Multidrug-resistant pathogens and ventilator-associated pneumonia in critically ill COVID-19 and non-COVID-19 patients: a prospective observational monocentric comparative study

被引:2
作者
Montrucchio, Giorgia [1 ,2 ]
Balzani, Eleonora [1 ]
Sales, Gabriele [1 ,2 ]
Vaninetti, Anna [1 ]
Grillo, Francesca [1 ]
Trompeo, Anna Chiara [2 ]
Zanierato, Marinella [2 ]
Fanelli, Vito [1 ,2 ]
Corcione, Silvia [3 ,4 ]
De Rosa, Francesco Giuseppe [3 ]
Curtoni, Antonio [5 ,6 ]
Costa, Cristina [5 ,6 ]
Brazzi, Luca [1 ,2 ]
机构
[1] Univ Turin, Dept Surg Sci, Turin, Italy
[2] Citta Salute & Sci Hosp, Dept Anesthesia Intens Care & Emergency, Turin, Italy
[3] Univ Turin, Dept Med Sci, Turin, Italy
[4] Tufts Univ, Sch Med, Boston, MA 02111 USA
[5] Univ Turin, Dept Publ Hlth & Paediat, Turin, Italy
[6] Citta Salute & Sci Hosp, Microbiol & Virol Lab, Corso Dogliotti 14, I-10126 Turin, Italy
关键词
COVID-19; Ventilator-acquired pneumonia; Critical care; Multidrug resistant organisms; Difficult to treat organisms; Antimicrobial resistance; DISEASE; ECMO;
D O I
10.1186/s12931-024-02779-1
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background The COVID-19 pandemic has increased the incidence of ventilator-associated pneumonia (VAP) among critically ill patients. However, a comparison of VAP incidence in COVID-19 and non-COVID-19 cohorts, particularly in a context with a high prevalence of multidrug-resistant (MDR) organisms, is lacking. Material and Methods We conducted a single-center, mixed prospective and retrospective cohort study comparing COVID-19 patients admitted to the intensive care unit (ICU) of the "Citt & agrave; della Salute e della Scienza" University Hospital in Turin, Italy, between March 2020 and December 2021 (COVID-19 group), with a historical cohort of ICU patients admitted between June 2016 and March 2018 (NON-COVID-19 group). The primary objective was to define the incidence of VAP in both cohorts. Secondary objectives were to evaluate the microbial cause, resistance patters, risk factors and impact on 28 days, ICU and in-hospital mortality, duration of ICU stay, and duration of hospitalization). Results We found a significantly higher incidence of VAP (51.9% - n = 125) among the 241 COVID-19 patients compared to that observed (31.2% - n = 78) among the 252 NON-COVID-19 patients. The median SOFA score was significantly lower in the COVID-19 group (9, Interquartile range, IQR: 7-11 vs. 10, IQR: 8-13, p < 0.001). The COVID-19 group had a higher prevalence of Gram-positive bacteria-related VAP (30% vs. 9%, p < 0.001), but no significant difference was observed in the prevalence of difficult-to-treat (DTR) or MDR bacteria. ICU and in-hospital mortality in the COVID-19 and NON-COVID-19 groups were 71% and 74%, vs. 33% and 43%, respectively. The presence of COVID-19 was significantly associated with an increased risk of 28-day all-cause hospital mortality (Hazard ratio, HR: 7.95, 95% Confidence Intervals, 95% CI: 3.10-20.36, p < 0.001). Tracheostomy and a shorter duration of mechanical ventilation were protective against 28-day mortality, while dialysis and a high SOFA score were associated with a higher risk of 28-day mortality. Conclusion COVID-19 patients with VAP appear to have a significantly higher ICU and in-hospital mortality risk regardless of the presence of MDR and DTR pathogens. Tracheostomy and a shorter duration of mechanical ventilation appear to be associated with better outcomes.
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