- Open Access
Corticosteroids for treatment of COVID-19: effect, evidence, expectation and extent
Beni-Suef University Journal of Basic and Applied Sciences volume 10, Article number: 78 (2021)
The World Health Organization (WHO) announced the COVID-19 occurrence as a global pandemic in March 2020. The treatment of SARS-CoV-2 patients is based on the experience gained from SARS-CoV and MERS-CoV infection during 2003. There is no clinically accepted therapeutic drug(s) accessible yet for the treatment of COVID-19.
Corticosteroids, i.e., dexamethasone, methylprednisolone, hydrocortisone and prednisone are used alone or in combination for the treatment of moderate, severe and critically infected COVID-19 patients who are hospitalized and require supplemental oxygen as per current management strategies and guidelines for COVID-19 published by the National Institutes of Health. Corticosteroids are recorded in the WHO model list of essential medicines and are easily accessible worldwide at a cheaper cost in multiple formulations and various dosage forms. Corticosteroid can be used in all age group of patients, i.e., children, adult, elderly and during pregnancy or breastfeeding women. Corticosteroids have potent anti-inflammatory and immunosuppressive effects in both primary and secondary immune cells, thereby reducing the generation of proinflammatory cytokines and chemokines and lowering the activation of T cells, monocytes and macrophages. The corticosteroids should not be used in the treatment of non-severe COVID-19 patients because corticosteroids suppress the immune response and reduce the symptoms and associated side effects such as slow recovery, bacterial infections, hypokalemia, mucormycosis and finally increase the chances of death.
Intensive research on corticosteroid therapy in COVID-19 treatment is urgently needed to elucidate their mechanisms and importance in contributing toward successful prevention and treatment approaches. Hence, this review emphasizes on recent advancement on corticosteroid therapy for defining their importance in overcoming SARS-CoV-2 pandemic, their mechanism, efficacy and extent of corticosteroids in the treatment of COVID-19 patients.
The World Health Organization (WHO) announced the coronavirus disease 2019 (COVID-19) occurrence as a global pandemic in March 2020. COVID-19 is an infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that appeared from Wuhan, Hubei province, China in Dec 2019 [1, 2]. The most frequent indications of COVID-19 infection include fever, cough and myalgia. The infected persons have some additional symptoms like diarrhea, nasal congestion, respiratory distress, sepsis, septic shock, loss of smell and taste [3,4,5].
The crown-like spikes on the outer surface representing corona were responsible for naming the virus as ‘Coronavirus.’ The causative virus belongs to the family, Coronaviridae, and order, Nidovirales; bearing a single-stranded genomic RNA . The SARS-CoV, SARS-CoV-2, H5N1 influenza, H1N12009 and Middle East Respiratory Syndrome Coronavirus (MERS-CoV) were earlier thought to infect only animals, but with the outbreak of 2003 SARS-CoV in China and MERS-CoV in Middle Eastern countries, the world witnessed its infectious ability in humans, causing severe pulmonary failure and sometimes fatality. The possible evidence of animal to human transmission of coronavirus was also established in the COVID-19 pandemic [7,8,9]. However, the scientific studies have reported human to human spread of SARS-CoV-2 via droplets or direct contact. The possibility of transmission increases rapidly through asymptomatic carriers .
The current treatment of SARS-CoV-2 infected persons is based on the experiences gained from SARS-CoV and MERS-CoV infection during 2003 along with the application of existing antiviral/antibiotic therapy and mechanical respiratory support . Remdesivir is the only FDA-authorized investigational drug in the treatment of COVID-19 that has displayed activity against SARS-CoV-2, significantly reducing the time to recovery and mortality, while not shown clinical improvement after 5 days and have no statistically significant effect on deaths. It is presently accessible in an inadequate number of pharmacies and hospitals around the world . There are no FDA-approved therapeutic medicines available yet for the treatment of COVID-19 . There is an urgent need for an effective drug for the treatment of COVID-19 patients which should be available globally at a low cost, reducing the recovery time and death rate of infected patients.
Corticosteroids in COVID-19 treatment
Corticosteroids are a class of natural, semi-synthetic and synthetic steroidal hormones that are produced in the adrenal cortex of vertebrates and are required for a variety of physiological functions such as immune response, stress response, control of inflammation, protein catabolism, carbohydrate metabolism and blood electrolyte concentrations . Corticosteroids, alone or in combination with ribavirin, were particularly efficient in the treatment of the SARS outbreak in 2003 [15, 16]. Various clinical studies have reported that corticosteroids, i.e., dexamethasone, prednisone, methylprednisolone and hydrocortisone (Fig. 1) can be used for the treatment of mild, moderate, severe and critically ill COVID-19 patients (Table 1). Most of the time, the death of COVID-19 patients is occurring due to an overactive immune response to the infection not due to the coronavirus. The corticosteroids control the immune system or cytokine storm, providing support for patients, whose lungs are damaged due to an overactive immune response that an occasionally found in the severe incidents of COVID-19. Nevertheless, corticosteroids have exhibited detrimental effects, including extended time for viral clearance and a higher possibility of infection. Corticosteroids decrease the time required on mechanical ventilation, the residing period in an intensive care unit (ICU) and importantly death rate in COVID-19 patients . Corticosteroids can be used in all age groups of patients, i.e., children, adults, the elderly and during pregnancy or breastfeeding women. The recovery trial employed oral and intravenous (IV) infusion of dexamethasone to COVID-19 patients, including pregnant or breastfeeding women . Corticosteroids are the part of WHO model list of essential medicines and are easily accessible worldwide at a cheaper cost, in multiple formulations and various dosage forms, such as tablet, injectable suspension, oral solution, oral concentrate and administered orally, intramuscular, intra-articular, direct IV injection or intra-lesional injections and inhalation. The corticosteroids can be administered by inhalation in patients suffering from asthma and chronic obstructive pulmonary disease (COPD) . Inhaled corticosteroids studies are going on in various clinical trials and still need to be studied for assessing their efficacy in COVID-19 . Intensive research on corticosteroid therapy in COVID-19 treatment is urgently needed to elucidate their mechanisms and importance in contributing toward successful prevention and treatment approaches. Hence, this review emphasizes on recent advancement on corticosteroid therapy for defining their importance in overcoming SARS-CoV-2 pandemic, their mechanism, efficacy and extent of corticosteroids in the treatment of COVID-19 patients.
Dexamethasone (MK-125) is a synthetic corticosteroid developed in 1957. Its chemical structure contains the cyclopentaphenanthrene ring substituted by fluorine at position 9, substituted by hydroxy groups at positions 11, 17 and 21, methyl group at position 10, 13 and 16 and oxo groups at positions 3 and 20 (Fig. 1). Dexamethasone is used in the treatment of many conditions, including different inflammatory conditions, immune system disorders such as immunosuppressive, allergic disorders, asthma, chronic obstructive lung disease, rheumatic problems, inflammation in brain, croup, eye pain following eye surgery, tuberculosis bowel disorders and some cancers. Dexamethasone has been a part of the WHO model list of essential medicines since 1977 in the form of numerous formulations with various dosage forms such as tablet, injectable suspension, oral solution and oral concentrate, readily available globally at a low cost and administered orally, intramuscular, intra-articular or direct IV injection [21, 22].
