首页 > 最新文献

2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)最新文献

英文 中文
Diabetic Foot Ulcers Classification using a fine-tuned CNNs Ensemble 使用微调cnn集合的糖尿病足溃疡分类
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00056
E. Santos, Francisco Santos, J. Almeida, K. Aires, J. M. R. Tavares, R. Veras
Diabetic Foot Ulcers (DFU) are lesions in the foot region caused by diabetes mellitus. It is essential to define the appropriate treatment in the early stages of the disease once late treatment may result in amputation. This article proposes an ensemble approach composed of five modified convolutional neural networks (CNNs) - VGG-16, VGG-19, Resnet-50, InceptionV3, and Densenet-201 - to classify DFU images. To define the parameters, we fine-tuned the CNNs, evaluated different configurations of fully connected layers, and used batch normalization and dropout operations. The modified CNNs were well suited to the problem; however, we observed that the union of the five CNNs significantly increased the success rates. We performed tests using 8,250 images with different resolution, contrast, color, and texture characteristics and included data augmentation operations to expand the training dataset. 5-fold cross-validation led to an average accuracy of 95.04%, resulting in a Kappa index greater than 91.85%, considered “Excellent”.
糖尿病足溃疡(DFU)是由糖尿病引起的足部病变。一旦晚期治疗可能导致截肢,在疾病的早期阶段确定适当的治疗是至关重要的。本文提出了一种由5个改进的卷积神经网络(cnn) VGG-16、VGG-19、Resnet-50、InceptionV3和Densenet-201组成的集成方法来对DFU图像进行分类。为了定义参数,我们对cnn进行了微调,评估了全连接层的不同配置,并使用了批处理归一化和dropout操作。改进后的cnn很适合这个问题;然而,我们观察到五个cnn的联合显著提高了成功率。我们使用8250张具有不同分辨率、对比度、颜色和纹理特征的图像进行测试,并包括数据增强操作来扩展训练数据集。5倍交叉验证平均准确率为95.04%,Kappa指数大于91.85%,为“优秀”。
{"title":"Diabetic Foot Ulcers Classification using a fine-tuned CNNs Ensemble","authors":"E. Santos, Francisco Santos, J. Almeida, K. Aires, J. M. R. Tavares, R. Veras","doi":"10.1109/CBMS55023.2022.00056","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00056","url":null,"abstract":"Diabetic Foot Ulcers (DFU) are lesions in the foot region caused by diabetes mellitus. It is essential to define the appropriate treatment in the early stages of the disease once late treatment may result in amputation. This article proposes an ensemble approach composed of five modified convolutional neural networks (CNNs) - VGG-16, VGG-19, Resnet-50, InceptionV3, and Densenet-201 - to classify DFU images. To define the parameters, we fine-tuned the CNNs, evaluated different configurations of fully connected layers, and used batch normalization and dropout operations. The modified CNNs were well suited to the problem; however, we observed that the union of the five CNNs significantly increased the success rates. We performed tests using 8,250 images with different resolution, contrast, color, and texture characteristics and included data augmentation operations to expand the training dataset. 5-fold cross-validation led to an average accuracy of 95.04%, resulting in a Kappa index greater than 91.85%, considered “Excellent”.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"30 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132173521","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: 5
Online reconstruction of fast dynamic MR imaging using deep low-rank plus sparse network 基于深度低秩加稀疏网络的快速动态MR图像在线重构
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00036
Che Wang, Seng Jia, Zhonghong Yan, Yijia Zheng, Shaonan Liu, Haifeng Wang, Dong Liang, Yanjie Zhu
In order to test the performance of online reconstruction of deep low-rank pulse sparse network (L+S-Net) for fast dynamic MR imaging. The L+S-Net was implemented on Gadgetron platform for online reconstruction of the scanner. Although L+S-net has a good image reconstruction performance., it takes a long time to estimate the coil sensitivity using ESPIRiT method. In this study, SigPy's signal processing software package was adopted to accelerate the calculation of coil sensitivity to speed up the online reconstruction. The results of experiments showed that compared with the CPU based method., the time of the coil sensitivity estimation could be shortened more than 100 times by using the gridding reconstruction method based on SigPy GPU. The reconstruction performance is stable and can realize online fast dynamic MR imaging reconstruction within 10 seconds.
