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In VAP patients, we found no differences in CRP kinetics between early and late VAP (p = 0.304).
The mortality rate in VAP was 16% as compared with 0.2% in non-VAP cases (p < 0.001).
This way we could assess the kinetics of biomarkers in VAP prediction.
Among the studied biomarkers, CRP and CRP ratio showed the best performance in VAP prediction.
PCT was also significantly higher in VAP (0.64 ng/dl and 2.1 ng/dl, p < .001).001
Prediction of GPc or GNr bacteria involved in VAP has poor accuracy excepted for GNr specificity.
The two versions of the ALINEA approach are coded in VAP.
Our aim was to assess the value of biomarker kinetics in VAP prediction.
Why did the reduction in VAP prevalence not occur in 2013?
In our CDH cohort, we observed a microbiological shift in VAP pathogen.
In VAP, some studies have previously looked at PCT and/or CRP concentration changes before diagnosis.
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