Horby et al. performed controlled trials of corticosteroids as a potential treatment of COVID-19 in March 2020 called RECOVERY trial, for testing a range of potential therapies (Table 1). The dexamethasone 6 mg/day was either administered orally or IV injection for 10 days for randomly selected 2104 patients and compared with 4321 patients who concurrently received standard care for COVID-19 infection [23, 24]. During these studies, dexamethasone showed the remarkable results in critically ill patients who received mechanical ventilation by ventilators and who received oxygen therapy. Dexamethasone declined mortality by 33% in patients taking invasive mechanical ventilation and 20% in patients getting oxygen lacking invasive mechanical ventilation. The application of dexamethasone showed no effect in less severe cases of COVID-19 and has not reduced mortality in these patients [23, 24]. The treatments were comprised of short duration, recommended doses by doctors, and no serious side effects were observed, the potentially higher blood glucose level (hyperglycemia) was a temporary condition. However, prolonged application, i.e., more than 2 weeks has been found to produce undesirable events namely, glaucoma, hypertension, fluid retention, cataract, weight gain, elevated threat of infections, osteoporosis and psychological effects, e.g., mood swings, confusion or irritation and memory issues [18, 23, 24].
Tomazini et al. studied the effect of dexamethasone on mild ill COVID-19 patients who do not receive mechanical ventilation nor associated with Moderate or Severe Acute Respiratory Distress Syndrome (ARDS). The continuous IV infusion of dexamethasone 20 mg/daily was administered for 5 days subsequently 10 mg/daily for 5 days or until ICU discharge, in addition to standard care. This treatment enhanced the efficacy and significantly no adverse effect was observed (Table 1) [25, 26].
Dr. Negrin University Hospital studied the effectiveness of dexamethasone in patients with ARDS caused by COVID-19 under a clinical trial named DEXA-COVID19 with 200 participants in Spain. An IV dose of dexamethasone, i.e., 20 mg/day for the first 5 days, subsequently 10 mg/day for the next 6–10 days was administered. The primary outcome was 60-day mortality and the mortality outcome was 28 days, when compared with standard care as control of intervention (Table 1) .
Methylprednisolone is a synthetic corticosteroid first described in the literature in 1950 [28, 29]. The chemical structure contains the cyclopentaphenanthrene ring substituted by hydroxy groups at positions 11, 17 and 21, methyl group at positions 6, 10, 13 and oxo groups at positions 3 and 20 (Fig. 1). Methylprednisolone is being used for the treatment of many conditions like endocrine, ophthalmic, respiratory, rheumatic, skin disorders, blood disorders, fluid retention in body tissues, alopecia areata and discoid lupus erythematosus. Methylprednisolone has been recorded in the WHO model list of Essential Medicines in numerous formulations with various dosage forms such as tablet, injectable suspension, oral solution, oral concentrate, readily available globally at a low cost and administered orally, intramuscular, intra-articular, direct IV injection or intra-lesional injections. Methylprednisolone is the second drug in the class of corticosteroids, which has shown promising results in lowering mortalities after successful use of dexamethasone in critically ill COVID-19 patients [22, 30].
Wang et al. studied the application of methylprednisolone as possible treatment in severe patients with COVID-19 pneumonia. The IV injection of methylprednisolone 2 mg/kg/day for 5–7 days was administered to the patients. These studies showed that the application of methylprednisolone reduces the length of ICU hospitalization, while it did not show significant difference in death rate of COVID-19 patients (Table 1) .
Liu et al. studied the effect of methylprednisolone in severe and critically ill COVID-19 patients. A single dosage of 40–500 mg methylprednisolone as per the harshness of COVID-19 improved the lung performance without decreasing the generation of specific IgG antibodies against SARS-CoV-2 infection, while successfully halting the inflammatory cascade (Table 1) .
Beijing Chao Yang Hospital studied the efficacy and safety of methylprednisolone therapy against new coronavirus pneumonia. The dosage schedule was IV injection of methylprednisolone 1 mg/kg/day for 7 days. This study employed a lower dose of methylprednisolone, which did not show significant improvement in patient conditions during first 14 days. After 14th day, recovery in patient condition along with alleviation of clinical symptoms and signs was noticed and the patient did not require any additional or alternative treatment (Table 1) .
Corral et al. evaluated the efficacy of methylprednisolone in serious patients with COVID-19 pneumonia. The dosage schedule employed was IV infusion of methylprednisolone 40 mg/12 h for 3 days, after that 20 mg/12 h for 3 days. This 6 days course of methylprednisolone showed a beneficial effect along with decreased risk of admission to ICU, NIV or death (Table 1) .
Jeronimo et al. evaluated the efficacy of methylprednisolone in suspected COVID-19 infected persons with IV infusion of methylprednisolone in dose of 0.5 mg/kg twice in a day, for 5 days. This short course treatment schedule of methylprednisolone was not able to reduce mortality in COVID-19 patients (Table 1) [35, 36].
Peking Union Medical College hospital carried out clinical trial comprising of 80 patients for evaluating the effectiveness and safety of methylprednisolone in COVID-19 critically ill patients with Severe Acute Respiratory Failure. The dosage schedule was comprised of IV administration of 40 mg methylprednisolone every 12 h for 5 days. The outcome of studies was lesser lung injury at 7 and 14 days as determined using Murray lung injury score. The significant adverse effects noticed were secondary bacterial infections, severe hyperglycemia, GI bleeding and attained disability (Table 1) .
Hydrocortisone (cortisol or 17-hydroxycorticosterone) is a synthetic or semi-synthetic analog of naturally occurring glucocorticoid produced by the adrenal cortex, discovered in the 1930s by Edward Kendall. The chemical structure contains the cyclopentaphenanthrene ring, substituted by hydroxy groups at positions 11, 17 and 21, methyl group at positions 10, 13 and oxo groups at position 3 (Fig. 1). Hydrocortisone is employed in the treatment of inflammation, allergy, asthma, adrenocortical deficiency and few cancerous circumstances [22, 30].
Petersen et al. performed the clinical trial to investigate the effects of low-dose hydrocortisone in COVID-19 and critical hypoxic patients not supplied with life-support system, i.e., mechanical ventilation, circulatory support or renal replacement therapy. The continuous IV infusion of hydrocortisone 200 mg/daily was administered for 7 days beside the standard care. After 28 days, critical side effects, i.e., anaphylactic reaction, invasive fungal infection and gastrointestinal hemorrhage were observed (Table 1) [17, 38].
REMAP-CAP investigators reported the consequences of hydrocortisone on death rate and organ support in patients with severe infection of COVID-19 using data from 121 sites spread over 8 countries. The hydrocortisone was administered IV in the dose of 50 mg/day for 7 days or 100 mg every 6 h for 7 days, a shock-dependent course comprising of 50 mg every 6 h for 7 days when the shock was clinically apparent. This treatment employing hydrocortisone, when compared with no hydrocortisone, showed 93% and 80% chances of progress in organ support free days within 21 days (Table 1) [39,40,41].
Dequin et al. reported multicenter randomized double-blind clinical trial performed in France to examine the effect of hydrocortisone in seriously ill COVID-19 persons for monitoring the 21-day death rate or respiratory support requirement. These studies were carried out to find out hydrocortisone as a possible therapeutic option for treatment of severe lung damage occurring in COVID-19. The IV infusion of hydrocortisone 200 mg/daily was administered for 7 days followed by decreased dose to 100 mg/day for 4 days and 50 mg/day for 3 days, for a total of 14 days. This clinical trial employing low dose hydrocortisone, when compared with placebo did not significantly reduce the infection on day 21 (Table 1) [42, 43].
