Experience with hemoadsorption (CytoSorb®) in the management of septic shock patients

Abstract

BACKGROUND

Cytokines and inflammatory mediators are the hallmarks of sepsis. Extracorporeal cytokine hemoadsorption devices are the newer clinical support system to overcome the cytokine storm during sepsis.

AIM

To retrospectively evaluate the clinical outcomes of patients admitted in intensive care unit with septic shock with different etiologies.

METHODS

The laboratory parameters including biomarkers such as procalcitonin, serum lactate and C-reactive protein; and the hemodynamic parameters; mean arterial pressure, vasopressor doses, sepsis scores, cytokine levels and other vital parameters were evaluated. We evaluated these outcomes among survivors and non-survivors.

RESULTS

Of 100 patients evaluated, 40 patients survived. Post treatment, the vasopressors dosage remarkably decreased though it was not statistically different; 34.15% (P = 0.0816) for epinephrine, 20.5 % for norepinephrine (P = 0.3099) and 51% (P = 0.0678) for vasopressin. In the survivor group, a remarkable reduction of biomarkers levels; procalcitonin (65%, P = 0.5859), C-reactive protein (27%, P = 0.659), serum lactate (27%, P = 0.0159) and bilirubin (43.11%; P = 0.0565) were observed from baseline after CytoSorb^® therapy. A significant reduction in inflammatory markers; interleukin 6 and interleukin 10; (87% and 92%, P < 0.0001) and in tumour necrosis factor (24%, P = 0.0003) was also seen. Overall, 28 (28%) patients who were given CytoSorb^® therapy less than 48 h after onset of septic shock survived and the maximum duration of stay for 70% of these patients in intensive care unit was less than 15 d.

CONCLUSION

CytoSorb^® is a safe and well tolerated rescue therapy option in patients with septic shock. However, early (preferably within < 48 h after onset of septic shock) initiation could result in better clinical outcomes. Further randomized trials are needed to define the potential benefits of this new treatment modality.

Key Words: Hemoadsorption; Sepsis; Cytokines; Clinical conditions; Inflammation and extracorporeal

Core tip: CytoSorb^® is a promising new extracorporeal cytokine hemoadsorption device that can modulate the cytokine storm during sepsis. This retrospective study evaluated clinical outcomes after CytoSorb^® therapy of 100 patients admitted to intensive care unit with sepsis. We observed a significant reduction in vasopressors dosage in 40 patients who survived. The survivors also had a reduction in all the biomarker levels (procalcitonin, C-reactive protein, serum lactate and bilirubin) and inflammatory markers (interleukin 6, interleukin 10 and tumour necrosis factor) after CytoSorb^® therapy. Notably, 28% of patients who were given CytoSorb^® therapy < 48 h after onset of septic shock survived.

INTRODUCTION

Sepsis results due to complex interactive reactions between infecting microbe and the immune system of host. In patients admitted to intensive care units (ICU), sepsis is a major health problem worldwide and is associated with high mortality rates. Approximately, 30% of patients admitted to ICU have sepsis[1]. If not managed properly, sepsis can result in septic shock, systemic hyper inflammation and multiple organ failure[2]. Use of inappropriate antibiotics, virulence of bacteria and host response aggravates the activation of the inflammatory response which leads to dysregulation of inflammatory homeostasis with increased levels of both pro-inflammatory [interleukin (IL)-1β and tumour necrosis factor (TNF) α] and anti-inflammatory (IL-6, IL-8, IL-10) plasma mediators[3]. It results in major complications such as hypotension, reduced organ perfusion, need of organ support system like dialysis and mechanical ventilation[4,5].

Various extracorporeal blood purification therapies have been used to remove excess of inflammatory mediators or microbial toxins to improve health outcomes of patients with severe sepsis. Assuring results are obtained by various techniques including hemoperfusion, immunoglobulin therapy, endotoxin- binding polymyxin B hemoperfusion, high-volume hemofiltration, high cut-off membrane hemofiltration /hemodialysis, plasma exchange, and coupled plasma filtration adsorption dialysis and plasma filtration etc. However, the mortality rate still remains high with these techniques as observed in the recent EUPHRATES trial[6-9].

