10
views
0
recommends
+1 Recommend
2 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      The ten reasons why corticosteroid therapy reduces mortality in severe COVID-19

      editorial

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The recent finding of the effectiveness of corticosteroid therapy in reducing mortality in patients with severe coronavirus disease-19 (COVID-19) is a welcome breakthrough [1–6]. In this article, we highlight the current understanding of the effect of corticosteroid therapy in severe COVID-19. Evidence of effectiveness from randomized controlled trials in hospitalized patients with COVID-19. The RECOVERY randomized controlled trial (RCT) demonstrated that dexamethasone (6 mg daily for 10 days) in hospitalized patients with COVID-19 reduced (i) 28-day mortality (rate ratio 0.83; 95% confidence interval [CI], 0.75–0.93), (ii) duration of hospitalization and (iii) progression to invasive mechanical ventilation [1]. The greatest mortality reduction was observed in those receiving oxygen supplementation or invasive mechanical ventilation; no improvement was observed in those without respiratory support [1]. A prospective meta-analysis of 7 RCTs further confirmed the benefit of corticosteroid therapy in reducing mortality critically ill patients with COVID-19 (summary odds ratio [OR] 0.66, 95% CI, 0.53-0.82) [2]. This is the best direct evidence supporting corticosteroid therapy in severe COVID-19. Evidence of effectiveness in non-viral acute respiratory distress syndrome (ARDS). A recent Spanish RCT (n = 277) of patients with moderate-to-severe ARDS, found that dexamethasone (20 mg and 10 mg for 5 days each), in comparison to placebo, was associated with more mechanical ventilation-free days and lower mortality. An updated meta-analysis of ten RCTs shows that corticosteroid therapy initiated before day 14 of ARDS was associated with a significant reduction in duration of mechanical ventilation and hospital mortality (risk ratio [RR] 0.67; 95% CI 0.52–0.87) [7]. Evidence of effectiveness in community-acquired pneumonia. Several systematic reviews demonstrated that in patients hospitalized with community-acquired pneumonia (CAP), corticosteroid therapy was associated with reduction in mortality, length of stay and time to clinical stability [8]. Dysregulated immune response in COVID-19. Corticosteroid therapy aims to support the central regulatory function of the activated glucocorticoid receptor α (GC-GRα) throughout disease development and resolution. The dysregulated immune response observed in COVID-19 is qualitatively similar to that of multifactorial ARDS [9]. In patients with severe COVID-19, glucocorticoid receptor expression in bronchoalveolar lavage myeloid cells is negatively related to lung neutrophilic inflammation, NETosis, and severity of symptoms [10]. Translational research in ARDS patients randomized to methylprednisolone has demonstrated the ability of corticosteroid therapy to rescue the cellular concentrations and functions of activated GC-GRα leading to downregulation of systemic and pulmonary nuclear factor- κB-activated markers of inflammation, coagulation, and fibroproliferation [11, 12]. Biological improvement was associated with accelerated disease resolution [11]. Further work is needed to understand the effect of corticosteroid therapy on the immune response to COVID-19. Computed tomographic and pathology findings. Computed tomographic findings of ground glass appearance and histopathologic features (post-mortem studies) of diffuse alveolar damage and acute fibrinous and organizing pneumonia [13] are consistent with corticosteroid-responsive inflammatory lung diseases. The role of hypothalamic–pituitary–adrenal axis. Evidence from studies of severe acute respiratory syndrome (SARS) suggest that infection with SARS-CoV-2 is associated with impaired cortisol stress response (Fig. 1). Microthrombi and coagulopathy. The pathogenesis of COVID-19 illness appears to be induced by dysregulated systemic and pulmonary inflammation, along with endothelial injury, hypercoagulability and thrombosis [14, 15]. Platelet–fibrin thrombi formation in small arterial vessels are commonly observed in post-mortem examination of the lungs from patients with COVID-19 [16]. Emerging data indicate that hypercoagulability in COVID-19 is induced by dysregulated release of neutrophil extracellular traps (NETs). In an equine experimental model, dexamethasone decreased NETs formation [17], which may contribute to the observed benefit from corticosteroid therapy in COVID-19. Acceptable safety profile. Short-term (up to 4 weeks) corticosteroid therapy in patients with life-threatening systemic inflammation is well-tolerated. Data from systematic reviews in CAP and ARDS showed that corticosteroid therapy was associated with transient hyperglycemia but did not increase the frequency of gastrointestinal hemorrhage, neuromuscular