Viral clearance after early corticosteroid treatment in patients with moderate or severe covid-19

Abstract

The aim of this study was to evaluate the impact of early treatment with corticosteroids on SARS-CoV-2 clearance in hospitalized COVID-19 patients. Retrospective analysis on patients admitted to the San Raffaele Hospital (Milan, Italy) with moderate/severe COVID-19 and availability of at least two nasopharyngeal swabs. The primary outcome was the time to nasopharyngeal swab negativization. A multivariable Cox model was fitted to determine factors associated with nasopharyngeal swab negativization. Of 280 patients included, 59 (21.1%) patients were treated with steroids. Differences observed between steroid users and non-users included the proportion of patients with a baseline PaO2/FiO2 ≤ 200 mmHg (45.8% vs 34.4% in steroids and non-steroids users, respectively; p = 0.023) or ≤ 100 mmHg (16.9% vs 12.7%; p = 0.027), and length of hospitalization (20 vs 14 days; p < 0.001). Time to negativization of nasopharyngeal swabs was similar in steroid and non-steroid users (p = 0.985). According to multivariate analysis, SARS-CoV-2 clearance was associated with age ≤ 70 years, a shorter duration of symptoms at admission, a baseline PaO2/FiO2 > 200 mmHg, and a lymphocyte count at admission > 1.0 × 109/L. SARS-CoV-2 clearance was not associated with corticosteroid use. Our study shows that delayed SARS-CoV-2 clearance in moderate/severe COVID-19 is associated with older age and a more severe disease, but not with an early use of corticosteroids.

Introduction

As of October 26 2020, the ongoing pandemic of severe acute respiratory syndrome-Coronavirus 2 (SARS-CoV-2) has caused more than 43 million cases of Coronavirus disease-19 (COVID-19), resulting in more than 1,150,000 deaths1. Severe forms of COVID-19 are typically characterized by bilateral interstitial pneumonia and hyperactivation of the inflammatory cascade2. Considering the current lack of proven antiviral therapy, several different immunosuppressive agents have been evaluated with the aim of reducing the hyperinflammatory status associated with COVID-19 and improving the patients’ prognosis3.

Corticosteroids are inexpensive and readily available agents that are widely used for their anti-inflammatory effects in patients with respiratory infections. Earlier studies indicated that the use of corticosteroids in patients with SARS and MERS was associated with delayed viral clearance, and no clear benefits in term of survival, length of hospitalization, or use of mechanical ventilation4.

For these reasons, in the initial phase of SARS-CoV-2 pandemic, use of corticosteroids for the management of COVID-19 patients was not recommended. However, findings from non-randomized studies demonstrated a lower mortality in patients with COVID-19 when treated with corticosteroids5, 6. These preliminary findings were confirmed by a recent prospective meta-analysis7, including 7 randomized clinical trials7,8,9,10,11,12 that showed a clear survival benefit in critically ill patients with COVID-19 who received corticosteroids.

According to these findings, World Health Organization (WHO) now recommend systemic corticosteroids for the treatment of patients with severe and critical COVID-1913.

However, very little data on SARS-CoV-2 viral clearance after steroid treatment is currently available14, 15. The aim of this study was to evaluate the impact of an early treatment with corticosteroids on SARS-CoV-2 viral clearance in hospitalized COVID-19 patients.

Results

Two-hundred and eighty patients were included in this study. The median age was 63.5 (53.5–74.0) years, 34% of patients were > 70 years, 78% were males, 92% Caucasian, 3% were active smokers, 74% were overweight, and 66% had at least one comorbidity (including diabetes (18%), hypertension (45%), and any cardiovascular (29%), neoplastic (15%) or respiratory (9%) disease). At hospital admission, COVID-19 associated symptoms had been present for 7 days (4–10), while 36.8% and 13.6% of patients had a PaO2/FiO2 ≤ 200 mmHg or ≤ 100 mmHg, respectively. Serum levels of C-reactive Protein (CRP), lactate dehydrogenase (LDH) and ferritin were 70.9 (28.2–121.6) mg/L, 340 (275–449) U/L, and 1068 (561–1876) ng/mL, respectively; plasma D-dimer levels were 1.01 (0.59–2.05) µg/mL, total lymphocytes were 1.0 (0.8–1.3) × 109/L, and the neutrophils/lymphocytes ratio was 5.0 (3.1–8.6). Baseline characteristics of patients according to steroid use are reported in Table 1.

