Evidence map›Paper›PMID 25753640›Full record

ArticleAntimicrobial agents and chemotherapy2015

Influence of renal function estimation on pharmacokinetic modeling of vancomycin in elderly patients.

Anaïs Glatard, Laurent Bourguignon, Roger W Jelliffe, Pascal Maire, Michael N Neely, Sylvain Goutelle

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 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
2.0field-weighted citation impact, top 14% 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, 27 citations in OpenAlex.

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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 3 institutions in 1 country.

Anaïs GlatardService pharmaceutique-ADCAPT, Groupement Hospitalier de Gériatrie, Hospices Civils de Lyon, Lyon, France.
Laurent BourguignonService pharmaceutique-ADCAPT, Groupement Hospitalier de Gériatrie, Hospices Civils de Lyon, Lyon, France Laboratoire de Biométrie et Biologie Evolutive, CNRS UMR 5558, Université Lyon 1, Villeurbanne, France.
Roger W JelliffeLaboratory of Applied Pharmacokinetics, USC School of Medicine, Los Angeles, California, USA.
Pascal MaireService pharmaceutique-ADCAPT, Groupement Hospitalier de Gériatrie, Hospices Civils de Lyon, Lyon, France Laboratoire de Biométrie et Biologie Evolutive, CNRS UMR 5558, Université Lyon 1, Villeurbanne, France.
Michael N NeelyLaboratory of Applied Pharmacokinetics, USC School of Medicine, Los Angeles, California, USA sylvain.goutelle@chu-lyon.fr mneely@usc.edu.
Sylvain GoutelleService pharmaceutique-ADCAPT, Groupement Hospitalier de Gériatrie, Hospices Civils de Lyon, Lyon, France Laboratoire de Biométrie et Biologie Evolutive, CNRS UMR 5558, Université Lyon 1, Villeurbanne, France Faculté de Pharmacie de Lyon-ISPB, Université Lyon 1, Lyon, France sylvain.goutelle@chu-lyon.fr mneely@usc.edu.
Centre National de la Recherche Scientifique · FRHospices Civils de Lyon · FRLaboratoire de Biométrie et Biologie Evolutive · FR

Funding

Populaton Pharmacokinetic Modeling and Optimal ControlR01GM068968 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI NEELY, MICHAEL N. · 2003 to 2015
$3.9M
NIGMS NIH HHS R01 GM068968
6 · The paper itself

Abstract

Vancomycin is a renally excreted drug, and its body clearance correlates with creatinine clearance. However, the renal function estimation equation that best predicts vancomycin clearance has not been established yet. The objective of this study was to compare the abilities of different renal function estimation equations to describe vancomycin pharmacokinetics in elderly patients. The NPAG algorithm was used to perform population pharmacokinetic analysis of vancomycin concentrations in 78 elderly patients. Six pharmacokinetic models of vancomycin clearance were built, based on the following equations: Cockcroft-Gault (CG), Jelliffe (JEL), Modification of Diet in Renal Disease (MDRD), Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) (both in milliliters per minute per 1.73 m(2)), and modified MDRD and CKD-EPI equations (both in milliliters per minute). Goodness-of-fit and predictive performances of the six PK models were compared in a learning set (58 subjects) and a validation set (20 patients). Final analysis was performed to estimate population parameters in the entire population. In the learning step, the MDRD-based model best described the data, but the CG- and JEL-based models were the least biased. The mean weighted errors of prediction were significantly different between the six models (P = 0.0071). In the validation group, predictive performances were not significantly different. However, the use of a renal function estimation equation different from that used in the model building could significantly alter predictive performance. The final analysis showed important differences in parameter distributions and AUC estimation across the six models. This study shows that methods used to estimate renal function should not be considered interchangeable for pharmacokinetic modeling and model-based estimation of vancomycin concentrations in elderly patients.

Indexed as

Models, TheoreticalAgedAged, 80 and overFemaleGlomerular Filtration RateHumansKidney Function TestsMaleRetrospective StudiesVancomycinVancomycin

Identifiers

PMID25753640
PMCPMC4432143
OpenAlexW2092735046

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.