Abstract

Carriage of Staphylococcus aureus is associated with S aureus infection. However, associations between S aureus carriage and the development of S aureus intensive care unit (ICU) pneumonia (SAIP) have not been quantified accurately, and interpretation of available data is hampered because of variations in definitions. To quantify associations of patient-related and contextual factors, including S aureus colonization status, with the occurrence of SAIP. This cohort study was conducted in ICUs of 30 hospitals in 11 European countries, geographically spread across 4 regions. Among patients with an anticipated length of stay 48 hours or longer who were undergoing mechanical ventilation at ICU admission, S aureus colonization was ascertained in the nose and lower respiratory tract. From this group, S aureus-colonized and noncolonized patients were enrolled into the study cohort in a 1:1 ratio. Data analysis was performed from May to November 2019. SAIP was defined as any pneumonia during the ICU stay developing 48 hours or more after ICU admission with S aureus isolated from lower respiratory tract specimens or blood samples. The incidence of SAIP was derived in the study cohort and estimated on the weighted incidence calculation for the originating overarching population, while taking competing events into account. Weighted risk factor analysis was performed using Cox multivariable regression. The study cohort consisted of 1933 patients (mean [SD] age, 62.0 [16.0] years); 1252 patients (64.8%) were men, and 950 patients (49.1%) were S aureus carriers at ICU admission. In all, 304 patients (15.7%) developed ICU-acquired pneumonia, of whom 131 patients (6.8%) had SAIP. Weighted SAIP incidences were 11.7 events per 1000 patient-days in the ICU for S aureus-colonized patients and 2.9 events per 1000 patient-days in the ICU for noncolonized patients (overall incidence, 4.9 events per 1000 patient-days in the ICU). The only factor independently associated with SAIP was S aureus colonization status at ICU admission (cause-specific hazard ratio, 3.6; 95% CI, 2.2-6.0; P < .001). There were marked regional differences in SAIP incidence and cause-specific hazard ratios for colonization status. SAIP incidence was 4.9 events per 1000 ICU patient-days for patients undergoing mechanical ventilation at ICU admission (or shortly thereafter). The daily risk of SAIP was 3.6 times higher in patients colonized with S aureus at ICU admission compared with noncolonized patients.

Highlights

  • Staphylococcus aureus is both a human commensal and an opportunistic pathogen

  • The only factor independently associated with SAIP was S aureus colonization status at intensive care unit (ICU) admission

  • The daily risk of SAIP was 3.6 times higher in patients colonized with S aureus at ICU admission compared with noncolonized patients

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Summary

Introduction

Staphylococcus aureus is both a human commensal and an opportunistic pathogen. Healthy people carry the bacterium on the skin or in the respiratory tract, with a preference for the nose. Reported rates of nasal carriage are approximately 25% to 30% of healthy individuals.[1,2] For healthy people, S aureus carriage is not a direct risk for infection,[3] but this changes in case of surgery or serious illness, such as when being treated in an intensive care unit (ICU). S aureus infections do occur in noncarriers, they occur far more frequently in those who are colonized with S aureus.[4,5] Nosocomial pneumonia caused by S aureus frequently complicates hospitalization and may lead to severe consequences, especially when acquired in the ICU.[6,7]

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