Biomedical subjects

X George Xu

Publications and source records attributed to X George Xu.

15 recordsLinked to original sources

PubMed2006

Effective dose equivalent for point gamma sources located 10 cm near the body.

The key component in the so-called EPRI effective dose equivalent (EDE) methodology is an algorithm that utilizes two dosimeters (instead of multiple dosimeters) to predict the EDE for external photon exposures. The exposure scenarios that were previously studied in deriving the algorithm include parallel photon beams and point sources 33 cm from the body surface. The motivation for this study was the need to investigate source locations within 33 cm from the body so the method is more widely applicable. The ORNL stylized mathematical human phantoms and the MCNP code were used to calculate organ doses in this study. This paper presents the EDE data for point gamma sources at 0.3, 1.0, and 1.5 MeV, respectively, which are located at 10 cm from the surface of the body. The results and analyses show that the locations ranging from the overhead to the foot have resulted in conservative ratios except for two general regions near the front upper thigh and directly overhead. If all locations considered in this study were averaged for each photon energy, the overall ratio is on the conservative side. These data suggest that the EPRI EDE methodology is still valid for sources located 10 cm from the body, although the chance for resulting in a non-conservative estimate of the EDE has increased in comparison with the sources located at 30 cm from the body. Finally, this paper provides recommendations on how to apply the EPRI EDE methodology.

Body Burden↗

PubMed2006

The EPRI EDE calculator--a software package for assessing effective dose equivalent from hot particles on the skin.

Whole body exposure from photon-emitting hot particles is receiving new attention because of changes in skin dose regulations. A recent study calculated and tabulated effective dose equivalent (EDE) and effective dose (ED) for photon energies between 0.1 MeV and 2 MeV for point sources at 74 locations on the skin. This technical note describes a software package called the EPRI EDE Calculator that allows a user to input exposure data and to calculate the EDE and ED automatically.

Algorithms↗

PubMed2006

An investigation of voxel geometries for MCNP-based radiation dose calculations.

Voxelized geometry such as those obtained from medical images is increasingly used in Monte Carlo calculations of absorbed doses. One useful application of calculated absorbed dose is the determination of fluence-to-dose conversion factors for different organs. However, confusion still exists about how such a geometry is defined and how the energy deposition is best computed, especially involving a popular code, MCNP5. This study investigated two different types of geometries in the MCNP5 code, cell and lattice definitions. A 10 cm x 10 cm x 10 cm test phantom, which contained an embedded 2 cm x 2 cm x 2 cm target at its center, was considered. A planar source emitting parallel photons was also considered in the study. The results revealed that MCNP5 does not calculate total target volume for multi-voxel geometries. Therefore, tallies which involve total target volume must be divided by the user by the total number of voxels to obtain a correct dose result. Also, using planar source areas greater than the phantom size results in the same fluence-to-dose conversion factor.

Humans↗

PubMed2005

PRDC--a software package for personnel radiation dose calculation.

To determine effective dose, we usually need to use a very complicated human body model and a sophisticated computer code to transport radiations in the body model and surrounding medium, which is not very easy to practicing health physicists in the field. This study develops and tests a software package, called PRDC (Personnel Radiation Dose Calculation), which calculates effective dose and radiation doses to various organs/tissues and personal dosemeters based on a series of interpolations.

Algorithms↗

PubMed2005

Simulation of organ-specific patient effective dose due to secondary neutrons in proton radiation treatment.

Cancer patients undergoing radiation treatment are exposed to high doses to the target (tumour), intermediate doses to adjacent tissues and low doses from scattered radiation to all parts of the body. In the case of proton therapy, secondary neutrons generated in the accelerator head and inside the patient reach many areas in the patient body. Due to the improved efficacy of management of cancer patients, the number of long term survivors post-radiation treatment is increasing substantially. This results in concern about the risk of radiation-induced cancer appearing at late post-treatment times. This paper presents a case study to determine the effective dose from secondary neutrons in patients undergoing proton treatment. A whole-body patient model, VIP-Man, was employed as the patient model. The geometry dataset generated from studies made on VIP-Man was implemented into the GEANT4 Monte Carlo code. Two proton treatment plans for tumours in the lung and paranasal sinus were simulated. The organ doses and ICRP-60 radiation and tissue weighting factors were used to calculate the effective dose. Results show whole body effective doses for the two proton plans of 0.162 Sv and 0.0266 Sv, respectively, to which the major contributor is due to neutrons from the proton treatment nozzle. There is a substantial difference among organs depending on the treatment site.

Computer Simulation↗

PubMed2005

Monte Carlo study of MOSFET dosemeter characteristics: dose dependence on photon energy, direction and dosemeter composition.

MOSFET dosemeters are emerging as a versatile tool in various medical physics and health physics dose measurements. It is an important but difficult task to understand their energy and directional dependences because of their unique features. This paper presents a study to characterise a MOSFET dosemeter using Monte Carlo simulation method. Monoenergetic photon beams ranging from 15 to 6 MeV were simulated to study the energy and angular dependences. The results were compared with published experimental data. The Monte Carlo model also provided insightful information on optimising the dosemeter design by examining how various regions of the dosemeter contributed to the dose. Detailed energy deposition processes were further analysed by tracking individual particles inside the dosemeter.