Table 1 Patients’ characteristics at the time of hospitalization for a moderate or severe COVID-19 infection.

During hospitalization, 12 (4.3%) patients died, 24 (8.6%) were admitted to the intensive care unit (ICU), and 95 (34%) required mechanical ventilation (invasive or non-invasive). Antiretrovirals, hydroxychloroquine, and immunomodulatory agents were administered to 222 (79%), 261 (93%), and 97 (35%) patients, respectively.

Fifty-nine (21.1%) patients were treated with steroids, after a median of 1 day (0–2) since admission, and for a total of 9 (7–16) days. Initially, intravenous methylprednisolone was used in 55 (93.2%) cases, oral prednisone in 3 (5.1%) cases, and intravenous dexamethasone in 1 (1.7%) case of steroid use. Initial steroid methylprednisolone-equivalent dosage was 0.87 (0–51 to 1.0) mg/Kg.

At steroid discontinuation, 44 (74.6%) steroid users were receiving intravenous methylprednisolone, 10 (16.9%) oral prednisone, and 5 (8.5%) intravenous dexamethasone. Methylprednisolone-equivalent dosage was 0.38 (0.21–0.53) mg/Kg.

Differences between steroid users and non-users were observed with regard to the proportion of patients with a baseline PaO2/FiO2 ≤ 200 mmHg (45.8% vs 34.4% in steroids and non-steroids users, respectively; p = 0.023) and ≤ 100 mmHg (16.9% vs 12.7%, p = 0.027), and with regard to the length of hospitalization (20 vs 14 days; p < 0.001). Although steroid users had a higher proportion of severe respiratory impairment at admission than non-users, no significant differences between the two groups were found with regard to mortality (6.8% vs 3.6%; p = 0.29), use of mechanical ventilation (36% vs 34%; p = 0.76), and risk of subsequent infections (10.4% in both groups; p = 0.87). Among 47/59 steroid users without a previous diabetes mellitus diagnosis, 2 (4.3%) steroid users developed new-onset diabetes during hospitalization.

During follow-up, each patient underwent 4 (3–5) consecutive nasopharyngeal swabs. The distribution of follow-up nasopharyngeal swabs, and the proportion of negative samples according to days since first positive swab and use of steroids are reported in Fig. 1. Time to negativization of nasopharyngeal swabs according to the use of steroids, immunomodulatory agents, baseline lymphocyte cell count, PaO2/FiO2, age and days from symptoms occurrence to hospital admission is also shown in Figs. 1 and 2.

Figure 1
figure1

Distribution of follow-up nasopharyngeal swabs according to days since first positive swab and use of steroid (A); time to negativization of nasopharyngeal swab according to the use of steroid (B).

Figure 2
figure2

Time to negativization of nasopharyngeal swab according to: age (A); body mass index (B); days from symptoms to hospital admission (C); PaO2/FiO2 at hospital admission (D); total lymphocytes count at hospital admission (E); use of immunomodulatory drugs (F).

Using multivariate analysis (Table 2), SARS-CoV-2 clearance was associated with age ≤ 70 years (aHR = 1.57, CI 1.11–2.23; p = 0.011), shorter symptoms duration at hospital admission (aHR for 7-days longer = 0.76 (0.61–0.94); p = 0.013), baseline PaO2/FiO2 > 200 mmHg (aHR = 1.42, CI 1.03–1.97; p = 0.035), and a lymphocyte count at admission > 1.0 × 109/L (aHR = 1.55, CI 1.12–2.15; p = 0.009). Use of corticosteroids did not impact on viral clearance (p = 0.162).

