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Candida spp. co-infection in COVID-19 patients with severe pneumonia: Prevalence study and associated risk factors. | LitMetric

AI Article Synopsis

  • Invasive fungal infections, particularly from Aspergillus, have increased among COVID-19 patients, while reports of Candida infections are still emerging.
  • The study found a 14.4% prevalence of systemic candidiasis in ICU patients with severe pneumonia due to SARS-CoV-2, primarily involving C. albicans and C. parapsilosis.
  • Those with candidiasis experienced longer ICU stays, higher mortality rates, and worse clinical outcomes, potentially linked to treatments like tocilizumab.

Article Abstract

Background: Invasive fungal infections (IFI) are increasing in prevalence in recent years. In the last few months, the rise of COVID-19 patients has generated a new escalation in patients presenting opportunistic mycoses, mainly by Aspergillus. Candida infections are not being reported yet.

Objectives: We aimed to determine the prevalence of systemic candidiasis in patients admitted to ICUs due to severe pneumonia secondary to SARS-CoV-2 infection and the existence of possible associated risk factors that led these patients to develop candidiasis.

Patients/methods: We designed a study including patients with a confirmed diagnosis of COVID-19.

Results: The prevalence of systemic candidiasis was 14.4%, and the main isolated species were C. albicans and C. parapsilosis. All patients that were tested positive for Candida spp. stayed longer in the ICU in comparison to patients who tested negative. Patients with candidiasis had higher MuLBSTA score and mortality rates and a worse radiological involvement. In our study, Candida spp. isolates were found in patients that were submitted to: tocilizumab, tocilizumab plus systemic steroids, interferon type 1β and Lopinavir-Ritonavir.

Conclusions: Results suggested a high prevalence of systemic candidiasis in severe COVID-19-associated pneumonia patients. Patients with Candidiasis had the worst clinical outcomes. Treatment with tocilizumab could potentialize the risk to develop systemic candidiasis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445759PMC
http://dx.doi.org/10.1016/j.rmed.2021.106619DOI Listing

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