Prednisone is a synthetic glucocorticoid analog of cortisone. The chemical structure contains the cyclopentaphenanthrene ring, substituted by hydroxy groups at positions 17 and 21, a methyl group at positions 10, 13 and oxo groups at positions 3, 11 (Fig. 1). Prednisone is used for its immunosuppressive activity in allergic, skin, blood, gastrointestinal, nervous system, kidney, respiratory disorders and organ transplantation [22, 30].
Keller et al.  reported that glucocorticoid formulations of prednisone can give the same life-saving benefits in COVID-10 treatment as dexamethasone, methylprednisolone and hydrocortisone (Table 1). Bozzette et al.  reported that prednisone used in patients with pneumonia and hypoxia reduces the risk of death (Table 1).
The combination of corticosteroids with other drugs for treatment of COVID-19 infection
Corticosteroids plus Remdesivir
The dexamethasone plus remdesivir combination is used to treat hospitalized patients, who require increasing amounts of supplemental oxygen, high-flow oxygen or noninvasive ventilation, but it is not recommended in patients who require invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO) . The safety and efficacy of the combination of dexamethasone and remdesivir have not been adequately examined in clinical studies; consequently, there is insufficient clinical data to justify the use of this combination medication. The combination of dexamethasone and remdesivir is recommended because there are theoretical considerations, according to scientists, that corticosteroids have potent anti-inflammatory effects to prevent hyperinflammatory effects and that remdesivir has an antiviral effect. The combination may treat the viral infection and dampen the potentially injurious inflammatory response that is a consequence of the infection. However, the data on clinical outcomes for patients who received this combination are currently limited . If dexamethasone isn't accessible, other corticosteroids like prednisone, methylprednisolone or hydrocortisone can be used in place of it.
Corticosteroids plus Tocilizumab
The dexamethasone or another corticosteroid at an equivalent dose plus tocilizumab combination is used for the treatment of recently hospitalized patients who require supplemental oxygen, invasive mechanical ventilation or ECMO have either been admitted to the ICU within the prior 24 h or have significantly increased inflammatory markers of inflammation . The COVID-19 viral infection of some severe patients suffers from cytokine storm syndrome (CSS) causing hypotension, fever and high levels of C-reactive protein (CRP), abnormal coagulation, uncontrolled inflammatory response, shock and multiorgan system failure. The patients suffer CSS elevated levels of cytokines thus raising interleukin-6 (IL-6), interleukin-10 (IL-10) and interferon-gamma (IFN-γ). The scientific reports indicate that the SARS-CoV-2 infection is associated with a significant increase in IL-6 [51, 52]. Tocilizumab is a monoclonal antibody that inhibits IL-6, and the FDA has already granted emergency use authorization for the management of COVID-19 related CSS and organ failure. Sarilumab is another IL-6 inhibitor that has been recommended as a replacement for tocilizumab .
Corticosteroid plus Baricitinib
The combination of dexamethasone or another corticosteroid at an equivalent dose plus baricitinib is used for recently hospitalized patients (within 3 days of hospital admission) who have rapidly increasing oxygen needs, require high-flow oxygen or noninvasive ventilation and have increased markers of inflammation, as well as selected patients, who are on low-flow oxygen but are progressing toward needing higher levels of respiratory support . Baricitinib is an oral Janus kinase (JAK) inhibitor for the treatment of rheumatoid arthritis and granted an emergency use authorization for the treatment of COVID-19 in the USA. Baricitinib has immunomodulatory, antiviral effects and is able to prevent the poorly regulated production of proinflammatory cytokines in severe or critical COVID-19 patients . The baricitinib in combination with tocilizumab for the treatment of COVID-19 is strictly prohibited because both are potent immunosuppressants, there is the potential for an additive risk of infection. If baricitinib isn't accessible, tofacitinib, another JAK inhibitor, could be used instead [46, 53].
Current management strategies and guidelines for the use of corticosteroids in COVID-19
The National Institutes of Health (NIH) has published treatment guidelines for COVID-19 that includes the use of corticosteroids. The patients with asymptomatic/presymptomatic and mild infection of COVID-19 exhibit a variety of symptoms such as fever, sore throat, cough, loss of taste and smell, headache, muscle pain, malaise, nausea, vomiting and diarrhea; The corticosteroids should not be used in asymptomatic/ presymptomatic and mild infection of COVID-19 (Table 2). The COVID-19 patients already receiving dexamethasone or another corticosteroid may suffer from another disease including different inflammatory conditions, immune system disorders as immunosuppressive, allergic disorders, asthma, chronic obstructive lung disease, rheumatoid arthritis (RA), inflammation in brain, croup, eye pain following eye surgery, tuberculosis bowel disorders and some cancers should continue therapy as directed by their treatment center .
The patients with moderate infection of COVID-19 have the lower respiratory disease during clinical assessment or imaging and an oxygen saturation (SpO2) 90% to < 93% on room air at sea level, respiratory rate > 24/min, breathlessness but not require supplemental oxygen. It is advised not to use corticosteroids for the treatment of COVID-19 patients . However, the patients who require supplemental oxygen but who do not require oxygen delivery through a high-flow device, noninvasive ventilation can be treated with dexamethasone 6 mg once daily plus standard of care for up to 10 days or until hospital discharge, whichever came first. If dexamethasone is not available, an alternative corticosteroid such as prednisone 40 mg/methylprednisolone 32 mg administered once daily or in two divided doses daily, or hydrocortisone 160 mg administered in two to four divided doses daily can be used (Table 2) . The combination of dexamethasone and remdesivir for anti-inflammatory effects and antiviral effect, respectively, is recommended as a treatment option for patients of this group .
The patients with COVID-19 are considered to have severe infection of COVID-19, if they have SpO2 < 90% on room air at sea level, a respiratory rate > 30 breaths/min, PaO2/FiO2 < 300 mm Hg or lung infiltrates > 50%. These patients may experience rapid clinical deterioration. Oxygen should be administered immediately through a high-flow device or noninvasive ventilation but not invasive mechanical ventilation or extracorporeal membrane oxygenation. The severe infection of COVID-19 should be treated with dexamethasone alone or an alternative corticosteroid such as prednisone/ methylprednisolone/ hydrocortisone or dexamethasone plus remdesivir. The COVID-19 patients, who have been recently hospitalized with rapidly increasing oxygen needs, require high-flow oxygen or noninvasive ventilation and have increased markers of inflammation, within 3 days of hospital admission should be treated with baricitinib or tocilizumab plus dexamethasone alone or baricitinib or tocilizumab plus dexamethasone plus remdesivir (Table 2). The combination of baricitinib with tocilizumab for the treatment of COVID-19 is strictly prohibited as both the drugs are potent immunosuppressants and may have a potential for an additive risk of infection .
The critical infection of COVID-19 patients may have acute respiratory distress syndrome, septic shock, cardiac dysfunction, an exaggerated inflammatory response and/or multiple organ dysfunction. The patients who require invasive mechanical ventilation or extracorporeal membrane oxygenation are treated with dexamethasone alone. If dexamethasone is not available, equivalent doses of alternative corticosteroids prednisone, methylprednisolone or hydrocortisone may be used. The patients who are admitted within 24 h of admission to the ICU are treated with dexamethasone plus tocilizumab (Table 2) .
