scholarly journals A method of rapid quantification of patient‐specific organ doses for CT using deep‐learning‐based multi‐organ segmentation and GPU‐accelerated Monte Carlo dose computing

2020 ◽  
Vol 47 (6) ◽  
pp. 2526-2536 ◽  
Author(s):  
Zhao Peng ◽  
Xi Fang ◽  
Pingkun Yan ◽  
Hongming Shan ◽  
Tianyu Liu ◽  
...  
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.


2015 ◽  
Vol 108 (1) ◽  
pp. 44-52 ◽  
Author(s):  
Osamu Kamei ◽  
Mitsuaki Ojima ◽  
Takayasu Yoshitake ◽  
Koji Ono ◽  
Kohjiro Nishijima ◽  
...  

2021 ◽  
Vol 60 (1) ◽  
pp. 93-113
Author(s):  
Nina Petoussi-Henss ◽  
Daiki Satoh ◽  
Helmut Schlattl ◽  
Maria Zankl ◽  
Vladimir Spielmann

AbstractThis article presents nuclide-specific organ dose rate coefficients for environmental external exposures due to soil contamination assumed as a planar source at a depth of 0.5 g cm−2 in the soil and submersion to contaminated air, for a pregnant female and its fetus at the 24th week of gestation. Furthermore, air kerma free-in-air coefficient rates are listed. The coefficients relate the organ equivalent dose rates (Sv s−1) to the activity concentration of environmental sources, in Bq m−2 or Bq m−3, allowing to time-integrate over a particular exposure period. The environmental radiation fields were simulated with the Monte Carlo radiation transport codes PHITS and YURI. Monoenergetic organ dose rate coefficients were calculated employing the Monte Carlo code EGSnrc simulating the photon transport in the voxel phantom of a pregnant female and fetus. Photons of initial energies of 0.015–10 MeV were considered including bremsstrahlung. By folding the monoenergetic dose coefficients with the nuclide decay data, nuclide-specific organ doses were obtained. The results of this work can be employed for estimating the doses from external exposures to pregnant women and their fetus, until more precise data are available which include coefficients obtained for phantoms at different stages of pregnancy.


2020 ◽  
Author(s):  
Luciano Melodia

The distribution of energy dose from Lu177 radiotherapy can be estimated by convolving an image of a time-integrated activity distribution with a dose voxel kernel (DVK) consisting of different types of tissues. This fast and inacurate approximation is inappropriate for personalized dosimetry as it neglects tissue heterogenity. The latter can be calculated using different imaging techniques such as CT and SPECT combined with a time consuming monte-carlo simulation. The aim of this study is, for the first time, an estimation of DVKs from CT-derived density kernels (DK) via deep learning in convolutional neural networks (CNNs). The proposed CNN achieved, on the test set, a mean intersection over union (IOU) of =0.86 after 308 epochs and a corresponding mean squared error (MSE) =1.24⋅10−4. This generalization ability shows that the trained CNN can indeed learn the difficult transfer function from DK to DVK. Future work will evaluate DVKs estimated by CNNs with full monte-carlo simulations of a whole body CT to predict patient specific voxel dose maps.


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.


2020 ◽  
Vol 191 (1) ◽  
pp. 1-8
Author(s):  
W J Garzón ◽  
D F A Aldana ◽  
V F Cassola

Abstract The aim of this work was to estimate patient’s organ absorbed doses from pediatric helical head computed tomography (CT) examinations using the Size-Specific Dose Estimate (SSDE) methodology and to determine organ dose to SSDE conversion coefficients for clinical routine. Patient-specific organ and tissue absorbed doses from 139 Head CT scans performed in pediatric patients from 0 to 15 years old in a Public Hospital in Tunja, Colombia were estimated. The calculations were made through Monte Carlo simulations, based on patient-specific information, dosimetric CT quantities (CTDIvol, DLP) and age-specific computational human phantoms matched to patients on the basis of gender and size. SSDE showed to be a good quantity for estimate patient-specific organ doses from pediatric head CT examinations when appropriate phantom’s attenuation-based size metrics are chosen to match for any patient size. Strong correlations between absorbed dose and SSDE were found for skin (R2 = 0.99), brain (R2 = 0.98) and eyes (R2 = 0.97), respectively. Besides, a good correlation between SSDE and absorbed dose to the red bone marrow (tissue extended outside the scan coverage) was observed (R2 = 0.94). SSDE-to-organ-dose conversion coefficients obtained in this study provide a practical way to estimate patient-specific organ head CT doses.


2008 ◽  
Vol 35 (6Part24) ◽  
pp. 2949-2949
Author(s):  
X Li ◽  
B Liu

2019 ◽  
Vol 5 (1) ◽  
pp. 223-226
Author(s):  
Max-Heinrich Laves ◽  
Sontje Ihler ◽  
Tobias Ortmaier ◽  
Lüder A. Kahrs

AbstractIn this work, we discuss epistemic uncertainty estimation obtained by Bayesian inference in diagnostic classifiers and show that the prediction uncertainty highly correlates with goodness of prediction. We train the ResNet-18 image classifier on a dataset of 84,484 optical coherence tomography scans showing four different retinal conditions. Dropout is added before every building block of ResNet, creating an approximation to a Bayesian classifier. Monte Carlo sampling is applied with dropout at test time for uncertainty estimation. In Monte Carlo experiments, multiple forward passes are performed to get a distribution of the class labels. The variance and the entropy of the distribution is used as metrics for uncertainty. Our results show strong correlation with ρ = 0.99 between prediction uncertainty and prediction error. Mean uncertainty of incorrectly diagnosed cases was significantly higher than mean uncertainty of correctly diagnosed cases. Modeling of the prediction uncertainty in computer-aided diagnosis with deep learning yields more reliable results and is therefore expected to increase patient safety. This will help to transfer such systems into clinical routine and to increase the acceptance of machine learning in diagnosis from the standpoint of physicians and patients.


Sign in / Sign up

Export Citation Format

Share Document