Electrons↗

PubMed2005

Adjoint Monte Carlo method for prostate external photon beam treatment planning: an application to 3D patient anatomy.

Recently, the theoretical framework of the adjoint Monte Carlo (AMC) method has been developed using a simplified patient geometry. In this study, we extended our previous work by applying the AMC framework to a 3D anatomical model called VIP-Man constructed from the Visible Human images. First, the adjoint fluxes for the prostate (PTV) and rectum and bladder (organs at risk (OARs)) were calculated on a spherical surface of 1 m radius, centred at the centre of gravity of PTV. An importance ratio, defined as the PTV dose divided by the weighted OAR doses, was calculated for each of the available beamlets to select the beam angles. Finally, the detailed doses in PTV and OAR were calculated using a forward Monte Carlo simulation to include the electron transport. The dose information was then used to generate dose volume histograms (DVHs). The Pinnacle treatment planning system was also used to generate DVHs for the 3D plans with beam angles obtained from the AMC (3D-AMC) and a standard six-field conformal radiation therapy plan (3D-CRT). Results show that the DVHs for prostate from 3D-AMC and the standard 3D-CRT are very similar, showing that both methods can deliver prescribed dose to the PTV. A substantial improvement in the DVHs for bladder and rectum was found for the 3D-AMC method in comparison to those obtained from 3D-CRT. However, the 3D-AMC plan is less conformal than the 3D-CRT plan because only bladder, rectum and PTV are considered for calculating the importance ratios. Nevertheless, this study clearly demonstrated the feasibility of the AMC in selecting the beam directions as a part of a treatment planning based on the anatomical information in a 3D and realistic patient anatomy.

Dose-Response Relationship, Radiation↗

PubMed2005

Development of a simulator for radiographic image optimization.

A software package, incorporating two computational patient phantoms, has been developed for optimizing X-ray radiographic imaging. A tomographic phantom, visible photographic Man tomographic phantom (VIP-Man), constructed from Visible Human anatomical color images is used to simulate the scattered portion of an X-ray system using the Electron Gamma Shower National Research Council (EGSnrc) Monte Carlo code. The primary portion of an X-ray image is simulated using the projection ray-tracing method through the Visible Human CT data set. To produce a realistic image, the software simulates quantum noise, blurring effects, lesions, detector absorption efficiency, and other imaging artifacts. The primary and scattered portions of an X-ray chest image are combined to form a final image for future observer studies and image quality analysis. Absorbed doses in organs and tissues of the segmented VIP-Man phantom were also obtained from the Monte Carlo simulations. This paper presents methods of the simulator and preliminary results.

Computers↗

PubMed2005

Comparison of effective doses from various monoenergetic particles based on the stylised and the VIP-Man tomographic models.

This study compares the effective doses from a MIRD-type stylised model with those derived from the scaled-down version of the tomographic VIP-Man model for photon, electron, neutron and proton beams. The effective dose results from these two models show that they differ from each other within approximately 10% for common high-energy photon beams, within approximately 16% for neutrons, and within approximately 4% for high-energy proton beams. However, for low-energy protons and common electron beams, the effective doses can be different in >100%. It is concluded that the use of a single tomographic models will not improve the operational radiation protection dosimetry involving external beam exposures.

Adult↗

PubMed2005

Effective dose for patients undergoing coronary and femoral intravascular radiotherapy involving an HDR 192Ir source.

Effective dose equivalent (EDE), and effective dose (ED) for coronary and femoral Intravascular brachytherapy (IVBT) procedures involving a 370 GBq (10 Ci) HDR 192Ir gamma source are tabulated. MIRD stylised models and the MCNP Monte Carlo code were used for the calculations. For coronary irradiation, the normalised EDE is 0.18 mSv (GBq min)(-1) and the ED is 0.056 mSv (GBq min)(-1). For femoral IVBT, the normalised EDE is 0.01629 mSv (GBq min)(-1) and the ED is 0.01195 mSv (GBq min)(-1). Although the medical benefits to a patient undergoing IVBT are often significant and justified, patient doses are high compared with dose limits for radiation protection purposes. As IVBT is becoming a routine procedure, data in this paper could be useful to manage the procedures efficiently.

Brachytherapy↗

PubMed2005

The effective dose equivalent and effective dose for hot particles on the skin.

Whole body exposure from photon-emitting hot particles is a relatively new problem. Until recently, the U.S. Nuclear Regulatory Commission required the use of deep dose equivalent (DDE) to estimate and report whole body exposures from hot particles. In this study, effective dose equivalent (EDE) and effective dose (ED) were calculated for point sources with photon energies between 0.1 MeV to 2.0 MeV for 74 locations covering the entire body surface, using the MCNP code and the MIRD-type stylized phantoms. Tabulated data show that the sources located near the upper chest and the lower waist have the highest EDE and ED, while sources near the top of head and feet yielded the smallest. The calculated DDE values are much higher than the EDE values. For an exposure of 75 microCi h(-1) to a 60Co source located at the center upper chest area, the EDE is 36.5 microSv (3.65 mrem), which is a factor of 240 smaller than the corresponding DDE. EDE and ED data are tabulated for quick reference by users in nuclear power plants.