Inhaled corticosteroids (ICS) are a major course of treatment for asthma patients. Corticosteroids may have two major effects, (a) they can prevent excessive inflammation in the host, including cytokine storming, and (b) they can also induce coronavirus multiplication by suppressing innate immunity. As per WHO guidelines, systemic corticosteroids should be administered with caution and only in certain situations. Several recent Japanese researches have shown that ciclesonide, a form of ICS, may be beneficial in the treatment and prognosis of COVID-19 patients with asthma [47, 48]. The worldwide asthma guideline, Global Initiative for Asthma (GINA), advises that asthma sufferers should keep on using ICS and oral corticosteroids, even during the COVID-19 pandemic period. Yet, no research supporting this recommendation has been published so far. One of the independent studies revealed that administration of asthma medicine had no prognosis effect on COVID-19 clinical outcomes and that further research is required .
Mode of action of corticosteroids in COVID-19 treatment
Though mainstream patients endure an uneventful reclamation, around 19% patients show progressive worsening with severe pneumonia , followed by severe dyspnea, ARDS, multiple organ dysfunction and sometimes death [55, 56]. The condition worsens with the unstoppable arrival of ‘cytokine storm’ in infected individuals. Earlier studies on SARS-CoV and MERS-CoV infected patients show an excessive generation and release of proinflammatory cytokines and chemokines like tumor necrosis factor-α, IL-1, IL-2, IL-6, IL-8, IL-12, INF-α, INF-β, INF-γ, monocyte chemoattractant protein 1 (MCP1), INF-γ-induced protein 10 (IP10)  in their serological findings. The similar findings were also evident in individuals with COVID-19.
Initially, with the invasion of SARS-CoV-2 through the angiotensin-converting enzyme 2 receptor in the body, the virus vigorously replicates infecting airway and alveolar epithelial cells at the prior stage. This stimulates the specific immune cells (like monocytes, T cells, B cells, natural killer cells) promoting colossal production of cytokines and chemokines, hence bringing ‘cytokine storm.’ The cytokine storm upholds the bulk movement of inflammatory cells into the lungs, accompanying with enormous vascular inflammation, shock and hypotension, causing multi-organ failure and death. On one end, the balanced immune response of the body tries to keep and manage the infection under control, but on contrary, the exaggerated immune response favors pulmonary damage and failure [12, 57]. The involvement of immune response in COVID-19 pathophysiology raised a thought in the researcher’s mind that intervention of corticosteroids in COVID-19 therapy may prove to be a beneficial and life-saving measure for critically infected individuals from this global pandemic.
Corticosteroid treatment may serve as a sailor for drowning life of patients with severe pneumonia in presence of COVID-19. Though it’s an immune-suppressive property impairing the innate immunity may worsen the intensity of viral propagation. Conversely, patients undergoing long term maintenance dose of steroids exhibits attained encouraging outcome without any increased occurrence of development of serious COVID-19 pneumonia . Therefore, caution should be adopted before including corticosteroids in the COVID-19 treatment regimen.
The count of specific immune cells like macrophages, monocytes, natural killer cells, T cells, B cells, etc. is markedly affected in individuals with COVID-19. Lymphopenia seems to be a precarious factor related to disease harshness and modality. The results of a pilot study conducted by Guo and co-workers revealed a noticeable decrease in the number of CD3+ T cells, CD3+ CD4+ T cells and CD3+ CD8+ T cells in the patients who died with viral pneumonia. The results suggested that the cellular immune function of such individuals was significantly inhibited. The CD4+ T cells are responsible for maintaining immunity through T cells antiviral response. The researches even showed that an increased concentration of both extremely proinflammatory CCR6+ Th17 in CD4 T cells and cytotoxic granules in CD8 T cells. The over-activated T cells severely cause immune injury accompanied with elevated Th17 and high cytotoxicity of CD8 T cells. In such individuals, corticosteroids usage may hinder T cells immunity and result in tenacious viral replication and subsequent delay in clearance . Systemic corticosteroids appear to aggravate the viral load due to their immune-suppressive effect and delay the viral excretion. Nevertheless, recent reports highlight the fact that corticosteroids may possess a stimulatory as well as inhibitory action on the immune response depending upon the duration and their blood concentration . The possible mechanism of action of corticosteroids in COVID-19 treatment is depicted in Fig. 2.
Caution against corticosteroid-based COVID-19 treatment
The corticosteroids should be used under the supervision of a clinician for the treatment of COVID-19 patients. The use of corticosteroid in the treatment of COVID-19 treatment is controversial, some scientific reports do not support corticosteroid treatment due to the huge side effects such as increased mortality [60, 61], obstructed clearance of viral RNA from the respiratory tract , slow clearance of viral RNA from blood , psychosis , induced diabetes , avascular necrosis in survivors , induced lung injury or shock . However, some scientific reports support the application of corticosteroids at low-to-average amount for a shorter period as it declines the death rate and minimizes the duration of hospitalization for seriously ill patients with COVID-19 without causing secondary infection and other side effects (Table 1) [17, 67]. The RECOVERY trial noticed a noteworthy decline in death with dexamethasone only in serious cases of COVID-19 [23, 24]. The WHO published guidance on September 02, 2020, regarding the use of corticosteroids in patients with COVID-19. According to these guidelines, corticosteroids are recommended for the treatment of patients with severe and critical COVID-19. The corticosteroids should not be used in the treatment of non-severe COVID-19 patients because corticosteroids suppress the immune response and reduce the symptoms and associated side effects such as slow recovery, bacterial infections, hypokalemia and finally increase the chances of death . Salinas et al. and Saiz-Rodríguez et al. studied the effect of early use of corticosteroids in non-critical COVID-19 patients, the primary result indicated serious side effect to patients such as respiratory deterioration, worsening of the glycemic profile, delirium, pneumonia, urinary tract infection, device-associated infections, need to admission to ICU, mechanical ventilation or death by day 28. The COVID-19 pandemic has been reported with very high incidence of mucormycosis (black fungus infection) among COVID-19 patients, especially in those who have had treatment with higher doses or longer courses of steroids or who are diabetic or cancer or HIV or have weak immune systems and have received steroids [68, 69].
The corticosteroids can intensify the possibility of osteonecrosis of the femoral head (ONFH) and it should be prevented by avoiding their use and/or minimizing the dose and duration of corticosteroids. The COVID-19 patients being treated with corticosteroids should also be prescribed with biphosphates and vitamin E. The latter drugs could also be replaced with vasodilators, anticoagulants or traditional Chinese medicine [70, 71].