CytoSorb^® is an European CE mark approved and ISO certified hemoadsorption device which helps in reduction of excess inflammatory cytokines in the blood[10,11]. This unique therapy can eliminate bacterial exotoxins, myoglobin, free hemoglobin, bilirubin, activated complement and hosts of other inflammatory agents which can lead to fatal systemic inflammatory response syndrome (SIRS)[11]. Its clinical utility is also observed in various other clinical conditions including cardiac surgeries, liver failure, respiratory failures and various autoimmune diseases and infections[11-13]

In previous studies, CytoSorb^® therapy has shown clinical benefits if used early (< 24 h) in patients with septic shock[14,15]. The aim of the present study was to evaluate the clinical outcomes after CytoSorb^® therapy in patients admitted to ICU with septic shock due to different clinical conditions.

MATERIALS AND METHODS

Study design

This retrospective and observational study was conducted at Medanta medicity, Gurgaon, India for duration of 2 years (2016-2018). The study was approved by an institutional ethics committee and conducted in compliance with the current International Council for Harmonization, good clinical practice, Schedule Y, and Indian Council of Medical Research guidelines. A written informed consent was obtained from all patients’ relatives before initiating the therapy. The patients/caretakers were briefed about the usage, advantages and disadvantages of treatment. CytoSorb^® is a whole blood perfusion cartridge meant for single use. It is made up of biocompatible, polystyrene and divinylbenzene polymer beads with a large surface area. It can be easily used in conjunction with various renal replacement therapies and as a standalone therapy as well. The cartridge is attached in a close loop circuit with a pump. Venous blood of the patient enters at one end of the hemadsorption cartridge, and reinfused from the other port of dialysis catheter. It can be used maximum for 24 h. It removes hydrophobic molecules between 5-60 Kda by adsorption. Molecules beyond this range remain unaffected. Its use may be challenging in patients with contraindication to systemic anticoagulation. It is associated with decrease in platelet levels, though this has not been found to be clinically significant[12].

Study characteristics

Inclusion/exclusion criteria: The medical records of the patients who had received CytoSorb^® therapy following diagnosis of sepsis or septic shock (as per the surviving sepsis guidelines) and hospitalized in ICU between 2016 and 2018 were included. We selected the patients with acute kidney injury and sepsis for dialysis and CytoSorb^® combination therapy.

Evaluation of application of CytoSorb^® scoring system for patient selection to start the therapy: We retrospectively evaluated the application of the CytoSorb^® scoring (CS) system developed by a group of clinicians for initiating CytoSorb^® therapy on the basis of their practical experience. The scoring system was derived from five parameters (hemodynamic, renal, respiratory, laboratory and sepsis scores), representing five different organ system which get affected in sepsis patients. At the end, final scores were calculated by adding all the individual organ system scores. Supplementary Table 1 presents the CS system. Scores of 8-13 were considered ideal for recommending CytoSorb^® therapy. Scores > 13 implied that the patient condition was critical and required aggressive therapy.

Table 1 Baseline characteristics of all the patients, survivors and non-survivors before initiating the therapy (mean ± SD).

Baseline characteristics	Survivors (n = 40)	Non-survivors (n = 60)	P value (survivors vs non-survivors)
Age (yr)	51.3 ± 16.66	53.66 ± 16.47	0.4864
Urine output (mL/d)	551.13 ± 524.60	666.48 ± 595.25	0.3224
MAP (mmHg)	62.82 ± 9.73	66.31 ± 9.48	0.0774
GCS	6.26 ± 3.67	6.12 ± 4.56	0.8715
APACHE-II	24.6 ± 7.32	27.61 ± 9.29	0.0881
SOFA	12.3 ± 3.17	15.05 ± 3.35	0.0001
Leucocytes (cells/mm3)	15.60 ± 8.56	21.40 ± 26.17	0.1794
Platelets (cells/mm3)	123.95 ± 51.42	110.53 ± 50.18	0.1976
BUN	58.45 ± 36.94	108.55 ± 92.10	0.0015
SGOT(U/L)	1135.74 ± 2206.67	616.25 ± 1353.71	0.1477
SGPT(U/L)	504.63 ± 876.89	540.93 ± 1216.70	0.8712
S. Creatinine (mg/dL)	2.73 ± 1.86	7.01 ± 23.41	0.2521
S. Lactate (mg/dL)	3.71 ± 2.30	4.18 ± 3.23	0.3812
PaCO2	38.46 ± 14.51	40.89 ± 12.20	0.3682
PaO2	96.78 ± 41.42	84.50 ± 48.56	0.1920
FiO2	49.32 ± 18.71	69.15 ± 67.74	0.0744

MAP: Mean arterial pressure; GCS: Glasgow coma scale; APACHE: Acute physiology and chronic health evaluation; SOFA: Sequential organ failure assessment; BUN: Blood urea nitrogen; SGOT: Serum glutamic oxaloacetic transaminase; SGPT: Serum glutamic pyruvic transaminase.

