Evidence map›Paper›PMID 32307575›Full record

Trial reportEuropean journal of clinical pharmacology2020

Population pharmacokinetics and target attainment of ciprofloxacin in critically ill patients.

Alan Abdulla, Omar Rogouti, Nicole G M Hunfeld, Henrik Endeman, Annemieke Dijkstra, Teun van Gelder, Anouk E Muller, Brenda C M de Winter, Birgit C P Koch

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in European journal of clinical pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 35 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

9 authors at 4 institutions in 1 country.

Alan AbdullaDepartment of Hospital Pharmacy, Erasmus University Medical Center, P.O. Box 2040, 3000 CA, Rotterdam, The Netherlands. a.abdulla@erasmusmc.nl.
Omar RogoutiDepartment of Hospital Pharmacy, Erasmus University Medical Center, P.O. Box 2040, 3000 CA, Rotterdam, The Netherlands.
Nicole G M HunfeldDepartment of Hospital Pharmacy, Erasmus University Medical Center, P.O. Box 2040, 3000 CA, Rotterdam, The Netherlands.
Henrik EndemanDepartment of Intensive Care, Erasmus University Medical Center, Rotterdam, The Netherlands.
Annemieke DijkstraDepartment of Intensive Care, Maasstad Hospital, Rotterdam, The Netherlands.
Teun van GelderDepartment of Hospital Pharmacy, Erasmus University Medical Center, P.O. Box 2040, 3000 CA, Rotterdam, The Netherlands.
Anouk E MullerDepartment of Medical Microbiology and Infectious Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
Brenda C M de WinterDepartment of Hospital Pharmacy, Erasmus University Medical Center, P.O. Box 2040, 3000 CA, Rotterdam, The Netherlands.
Birgit C P KochDepartment of Hospital Pharmacy, Erasmus University Medical Center, P.O. Box 2040, 3000 CA, Rotterdam, The Netherlands.
Erasmus MC · NLLeiden University Medical Center · NLMaasstad Ziekenhuis · NLMedisch Centrum Haaglanden · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo develop and validate a population pharmacokinetic model of ciprofloxacin intravenously in critically ill patients, and determine target attainment to provide guidance for more effective regimens.

methodsNon-linear mixed-effects modelling was used for the model development and covariate analysis. Target attainment of an ƒAUC

resultsA total of 204 blood samples were collected from 42 ICU patients treated with ciprofloxacin 400-1200 mg/day, with median values for age of 66 years, APACHE II score of 22, BMI of 26 kg/m

conclusionsThe model described the pharmacokinetics of ciprofloxacin in ICU patients adequately. No significant covariates were found and high inter-individual variability of ciprofloxacin pharmacokinetics in ICU patients was observed. The poor target attainment supports the use of higher doses such as 1200 mg/day in critically ill patients, while the variability of inter-individual pharmacokinetics parameters emphasizes the need for therapeutic drug monitoring to ensure optimal exposure.

Indexed as

Models, BiologicalAdministration, IntravenousAgedAnti-Bacterial AgentsCiprofloxacinComputer SimulationCritical IllnessFemaleHumansMaleMicrobial Sensitivity TestsMiddle AgedMonte Carlo MethodPseudomonas aeruginosaAnti-Bacterial AgentsCiprofloxacinCiprofloxacinCritically ill patientsNONMEMPopulation pharmacokineticsTarget attainment

Identifiers

PMID32307575
PMCPMC7306030
OpenAlexW3016656351

What OpenQuestion holds

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LicenceCC BY
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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.