Table 2 Multivariable analysis (stepwise Cox proportional hazard model): factors associated with the risk of negativization of nasopharyngeal swab.

Discussion

A concern against the use of corticosteroids in COVID-19 is the potential negative impact of steroids on the control of SARS-CoV-2 viral replication and the consequent delayed viral clearance, as reported in other viral pneumonia4. Our study shows that steroid treatment has no impact on viral clearance in patients with moderate or severe COVID-19. Our results are similar to those reported in two other studies on smaller cohorts of patients14, 15.

In our study, we also observed an association between delayed viral clearance and older age. The characteristic age-related immune decline observed in elderly patients16 may impair their ability to control SARS-CoV-2 infection, potentially explaining the higher risk of viral persistence observed in subjects ≥ 70 years. A delayed viral clearance was also related with a longer duration of symptoms before hospitalization and with respiratory impairment and lymphopenia at admission. All these different factors may reflect a more severe disease and consequently a higher probable viral load in the respiratory tract17.

Moreover, we observed a longer length of hospitalization in steroid-users compared to non-users. We think that this difference may be explained by the higher degree of baseline respiratory impairment, as documented by the higher proportion of patients with PaO2/FiO2 ≤ 200 and ≤ 100, in steroid users.

The pathophysiological mechanism associated with the development of progressive lung damage associated with respiratory failure in COVID-19 is related to an unregulated pro-inflammatory cytokine response18.

At this regard, the steroid anti-inflammatory effect plays a role in mitigating the hyper-inflammatory status that characterizes the disease progression. Currently, randomized clinical trials7,8,9,10,11,12 demonstrated the benefit in overall survival in critically-ill patients with COVID-19 accordingly to this biological mechanism.

Potential concerns regarding the use of steroids in COVID-19 management include side-effects, in particular metabolic disorders and secondary infections. However, in patients with severe/critical illness, the benefit of steroid administration overcome the potential risks.

Our study has several limitations. First, we cannot exclude a potential selection bias, given that the included patients need to have at least two nasopharyngeal swabs. This criterion excluded patients showing a more aggressive course who unfortunately died within a few days of hospital admission (leading also to an underestimation of the number of observed deaths). Second, treatment with steroids was not standardized, and the decision to administer this drug and the timing of administration was at the discretion of the different physicians. This approach might be associated with a potential indication bias.

Third, we had not available data on baseline SARS-CoV-2 viral load (cycle threshold (Ct) values) that might confound the association between corticosteroid treatment and viral clearance.

In conclusion, our study showed that delayed SARS-CoV-2 clearance in moderate/severe COVID-19 was associated with older age and a more severe disease, but not with an early use of corticosteroids. Considering the growing body of scientific evidences5,6,7,8,9,10,11,12 on steroid efficacy in improving survival in COVID-19 patients, our findings may reassure clinicians on the concern of a potential delayed viral clearance.

Methods

For this retrospective analysis, we considered all patients admitted between February 25th 2020 and May 19th 2020 to the Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) San Raffaele (Milan, Italy) with moderate or severe COVID-19, a definite outcome (discharge or death), complete information on therapies administered during hospitalization, and the availability of at least two nasopharyngeal swabs (one at hospital admission and ≥ 1 thereafter).

We obtained data from the COVID-BioB clinical database of the IRCCS San Raffaele Hospital. The study was approved by the Ethics Committee of San Raffaele Hospital (protocol No. 34/int/2020) and was registered on ClinicalTrials.gov (NCT04318366). All patients signed an informed consent form. Our research was in compliance to the Declaration of Helsinki.