为了测试深度低秩脉冲稀疏网络(L+S-Net)用于快速动态磁共振成像的在线重构性能。L+S-Net在Gadgetron平台上实现,用于扫描仪的在线重建。虽然L+S-net具有良好的图像重建性能。采用ESPIRiT方法估算线圈灵敏度需要较长时间。本研究采用SigPy的信号处理软件包,加速线圈灵敏度的计算,加快在线重建速度。实验结果表明,与基于CPU的方法进行了比较。,采用基于SigPy GPU的网格重建方法,线圈灵敏度估计时间可缩短100倍以上。重建性能稳定,可在10秒内实现在线快速动态磁共振成像重建。
{"title":"Online reconstruction of fast dynamic MR imaging using deep low-rank plus sparse network","authors":"Che Wang, Seng Jia, Zhonghong Yan, Yijia Zheng, Shaonan Liu, Haifeng Wang, Dong Liang, Yanjie Zhu","doi":"10.1109/CBMS55023.2022.00036","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00036","url":null,"abstract":"In order to test the performance of online reconstruction of deep low-rank pulse sparse network (L+S-Net) for fast dynamic MR imaging. The L+S-Net was implemented on Gadgetron platform for online reconstruction of the scanner. Although L+S-net has a good image reconstruction performance., it takes a long time to estimate the coil sensitivity using ESPIRiT method. In this study, SigPy's signal processing software package was adopted to accelerate the calculation of coil sensitivity to speed up the online reconstruction. The results of experiments showed that compared with the CPU based method., the time of the coil sensitivity estimation could be shortened more than 100 times by using the gridding reconstruction method based on SigPy GPU. The reconstruction performance is stable and can realize online fast dynamic MR imaging reconstruction within 10 seconds.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"353 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115889936","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
Experiences in Development and Support of a Multi-technology Skin Conditions Clinical Trial Platform 多技术皮肤病临床试验平台的开发与支持经验
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00087
R. Sinnott, William Hu
Clinical trials depend upon secure and robust data collection. Often this data is longitudinal in nature and can include clinical information captured in clinical/hospital settings as well as patient reported information. This paper describes a web application and associated mobile applications (iPhone/Android) developed to support a clinical trial focused on the application of a commercially available tropical fruit-based ointment applied to a range of skin conditions including eczema and skin rashes, cracked/dry skin on heels, sunburn and insect bites: the LPR Study. The LPR study involved 138 participants in four cohorts with treatments over different time periods (10–21 days) depending on their associated skin condition. The paper describes the solution that was developed and the practical experiences and challenges that were faced and overcome in delivery of the underpinning platform.