The COVID-19 pandemic is uncontrolled, unabated and untreatable at present; no potential therapeutic drug is available yet for its treatment. The treatments of SARS-CoV-2 infected patients are based on the experiences gained from SARS-CoV and MERS-CoV infection during 2003. There is an urgent need for a suitable drug, i.e., readily available around the globe with low cost, highly efficacious with lesser side effects for the treatment of COVID-19. Corticosteroids are off-patent and are the part of WHO model list of essential medicines, smoothly accessible worldwide at a cheaper cost, in multiple formulations and various dosage forms. The WHO and several countries have approved dexamethasone as the first treatment shown to decline death rate in patients with COVID-19 requiring oxygen or ventilator assistance. The methylprednisolone, hydrocortisone and prednisolone are the other drugs belonging to the class of corticosteroids, that have shown significant results in the treatment of COVID-19 patients. The corticosteroids restrain the immune system or cytokine storm, which possibly imparts relief to patients, whose lungs are damaged by an intense immune response sometimes observed in critically ill COVID-19 patients. The corticosteroid can be used for all age of patients, i.e., children, adults, the elderly and pregnant or breastfeeding women. Current management strategies and guidelines published by NIH recommend the use of corticosteroids alone or in combination for moderate, severe and critical infected COVID-19 patients, who are hospitalized and require supplemental oxygen. However, the use of corticosteroids is strictly prohibited for asymptomatic/presymptomatic mild and moderate infections of COVID-19 patients, who require supplemental oxygen but who do not require oxygen delivery. Another opinion about use of corticosteroids in COVID-19 is somehow different, i.e., some scientific reports consider it controversial due to its enormous side effects such as increased mortality, slow clearance of viral RNA from the respiratory tract, obstructed clearance of viral RNA from blood, psychosis, induced diabetes, avascular necrosis in survivors, induced lung damage or shock. While considering the fact of their side effects, some scientific reports support the application of corticosteroids at low-to-average dose for a shorter duration as it reduces the death rate and minimizes the duration of hospitalization for seriously ill patients with COVID-19 without showing secondary infection and other adverse effects. In conclusion, corticosteroid drugs are beneficial in COVID-19 with some limitations; however, some additional clinical studies are required to establish their role in the treatment of COVID-19 patients.
Future prospect and future research
WHO has approved dexamethasone as the first corticosteroid drug used for the treatment of critically ill patients with COVID-19 necessitating oxygen or ventilator assistance to reduce mortality. Methylprednisolone and hydrocortisone are other drugs belonging to the class of corticosteroids, which have exhibited promising results in lowering mortalities. The corticosteroids open the new door, and future research may concentrate on the development of known and novel corticosteroids analogs for the treatment of COVID-19 patients. The use of corticosteroid for the treatment of COVID-19 treatment is controversial, unclear needs more scientific evidence and may be studied further. The use of systemic corticosteroids for longer duration and its effect on death rate and functional consequence in COVID-19 patients is unknown and will be the subject of future investigations. The use of corticosteroids in combination with other potent drugs found effective against COVID-19 such as immunomodulators: interferon-β, peginterferon alpha-2a and -2b, tocilizumab and BMS-986253; antiviral drugs: favipiravir, remdesivir, ribavirin, triazavirin and umifenovir; antiparasitic drugs: chloroquine, hydroxychloroquine and mefloquine; antibiotics: teicoplanin, oritavancin, dalbavancin, monensin and azithromycin need to be studied to evaluate how these drugs interact/potentiate/decrease with effect of corticosteroids. Moreover, the effect and efficacy of corticosteroids also need to be established when used alone versus in combination with the aforementioned drugs. Additionally, scientists are also required to further study about various uncertainties including steroid preparation, dosing, maximum dose duration and corticosteroids effect on viral replication for finding out a better treatment option for COVID-19 patients.
Availability of data and materials
All the data generated and analyzed during the study are included in the manuscript.
World Health Organization
Severe Acute Respiratory Syndrome Coronavirus 2
Middle East Respiratory Syndrome Coronavirus
Intensive Care Unit
Chronic Obstructive Pulmonary Disease
Acute Respiratory Distress Syndrome
Extracorporeal Membrane Oxygenation
Cytokine Storm Syndrome
Osteonecrosis of the Femoral Head
WHO Organization. Coronavirus disease 2019 (COVID-19): situation report, 72. www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports (2020).
Wu Z, McGoogan JM (2020) Characteristics of and important lessons from the Coronavirus Disease 2019 (COVID-19) outbreak in China: Summary of a report of 72 314 cases from the Chinese Center for Disease Control and Prevention. JAMA 323(13):1239–1242. https://doi.org/10.1001/jama.2020.2648
Veronese N, Demurtas J, Yang L, Tonelli R, Barbagallo M, Lopalco P, Lagolio E, Celotto S, Pizzol D, Zou L, Tully MA, Ilie PC, Trott M, López-Sánchez GF, Smith L (2020) Use of corticosteroids in Coronavirus Disease 2019 Pneumonia: a systematic review of the literature. Front Med 7:170. https://doi.org/10.3389/fmed.2020.00170
Wang C, Horby PW, Hayden FG, Gao GF (2020) A novel coronavirus outbreak of global health concern. Lancet 395(10223):470–473. https://doi.org/10.1016/S0140-6736(20)30185-9
Chan JF-W, Yuan S, Kok K-H, To KK-W, Chu H, Yang J, Xing F, Liu J, Yip CC-Y, Poon RW-S (2020) A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster. Lancet 395(10223):514–523. https://doi.org/10.1016/S0140-6736(20)30154-9
Weiss SR, Navas-Martin S (2005) Coronavirus pathogenesis and the emerging pathogen severe acute respiratory syndrome coronavirus. Microbiol Mol Biol Rev 69(4):635–664. https://doi.org/10.1128/MMBR.69.4.635-664.2005
Shereen MA, Khan S, Kazmi A, Bashir N, Siddique R (2020) COVID-19 infection: origin, transmission, and characteristics of human coronaviruses. J Adv Res 24:91–98. https://doi.org/10.1016/j.jare.2020.03.005
Zhong N, Zheng B, Li Y, Poon L, Xie Z, Chan K, Li P, Tan S, Chang Q, Xie J (2003) Epidemiology and cause of severe acute respiratory syndrome (SARS) in Guangdong, People’s Republic of China, in February, 2003. Lancet 362(9393):1353–1358. https://doi.org/10.1016/s0140-6736(03)14630-2
