Evidence map›Paper›PMID 41983018›Full record

ArticleThe journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG2026

Albumin and Other Plasma Proteins in Pediatric Patients: What, When, and How Much They Influence Antimicrobial Pharmacology.

Jacopo Angelini, Francesco Russiani, Sara Ferin, Sarah Flammini, Carlo Tascini, Jason A Roberts, Massimo Baraldo, Simone Giuliano

Abstract read
In one paragraph

Article in The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jacopo AngeliniClinical Pharmacology Institute (JA, FR, MB), University Hospital Friuli Centrale, Udine, Italy.
Francesco RussianiClinical Pharmacology Institute (JA, FR, MB), University Hospital Friuli Centrale, Udine, Italy.
Sara FerinInfectious Diseases Clinic (SFe, SFl, CT, SG), Department of Medicine, University of Udine and Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.
Sarah FlamminiInfectious Diseases Clinic (SFe, SFl, CT, SG), Department of Medicine, University of Udine and Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.
Carlo TasciniInfectious Diseases Clinic (SFe, SFl, CT, SG), Department of Medicine, University of Udine and Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.
Jason A RobertsFaculty of Medicine The University of Queensland (JAR), University of Queensland Centre for Clinical Research, Brisbane, Australia.
Massimo BaraldoClinical Pharmacology Institute (JA, FR, MB), University Hospital Friuli Centrale, Udine, Italy.
Simone GiulianoInfectious Diseases Clinic (SFe, SFl, CT, SG), Department of Medicine, University of Udine and Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasma proteins play a critical role in antimicrobial drug exposure, particularly in special populations where protein concentrations and binding capacity may be altered. This review summarizes current knowledge on age-related changes in plasma protein concentrations and protein-binding variability, with a specific focus on pediatric populations. This variability can lead to substantial alterations in the unbound fraction of many antimicrobials, especially those that are highly protein-bound. Understanding these pharmacokinetic changes is fundamental for safe and effective antimicrobial dosing in particular patients such as pediatric patients, who may require specific dose adjustments based on the various stages of their physiological development, from birth to adolescence. During this growth period, each developmental stage may represent a clinical setting with distinctive characteristics that clinicians must consider when choosing the drug and its dosage, because pharmacokinetic parameters may change within a shorter and more variable time frame than observed in adult patients. In this context therapeutic drug monitoring (TDM) represents a key strategy for optimizing drug dosing and achieving target therapeutic drug concentrations.

Indexed as

albuminantimicrobialinfectious diseasepediatricpharmacokineticsprotein-binding

Identifiers

PMID41983018
PMCPMC13075404

What OpenQuestion holds

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Registered trials

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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.