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Risk factors associated with development of coinfection in critically Ill patients with COVID-19.
Orsini, Erica M; Sacha, Gretchen L; Han, Xiaozhen; Wang, Xiaofeng; Duggal, Abhijit; Rajendram, Prabalini.
  • Orsini EM; Department of Critical Care, Cleveland Clinic, Cleveland, OH, USA.
  • Sacha GL; Department of Pharmacy, Cleveland Clinic, Cleveland, OH, USA.
  • Han X; Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, USA.
  • Wang X; Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, USA.
  • Duggal A; Department of Critical Care, Cleveland Clinic, Cleveland, OH, USA.
  • Rajendram P; Department of Anesthesiology and Critical Care, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Acute Crit Care ; 37(3): 312-321, 2022 Aug.
Article in English | MEDLINE | ID: covidwho-2030176
ABSTRACT

BACKGROUND:

At outset of the coronavirus disease 2019 (COVID-19) pandemic, the significance of bacterial and fungal coinfections in individuals with COVID-19 was unknown. Initial reports indicated that the prevalence of coinfection in the general population was low, but there was uncertainty regarding the risk of coinfection in critically ill patients.

METHODS:

Nine hundred critically ill adult patients with COVID-19 infection were enrolled in this observational case-control study. Patients with a coinfection (case) and patients without a coinfection (control) were compared using univariate and multivariable analyses. A subgroup analysis was performed on patients with coinfection, dividing them into early (infection within 7 days) and late (infection after 7 days) infection groups.

RESULTS:

Two hundred and thirty-three patients (25.9%) had a bacterial or fungal coinfection. Vasopressor use (P<0.001) and severity of illness (higher Acute Physiology and Chronic Health Evaluation III score, P=0.009) were risk factors for the development of a coinfection. Patients with coinfection had higher mortality and length of stay. Vasopressor and corticosteroid use and central line and foley catheter placement were risk factors for late infection (>7 days). There were high rates of drug-resistant infections.

CONCLUSIONS:

Critically ill patients with COVID-19 are at risk for both community-acquired and hospital-acquired infections throughout their hospitalization for COVID-19. It is important to consider the development of a coinfection in clinically worsening critically ill patients with COVID-19 and consider the likelihood of drug-resistance when choosing an empiric regimen.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Acute Crit Care Year: 2022 Document Type: Article Affiliation country: Acc.2022.00136

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Acute Crit Care Year: 2022 Document Type: Article Affiliation country: Acc.2022.00136