临床试验依赖于安全可靠的数据收集。这些数据通常是纵向的,可以包括在临床/医院环境中捕获的临床信息以及患者报告的信息。本文描述了一个web应用程序和相关的移动应用程序(iPhone/Android),该应用程序开发用于支持一项临床试验,该试验侧重于将一种市售热带水果软膏应用于一系列皮肤状况,包括湿疹和皮疹、脚跟皮肤皲裂/干燥、晒伤和昆虫叮咬:LPR研究。LPR研究涉及四个队列的138名参与者,根据他们相关的皮肤状况在不同的时间段(10-21天)进行治疗。本文介绍了开发的解决方案,以及在基础平台交付过程中所面临和克服的实践经验和挑战。
{"title":"Experiences in Development and Support of a Multi-technology Skin Conditions Clinical Trial Platform","authors":"R. Sinnott, William Hu","doi":"10.1109/CBMS55023.2022.00087","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00087","url":null,"abstract":"Clinical trials depend upon secure and robust data collection. Often this data is longitudinal in nature and can include clinical information captured in clinical/hospital settings as well as patient reported information. This paper describes a web application and associated mobile applications (iPhone/Android) developed to support a clinical trial focused on the application of a commercially available tropical fruit-based ointment applied to a range of skin conditions including eczema and skin rashes, cracked/dry skin on heels, sunburn and insect bites: the LPR Study. The LPR study involved 138 participants in four cohorts with treatments over different time periods (10–21 days) depending on their associated skin condition. The paper describes the solution that was developed and the practical experiences and challenges that were faced and overcome in delivery of the underpinning platform.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"48 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117268484","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
Integrating Residual, Dense, and Inception Blocks into the nnUNet 将残差块、密集块和盗梦块集成到nnUNet中
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00045
Niccolò McConnell, A. Miron, Zidong Wang, Yongmin Li
The nnUNet is a fully automated and generalisable framework which automatically configures the full training pipeline for the segmentation task it is applied on, while taking into account dataset properties and hardware constraints. It utilises a basic UNet type architecture which is self-configuring in terms of topology. In this work, we propose to extend the nnUNet by integrating mechanisms from more advanced UNet variations such as the residual, dense, and inception blocks, resulting in three new nnUNet variations, namely the Residual-nnUNet, Dense-nnUNet, and Inception-nnUNet. We have evaluated the segmentation performance on eight datasets consisting of 20 target anatomical structures. Our results demonstrate that altering network architecture may lead to performance gains, but the extent of gains and the optimally chosen nnUNet variation is dataset dependent.
nnUNet是一个完全自动化和通用的框架,在考虑数据集属性和硬件约束的同时,它会自动为它应用的分割任务配置完整的训练管道。它利用基本的UNet类型架构,在拓扑方面是自配置的。在这项工作中,我们建议通过集成来自更高级的UNet变体(如残差、密集和初始块)的机制来扩展nnUNet,从而产生三种新的nnUNet变体,即残差-nnUNet、密集-nnUNet和初始-nnUNet。我们评估了由20个目标解剖结构组成的8个数据集的分割性能。我们的结果表明,改变网络架构可能会导致性能提高,但提高的程度和最优选择的nnUNet变化取决于数据集。
{"title":"Integrating Residual, Dense, and Inception Blocks into the nnUNet","authors":"Niccolò McConnell, A. Miron, Zidong Wang, Yongmin Li","doi":"10.1109/CBMS55023.2022.00045","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00045","url":null,"abstract":"The nnUNet is a fully automated and generalisable framework which automatically configures the full training pipeline for the segmentation task it is applied on, while taking into account dataset properties and hardware constraints. It utilises a basic UNet type architecture which is self-configuring in terms of topology. In this work, we propose to extend the nnUNet by integrating mechanisms from more advanced UNet variations such as the residual, dense, and inception blocks, resulting in three new nnUNet variations, namely the Residual-nnUNet, Dense-nnUNet, and Inception-nnUNet. We have evaluated the segmentation performance on eight datasets consisting of 20 target anatomical structures. Our results demonstrate that altering network architecture may lead to performance gains, but the extent of gains and the optimally chosen nnUNet variation is dataset dependent.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"18 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123688364","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: 5
Measuring the Left Ventricular Ejection Fraction using Geometric Features 用几何特征测量左心室射血分数
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00008
Athanasios Lagopoulos, D. Hristu-Varsakelis
One of the crucial indicators of the heart's functioning, is the so-called left ventricular ejection fraction (LVEF), which measures the heart's ability to pump blood, and corresponds to the relative change in volume within the heart's left ventricle between it's most expanded (end-diastole) and most contracted state (end-systole) during a cardiac cycle. A reduced LVEF is a key indicator of heart failure, and as such, its accurate measurement plays a prominent role in cardiology. This work proposes a machine learning approach for estimating the LVEF from short echocardiogram videos. Our model, based on gradient-boosted trees, is significantly simpler than the state of the art, but is competitive in terms of accuracy and has a higher degree of explainability. The proposed model operates on a set of geometric features of the heart's left ventricle, tracking its evolution during the cardiac cycle; some of these features are novel and are proposed here for the first time. We discuss the performance of our model on a dataset of over 10,000 samples, including the relative importance of our proposed features, and show that the model's estimation error is well within the margin of variation that occurs when the same LVEF is measured by different experts.