Study procedure

Evaluation of laboratory and vital parameters: Baseline patient data including relevant demographic details, vitals, clinical diagnosis were recorded in the case record form. The related laboratory tests for renal, liver and metabolic parameters were evaluated in both pre and post CytoSorb^® therapy and a comparison was done between the survivor and the non-survivor group. All the laboratory parameters’ limits (values) were categorized as per the scoring system (Supplementary Table 1). Routine ICU monitoring parameters were also noted like routine biochemical investigations, and clinical parameters like Glasgow Coma Scale (GCS). GCS is a neurological scale used as a part of several ICU scoring systems for assessment of central nervous system.

Vasopressors dose and hemodynamic parameters: We compared the mean arterial pressure (MAP) improvement and vasopressor dose (percentage reduction) between pre and post CytoSorb^® therapy among survivors and non-survivors. Post therapy, the percentage decrease in number of patients needing both reduced number and doses of vasopressor drugs, i.e., norepinephrine (NE), epinephrine (E), and vasopressin (V) was evaluated.

Evaluation of other outcomes: Inflammatory parameters including interleukins; IL1, IL6, IL10, TNF and sequential organ failure assessment (SOFA) score were recorded pre and post therapy. Acute physiology and chronic health evaluation (APACHE II) were also recorded. Survival outcomes were determined on the basis of time taken (< 48 h or > 48 h) to initiate CytoSorb^® therapy after admitting in ICU. Length of patients’ stay in ICU (total number of days spent by the patient in ICU before, during and post CytoSorb^® therapy) was also recorded. Predicted percentage mortality calculated using APACHE-II calculator was used as a severity score and mortality estimation tool[16].

Statistical analysis

The continuous data were presented as mean ± SD and categorical as frequency and percentage (%). The analysis was performed using paired t test. P < 0.05 was considered to be statistically significant.

RESULTS

Study population

A total of 100 patients were included in the study. The mean age of all the patients was 52.53 ± 16.46 years. Majority of the patients were men (77.0%) with mean age of 51.33 ± 17.11 years. The mean age of women patients was 56.52 ± 13.62 years. Of these 100 patients, 40 (40%) patients survived (survivor group). The baseline characteristics of all the patients in both the groups are presented in Table 1.

Study outcomes

Effect of CytoSorb^® therapy on vasopressor dose and MAP levels: In the survivor group, an improvement in post CytoSorb^® therapy MAP (68.23 ± 7.50 mmHg) as compared to pre CytoSorb^® MAP (62.82 ± 9.73 mmHg; P = 0.1805) was observed.

We also observed a reduction in doses of E (post CytoSorb^® therapy: 12.76 ± 7.36 mcg/ min vs pre CytoSorb^® therapy: 19.38 ± 9.91 mcg/ min; P = 0.0816), NE (post CytoSorb^® therapy: 14.04 ± 10.46 mcg/ min vs pre CytoSorb^® therapy: 17.68 ± 15.45 mcg/min; P = 0.3099) and V (post CytoSorb^® therapy: 1.33 ± 0.93 mcg/min vs pre CytoSorb^® therapy: 2.01 ± 1.13 mcg/min; P = 0.0678).

In the non-survivor group, there was no improvement in MAP (64.31 ± 10.88 mmHg vs 66.31 ± 9.48 mmHg) post CytoSorb^® therapy vs pre post CytoSorb^® therapy. Further, no reduction in vasopressor dose was reported post CytoSorb^® therapy. Figure 1 shows the comparison of mean percentage reduction in doses of vasopressor drugs for the patients in the survivor and non-survivor groups.

Figure 1 Comparison of percentage reduction in vasopressor doses among survivor and non-survivor patients.

Evaluation of CytoSorb scores and number of CytoSorb^® devices required: Prior to CytoSorb^® therapy, majority of the patients were on dialysis and continued to be on dialysis post therapy. In the survivor group, patients were on different types of dialysis treatment CRTT (n = 42), HD (n = 24) and SLED (n = 34). The number of CytoSorb^® devices used per patient varied between 1-3.

