Abstract

The ideal biomarker to assess response and prognostic assessment in the infected critically ill patient is still not available.The aims of our study were to analyze the association between early C-reactive protein kinetics and duration and appropriatenessof antibiotic therapy and its usefulness in predicting mortality in infected critically ill patients. We have carried out an observational retrospective study in a cohort of 60 patients with community-acquiredpneumonia, aspiration pneumonia and bacteremia at an intensive care unit. We have collected C-reactive protein consecutive serumlevels for eight days as well as duration and appropriateness of initial antibiotic therapy. C-reactive protein kinetic groups were definedbased on the levels at days 0, 4 and 7. With a follow-up of one year, we have evaluated mortality at different time-points. We have obtained three different C-reactive protein kinetic groups from the sample: fast response, delayed but fast responseand delayed and slow response. We did not find statistically significant associations between C-reactive protein kinetics and early (intensivecare unit, hospital and 28-days) or late (six months and one year) mortality and antibiotic therapy duration (p > 0.05). Althoughthere were no statistically significant differences between the appropriateness of antibiotic therapy and the defined groups (p = 0.265),no patient with inappropriate antibiotic therapy presented a fast response pattern. Several studies suggest the importance of this protein in infection. Early C-reactive protein kinetics is not associated with response and prognostic assessment in infected critically ill patients.Nevertheless, a fast response pattern tends to exclude initial inappropriate antibiotic therapy.

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