Hemoadsorption in 'Liver Indication'-Analysis of 109 Patients' Data from the CytoSorb International Registry.

CytoSorb bilirubin blood purification cytokine adsorption hemoadsorption liver failure liver support

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
05 Nov 2021
Historique:
received: 28 09 2021
revised: 01 11 2021
accepted: 03 11 2021
entrez: 13 11 2021
pubmed: 14 11 2021
medline: 14 11 2021
Statut: epublish

Résumé

Our aim is to report the results of the 'liver indication' subset of patients in the CytoSorb International Registry. Structured data were recorded. Treatment characteristics and changes from T1 (start of hemoadsorption) to T2 (termination) were evaluated with a special focus on bilirubin, C-reactive protein, procalcitonin, interleukin-6, platelet levels, SOFA scores, mortality, and subjective assessment by the attending physicians. Until January 2021, from the total 1434 patients, 109 (age: 49.2 ± 17.1 years, 57.8% males) received treatment for hyperbilirubinemia. APACHE II-predicted mortality was 49.6 ± 26.8%. In the study, 91% of patients were alive at the termination of hemoadsorption and improvement was observed by the physicians in 75 cases. Overall, 65 (59.6%) patients died in the hospital, and 60 (55.0%) died in the ICU. Patients received a median of two treatments for a median of 43 h (interquartile range: 24-72 h) in total. Serum bilirubin levels reduced significantly to -4.6 (95% CI: -6.329 to -2.8) mg/dL. Thrombocytopenia was reported in four patients as an adverse event. We report the largest case series on hemoadsorption for 'liver indication' from the CytoSorb International Registry. The finding of significant bilirubin removal observed in our study could have substantial impact in designing and executing further studies on the effects of hemoadsorption in liver dysfunction, which are certainly warranted.

Sections du résumé

BACKGROUND BACKGROUND
Our aim is to report the results of the 'liver indication' subset of patients in the CytoSorb International Registry.
METHODS METHODS
Structured data were recorded. Treatment characteristics and changes from T1 (start of hemoadsorption) to T2 (termination) were evaluated with a special focus on bilirubin, C-reactive protein, procalcitonin, interleukin-6, platelet levels, SOFA scores, mortality, and subjective assessment by the attending physicians.
RESULTS RESULTS
Until January 2021, from the total 1434 patients, 109 (age: 49.2 ± 17.1 years, 57.8% males) received treatment for hyperbilirubinemia. APACHE II-predicted mortality was 49.6 ± 26.8%. In the study, 91% of patients were alive at the termination of hemoadsorption and improvement was observed by the physicians in 75 cases. Overall, 65 (59.6%) patients died in the hospital, and 60 (55.0%) died in the ICU. Patients received a median of two treatments for a median of 43 h (interquartile range: 24-72 h) in total. Serum bilirubin levels reduced significantly to -4.6 (95% CI: -6.329 to -2.8) mg/dL. Thrombocytopenia was reported in four patients as an adverse event.
CONCLUSIONS CONCLUSIONS
We report the largest case series on hemoadsorption for 'liver indication' from the CytoSorb International Registry. The finding of significant bilirubin removal observed in our study could have substantial impact in designing and executing further studies on the effects of hemoadsorption in liver dysfunction, which are certainly warranted.

Identifiants

pubmed: 34768702
pii: jcm10215182
doi: 10.3390/jcm10215182
pmc: PMC8584981
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : CytoSorbents Europe GmbH
ID : unrestricted
Organisme : European Union
ID : "GINOP-2.3.2-15-2016-00048 - STAY ALIVE"
Organisme : European Union
ID : EFOP 3.6.2-16-2017-00006 - LIVE LONGER
Organisme : Hungarian National Research, Development and Innovation Office
ID : K 138816

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Auteurs

Klementina Ocskay (K)

Institute for Translational Medicine, Medical School, University of Pécs, 7624 Pécs, Hungary.

Dana Tomescu (D)

Anesthesiology and Intensive Care, Fundeni Clinical Institute, 022328 Bucharest, Romania.

Andreas Faltlhauser (A)

Medizinische Klinik I, Kliniken Nordoberpfalz AG, Klinikum Weiden, 92637 Weiden, Germany.

David Jacob (D)

Klinik für Anaesthesiologie und Intensivtherapie, Universitätsklinikum Magdeburg, 39120 Magdeburg, Germany.

Sigrun Friesecke (S)

Klinik und Poliklinik für Innere Medizin B, Universitätsmedizin Greifswald, 17475 Greifswald, Germany.

Manu Malbrain (M)

Intensive Care Chief Medical Officer, AZ Jan Palfijn, 9000 Gent, Belgium.
First Department of Anaesthesia and Intensive Therapyx, Medical University of Lublin, 20059 Lublin, Poland.

Klaus Kogelmann (K)

Hans-Susemihl-Krankenhaus GmbH, Klinik für Anästhesiologie und Intensivmedizin, 26721 Emden, Germany.

Ralph Bogdanski (R)

Klinikum Rechts der Isar der TU München, Klinik für Anästhesiologie, 81675 München, Germany.

Friedhelm Bach (F)

Evangelisches Krankenhaus Bielefeld, Klinik für Anästhesiologie, Intensiv-, Notfallmedizin, Transfusionsmedizin und Schmerztherapie, Kantensiek 11, 33617 Bielefeld, Germany.

Harald Fritz (H)

Krankenhaus Martha Maria Halle, Klinik für Anaesthesiologie und Intensivmedizin, Röntgenstr. 1, 06120 Halle, Germany.

Andreas Hartjes (A)

Krankenhaus der Barmherzigen Schwestern Ried, Anästhesie, Intensiv- und Palliativmedizin, Schlossberg 1, 4933 Ried im Innkreis, Austria.

Andreas Kortgen (A)

Klinik für Anästhesiologie und Intensivmedizin, Universitätsklinikum Jena, 07747 Jena, Germany.

Jens Soukup (J)

Carl-Thiem-Klinikum Cottbus, Klinik für Anästhesiologie, Intensivtherapie und Palliativmedizin, Thiemstr. 111, 03048 Cottbus, Germany.

Stefan Utzolino (S)

Abteilung Allgemein- und Viszeralchirurgie, Universitätsklinikum Freiburg, 79106 Freiburg, Germany.

Martijn van Tellingen (M)

Intensive Care, Ziekenhuis de Tjongerschans, 8441 PW Heerenveen, The Netherlands.

Karl Träger (K)

Kardioanasthesiologie, Universitätsklinikum Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany.

Ulrike Schumacher (U)

Zentrum für Klinische Studien, Universitätsklinikum Jena, 07747 Jena, Germany.

Frank M Brunkhorst (FM)

Zentrum für Klinische Studien, Klinik für Anästhesiologie und Intensivtherapie, Universitätsklinikum Jena, Am Klinikum 1, 07747 Jena, Germany.

Zsolt Molnar (Z)

Department of Anaesthesiology and Intensive Therapy, Faculty of Medicine, Poznan University for Medical Sciences, 60355 Poznan, Poland.
Department of Anaesthesiology and Intensive Therapy, Semmelweis University, 1082 Budapest, Hungary.

Classifications MeSH