- 1Department of Intensive Care, Vall d'Hebron University Hospital, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain
- 2Shock, Organ Dysfunction and Resuscitation Research Group, Vall d'Hebron Research Institute (VHIR), Vall d'Hebron University Hospital, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain
- 3Departament de Medicina, Universitat Autonoma de Barcelona, Barcelona, Spain
- 4Department of Immunology, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain
Introduction: A dysregulated inflammatory response, known as “cytokine storm”, plays an important role in the pathophysiology of coronavirus 2019 disease (COVID-19). Identifying patients with a dysregulated inflammatory response and at high risk for severe respiratory failure, organ dysfunction, and death is clinically relevant, as they could benefit from the specific therapies, such as cytokine removal by hemoadsorption. This study aimed to evaluate cytokine hemoadsorption as rescue therapy in critically ill patients with SARS-CoV-2 pneumonia, severe respiratory failure refractory to prone positioning, and hypercytokinemia.
Methods: In this single center, observational and retrospective study, critically ill patients with SARS-CoV-2 pneumonia, severe acute respiratory failure, and hypercytokinemia were analyzed. All the patients underwent cytokine hemoadsorption using CytoSorb® (Cytosorbents Europe, Berlin, Germany). The indication for treatment was acute respiratory failure, inadequate clinical response to the prone position, and hypercytokinemia.
Results: Among a total of 343 patients who were admitted to the intensive care unit (ICU) due to SARS-CoV-2 infection between March 3, 2020 and June 22, 2020, six patients received rescue therapy with cytokine hemoadsorption. All the patients needed invasive mechanical ventilation and prone positioning. A significant difference was found in the pre- and post-treatment D-dimer (17,868 mcg/ml [4,196–45,287] vs. 4,488 mcg/ml [3,166–17,076], p = 0.046), C-reactive protein (12.9 mg/dl [10.6] vs. 3.5 mg/dl [2.8], p = 0.028), ferritin (1,539 mcg/L [764–27,414] vs. 1,197 ng/ml [524–3,857], p = 0.04) and interleukin-6 (17,367 pg/ml [4,539–22,532] vs. 2,403 pg/ml [917–3,724], p = 0.043) levels. No significant differences in the pre- and post-treatment interleukin-10 levels (22.3 pg/ml [19.2–191] vs. 5.6 pg/ml [5.2–36.6], p = 0.068) were observed. Improvements in oxygenation (prehemoadsorption PaO2/FIO2 ratio 103 [18.4] vs. posthemoadsorption PaO2/FIO2 ratio 222 [20.9], p = 0.029) and in the organ dysfunction (prehemoadsorption SOFA score 9 [4.75] vs. posthemoadsorption SOFA score 7.7 [5.4], p = 0.046) were observed. ICU and in-hospital mortality was 33.7%.
Conclusions: In this case series, critically ill patients with COVID-19 with severe acute respiratory failure refractory to prone positioning and hypercytokinemia who received adjuvant treatment with cytokine hemoadsorption showed a significant reduction in IL-6 plasma levels and other inflammatory biomarkers. Improvements in oxygenation and SOFA score were also observed.
Introduction
Clinicians face several challenges when taking care of patients with coronavirus 2019 disease (COVID-19) (1), as the disease presents three distinct stages of disease progression. Each stage corresponds to the different clinical profiles according to individual responses to therapy and different prognoses (2). These three stages determine the severity of SARS-CoV-2 pneumonia: early, pulmonary, and hyperinflammatory. The hyperinflammatory stage is characterized by a multisystemic inflammatory syndrome, in which serum levels of inflammatory biomarkers increase, resulting in a high risk of organ dysfunction and death (3). The “cytokine storm” plays a central role in the pathophysiology of the disease (4). In the former reports from China, the cytokine storm was recognized as a clinical feature associated with the severity of the clinical condition (5).
As a consequence, the resulting inflammatory response is not homogeneous throughout the course of the disease (6, 7). During the asymptomatic phase, hypercytokinemia is not clinically evident, and, in the subsequent stages, massive cytokine release worsens the clinical course of the disease (8). This progression correlates with the fact that although an important cytokine elevation begins in the first 24 or 48 h of presentation, the clinical hyperinflammatory state becomes evident on days 7–10 from the onset of symptoms. At this stage, clinical deterioration is ubiquitous, and acute respiratory failure occurs progressively. In the lung, hypercytokinemia leads to diffuse alveolar damage, hyaline membrane formation, thrombus formation, fibrin exudates, and fibrotic healing (9), resulting in acute respiratory distress syndrome (ARDS) (10), whose frequency is up to 26% in SARS-CoV-2 infection (11, 12).