Using the clinicians’ designed scoring system for initiation of CytoSorb^® therapy, we tried to retrospectively validate this scoring system in our patients. Through this scoring system, we observed that the patients in the survivor group had mean score of 12 as compared to those in the non-survivor group with mean score of 14. Patients with CytoSorb (CS) scores of 10 and 11 had mostly received one CytoSorb^® device. Overall, there were 79 patients (32 from survivor and 47 from non-survivor group) with high CS score (12-14) and were recommended more than one CytoSorb^® device. Only one patient each with CS score 13 and CS score 14 were recommended 3 CytoSorb^® devices. The correlation of CS scores with number of devices recommended for both the groups is shown in Table 2.

Table 2 CytoSorb scores and number of Cytosorb^® devices used (survivor vs non-survivor group).

CS score	Survivor (n)	CS score (n, number of devices used)	Non-survivor (n)	CS score (n, number of devices used)
< 8	0	-	0	-
8-13	35	10 (n = 1, 1)	21	11 (n = 1, 1)
		11 (n = 7, 1)		12 (n = 6, 1)
		12 (n = 19; 18 = 1, 1 = 2)		13 (n = 14; 13 = 1, 1 = 3)
		13 (n = 8; 1 = 1, 3 = 2, 1 = 3)
> 13	5	14 (n = 5; 1 = 1, 3 = 2, 1 = 3)	39	14 (n = 27; 21 = 1, 6 = 2)
				15 (n = 12; 11 = 1, 4 = 2)

CS: CytoSorb.

Effect of CytoSorb^® therapy on laboratory and vital parameters: In the survivor group, 16% decrease (from 15.60 ± 8.56 cells/mm³ to 13.09 ± 6.71 cells/mm³, P = 0.1484) in total leucocyte count was reported post CytoSorb^® therapy. The platelet count decreased slightly by 4.2% (from 123.95 ± 51.42 cells/mm³ to 118.75 ± 48.33 cells/mm³, P = 0.6425). Serum creatinine and Serum lactate reduced by 17% (from 2.73 ± 1.86 mg/dL to 2.27 ± 1.31 mg/dL, P = 0.2048) and 27% (from 3.71 ± 2.30 mg/dL to 2.28 ± 0.89 mg/dL, P = 0.0159), respectively. Procalcitonin (PCT) levels reduced by 65% (from 121.56 ± 421.20 ng/dL to 42.80 ± 69.89 ng/dL), C-reactive protein (CRP) levels reduced by 27% (from 165.68 ± 169.26 mg/dL to 120.33 ± 63.72 mg/dL) and bilirubin levels dropped by 43% (from 3.27 ± 2.67 mg/dL to 1.86 ± 1.51 mg/dL, P = 0.05).

Improvement was also reported in GCS in the patients in survivor group as compared with patients in the non-survivor group. One patient showed an improvement of more than 50% (from score 5 to 10) and one patient showed an improvement of 75% (from score 3 to 12). There was an overall 22.3% (8.05 ± 3.91) improvement in GCS. Slight improvement in other vital parameters like heart rate, respiratory rate, BP and body temperature was also reported.

Among non-survivors, a significant reduction in serum creatinine (25%, P = 0.008) was observed. Other laboratory and vital parameters except GCS (30%, P = 0.0129) did not show any significant improvement. Change in the laboratory and vital parameters pre and post therapy among survivors and non survivors is shown in Tables 3 and 4.

Table 3 Change in laboratory and vital parameters (survivors).