心脏功能的关键指标之一是所谓的左心室射血分数(LVEF),它衡量心脏泵血的能力,对应于心脏周期中左心室最大扩张状态(舒张末期)和最大收缩状态(收缩期末期)之间的相对体积变化。LVEF降低是心衰的关键指标,因此,准确测量LVEF在心脏病学中起着重要作用。这项工作提出了一种机器学习方法来估计短超声心动图视频的LVEF。我们的模型基于梯度增强树,比现有的模型简单得多,但在准确性方面具有竞争力,并且具有更高的可解释性。该模型基于左心室的一组几何特征,跟踪其在心脏周期中的演变;其中一些特性是新颖的,在这里是第一次提出。我们讨论了我们的模型在超过10,000个样本的数据集上的性能,包括我们提出的特征的相对重要性,并表明模型的估计误差完全在由不同专家测量相同LVEF时发生的变化范围内。
{"title":"Measuring the Left Ventricular Ejection Fraction using Geometric Features","authors":"Athanasios Lagopoulos, D. Hristu-Varsakelis","doi":"10.1109/CBMS55023.2022.00008","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00008","url":null,"abstract":"One of the crucial indicators of the heart's functioning, is the so-called left ventricular ejection fraction (LVEF), which measures the heart's ability to pump blood, and corresponds to the relative change in volume within the heart's left ventricle between it's most expanded (end-diastole) and most contracted state (end-systole) during a cardiac cycle. A reduced LVEF is a key indicator of heart failure, and as such, its accurate measurement plays a prominent role in cardiology. This work proposes a machine learning approach for estimating the LVEF from short echocardiogram videos. Our model, based on gradient-boosted trees, is significantly simpler than the state of the art, but is competitive in terms of accuracy and has a higher degree of explainability. The proposed model operates on a set of geometric features of the heart's left ventricle, tracking its evolution during the cardiac cycle; some of these features are novel and are proposed here for the first time. We discuss the performance of our model on a dataset of over 10,000 samples, including the relative importance of our proposed features, and show that the model's estimation error is well within the margin of variation that occurs when the same LVEF is measured by different experts.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"37 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116799807","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: 2
Deep Model for Anticancer Drug Response through Genomic Profiles and Compound Structures 基于基因组图谱和化合物结构的抗癌药物反应深度模型
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00050
Filipa G. Carvalho, Maryam Abbasi, B. Ribeiro, Joel P. Arrais
Cancer is among the deadliest diseases, enhancing the need for its detection and treatment. In the era of precision medicine, the main goal is to take into account individual vari-ability in order to choose more accurately which treatment and prevention strategies suit each person. However, drug response prediction for cancer therapy remains a challenge. In this work, we propose a deep neural network model to predict the effect of anticancer drugs in tumors through the half-maximal inhibitory concentration (IC50). The model can be seen as two-fold: first, we pre-trained two autoencoders with high-dimensional gene expression and mutation data to capture the crucial features from tumors; then, this genetic background is translated to cancer cell lines to predict the impact of the genetic variants on a given drug. Moreover, SMILES structures were introduced so that the model can apprehend relevant features regarding the drug compound. Finally, we use drug sensitivity data correlated to the genomic and drugs data to identify features that predict the IC50 value for each pair of drug-cell line. The obtained results demonstrate the effectiveness of the extracted deep representations in the prediction of drug-target interactions, achieving a performance of a mean squared error of 1.07 and surpassing previous state-of-the-art models.