weakness, or nosocomial infections [8, 12]. Hyperglycemia did not affect outcome. Recent data have provided evidence that the GRα is essential for activation and reinforcement of innate immunity and when applied correctly (i.e., appropriate duration of corticosteroid administration) is associated with restoration of anatomy and function of the affected tissues, along with a parallel support of adaptive immunity. Corticosteroid treatment-associated downregulation of systemic and pulmonary inflammation might lower the risk of developing nosocomial infections by (i) decreasing duration of mechanical ventilation, (ii) achieving an inflammatory milieu less favorable to intra- and extra- cellular growth of bacterial pathogens frequently encountered in ARDS (Staphylococcus aureus, Pseudomonas aeruginosa, and Acinetobacter sps.), and (iii) improving opsonization-dependent phagocytic neutrophil function and intracellular killing [18]. (Online Supplement for Supplementary References). Long-term outcome. In RCTs of ARDS patients, corticosteroid therapy was associated with survival benefit that persisted after up to one year of hospital discharge (limit of measurement) [19]. Extensive literature suggests pro-inflammatory cytokines do influence the brain, and may be involved in the pathogenesis of depression and post-traumatic stress disorder (PTSD). Data from five small RCTs (n = 292) suggest that longer duration of corticosteroid therapy may be associated with lower anxiety scores and improved PTSD symptomatology. Corticosteroid therapy-associated reduction in duration of mechanical ventilation and sedation may also have a positive impact on long-term PTSD symptoms and cognitive function. (Online Supplement for Supplementary References). Scalability. The low cost and wide availability make corticosteroid therapy easily equitable and available globally across different income settings. Recent data on corticosteroid therapy represent a milestone in the of management of COVID-19, while many questions remain. Efforts for worldwide implementation of corticosteroid therapy protocols should be supported by data regarding generalizability of the observed effect in randomized controlled trials across subgroups of patients, different populations, and resource settings. More data are needed to evaluate the impact of type of corticosteroid, timing of initiation, dose, mode of administration, duration, and dose tapering on outcome. And also to (i) identify modalities to adjust treatment dose and duration based on laboratory parameters of oxygenation and inflammation, and (ii) to evaluate the impact of co-interventions directed at improving response to corticosteroid therapy [20]. Limited data are presently available on the impact of corticosteroid therapy on SARS CoV-2 replication, and on the potential benefits of concomitant antiviral treatment. The interaction between corticosteroid therapy and other COVID-19 therapeutics, such as interferons (IFNs) [21] and anticoagulation should be explored. In conclusion, corticosteroid therapy is a safe and effective intervention in downregulating the integrated pathways of inflammation-coagulation-fibroproliferation, in the lung and systemically, in COVID-19 patients. There is an ethical urgency to invest in this field of research. Fig. 1 Hypothalamic–pituitary–adrenal (HPA) response in COVID-19. The left panel shows an intact HPA axis response to stress leading to the downregulation of NF-kB. The right panel shows mechanisms potentially involved in an impaired HPA axis response to stress in COVID-19. COVID-19 may be associated with CIRCI, as a result of inhibition of the hypothalamic–pituitary–adrenal (HPA) axis at any or all of its levels, as shown by the red X’s: (1) Hypothalamus (CRH/AVP), (2) pituitary gland (ACTH/AT2/ACE2), (3) adrenal cortex (cortisol), and (4), target tissues (Glucocorticoid receptor signaling system). In CIRCI, target tissue resistance to glucocorticoids may occur even in the presence of elevated levels of circulating cortisol. SARS -CoV-2 has an epitope that binds the ACE2 enzyme facilitating entry into host cells, which might influence the function of the HPA axis at level (2). SARS-CoV-2 may have an ACTH-mimic peptide that could act as an agonist or antagonist at the ACTH receptor at level (3). Prolonged glucocorticoid treatment is indicated when cortisol production and/or target tissue sensitivity to cortisol are compromised (Online Supplement for Supplementary References). CIRCI Critical illness-related corticosteroid insufficiency, CRH corticotropin-releasing hormone, AVP arginine-vasopressin, ACE2 angiotensin-converting enzyme 2, AT2 angiotensin 2, ACTH corticotropin, GR glucocorticoid receptor–alpha, HSP heat shock protein, FKBP immunophilin, GRIP1 coactivator, p65/p50 nuclear factor (NF)-kB Electronic supplementary material Below is the link to the electronic supplementary material. Supplementary file1 (DOCX 27 kb)