Parameters	Pre CytoSorb® therapy	Post CytoSorb® therapy	Percentage change	P value
Urine output (mL/d)	551.13 ± 524.60	862.88 ± 682.46	56.56	0.0247a
CRP (mg/dL)	165.68 ± 169.26	120.33 ± 63.72	-27.4	0.6590
PCT (ng/dL)	121.56 ± 421.20	42.81 ± 69.89	-65	0.5859
MAP (mm/Hg)	62.82 ± 9.73	68.23 ± 7.50	8.6	0.1805
GCS	6.26 ± 3.67	8.05 ± 3.92	22.36	0.0417c
Leucocytes (cells/mm3)	15.60 ± 8.56	13.09 ± 6.71	-16.02	0.1484
Platelets (cells/mm3)	123.95 ± 51.42	118.75 ± 48.33	-4.2	0.6425
S. Creatinine (mg/dL)	2.73 ± 1.86	2.27 ± 1.31	-16.84	0.2048
S. Lactate (mmol/L)	3.71 ± 2.30	2.28 ± 0.89	-26.66	0.0159a
SGOT (U/L)	1135.74 ± 2206.67	1078.92 ± 1890.45	-5.00	0.9222
SGPT (U/L)	504.63 ± 876.89	316.59 ± 645.41	-37.26	0.3796
BUN	58.45 ± 36.94	56.67 ± 28.24	-3.05	0.8266
Bilirubin (mg/dL)	3.27 ± 2.67	1.86 ± 1.51	-43.11	0.0565a
Sodium (mmol/L)	136.59 ± 24.49	136.31 ± 24.22	-0.20	0.9615
Potassium (mmol/L)	4.22 ± 0.65	3.75 ± 0.56	-11.14	< 0.0001a
Albumin (g/L)	2.64 ± 0.58	2.65 ± 0.62	0.38	0.9412
Arterial pH	7.33 ± 0.13	7.37 ± 0.13	0.55	0.1727
Bicarbonate	20.32 ± 4.05	22.825 ± 3.86	12.35	0.0060a
PaO2	96.78 ± 41.42	85.88 ± 27.89	-11.26	0.1714
PaCO2	38.46 ± 14.51	38.36 ± 14.53	-0.26	0.9755
FiO2	49.32 ± 18.71	41.95 ± 13.71	-14.94	0.0550

^aP < 0.05, significant decrease;

^cP < 0.05, significant rise. All values are defined as mean ± SD. Hb: Haemoglobin; SGOT: Serum glutamic oxaloacetic transaminase; SGPT: Serum glutamic-pyruvic transaminase; BUN: Blood urea nitrogen; CRP: C-reactive protein; PCT: Procalcitonin test; MAP: Meanarterial pressure; GCS: Glasgow Coma Scale.

Table 4 Change in laboratory and vital parameters (non-survivor group).

Parameters	Pre CytoSorb® therapy	Post CytoSorb® therapy	Percentage change	P value
Urine output (mL/d)	666.48 ± 595.25	493.85 ± 433.11	-25.90	0.0718
CRP (mg/dL)	1175.22 ± 126.60	-	-	-
PCT (ng/dL)	24.91 ± 24.51	48.97 ± 57.57	96.58	0.0766
MAP (mm/Hg)	66.13 ± 9.485	64.31 ± 10.87	-2.75	0.3304
GCS	6.12 ± 4.56	4.27 ± 2.91	-30.23	0.0129a
Leucocytes (cells/mm3)	21.40 ± 26.17	20.25 ± 18.25	-5.34	0.7327
Platelets (cells/mm3)	110.53 ± 50.18	99.67 ± 47.81	-9.83	0.2273
S. Creatinine (mg/dL)	7.01 ± 23.41	5.27 ± 23.19	-24.82	0.0088a
S. Lactate (mmol/L)	4.18 ± 3.23	5.05 ± 3.75	17.2	0.1759
SGOT (U/L)	616.25 ± 1353.71	1418.14 ± 2068	130.12	0.0693
SGPT (U/L)	540.93 ± 1216.70	577.38 ± 945.94	6.74	0.9048
BUN	108.55 ± 92.10	95.02 ± 84.83	-12.46	0.4362
Bilirubin (mg/dL)	5.15 ± 14.19	3.84 ± 4.09	-25.44	0.6543
Sodium (mmol/L)	133.79 ± 26.22	139.51 ± 7.32	4.28	0.1244
Potassium (mmol/L)	4.43 ± 1.03	4.15 ± 1.03	-6.32	0.1392
Albumin (g/L)	3.03 ± 1.07	2.85 ± 0.80	-5.94	0.2988
Arterial pH	7.28 ± 0.14	7.22 ± 0.18	-0.82	0.0438
Bicarbonate	24.52 ± 24.21	22.16 ± 22.19	-9.62	0.6560
PaO2	84.50 ± 48.56	90.42 ± 51.14	7.01	0.5256
PaCO2	40.89 ± 12.20	45.05 ± 33.71	10.17	0.3760
FiO2	69.15 ± 67.74	62.6 ± 28.61	-9.47	0.5016

^aP < 0.05, significant decrease, all values are defined as mean ± SD. Hb: Haemoglobin; SGOT: Serum glutamic oxaloacetic transaminase; SGPT: Serum glutamic-pyruvic transaminase; BUN: Blood urea nitrogen; CRP: C-reactive protein; PCT: Procalcitonin test; MAP: Mean arterial pressure; GCS: Glasgow Coma Scale.

