首页 > 最新文献

IEEE Transactions on Radiation and Plasma Medical Sciences最新文献

英文 中文
Unified Feature Consistency of Under-Performing Pixels and Valid Regions for Semi-Supervised Medical Image Segmentation
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-23 DOI: 10.1109/TRPMS.2024.3465561
Tao Lei;Yi Wang;Xingwu Wang;Xuan Wang;Bin Hu;Asoke K. Nandi
Existing semi-supervised medical image segmentation methods based on the teacher-student model often employ unweighted pixel-level consistency loss, neglecting the varying difficulties of different pixels and resulting in significant deficits in segmenting challenging regions. Additionally, consistency learning often excludes pixels with high uncertainty, which destroys the semantic integrity of a medical image. To address these issues, we propose a novel unified feature consistency (UFC) of under-performing pixels (UPPs) and valid regions for semi-supervised medical image segmentation: 1) high-performing pixels (HPPs) and UPPs are distinguished by confidence differences between the student and teacher models, and then UPPs are mapped into a latent feature space to improve consistency learning effect (UPPFC); 2) in order to obtain richer semantic information from a medical image, vectors of valid regions are selected from both image- and patch-level class feature vectors by using the output probabilities of the teacher model; and 3) these vectors are mapped into the latent feature space for class feature consistency (CFC) learning as a supplement to UPPFC which only focuses on challenging regions for pixel-level consistency learning, thereby enhancing the model’s ability to learn structured semantic information from images themselves. Experimental results demonstrate that the proposed UFC achieves sufficient learning for challenging regions and retains the semantic integrity of medical images. Encouragingly, our proposed UFC provides better-segmentation results than the current state-of-the-art methods on three publicly available datasets. Our codes will be released at: https://github.com/SUST-reynole.
{"title":"Unified Feature Consistency of Under-Performing Pixels and Valid Regions for Semi-Supervised Medical Image Segmentation","authors":"Tao Lei;Yi Wang;Xingwu Wang;Xuan Wang;Bin Hu;Asoke K. Nandi","doi":"10.1109/TRPMS.2024.3465561","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3465561","url":null,"abstract":"Existing semi-supervised medical image segmentation methods based on the teacher-student model often employ unweighted pixel-level consistency loss, neglecting the varying difficulties of different pixels and resulting in significant deficits in segmenting challenging regions. Additionally, consistency learning often excludes pixels with high uncertainty, which destroys the semantic integrity of a medical image. To address these issues, we propose a novel unified feature consistency (UFC) of under-performing pixels (UPPs) and valid regions for semi-supervised medical image segmentation: 1) high-performing pixels (HPPs) and UPPs are distinguished by confidence differences between the student and teacher models, and then UPPs are mapped into a latent feature space to improve consistency learning effect (UPPFC); 2) in order to obtain richer semantic information from a medical image, vectors of valid regions are selected from both image- and patch-level class feature vectors by using the output probabilities of the teacher model; and 3) these vectors are mapped into the latent feature space for class feature consistency (CFC) learning as a supplement to UPPFC which only focuses on challenging regions for pixel-level consistency learning, thereby enhancing the model’s ability to learn structured semantic information from images themselves. Experimental results demonstrate that the proposed UFC achieves sufficient learning for challenging regions and retains the semantic integrity of medical images. Encouragingly, our proposed UFC provides better-segmentation results than the current state-of-the-art methods on three publicly available datasets. Our codes will be released at: <uri>https://github.com/SUST-reynole</uri>.","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"9 2","pages":"169-181"},"PeriodicalIF":4.6,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10685517","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143106268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Finite Element Method-Based Hybrid MRI/CBCT Generation to Improve Liver Stereotactic Body Radiation Therapy Targets Localization Accuracy
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-23 DOI: 10.1109/TRPMS.2024.3466184
Zeyu Zhang;Mark Chen;Ke Lu;Dongyang Guo;Zhuoran Jiang;Hualiang Zhong;Jason Molitoris;Phuoc T. Tran;Fang-Fang Yin;Lei Ren
Cone-beam CT (CBCT) is commonly used in treatment imaging, but its limited soft tissue contrast presents challenges for liver tumor localization. As a result, indirect localization methods relying on the liver’s boundary are commonly utilized, which have limited accuracy for tumor localization. On-board MRI offers superior soft tissue contrast but is limited by the cost. To address this, we devised a method to generate onboard virtual MRI by integrating pretreatment MRI with onboard CBCT, enhancing liver stereotactic body radiation therapy (SBRT) tumor localization accuracy. We employed a finite element method (FEM) for deformable mapping, deforming prior liver MR images onto CBCT geometry to create a virtual MRI. This hybrid virtual-MRI/CBCT (hMRI-CBCT) approach was evaluated in a pilot study involving 48 patients. The hMRI-CBCT demonstrated superb soft-tissue contrast with clear tumor visualization. Registration accuracy of hMRI-CBCT to planning CT significantly surpasses the onboard CBCT to planning CT registration, particularly for tumors not near the liver boundary, with an average error reduction of $1.53~pm ~2$ .16 mm. Our study demonstrated that hybrid MRI/CBCT can apparently reduce localization errors in liver SBRT, potentially improving tumor control and reducing toxicities, and opening avenues for further margin reduction and dose escalation.
