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Epidemiology and Determinants of Outcomes of Hospital Acquired Blood Stream Infections in the Intensive Care

Epidemiology and Determinants of Outcomes of Hospital Acquired Blood Stream Infections in the Intensive Care: the Eurobact II Multinational Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03937245
Acronym
EurobactII
Enrollment
3058
Registered
2019-05-03
Start date
2019-08-30
Completion date
2021-06-03
Last updated
2021-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bacteremia, Hospital Acquired Condition, Resistance Bacterial, Sepsis

Keywords

Hospital-acquired infection, Blood stream infection, Bacteremia, Intensive care

Brief summary

Eurobact II will investigate the mortality and morbidity of hospital-acquired blood stream infections in patients treated in intensive care units (ICU). It will investigate the effects of the micro-organism and its characteristics, such as type and resistance to antibiotics on the infection and its consequences. It will also investigate the effects of the antibiotics and other treatments on survival of patients. Eurobact II will include patients from multiple ICUs in multiple countries.

Detailed description

Eurobact II is a multinational multicentre cohort study that will include patients with hospital-acquired blood stream infections (HA-BSI) treated in ICUs around the globe. It will provide with an update of the epidemiology of HA-BSI since the Eurobact I study. It is designed to investigate the effects of HA-BSI on mortality at day 28. To describe the determinants of outcomes of HA-BSI, specifically the effects of the source of infection, the microorganism, the characteristics of antimicrobial therapy and of source control. It will investigate patient specific and organizational factors and will describe the determinants of management of HA-BSI in ICUs.

Interventions

None listed

Sponsors

European Society of Intensive Care Medicine
CollaboratorOTHER
European Society of Clinical Microbiology and Infectious Diseases
CollaboratorOTHER
Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Outcome Rea
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 Years. * Hospital Acquired Bloodstream Infection (HA-BSI). * Treated in the ICU. * ICU acquired OR * Hospital acquired prior to ICU admission

Exclusion criteria

* Patients that had a positive blood culture in the hospital and transferred to ICU for a different reason than specific treatment of the causes or consequences of HA-BSI. * Previous inclusion in the study. * HA-BSI is defined as a positive blood culture (BC) sampled after 48 hours following hospital admission.

Design outcomes

Primary

MeasureTime frameDescription
Mortality28 daysVital status

Secondary

MeasureTime frameDescription
Clinical cure7 days, 28 daysAs evaluated by the treating clinician
Microbiological cure7 days, 28 daysPresence of persisting or relapsing blood stream infection
Progress of organ failures7 daysAssessed by the components of the SOFA score
Days free or organ supportive therapy28 daysDays free of renal replacement therapy, mechanical ventilation, vasopressors, intensive care unit

Countries

Australia, France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026