Wang N, Shi X, Jiang L, Zhang S, Wang D, Tong P, Guo D, Fu L, Cui Y, Liu X (2013) Structure of MERS-CoV spike receptor-binding domain complexed with human receptor DPP4. Cell Res 23(8):986–993. https://doi.org/10.1038/cr.2013.92
Lai C-C, Shih T-P, Ko W-C, Tang H-J, Hsueh P-R (2020) Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and coronavirus disease-2019 (COVID-19): the epidemic and the challenges. Int J Antimicrob Agents 55(3):105924. https://doi.org/10.1016/j.ijantimicag.2020.105924
Yang Y, Islam MS, Wang J, Li Y, Chen X (2020) Traditional Chinese medicine in the treatment of patients infected with 2019-New Coronavirus (SARS-CoV-2): a review and perspective. Int J Biol Sci 16(10):1708–1717. https://doi.org/10.7150/ijbs.45538
Beigel JH, Tomashek KM, Dodd LE, Mehta AK, Zingman BS, Kalil AC, Hohmann E, Chu HY, Luetkemeyer A, Kline S, Lopez de Castilla D, Finberg RW, Dierberg K, Tapson V, Hsieh L, Patterson TF, Paredes R, Sweeney DA, Short WR, Touloumi G, Lye DC, Ohmagari N, Oh M-d, Ruiz-Palacios GM, Benfield T, Fätkenheuer G, Kortepeter MG, Atmar RL, Creech CB, Lundgren J, Babiker AG, Pett S, Neaton JD, Burgess TH, Bonnett T, Green M, Makowski M, Osinusi A, Nayak S, Lane HC (2020) Remdesivir for the treatment of COVID-19-preliminary report. N Engl J Med 383:1813–1826. https://doi.org/10.1056/NEJMoa2007764
Li H, Liu S-M, Yu X-H, Tang S-L, Tang C-K (2020) Coronavirus disease 2019 (COVID-19): current status and future perspectives. Int J Antimicrob Agents 55(5):105951. https://doi.org/10.1016/j.ijantimicag.2020.105951
Nussey S, Whitehead S (2001) Endocrinology: an integrated approach. BIOS Scientific Publishers, Oxford
Stockman LJ, Bellamy R, Garner P (2006) SARS: systematic review of treatment effects. PLoS Med 3(9):e343–e343. https://doi.org/10.1371/journal.pmed.0030343
Yu WC, Hui DSC, Chan-Yeung M (2004) Antiviral agents and corticosteroids in the treatment of severe acute respiratory syndrome (SARS). Thorax 59(8):643. https://doi.org/10.1136/thx.2003.017665
Petersen MW, Meyhoff TS, Helleberg M, Kjær M-BN, Granholm A, Hjortsø CJS, Jensen TS, Møller MH, Hjortrup PB, Wetterslev M, Vesterlund GK, Russell L, Jørgensen VL, Tjelle K, Benfield T, Ulrik CS, Andreasen AS, Mohr T, Bestle MH, Poulsen LM, Hitz MF, Hildebrandt T, Knudsen LS, Møller A, Sølling CG, Brøchner AC, Rasmussen BS, Nielsen H, Christensen S, Strøm T, Cronhjort M, Wahlin RR, Jakob S, Cioccari L, Venkatesh B, Hammond N, Jha V, Myatra SN, Gluud C, Lange T, Perner A (2020) Low-dose hydrocortisone in patients with COVID-19 and severe hypoxia (COVID STEROID) trial—protocol and statistical analysis plan. Acta Anaesthesiol Scand 64(9):1365–1375. https://doi.org/10.1111/aas.13673
Horby P, Lim WS, Emberson J, Mafham M, Bell J, Linsell L, Staplin N, Brightling C, Ustianowski A, Elmahi E, Prudon B, Green C, Felton T, Chadwick D, Rege K, Fegan C, Chappell LC, Faust SN, Jaki T, Jeffery K, Montgomery A, Rowan K, Juszczak E, Baillie JK, Haynes R, Landray MJ (2020) Effect of dexamethasone in hospitalized patients with COVID-19: preliminary report. medRxiv. https://doi.org/10.1101/2020.06.22.20137273
Schultze A, Walker AJ, MacKenna B, Morton CE, Bhaskaran K, Brown JP, Rentsch CT, Williamson EJ, Drysdale H, Croker R, Bacon S, Hulme WJ, Bates C, Curtis HJ, Mehrkar A, Evans D, Inglesby P, Cockburn J, McDonald HI, Tomlinson L, Mathur R, Wing K, Wong AY, Forbes H, Parry J, Hester F, Harper S, Evans SJ, Quint J, Smeeth L, Douglas IJ, Goldacre B (2020) Inhaled corticosteroid use and risk COVID-19 related death among 966,461 patients with COPD or asthma: an OpenSAFELY analysis. medRxiv. https://doi.org/10.1101/2020.06.19.20135491
Nicolau DV, Bafadhel M (2020) Inhaled corticosteroids in virus pandemics: a treatment for COVID-19? Lancet Respir Med 8(9):846–847. https://doi.org/10.1016/S2213-2600(20)30314-3
Cohen EM (1973) Dexamethasone. In: Florey K (ed) Analytical profiles of drug substances, vol 2. Academic Press, Cambridge, pp 163–197
Ericson-Neilsen W, Kaye AD (2014) Steroids: pharmacology, complications, and practice delivery issues. Ochsner J 14(2):203–207
Horby P, Lim WS, Emberson JR, Mafham M, Bell JL, Linsell L, Staplin N, Brightling C, Ustianowski A, Elmahi E, Prudon B, Green C, Felton T, Chadwick D, Rege K, Fegan C, Chappell LC, Faust SN, Jaki T, Jeffery K, Montgomery A, Rowan K, Juszczak E, Baillie JK, Haynes R, Landray MJ (2020) Dexamethasone in hospitalized patients with COVID-19—preliminary report. N Eng J Med. https://doi.org/10.1056/NEJMoa2021436
National Library of Medicine (US), ClinicalTrials.gov identifier: NCT04381936. Randomised evaluation of COVID-19 therapy (RECOVERY). https://clinicaltrials.gov/ct2/show/NCT04381936. Accessed 05 Aug 2021.
Tomazini BM, Maia IS, Cavalcanti AB, Berwanger O, Rosa RG, Veiga VC, Avezum A, Lopes RD, Bueno FR, Silva MVAO, Baldassare FP, Costa ELV, Moura RAB, Honorato MO, Costa AN, Damiani LP, Lisboa T, Kawano-Dourado L, Zampieri FG, Olivato GB, Righy C, Amendola CP, Roepke RML, Freitas DHM, Forte DN, Freitas FGR, Fernandes CCF, Melro LMG, Junior GFS, Morais DC, Zung S, Machado FR, Azevedo LCP, for the COALITION COVID-19 Brazil III Investigators (2020) Effect of dexamethasone on days alive and ventilator-free in patients with moderate or severe acute respiratory distress syndrome and COVID-19: The CoDEX Randomized Clinical Trial. JAMA 324:1307–1316. https://doi.org/10.1001/jama.2020.17021
National Library of Medicine (US), ClinicalTrials.gov identifier: NCT04327401. COVID-19-associated ARDS treated with dexamethasone: alliance Covid-19 Brasil III (CoDEX). https://clinicaltrials.gov/ct2/show/NCT04327401. Accessed 05 Aug 2021.
National Library of Medicine (US), ClinicalTrials.gov identifier: NCT04325061. Efficacy of dexamethasone treatment for patients with ARDS caused by COVID-19 (DEXA-COVID19). https://clinicaltrials.gov/ct2/show/NCT04325061. Accessed 05 Aug 2021.
Feinberg SM, Feinberg AR, Pruzansky J, Fisherman EW (1957) Methylprednisolone (medrol), a potent new anti-inflammatory steroid; therapeutic results in allergic diseases. JAMA 165(12):1560–1562. https://doi.org/10.1001/jama.1957.72980300006009b
Boland EW, Liddle GW (1957) Metabolic and antirheumatic activities of 6-methylprednisolone (medrol). Ann Rheum Dis 16(3):297–306. https://doi.org/10.1136/ard.16.3.297
Vardanyan RS, Hruby VJ (2006) 27—corticosteroids. In: Vardanyan RS, Hruby VJ (eds) Synthesis of essential drugs. Elsevier, Amsterdam, pp 349–363
Wang Y, Jiang W, He Q, Wang C, Wang B, Zhou P, Dong N, Tong Q (2020) A retrospective cohort study of methylprednisolone therapy in severe patients with COVID-19 pneumonia. Signal Transduct Target Ther 5(1):57. https://doi.org/10.1038/s41392-020-0158-2
Liu J, Zheng X, Huang Y, Shan H, Huang J (2020) Successful use of methylprednisolone for treating severe COVID-19. J Allergy Clin Immunol 146(2):325–327. https://doi.org/10.1016/j.jaci.2020.05.021
National Library of Medicine, ClinicalTrials.gov identifier (NCT number): NCT04273321. https://clinicaltrials.gov/ct2/show/NCT04273321.
