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Journal of Fungi logoLink to Journal of Fungi
. 2020 Nov 13;6(4):286. doi: 10.3390/jof6040286

Is the Frequency of Candidemia Increasing in COVID-19 Patients Receiving Corticosteroids?

Cezar V W Riche 1,3, Renato Cassol 2, Alessandro C Pasqualotto 3,4,*
PMCID: PMC7712895  PMID: 33203016

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.

Characteristics of patients who had candidemia following corticosteroid use for severe COVID-19.

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.

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