However, potentially useful adjuvant treatments do not fit all the patients. Early in the course of COVID-19, avoiding immunosuppression is recommended. In advanced stages, immunomodulation is a cornerstone for treatment interventions. Thus, it is relevant to identify the subgroup of patients who develop a hyperinflammatory response (13), as they could benefit from specific therapies, such as immunomodulation using blood purification strategies (14). Cytokine hemoadsorption therapy could be a promising therapeutic intervention in patients with severe acute respiratory failure (15–17).
This study hypothesizes that cytokine hemoadsorption may improve the hyperinflammatory profile and organ dysfunction in the selected critically ill COVID-19 patients. This study aimed to evaluate cytokine hemoadsorption as rescue therapy in critically ill patients with severe SARS-CoV-2 pneumonia, acute respiratory failure refractory to standard maneuvers, and hypercytokinemia.
Methods
Patients and Ethics Approval
In this single center, observational, and retrospective study, critically ill patients with COVID-19 who received cytokine hemoadsorption using CytoSorb® (Cytosorbents Europe, Berlin, Germany) adsorbent, between March 3, 2020 and June 22, 2020 were eligible. All patients were admitted to the ICU of Vall d'Hebron University Hospital, Barcelona, Spain. The study was approved by the local Clinical Research Ethics Committee (PR (AG) 270/2020), and the need for informed consent was waived.
Inclusion and Exclusion Criteria
The inclusion criteria were the presence of acute respiratory failure (PaO2/FIO2 [arterial oxygen pressure (PaO2), inspired fraction of oxygen (FIO2)] ratio <150) with poor response to the prone position, hyperinflammatory state, manifested as interleukin-6 (IL-6) hypercytokinemia (IL-6 > 1,000 pg/ml), and increased levels of ferritin and D-dimer (DD). Poor response to prone positioning was considered when PaO2/FiO2 ratio remained <150 after the prone position. The exclusion criteria were all patients who did not meet the aforementioned criteria or had a limitation of life-sustaining care, pregnant patients, or patients who had other indications for cytokine hemoadsorption.
Analyzed Data and Scores
The plasma concentrations of inflammatory biomarkers were analyzed, including IL-6, IL-10, DD, and C-reactive protein (CRP) on ICU admission, immediately before hemoadsorption initiation (prehemoadsorption), and after the procedure (posthemoadsorption). The severity of the disease was evaluated with the Acute Physiology and Chronic Health disease Classification System (APACHE) II (18) and Sequential Organ Failure Assessment (SOFA) scores (19). Both scores were calculated using the worst parameters measured during the first 24 h of admission. Organ dysfunction was assessed by calculating the SOFA score before and after the treatment with hemoadsorption.
Acute respiratory distress syndrome was defined according to the Berlin definition criteria (20). Data on the incidence of acute kidney injury (AKI) or failure, and the need for the continuous renal replacement therapy (CRRT), were collected according to the latest kidney disease: Improving Global Outcomes (KDIGO) Clinical Practice Guideline criteria (21). PaO2/FIO2 ratio was calculated before and after each hemoadsorption session. Also, the use of high doses of methylprednisolone (~1.5–2 mg/kg), systemic anticoagulation (22), number of days on mechanical ventilation, duration of ICU stay, and ICU and in-hospital mortality were collected. The study fulfilled the “Strengthening the reporting of observational studies in epidemiology (STROBE)” checklist for the observational studies (23).
CytoSorb® and Continuous Renal Replacement Therapy
CytoSorb® is a highly bio- and hemocompatible cytokine adsorber approved for use in conditions with increased levels of cytokines. The device is composed of porous polymer beads within a huge and efficient surface area. It allows for adsorption and permanent binding of molecules in the 5–60 kDa range. This range includes the vast majority of cytokines and other inflammatory molecules.
The CytoSorb® filter was connected posthemofilter via a close loop circuit to the CRRT pump (Prismaflex, Gambro Lundia AB, Lund, Sweden). CRRT was delivered using the continuous hemodiafiltration mode using an MA 150® hemofilter (Baxter, Illinois, US) at a blood flow rate of 200 ml/min. Anticoagulation was performed with citrate or heparin.