{"title":"Finite Element Method-Based Hybrid MRI/CBCT Generation to Improve Liver Stereotactic Body Radiation Therapy Targets Localization Accuracy","authors":"Zeyu Zhang;Mark Chen;Ke Lu;Dongyang Guo;Zhuoran Jiang;Hualiang Zhong;Jason Molitoris;Phuoc T. Tran;Fang-Fang Yin;Lei Ren","doi":"10.1109/TRPMS.2024.3466184","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3466184","url":null,"abstract":"Cone-beam CT (CBCT) is commonly used in treatment imaging, but its limited soft tissue contrast presents challenges for liver tumor localization. As a result, indirect localization methods relying on the liver’s boundary are commonly utilized, which have limited accuracy for tumor localization. On-board MRI offers superior soft tissue contrast but is limited by the cost. To address this, we devised a method to generate onboard virtual MRI by integrating pretreatment MRI with onboard CBCT, enhancing liver stereotactic body radiation therapy (SBRT) tumor localization accuracy. We employed a finite element method (FEM) for deformable mapping, deforming prior liver MR images onto CBCT geometry to create a virtual MRI. This hybrid virtual-MRI/CBCT (hMRI-CBCT) approach was evaluated in a pilot study involving 48 patients. The hMRI-CBCT demonstrated superb soft-tissue contrast with clear tumor visualization. Registration accuracy of hMRI-CBCT to planning CT significantly surpasses the onboard CBCT to planning CT registration, particularly for tumors not near the liver boundary, with an average error reduction of <inline-formula> <tex-math>$1.53~pm ~2$ </tex-math></inline-formula>.16 mm. Our study demonstrated that hybrid MRI/CBCT can apparently reduce localization errors in liver SBRT, potentially improving tumor control and reducing toxicities, and opening avenues for further margin reduction and dose escalation.","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"9 3","pages":"372-381"},"PeriodicalIF":4.6,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143553150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Test-Time Adaptation via Orthogonal Meta-Learning for Medical Imaging
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-17 DOI: 10.1109/TRPMS.2024.3462542
Zhiwen Wang;Zexin Lu;Tao Wang;Ziyuan Yang;Hui Yu;Zhongxian Wang;Yinyu Chen;Jingfeng Lu;Yi Zhang
Deep learning (DL) models, which have significantly promoted medical imaging, typically assume that training and testing data come from the same domain and distribution. However, these models struggle with unseen testing variations, like different imaging scanners or protocols, leading to suboptimal results from distribution mismatches between training and testing data. Despite extensive research, the issue of distribution mismatch in DL-based medical imaging has been largely overlooked in current literature. To improve the performance with mismatched testing data, this article proposes an orthogonal meta-learning (OML) framework for test-time adaptation (TTA) in medical imaging. Specifically, during training, we develop supervised meta-training reconstruction tasks to guide the self-supervised meta-testing task. Additionally, we introduce an orthogonal learning strategy to enforce orthogonality of pretrained parameters during training, which accelerates convergence during TTA and enhances performance. During the testing stage, the fine-tuned meta-learned parameters effectively reconstruct new, unseen testing data. Extensive experiments on magnetic resonance imaging and computed tomography datasets were conducted to validate our method’s effectiveness against other state-of-the-art methods, including supervised ones, in various mismatch scenarios.
