Evidence map›Paper›PMID 29382394›Full record

Observational studyCritical care (London, England)2018

Pharmacokinetics of meropenem in septic patients on sustained low-efficiency dialysis: a population pharmacokinetic study.

Stephan Braune, Christina König, Jason A Roberts, Axel Nierhaus, Oliver Steinmetz, Michael Baehr, Stefan Kluge, Claudia Langebrake

Registry-linked trialOpen access · goldAbstract readObservational Study
In one paragraph

Observational study in Critical care (London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02287493 (Pharmacokinetics of Selected Antiinfectives During Sustained Low-efficiency Dialysis), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.1field-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.

NCT02287493 completednot on this map

Pharmacokinetics of Selected Antiinfectives During Sustained Low-efficiency Dialysis (SLED)

TypeobservationalSponsorUniversitätsklinikum Hamburg-EppendorfRan2013 to 2016Enrolled35ConditionsReplacement Therapy, RenalArmsPharmacokinetic Analysis
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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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

8 authors at 2 institutions in 2 countries.

Stephan BrauneDepartment of Intensive Care Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. s.braune@uke.de.ORCID 0000-0003-4984-9083
Christina KönigDepartment of Intensive Care Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Jason A RobertsUniversity of Queensland Centre for Clinical Research, Faculty of Medicine and Centre for Translational Anti-infective Pharmacodynamics, School of Pharmacy, The University of Queensland, Brisbane, Australia and Royal Brisbane and Women's Hospital, The University of Queensland, Brisbane, QLD, Australia.
Axel NierhausDepartment of Intensive Care Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Oliver SteinmetzIII. Medical Clinic and Polyclinic, Department of Nephrology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Michael BaehrHospital Pharmacy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Stefan KlugeDepartment of Intensive Care Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Claudia LangebrakeHospital Pharmacy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Universität Hamburg · DEThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of the study was to describe the population pharmacokinetics (PK) of meropenem in critically ill patients receiving sustained low-efficiency dialysis (SLED).

methodsProspective population PK study on 19 septic patients treated with meropenem and receiving SLED for acute kidney injury. Serial blood samples for determination of meropenem concentrations were taken before, during and after SLED in up to three sessions per patient. Nonparametric population PK analysis with Monte Carlo simulations were used. Pharmacodynamic (PD) targets of 40% and 100% time above the minimal inhibitory concentration (f T

resultsA two-compartment linear population PK model was most appropriate with residual diuresis supported as significant covariate affecting meropenem clearance. In patients without residual diuresis the PTA for both targets (40% and 100% f T

conclusionsWe found a relevant PK variability for meropenem in patients on SLED, which was significantly influenced by the degree of residual diuresis. As a result dosing recommendations for meropenem in patients on SLED to achieve adequate PD targets greatly vary. Therapeutic drug monitoring may help to further optimise individual dosing.

trial registrationClincialtrials.gov, NCT02287493 .

Indexed as

Acute Kidney InjuryAdultAgedCritical IllnessDialysisFemaleGermanyHumansMaleMeropenemMicrobial Sensitivity TestsMiddle AgedMonte Carlo MethodOrgan Dysfunction ScoresProspective StudiesSepsisMeropenemThienamycinsAcute renal failureMeropenemPharmacokineticsSepsisSustained low-efficiency dialysis

Identifiers

PMID29382394
PMCPMC5791175
OpenAlexW2794244996

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.