Measurement of Plasmatic Levels of Cytokines
Plasmatic levels of IL-6 were measured using the automated quantitative immunoassay Cobas® (Roche diagnostics International Ltd, Switzerland), following the instructions of the manufacturer. Circulating levels of IL-10 and soluble CD25 (IL-2Ra) were determined using the microfluidics-based quantitative immunoassay, ELLA® (ProteinSimple, California, US), following the instructions of the manufacturer.
Statistical Analysis
According to the variable distribution, descriptive data were expressed as mean (SD) or median (interquartile range [IQR], 25–75%). Mann-Whitney U-test was used to compare continuous variables and Fisher's test for categorical variables. All the statistical tests were 2-sided, and a p-value < 0.05 was considered statistically significant. An analysis of the required sample size was not performed because of the observational characteristics of the study. Data analysis was conducted using the statistical software package PASW Statistics for Windows, Version 18.0 (SPSS Inc, Chicago, Illinois, US).
Results
Characteristics of the Study Population
Among a total of 343 patients who were admitted to the ICU due to severe infection of SARS-CoV-2, six patients received treatment with CytoSorb® (Table 1). During the study period, hemoadsorption was performed in another patient whose indication was refractory septic shock secondary to the intestinal perforation. This patient was excluded from this study.
From a total of six patients, 5 (83.0%) were male; mean age 57.0 years (10.5). Patient characteristics, other treatments received, and outcomes are presented in Table 1. All the patients fulfilled the Berlin criteria for severe ARDS. All patients required mechanical ventilation and prone positioning. The mean SOFA score was 5.2 (1.5) at ICU admission, and the mean PaO2/FiO2 ratio was 97.5 (14.6). The levels of DD were 559 mcg/ml (254–2,643), CRP 19.5 mg/dl (13.4), ferritin 967 mcg/L (682–2,116) and IL-6 1,163 pg/ml (52–2,775).
The mean duration of the mechanical ventilation was 15.2 days (7.2). Three (50%) patients developed COVID-19-associated AKI and required CRRT. The mean ICU stay was 17.2 days (8.0), and ICU and in-hospital mortality was 33.7%.
Hemoadsorption
Patient eligibility for the cytokine hemoadsorption was assessed between days 3 and 4 of ICU admission. At inclusion, clinical parameters of the organ dysfunction and inflammation had worsened in all patients. The mean SOFA score was 9 (4.75), and PaO2/FiO2 ratio was 103 (18.4). Levels of DD were 17,868 mcg/ml (4,196–45,287), CPR 12.9 mg/dl (10.6), ferritin 1,539 mcg/L (764–27,414), IL-6 17,367 pg/ml (4,539–22,532), and IL-10 22.3 pg/ml (19.2–191) (Table 2). All the patients underwent cytokine hemoadsorption (5 patients received one session of CytoSorb® hemoadsorption [each session of variable duration], and one patient received two 24-h sessions). The mean perfusion time was 16 (9) h. The circuit patency determined the duration of hemoadsorption sessions in 3 patients (circuit clotting occurred at 3, 8, and 16 h).
Inflammatory Parameters and Organ Dysfunction
All inflammatory parameters, except for IL-10 levels, significantly decreased after treatment (posthemoadsorption DD levels 4,488 mcg/ml [3,166–17,076], p = 0.046; posthemoadsorption CRP 3.5 mg/dl [2.8], p = 0.028; posthemoadsorption ferritin levels 1,197 mcg/L [524–3,857], p = 0.046; posthemoadsorption IL-6 levels 2.403 pg/ml [917–3.724], p = 0.043; and posthemoadsorption IL-10 levels 5.6 pg/ml [5.2–36.6], p = 0.068).
Improvements in oxygenation (posthemoadsorption PaO2/FiO2 ratio 222 (20.9), p = 0.029) and the organ dysfunction were also observed (posthemoadsorption SOFA score 7.7 [5.4], p = 0.046) (Table 2).
Discussion
Main Findings of This Study
This retrospective study describes the potential benefits of CytoSorb® hemoadsorption in critically ill patients with refractory acute respiratory failure due to COVID-19 and hypercytokinemia. Hemoadsorption was associated with a reduction in inflammatory biomarkers, improved oxygenation, and multiorgan dysfunction.
