Pneumologie 2014; 68 - P24
DOI: 10.1055/s-0034-1367795

Can Procalcitonin help to distinguish between an acute bacterial pneumonia and influenza A (H1N1) pneumonia on an intensive care unit?

R Pfister 1, M Kochanek 2, T Leygeber 1, C Brun-Buisson 3, E Cuquemelle 3, M Benevides Paiva Machado 4, E Piacentini 5, N Hammond 6, P Ingram 7, G Michels 1
  • 1Department of Internal Medicine III, University of Cologne, Germany
  • 2Department of Internal Medicine I, University of Cologne, Germany
  • 3Service de Réanimation Médicale, Medical Intensive Care Unit, Université Paris-Est Créteil, Créteil, France
  • 4Universidade Federal de Minas Gerais, Faculdade de Medicina (Ufmg), Hospital Das Clinicas Ufmg, Unidade Coronariana, Belo Horizonte/Mg, Brazil
  • 5Intensive Care Unit, Hospital Universitario Mútua de Terrassa, Terrassa, Spain
  • 6Department of Intensive Care Medicine, The Prince Charles Hospital, and Queensland University of Technology, School of Public Health, Rode Road, Brisbane, Australia
  • 7Department of Microbiology and Infectious Diseases, Royal Perth Hospital, Perth, Australia

Procalcitonin (PCT) is helpful for diagnosing bacterial infections. The diagnostic utility of PCT has not been examined thoroughly in critically ill patients with suspected H1N1 influenza. We prospectively assessed the clinical characteristics and PCT in patients admitted with lower respiratory tract infection to the medical intensive care unit (ICU) of the University hospital of Cologne during the 2009 and 2010 influenza seasons. Additionally, we performed a literature search to identify studies on the diagnostic role of PCT in ICU patients with suspected H1N1 influenza. Individual patient-data meta-analysis was conducted using data from our cohort (n = 46) combined with data from 5 eligible studies, with a total of 182 patients analyzed. PCT levels assessed during the first 48 hours after admission differed significantly between patients with and without bacterial pneumonia, but not H1N1 influenza status. The area under the curve of the ROC curve of PCT was 0.71 (95% CI 0.64 – 0.79, p < 0.0001) for diagnosis of bacterial pneumonia but increased to 0.76 (95% CI 0.68 – 0.84, p < 0.0001) when patients with hospital acquired pneumonia and immune-compromising disorders were excluded. A cut-off of procalcitonin of 0.5 µg/L had a sensitivity and a negative predictive value for diagnosis of bacterial pneumonia of 80.5% and 76.6% respectively, which increased to 85.5% and 84.6% in patients without hospital acquired pneumonia or immune-compromising disorder. In critically ill patients with suspected lower respiratory tract infection during the influenza season, PCT is a sensitive marker with high negative predictive value for detection of bacterial pneumonia particularly in patients with community acquired disease and without immune-compromising disorders.