Cytokine assay

There was a significant reduction in levels of inflammatory markers IL6, IL10 and TNF in the survivor group. A high percentage reduction in IL6 and IL10; (87% and 92%, P < 0.0001) and in TNF (24%, P = 0.0003) was observed. Among non-survivors, there was no improvement in any of the cytokine levels. Tables 5 and 6 show the cytokine assay data for patients in survivor and non-survivor group

Table 5 Cytokine assay (survivor group) (mean ± SD).

Cytokine (pg)	Pre CytoSorb® therapy	Post CytoSorb® therapy	Percentage decrease	P value
IL-1	3.82 ± 3.12	2.97 ± 2.99	22.25	0.2172
IL-6	1962.04 ± 229.09	254.09 ± 223.62	87	< 0.0001a
IL-10	293.75 ± 176.28	124.33 ± 73.61	91.7	< 0.0001a
TNF	20.82 ± 5.74	15.86 ± 6.11	23.82	0.0003a

^aP < 0.05, significant value. IL: Interleukin; TNF: Tumour necrosis factor.

Table 6 Cytokine assay (non-survivor group) (mean ± SD).

Cytokine (pg)	Pre CytoSorb® therapy	Post CytoSorb® therapy	Percentage change	P value
IL-1	5.52 ± 2.59	5.79 ± 2.55	4.89	0.7364
IL-6	2273.51 ± 1212.82	2638.24 ± 1518.26	16.04	0.1486
IL-10	296.00 ± 146.4	295.67 ± 112.00	-0.111	0.9894
TNF	19.43 ± 6.07	20.40 ± 6.26	5.00	0.3914

IL: Interleukin; TNF: Tumour necrosis factor.

Sepsis scores

Post therapy 16.2% (P = 0.0070) fall in SOFA scores was observed in the survivor group. Among non-survivors1% rise in SOFA score, was observed after therapy. Figure 2 shows the change in APACHE II and SOFA scores in both groups for pre and post CytoSorb^® therapy.

Figure 2 Comparison of sepsis scores among survivor and non-survivor patients. Significant reduction in acute physiology and chronic health evaluation II (P < 0.0001) and sequential organ failure assessment (P = 0.0070) scores in survivor group. APACHE: Acute physiology and chronic health evaluation; SOFA: Sequential organ failure assessment.

Predicted percentage mortality

As per APACHEII calculator[16], the mean predicted percentage mortality was 54% (53.68 ± 28.84) for the survivor group and 62% (62.32 ± 29.44) for the non-survivor group.

Survival outcomes: Initiation of therapy after onset of shock and number of days spent in ICU

CytoSorb^® therapy was started as per the severity of septic shock and clinical parameters of patients. From an overall pool of patients (n = 100), 60 patients were started with CytoSorb^® therapy within 48 h of ICU admission and 40 patients more than 48h of ICU admission. We observed that in the survivor group (n = 40), 70% (n = 28) of patients received CytoSorb^® therapy within 48 h of ICU admission as compared to 72% of non survivors (n = 43/60) in whom CytoSorb^® was initiated after 48 h after ICU admission. Figure 3 and Figure 4 show the patient survival data for both the groups.

Figure 3 Initiation of CytoSorb^® treatment after onset of septic shock. ICU: Intensive care units.

Figure 4 Length of patients’ stay in intensive care units (d). ICU: Intensive care units.

