Evidence map›Paper›PMID 28584142›Full record

ArticleAntimicrobial agents and chemotherapy2017

Micafungin Plasma Levels Are Not Affected by Continuous Renal Replacement Therapy: Experience in Critically Ill Patients.

M G Vossen, D Knafl, M Haidinger, R Lemmerer, M Unger, S Pferschy, W Lamm, A Maier-Salamon, W Jäger, F Thalhammer

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2017. 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
2.1field-weighted citation impact, top 13% 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, 23 citations in OpenAlex.

  1. Trial
  2. Trial
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  4. Successful Management ofClinical case reports · 2026
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  6. Observational
  7. Article
  8. Review
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  10. Antifungal Drugs Influence Neutrophil Effector Functions.Antimicrobial agents and chemotherapy · 2019
    Article
  11. 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

10 authors at 2 institutions in 1 country.

M G VossenClinical Division of Infectious Disease, Department of Medicine I, Medical University of Vienna, Vienna, Austria matthias.vossen@meduniwien.ac.at.ORCID 0000-0002-4350-7173
D KnaflClinical Division of Infectious Disease, Department of Medicine I, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-6810-615X
M HaidingerInternistisches Zentrum Nord, Vienna, Austria.
R LemmererClinical Division of Infectious Disease, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
M UngerClinical Division of Rheumatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
S PferschyClinical Division of Infectious Disease, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
W LammDepartment of Internal Medicine I-Intensive Care Unit 13i2, Medical University of Vienna, Vienna, Austria.
A Maier-SalamonDepartment of Clinical Pharmacy and Diagnostics, University of Vienna, Vienna, Austria.
W JägerDepartment of Clinical Pharmacy and Diagnostics, University of Vienna, Vienna, Austria.
F ThalhammerClinical Division of Infectious Disease, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATUniversity of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Critically ill patients often experience acute kidney injury and the need for renal replacement therapy in the course of their treatment in an intensive care unit (ICU). These patients are at an increased risk for candidiasis. Although there have been several reports of micafungin disposition during renal replacement therapy, to this date there are no data describing the elimination of micafungin during high-dose continuous venovenous hemodiafiltration with modified AN69 membranes. The aim of this prospective open-label pharmacokinetic study was to assess whether micafungin plasma levels are affected by continuous hemodiafiltration in critical ill patients using the commonly employed AN69 membrane. A total of 10 critically ill patients with micafungin treatment due to suspected or proven candidemia were included in this trial. Prefilter/postfilter micafungin clearance was measured to be 46.0 ml/min (±21.7 ml/min;

Indexed as

Acute Kidney InjuryAdultAgedAntifungal AgentsCandidemiaCritical IllnessEchinocandinsFemaleHemodiafiltrationHumansIntensive Care UnitsLipopeptidesMaleMetabolic Clearance RateMicafunginMiddle AgedAntifungal AgentsEchinocandinsLipopeptidesMicafunginantifungal agentcontinuous renal replacement therapycontinuous venovenous hemodiafiltrationmicafunginpharmacokinetics

Identifiers

PMID28584142
PMCPMC5527635
OpenAlexW2623047176

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.