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No statistical differences were found between mean doses and dose distributions in patients with and without pathologic uptakes.
Similarly, no statistical differences were found between mean doses and dose distributions (represented by DVHs) in patients with and without pathologic uptakes.
This was performed by a direct, i.e., Gy-to-Gy, comparison between intended tumor mean doses and post-radioembolization tumor mean doses by 90Y PET, expressed as relative percentage errors.
For all vasopressors/inotropes administered, both the mean doses and the peak doses were recorded.
Specific SRI's, mean doses and dose range are provided in Table 1.
For PTVs, RA-C delivered lower maximum and mean doses and improved conformity and homogeneity compared with RA-FFF.
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Mean dose and dose volume histogram is a most convenient tool for incorporating such constraints.
We found that the EUD parameter has strong dependence on the parameters that characterize the distribution, namely the mean dose and the standard deviation around the mean.
For each investigated organ and tumor, its mean dose and dose distribution (represented by the cumulated dose-volume histograms DVHs) were estimated using the voxel-S approach.
The mean dose and V50 of the heart were maintained at < 40 Gy and 50%%, respectively.
The mean dose and ID deposited in the OARs and NT were also compared.
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CEO of Professional Science Editing for Scientists @ prosciediting.com