Surveillance for multidrug-resistant organisms Infections and Infestations
Conditions
Interventions
All patients admitted to ICU during the study period will be screened for MDRO and clinical data on infections and antimicrobial use will be collected.
Participants will be screened f
Sponsors
Cambridge University Hospitals NHS Foundation Trust
University of Cambridge
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Aged 18 years old or older 2. Male or female 3. Admitted to the John Farman Intensive Care Unit during the study period
Exclusion criteria
Exclusion criteria: Does not fulfil study inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measured using patient records during the study period: 1. Number of patients colonised with multidrug-resistant organisms 2. Number of patients with clinical evidence of infection with multidrug-resistant organisms 3. Number of transmission events of multidrug-resistant organisms | — |
Secondary
| Measure | Time frame |
|---|---|
| Measured using patient records during the study period: 1. Risk factors for colonisation / infection with multidrug-resistant organisms 2. Outcome of patients colonised / infected with multidrug-resistant organisms 3. Cost-consequences of whole-genome sequencing versus standard epidemiological investigation / typing for surveillance and investigation of suspected outbreaks and the management of confirmed outbreaks | — |
Countries
United Kingdom
Outcome results
None listed