4.2 Article

Acute Inflammatory Response of Patients with Pseudomonas aeruginosa Infections: A Prospective Study

Journal

MICROBIAL DRUG RESISTANCE
Volume 23, Issue 4, Pages 523-530

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/mdr.2016.0144

Keywords

Pseudomonas aeruginosa; microbial drug resistance; nosocomial infections; infections

Funding

  1. National Health Service grant from the Fondo de Investigacion Sanitarias, Instituto de Salud Carlos III [FIS 11/00164]
  2. FEDER funds/European Regional Development Fund (ERDF), a way to build Europe
  3. Spanish Network for Research in Infectious Diseases (REIPI)
  4. Ciber de Enfermedades Respiratorias [CB06/06/0037]

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The severity of Pseudomonas aeruginosa (PA) infection may be determined by the interaction with the host immune system. We designed a prospective study to assess the relationship between the inflammatory response and the clinical presentation and outcome of PA infection. We also investigated whether there are differences in the inflammatory response depending on the resistance profile of PA. Interleukin-6 (IL-6), IL-10, procalcitonin (PCT), and C-reactive protein (CRP) were measured. Sixty-nine infection episodes were recorded; 40 caused by non-multidrug-resistant (non-MDR) strains [29 (73%) respiratory; 8 (20%) bacteremia], 12 by MDR nonextensively drug-resistant (MDR-non-XDR) [9 (75%) respiratory; 3 (25%) bacteremia], and 17 by XDR strains [9 (53%) respiratory; 7 (41%) bacteremia]. All inflammatory parameters were significantly higher in patients who developed acute organ dysfunction and bacteremia. PCT levels were higher in patients with early mortality [p = 0.050]. Inflammatory biomarkers were higher in patients with XDR than in those with non-MDR PA [IL-6 430 (67-951) vs. 77 (34-216), p = 0.02; IL-10 3.3 (1.5-16.3) vs. 1.3 (0-3.9), p = 0.02; and PCT 1.1 (0.6-5.2) vs. 0.3 (0.1-1.0), p = 0.008]. The intensity of inflammatory response was associated with the severity of PA infection, particularly if bacteremia occurred. Only PCT was documented useful to predict the outcome. XDR infections presented a higher inflammatory response; related in part to the larger number of bloodstream infections in this group.

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