Evidence map›Paper›PMID 41235813›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2025

Feasibility and Safety of Cytosorb Application in Patients With Acute Liver Failure.

Patrick Haselwanter, Seanna Fairfield, Riva Reinhold, Marlene Riedl-Wewalka, Monika Schmid, Lorenz Balcar, Albert Friedrich Stättermayer, Thomas Reiberger, Michael Trauner, Christian Zauner and 1 more

Abstract read
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 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

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

1 citing paper in PubMed.

  1. Feasibility and Safety of Cytosorb Application in Patients With Acute Liver Failure.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
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

11 authors.

Patrick HaselwanterDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.
Seanna FairfieldDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.
Riva ReinholdDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.
Marlene Riedl-WewalkaDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.
Monika SchmidDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.
Lorenz BalcarDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-6708-3061
Albert Friedrich StättermayerDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.
Thomas ReibergerDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-4590-3583
Michael TraunerDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.
Christian ZaunerDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.
Mathias Schneeweiss-GleixnerDepartment of Medicine III, Division of Gastroenterology and Hepatology, Intensive Care Unit 13H1, Medical University of Vienna, Vienna, Austria.ORCID 0009-0001-5296-1212

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsAcute liver failure (ALF) is a rare, life-threatening condition with high mortality and limited therapeutic options beyond liver transplantation. Cytosorb adsorber can be easily applied to continuous renal replacement therapy (CRRT) and potentially support liver function by removing bilirubin and cytokines.

methodsThis retrospective single-centre study included all ALF patients admitted to the intensive care unit (ICU) at the Division of Gastroenterology and Hepatology of the Vienna General Hospital from 2012 to 2025 receiving CRRT.

resultsTwenty-eight ALF patients (median SOFA 11, SAPS II 43) were included, with high incidences of vasopressor use (82.1%) and invasive ventilation (85.7%). Fourteen received adjunctive Cytosorb therapy. Complications (hemodynamic instability, citrate accumulation, bleeding, hypofibrinogenemia, thrombocytopenia) were similar in patients with or without Cytosorb. Bilirubin levels significantly decreased after Cytosorb initiation (from 20.85 to 12.32 mg/dL at 24 h, and to 9.46 mg/dL after treatment; p < 0.001), GGT, ALAT, and platelets also declined post-treatment. Cytosorb patients had lower SAPS II scores (median: 38.5 vs. 45.5, p = 0.039), were more often listed for HU-LTx (92.9% vs. 42.9%, p = 0.005), and had higher transplantation rates (64.3% vs. 28.6%, p = 0.058). Therefore, ICU survival (71.4% vs. 42.9%; p = 0.127) and 6-month survival (71.4% vs. 28.6%; p = 0.023) were higher in the Cytosorb group.

conclusionsCytosorb appeared to be a feasible and well-tolerated blood purification tool with potential beneficial effects in ALF patients. Improved survival with Cytosorb likely reflects confounding by patient selection and higher HU-LTx rates. Prospective studies are warranted to clarify the clinical impact of adjunctive Cytosorb therapy in ALF patients.

Indexed as

Continuous Renal Replacement TherapyLiver Failure, AcuteSorption DetoxificationAdultAustriaBilirubinFeasibility StudiesFemaleHumansIntensive Care UnitsMaleMiddle AgedRetrospective StudiesTreatment OutcomeBilirubin

Identifiers

PMID41235813
PMCPMC12617026

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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.