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Details

Autor(en) / Beteiligte
Titel
Normalized glandular dose coefficients in mammography, digital breast tomosynthesis and dedicated breast CT
Ist Teil von
  • Physica medica, 2018-11, Vol.55, p.142-148
Ort / Verlag
Italy: Elsevier Ltd
Erscheinungsjahr
2018
Quelle
MEDLINE
Beschreibungen/Notizen
  • •Modeling a breast compressed in MLO view instead of in CC view does not produce any significant differences in MGD estimates.•Skin model presents a noticeable influence on T-factor in DBT.•Correction factor for taking into account the ion-chamber model in MGD estimates in BCT was calculated. To provide mean glandular dose (MGD) estimates via Monte Carlo (MC) simulations as a function of the breast models and scan parameters in mammography, digital breast tomosynthesis (DBT) and dedicated breast CT (BCT). The MC code was based on GEANT4 toolkit. The simulated compressed breast was either a cylinder with a semi-circular section or ad hoc shaped for oblique view (MLO). In DBT we studied the influence of breast models and exam parameters on the T-factors (i.e. the conversion factor for the calculation of the MGD in DBT from that for a 0-degree projection), and in BCT we investigated the influence on the MGD estimates of the ion chamber volume used for the air kerma measurements. In mammography, a model representative of a breast undergoing an MLO view exam did not produce substantial differences (0.4%) in MGD estimates, when compared to a conventional cranio-caudal (CC) view breast model. The beam half value layer did not present a significant influence on T-factors in DBT (<0.8%), while the skin model presented significant influence on MGD estimates (up to 3.3% at 30 degrees scan angle), increasing for larger scan angles. We derived a correction factor for taking into account the different ion chamber volume used in MGD estimates in BCT. A series of MC code modules for MGD estimates in 2D and 3D breast imaging have been developed in order to take into account the most recent advances in breast models.
Sprache
Englisch
Identifikatoren
ISSN: 1120-1797
eISSN: 1724-191X
DOI: 10.1016/j.ejmp.2018.09.002
Titel-ID: cdi_proquest_miscellaneous_2119920383

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