TY - JOUR
T1 - ICU-acquired pneumonia in immunosuppressed patients with acute hypoxemic respiratory failure
T2 - A post-hoc analysis of a prospective international cohort study
AU - Efraim investigators and the Nine-I study group
AU - Martin-Loeches, Ignacio
AU - Darmon, Michael
AU - Demoule, Alexandre
AU - Antonelli, Massimo
AU - Schellongowski, Peter
AU - Pickkers, Peter
AU - Soares, Marcio
AU - Rello, Jordi
AU - Bauer, Philippe
AU - van de Louw, Andry
AU - Lemiale, Virgine
AU - Grimaldi, David
AU - Balik, Martin
AU - Mehta, Sangeeta
AU - Kouatchet, Ac
AU - Barratt-Due, Andreas
AU - Valkonen, Miia
AU - Reignier, Jean
AU - Metaxa, Victoria
AU - Moreau, Anne Sophie
AU - Burghi, Gaston
AU - Mokart, Djamel
AU - Azoulay, Elie
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2021/6
Y1 - 2021/6
N2 - Objective: Intensive Care Units (ICU) acquired Pneumonia (ICU-AP) is one of the most frequent nosocomial infections in critically ill patients. Our aim was to determine the effects of having an ICU-AP in immunosuppressed patients with acute hypoxemic respiratory failure. Design: Post-hoc analysis of a multinational, prospective cohort study in 16 countries. Settings: ICU. Patients: Immunosuppressed patients with acute hypoxemic respiratory failure. Intervention: None. Measurements and main results: The original cohort had 1611 and in this post-hoc analysis a total of 1512 patients with available data on hospital mortality and occurrence of ICU-AP were included. ICU-AP occurred in 158 patients (10.4%). Hospital mortality was higher in patients with ICU-AP (14.8% vs. 7.1% p < 0.001). After adjustment for confounders and centre effect, use of vasopressors (Odds Ratio (OR) 2.22; 95%CI 1.46–3.39) and invasive mechanical ventilation at day 1 (OR 2.12 vs. high flow oxygen; 95%CI 1.07–4.20) were associated with increased risk of ICU-AP while female gender (OR 0.63; 95%CI 0.43–94) and chronic kidney disease (OR 0.43; 95%CI 0.22–0.88) were associated with decreased risk of ICU-AP. After adjustment for confounders and centre effect, ICU-AP was independently associated with mortality (Hazard Ratio 1.48; 95%CI 14.–1.91; P = 0.003). Conclusions: The attributable mortality of ICU-AP has been repetitively questioned in immunosuppressed patients with acute respiratory failure. This manuscript found that ICU-AP represents an independent risk factor for hospital mortality.
AB - Objective: Intensive Care Units (ICU) acquired Pneumonia (ICU-AP) is one of the most frequent nosocomial infections in critically ill patients. Our aim was to determine the effects of having an ICU-AP in immunosuppressed patients with acute hypoxemic respiratory failure. Design: Post-hoc analysis of a multinational, prospective cohort study in 16 countries. Settings: ICU. Patients: Immunosuppressed patients with acute hypoxemic respiratory failure. Intervention: None. Measurements and main results: The original cohort had 1611 and in this post-hoc analysis a total of 1512 patients with available data on hospital mortality and occurrence of ICU-AP were included. ICU-AP occurred in 158 patients (10.4%). Hospital mortality was higher in patients with ICU-AP (14.8% vs. 7.1% p < 0.001). After adjustment for confounders and centre effect, use of vasopressors (Odds Ratio (OR) 2.22; 95%CI 1.46–3.39) and invasive mechanical ventilation at day 1 (OR 2.12 vs. high flow oxygen; 95%CI 1.07–4.20) were associated with increased risk of ICU-AP while female gender (OR 0.63; 95%CI 0.43–94) and chronic kidney disease (OR 0.43; 95%CI 0.22–0.88) were associated with decreased risk of ICU-AP. After adjustment for confounders and centre effect, ICU-AP was independently associated with mortality (Hazard Ratio 1.48; 95%CI 14.–1.91; P = 0.003). Conclusions: The attributable mortality of ICU-AP has been repetitively questioned in immunosuppressed patients with acute respiratory failure. This manuscript found that ICU-AP represents an independent risk factor for hospital mortality.
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U2 - 10.1016/j.jcrc.2020.09.027
DO - 10.1016/j.jcrc.2020.09.027
M3 - Article
C2 - 33012580
AN - SCOPUS:85092244418
SN - 0883-9441
VL - 63
SP - 243
EP - 245
JO - Journal of Critical Care
JF - Journal of Critical Care
ER -