Beta-particle dosimetry of the trabecular skeleton using Monte Carlo transport within 30 digital images

Citation
Dw. Jokisch et al., Beta-particle dosimetry of the trabecular skeleton using Monte Carlo transport within 30 digital images, MED PHYS, 28(7), 2001, pp. 1505-1518
Citations number
49
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
MEDICAL PHYSICS
ISSN journal
00942405 → ACNP
Volume
28
Issue
7
Year of publication
2001
Pages
1505 - 1518
Database
ISI
SICI code
0094-2405(200107)28:7<1505:BDOTTS>2.0.ZU;2-P
Abstract
Presently, skeletal dosimetry models utilized in clinical medicine simulate electron path lengths through skeletal regions based upon distributions of linear chords measured across bone trabeculae and marrow cavities. In this work, a human thoracic vertebra has been imaged via nuclear magnetic reson ance (NMR) spectroscopy yielding a three-dimensional voxelized representati on of this skeletal site. The image was then coupled to the radiation trans port code EGS4 allowing for 3D tracing of electron paths within its true 3D structure. The macroscopic boundaries of the trabecular regions, as well a s the cortex of cortical bone surrounding the bone site, were explicitly co nsidered in the voxelized transport model. For the case of a thoracic verte bra, energy escape to the cortical bone became significant at source energi es exceeding similar to2 MeV. Chord-length distributions were acquired From the same NMR image, acid subsequently used as input for a chord-based dosi metry model. Differences were observed in the absorbed fractions given by t he chord-based model and the voxel transport model, suggesting that some of the input chord distributions for the chord-based models may not be accura te. Finally, this work shows that skeletal mass estimates can be made from the same NMR image in which particle transport is performed. This feature a llows one to determine a skeletal S-value using absorbed fraction and mass data taken from the same anatomical tissue sample. The techniques developed in this work may be applied to a variety of skeletal sites, thus allowing for the development of skeletal dosimetry models at all skeletal sites for both males and females and as a function of subject age. (C) 2001 American Association of Physicists in Medicine.