B00
Conditions
Interventions
Group 1: Retrospective analysis of all patients aged over 18 who were treated for SARS-CoV-2 infection in the anesthesiology intensive care unit of University Hospital Essen, Germany, between March 20
Sponsors
Universitätsklinikum Essen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Inclusion criteria were admission to the ICU and a confirmed positive test for SARS-CoV-2.
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint was defined as ICU mortality . Mortality was defined as death from any cause occurring during the initial ICU admission. Secondary endpoints included the crude incidence of HSV, CMV, candida and aspergillus co-presence, the use of antiviral and antifungal therapy, organ failure, need for mechanical ventilation and need for venovenous extracorporal membrane oxygenation (vvECMO) support. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints included the crude incidence of HSV, CMV, candida and aspergillus co-presence, the use of antiviral and antifungal therapy, organ failure, need for mechanical ventilation and need for venovenous extracorporal membrane oxygenation (vvECMO) support. | — |
Countries
Germany
Contacts
Public ContactSimon Dubler
Universitätsklinikum Essen
Outcome results
None listed