The passive leg raising (PLR) test is a reversible preload challenge of around 300 mL of blood that can be repeated as frequently as required without infusing a drop of fluid. Two recent meta-analyses of many studies have confirmed the reliability of the PLR test to predict fluid responsiveness in patients with acute circulatory failure. Nevertheless, the effects of the PLR must be assessed by the direct measurement of cardiac output since changes in arterial pressure do not allow the assessment of the PLR hemodynamic effects with reliability. Moreover, cardiac output must be measured continuously and in real time. In clinical practice, cardiac output measurement can be difficult for different reasons such as the unavailability of the echocardiography machine, or the absence of any continuous cardiac output monitoring technique at the time of acute circulatory failure occurrence. Recently, it was shown that the decrease in pulse pressure variation (PPV) induced by the mini-fluid challenge (100 mL of colloid solution infused in 1 min) was able to predict fluid responsiveness with reliability in patients ventilated with low tidal volume (\<8 mL/kg of ideal body weight). Therefore, the investigators hypothesize that the changes in PPV induced by PLR test could be able to predict fluid responsiveness with reliability in mechanically ventilated patients with acute circulatory failure.
Study Type
OBSERVATIONAL
Enrollment
286
Infusion of 500 mL of crystalloid solution in less than 15 minutes
This intervention is done before the fluid loading in order to predict fluid responsiveness.
CHU d'Amiens - Réanimation Cardio-Thoracique-Vasculaire
Amiens, France
CHU d'Amiens - Réanimation chirurgicale
Amiens, France
Centre Hospitalier d'Arras
Arras, France
Centre Hospitalier de Béthune
Béthune, France
CH Boulogne-sur-mer
Boulogne-sur-Mer, France
CHU de Caen
Caen, France
Centre Hospitalier de Cambrai
Cambrai, France
CHU de Dijon
Dijon, France
Centre Hospitalier de Lens - Anesthésie-Réanimation
Lens, France
Centre Hospitalier de Lens - Réanimation
Lens, France
...and 2 more locations
Increase in cardiac output in all mechanically ventilated patients
The primary endpoint is the increase in cardiac output of more than or equal to 15% after 500 mL of volume expansion. All included patients are concerned by the primary outcome.
Time frame: Cardiac output will be measured immediately after the end of the volume expansion
Increase in cardiac output in mechanically ventilated patients with spontaneous breathing activities
The secondary endpoint is the increase in cardiac output of more than or equal to 15% after 500 mL of volume expansion. Only patients with spontaneous breathing activities are concerned by this secondary outcome.
Time frame: Cardiac output will be measured immediately after the end of the volume expansion
Increase in cardiac output in mechanically ventilated patients with low tidal ventilation and/or low respiratory compliance
The secondary endpoint is the increase in cardiac output of more than or equal to 15% after 500 mL of volume expansion. Only patients with low tidal ventilation (\<8mL/kg of ideal body weight) and/or low respiratory compliance (\<30mL/cmH2O) are concerned by this secondary outcome.
Time frame: Cardiac output will be measured immediately after the end of the volume expansion
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