| Literature DB >> 33546093 |
Daniele Roberto Giacobbe1, Denise Battaglini2, Elisa Martina Enrile2,3, Chiara Dentone1, Antonio Vena1, Chiara Robba2,3, Lorenzo Ball2,3, Michele Bartoletti4, Irene Coloretti5, Stefano Di Bella6, Antonio Di Biagio1,7, Iole Brunetti2, Malgorzata Mikulska1,7, Novella Carannante8, Andrea De Maria1,7, Laura Magnasco1,7, Alberto Enrico Maraolo9, Michele Mirabella1,7, Giorgia Montrucchio10,11, Nicolò Patroniti2,3, Lucia Taramasso1, Giusy Tiseo12, Giacomo Fornaro4, Fiorentino Fraganza13, Luca Monastra13, Erik Roman-Pognuz6,14, Giacomo Paluzzano6, Giuseppe Fiorentino15, Antonio Corcione16, Linda Bussini4, Renato Pascale4, Silvia Corcione17, Tommaso Tonetti18, Matteo Rinaldi4, Marco Falcone12, Emanuela Biagioni5, Vito Marco Ranieri18, Maddalena Giannella4, Francesco Giuseppe De Rosa17, Massimo Girardis5, Francesco Menichetti12, Pierluigi Viale4, Paolo Pelosi2,3, Matteo Bassetti1,7.
Abstract
The primary objective of this multicenter, observational, retrospective study was to assess the incidence rate of ventilator-associated pneumonia (VAP) in coronavirus disease 2019 (COVID-19) patients in intensive care units (ICU). The secondary objective was to assess predictors of 30-day case-fatality of VAP. From 15 February to 15 May 2020, 586 COVID-19 patients were admitted to the participating ICU. Of them, 171 developed VAP (29%) and were included in the study. The incidence rate of VAP was of 18 events per 1000 ventilator days (95% confidence intervals [CI] 16-21). Deep respiratory cultures were available and positive in 77/171 patients (45%). The most frequent organisms were Pseudomonas aeruginosa (27/77, 35%) and Staphylococcus aureus (18/77, 23%). The 30-day case-fatality of VAP was 46% (78/171). In multivariable analysis, septic shock at VAP onset (odds ratio [OR] 3.30, 95% CI 1.43-7.61, p = 0.005) and acute respiratory distress syndrome at VAP onset (OR 13.21, 95% CI 3.05-57.26, p < 0.001) were associated with fatality. In conclusion, VAP is frequent in critically ill COVID-19 patients. The related high fatality is likely the sum of the unfavorable prognostic impacts of the underlying viral and the superimposed bacterial diseases.Entities:
Keywords: COVID-19; SARS-CoV-2; VAP; coronavirus; ventilation
Year: 2021 PMID: 33546093 PMCID: PMC7913191 DOI: 10.3390/jcm10040555
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241