Evidence map›Paper›PMID 34811403›Full record

ArticleScientific reports2021

Advancement of pharmacokinetic models of iohexol in patients aged 70 years or older with impaired kidney function.

Max Taubert, Elke Schaeffner, Peter Martus, Markus van der Giet, Uwe Fuhr, Amina Lösment, Natalie Ebert

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

7 authors at 3 institutions in 1 country.

Max TaubertClinical Pharmacology Unit, Department I of Pharmacology, Faculty of Medicine and University Hospital Cologne, Center for Pharmacology, University Hospital Cologne (AöR), Gleueler Straße 24, 50931, Cologne, Germany. max.taubert@uk-koeln.de.
Elke SchaeffnerInstitute of Public Health, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Peter MartusInstitute for Clinical Epidemiology and Applied Biostatistics, University Hospital Tübingen, Tübingen, Germany.
Markus van der GietDepartment of Nephrology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Uwe FuhrClinical Pharmacology Unit, Department I of Pharmacology, Faculty of Medicine and University Hospital Cologne, Center for Pharmacology, University Hospital Cologne (AöR), Gleueler Straße 24, 50931, Cologne, Germany.
Amina LösmentDepartment of Nephrology, Vivantes Klinikum Im Friedrichshain, Berlin, Germany.
Natalie EbertInstitute of Public Health, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Charité - Universitätsmedizin Berlin · DEUniversity Hospital Cologne · DEKlinikum im Friedrichshain · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasma clearance of iohexol is a pivotal metric to quantify glomerular filtration rate (GFR), but the optimal timing and frequency of plasma sampling remain to be assessed. In this study, we evaluated the impact of a Bayesian estimation procedure on iohexol clearance estimates, and we identified an optimal sampling strategy based on data in individuals aged 70+. Assuming a varying number of random effects, we re-estimated previously developed population pharmacokinetic two- and three-compartment models in a model development group comprising 546 patients with iohexol concentration data up to 300 min post injection. Model performance and optimal sampling times were assessed in an evaluation group comprising 104 patients with reduced GFR and concentration data up to 1440 min post injection. Two- and three-compartment models with random effects for all parameters overestimated clearance values (bias 5.07 and 4.40 mL/min, respectively) and underpredicted 24-h concentrations (bias - 14.5 and - 12.0 µg/ml, respectively). Clearance estimates improved distinctly when limiting random effects of the three-compartment model to clearance and central volume of distribution. Two blood samples, one early and one 300 min post injection, were sufficient to estimate iohexol clearance. A simplified three-compartment model is optimal to estimate iohexol clearance in elderly patients with reduced GFR.

Indexed as

AgedBayes TheoremContrast MediaCreatinineFemaleGlomerular Filtration RateHumansIohexolKidneyKidney DiseasesKidney Function TestsMaleModels, StatisticalProbabilityContrast MediaCreatinineIohexol

Identifiers

PMID34811403
PMCPMC8608910
OpenAlexW3214781290

What OpenQuestion holds

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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.