DISCUSSION

In the management of sepsis, it is necessary to stabilize the hemodynamic levels in patients undergoing treatment for septic shock. Resuscitation in septic shock can be rapidly achieved by restoration of perfusion by administration of intravenous fluids, inotropic supports, and vasopressor drugs. It is of utmost importance to maintain the appropriate MAP levels[17]. Some studies have also shown successful and effective results in the treatment of hemodynamics accompanied by a decrease in vasopressor doses with CytoSorb^® therapy[14]. For evaluating the hemodynamic parameters, we used multiple vasopressor drugs; NE, E and V in patients with septic shock > 48 h having MAP > 65 mmHg. Post therapy, in the survivor group, we observed hemodynamic stability with improvement in MAP as compared to pre CytoSorb^® therapy. We also observed significant reduction in mean percentage doses of all vasopressors. Post CytoSorb^® therapy, the survival rate was 40%. Patients in the survivor group showed better clinical outcomes than non-survivor group in all aspects of laboratory, vital parameters, sepsis scores, cytokine levels and vasopressor needs. A crucial aspect of this study was to look for the patients’ suitability for this therapy and to determine the extent of improvement in laboratory and hemodynamic parameters post therapy. Therefore, our clinical team designed a scoring system based on patients’ baseline characteristics including five parameters which directly affect the body’s main organ system that are prone to undergo dysfunction during sepsis (Supplementary Table 1). As per the CS scoring system, CytoSorb^® therapy should be recommended to the patients with scores between 8-13. For patients with CS between 10-14, dialysis in combination with one or more CytoSorb^® device depending on their clinical outcomes should be followed.

Laboratory parameters such as PCT, CRP and serum lactate are well known biomarkers that indicate cytokine storm[18-20]. We evaluated these parameters considering the target cut off for maximum severity score 3 as PCT (> 3 ng/mL), serum lactate (> 4 mmol) and CRP (> 200 mg/dL). In our study results, we reported remarkable reduction in patients’ PCT (65%), CRP (27%), bilirubin (43%, P = 0.05), and serum lactate (27%, P = 0.0159) levels post CytoSorb^® therapy. CytoSorb^® device is capable of removing more than 90% bilirubin (0.7 kDa), PCT (13 kDa), and IL-6 (26 kDa)[21,22]. Our study reports were consistent with the study conducted by Hawchar et al[23], in 20 patients (CytoSorb^® and control group; n = 10 each) on mechanical ventilation with baseline PCT > 3 ng/mL and serum lactate > 2.0 mmol/L. CytoSorb^® therapy was initiated within 24 h of septic shock and resulted in significant improvement in patients for PCT levels; T₀ = 20.6 [QR: 6.5-144.5] ng/mL, T₄₈ = 5.6 [QR: 1.9-54.4] ng/mL, P = 0.004. In the control group, PCT levels improved as; T₀ = 13.2 [QR: 7.6-47.8] ng/mL, T₄₈ = 9.2 [QR: 3.8-44.2] ng/mL. Serum lactate was reduced by 33% in CytoSorb^® group and 53.3% in control group. However, no significant difference was observed in both the groups for CRP concentration. This could be due to high molecular weight of CRP around 25 kDa that might not be absorbed by CytoSorb^® as efficiently as PCT. Both groups showed a decrease of CRP by T₄₈[23].

Elevation of proinflammatory cytokines such as TNF and interleukins is a potential marker of the hyper-inflammatory phase of sepsis[20]. In this study, IL6 and IL10 showed significant reduction (P < 0.0001) after the therapy in survivor group. Our results were supported by Mitzner and coworkers’ study who reported that the use of CytoSorb^® within 24 h in a patient with septic shock and chronic kidney failure decreased the levels of IL-6, CRP, serum creatinine, PCT, and leukocytes during the treatment and in the following days. CytoSorb^® hemoadsorber treatment appeared to be safe and was well tolerated by the patient as reported by them[24].

Our study showed a significant improvement in SOFA (P = 0.0070) score in survivor group. Improvement in SOFA scores indicated improvement in clinical condition including laboratory and hemodynamic parameters.

We also studied the correlation between early use of CytoSorb^® therapy (< 48 h and > above) with better outcome and evaluated the survival outcomes on the basis of number of days spent in ICU by patients. Two patients were discharged within a day of treatment. Our results were well supported by other studies which reported that use of this therapy within 24h of sepsis diagnosis could lead to decreased mortality in both medical and post-surgical patients[14,15,25].

Overall, the study showed a reduction in the vasopressor dose, a significant reduction in cytokine levels, remarkable reduction in diagnostic markers such as PCT, CRP, bilirubin in and serum lactate after using CytoSorb^® therapy. However, the current study has some limitations. First, the present study was a small, single-center retrospective study and underpowered for any significant outcome analysis. Further studies with a larger patient group are needed to deal with this question. Second, the lack of a control group precludes conclusions about effectiveness and cause of the therapy applied. Furthermore appropriate time of initiation of therapy needs to be well defined.

