Abstract
Corticosteroids have potent anti-inflammatory and immunosuppressive effects. Recently, these medications have gained importance in the treatment of severe COVID-19. Here we present data demonstrating a marked (10-fold) increase in frequency of candidemia in hospitalized patients with COVID-19 receiving corticosteroids in Brazil. Overall mortality was 72.7%, despite antifungal therapy. Physicians should be aware of the potential risk for candidemia among severely ill COVID-19 patients receiving high-doses of corticosteroids.
Keywords: COVID-19, candidemia, steroids
1. Introduction
Recent trials have demonstrated the benefit of corticosteroids in the treatment of severe COVID-19 [1,2,3,4], which is likely to result in a marked increase in steroids prescriptions in clinical practice. Steroids are known to increase the risks for a variety of infections, but data on serious fungal diseases in critically ill patients receiving corticosteroids for COVID-19 remains scarce. In the Randomized, Embedded, Multifactorial, Adaptive Platform trial for Community-Acquired Pneumonia (REMAP-CAP), despite the benefits observed with hydrocortisone treatment, the authors demonstrated a higher number of serious adverse events in both hydrocortisone groups [2], even though only one patient had documented fungemia in the trial.
The relationship between corticosteroid treatment and fungal infections is well established. Corticosteroids may promote fungal growth in vitro [5]. Moreover, use of corticosteroids have been associated with increased risk for most serious fungal diseases including candidemia, invasive aspergillosis, fusariosis, and mucormycosis [6]. He we present provocative results of a series of candidemia cases following COVID-19, in which the use of steroids was suggested as the main risk factor for fungal infection.
2. Materials and Methods
This was a case series of candidemia following COVID-19 in two tertiary care hospitals located in Porto Alegre, Southern Brazil. COVID-19 was diagnosed based on a positive real time PCR test in a patient with appropriate signs and symptoms, according to the criteria established by the Brazilian National as well as the Regional Sanitary Surveillance agencies [7,8]. Candidemia was defined as the presence of one or more Candida species in blood cultures, in patients with temporally clinical manifestations. Patients were included only once in the study. Yeasts were identified at the species level either by Phoenix Automated Microbiology System (Becton Dickinson, Franklin Lakes, NJ, USA) or Vitek-2 System (bioMérieux, Marcy-l’Étoile, France).
Data were retrospectively collected in the year 2020 between March 16 (date of the first COVID-19 admission in the participant hospitals) and August 31. Data were obtained from infection control records, as well as patients’ electronic charts. The Chi-square test with Yates correction was used to compare proportions—WINPEPI v. 11.65 (Abramson, JH) [9], and p values of < 5% were considered statistically significant.
3. Results
Since the beginning of the COVID-19 pandemic, an increase in the frequency of candidemia was observed in two of the hospitals in which authors (CVWR, and RC) were based. During the period of study, incidence of candidemia was 1.43 (hospital 1) and 1.15 (hospital 2) in patients who did not have COVID-19, both per 1000 patients-day. These frequencies were unaltered in comparison to previous year. In contrast, the incidence of candidemia in patients with COVID-19 were 11.83 (hospital 1) and 10.23 (hospital 2) per 1000 patients-day, during the same period (p = 0.001 in comparison to the prevalence of candidemia in non-COVID-19 patients). In patients with COVID-19, all cases of candidemia occurred after the use of high-doses of corticosteroids for severe disease. Table 1 summarizes the main clinical findings for these 11 patients. These were mostly male (n = 7; 63.6%), with a median age of 59 years-old (interquartile range, IQR, 49–70 years-old), and a median Charlson score of 4 (IQR, 1–4). Four patients had diabetes, and one was HIV-positive. Ten patients (90.9%) had central venous catheters in place. These were all non-surgical patients with limited antibiotic exposure, and additional risk factors for candidemia were virtually absent. Candidemia occurred in intensive care for 8/11 patients (72.7%), and after a median length of admission to the intensive care unit of 8.7 days. Overall mortality of candidemia following steroid use in COVID-19 was 72.7% (8/11), while 3/11 patients (22.3%) were discharged from the hospital. Overall mortality in COVID-19 patients who did not develop candidemia was 17.7% (hospital 1) and 22.0% (hospital 2).
Table 1.
