J10 U07.1
Conditions
Interventions
Group 1: conventional influenza testing in the central laboratory
Group 2: rapid (<30 Min) and early (< 2 hours after admission) influenza testing ´directly in the emergency department
Sponsors
Charité Universitätsmedizin Berlin; Notfall- und Akutmedizin (CVK, CCM)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: All patients attending the Emergency Departments during the study period with any influenza symptom and fever (=38.0°C) will be eligible to participate in the study. No exclusion criteria will be applied.
Exclusion criteria
Exclusion criteria: < 18 years of age
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| length of hospital stay, in-hospital mortality, proportion of patients tested, ICU admission, proportion of patients with a final diagnosis of influenza or pneumonia, proportion of secondary infections, Aspergillus infections, pneumococci infections, between presentation to the ED and antiviral/antibiotic treatment, time to disposition, admission/discharge rate, medical procedures, laboratory tests performed, transmission rate on other patients. turn-around-time until test result is available. Physician decision making (disposition, medical procedures, antiviral/antibiotic therapy, laboratory parameters). | — |
Primary
| Measure | Time frame |
|---|---|
| 1. sick days of personnel 2. Proportion of patients treated with antibiotic and antiviral therapy | — |
Countries
Germany
Contacts
Public ContactMartin Möckel
Charité Universitätsmedizin BerlinNotfall- und Akutmedizin (CVK, CCM)
Outcome results
None listed