Biomarkers for Ventilator-associated Pneumonia
- Conditions
- Pneumonia, Ventilator-Associated
- Registration Number
- NCT05117125
- Lead Sponsor
- Region Skane
- Brief Summary
The purpose of this study is to evaluate different peptide biomarkers, variations in the microbiome and patterns in the bacterial transcriptome as prognostic or diagnostic biomarkers of VAP.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 1000
- Admission to an intensive care unit
- Intubation within last 24 hours
- Anticipated mechanical ventilation of at least 48 hours
- FiO2 above 70% or PEEP above 15
- Severe coagulopathy (spontaneous PK(INR) >1.8 or thrombocytes <50). Prophylaxis treatment dose of LMWH or factor Xa inhibitors/NOAC is not an exclusion criteria. If higher doses of these substances are administered, the responsible clinician should be consulted before sample collection.
- Ongoing infection of the lungs at admission to the ICU.
- Severely elevated or instable intracranial pressure.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in HBP concentration over time Day 1, 3 and in selected patients day 7 and 14. In patients with VAP also VAP day 1, 3 and 7. Change in concentration (ng/ml) compared to baseline.
Change in IL-26 over time Day 1, 3 and in selected patients day 7 and 14. In patients with VAP also VAP day 1, 3 and 7. Change in concentration (ng/ml) compared to baseline.
IL-26 at VAP diagnosis VAP day 1 compared to No VAP day 3 Concentration at VAP day 1, compared to day 3 in patients with no VAP. ROC curves, specificity and sensitivity as diagnostic biomarker.
HBP at VAP diagnosis VAP day 1 compared to No VAP day 3 Concentration at VAP day 1, compared to day 3 in patients with no VAP. ROC curves, specificity and sensitivity as diagnostic biomarker.
- Secondary Outcome Measures
Name Time Method Bacterial transcriptome patterns VAP day 1 Patterns in the bacterial gene expression that predict antibiotic drug treatment failure.
Diversity of microbiome Day 1 and 3, and VAP day 1. Changes in alpha and beta diversity as prognostic biomarker for VAP. Cases that develop VAP are compared to cases with no VAP.
Trial Locations
- Locations (5)
Vestre Viken
🇳🇴Drammen, Norway
Hospital de São Francisco Xavier
🇵🇹Lisbon, Portugal
Skåne University Hospital, Dept. of Infectious diseases
🇸🇪Lund, Sweden
Skåne university Hospital, ICU
🇸🇪Malmö, Sweden
Karolinska University Hospital, ICU
🇸🇪Solna, Sweden
Vestre Viken🇳🇴Drammen, NorwayKarl-Erik Müller, MD PhDContact+4703525kamull@vestreviken.no