Adult↗

PubMed2005

Dose mapping using MCNP5 mesh tallies.

Rensselaer Polytechnic Institute has a 69.6 GBq (1.88 Ci) (137)Cs source that is used for research, calibration of various instruments, and teaching. Recently it was calibrated using ion chambers. The source and room were also modeled in Monte Carlo N-Particle transport code (MCNP5) to determine if the use of a new feature called mesh tallies produces a dose map in the entire room that agrees with the measured results. The dose rate in the hallway, while the source is exposed, was also calculated. It was found that the dose rates calculated from the MCNP5 are in reasonable agreement with the measured results and theoretical predictions. It was also confirmed that the dose rates where the user often stays during the measurement are well below the annual limits. This project shows that the MCNP5 mesh tallies are useful tool for dose mapping in many operational radiation protection situations.

Cesium Radioisotopes↗

PubMed2004

S-values calculated from a tomographic head/brain model for brain imaging.

A tomographic head/brain model was developed from the Visible Human images and used to calculate S-values for brain imaging procedures. This model contains 15 segmented sub-regions including caudate nucleus, cerebellum, cerebral cortex, cerebral white matter, corpus callosum, eyes, lateral ventricles, lenses, lentiform nucleus, optic chiasma, optic nerve, pons and middle cerebellar peduncle, skull CSF, thalamus and thyroid. S-values for C-11, O-15, F-18, Tc-99m and I-123 have been calculated using this model and a Monte Carlo code, EGS4. Comparison of the calculated S-values with those calculated from the MIRD (1999) stylized head/brain model shows significant differences. In many cases, the stylized head/brain model resulted in smaller S-values (as much as 88%), suggesting that the doses to a specific patient similar to the Visible Man could have been underestimated using the existing clinical dosimetry.

Algorithms↗

PubMed2004

Use of the VIP-Man model to calculate energy imparted and effective dose for x-ray examinations.

A male human tomographic model was used to calculate values of energy imparted (epsilon) and effective dose (E) for monoenergetic photons (30-150 keV) in radiographic examinations. Energy deposition in the organs and tissues of the human phantom were obtained using Monte Carlo simulations. Values of E/epsilon were obtained for three common projections [anterior-posterior (AP), posterior-anterior (PA), and lateral (LAT)] of the head, cervical spine, chest, and abdomen, respectively. For head radiographs, all three projections yielded similar E/epsilon values. At 30 keV, the value of E/epsilon was approximately 1.6 mSv J(-1), which is increased to approximately 7 mSv J(-1) for 150 keV photons. The AP cervical spine was the only projection investigated where the value of E/epsilon decreased with increasing photon energy. Above 70 keV, cervical spine E/epsilon values showed little energy dependence and ranged between approximately 8.5 mSv J(-1) for PA projections and approximately 17 mSv J(-1) for AP projections. The values of E/epsilon for AP chest examinations showed very little variation with photon energy, and had values of approximately 23 mSv J(-1). Values of E/epsilon for PA and LAT chest projections were substantially lower than the AP projections and increased with increasing photon energy. For abdominal radiographs, differences between the PA and LAT projections were very small. All abdomen projections showed an increase in the E/epsilon ratio with increasing photon energy, and reached a maximum value of approximately 13.5 mSv J(-1) for AP projections, and approximately 9.5 mSv J(-1) for PA/lateral projections. These monoenergetic E/epsilon values can generate values of E/epsilon for any x-ray spectrum, and can be used to convert values of energy imparted into effective dose for patients undergoing common head and body radiological examinations.

Adult↗

PubMed2004

Development of a 30-week-pregnant female tomographic model from computed tomography (CT) images for Monte Carlo organ dose calculations.

Assessment of radiation dose and risk to a pregnant woman and her fetus is an important task in radiation protection. Although tomographic models for male and female patients of different ages have been developed using medical images, such models for pregnant women had not been developed to date. This paper reports the construction of a partial-body model of a pregnant woman from a set of computed tomography (CT) images. The patient was 30 weeks into pregnancy, and the CT scan covered the portion of the body from above liver to below pubic symphysis in 70 slices. The thickness for each slice is 7 mm, and the image resolution is 512x512 pixels in a 48 cm x 48 cm field; thus, the voxel size is 6.15 mm3. The images were segmented to identify 34 major internal organs and tissues considered sensitive to radiation. Even though the masses are noticeably different from other models, the three-dimensional visualization verified the segmentation and its suitability for Monte Carlo calculations. The model has been implemented into a Monte Carlo code, EGS4-VLSI (very large segmented images), for the calculations of radiation dose to a pregnant woman. The specific absorbed fraction (SAF) results for internal photons were compared with those from a stylized model. Small and large differences were found, and the differences can be explained by mass differences and by the relative geometry differences between the source and the target organs. The research provides the radiation dosimetry community with the first voxelized tomographic model of a pregnant woman, opening the door to future dosimetry studies.

Body Burden↗