Pt | Age/Sex | Underlying Conditions | Date of Admission | COVID-19 Management | ICU Days until Isolation/Candida Species | Risk Factors for Candidemia | Treatment and Outcome |
---|---|---|---|---|---|---|---|
1 | 44/M | DM, dyslipidemia, psoriasis, schizophrenia | 13 April 2020 | Chloroquine 4 d AZI, IVE MPD 1 g qd 2 d, then 80 mg bid 9 d and reduction |
No ICU admission C. albicans |
DM CVC 20 days PTZ 5 days MEM 8 days |
AFG Discharged |
2 | 71/F | HT, coronary artery disease | 14 May 2020 | AZI MPD 62.5 mg bid 2 d |
1 day C. glabrata |
CVC 7 days Ceftriaxone 2 d. PTZ 7 days |
Death prior to treatment |
3 | 69/F | DM, HT, obesity, cardiac failure, COPD |
16 May 2020 | HCQ 1 day a/AZI MPD 62.5 mg tid 7 d |
9 days C. glabrata |
DM, CVC 9 days Oxacillin 4 days PTZ 7 days |
AFG Death |
4 | 37/F | Asthma | 1 July 2020 | AZI, IVE MPD 62.5 mg tid 2 d., then DXM 6 mg qd 3 d., MPD 62.5 mg quad 8 d |
8 days C. albicans |
CVC 8 days AMC 5 days PTZ 7 days |
AMB-d FLC Death |
5 | 87/F | HT, atrial fibrillation |
10 July 2020 | AZI, IVE MPD 62.5 mg tid 2 d., bid 2 d., and qd 3 d |
6 days C. tropicalis |
CVC 7 days PTZ 6 days |
AFG Death |
6 | 66/M | HT | 26 July 2020 | AZI, IVE MPD 1 g qd 2 d., then 500 mg qd 1 day, DXM 6 mg qd 9 d |
14 days C. albicans |
CVC 14 days Cefuroxime 5 d. PTZ 8 days MEM 3 days |
AFG Discharged |
7 | 91/M | Asthma | 29 July 2020 | MPD 250 mg qd 1 d., then DXM 6 mg qd 7 d | 7 days C. albicans |
CVC 7 days Amoxicillin 5 d. PTZ 7 days |
AFG Death |
8 | 54/M | DM, HT, obesity, Raynaud synd., depression |
8 August 2020 | AZI DXM 6 mg qd 5 d |
Day of ICU admission C. albicans |
DM AMC 6 days PTZ 2 days |
FLC Discharged |
9 | 41/M | HIV, HCV, myocardiopathy | 15 August 2020 | Prednisone 40 mg qd 4 d | Day of ICU admission C. albicans |
HIV CVC 10 days |
FLC Death |
10 | 57/M | DM, HT | 23 July 2020 b | AZI DXM 6 mg qd 10 d |
22 days C. albicans |
DM CVC 22 days AMC 5 days PTZ 8 days |
Voriconazole AFG Death |
11 | 59/M | HT, chronic renal disease, mental impairment | 23 August 2020 | DXM 6 mg qd 3 d., then Hydrocortisone 50 mg qid 4 d | 3 days C. albicans |
CVC 4 days AMC 4 days |
FLC Death |
Abbreviations: F, female; M, male; Pt, patient; COPD, chronic obstructive pulmonary disease; DM, Diabetes mellitus; HCV, hepatitis C virus; HT, hypertension; AZI, Azithromycin; DMX, dexamethasone; days, d.; HQC, hydroxychloroquine; IVE, Ivermectin; ICU, intensive care unit; MPD, methylprednisolone; AMC, Amoxicillin/clavulanate; AMB-d, Amphotericin B deoxycholate; AFG, Anidulafungin; CVC central venous catheter; FLC, Fluconazole; MEM, Meropenem; PTZ, Piperacillin/tazobactam. a Hydroxychloroquine was stopped because of cardiac arrythmia. b COVID-19 symptoms began after hospital admission.
4. Discussion
In this small case series, we observed a 10-fold increase in the frequency of candidemia in two medical centers in Brazil, in COVID-19 patients taking high doses of steroids. The in-hospital mortality among COVID-19 patients in the study was similar to the published findings of others [10], and even lower than other studies conducted in the same region in Brazil [11]. He observed an impressively high mortality in these patients. It should be noted, however, that our study is limited—mostly by its small sample size, in addition to its retrospective design and its short duration of observation.
Current data suggest low frequency of both bacterial and fungal infections in COVID-19 cases presenting early at the hospital [12]. However, the use of steroids may dramatically change such scenarios. Fungal infections are known to occur after COVID-19, with most studies so far focusing on invasive aspergillosis [13]. In our perspective, the real frequencies and organisms associated with COVID-19 superinfections must be further evaluated and might be increased by immunosuppressive treatments.
In conclusion, steroids are a lifesaving treatment option in COVID-19 pneumonia, but the right dose and timing of such interventions remain to be determined. High corticosteroid doses might be associated with severe superinfections. Physicians should be aware of the potential increase in the frequency of candidemia in patients with COVID-19 treated with corticosteroids.