Previous Experience With Cytokine Hemoadsorption
Several recommendations regarding the use of cytokine hemoadsorption in SARS-CoV-2 pneumonia have been published recently. The National Health Commission and National Administration of Traditional Chinese Medicine recommends CytoSorb® hemoadsorption to treat severe and critical cases of COVID-19 (24). The Brescia Renal Covid Task Force recommends CytoSorb® hemoadsorption in the patients with COVID-19 admitted to ICU who have ARDS or AKI-requiring CRRT (25). The Panamanian Association of Critical Medicine and Intensive Therapy recommends using CytoSorb® in patients with hyperlactatemia and high-dose vasopressors who do not respond to standard therapy. Patients with severe ARDS with high-ventilatory support requirements or candidates for the use of extracorporeal membrane oxygenation (ECMO) therapy are also considered (26). The Colombian consensus suggests using CytoSorb® in patients with cytokine storm syndrome when there is a lack of treatment response, and while evaluating the individual prognosis of the patient (27). On April 10, 2020, the United States of America Food and Drug Administration issued an Emergency Use Authorization for CytoSorb® to treat patients with 18 years of age or older with confirmed COVID-19 admitted to the ICU with confirmed or imminent respiratory failure and specifically early ARDS, severe disease or life-threatening disease defined as respiratory failure, septic shock or the multiorgan dysfunction (28). Despite these recommendations, clinical experience is scarce and comes mainly from case reports and some case series (29–31).
Characteristics of the Study Population. Target Patient Population
The selection of patients with COVID-19 for receiving cytokine hemoadsorption is critical and should be individualized. There are two clinical phenotypes of the patients with COVID-19 (11). One phenotype is characterized by a mild or moderate disease with low-viral loads. These patients have preserved interferon responses with regulated production of cytokines and show rapid recovery from initial lymphopenia. Thus, they are unlikely to benefit from cytokine hemoadsorption. However, selected patients in the second phenotype, characterized by a severe disease with a high risk of death, high-viral loads, insufficient interferon response, sustained lymphopenia, and a very significant elevation of cytokines, could benefit from cytokine hemoadsorption. In this study, patients were more suitable to receive cytokine hemoadsorption if they were more severely ill and developed severe acute respiratory failure refractory or poorly responsive to prone positioning, in association with a hyperinflammatory state (determined by very high levels of biomarkers, such as IL-6, ferritin, and DD). All patients in this study presented a considerable deleterious clinical condition, with a mean PaO2/FIO2 ratio of 103 (18.4).
There is a lack of studies evaluating cytokine hemadsorption in critically ill patients with COVID-19, and some of them have included heterogeneous populations of critically ill patients. Rampino et al. (32) reported a case series of 9 consecutive critically ill patients with SARS-CoV-2 and acute respiratory failure requiring continuous positive airway pressure. In this study, no patients required invasive mechanical ventilation. Their eligibility criteria were confirmed SARS-CoV-2 pneumonia and a sum of PaO2/FiO2 ratio < 200 mm Hg, CRP levels >10 mg/dl, and a lymphocyte count <1,500/mm3. Damiani et al. (33) delivered hemoadsorption with CytoSorb® for 24 to 48-h sessions to 11 patients with COVID-19 requiring mechanical ventilation due to rapidly progressive ARDS after a median of 3 days (range 0–4 days) from hospital admission. Nassiri et al. (34) used CytoSorb® in 26 patients with COVID-19-associated moderate ARDS (PaO2/FiO2 ratio <200) and hyper inflammation (CRP > 50 mg/L and ferritin > 1,500 mcg/L). Of all patients, 46.2% received mechanical ventilation. Paisey et al. (35) reported a case series of 15 patients with severe COVID-19 that received cytokine hemoadsorption (five HA-330 cartridges and 10 CytoSorb® adsorbents). All the patients needed invasive mechanical ventilation and CRRT, and 11 received ECMO support. In a multicenter study, Villa et al. (36) evaluated 37 patients who had received cytokine hemoadsorption using the oXiris® membrane. The indication for oXiris® was biochemical and clinical evidence of systemic inflammation associated with AKI, hemodynamic instability, or multiorgan dysfunction. All the patients received mechanical ventilation.
Biomarker Levels and Organ Dysfunction Throughout Hemoadsorption in Relation to Outcomes
In general, critically ill patients with COVID-19 do not show increased plasma levels of biomarkers as other populations of critically ill patients (e.g., septic shock or sepsis with patients with ARDS). Previous studies have found mild-to-moderate elevations of CRP, IL-6, and ferritin. (37) However, there are no well-defined thresholds of biomarkers to consider the initiation of cytokine hemoadsorption. Given the heterogeneity of individual responses and the numerous underlying factors that affect levels of biomarker, it is uncertain whether valid thresholds will be determined shortly.