In conclusion, the study showed that the CytoSorb^® is a safe and well tolerated rescue therapy option in patients with severe septic shock. However, early (preferably within < 48 h after onset of septic shock) initiation might result in better clinical outcomes. These results may provide important support and guidance to future protocol designs and can help to define the appropriate study end points. Further, prospective randomized controlled trials should be performed to substantiate this hypothesis.

ARTICLE HIGHLIGHTS

Research background

Sepsis is one of the world’s leading cause of death in the intensive care unit (ICU) and yet remains the most significant unmet medical need. Sepsis results due to complex interactive reactions between infecting microbe and the immune system of host. CytoSorb^® is an European CE mark approved and ISO certified hemoadsorption device which helps in reducing cytokine storm in the blood. In this study, clinical outcomes were evaluated after the use CytoSorb^® device as an adjuvant therapy in patients who were admitted in ICU with sepsis between 2016 and 2018.

Research motivation

Most of the patients with septic shock end up dying even though control of inflammation has been attempted through various means. CytoSorb^® is an emerging extracorporeal hemadsorption device but there is a paucity of clinical evidence supporting its benefits and clinical outcomes after use. Previous individual studies have shown promising results after use of CytoSorb^® therapy in patients with sepsis and septic shock. We used CytoSorb^® in 100 patients admitted to ICU with sepsis a rescue therapy but had not analyzed the data to evaluate clinical outcomes in these patients. This study will serve as an important link to guide doctors about the usage of CytoSorb^® and possible clinical outcomes. Further, this study will help answer an important question of when to start the CytoSorb^® therapy after the onset of septic shock and how many devices are optimums for patients.

Research objectives

The objective of this study was to evaluate the clinical benefits of CytoSorb^® therapy in critically ill patients admitted in ICU. We looked for the patients’ suitability for this therapy and determined the extent of improvement in laboratory and hemodynamic parameters post therapy with CytoSorb^®. Future research should have the objective of a comparative study with a control group and a prospective randomized controlled trial should be performed to provide more evidence.

Research methods

A retrospective observational study was carried out over a period of 2 years. We used the CytoSorb^® scoring (CS) system that was developed by group of clinicians for initiating CytoSorb^® therapy on the basis of their practical experience for the evaluation of patients. The scoring system was derived from five parameters (hemodynamic, renal, respiratory, lab and sepsis scores), representing five different organ system which get affected in sepsis patients. At the end, final scores were calculated by adding all the individual organ system scores. We evaluated the vitals, laboratory and other parameters by observing the data pre and post CytoSorb^® administration.

Research results

The survivor group had a decrease in total leucocyte count, serum creatinine, serum lactate and platelet count. In the non-survivor group, serum creatinine levels and other parameters did not improve. We also observed that there was a significant decrease in inflammatory markers in the survivor group. Another major observation is that 70% of those who received the CytoSorb^® therapy within 48 h had better chances of survival.

Research conclusions

CytoSorb^® score used in this study is a newly devised scoring system that can guide doctors about usage of CytoSorb^® therapy. This study proposes that the CytoSorb^® therapy should be recommended to the patients with scores between 8-13. For patients with CS between 10-14; dialysis in combination with one or more CytoSorb^® device depending on their clinical outcomes should be followed. In summary, this study showed a reduction in the vasopressor dose, a significant reduction in cytokine levels, remarkable reduction in diagnostic markers such as PCT, CRP, bilirubin and serum lactate after the usage of CytoSorb^® therapy. The new hypothesis that this study proposed is there is an improvement in MAP levels, vasopressor dose and other laboratory and clinical parameters when the CytoSorb^® therapy is initiated early after onset of septic shock. We used a newly devised scoring system called CytoSorb^® score that was derived from five parameters (hemodynamic, renal, respiratory, laboratory and sepsis scores), representing five different organ system which get affected in sepsis patients. Through this study, we reinforced that the CytoSorb^® is a safe and well tolerated rescue therapy option in patients with severe septic shock.

Research perspectives

The lesson learnt from this study is that CytoSorb^® therapy should be initiated early in critically ill patients with sepsis and septic shock. In the future, we should design randomized clinical studies that can compare the results with control population. The best method would be to use CS score to decide the usage of CytoSorb^® therapy.

ACKNOWLEDGEMENTS

The authors acknowledge Mr. Pradeep Yanamala for end to end coordination and extended support in formatting of this paper and in that line improved the manuscript significantly and Knowledge Isotopes Pvt. Ltd (https://www. knowledgeisotopes.com) for the medical writing assistance.