Hemoadsorption in the critically ill-Final results of the International CytoSorb Registry.
Fatime HawcharDana Rodica TomescuKarl TrägerDominik JoskowiakKlaus KogelmannJens SoukupSingrun FrieseckeDavid JacobJan GummertAndreas FaltlhauserFilippo AucellaMartijn van TellingenManu L N G MalbrainRalph BogdanskiGünter WeissAndreas HerbrichStefan UtzolinoAxel NierhausAndreas BaumannAndreas HartjesDietrich HenzlerEvgeny GrigoryevHarald FritzFriedhelm BachStefan SchröderAndreas WeylandUdo GottschaldtMatthias MenzelOlivier ZachariaeRadovan NovakJernej BerdenHendrik HaakeMichael QuintelStephan KloeselAndreas KortgenStephanie StecherPatricia TortiFrieder NestlerMarkus NitschDetlef OlboeterPhilip MuckMichael FindeisenDiane BitzingerJens KraßlerMartin BenadMartin SchottUlrike SchumacherZsolt MolnarFrank Martin BrunkhorstPublished in: PloS one (2022)
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).
Keyphrases
- cardiac surgery
- end stage renal disease
- acute kidney injury
- septic shock
- cardiovascular events
- chronic kidney disease
- newly diagnosed
- ejection fraction
- risk factors
- prognostic factors
- peritoneal dialysis
- healthcare
- clinical trial
- type diabetes
- coronary artery disease
- deep learning
- patient reported outcomes
- electronic health record
- big data
- data analysis