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Published on: January 20, 2023
Fluid Responsiveness in Critically Ill Patients Using Carotid Peak Systolic Velocity Variability: A New Frontier
Abhinob Roy1, Anant Vikram Pachisia2, Deepak Govil3
1Critical Care Medicine, Paras Hospital, Gurugram, IND.
Carotid peak systolic velocity (CPSV) variation significantly decreases after fluid administration in fluid responders, mirroring changes in Left Ventricular Outflow Tract (LVOT) velocity time integral (VTI) variation. This suggests CPSV variation is a potential surrogate for assessing fluid responsiveness.
Area of Science:
- Critical care medicine
- Cardiovascular physiology
- Hemodynamic monitoring
Background:
- Fluid responsiveness assessment is crucial in critical care.
- Left Ventricular Outflow Tract (LVOT) velocity time integral (VTI) variability is a common but often difficult-to-obtain parameter for fluid responsiveness.
- Carotid Peak Systolic Velocity (CPSV) variation is explored as a potentially more accessible surrogate marker.
Purpose of the Study:
- To evaluate the utility of CPSV variation as a surrogate marker for fluid responsiveness.
- To assess changes in CPSV variation in patients already identified as fluid responders.
Main Methods:
- Adult patients receiving fluid bolus therapy were studied.
- LVOT VTI and CPSV variation were measured before and after a 6 ml/kg fluid bolus.
- Hemodynamic variables and breathing modes (spontaneous vs. mechanical ventilation) were recorded.
Main Results:
- CPSV variation significantly decreased post-fluid administration in both spontaneously breathing (14.1 ± 3.4 to 5.4 ± 2.6, p < 0.05) and mechanically ventilated patients (15 ± 5.3 to 6.5 ± 3.1, p < 0.005).
- A significant positive correlation was found between LVOT VTI variation and CPSV variation before fluid therapy (r=0.56, p=0.001) and a moderate positive correlation after (r=0.37, p=0.043).
Conclusions:
- CPSV variation decreases significantly after fluid administration in fluid responders.
- CPSV variation shows potential as a non-invasive, easily obtainable surrogate marker for assessing fluid responsiveness, complementing LVOT VTI.
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