Evidence map›Paper›PMID 31932366›Full record

ArticleAntimicrobial agents and chemotherapy2020

Population Pharmacokinetics of Teicoplanin in Preterm and Term Neonates: Is It Time for a New Dosing Regimen?

A Kontou, K Sarafidis, O Begou, H G Gika, A Tsiligiannis, K Ogungbenro, A Dokoumetzidis, E Agakidou, E Roilides

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Use of Antibiotics in Preterm Newborns.Antibiotics (Basel, Switzerland) · 2022
    Review
  9. Observational
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

9 authors at 4 institutions in 2 countries.

A Kontou1st Department of Neonatology, Aristotle University School of Health Sciences, Hippokration General Hospital, Thessaloniki, Greece.
K Sarafidis1st Department of Neonatology, Aristotle University School of Health Sciences, Hippokration General Hospital, Thessaloniki, Greece.
O BegouLaboratory of Analytical Chemistry, School of Chemistry, Aristotle University of Thessaloniki, Thessaloniki, Greece.
H G GikaDepartment of Medicine, Laboratory of Forensic Medicine & Toxicology, Aristotle University School of Health Sciences, Thessaloniki, Greece.
A TsiligiannisDepartment of Pharmacy, University of Athens, Athens, Greece.
K OgungbenroDivision of Pharmacy and Optometry, School of Health Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
A DokoumetzidisDepartment of Pharmacy, University of Athens, Athens, Greece.
E Agakidou1st Department of Neonatology, Aristotle University School of Health Sciences, Hippokration General Hospital, Thessaloniki, Greece.
E RoilidesInfectious Diseases Unit, 3rd Department of Pediatrics, Aristotle University School of Health Sciences, Hippokration General Hospital, Thessaloniki, Greece roilides@med.auth.gr.ORCID 0000-0002-0202-364X
Hippocration General Hospital · GRAristotle University of Thessaloniki · GRNational and Kapodistrian University of Athens · GRManchester Academic Health Science Centre · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our objective was to develop a population pharmacokinetic (PK) model in order to evaluate the currently recommended dosing regimen in term and preterm neonates. By using an optimal design approach, a prospective PK study was designed and implemented in 60 neonates with postmenstrual ages (PMA) of 26 to 43 weeks. A loading dose of 16 mg/kg was administered at day 1, followed by a maintenance dose of 8 mg/kg daily. Plasma concentrations were quantified by high-pressure liquid chromatography-mass spectrometry. Population PK (popPK) analysis was performed using NONMEM software. Monte-Carlo (MC) simulations were performed to evaluate currently recommended dosing based on a pharmacodynamic index of area under the concentration-time curve (AUC)/MIC ratio of ≥400. A two-compartment model with linear elimination best described the data by the following equations: clearance (CL) = 0.0227 × (weight [wt]/1,765)

Indexed as

Anti-Bacterial AgentsFemaleGestational AgeHumansInfant, NewbornMaleMicrobial Sensitivity TestsMonte Carlo MethodPremature BirthSepsisStaphylococcal InfectionsStaphylococcusTeicoplaninAnti-Bacterial AgentsTeicoplaninMonte Carlo simulationneonatespopulation pharmacokineticspremature neonatespreterm neonatesteicoplanin

Identifiers

PMID31932366
PMCPMC7179285
OpenAlexW2998780671

What OpenQuestion holds

Textmetadata
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.