Corral L, Bahamonde A, delas Revillas FA, Gomez-Barquero J, Abadia-Otero J, Garcia-Ibarbia C, Mora V, Cerezo-Hernandez A, Hernandez JL, Lopez-Muniz G, Hernandez-Blanco F, Cifrian JM, Olmos JM, Carrascosa M, Farinas MC, Riancho JA (2020) GLUCOCOVID: a controlled trial of methylprednisolone in adults hospitalized with COVID-19 pneumonia. medRxiv. https://doi.org/10.1101/2020.06.17.20133579
Jeronimo CMP, Farias MEL, Val FFA, Sampaio VS, Alexandre MAA, Melo GC, Safe IP, Borba MGS, Abreu-Netto RL, Maciel ABS, Neto JRS, Oliveira LB, Figueiredo EFG, Dinelly KMO, Rodrigues MGA, Brito M, Mourao MPG, Pivoto João GA, Hajjar LA, Bassat Q, Romero GAS, Naveca FG, Vasconcelos HL, Tavares MA, Brito-Sousa JD, Costa FTM, Nogueira ML, Baía-da-Silva D, Xavier MS, Monteiro WM, Lacerda MVG, the Metcovid Team (2020) Methylprednisolone as adjunctive therapy for patients hospitalized with COVID-19 (Metcovid): a randomised, double-blind, phase IIb, placebo-controlled trial. Clin Infect Dis 72:e373–e381. https://doi.org/10.1093/cid/ciaa1177
National Library of Medicine (US), ClinicalTrials.gov identifier: NCT04244591. Glucocorticoid therapy for COVID-19 critically ill patients with severe acute respiratory failure. https://www.clinicaltrials.gov/ct2/show/NCT04244591.
National Library of Medicine (US), ClinicalTrials.gov identifier: NCT04343729. Methylprednisolone in the treatment of patients with signs of severe acute respiratory syndrome in COVID-19 (MetCOVID). https://clinicaltrials.gov/ct2/show/NCT04343729.
National Library of Medicine (US), ClinicalTrials.gov identifier: NCT04348305. Hydrocortisone for COVID-19 and severe hypoxia (COVID STEROID). https://clinicaltrials.gov/ct2/show/NCT04348305.
Angus DC, Berry S, Lewis RJ, Al-Beidh F, Arabi Y, van Bentum-Puijk W, Bhimani Z, Bonten M, Broglio K, Brunkhorst F, Cheng AC, Chiche JD, De Jong M, Detry M, Goossens H, Gordon A, Green C, Higgins AM, Hullegie SJ, Kruger P, Lamontagne F, Litton E, Marshall J, McGlothlin A, McGuinness S, Mouncey P, Murthy S, Nichol A, O’Neill GK, Parke R, Parker J, Rohde G, Rowan K, Turner A, Young P, Derde L, McArthur C, Webb SA (2020) The REMAP-CAP (Randomized Embedded Multifactorial Adaptive Platform for Community-acquired Pneumonia) Study. Rationale and Design. Ann Am Thorac Soc 17(7):879–891. https://doi.org/10.1513/AnnalsATS.202003-192SD
The Writing Committee for the R-CAPI (2020) Effect of hydrocortisone on mortality and organ support in patients with severe COVID-19: the REMAP-CAP COVID-19 Corticosteroid Domain Randomized Clinical Trial. JAMA 324:1317–1329. https://doi.org/10.1001/jama.2020.17022
National Library of Medicine (US), ClinicalTrials.gov identifier: NCT02735707. Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community-Acquired Pneumonia (REMAP-CAP). https://clinicaltrials.gov/ct2/show/NCT02735707.
Dequin P-F, Heming N, Meziani F, Plantefève G, Voiriot G, Badié J, François B, Aubron C, Ricard J-D, Ehrmann S, Jouan Y, Guillon A, Leclerc M, Coffre C, Bourgoin H, Lengellé C, Caille-Fénérol C, Tavernier E, Zohar S, Giraudeau B, Annane D, Le Gouge A, for the CAPE COVID Trial Group and the CRICS-TriGGERSep Network (2020) Effect of hydrocortisone on 21-day mortality or respiratory support among critically ill patients with COVID-19: a randomized clinical trial. JAMA 324:1298–1306. https://doi.org/10.1001/jama.2020.16761
National Library of Medicine (US), ClinicalTrials.gov identifier: NCT02517489. Community-acquired pneumonia: Evaluation of corticosteroids (CAPE_COD). https://clinicaltrials.gov/ct2/show/NCT02517489.
Keller MJ, Kitsis EA, Arora S, Chen JT, Agarwal S, Ross MJ, Tomer Y, Southern W (2020) Effect of systemic glucocorticoids on mortality or mechanical ventilation in patients with COVID-19. J Hosp Med 15(8):489–493. https://doi.org/10.12788/jhm.3497
Bozzette SA, Sattler FR, Chiu J, Wu AW, Gluckstein D, Kemper C, Bartok A, Niosi J, Abramson I, Coffman J et al (1990) A controlled trial of early adjunctive treatment with corticosteroids for Pneumocystis carinii pneumonia in the acquired immunodeficiency syndrome. California Collaborative Treatment Group. N Engl J Med 323(21):1451–1457. https://doi.org/10.1056/nejm199011223232104
National Institute of Health (2021) Therapeutic management of hospitalized adults with COVID-19. https://www.covid19treatmentguidelines.nih.gov/management/clinical-management/hospitalized-adults--therapeutic-management/. Accessed 13 July 2021.
Matsuyama S, Kawase M, Nao N, Shirato K, Uijke M, Kamitani W, Shimojima M, Fukushi S (2020) The inhaled corticosteroid ciclesonide blocks coronavirus RNA replication by targeting viral NSP15. bioRxiv. https://doi.org/10.1101/2020.03.11.987016
Kumar K, Hinks TSC, Singanayagam A (2020) Treatment of COVID-19 exacerbated asthma: should systemic corticosteroids be used? Am J Physiol Lung Cell Mol Physiol 318:L1244–L1247. https://doi.org/10.1152/ajplung.00144.2020
Choi YJ, Park JY, Lee HS, Suh J, Song JY, Byun MK, Cho JH, Kim HJ, Lee J-H, Park J-W, Park HJ (2021) Effect of asthma and asthma medication on the prognosis of patients with COVID-19. Eur Respir J 57:2002226. https://doi.org/10.1183/13993003.02226-2020
Benfield T, Bodilsen J, Brieghel C, Harboe ZB, Helleberg M, Holm C, Israelsen SB, Jensen J, Jensen TØ, Johansen IS, Johnsen S, Madsen BL, Lundgren J, Meyer CN, Mohey R, Pedersen LM, Nielsen H, Nielsen SL, Obel N, Omland LH, Podlekareva D, Poulsen BK, Ravn P, Sandholdt H, Starling J, Storgaard M, Søborg C, Søgaard OS, Tranborg T, Wiese L, Christensen HR (2021) Improved survival among hospitalized patients with COVID-19 treated with remdesivir and dexamethasone. A nationwide population-based cohort study. Clin Infect Dis. https://doi.org/10.1093/cid/ciab536
Alkofide H, Almohaizeie A, Almuhaini S, Alotaibi B, Alkharfy KM (2021) Tocilizumab and systemic corticosteroids in the management of COVID-19 patients: a systematic review and meta-analysis. Int J Infect Dis. https://doi.org/10.1016/j.ijid.2021.07.021
Xiong M, Liang X, Wei YD (2020) Changes in blood coagulation in patients with severe coronavirus disease 2019 (COVID-19): a meta-analysis. Br J Haematol 189:1050–1052. https://doi.org/10.1111/bjh.16725
National Institute of Health. Kinase inhibitors: Baricitinib and other Janus kinase inhibitors, and Bruton’s tyrosine kinase inhibitors (2021). https://www.covid19treatmentguidelines.nih.gov/therapies/immunomodulators/kinase-inhibitors. Accessed 04 Aug 2021.
