A41.0 A41.1
Conditions
Interventions
Group 1: HELP App (CDSS
digital book)
Group 2: TAU ("treatment as usual")
Sponsors
Universitätsklinikum Jena
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Staphylococcus spp. bacteremia
Exclusion criteria
Exclusion criteria: Patients from psychiatric wards, pediatric wards and obstetric wards. If treated according to KNS arm: death of patient within 72h after collection of first blood culture.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Coprimary endpoints (confirmatory test in the hierarchical order given here): - mortality and relapse rate due to S. aureus within 90 days in the SAB arm (non-inferiority test) and - the cumulative consumption of vancomycin in the CNS arm (superiority test) | — |
Secondary
| Measure | Time frame |
|---|---|
| - acute renal failure (KDIGO clinical practice guideline for acute kidney injury) - cumulative consumption of vancomycin, linezolid, teicoplanin, daptomycin, rifampicin, fosfomycin, flucloxacillin, cefazolin - incoming blood culture sets per institution and year - estimation of treatment costs based on ID consultation times and frequencies (only for complicated SAB) as well as technical and process-oriented endpoints from questionnaires (user survey) | — |
Countries
Germany
Contacts
Public ContactAndré Scherag
Institut für Medizinische Statistik, Informatik und Datenwissenschaften (IMSID), Universitätsklinikum Jena
Outcome results
None listed