The results of this study are engaging and coincide with the previous studies. Rampino et al. (32) documented reductions in proinflammatory cytokines (e.g., IL-6) in patients receiving cytokine hemoadsorption therapy. All patients who received the treatment survived, and only two of them needed endotracheal intubation. Damiani et al. (33) showed the median values of IL-6 before hemoadsorption were 355 pg/ml (IQR 263–466), 118 pg/ml (IQR 19–221, p = 0.003) at treatment end and 169 pg/ml (IQR 61–253, p = 0.03) 24 h after therapy. A significant decrease in CRP and an increase in PaO2/FiO2 ratio were also observed. The improvement in the inflammatory profile was associated with progressive improvements in the respiratory function. Nassiri et al. (34) reported that the PaO2/FiO2 ratio, SOFA score, and inflammatory biomarkers (procalcitonin, CRP, and ferritin) improved significantly, and the authors reported a mortality rate of 19.2%. A potential limitation of this study is that cytokine levels were not reported. Paisey et al. (35) proposed hemoadsorption as an adjunctive treatment leading to a reduction in ferritin, CRP, procalcitonin, and lactate levels. Yet, no significant differences were found in IL-6 and IL-10 pre- and post-treatment levels. In these patients, hypercytokinemia was moderate, although they showed a hyperinflammatory profile based on ferritin and CPR levels. Villa et al. (36) delivered the hemoadsorption therapy after a median of 3.6 days (IQR 3.7) from ICU admission and 14 days (IQR 10.0) from the symptom onset. The decrease of IL-6 concentration was significant, especially during the first 24 h of treatment (from baseline levels of 1,230 pg/ml [IQR 895] to 479 pg/ml [IQR 531] at 24 h after treatment, 320 pg/ml [IQR 259] at 48 h, and 160 pg/ml [IQR 141] at 72 h [p = 0.001 for each time point]). The reduction in serum IL-6 concentration levels correlated with improved organ function, particularly hemodynamic and pulmonary function. A slight decrease in the observed mortality rate compared with the predicted mortality rate, calculated by the APACHE IV score, was also observed.
The results of this study are different from the recently published CYCOV trial (38), in which 34 patients with severe COVID-19 pneumonia requiring ECMO were included. Seventeen patients were treated with cytokine hemoadsorption for 72 h. No significant differences in IL-6 levels were observed between the two groups after 72 h of cytokine hemoadsorption. The median IL-6 concentrations decreased from 357 pg/ml (IQR 177.4–118.0) to 98.6 pg/ml (71–192.8) in the cytokine adsorption group and from 289.0 pg/ml (87–787.0) to 110.0 pg/ml (48–198.5) in the control group. In contrast, the median baseline IL-6 levels were very high (17,367 pg/ml [4,539–22,532]), and the reduction in IL-6 levels and inflammatory biomarkers was substantial. The results of the CYVOV trial are not comparable with the results of this study, as the rate of cytokine removal by hemoadsorption depends on the presence of baseline high-concentration levels of cytokines in plasma (39).
In this study, the strategy for delivering cytokine hemadsorption was different from other studies that used fixed hemoadsorption regimens. Single 24-h sessions of hemoadsorption were planned to be delivered (only one patient required two sessions of 24 h). Real-time IL-6 levels were monitored during the hemoadsorption sessions, which allowed us to withhold the treatment at 24 h if IL-6 levels had been reduced, and the patient had clinical improvement. As observed by Damiani et al. (33) and Paisey et al. (37), no significant differences were found in the reduction of IL-10 levels. However, the lack of effect over IL-10 levels may be secondary to the slightly increased baseline levels and the small sample size.
Cytokine hemoadsorption could be considered an effective and safe rescue therapy for highly selected critically ill patients with COVID-19. Further studies and randomized controlled trials in critically ill patients with COVID-19 with refractory acute respiratory failure and hypercytokinemia should be conducted to accurately narrow the indications and clinical benefits of the cytokine hemoadsorption.