COVID-19 was diagnosed in all patients with a SARS-CoV-2 positive real-time reverse-transcriptase polymerase chain reaction (RT-PCR; Roche Cobas Systems) assay result from a nasopharyngeal swab and compatible signs, symptoms, and/or radiological findings. All nasopharyngeal samples were submitted to the San Raffaele Scientific Institute Laboratory for RT-PCR testing, yielding qualitative results (positive or negative).

Moderate COVID-19 was defined as the presence, during hospitalization, of: (1) at least one arterial oxygen partial pressure (PaO2)/fraction inspired oxygen (FiO2) ratio < 300 mmHg, as determined by arterial blood gas analysis; or (2) supplemental oxygen use; or (3) a peripheral saturation of oxygen < 94%.

Severe COVID-19 was defined as: requiring the need of mechanical ventilation (both invasive and non-invasive). Only steroid treatment within 7 days of admission was considered for this analysis. Patients on chronic steroid therapy were excluded.

Use of corticosteroids in patients with COVID-19 was at the discretion of the different medical teams. All corticosteroids were converted to methylprednisolone-equivalent doses and dosing was reported in mg/Kg. Other treatments considered in the analysis included immunomodulatory agents (tocilizumab, sarilumab, mavrilimumab, and anakinra), hydroxychloroquine, and antiretrovirals (lopinavir/ritonavir and darunavir/cobicistat).

The primary outcome of this study was the time to nasopharyngeal swab negativization defined by: (i) the occurrence of two consecutive negative swabs after hospital admission (baseline), in cases of multiple nasopharyngeal swabs; or (ii) the occurrence of a negative swab prior to discharge or death, in cases without multiple nasopharyngeal swabs. In patients treated with corticosteroids, swab negativization (if shown) was attributed to corticosteroid treatment only if it had occurred after steroid introduction.

Statistical analyses

Results were reported as median (interquartile range, IQR) and frequency (%).

Distributions of continuous variables were compared between patients treated with or not treated with steroids using the Wilcoxon rank-sum test or the chi-square/Fisher exact test for categorical variables.

Time to nasopharyngeal swab negativization was estimated by the use of Kaplan–Meier curves; estimates were provided according to different factors and compared by the log-rank test. Follow-up started at baseline and ended at the date of first nasopharyngeal swab negativization, or the date of discharge, or death (whichever occurred first), and was right censored 60 days after baseline owing to the low number of cases thereafter; there were no competing events.

A multivariable Cox proportional hazard model was fitted to determine factors associated with the risk of nasopharyngeal swab negativization; the adjusted hazard ratio (aHR) with the corresponding 95% CI were reported. The considered covariates were fitted as time-fixed and measured at baseline. A backward elimination variable selection algorithm with entry and stay criteria of 0.10 and 0.05, respectively, was applied; adjusted hazard ratios (aHR) of nasopharyngeal swab negativization were reported with the corresponding 95% CI for significant covariates. The assumption of the proportional hazard was examined by use of interactions of the predictors and the function of time; it was confirmed for all the significant covariates.

For the analyses, two-sided p-values < 0.05 were considered statistically significant. All analyses were performed using the SAS Software, release 9.4 (SAS Institute, Cary, NC).

Data availability

The datasets used and analysed during the current study are available from the corresponding author on reasonable request.

References

  1. 1.

    Coronavirus Resource Center. Johns Hopkins University. https://coronavirus.jhu.edu/map.html. (2020).

  2. 2.

    Huang, C. et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 395, 497–506 (2020).

    CAS  Article  Google Scholar 

  3. 3.

    Salvi, R. & Patankar, P. Emerging pharmacotherapies for COVID-19. Biomed. Pharmacother. 128, 11026 (2020).

    Article  Google Scholar 

  4. 4.

    Li, H. et al. Impact of corticosteroid therapy on outcomes of persons with SARS-CoV-2, SARS-CoV, or MERS-CoV infection: a systematic review and meta-analysis. Leukemia 34, 1503–1511 (2020).

