Evidence map›Paper›PMID 31016671›Full record

ArticleClinical pharmacokinetics2019

A Prospective Clinical Study Characterizing the Influence of Morbid Obesity on the Pharmacokinetics of Gentamicin: Towards Individualized Dosing in Obese Patients.

Cornelis Smit, Roeland E Wasmann, Sebastiaan C Goulooze, Eric J Hazebroek, Eric P A Van Dongen, Desiree M T Burgers, Johan W Mouton, Roger J M Brüggemann, Catherijne A J Knibbe

Open access · hybridAbstract readControlled Clinical Trial
In one paragraph

Article in Clinical pharmacokinetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Population pharmacokinetics of oral fosfomycin calcium in healthy women.The Journal of antimicrobial chemotherapy · 2024
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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

9 authors at 6 institutions in 1 country.

Cornelis SmitDepartment of Clinical Pharmacy, St. Antonius Hospital, Koekoekslaan 1, 3435 CM, Nieuwegein, The Netherlands.
Roeland E WasmannDepartment of Pharmacy, Radboud Institute for Health Sciences, Radboudumc, Geert Grooteplein Zuid 8, 6525 GA, Nijmegen, The Netherlands.
Sebastiaan C GouloozeDepartment of Systems Biomedicine and Pharmacology, Leiden Academic Centre for Drug Research, Leiden University, Einsteinweg 55, 2333 CC, Leiden, The Netherlands.
Eric J HazebroekDepartment of Surgery, St. Antonius Hospital, Koekoekslaan 1, 3435 CM, Nieuwegein, The Netherlands.
Eric P A Van DongenDepartment of Anesthesiology, St. Antonius Hospital, Koekoekslaan 1, 3435 CM, Nieuwegein, The Netherlands.
Desiree M T BurgersDepartment of Clinical Pharmacy, St. Antonius Hospital, Koekoekslaan 1, 3435 CM, Nieuwegein, The Netherlands.
Johan W MoutonDepartment of Medical Microbiology and Infectious Diseases, Erasmus MC, Doctor Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
Roger J M BrüggemannDepartment of Pharmacy, Radboud Institute for Health Sciences, Radboudumc, Geert Grooteplein Zuid 8, 6525 GA, Nijmegen, The Netherlands.
Catherijne A J KnibbeDepartment of Clinical Pharmacy, St. Antonius Hospital, Koekoekslaan 1, 3435 CM, Nieuwegein, The Netherlands. c.knibbe@antoniusziekenhuis.nl.
St. Antonius Ziekenhuis · NLLeiden University · NLCentre for Human Drug Research · NLErasmus MC · NLRadboud Institute for Molecular Life Sciences · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveGentamicin is an aminoglycoside antibiotic predominantly used in bloodstream infections. Although the prevalence of obesity is increasing dramatically, there is no consensus on how to adjust the dose in obese individuals. In this prospective clinical study, we study the pharmacokinetics of gentamicin in morbidly obese and non-obese individuals to develop a dosing algorithm that results in adequate drug exposure across body weights.

methodsMorbidly obese subjects undergoing bariatric surgery and non-obese healthy volunteers received one intravenous dose of gentamicin (obese: 5 mg/kg based on lean body weight, non-obese: 5 mg/kg based on total body weight [TBW]) with subsequent 24-h sampling. All individuals had a normal renal function. Statistical analysis, modelling and Monte Carlo simulations were performed using R version 3.4.4 and NONMEM

resultsA two-compartment model best described the data. TBW was the best predictor for both clearance [CL = 0.089 × (TBW/70)

conclusionsIn this study in morbidly obese and non-obese individuals ranging from 53 to 221 kg we identified body weight as an important determinant for both gentamicin CL and V

trial registrationRegistered in the Dutch Trial Registry (NTR6058).

Indexed as

Administration, IntravenousAdultAnti-Bacterial AgentsBody WeightFemaleGentamicinsHumansMaleMiddle AgedModels, BiologicalObesity, MorbidPrecision MedicineYoung AdultAnti-Bacterial AgentsGentamicins

Identifiers

PMID31016671
PMCPMC6768900
OpenAlexW2941102003

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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.