{"title":"Test-Time Adaptation via Orthogonal Meta-Learning for Medical Imaging","authors":"Zhiwen Wang;Zexin Lu;Tao Wang;Ziyuan Yang;Hui Yu;Zhongxian Wang;Yinyu Chen;Jingfeng Lu;Yi Zhang","doi":"10.1109/TRPMS.2024.3462542","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3462542","url":null,"abstract":"Deep learning (DL) models, which have significantly promoted medical imaging, typically assume that training and testing data come from the same domain and distribution. However, these models struggle with unseen testing variations, like different imaging scanners or protocols, leading to suboptimal results from distribution mismatches between training and testing data. Despite extensive research, the issue of distribution mismatch in DL-based medical imaging has been largely overlooked in current literature. To improve the performance with mismatched testing data, this article proposes an orthogonal meta-learning (OML) framework for test-time adaptation (TTA) in medical imaging. Specifically, during training, we develop supervised meta-training reconstruction tasks to guide the self-supervised meta-testing task. Additionally, we introduce an orthogonal learning strategy to enforce orthogonality of pretrained parameters during training, which accelerates convergence during TTA and enhances performance. During the testing stage, the fine-tuned meta-learned parameters effectively reconstruct new, unseen testing data. Extensive experiments on magnetic resonance imaging and computed tomography datasets were conducted to validate our method’s effectiveness against other state-of-the-art methods, including supervised ones, in various mismatch scenarios.","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"9 2","pages":"215-227"},"PeriodicalIF":4.6,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143106335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Implementation of a FPGA-Based Time-to-Digital Converter Utilizing Opposite-Transition Propagation and Virtual Bin Method
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-10 DOI: 10.1109/TRPMS.2024.3457618
Daehee Lee;Sun Il Kwon
We propose an field-programmable gate array (FPGA)-based time-to-digital converter (TDC) that utilizes a virtual bin (VB) approach with opposite-transition (OT) inputs on two tapped-delay lines (TDLs) to obtain less-correlated time bins. The VBs from the proposed OT TDC were obtained by comparing and segmenting the less-correlated bins collected from the two TDLs. The OT TDC was implemented on a 7-series FPGA (Xilinx) to verify performance. A conventional monotonic-transition (MT) TDC, which used identical transition inputs (0-to-1 or 1-to-0 transition) for the two TDLs, was also implemented as a control group. The results were compared with those from the MT TDC and other studies. The proposed method effectively improves time resolution and integral linearity while keeping resource usage low by exploiting these characteristics. The average bin size and RMS value were 5.5 and 4.2 ps, respectively. Moreover, the proposed method exhibits stable performance under temperature variations and implementation location changes. The VB OT TDC, which applies the VB method to the OT TDC, successfully measures detection time differences of two signals from two Cerenkov radiator integrated microchannel plate photomultiplier tubes (CRI-MCP-PMTs) with a high-timing precision of sub-100 ps. The VB OT TDC can be used for next-generation applications that require fast-timing measurements.
