Hemoadsorption in the critically ill—Final results of the International CytoSorb Registry
Author:
Hawchar FatimeORCID, Tomescu DanaORCID, Träger Karl, Joskowiak Dominik, Kogelmann Klaus, Soukup Jens, Friesecke Singrun, Jacob David, Gummert Jan, Faltlhauser Andreas, Aucella Filippo, van Tellingen Martijn, Malbrain Manu L. N. G., Bogdanski Ralph, Weiss Günter, Herbrich Andreas, Utzolino Stefan, Nierhaus Axel, Baumann AndreasORCID, Hartjes Andreas, Henzler Dietrich, Grigoryev Evgeny, Fritz Harald, Bach Friedhelm, Schröder StefanORCID, Weyland Andreas, Gottschaldt Udo, Menzel Matthias, Zachariae Olivier, Novak Radovan, Berden Jernej, Haake Hendrik, Quintel Michael, Kloesel StephanORCID, Kortgen Andreas, Stecher Stephanie, Torti Patricia, Nestler Frieder, Nitsch Markus, Olboeter Detlef, Muck Philip, Findeisen Michael, Bitzinger Diane, Kraßler Jens, Benad Martin, Schott MartinORCID, Schumacher Ulrike, Molnar Zsolt, Brunkhorst Frank Martin
Abstract
The aim of the current paper is to summarize the results of the International CytoSorb Registry. Data were collected on patients of the intensive care unit. The primary endpoint was actual in-hospital mortality compared to the mortality predicted by APACHE II score. The main secondary endpoints were SOFA scores, inflammatory biomarkers and overall evaluation of the general condition. 1434 patients were enrolled. Indications for hemoadsorption were sepsis/septic shock (N = 936); cardiac surgery perioperatively (N = 172); cardiac surgery postoperatively (N = 67) and “other” reasons (N = 259). APACHE-II-predicted mortality was 62.0±24.8%, whereas observed hospital mortality was 50.1%. Overall SOFA scores did not change but cardiovascular and pulmonary SOFA scores decreased by 0.4 [-0.5;-0.3] and -0.2 [-0.3;-0.2] points, respectively. Serum procalcitonin and C-reactive protein levels showed significant reduction: -15.4 [-19.6;-11.17] ng/mL; -17,52 [-70;44] mg/L, respectively. In the septic cohort PCT and IL-6 also showed significant reduction: -18.2 [-23.6;-12.8] ng/mL; -2.6 [-3.0;-2.2] pg/mL, respectively. Evaluation of the overall effect: minimal improvement (22%), much improvement (22%) and very much improvement (10%), no change observed (30%) and deterioration (4%). There was no significant difference in the primary outcome of mortality, but there were improvements in cardiovascular and pulmonary SOFA scores and a reduction in PCT, CRP and IL-6 levels.
Trial registration: ClinicalTrials.gov Identifier: NCT02312024 (retrospectively registered).
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Cited by
18 articles.
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