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Club Cell protein: a candidate diagnostic biomarker of Pseudomonas aeruginosa nosocomial pneumonia
Critical Care volume 18, Article number: P218 (2014)
Introduction
Early etiological diagnosis of nosocomial pneumonia (NP) determines prompt targeted treatment. The aim of this study was to investigate the role of Club Cell protein (CCP) as a candidate diagnostic biomarker of Pseudomonas aeruginosa (PA) NP.
Methods
The observational study in ICU ventilated septic patients with peritonitis (65%), pancreonecrosis (20%) and mediastinitis (15%) was performed in 2010 and 2013. Diagnosis of NP was made according to the standard clinical criteria. Associations of multiresistant Gram- negative bacteria were detected in sputum of all patients. PA was detected in 75% of patients. Plasma CCP was measured on the day of NP diagnosis (day 0) and days 3, 5 and 7 by the immunoenzyme essay (BioVendor, USA). Data were statistically analyzed by STATISTICA 7.0, ANOVA method, and presented as Me and 25 to 75 percentiles, ng/ml; P < 0.05 was considered significant. Areas under the receiver operating curves (ROC) were calculated.
Results
Ninety patients (out of 350 screened) were enrolled in the study according to the inclusion/exclusion criteria. Patients were assigned to groups: NP (n = 50, 45 ± 4.3 years old, M/F 36/14) and noNP (n = 40, 48 ± 7.2 years old, M/F 30/10). Groups were comparable in APACHE II and CPIS scores. In patients with PA NP (n = 30), plasma CCP was significantly lower at all points than in the patients with no PA detected (n = 20; Figure 1). Plasma CCP on day 0 had a good capacity for the diagnosis of PA NP: CCP on day 0 ≤ 17.5 ng/ml yielded a sensitivity of 86.5% and specificity of 66.7% (AUC 0.74; 95% CI 0.630 to 0.829; P = 0.0001; Figure 2).
Conclusion
Plasma CCP level ≤17.5 ng/ml is a sensitive and specific candidate diagnostic biomarker of PA NP.
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Moroz, V., Kuzovlev, A. & Polovnikov, S. Club Cell protein: a candidate diagnostic biomarker of Pseudomonas aeruginosa nosocomial pneumonia. Crit Care 18 (Suppl 1), P218 (2014). https://doi.org/10.1186/cc13408
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DOI: https://doi.org/10.1186/cc13408