Limitations
This study has some limitations. First, this is a single-center study including a small number of patients with no control group. Thus, the findings of this study should be confirmed in larger comparative studies and cannot be extrapolated to other ICU settings; moreover, the complexity of the conferred difficulty of the patients in determining the effect of CytoSorb® alone on patient outcomes. Second, the patient inclusion process was not consecutive. Given the unprecedented pandemic situation, it was impossible to ensure that all patients meeting the inclusion criteria were evaluated for eligibility. Third, we have not performed the sample size calculation because of the observational characteristics of the study.
Conclusions
In this case series, critically ill patients with COVID-19 with severe acute respiratory failure refractory to prone positioning and hypercytokinemia who received adjuvant treatment with cytokine hemoadsorption showed a significant reduction in IL-6 plasma levels and other inflammatory biomarkers. Improvements in oxygenation and SOFA score were also observed. Cytokine hemoadsorption could be a safe and effective rescue therapy for patients with refractory COVID-19 acute respiratory failure.
Data Availability Statement
The original contributions presented in the study are included in the article/supplementary materials, further inquiries can be directed to the corresponding author/s.
Ethics Statement
The study was approved by the Local Clinical Research Ethics Committee (PR (AG) 270/2020), and the need for informed consent was waived. The patients/participants provided their written informed consent to participate in this study.
Author Contributions
All authors involved in providing care for the patient and writing and reviewing the manuscript.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1. Bouadma L, Lescure FX, Lucet JC, Yazdanpanah Y, Timsit JF. Severe SARS-CoV-2 infections: practical considerations and management strategy for intensivists. Intensive Care Med. (2020) 46:579–82. doi: 10.1007/s00134-020-05967-x
2. Siddiqi HK, Mehra MR. COVID-19 illness in native and immunosuppressed states: a clinical-therapeutic staging proposal. J Heart Lung Transplant. (2020) 39:405–7. doi: 10.1016/j.healun.2020.03.012
3. Robba C, Battaglini D, Pelosi P, Rocco PRM. Multiple organ dysfunction in SARS-CoV-2: MODS-CoV-2. Expert Rev Respir Med. (2020) 14:865–8. doi: 10.1080/17476348.2020.1778470
4. Kox M, Waalders NJB, Kooistra EJ, Gerretsen J, Pickkers P. Cytokine levels in critically Ill patients with COVID-19 and other conditions. JAMA. (2020) 324:1565–7. doi: 10.1001/jama.2020.17052
5. Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. (2020) 395:497–506. doi: 10.1016/S0140-6736(20)30183-5
6. Osuchowski MF, Winkler MS, Skirecki T, Cajander S, Shankar-Hari M, Lachmann G, et al. The COVID-19 puzzle: deciphering pathophysiology and phenotypes of a new disease entity. Lancet Respir Med. (2021) 9:622–42. doi: 10.1016/S2213-2600(21)00218-6
7. Lopes-Pacheco M, Silva PL, Cruz FF, Battaglini D, Robba C, Pelosi P, et al. Pathogenesis of multiple organ injury in COVID-19 and potential therapeutic strategies. Front Physiol. (2021) 12:593223. doi: 10.3389/fphys.2021.593223
8. Pedersen SF, Ho YC. SARS-CoV-2: a storm is raging. J Clin Invest. (2020) 130:2202–5. doi: 10.1172/JCI137647
9. Dolhnikoff M, Duarte-Neto AN, de Almeida Monteiro RA, da Silva LFF, de Oliveira EP, Saldiva PHN, et al. Pathological evidence of pulmonary thrombotic phenomena in severe COVID-19. J Thromb Haemost. (2020) 18:1517–9. doi: 10.1111/jth.14844
10. Liu Q, Zhou YH, Yang ZQ. The cytokine storm of severe influenza and development of immunomodulatory therapy. Cell Mol Immunol. (2016) 13:3–10. doi: 10.1038/cmi.2015.74