{"title":"Implementation of a FPGA-Based Time-to-Digital Converter Utilizing Opposite-Transition Propagation and Virtual Bin Method","authors":"Daehee Lee;Sun Il Kwon","doi":"10.1109/TRPMS.2024.3457618","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3457618","url":null,"abstract":"We propose an field-programmable gate array (FPGA)-based time-to-digital converter (TDC) that utilizes a virtual bin (VB) approach with opposite-transition (OT) inputs on two tapped-delay lines (TDLs) to obtain less-correlated time bins. The VBs from the proposed OT TDC were obtained by comparing and segmenting the less-correlated bins collected from the two TDLs. The OT TDC was implemented on a 7-series FPGA (Xilinx) to verify performance. A conventional monotonic-transition (MT) TDC, which used identical transition inputs (0-to-1 or 1-to-0 transition) for the two TDLs, was also implemented as a control group. The results were compared with those from the MT TDC and other studies. The proposed method effectively improves time resolution and integral linearity while keeping resource usage low by exploiting these characteristics. The average bin size and RMS value were 5.5 and 4.2 ps, respectively. Moreover, the proposed method exhibits stable performance under temperature variations and implementation location changes. The VB OT TDC, which applies the VB method to the OT TDC, successfully measures detection time differences of two signals from two Cerenkov radiator integrated microchannel plate photomultiplier tubes (CRI-MCP-PMTs) with a high-timing precision of sub-100 ps. The VB OT TDC can be used for next-generation applications that require fast-timing measurements.","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"9 2","pages":"148-156"},"PeriodicalIF":4.6,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143106285","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Silicon-Pixel Paradigm for PET
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-09 DOI: 10.1109/TRPMS.2024.3456241
Aleix Boquet-Pujadas;Jihad Saidi;Mateus Vicente;Lorenzo Paolozzi;Jonathan Dong;Pol Del Aguila Pla;Giuseppe Iacobucci;Michael Unser
Positron emission tomography (PET) scanners use scintillation crystals to stop high-energy photons. The ensuing lower-energy photons are then detected via photomultipliers. We study the performance of a stack of monolithic silicon-pixel detectors as an alternative to the combination of crystals and photomultipliers. The resulting design allows for pitches as small as $100~ {mu }$ m and greatly mitigates depth-of-interaction problems. We develop a theory to optimize the sensitivity of these and other scanners under design constraints. The insight is complemented by Monte Carlo simulations and reconstructions thereof. Experiments and theory alike suggest that our approach has the potential to move PET closer to the microscopic scale. The volumetric resolution is an order of magnitude better than that of the state of the art and the parallax error is very small. A small-animal scanner is now under construction.
{"title":"A Silicon-Pixel Paradigm for PET","authors":"Aleix Boquet-Pujadas;Jihad Saidi;Mateus Vicente;Lorenzo Paolozzi;Jonathan Dong;Pol Del Aguila Pla;Giuseppe Iacobucci;Michael Unser","doi":"10.1109/TRPMS.2024.3456241","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3456241","url":null,"abstract":"Positron emission tomography (PET) scanners use scintillation crystals to stop high-energy photons. The ensuing lower-energy photons are then detected via photomultipliers. We study the performance of a stack of monolithic silicon-pixel detectors as an alternative to the combination of crystals and photomultipliers. The resulting design allows for pitches as small as <inline-formula> <tex-math>$100~ {mu }$ </tex-math></inline-formula>m and greatly mitigates depth-of-interaction problems. We develop a theory to optimize the sensitivity of these and other scanners under design constraints. The insight is complemented by Monte Carlo simulations and reconstructions thereof. Experiments and theory alike suggest that our approach has the potential to move PET closer to the microscopic scale. The volumetric resolution is an order of magnitude better than that of the state of the art and the parallax error is very small. A small-animal scanner is now under construction.","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"9 2","pages":"228-246"},"PeriodicalIF":4.6,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10669392","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143106262","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
IEEE Transactions on Radiation and Plasma Medical Sciences Publication Information 电气和电子工程师学会辐射与等离子体医学科学杂志》(IEEE Transactions on Radiation and Plasma Medical Sciences)出版信息
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-06 DOI: 10.1109/TRPMS.2024.3449313
{"title":"IEEE Transactions on Radiation and Plasma Medical Sciences Publication Information","authors":"","doi":"10.1109/TRPMS.2024.3449313","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3449313","url":null,"abstract":"","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"8 7","pages":"C3-C3"},"PeriodicalIF":4.6,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10669124","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142143580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
IEEE Transactions on Radiation and Plasma Medical Sciences Information for Authors 电气和电子工程师学会《辐射与等离子体医学科学杂志》作者须知
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-06 DOI: 10.1109/TRPMS.2024.3449311