Author Contributions
Conceptualization, C.V.W.R., A.C.P.; investigation, C.V.W.R., R.C.; writing—original draft preparation, C.V.W.R., A.C.P.; writing—reviewing and editing C.V.W.R., R.C., A.C.P. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Conflicts of Interest
Pasqualotto has received research grants from Gilead, Pfizer, and MSD. He has also given paid talks on behalf of Gilead, Pfizer, MSD, Astellas, United Medical, Teva, and IMMY.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.The RECOVERY Collaborative Group. Horby P., Lim W.S., Emberson J.R., Mafham M., Bell J.L., Linsell L., Staplin N., Brightling C., Ustianowski A., et al. Dexamethasone in hospitalized patients with Covid-19-Preliminary report. N. Engl. J. Med. 2020 doi: 10.1056/nejmoa2021436. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.The Writing Committee for the REMAP-CAP Investigators. Angus D.C., Derde L., Al-Beidh F., Annane D., Arabi Y., Beane A., Van Bentum-Puijk W., Berry L., Bhimani Z., et al. Effect of hydrocortisone on mortality and organ support in patients with severe COVID-19. JAMA. 2020;324:1317. doi: 10.1001/jama.2020.17022. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Tomazini B.M., Maia I.S., Cavalcanti A.B., Berwanger O., Rosa R.G., Veiga V.C., Avezum A., Lopes R.D., Bueno F.R., Silva M.V.A.O., et al. Effect of Dexamethasone on days alive and ventilator-free in patients with moderate or severe acute respiratory distress syndrome and COVID-19. JAMA. 2020;324:1307. doi: 10.1001/jama.2020.17021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Dequin P.-F., Heming N., Meziani F., Plantefève G., Voiriot G., Badié J., François B., Aubron C., Ricard J.-D., Ehrmann S., et al. Effect of hydrocortisone on 21-day mortality or respiratory support among critically ill patients with COVID-19. JAMA. 2020;324:1298. doi: 10.1001/jama.2020.16761. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Ng T.T., Robson G.D., Denning D.W. Hydrocortisone-enhanced grow of Aspergillus spp.: Implications for pathogenesis. Microbiology. 1994;140:2475–2479. doi: 10.1099/13500872-140-9-2475. [DOI] [PubMed] [Google Scholar]
- 6.Lionakis M.S., Kontoyiannis D.P. Glucocorticoids and invasive fungal infections. Lancet. 2003;362:1828–1838. doi: 10.1016/S0140-6736(03)14904-5. [DOI] [PubMed] [Google Scholar]
- 7.Brazilian Health Regulatory Agency—ANVISA . Guidelines for Prevention and Epidemiologic Surveillance of SARS-CoV-2 (COVID-19) Infections within Health Services. Brazilian Health Regulatory Agency—ANVISA; Brasilia, Brazil: 2020. Technical Note GVIMS/GGTES/ANVISA No 07/2020. [Google Scholar]
- 8.Emergency Operations Center in Public Health—COE/SES-RS . Surveillance of Influenza-like Syndrome and Severe Acute Respiratory Syndrome (SARS) Related to COVID-19 Human Infection, Surveillance Systems, Laboratory Network and Testing Strategies. Emergency Operations Center in Public Health—COE/SES-RS; Porto Alegre, Brazil: 2020. Informative Note 24 COE/SES-RS. [Google Scholar]
- 9.Abramson J.H. WINPEPI updated: Computer programs for epidemiologists, and their teaching potential. Epidemiol. Perspect. Innov. 2011;8:1. doi: 10.1186/1742-5573-8-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Zhou F., Yu T., Du R., Fan G., Liu Y., Liu Z., Xiang J., Wang Y., Song B., Gu X., et al. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: A retrospective cohort study. Lancet. 2020;395:1054–1062. doi: 10.1016/S0140-6736(20)30566-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Baqui P., Bica I., Marra V., Ercole A., Van Der Schaar M. Ethnic and regional variations in hospital mortality from COVID-19 in Brazil: A cross-sectional observational study. Lancet Glob. Health. 2020;8:e1018–e1026. doi: 10.1016/S2214-109X(20)30285-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Hughes S., Troise O., Donaldson H., Mughal N., Moore L. Bacterial and fungal coinfection among hospitalized patients with COVID-19: A retrospective cohort study in a UK secondary-care setting. Clin. Microbiol. Infect. 2020;26:1395–1399. doi: 10.1016/j.cmi.2020.06.025. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Lansbury L., Lim B., Baskaran V., Lim W.S. Co-infections in people with COVID-19: A systematic review and meta-analysis. J. Infect. 2020;81:266–275. doi: 10.1016/j.jinf.2020.05.046. [DOI] [PMC free article] [PubMed] [Google Scholar]