We hypothesized that Ventilator-Associated Event (VAE) within 28 days upon admission to medical intensive care units (ICUs) can be a predictor for poor outcomes in sepsis patients. We aimed to determine the risk factors and associated outcomes of VAE. A total of 453 consecutive mechanically ventilated (MV) sepsis patients were enrolled. Of them, 136 patients had immune profile study. Early VAE (< 7-day MV, n = 33) was associated with a higher mortality (90 days: 81.8% vs. 23.0% [non-VAE], P < 0.01), while late VAE (developed between 7 and 28 days, n = 85) was associated with longer MV day (43.8 days vs. 23.3 days [non-VAE], P < 0.05). The 90-day Kaplan-Meier survival curves showed three lines that separate the groups (non-VAE, early VAE, and late VAE). Cox regression models with time-varying coefficient covariates (adjusted for the number of days from intubation to VAE development) confirmed that VAE which occurred within 28 days upon admission to the medical ICUs can be associated with higher 90-day mortality. The risk factors for VAE development include impaired immune response (lower human leukocyte antigen D-related expression, higher interleukin-10 expression) and sepsis progression with elevated SOFA score (especially in coagulation sub-score). Ventilator-associated event (VAE) 1,2 was proposed to overcome the limitations of only focusing on ventilatorassociated pneumonia (VAP) 3 surveillance in mechanically ventilated (MV) patients in the context of surveying quality improvement. The limitations of previous VAP surveillance, which is proven to be neither sensitive nor specific 4 , hindered its application in quality improvement programs 5. Although VAE surveillance was a promising early warning tool for VAP prevention 6 , VAP prevention bundle compliance was not associated with a reduced risk of VAE 7. VAEs are defined as respiratory deterioration after a period of improved or stable gas exchange. The definition of VAE shifted the focus of surveillance from pneumonia to all conditions caused by mechanical ventilation including infectious or noninfectious conditions. The purpose was to expand the scope of surveillance to include multiple serious complications in ventilated patients, not just pneumonia, as well as to make surveillance more objective, efficient, and suitable for electronic implementation. Sepsis patients developed life-threatening organ dysfunctions (e.g., acute respiratory failure) caused by dysregulated host immune response to infection 8-10. An increase in sequential organ failure assessment (SOFA) score (including respiratory and other five sub-scores) has prognostic accuracy for in-hospital mortality in sepsis patients in the intensive care units (ICUs) 11. Since mechanical ventilator support and aggressive fluid resuscitation