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Lingel, Maximilian P. ; Haus, Moritz ; Paschke, Lukas ; Foltan, Maik ; Lubnow, Matthias ; Gruber, Michael ; Krenkel, Lars ; Lehle, Karla

Clinical relevance of cell‐free DNA during venovenous extracorporeal membrane oxygenation

Lingel, Maximilian P., Haus, Moritz, Paschke, Lukas, Foltan, Maik , Lubnow, Matthias , Gruber, Michael , Krenkel, Lars und Lehle, Karla (2023) Clinical relevance of cell‐free DNA during venovenous extracorporeal membrane oxygenation. Artificial Organs.

Veröffentlichungsdatum dieses Volltextes: 07 Aug 2023 14:33
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.54563


Zusammenfassung

Background: Thrombosis remains a critical complication during venovenous extracorporeal membrane oxygenation (VV ECMO). The involvement of neutrophil extracellular traps (NETs) in thrombogenesis has to be discussed. The aim was to verify NETs in the form of cell-free DNA (cfDNA) in the plasma of patients during ECMO. Methods: A fluorescent DNA-binding dye (QuantifFluor((R)), Promega) was used to ...

Background: Thrombosis remains a critical complication during venovenous extracorporeal membrane oxygenation (VV ECMO). The involvement of neutrophil extracellular traps (NETs) in thrombogenesis has to be discussed. The aim was to verify NETs in the form of cell-free DNA (cfDNA) in the plasma of patients during ECMO. Methods: A fluorescent DNA-binding dye (QuantifFluor((R)), Promega) was used to detect cell-free DNA in plasma samples. cfDNA concentrations from volunteers (n = 21) and patients (n = 9) were compared and correlated with clinical/technical data before/during support, ECMO end and time of a system exchange. Results: Before ECMO, patients with a median (IQR) age of 59 (51/63) years, SOFA score of 11 (10/15), and ECMO run time of 9.0 (7.0/19.5) days presented significantly higher levels of cfDNA compared to volunteers (6.4 (5.8/7.9) ng/mu L vs. 5.9 (5.4/6.3) ng/mu L; p = 0.044). Within 2 days after ECMO start, cfDNA, inflammatory, and hemolysis parameters remained unchanged, while platelets decreased (p = 0.005). After ECMO removal at the end of therapy, cfDNA, inflammation, and coagulation data (except antithrombin III) remained unchanged. The renewal of a system resulted in known alterations in fibrinogen, d-dimers, and platelets, while cfDNA remained unchanged. Conclusion: Detection of cfDNA in plasma of ECMO patients was not an indicator of acute and circuit-induced thrombogenesis.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftArtificial Organs
Verlag:WILEY
Ort der Veröffentlichung:HOBOKEN
Datum1 August 2023
InstitutionenMedizin > Lehrstuhl für Anästhesiologie
Medizin > Lehrstuhl für Herz-, Thorax- und herznahe Gefäßchirurgie
Medizin > Lehrstuhl für Innere Medizin II
Identifikationsnummer
WertTyp
10.1111/aor.14616DOI
Stichwörter / KeywordsNEUTROPHIL EXTRACELLULAR TRAPS; THROMBOSIS; blood; cell-free DNA; coagulation; ECMO; inflammation; neutrophil extracellular traps
Dewey-Dezimal-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenZum Teil
URN der UB Regensburgurn:nbn:de:bvb:355-epub-545636
Dokumenten-ID54563

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