Evidence map›Paper›PMID 24839147›Full record

ArticleAmerican journal of perinatology2015

Optimization of vancomycin dosing in very low-birth-weight preterm neonates.

Theresa Madigan, Christine B Teng, Jena Koshaish, Kent R Johnson, Kevin K Graner, Ritu Banerjee

Abstract read
In one paragraph

Article in American journal of perinatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Observational
  5. Review
  6. Achieving Vancomycin Troughs Within Goal Range in Low Birth Weight Neonates.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2021
    Article
  7. Article
  8. Adverse consequences of neonatal antibiotic exposure.Current opinion in pediatrics · 2016
    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

6 authors at 5 institutions in 2 countries.

Theresa MadiganDepartment of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota.
Christine B TengDivision of Pediatric Infectious Diseases, Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota.
Jena KoshaishDepartment of Pharmacy, All Children's Hospital, St. Petersburg, Florida.
Kent R JohnsonPharmacy Services, Mayo Clinic, Rochester, Minnesota.
Kevin K GranerPharmacy Services, Mayo Clinic, Rochester, Minnesota.
Ritu BanerjeeDivision of Pediatric Infectious Diseases, Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota.
WinnMed · USJohns Hopkins All Children's Hospital · USMayo Clinic · USMayo Clinic in Florida · USNational University of Singapore · SG

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
NCATS NIH HHS UL1 TR000135
6 · The paper itself

Abstract

objectiveTo compare vancomycin serum trough concentrations and 24-hour area under the serum concentration-versus-time curve (AUC24) among very low-birth-weight (VLBW) premature infants before and after implementation of an institution-wide increase in neonatal vancomycin dosing. STUDY

designWe performed a retrospective analysis of vancomycin concentrations among preterm VLBW neonates before (2007-2010) and after (2010-2013) implementation of a new vancomycin dosing protocol consisting of increased vancomycin daily dose and frequency of administration.

resultsNeonates weighing < 1,500 g and receiving the new vancomycin dosing regimen had lower rates of undetectable trough concentrations (24 vs. 50%, p = 0.04), higher median trough concentrations (10.8 vs. 5.9 µg/mL, p = 0.003), a higher proportion of goal trough concentrations of 10 to 20 µg/mL (35 vs. 4%, p = 0.005), and a significantly higher vancomycin AUC24 (438 vs. 320 mg·h/L, p = 0.004) compared with historical controls.

conclusionIncreasing the vancomycin daily dose and dosing frequency led to an increase in vancomycin trough concentrations and AUC24, and a decrease in the proportion of undetectable (< 5.0 µg/mL) troughs, without an increase in toxicity among VLBW premature neonates.

Indexed as

Anti-Bacterial AgentsBacteremiaCohort StudiesEnterocolitis, NecrotizingFemaleHumansInfant, Extremely PrematureInfant, NewbornInfant, PrematureInfant, Very Low Birth WeightMaleRetrospective StudiesVancomycinAnti-Bacterial AgentsVancomycin

Identifiers

PMID24839147
PMCPMC4418186
OpenAlexW2313288342

What OpenQuestion holds

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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.