scholarly journals A new Monte Carlo tool for organ dose estimation in computed tomography

2020 ◽  
Vol 55 (2) ◽  
pp. 123-134
Author(s):  
C. Adrien ◽  
C. Le Loirec ◽  
S. Dreuil ◽  
J.-M. Bordy

The constant increase of computed tomography (CT) exams and their major contribution to the collective dose led to international concerns regarding patient dose in CT imaging. Efforts were made to manage radiation dose in CT, mostly with the use of the CT dose index (CTDI). However CTDI does not give access to organ dose information, while Monte Carlo (MC) simulation can provide it if detailed information of the patient anatomy and the source are available. In this work, the X-ray source and the geometry of the GE VCT Lightspeed 64 were modelled, based both on the manufacturer technical note and some experimental data. Simulated dose values were compared with measurements performed in homogeneous conditions with a pencil chamber and then in CIRS ATOM anthropomorphic phantom using both optically stimulated luminescence dosimeters (OSLD) for point doses and XR-QA Gafchromic® films for relative dose maps. Organ doses were ultimately estimated in the ICRP 110 numerical female phantom and compared to data reported in the literature. Comparison of measured and simulated values show that our tool can be used for a patient specific and organ dose oriented radiation protection tool in CT medical imaging.

2016 ◽  
Vol 36 (2) ◽  
pp. 215-229 ◽  
Author(s):  
Colin J Martin ◽  
Abdullah Abuhaimed ◽  
Marimuthu Sankaralingam ◽  
Mohamed Metwaly ◽  
David J Gentle

2020 ◽  
Author(s):  
Ying Huang ◽  
Yang Yang ◽  
Xin Chen ◽  
Yiming Gao ◽  
Weihai Zhuo ◽  
...  

BACKGROUND CT imaging is one of the most important contributors to medical radiation exposure(1). The frequency of CT scans and radiation doses accepted by patients attracted serious concerns for health physics researchers. The utilization of advanced technology ATCM has the potentials to reduce CT radiation doses while diagnostic image quality is maintained (2-7). As ATCM adjusted tube currents slice by slice it brought challenges to organ dose estimation using conversion factors derived from fixed tube current. Cross-system communication with hospital Picture Archive and Communication System (PACS),made it possible to read massive data automatically like the scanning parameters of each slice in each case. Monte Carlo simulations are probably the most reliable techniques which could be used for accurate dose assessment. [8-11]. However, specific patient model development and specific patient dose simulations are computationally demanding and may require dedicated hardware resources, this limitation constrained its application in large scale investigation. As an alternative method, patient specific organ doses could be calculated using the patient specific scan parameters and the Monte Carlo simulated organ doses with reference human phantom, and then correct the results with patient size factors. Dw is referred as the preferred patient size metric that determined the patient group and affected organ dose. The distance of the pathway traversed by the X-ray beam could provide the best approximation of tissue length traversed during the examination (12, 13),as CT image is a cross-sectional map normalized to the linear attenuation of water (14). The purpose of current study was to establish a method to access patient-specific organ dose associated with ATCM in chest computed tomography (CT) scans by combining Monte Carlo simulation with parameters contracted from clinical CT images of each patient underwent chest CT scan with ATCM. OBJECTIVE To explore a method to access patient-specific organ dose associated with automatic tube current modulation (ATCM) in chest computed tomography (CT) scans based on the information extracted from PACS automatically. METHODS 176cases of chest CT scans were read through cross-system communication with hospital PACS. A total of 8468 images were collected and analyzed automatically using in-house software. The scanning parameters (kVp, tube current, collimation width, etc.) of each CT examination were collected in real time, and a middle CT image of each case was collected for patient size(water equivalent diameter, Dw) calculation. Based on the reference human phantom, organ doses were simulated slice by slice using Monte Carlo method. The patient specific organ doses were calculated by combining tube currents of each patient slice with the simulated results, and doses were revised by correction factors that related to patient size. RESULTS A sum of 8468 slice of tube currents were extracted and analyzed in this study, the average mAs for large size patient group was about 1.6 times to the small size patient group. For organs that covered in the scan range like lung, breast, heart, the dose values were 18.30±2.91mGy, 15.13 ±2.75mGy and 17.87±2.96mGy in small size patients(Dw smaller than 22cm).The dose values of lung, breast, heart, in medium-sized patients (Dw from 22cm to 25cm) were 21.89±4.60mGy, 18.16 ±4.13mGy and 21.46±4.60mGy, while the values were 24.98±4.40mGy, 20.81±3.66mGy and 24.77±4.46mGy respectively in large size patients(Dw larger than 25cm). The organ doses increase with the patient size due to the increase of mAs. CONCLUSIONS The PACS-based method of large batch organ dose calculation to patients undergoing chest CT with ATCM was established. The methods and results may provide guidance to the design and optimization of chest CT protocols with ATCM.


