti-Bacterial AgentsArea Under CurveBacteriological Techniquesbeta-LactamsChildChild, PreschoolComputer SimulationDose-Response Relationship, DrugDrug Dosage CalculationsHumansInfantInfant, NewbornMeningitis, BacterialMicrobial Sensitivity TestsPediatricsAnti-Bacterial Agentsbeta-Lactams

Identifiers

PMID33521971
PMCPMC8358626
OpenAlexW3126174921

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.