- Meeting abstract
- Open Access
Inferior vena cava diameters and collapsibility index changes reveal early volume depletion in a healthy donor model
© Pasquero et al; licensee Springer. 2012
- Published: 18 December 2012
- Blood Loss
- Inferior Vena Cava
- Healthy Donor
- Renal Vein
- Post Processing
Measurement of the Inferior Vena Cava (IVC) diameters and collapsibility index (CI) for the detection of early volume depletion in healthy donors was recently investigated by Resnick et al. who showed no significant changes using different approaches after blood loss.
To investigate the usefulness of IVC diameters and CI measurement to detect early volume depletion after blood loss of 400-450 ml using different sonographic windows.
54 consecutive healthy donors were enrolled. 7 were excluded (1 for anaemia, 1 hypotension, 4 inadequate IVC visualization and 1 abnormal IVC dilatation).
Ultrasound measurements were obtained using M Mode, immediately before and as soon as possible after blood donation. Time from end of donation was recorded. Antero-posterior mid hepatic IVC diameter (long-axis and short-axis) were taken under the hepatic veins while distal IVC diameter was measured at the left renal vein junction. All data were fully recorded for a post processing study with an open source software (Image J).
47 donors (27 males, median age 38, median BMI 24.25) had satisfactory IVC visualization in 92.1%, 88.2%, 58.8% of cases for hepatic long-axis, hepatic short-axis and renal vein approach respectively.
No statistical difference between real time and post processing hepatic short-axis measurements was found. All mean IVC diameters decreased (-19.3%, -19.8%, -25.9% in maximal diameters; -30.3%, -32.4%, -34.7% in minimal diameters) and mean CI increased (+27.2%,+30.2%, +23.9%) for each window after blood letting (p<0.00). Mid hepatic IVC long-axis revealed a correlation between the time after donation and CI ( 20% CI decrease within 5 minutes until 0% after 20 minutes).
Both IVC diameters and CI changes identified volume depletion in a healthy donor model. The mid hepatic long-axis window showed the best correlation between the IVC-CI and early volume variations following blood loss and post-donation volume repletion.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.