National Institute of Health. Corticosteroids (2021). https://www.covid19treatmentguidelines.nih.gov/therapies/immunomodulators/corticosteroids/. Accessed 04 Aug 2021.
Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, Qiu Y, Wang J, Liu Y, Wei Y, Xia Ja YuT, Zhang X, Zhang L (2020) Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet 395(10223):507–513. https://doi.org/10.1016/S0140-6736(20)30211-7
Wang D, Hu B, Hu C, Zhu F, Liu X, Zhang J, Wang B, Xiang H, Cheng Z, Xiong Y, Zhao Y, Li Y, Wang X, Peng Z (2020) Clinical characteristics of 138 hospitalized patients with 2019 novel Coronavirus-infected pneumonia in Wuhan. China JAMA 323(11):1061–1069. https://doi.org/10.1001/jama.2020.1585
Yang JW, Yang L, Luo RG, Xu JF (2020) Corticosteroid administration for viral pneumonia: COVID-19 and beyond. Clin Microbiol Infect 26(9):1171–1177. https://doi.org/10.1016/j.cmi.2020.06.020
Isidori AM, Arnaldi G, Boscaro M, Falorni A, Giordano C, Giordano R, Pivonello R, Pofi R, Hasenmajer V, Venneri MA, Sbardella E, Simeoli C, Scaroni C, Lenzi A (2020) COVID-19 infection and glucocorticoids: update from the Italian society of endocrinology expert opinion on steroid replacement in adrenal insufficiency. J Endocrinol 43(8):1141–1147. https://doi.org/10.1007/s40618-020-01266-w
Singh AK, Majumdar S, Singh R, Misra A (2020) Role of corticosteroid in the management of COVID-19: a systemic review and a clinician’s perspective. Diabetes Metab Synd 14(5):971–978. https://doi.org/10.1016/j.dsx.2020.06.054
Ni YN, Chen G, Sun J, Liang BM, Liang ZA (2019) The effect of corticosteroids on mortality of patients with influenza pneumonia: a systematic review and meta-analysis. Crit Care 23(1):99. https://doi.org/10.1186/s13054-019-2395-8
Arabi YM, Mandourah Y, Al-Hameed F, Sindi AA, Almekhlafi GA, Hussein MA, Jose J, Pinto R, Al-Omari A, Kharaba A, Almotairi A, Al Khatib K, Alraddadi B, Shalhoub S, Abdulmomen A, Qushmaq I, Mady A, Solaiman O, Al-Aithan AM, Al-Raddadi R, Ragab A, Balkhy HH, Al Harthy A, Deeb AM, Al Mutairi H, Al-Dawood A, Merson L, Hayden FG, Fowler RA (2018) Corticosteroid therapy for critically ill patients with middle East respiratory syndrome. Am J Respir Crit 197(6):757–767. https://doi.org/10.1164/rccm.201706-1172OC
Lee N, Allen Chan KC, Hui DS, Ng EK, Wu A, Chiu RW, Wong VW, Chan PK, Wong KT, Wong E, Cockram CS, Tam JS, Sung JJ, Lo YM (2004) Effects of early corticosteroid treatment on plasma SARS-associated Coronavirus RNA concentrations in adult patients. J Clin Virol 31(4):304–309. https://doi.org/10.1016/j.jcv.2004.07.006
Lee DT, Wing YK, Leung HC, Sung JJ, Ng YK, Yiu GC, Chen RY, Chiu HF (2004) Factors associated with psychosis among patients with severe acute respiratory syndrome: a case–control study. Clin Infect Dis 39(8):1247–1249. https://doi.org/10.1086/424016
Xiao JZ, Ma L, Gao J, Yang ZJ, Xing XY, Zhao HC, Jiao JS, Li GW (2004) Glucocorticoid-induced diabetes in severe acute respiratory syndrome: the impact of high dosage and duration of methylprednisolone therapy. Zhonghua Nei Ke Za Zhi 43(3):179–182
Li YM, Wang SX, Gao HS, Wang JG, Wei CS, Chen LM, Hui WL, Yuan SL, Jiao ZS, Yang Z, Su B (2004) Factors of avascular necrosis of femoral head and osteoporosis in SARS patients’ convalescence. Zhonghua Yi Xue Za Zhi 84(16):1348–1353. https://doi.org/10.3760/j:issn:0376-2491.2004.16.014
Russell CD, Millar JE, Baillie JK (2020) Clinical evidence does not support corticosteroid treatment for 2019-nCoV lung injury. Lancet 395(10223):473–475. https://doi.org/10.1016/S0140-6736(20)30317-2
Shang L, Zhao J, Hu Y, Du R, Cao B (2020) On the use of corticosteroids for 2019-nCoV pneumonia. Lancet 395(10225):683–684. https://doi.org/10.1016/S0140-6736(20)30361-5
Salinas M, Andino P, Palma L, Valencia J, Figueroa E, Ortega J (2021) Early use of corticosteroids in non-critical patients with COVID-19 pneumonia (PREDCOVID): a structured summary of a study protocol for a randomised controlled trial. Trials 22:92. https://doi.org/10.1186/s13063-021-05046-6
Saiz-Rodríguez M, Pena T, Lázaro L, González A, Martinez A, Cordero JA, Vicente JT, Richard F, Coma MJ, Frutos M, Labrador J, Pueyo A (2020) Outpatient treatment of COVID-19 with steroids in the phase of mild pneumonia without the need for admission as an opportunity to modify the course of the disease: a structured summary of a randomised controlled trial. Trials 2:632. https://doi.org/10.1186/s13063-020-04575-w
Shirbhate E, Patel P, Patel VK, Veerasamy R, Sharma PC, Sinha BN, Rajak H (2020) Synthetic and semi-synthetic drugs as promising therapeutic option for the treatment of COVID-19. Min Rev Med Chem 21:1004–1016. https://doi.org/10.2174/1389557520666201204162103
Tang C, Wang Y, Lv H, Guan Z, Gu J (2020) Caution against corticosteroid-based COVID-19 treatment. Lancet 395(10239):1759–1760. https://doi.org/10.1016/S0140-6736(20)30749-2
All authors wish to express their gratitude to Guru Ghasidas University, Bilaspur, India, for providing library facilities. The permission to access electronic database available at National Medical Library, New Delhi, is also acknowledged.
The first author Vijay K Patel is grateful to Indian Council for Medical Research (ICMR), New Delhi, for providing financial support in the form of Research Associateship (Grant Number: 45/05/2019-PHA-BMS). One of the authors, Harish Rajak, is thankful to ICMR, New Delhi, India for providing financial assistance in the form of an Extra-Mural Research project (ICMR/2020/2817).
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Patel, V.K., Shirbhate, E., Patel, P. et al. Corticosteroids for treatment of COVID-19: effect, evidence, expectation and extent. Beni-Suef Univ J Basic Appl Sci 10, 78 (2021). https://doi.org/10.1186/s43088-021-00165-0