Evidence map›Paper›PMID 40186392›Full record

ArticleArtificial organs2025

In Vitro Evaluation of Liposomal Amphotericin B Adsorption With Different Hemofilters for Continuous Hemofiltration.

Toshihisa Hiraiwa, Naohide Kuriyama, Kazuhiro Moriyama, Shigeki Yamada, Tomoyuki Nakamura, Osamu Nishida

Abstract read
In one paragraph

Article in Artificial organs, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. Review
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

6 authors.

Toshihisa HiraiwaDepartment of Anesthesiology and Clinical Care Medicine, Fujita Health University School of Medicine, Aichi, Japan.ORCID https://orcid.org/0000-0003-3326-4398
Naohide KuriyamaDepartment of Anesthesiology and Clinical Care Medicine, Fujita Health University School of Medicine, Aichi, Japan.
Kazuhiro MoriyamaDepartment of Anesthesiology and Clinical Care Medicine, Fujita Health University School of Medicine, Aichi, Japan.
Shigeki YamadaDepartment of Pharmacy, Fujita Health University Hospital, Aichi, Japan.
Tomoyuki NakamuraDepartment of Anesthesiology and Clinical Care Medicine, Fujita Health University School of Medicine, Aichi, Japan.ORCID https://orcid.org/0000-0002-8348-4092
Osamu NishidaDepartment of Anesthesiology and Clinical Care Medicine, Fujita Health University School of Medicine, Aichi, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFungemia is an infectious disease with a poor prognosis. Continuous hemofiltration (CHF) is widely used for the treatment of acute kidney injury associated with fungemia. However, the effect of hemofiltration membranes for CHF on antifungal drug concentrations remains poorly understood. Therefore, clarifying the adsorption of antifungal drugs onto these membranes is important. We investigated the adsorption properties of liposomal amphotericin B on different hemofiltration membranes using closed-circulation hemofiltration.

methodsWe performed hemofiltration with each solution adjusted to liposomal amphotericin B as a closed circulatory circuit using polyacrylonitrile (AN69ST), polymethyl methacrylate (PMMA), and polysulfone (PS) membranes. Only this circuit was used as a control. Amphotericin B concentration at the inlet and in the effluent of the hemofiltration membrane was measured. The adsorption rate (Ra) of amphotericin B was then calculated.

resultsThe concentration of amphotericin B decreased in the PS membranes compared to that in the controls after 15 min (p = 0.03). The Ra of amphotericin B was higher in PS membranes than in the controls (p = 0.02). Amphotericin B was not adsorbed onto the PMMA or AN69ST membranes. The concentration of amphotericin B in these membranes showed no change compared with that in the control after 1440 min. Liposomal amphotericin B was temporarily absorbed on PS membranes, but at clinical doses, it did not appear to affect the antifungal doses.

conclusionsDifferent blood purification membranes can be used to treat CHF without affecting the administration of antifungal drugs.

Indexed as

Amphotericin BAntifungal AgentsContinuous Renal Replacement TherapyHemofiltrationMembranes, ArtificialAcrylic ResinsAdsorptionHumansPolymersPolymethyl MethacrylateSulfonesAcrylic ResinsAmphotericin BAntifungal Agentsliposomal amphotericin BMembranes, ArtificialpolyacrylonitrilePolymersPolymethyl Methacrylatepolysulfone P 1700Sulfonesadsorptionamphotericin Bexperimental modelhemofilter

Identifiers

PMID40186392
PMCPMC12179754

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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.