癌症是最致命的疾病之一,因此更需要对其进行检测和治疗。在精准医疗时代,主要目标是考虑到个体的可变性,以便更准确地选择适合每个人的治疗和预防策略。然而,癌症治疗的药物反应预测仍然是一个挑战。在这项工作中,我们提出了一个深度神经网络模型,通过半最大抑制浓度(IC50)来预测抗癌药物在肿瘤中的作用。该模型可以看作是双重的:首先,我们预先训练了两个具有高维基因表达和突变数据的自编码器,以捕获肿瘤的关键特征;然后,将这种遗传背景转化为癌细胞系,以预测遗传变异对给定药物的影响。此外,引入了SMILES结构,使模型能够理解药物化合物的相关特征。最后,我们使用与基因组和药物数据相关的药物敏感性数据来确定预测每对药物细胞系IC50值的特征。获得的结果证明了提取的深度表征在预测药物-靶标相互作用方面的有效性,实现了均方误差为1.07的性能,超过了以前最先进的模型。
{"title":"Deep Model for Anticancer Drug Response through Genomic Profiles and Compound Structures","authors":"Filipa G. Carvalho, Maryam Abbasi, B. Ribeiro, Joel P. Arrais","doi":"10.1109/CBMS55023.2022.00050","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00050","url":null,"abstract":"Cancer is among the deadliest diseases, enhancing the need for its detection and treatment. In the era of precision medicine, the main goal is to take into account individual vari-ability in order to choose more accurately which treatment and prevention strategies suit each person. However, drug response prediction for cancer therapy remains a challenge. In this work, we propose a deep neural network model to predict the effect of anticancer drugs in tumors through the half-maximal inhibitory concentration (IC50). The model can be seen as two-fold: first, we pre-trained two autoencoders with high-dimensional gene expression and mutation data to capture the crucial features from tumors; then, this genetic background is translated to cancer cell lines to predict the impact of the genetic variants on a given drug. Moreover, SMILES structures were introduced so that the model can apprehend relevant features regarding the drug compound. Finally, we use drug sensitivity data correlated to the genomic and drugs data to identify features that predict the IC50 value for each pair of drug-cell line. The obtained results demonstrate the effectiveness of the extracted deep representations in the prediction of drug-target interactions, achieving a performance of a mean squared error of 1.07 and surpassing previous state-of-the-art models.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"12 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130182720","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
Aerobic Exercise System for Home Telerehabilitation 家庭远程康复有氧运动系统
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00059
Aref Smiley, J. Finkelstein
The COVID-19 pandemic has impacted every aspect of health delivery and encouraged to replace in-person clinical visits with telecommunications. By providing wireless communication between embedded electronic devices and sensors, telerehabilitation enables constant monitoring of vital body functions, and tracking of physical activities of a person and aids physical therapy. In this paper, we designed and tested two remotely controlled versions of interactive bike (iBikE) systems which communicate through either Wi-Fi or BLE and give the clinical team the capability to monitor exercise progress in real time using simple graphical representation. We used the same hardware and user interface for both designs. The software uses either Wi-Fi or BLE protocol to connect the iBikE equipment and PC tablet. The bike can be used for upper or lower limb rehabilitation. A customized tablet app was developed to provide user interface between the app and the bike sensors. Both bikes were tested with a single group of nine individuals in two separate sessions. Each individual was asked to hand-cycle for three separate sub-sessions (1 minute each for slow, medium, and fast pace) with one-minute rest. During each sub-session, speed of the bikes was measured continuously using a tachometer, in addition to reading speed values from the iBikE app, to compare the functionality and accuracy of the measured data. Measured RPMs in each sub-session from iBikE and tachometer were further divided into 4 categories: 10-second bins (6 bins), 20-second bins (3 bins), 30-second bins (2 bins), and RPMs in each sub-session (1 minute, 1 bin). Then, the mean difference of each category (iBikE, tachometer) was calculated for each sub-session. Finally, mean and standard deviation (SD) of the calculated mean differences were reported for all individuals. We saw decreasing trend in both mean and SD from 10 second to 1 minute measurement. For BLE iBikE system, minimum mean RPM difference was $0.2 pm 0.3$ in one-minute sub-session with medium speed. This number was $0.21 pm 0.21$ in one-minute sub-session with slow speed for Wi-Fi iBikE system. Thus, testing confirmed high accuracy of our interfaces.
