About this trial
The objective of the study is to determine whether rapid multiplex PCR testing of respiratory samples can reduce exposure to broad-spectrum antibiotics in intensive care unit patients with suspected or confirmed ventilator-associated pneumonia, compared to standard diagnostic methods.
As secondary objectives, the investigators will study antibiotic management and overall antibiotic consumption, as well as escalation or de-escalation events. The investigators will study the potential clinical impact of using multiplex PCR to see if the length of stay in the intensive care unit is reduced, as well as the duration of mechanical ventilation.
Eligibility criteria
Qualifiers
Adult patients (≥ 18 years old)
Hospitalized in intensive care with invasive mechanical ventilation ≥ 48 hours
Administration of antimicrobial therapy for suspected VAP at the time of inclusion.
Expected survival > 96 hours.
Disqualifiers
Enrollment prior to the current trial
Participation in an interventional study on the management of AMR that has a direct impact on antibiotic therapy practices.
Trial design
Treatments tested in this trial
- PCR multiplex BioFire Pneumonia plus
Treatment groups
Sponsors and collaborators
University Hospital, Geneva
Lead sponsor
BioMérieux
Collaborator
Hospital Fribourg, Switzerland
Collaborator
Hôpital universitaire de Lausanne
Collaborator
Hospital of Neuchâtel
Collaborator
Centre Hospitalier du Centre du Valais
Collaborator
Hospital Lugano
Collaborator