U80.00 U80.3
Conditions
Interventions
Group 1: The preventions bundles are started 6 month after randomisation including stop of contact precautions, Patient participation, ABS measures and compliance observations of hand-hygienic procedu
Sponsors
Institut für Hygiene und Umweltmedizin, Charité Berlin
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All German Hospital which are willing to follow the study procedures are welcome to participate in ISO-ADE. Units which can not participate because of their specialisation are summarized in exclusion criteria.
Exclusion criteria
Exclusion criteria: Following Units can not be included: intensive care unit, pediatrics, HEENT; ophtalomogy, psychiatric, gynecologic, oncologic, hematologic. Hospitals which have the intervention bundle already established as a standard operation procedure.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of the overall incidence of MRSA/VRE in the interventional and the observational study period. | — |
Secondary
| Measure | Time frame |
|---|---|
| Compliance of Hand Hygiene, incidence of infection with MRSA/VRE, prevalence of MRSA/VRE in newly admitted patients, Depression score of patients with and without contact precautions | — |
Countries
Germany
Contacts
Public ContactBeate Schlosser
Charité, Campus Benjamin Franklin
Outcome results
None listed