2019 ◽  
Author(s):  
Chena Lee ◽  
Jeongmin Yoon ◽  
Sang-Sun Han ◽  
Ji Yeon Na ◽  
Jeong-Hee Lee ◽  
...  

AbstractThe usage and the model variety of CBCT machine has been rapidly increasing, the dose evaluation of individual devices became an important issue. Patient dose from CBCT was assessed with two different methods, optically stimulated luminescence dosimeter (OSLD) measured and monte carlo (MC) simulation, in four different examination modes. Through the measurement process and obtained value, more practical and efficient method in acquiring CBCT effective dose would be suggested. Twenty-five OSLD were calibrated and equipped in human phantom of head and neck organs. This was exposed on 2 CBCT units, CS9300 (Carestream Dental LLC, Atlanta, Georgia) and RAYSCAN α+ (Ray Co. Ltd, Hwaseong-si, Korea) with 2 different examination modes. Dose recorded in dosimetry was obtained and organ dose as well as an effective dose were obtained in each units of examination modes. Those values were also calculated using MC software, PCXMC (STUK, Helsinki, Finland). The organ doses and effective doses from both methods were compared by each examination mode of individual unit. OSLD measured effective dose value was higher than that obtained with MC method in each examination mode, except dual jaw mode of CS9300. The percent difference of effective dose between the two methods were ranged from 4.0 to 14.3 %. The dose difference between the methods was decreased as the examination FOV decreased. Organ dose values were varied according to the method, while overall trend was similar in both methods. The organs showing high dose were mostly consistent in both methods. In this study, the effective dose obtained by OSLD measurement and MC simulation were compared and both methods were described in detail. Consequently, as relatively efficient and easy-handling method, we carefully suggest MC simulation for further dose evaluation.


2013 ◽  
Vol 64 (2) ◽  
pp. 119-129 ◽  
Author(s):  
Aaron Sodickson

Many tools and strategies exist to enable reduction of radiation exposure from computed tomography (CT). The common CT metrics of x-ray output, the volume CT dose index and the dose-length product, are explained and serve as the basis for monitoring radiation exposure from CT. Many strategies to dose-optimize CT protocols are explored that, in combination with available hardware and software tools, allow robust diagnostic quality CT to be performed with a radiation exposure appropriate for the clinical scenario and the size of the patient. Specific emergency department example protocols are used to demonstrate these techniques.


Author(s):  
Delaram Pakravan ◽  
Farshid Babapour Mofrad ◽  
Mohammad Reza Deevband ◽  
Mahdi Ghorbani ◽  
Hamidreza Pouraliakbar

2018 ◽  
Vol 20 (1) ◽  
pp. 308-320 ◽  
Author(s):  
Louise Giansante ◽  
Juliana C. Martins ◽  
Denise Y. Nersissian ◽  
Karen C. Kiers ◽  
Fernando U. Kay ◽  
...  

2020 ◽  
Vol 6 (4) ◽  
pp. 045016
Author(s):  
Choonsik Lee ◽  
Jiamin Liu ◽  
Keith Griffin ◽  
Les Folio ◽  
Ronald M Summers

Author(s):  
Keith T. Griffin ◽  
Tatsuhiko Sato ◽  
Sachiyo Funamoto ◽  
Konstantin Chizhov ◽  
Sean Domal ◽  
...  

AbstractThe radiation exposure estimates for the atomic bomb survivors at Hiroshima and Nagasaki have evolved over the past several decades, reflecting a constant strive by the Radiation Effects Research Foundation (RERF) to provide thorough dosimetry to their cohort. Recently, a working group has introduced a new series of anatomical models, called the J45 phantom series, which improves upon those currently used at RERF through greater age resolution, sex distinction, anatomical realism, and organ dose availability. To evaluate the potential dosimetry improvements that would arise from their use in an RERF Dosimetry System, organ doses in the J45 series are evaluated here using environmental fluence data for 20 generalized survivor scenarios pulled directly from the current dosimetry system. The energy- and angle-dependent gamma and neutron fluences were converted to a source term for use in MCNP6, a modern Monte Carlo radiation transport code. Overall, the updated phantom series would be expected to provide dose improvements to several important organs, including the active marrow, colon, and stomach wall (up to 20, 20, and 15% impact on total dose, respectively). The impacts were especially significant for neutron dose estimates (up to a two-fold difference) and within organs which were unavailable in the previous phantom series. These impacts were consistent across the 20 scenarios and are potentially even greater when biological effectiveness of the neutron dose component is considered. The entirety of the dosimetry results for all organs are available as supplementary data, providing confident justification for potential future DS workflows utilizing the J45 phantom series.


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