Septic shock and the underlying dysregulated inflammatory host-response remain a major contributor to mortality in critically ill patients. Cytokine adsorption represents an attractive approach to the treatment of septic shock. Nevertheless, its effect on circulating cytokine levels, as well as on the course of disease remains largely unassessed.
Cytokine-release plays an important role in the physiology of immune response to pathologic influences by recruiting immune cells to the pathogenic loci, be they of infectious or of non-infectious nature. Once at the focus, the activated immune cells can in turn release more cytokines if a more extensive immune response is needed. This extremely important mechanism for the organism, can however become pathological if the positive feedback loop between immune cells and cytokines, for any reason, overshoots in form of a so called cytokine storm and substantial amounts of released cytokines gain a systemic influence. The acute complication of this immune over-reaction is a SIRS, which can critically escalate into a potentially lethal multiple organ dysfunction syndrome, thus requiring immediate intensive care treatment. It is, having this framework in mind, the reason why the CytoSorb-Adsorber has been developed as a new therapeutic milestone. Essentially a haemoperfusion-filter, which through its layering with polymer beads (Divinylbenzene/ Polyvinylpyrrolidone) can adsorb cytokines as well as multiple inflammatory mediators and thus effectively remove them from the bloodstream, reducing their possible systemic influence and hence improving the outcome for patients being treated with it. The CytoSorb-Adsorber is an already CE-approved product, which has demonstrated its capacity to significantly reduce cytokine-levels such as IL-6, IL-8, IL-10, TNFα, HMGB-1, IL-1ra in a variety of pre-clinical studies. As well as in a clinical randomised multicentre study, which tested the CytoSorb-Adsorber on a cohort of ALI/ ARDS and severely septic/ septically shocked patients. The results of the later study can be very positively assessed, first of all and most importantly showing, that no security concerns had to be had in regard to the haemoperfusion-filter, as no adverse-effects attributable to the device were found. And further, by proving an effect on systemic cytokine-levels in form of a significant reduction in IL-6, IL-8, MCP-1 and IL-1ra, as well as a reduction in mortality of those patients with high initial cytokine levels, effectively reducing the 60 day mortality rate from 60% to 17% in a pool of 14 patients. With the intention to further elucidate the usefulness and clinical importance of this device this study proposes a prospective recruitment of patients in severe refractory septic shock to test the efficiency of this device.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
48
Cytokine adsorption therapy will be provided continuously for 72 hours by means of the CytoSorb® (CytoSorbents Corporation, Monmouth Junction, USA) column, run in series to a veno-venous continuous hemodialysis system, which will be exchanged every 24 hours.
Standard intensive care of patients suffering septic shock
Change in circulating Interleukin-6 levels over time
Change in circulating Interleukin-6 levels, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 24, 48, 72 hours
Change in Vasopressor requirements over time
Change in the Vasopressor Dependency Index, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 2, 4, 8, 12 , 24, 48, 72 hours
Cumulative intensive care mortality at 30 days
Intensive care mortality assessment at day 30 between groups
Time frame: 30 days post fulfillment of inclusion criteria
Change in C-reactive protein levels over time
Change in C-reactive protein levels, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 24, 48, 72 hours
Change in Procalcitonin levels over time
Change in Procalcitonin levels, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 24, 48, 72 hours
Change in SOFA Score over time
Change in SOFA Score, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 24, 48, 72 hours
Change in arterial lactate levels over time
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Change in arterial lactate levels, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 2, 4, 8, 12 , 24, 48, 72 hours
Change in cardiac index over time
Change in cardiac index, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 2, 4, 8, 12 , 24, 48, 72 hours
Change in Extra Vascular Lung Water Index over time
Change in Extra Vascular Lung Water Index, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 24, 48, 72 hours
Change in daily Infused Volume over time
Change in daily Infused Volume, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 24, 48, 72 hours
Change in PaO2/ FiO2 Ratio over time
Change in PaO2/ FiO2 Ratio, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 2, 4, 8, 12 , 24, 48, 72 hours
Change in Serum Albumin levels over time
Change in Serum Albumin levels, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 24, 48, 72 hours
Change in Bilirubin levels over time
Change in Bilirubin levels, stratified by groups, over the initial 72 hours ensuing fulfillment of inclusion criteria
Time frame: Mixed Model Assessment at timepoints 0, 24, 48, 72 hours