Epidemiology of Bacteremia at Two Tertiary ICUs in Switzerland
Duration of Antimicrobial Treatment for Bloodstream Infections in Swiss Critically Ill Patients - Retrospective Double Center Study
1 other identifier
observational
395
1 country
1
Brief Summary
The objectives of the retrospective cohort study is to describe the actual current practice of antibiotic treatment duration for bloodstream infections in critically ill patients at two tertiary hospitals (ICU Inselspital Bern and ICU CHUV Lausanne), to examine patient, pathogen and infectious syndrome factors associated with selection of shortened treatment duration, and to describe the expected time course of clinical resolution among bacteremic patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2022
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 1, 2022
CompletedStudy Start
First participant enrolled
February 1, 2022
CompletedFirst Posted
Study publicly available on registry
February 11, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2022
CompletedJanuary 26, 2023
January 1, 2023
28 days
February 1, 2022
January 25, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Antibiotic Treatment Duration
Days of adequate antibiotic treatment in Patients with Bacteremia
Hospital discharge, expected to be on average ca. 15-20 days
Secondary Outcomes (2)
Days of ICU stay
ICU discharge, expected to be on average ca. 5-15 days
Days of hospital stay
Hospital discharge, expected to be on average ca. 15-25 days
Study Arms (2)
Bern ICU
Lausanne ICU
Interventions
Eligibility Criteria
Patient is critically ill at the time the blood culture was collected and was treated at the ICU/IMC at the time of blood culture collection or has been admitted to ICU/IMC in the 48 hours after blood culture collection.
You may qualify if:
- Patient has a positive blood culture with a pathogenic organism Patient is critically ill at the time the blood culture was collected as defined by the following:
- was treated at the ICU/IMC at the time of blood culture collection;
- or has been admitted to ICU/IMC in the 48 hours after blood culture collection
You may not qualify if:
- Patient has a single positive blood culture with a common contaminant organism:
- coagulase negative staphylococci;
- Bacillus spp.;
- Corynebacterium spp.;
- Propionibacterium spp.;
- Aerococcus spp.;
- Micrococcus spp.
- Explicit documentation that the patient does not want to participate in any study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Departement of Intensive Care Medicine
Bern, Switzerland
Related Publications (1)
Zuercher P, Moser A, Frey MC, Pagani JL, Buetti N, Eggimann P, Daneman N, Fowler R, Que YA, Prazak J. The effect of duration of antimicrobial treatment for bacteremia in critically ill patients on in-hospital mortality - Retrospective double center analysis. J Crit Care. 2023 Apr;74:154257. doi: 10.1016/j.jcrc.2023.154257. Epub 2023 Jan 23.
PMID: 36696827DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Josef Prazak, MD, PhD
Insel Gruppe AG, University Hospital Bern
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 1, 2022
First Posted
February 11, 2022
Study Start
February 1, 2022
Primary Completion
March 1, 2022
Study Completion
March 30, 2022
Last Updated
January 26, 2023
Record last verified: 2023-01