Extracorporeal adsorption of protective and toxic bile acids and bilirubin in patients with cholestatic liver dysfunction: a prospective study.

Bile acids Cholestasis Cholestatic liver failure Critically ill patients Cytosorb® Mass spectrometry

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
09 Nov 2023
Historique:
received: 14 06 2023
accepted: 27 09 2023
medline: 9 11 2023
pubmed: 9 11 2023
entrez: 9 11 2023
Statut: epublish

Résumé

The release of toxic bile acids (BAs) in the blood of critically ill patients with cholestatic liver dysfunction might lead to the damage of various organs. Their extracorporeal elimination using the cytokine adsorber Cytosorb The prospective Cyto-SOVLE study (NCT04913298) included 20 intensive care patients with cholestatic liver dysfunction, continuous kidney replacement therapy, total bilirubin concentration > 10 mg/dl and the application of CS into the dialysis circuit. Bilirubin and different BAs were measured pre- and post-CS at defined timepoints (10 min, 1, 3, 6, and 12 h after initiation). Relative reduction (RR, %) was calculated with: [Formula: see text]. The median RR for total and conjugated bilirubin after initiation was - 31.8% and - 30.3%, respectively, and decreased to - 4.5% and - 4.8% after 6 h. A high initial RR was observed for the toxic BAs GCA (- 97.4%), TCA (- 94.9%), GCDCA (- 82.5%), and TCDCA (- 86.0%), decreasing after 6 h to - 32.9%, - 32.7%, - 12.8%, and - 14.3%, respectively. The protective hydrophilic BAs showed a comparable RR after initiation (UDCA: - 77.7%, GUDCA: - 83.0%, TUDCA: - 91.3%) dropping after 6 h to - 7.4%, - 8.5%, and - 12.5%, respectively. Cytosorb

Sections du résumé

BACKGROUND BACKGROUND
The release of toxic bile acids (BAs) in the blood of critically ill patients with cholestatic liver dysfunction might lead to the damage of various organs. Their extracorporeal elimination using the cytokine adsorber Cytosorb
METHODS METHODS
The prospective Cyto-SOVLE study (NCT04913298) included 20 intensive care patients with cholestatic liver dysfunction, continuous kidney replacement therapy, total bilirubin concentration > 10 mg/dl and the application of CS into the dialysis circuit. Bilirubin and different BAs were measured pre- and post-CS at defined timepoints (10 min, 1, 3, 6, and 12 h after initiation). Relative reduction (RR, %) was calculated with: [Formula: see text].
RESULTS RESULTS
The median RR for total and conjugated bilirubin after initiation was - 31.8% and - 30.3%, respectively, and decreased to - 4.5% and - 4.8% after 6 h. A high initial RR was observed for the toxic BAs GCA (- 97.4%), TCA (- 94.9%), GCDCA (- 82.5%), and TCDCA (- 86.0%), decreasing after 6 h to - 32.9%, - 32.7%, - 12.8%, and - 14.3%, respectively. The protective hydrophilic BAs showed a comparable RR after initiation (UDCA: - 77.7%, GUDCA: - 83.0%, TUDCA: - 91.3%) dropping after 6 h to - 7.4%, - 8.5%, and - 12.5%, respectively.
CONCLUSIONS CONCLUSIONS
Cytosorb

Identifiants

pubmed: 37943350
doi: 10.1186/s13613-023-01198-7
pii: 10.1186/s13613-023-01198-7
pmc: PMC10635921
doi:

Banques de données

ClinicalTrials.gov
['NCT04913298']

Types de publication

Journal Article

Langues

eng

Pagination

110

Subventions

Organisme : Else Kröner-Fresenius-Stiftung
ID : 2021_EKEA.101

Informations de copyright

© 2023. The Author(s).

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Auteurs

Antonia Greimel (A)

Department of Anesthesiology, LMU Hospital, Marchioninistrasse 15, 81377, Munich, Germany.

Katharina Habler (K)

Institute of Laboratory Medicine, LMU Hospital, Munich, Germany.

Caroline Gräfe (C)

Department of Anesthesiology, LMU Hospital, Marchioninistrasse 15, 81377, Munich, Germany.

Nils Maciuga (N)

Department of Anesthesiology, LMU Hospital, Marchioninistrasse 15, 81377, Munich, Germany.

Clara Isabell Brozat (CI)

Department of Anesthesiology, LMU Hospital, Marchioninistrasse 15, 81377, Munich, Germany.

Michael Vogeser (M)

Institute of Laboratory Medicine, LMU Hospital, Munich, Germany.

Michael Zoller (M)

Department of Anesthesiology, LMU Hospital, Marchioninistrasse 15, 81377, Munich, Germany.

Felix L Happich (FL)

Institute of Laboratory Medicine, LMU Hospital, Munich, Germany.

Uwe Liebchen (U)

Department of Anesthesiology, LMU Hospital, Marchioninistrasse 15, 81377, Munich, Germany.

Sandra Frank (S)

Department of Anesthesiology, LMU Hospital, Marchioninistrasse 15, 81377, Munich, Germany.

Michael Paal (M)

Institute of Laboratory Medicine, LMU Hospital, Munich, Germany.

Christina Scharf (C)

Department of Anesthesiology, LMU Hospital, Marchioninistrasse 15, 81377, Munich, Germany. Christina.Scharf@med.uni-muenchen.de.

Classifications MeSH