11. Murthy S, Gomersall CD, Fowler RA. Care for critically Ill patients with COVID-19. JAMA. (2020) 323:1499–500. doi: 10.1001/jama.2020.3633
12. Wang D, Hu B, Hu C, Zhu F, Liu X, Zhang J, et al. Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected pneumonia in Wuhan, China. JAMA. (2020) 323:1061–9. doi: 10.1001/jama.2020.1585
13. Mehta P, McAuley DF, Brown M, Sanchez E, Tattersall RS, Manson JJ, et al. Across speciality collaboration, UK. COVID-19: consider cytokine storm syndromes and immunosuppression. Lancet. (2020) 395:1033–4. doi: 10.1016/S0140-6736(20)30628-0
14. Ingraham NE, Lotfi-Emran S, Thielen BK, Techar K, Morris RS, Holtan SG, et al. Immunomodulation in COVID-19. Lancet Respir Med. (2020) 8:544–6. doi: 10.1016/S2213-2600(20)30226-5
15. Schwindenhammer V, Girardot T, Chaulier K, Grégoire A, Monard C, Huriaux L, et al. oXiris® Use in septic shock: experience of two French Centres. Blood Purif. (2019) 47:1–7. doi: 10.1159/000499510
16. Bucciarelli S, Espinosa G, Cervera R, Erkan D, Gómez-Puerta JA, Ramos-Casals M, et al. European Forum on antiphospholipid antibodies. Mortality in the catastrophic antiphospholipid syndrome: causes of death and prognostic factors in a series of 250 patients. Arthritis Rheum. (2006) 54:2568–76. doi: 10.1002/art.22018
17. Zhang Y, Chen Y, Meng Z. Immunomodulation for severe COVID-19 pneumonia: the state of the art. Front Immunol. (2020) 11:577442. doi: 10.3389/fimmu.2020.577442
18. Knaus WA, Draper EA, Wagner DP, Zimmerman JE, APACHE II. A severity of disease classification system. Crit Care Med. (1985) 13:818–29. doi: 10.1097/00003246-198510000-00009
19. Vincent JL, Moreno R, Takala J, Willatts S, De Mendonça A, Bruining H, et al. The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med. (1996) 22:707–10. doi: 10.1007/BF01709751
20. ARDS Definition Task Force, Ranieri VM, Rubenfeld GD, Thompson BT, Ferguson ND, Caldwell E, et al. Acute respiratory distress syndrome: the Berlin Definition. JAMA. (2012) 307:2526–33. doi: 10.1001/jama.2012.5669
21. Khwaja A, KDIGO. clinical practice guidelines for acute kidney injury. Nephron Clin Pract. (2012) 120:c179–84. doi: 10.1159/000339789
22. Al-Samkari H, Karp Leaf RS, Dzik WH, Carlson JCT, Fogerty AE, Waheed A, et al. COVID-19 and coagulation: bleeding and thrombotic manifestations of SARS-CoV-2 infection. Blood. (2020) 136:489–500. doi: 10.1182/blood.2020006520
23. Vandenbroucke JP, von Elm E, Altman DG, Gøtzsche PC, Mulrow CD, Pocock SJ, et al. STROBE Initiative. Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): explanation and elaboration. PLoS Med. (2007) 4:e297. doi: 10.1371/journal.pmed.0040297
24. Diagnosis and Treatment Protocol for Novel Coronavirus Pneumonia (Trial Version 7). Chin Med J. (2020).133:1087–95. doi: 10.1097/CM9.0000000000000819
25. Alberici F, Del Barba E, Manenti C, Econimo L, Valerio F, Pola A, et al. Managing patients in dialysis and with kidney transplant infected with Covid-19. G Ital Nefrol. (2020) 37:2020-vol2.
26. Asociación Panameña de Medicina Critica y Terapia Intensiva. GUÍAS NACIONALES DE ATENCIÓN DE PACIENTES ADULTOS COVID-19 VERSION 2.0. Published on March 22nd on https://medcriticapanama.com
27. González C, Yama E, Yomayusa N, Vargas J, Rico J, Ariza A et al. Consenso colombiano de expertos sobre recomendaciones informadas en la evidencia para la prevención, el diagnóstico y el manejo de la lesión renal aguda por SARS-CoV-2/COVID-19. Rev Colomb Nefrol. (2020) 7:89–117. doi: 10.22265/acnef.7.Supl.2.473
28. U.S. Food and Drug Administration. CytoSorb ® 300 mL Device Approved by FDA for Emergency Treatment of COVID-19. Silver Spring, MD: FDA (2020).