          Related collections

          Most cited references19

          • Record: found
          • Abstract: found
          • Article: not found

          Dexamethasone in Hospitalized Patients with Covid-19 — Preliminary Report

          Abstract Background Coronavirus disease 2019 (Covid-19) is associated with diffuse lung damage. Glucocorticoids may modulate inflammation-mediated lung injury and thereby reduce progression to respiratory failure and death. Methods In this controlled, open-label trial comparing a range of possible treatments in patients who were hospitalized with Covid-19, we randomly assigned patients to receive oral or intravenous dexamethasone (at a dose of 6 mg once daily) for up to 10 days or to receive usual care alone. The primary outcome was 28-day mortality. Here, we report the preliminary results of this comparison. Results A total of 2104 patients were assigned to receive dexamethasone and 4321 to receive usual care. Overall, 482 patients (22.9%) in the dexamethasone group and 1110 patients (25.7%) in the usual care group died within 28 days after randomization (age-adjusted rate ratio, 0.83; 95% confidence interval [CI], 0.75 to 0.93; P<0.001). The proportional and absolute between-group differences in mortality varied considerably according to the level of respiratory support that the patients were receiving at the time of randomization. In the dexamethasone group, the incidence of death was lower than that in the usual care group among patients receiving invasive mechanical ventilation (29.3% vs. 41.4%; rate ratio, 0.64; 95% CI, 0.51 to 0.81) and among those receiving oxygen without invasive mechanical ventilation (23.3% vs. 26.2%; rate ratio, 0.82; 95% CI, 0.72 to 0.94) but not among those who were receiving no respiratory support at randomization (17.8% vs. 14.0%; rate ratio, 1.19; 95% CI, 0.91 to 1.55). Conclusions In patients hospitalized with Covid-19, the use of dexamethasone resulted in lower 28-day mortality among those who were receiving either invasive mechanical ventilation or oxygen alone at randomization but not among those receiving no respiratory support. (Funded by the Medical Research Council and National Institute for Health Research and others; RECOVERY ClinicalTrials.gov number, NCT04381936; ISRCTN number, 50189673.)
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study

            Little evidence of increased thrombotic risk is available in COVID-19 patients. Our purpose was to assess thrombotic risk in severe forms of SARS-CoV-2 infection.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found

              Association Between Administration of Systemic Corticosteroids and Mortality Among Critically Ill Patients With COVID-19: A Meta-analysis

              Effective therapies for patients with coronavirus disease 2019 (COVID-19) are needed, and clinical trial data have demonstrated that low-dose dexamethasone reduced mortality in hospitalized patients with COVID-19 who required respiratory support.
                Bookmark

                Author and article information

                Contributors
                yaseenarabi@yahoo.com
                Journal
                Intensive Care Med
                Intensive Care Med
                Intensive Care Medicine
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0342-4642
                1432-1238
                7 October 2020
                : 1-4
                Affiliations
                [1 ]GRID grid.412149.b, ISNI 0000 0004 0608 0662, Intensive Care Department, King Abdullah International Medical Research Center, , Ministry of National Guard Health Affairs, King Saud Bin Abdulaziz University for Health Sciences, ; Riyadh, Kingdom of Saudi Arabia
                [2 ]GRID grid.5216.0, ISNI 0000 0001 2155 0800, University Research Institute of Maternal and Child Health and Precision Medicine, Medical School, , National and Kapodistrian University of Athens, ; Athens, Greece
                [3 ]GRID grid.413847.d, ISNI 0000 0004 0420 4721, Memphis Veterans Affairs Medical Center Research Service and Pulmonary, Critical Care, and Sleep Medicine Service, ; Memphis, TN USA
                [4 ]GRID grid.267301.1, ISNI 0000 0004 0386 9246, Department of Medicine, , University of Tennessee Health Science Center, ; Memphis, TN USA
                Author information
                http://orcid.org/0000-0001-5735-6241
                Article
                6223
                10.1007/s00134-020-06223-y
                7538533
                33026460
                8d8f7073-de04-4650-9f35-4df0fee0e10d
                © Springer-Verlag GmbH Germany, part of Springer Nature 2020

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 29 July 2020
                : 19 August 2020
                Categories
                Editorial

                Emergency medicine & Trauma
                Emergency medicine & Trauma

                Comments

                Comment on this article