{"title":"IEEE Transactions on Radiation and Plasma Medical Sciences Information for Authors","authors":"","doi":"10.1109/TRPMS.2024.3449311","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3449311","url":null,"abstract":"","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"8 7","pages":"C2-C2"},"PeriodicalIF":4.6,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10669129","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142143652","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Member Get-a-Member (MGM) Program 会员注册(MGM)计划
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-06 DOI: 10.1109/TRPMS.2024.3453689
{"title":"Member Get-a-Member (MGM) Program","authors":"","doi":"10.1109/TRPMS.2024.3453689","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3453689","url":null,"abstract":"","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"8 7","pages":"850-850"},"PeriodicalIF":4.6,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10669127","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142143609","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
IEEE DataPort IEEE 数据端口
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-06 DOI: 10.1109/TRPMS.2024.3453691
{"title":"IEEE DataPort","authors":"","doi":"10.1109/TRPMS.2024.3453691","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3453691","url":null,"abstract":"","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"8 7","pages":"851-851"},"PeriodicalIF":4.6,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10669128","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142143678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthetic CT Generation via Variant Invertible Network for Brain PET Attenuation Correction
IF 4.6 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-05 DOI: 10.1109/TRPMS.2024.3453009
Yu Guan;Bohui Shen;Shirui Jiang;Xinchong Shi;Xiangsong Zhang;Bingxuan Li;Qiegen Liu
Attenuation correction (AC) is essential for the generation of artifact-free and quantitatively accurate positron emission tomography (PET) images. Nowadays, deep-learning-based methods have been extensively applied to PET AC tasks, yielding promising results. Therefore, this article develops an innovative approach to generate continuously valued CT images from nonattenuation corrected PET images for AC on brain PET imaging. Specifically, an invertible neural network combined with the variable augmentation strategy that can achieve the bidirectional inference processes is proposed for synthetic CT generation. On the one hand, invertible architecture ensures a bijective mapping between the PET and synthetic CT image spaces, which can potentially improve the robustness of the prediction and provide a way to validate the synthetic CT by checking the consistency of the inverse mapping. On the other hand, the variable augmentation strategy enriches the training process and leverages the intrinsic data properties more effectively. Therefore, the combination provides for superior performance in PET AC by preserving information throughout the network and by better handling of the data variability inherent PET AC. To evaluate the performance of the proposed algorithm, we conducted a comprehensive study on a total of 1480 2-D slices from 37 whole-body 18F-FDG clinical patients using comparative algorithms (such as cycle-generative adversarial network and Pix2pix). Perceptual analysis and quantitative evaluations illustrate that the invertible network for PET AC outperforms other existing AC models, which demonstrates the feasibility of achieving brain PET AC without additional anatomical information.
{"title":"Synthetic CT Generation via Variant Invertible Network for Brain PET Attenuation Correction","authors":"Yu Guan;Bohui Shen;Shirui Jiang;Xinchong Shi;Xiangsong Zhang;Bingxuan Li;Qiegen Liu","doi":"10.1109/TRPMS.2024.3453009","DOIUrl":"https://doi.org/10.1109/TRPMS.2024.3453009","url":null,"abstract":"Attenuation correction (AC) is essential for the generation of artifact-free and quantitatively accurate positron emission tomography (PET) images. Nowadays, deep-learning-based methods have been extensively applied to PET AC tasks, yielding promising results. Therefore, this article develops an innovative approach to generate continuously valued CT images from nonattenuation corrected PET images for AC on brain PET imaging. Specifically, an invertible neural network combined with the variable augmentation strategy that can achieve the bidirectional inference processes is proposed for synthetic CT generation. On the one hand, invertible architecture ensures a bijective mapping between the PET and synthetic CT image spaces, which can potentially improve the robustness of the prediction and provide a way to validate the synthetic CT by checking the consistency of the inverse mapping. On the other hand, the variable augmentation strategy enriches the training process and leverages the intrinsic data properties more effectively. Therefore, the combination provides for superior performance in PET AC by preserving information throughout the network and by better handling of the data variability inherent PET AC. To evaluate the performance of the proposed algorithm, we conducted a comprehensive study on a total of 1480 2-D slices from 37 whole-body 18F-FDG clinical patients using comparative algorithms (such as cycle-generative adversarial network and Pix2pix). Perceptual analysis and quantitative evaluations illustrate that the invertible network for PET AC outperforms other existing AC models, which demonstrates the feasibility of achieving brain PET AC without additional anatomical information.","PeriodicalId":46807,"journal":{"name":"IEEE Transactions on Radiation and Plasma Medical Sciences","volume":"9 3","pages":"325-336"},"PeriodicalIF":4.6,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10666843","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143553033","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
IEEE Transactions on Radiation and Plasma Medical Sciences
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1