Abstract
Purpose Our aim was to evaluate the role of biomarker kinetics in the assessment of ventilator-associated pneumonia (VAP) response to antibiotics. Materials and methods We performed a prospective, multicenter, observational study to evaluate in 37 microbiologically documented VAP, the kinetics of C-reactive protein (CRP), procalcitonin (PCT), mid-region fragment of pro-adrenomedullin (MR-proADM). The kinetics of each variable, from day 1 to 6 of therapy, was assessed with a time dependent analysis comparing survivors and non-survivors. Results During the study period kinetics of CRP as well as its relative changes, CRP-ratio, was significantly different between survivors and non-survivors (p = 0.026 and p = 0.005, respectively). On day 4 of antibiotic therapy, CRP of survivors was 47% of the initial value while it was 96% in non-survivors. The kinetics of other studied variables did not distinguish between survivors and non-survivors. In survivors the bacterial load also decreased markedly. Adequate initial antibiotic therapy was associated with lower mortality (p = 0.025) and faster CRP decrease (p = 0.029). Conclusions C-reactive protein kinetics can be used to identify VAP patients with poor outcome as soon as four days after the initiation of treatment. (Trial registration - NCT02078999; registered 3 August 2012). © 2017 Elsevier Inc.
Original language | English |
---|---|
Pages (from-to) | 91-97 |
Number of pages | 7 |
Journal | Journal of Critical Care |
Volume | 41 |
DOIs | |
Publication status | Published - 1 Oct 2017 |
Keywords
- C-reactive protein
- Mid-region fragment of pro-adrenomedullin
- Procalcitonin
- Prognosis
- Ventilator-associated pneumonia
- antibiotic agent
- biological marker
- C reactive protein
- proadrenomedullin
- procalcitonin
- adult
- antibiotic therapy
- Article
- bacterial infection
- bacterial load
- clinical article
- clinical assessment
- clinical effectiveness
- clinical evaluation
- disease association
- drug efficacy
- drug response
- female
- human
- male
- mortality
- multicenter study
- observational study
- protein blood level
- survivor
- ventilator associated pneumonia