
4 DISCUSSION
The tissue response to compression is subject-
specific. Deformation and accordingly calculated
strain depend on the site of actuation. If the actua-
tor is mounted on the side with varying layers of adi-
pose superficial tissue, or varying stiffness of muscle
because of involuntary movements of the leg the re-
actions to compression will be different. So the intra-
subject peculiarities of tissues are proposed to be con-
sidered with the initial adjustment of the strain thresh-
old. The automatic compressions are performed from
the back side of the thigh and result in smaller mod-
ulation of strain. Despite low modulation of strain,
the actuation on the thigh from the opposite side and
the use of rigid pre-shaped frames to mount the imag-
ing transducer and actuating bladders contribute to re-
ducing uncertainty in tissue response (reducing shear
deformation).
The whole B-mode image was used for the strain
estimate calculation and not justified to regions of
thigh tissues. Adjusting region for strain estimation
could potentially increase strain modulation and the
accuracy in quantifying compression amount. Pro-
vided experimental results are from a limited num-
ber of healthy subjects. The personal body charac-
teristics were not examined in detail, thus further re-
search is needed including a bigger group of subjects
with higher variability in body composition. Addi-
tionally, individualized calibration should be devel-
oped to perform long-term accurate monitoring of tis-
sue response.
5 CONCLUSIONS
In this study, an ultrasonography tissue compression
actuator for automated long-term monitoring of ve-
nous vessels in the lower extremities is proposed. The
actuator is controlled by a tissue strain parameter that
regulates compression. The results show a negative
correlation between venous vessel lumen closure and
the tissue strain parameter, suggesting that using tis-
sue strain as a feedback mechanism is feasible. How-
ever, the variability at a higher strain threshold is rel-
atively big, leaving room for improvement. Inter-
subject variability could be addressed through initial
calibration, while intra-subject variability for moni-
toring applications could be managed by defining a
more targeted region of interest.
ACKNOWLEDGEMENTS
This work is funded under the Horizon Europe In-
novation Action ThrombUS+ (Grant Agreement No.
101137227), co-funded by the European Union.
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