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. 2020 Nov 18;10(1):154.
doi: 10.1186/s13613-020-00772-7.

Adsorption therapy in critically ill with septic shock and acute kidney injury: a retrospective and prospective cohort study

Affiliations

Adsorption therapy in critically ill with septic shock and acute kidney injury: a retrospective and prospective cohort study

Gregor A Schittek et al. Ann Intensive Care. .

Abstract

Background: Haemoadsorption has been described as an effective way to control increased pro- and anti-inflammatory mediators ("cytokine storm") in septic shock patients. No prospective or randomised clinical study has yet confirmed these results. However, no study has yet prospectively specifically investigated patients in severe septic shock with sepsis-associated acute kidney injury (SA-AKI). Therefore, we aimed to examine whether haemoadsorption could influence intensive care unit (ICU) and hospital mortality in these patients. Furthermore, we examined the influence of haemoadsorption on length of stay in the ICU and therapeutic support.

Methods: Retrospective control group and prospective intervention group design in a tertiary hospital in central Europe (Germany). Intervention was the implementation of haemoadsorption for patients in septic shock with SA-AKI. 76 patients were included in this analysis.

Results: Severity of illness as depicted by APACHE II was higher in patients treated with haemoadsorption. Risk-adjusted ICU mortality rates (O/E ratios) did not differ significantly between the groups (0.80 vs. 0.83). We observed in patients treated with haemoadsorption a shorter LOS and shorter therapeutic support such as catecholamine dependency and duration of RRT. However, in multivariate analysis (logistic regression for mortality, competing risk for LOS), we found no significant differences between the two groups.

Conclusions: The implementation of haemoadsorption for patients in septic shock with acute renal failure did not lead to a reduction in ICU or hospital mortality rates. Despite univariate analysis delivering some evidence for a shorter duration of ICU-related treatments in the haemoadsorption group, these results did not remain significant in multivariate analysis. Trial registration CytoSorb® registry https://clinicaltrials.gov/ct2/show/NCT02312024 . December 9, 2014.

Database: https://www.cytosorb-registry.org/ (registration for content acquisition is necessary).

Keywords: Acute kidney injury; Cytosorb; Haemoadsorption; Mortality; Outcome; Sepsis; Septic shock.

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Conflict of interest statement

GAS has received financial travel support for attending a symposium organised by CytoSorbents Europe GmbH in 2016. All other authors declare that there are no potential conflicts of interest to disclose.

Figures

Fig. 1
Fig. 1
Blue: control group—patients without haemoadsorption (n = 11); red: patients with haemoadsorption (n = 12)
Fig. 2
Fig. 2
ICU length of catecholamine dependency for patients without (blue) and with (red) haemoadsorption. For ICU survivors, N = 11 (control group) vs. N = 12 (Cytosorb™ group). For ICU non-survivors, N = 22 vs. N = 31, respectively
Fig. 3
Fig. 3
Influence of haemoadsorption on the time to event for alive discharge from ICU vs. death in ICU unadjusted cumulative incidence plots. The confidence intervals overlap, showing no significant difference in the cumulative incidences

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