dc.contributor.author
Bünger, Victoria
dc.contributor.author
Hunsicker, Oliver
dc.contributor.author
Krannich, Alexander
dc.contributor.author
Balzer, Felix
dc.contributor.author
Spies, Claudia D.
dc.contributor.author
Kuebler, Wolfgang M.
dc.contributor.author
Weber-Carstens, Steffen
dc.contributor.author
Menk, Mario
dc.contributor.author
Graw, Jan A.
dc.date.accessioned
2025-08-12T10:23:40Z
dc.date.available
2025-08-12T10:23:40Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/48664
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-48388
dc.description.abstract
Background Hemolysis is associated with increased mortality in patients with sepsis, ARDS, or therapy with extracorporeal membrane oxygenation (ECMO). To quantify a critical threshold of hemolysis in patients with ARDS and treatment with veno-venous ECMO, we aimed to identify cutoff values for cell-free hemoglobin (CFH) and haptoglobin (Hp) plasma concentrations associated with a significant increase in ICU mortality.Methods Patients with ARDS admitted to a tertiary ARDS referral center between 01/2007 and 12/2018 and treatment with veno-venous ECMO were included. Cutoff values for mean CFH (mCFH) and mean Hp (mHp) plasma concentrations dividing the cohort into groups with significantly different ICU mortalities were calculated and patient characteristics were compared. A multiple logistic regression model with stepwise backward variable selection was included. In addition, cutoff values for vulnerable relative timespans for the respective CFH and Hp concentrations were calculated.Results A quantitative cutoff value of 11 mg/dl for mCFH separated the cohort (n = 442) regarding ICU mortality (mCFH <= 11 mg/dl: 38%, [95%-CI: 32.22-43.93] (n = 277) vs. mCFH > 11 mg/dl: 70%, [61.99-76.47] (n = 165), p < 0.001). Analogously, a mHp cutoff value <= 0.39 g/l was associated with a significant increase in ICU mortality (mHp <= 0.39 g/l: 68.7%, [60.91-75.61] (n = 163) vs. mHp > 0.39 g/l: 38.7%, [33.01-44.72] (n = 279), p < 0.001). The independent association of ICU mortality with CFH and Hp cutoff values was confirmed by logistic regression adjusting for confounders (CFH Grouping: OR 3.77, [2.51-5.72], p < 0.001; Hp Grouping: OR 0.29, [0.19-0.43], p < 0.001). A significant increase in ICU mortality was observed when CFH plasma concentration exceeded the limit of 11 mg/dl on 13.3% of therapy days (<= 13.3% of days with CFH > 11 mg/dl: 33%; [26.81-40.54] (n = 192) vs. > 13.3% of days with CFH > 11 mg/dl: 62%; [56.05-68.36] (n = 250), p < 0.001). Analogously, a mortality increase was detected when Hp plasma concentration remained <= 0.39 g/l for > 18.2% of therapy days (<= 18.2% days with Hp <= 0.39 g/l: 27%; [19.80-35.14] (n = 138) vs. > 18.2% days with Hp <= 0.39 g/l: 60%; [54.43-65.70] (n = 304), p < 0.001).Conclusions Moderate hemolysis with mCFH-levels as low as 11 mg/dl impacts mortality in patients with ARDS and therapy with veno-venous ECMO. Furthermore, a cumulative dose effect should be considered indicated by the relative therapy days with CFH-concentrations > 11 mg/dl. In addition, also Hp plasma concentrations need consideration when the injurious effect of elevated CFH is evaluated.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
organ replacement technology
en
dc.subject
erythrocyte pathology
en
dc.subject
red cell pathology
en
dc.subject
hemoglobin scavenger
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Potential of cell-free hemoglobin and haptoglobin as prognostic markers in patients with ARDS and treatment with veno-venous ECMO
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
15
dcterms.bibliographicCitation.doi
10.1186/s40560-023-00664-5
dcterms.bibliographicCitation.journaltitle
Journal of Intensive Care
dcterms.bibliographicCitation.number
1
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.volume
11
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
37081577
dcterms.isPartOf.eissn
2052-0492