29. Rizvi S, Danic M, Silver M, LaBond V. Cytosorb filter: an adjunct for survival in the COVID-19 patient in cytokine storm? A case report. Heart Lung. (2021) 50:44–50. doi: 10.1016/j.hrtlng.2020.09.007
30. Mezger M, Eitel I, Ensminger S, Pogorzalek D, Huang Z, Graf T. Sequential use of hemoadsorption using cytosorb and biosky filter-technology in A COVID-19 patient suffering from severe ARDS. Arch Clin Med Case Rep. (2020) 4:969–77. doi: 10.26502/acmcr.96550286
31. Berlot G, Tomasini A, Roman Pognuz E, Randino A, Chiella F, La Fata C, et al. The combined use of tocilizumab and hemoadsorption in a patient with SARS-COV-2-19-associated pneumonia: a case report. Nephron. (2020) 144:459–62. doi: 10.1159/000509738
32. Rampino T, Gregorini M, Perotti L, Ferrari F, Pattonieri EF, Grignano MA, et al. Hemoperfusion with CytoSorb as adjuvant therapy in critically Ill patients with SARS-CoV2 pneumonia. Blood Purif. (2021) 50:566–71. doi: 10.1159/000511725
33. Damiani M, Gandini L, Landi F, Borleri G, Fabretti F, Gritti G, et al. Extracorporeal cytokine hemadsorption in severe COVID-19 respiratory failure. Respir Med. (2021) 185:106477. doi: 10.1016/j.rmed.2021.106477
34. Nassiri AA, Hakemi MS, Miri MM, Shahrami R, Koomleh AA, Sabaghian T. Blood purification with CytoSorb in critically ill COVID-19 patients: a case series of 26 patients. Artif Organs. (2021) 45:1338–47. doi: 10.1111/aor.14024
35. Paisey C, Patvardhan C, Mackay M, Vuylsteke A, Bhagra SK. Continuous hemadsorption with cytokine adsorber for severe COVID-19: a case series of 15 patients. Int J Artif Organs. (2021) 44:664–74. doi: 10.1177/03913988211023782
36. Villa G, Romagnoli S, De Rosa S, Greco M, Resta M, Pomarè Montin D, et al. Blood purification therapy with a hemodiafilter featuring enhanced adsorptive properties for cytokine removal in patients presenting COVID-19: a pilot study. Crit Care. (2020) 24:605. doi: 10.1186/s13054-020-03322-6
37. Leisman DE, Ronner L, Pinotti R, Taylor MD, Sinha P, Calfee CS, et al. Cytokine elevation in severe and critical COVID-19: a rapid systematic review, meta-analysis, and comparison with other inflammatory syndromes”. Lancet Respir Med. (2020) 8:1233–44. doi: 10.1016/S2213-2600(20)30404-5
38. Supady A, Weber E, Rieder M, Lother A, Niklaus T, Zahn T, et al. Cytokine adsorption in patients with severe COVID-19 pneumonia requiring extracorporeal membrane oxygenation (CYCOV): a single centre, open-label, randomised, controlled trial. Lancet Respir Med. (2021) 9:755–62. doi: 10.1016/S2213-2600(21)00177-6
39. Kellum JA, Kong L, Fink MP, Weissfeld LA, Yealy DM, Pinsky MR, et al. GenIMS Investigators. Understanding the inflammatory cytokine response in pneumonia and sepsis: results of the Genetic and Inflammatory Markers of Sepsis (GenIMS) Study. Arch Intern Med. (2007) 167:1655–63. doi: 10.1001/archinte.167.15.1655
Keywords: SARS-CoV-2 pneumonia, hemoadsorption, acute respiratory distress syndrome (ARDS), hypercytokinemia, COVID-19
Citation: Ruiz-Rodríguez JC, Chiscano-Camón L, Ruiz-Sanmartin A, Palmada C, Paola Plata-Menchaca E, Franco-Jarava C, Pérez-Carrasco M, Hernández-González M and Ferrer R (2022) Cytokine Hemoadsorption as Rescue Therapy for Critically Ill Patients With SARS-CoV-2 Pneumonia With Severe Respiratory Failure and Hypercytokinemia. Front. Med. 8:779038. doi: 10.3389/fmed.2021.779038
Received: 17 September 2021; Accepted: 23 November 2021;
Published: 10 January 2022.
Edited by:
Luo Zhe, Fudan University, ChinaReviewed by:
Talha Bin Emran, Begum Gulchemonara Trust University, BangladeshDenise Battaglini, Ospedale San Martino (IRCCS), Italy
Copyright © 2022 Ruiz-Rodríguez, Chiscano-Camón, Ruiz-Sanmartin, Palmada, Paola Plata-Menchaca, Franco-Jarava, Pérez-Carrasco, Hernández-González and Ferrer. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Luis Chiscano-Camón, bGNoaXNjYW5vJiN4MDAwNDA7dmhlYnJvbi5uZXQ=