About this trial
This prospective single-center observational study aims to evaluate whether the ultrasound-measured femoral vein-to-femoral artery diameter ratio can predict fluid responsiveness in mechanically ventilated adult intensive care patients with acute circulatory failure or shock. Only patients who already have PiCCO monitoring as part of routine clinical care and for whom a fluid challenge is clinically indicated will be included. No additional invasive procedure will be performed for study purposes. Cardiac index will be measured with PiCCO before and after administration of 500 mL balanced crystalloid over 10 minutes, and femoral vein and femoral artery diameters will be measured by bedside ultrasonography. Fluid responsiveness will be defined as an increase of more than 10% in cardiac index after fluid administration. The study will assess the diagnostic performance of the femoral vein-to-femoral artery diameter ratio as a practical bedside parameter to support hemodynamic decision-making in critically ill patients.
Eligibility criteria
Qualifiers
Adult patients aged 18 years or older
Admission to the intensive care unit where the study is being conducted
Receiving invasive mechanical ventilation
Clinical indication for a fluid challenge due to acute circulatory failure or shock, as determined by the responsible intensive care physician
Disqualifiers
Age younger than 18 years
Failure to obtain written informed consent from the patient or legally authorized representative before enrollment
Absence of PiCCO monitoring as part of routine clinical care or no clinical plan for fluid challenge
Inability to complete pre- and post-fluid challenge measurements (e.g., early death, urgent surgery, transfer)
Trial design
Treatments tested in this trial
- Ultrasound Measurement of Femoral Vein-to-Femoral Artery Diameter Ratio