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               <dc:title>Bacteremia is an independent risk factor for mortality in nosocomial pneumonia: a prospective and observational multicenter study</dc:title>
               <dc:creator>Magret, Mònica</dc:creator>
               <dc:creator>Lisboa, Thiago</dc:creator>
               <dc:creator>Martín Loeches, Ignacio</dc:creator>
               <dc:creator>Máñez Mendiluce, Rafael</dc:creator>
               <dc:creator>Nauwynck, Marc</dc:creator>
               <dc:creator>Wrigge, Hermann</dc:creator>
               <dc:creator>Cardellino, Silvano</dc:creator>
               <dc:creator>Díaz, Emili</dc:creator>
               <dc:creator>Koulenti, Despina</dc:creator>
               <dc:creator>Rello, Jordi</dc:creator>
               <dc:subject>Pneumònia adquirida a la comunitat</dc:subject>
               <dc:subject>Bacteris gramnegatius</dc:subject>
               <dc:subject>Community-acquired pneumonia</dc:subject>
               <dc:subject>Gram-negative bacteria</dc:subject>
               <dc:description>Introduction: Since positive blood cultures are uncommon in patients with nosocomial pneumonia (NP), the responsible pathogens are usually isolated from respiratory samples. Studies on bacteremia associated with hospital-acquired pneumonia (HAP) have reported fatality rates of up to 50%. The purpose of the study is to compare risk factors, pathogens and outcomes between bacteremic nosocomial pneumonia (B-NP) and nonbacteremic nosocomial pneumonia (NB-NP) episodes. Methods: This is a prospective, observational and multicenter study (27 intensive care units in nine European countries). Consecutive patients requiring invasive mechanical ventilation for an admission diagnosis of pneumonia or on mechanical ventilation for > 48 hours irrespective of admission diagnosis were recruited. Results: A total of 2,436 patients were evaluated; 689 intubated patients presented with NP, 224 of them developed HAP and 465 developed ventilation-acquired pneumonia. Blood samples were extracted in 479 (69.5%) patients, 70 (14.6%) being positive. B-NP patients had higher Simplified Acute Physiology Score (SAPS) II score (51.5 +/- 19.8 vs. 46.6 +/- 17.5, P = 0.03) and were more frequently medical patients (77.1% vs. 60.4%, P = 0.01). Mortality in the intensive care unit was higher in B-NP patients compared with NB-NP patients (57.1% vs. 33%, P &lt; 0.001). B-NP patients had a more prolonged mean intensive care unit length of stay after pneumonia onset than NB-NP patients (28.5 +/- 30.6 vs. 20.5 +/- 17.1 days, P = 0.03). Logistic regression analysis confirmed that medical patients (odds ratio (OR) = 5.72, 95% confidence interval (CI) = 1.93 to 16.99, P = 0.002), methicillin-resistant Staphylococcus aureus (MRSA) etiology (OR = 3.42, 95% CI = 1.57 to 5.81, P = 0.01), Acinetobacter baumannii etiology (OR = 4.78, 95% CI = 2.46 to 9.29, P &lt; 0.001) and days of mechanical ventilation (OR = 1.02, 95% CI = 1.01 to 1.03, P &lt; 0.001) were independently associated with B-NP episodes. Bacteremia (OR = 2.01, 95% CI = 1.22 to 3.55, P = 0.008), diagnostic category (medical patients (OR = 3.71, 95% CI = 2.01 to 6.95, P = 0.02) and surgical patients (OR = 2.32, 95% CI = 1.10 to 4.97, P = 0.03)) and higher SAPS II score (OR = 1.02, 95% CI = 1.01 to 1.03, P = 0.008) were independent risk factors for mortality. Conclusions: B-NP episodes are more frequent in patients with medical admission, MRSA and A. baumannii etiology and prolonged mechanical ventilation, and are independently associated with higher mortality rates.</dc:description>
               <dc:date>2018-12-07T11:18:57Z</dc:date>
               <dc:date>2018-12-07T11:18:57Z</dc:date>
               <dc:date>2011-02-16</dc:date>
               <dc:date>2018-07-24T13:02:17Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.1186/cc10036</dc:relation>
               <dc:relation>Critical Care, 2011, vol. 15, num. R62</dc:relation>
               <dc:relation>https://doi.org/10.1186/cc10036</dc:relation>
               <dc:rights>cc by (c) Magret et al., 2011</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>BioMed Central</dc:publisher>
               <dc:source>Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))</dc:source>
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