    CAS  Article  Google Scholar 

  5. 5.

    Shang, L., Zhao, Y., Hu, Y., Du, R. & Cao, B. On the use of corticosteroids for 2019-nCoV pneumonia. Lancet 395, 683–684 (2020).

    CAS  Article  Google Scholar 

  6. 6.

    Fadel, R. et al. Early short course corticosteroids in hospitalized patients with COVID-19. Clin. Infect. Dis. 71, 2114–2120 (2020).

    CAS  PubMed  Google Scholar 

  7. 7.

    The WHO Rapid Evidence Appraisal for COVID-19 Therapies (REACT) Working Group. Association between administration of systemic corticosteroids and mortality among critically Ill patients with COVID-19. A meta-analysis. JAMA 324, 1330–1341 (2020).

    Article  Google Scholar 

  8. 8.

    Horby, P. et al. RECOVERY Collaborative Group. Dexamethasone in hospitalized patients with Covid-19—preliminary report. N. Engl. J. Med. 1, 4. https://doi.org/10.1056/NEJMoa2021436 (2020).

    Article  Google Scholar 

  9. 9.

    Dequin, P. F. et al. Effect of hydrocortisone on 21-day mortality or respiratory support among critically ill patients with COVID-19: a randomized clinical trial. JAMA 324, 1–9 (2020).

    Article  Google Scholar 

  10. 10.

    Angus, D. C. et al. The REMAP-CAP (Randomized Embedded Multifactorial Adaptive Platform for Community-acquired Pneumonia) study. Ann. Am. Thorac. Soc. 17, 879–891 (2020).

    Article  Google Scholar 

  11. 11.

    The Writing Committee for the REMAP-CAP Investigators. 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 (2020).

    Article  Google Scholar 

  12. 12.

    Tomazini, B. M. et al. 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, 1–11 (2020).

    Article  Google Scholar 

  13. 13.

    https://www.who.int/news-room/feature-stories/detail/who-updates-clinical-care-guidance-with-corticosteroid-recommendations. (2020).

  14. 14.

    Fang, X. et al. Low-dose corticosteroid therapy does not delay viral clearance in patients with COVID-19. J Infect. https://doi.org/10.1016/j.jinf.2020.03.039 (2020).

    Article  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Zha, L. et al. Corticosteroid treatment of patients with coronavirus disease 2019 (COVID-19). Med J Aust. 212, 416–420 (2020).

    Article  Google Scholar 

  16. 16.

    Kumar, R. & Burns, E. A. Age-related decline in immunity: implications for vaccine responsiveness. Expert Rev Vaccines. 7, 467–479 (2008).

    Article  Google Scholar 

  17. 17.

    Zheng, S. et al. Viral load dynamics and disease severity in patients infected with SARS-CoV-2 in Zhejiang province, China, January-March 2020: retrospective cohort study. BMJ 369, m1443 (2020).

    Article  Google Scholar 

  18. 18.

    Siddiqi, H. K. & Mehra, M. R. COVID-19 illness in native and immunosuppressed states: a clinical–therapeutic staging proposal. J. Heart Lung Transplant. 39, 405–407 (2020).

    Article  Google Scholar 

Download references

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Author information

Affiliations

Authors

Consortia

Contributions

V.S. and M.G. conceived the study, collected and reviewed data, wrote the first draft of the manuscript; A.C., P.R.Q., M.R., P.S., M.C., M.T., L.D., A.L. A.Z. and F.C. collected and reviewed data, reviewed and edited the manuscript; A.P. and L.G. collected and reviewed data and performed statistical analyses.

Corresponding author

Correspondence to V. Spagnuolo.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Spagnuolo, V., Guffanti, M., Galli, L. et al. Viral clearance after early corticosteroid treatment in patients with moderate or severe covid-19. Sci Rep 10, 21291 (2020). https://doi.org/10.1038/s41598-020-78039-1

Download citation

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing