Clinical Q, Bottom Line, Primary Outcome 1)ARDS Flashcards
ACURASYS Clinical Questions
Does administration of cisatracurium improve survival when compared to placebo in ICU patients undergoing mechanical ventilation for early severe ARDS?
ACURASYS Bottom Line
Paralysis with cisatracurium for 48 hours in patients with early severe ARDS improves 90 day survival and increases ventilator-free days.
ACURASYS Primary Outcome
Mortality before discharge or 90 days
ARDSNet Clinical Q
In patients with ALI/ARDS receiving mechanical ventilation, how does a lung protective strategy using lower tidal volumes compare with traditional ventilation protocols in decreasing mortality and ventilator-free days?
ARDSNet Bottomline
In patients with ARDS, low tidal volume ventilation (initial TV 6ml/kg PBW) had lower mortality and more ventilator-free days.
ARDSNet Primary Outcome
ventilator free days, mortality at 120 days
FACTT Clinical Q
In patients with ALI/ARDS that are intubated and receiving positive pressure ventilation, how does the conservative compare to the liberal fluid management strategy in reducing mortality?
FACTT Bottom Line
Among patients with ALI/ARDS, a conservative fluid management strategy targeting a CVP <4 mmHg improves lung function, decreases ventilator days, and reduces ICU days compared to a liberal strategy.
FACTT primary outcome
All cause mortality at 60 days
Dialysis at 60 days
Clinical Question OSCILLATE
In patients is moderate to severe early ARDS, does high-frequency oscillatory ventilation reduce in-hospital mortality?
OSCILLATE Bottom Line
In patients with moderate to severe early ARDS, early high-frequency oscillatory ventilation might increase in-hospital mortality
OSCILLATE Primary outcome
In-hospital mortality
PROSEVA Clinical Question
Among patients with severe ARDS, does prone positioning reduce all-cause mortality at 28 days when compared to supine-only positioning?
PROSEVA Bottom Line
Among patients with severe ARDS (P:F ratio <150 mmHg), prone positioning reduces 28-day mortality.
PROSEVA Primary Outcome
All-cause mortality at 28 days