COVID-19大流行影响了卫生服务的各个方面,并鼓励人们用电信代替亲自就诊。通过在嵌入式电子设备和传感器之间提供无线通信,远程康复能够持续监测身体的重要功能,跟踪一个人的身体活动,并有助于物理治疗。在本文中,我们设计并测试了两种远程控制版本的交互式自行车(iBikE)系统,它们通过Wi-Fi或BLE进行通信,并使临床团队能够使用简单的图形表示实时监控运动进度。我们在两个设计中使用了相同的硬件和用户界面。该软件使用Wi-Fi或BLE协议连接iBikE设备和PC平板电脑。该自行车可用于上肢或下肢康复。开发了定制的平板电脑应用程序,以提供应用程序和自行车传感器之间的用户界面。这两款自行车都是由一组9人在两个单独的时段进行测试的。每个人被要求进行三个独立的分阶段(慢速、中速和快速各1分钟),休息一分钟。在每一个分阶段,除了从iBikE应用程序读取速度值外,还使用转速计连续测量自行车的速度,以比较测量数据的功能和准确性。将iBikE和转速计测得的每个子会话转速进一步分为4类:10秒组(6个)、20秒组(3个)、30秒组(2个)和每个子会话转速(1分钟,1个)。然后,计算每个子会话的每个类别(iBikE, tachometer)的平均差值。最后,报告所有个体计算的平均差异的均值和标准差(SD)。从10秒到1分钟的测量,我们看到平均值和标准差都呈下降趋势。对于BLE iBikE系统,在1分钟的中速次会话中,最小平均RPM差异为0.2美元/ pm 0.3美元。在低速Wi-Fi iBikE系统的1分钟次会话中,该数字为0.21美元/分0.21美元。因此,测试证实了我们的接口具有很高的准确性。
{"title":"Aerobic Exercise System for Home Telerehabilitation","authors":"Aref Smiley, J. Finkelstein","doi":"10.1109/CBMS55023.2022.00059","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00059","url":null,"abstract":"The COVID-19 pandemic has impacted every aspect of health delivery and encouraged to replace in-person clinical visits with telecommunications. By providing wireless communication between embedded electronic devices and sensors, telerehabilitation enables constant monitoring of vital body functions, and tracking of physical activities of a person and aids physical therapy. In this paper, we designed and tested two remotely controlled versions of interactive bike (iBikE) systems which communicate through either Wi-Fi or BLE and give the clinical team the capability to monitor exercise progress in real time using simple graphical representation. We used the same hardware and user interface for both designs. The software uses either Wi-Fi or BLE protocol to connect the iBikE equipment and PC tablet. The bike can be used for upper or lower limb rehabilitation. A customized tablet app was developed to provide user interface between the app and the bike sensors. Both bikes were tested with a single group of nine individuals in two separate sessions. Each individual was asked to hand-cycle for three separate sub-sessions (1 minute each for slow, medium, and fast pace) with one-minute rest. During each sub-session, speed of the bikes was measured continuously using a tachometer, in addition to reading speed values from the iBikE app, to compare the functionality and accuracy of the measured data. Measured RPMs in each sub-session from iBikE and tachometer were further divided into 4 categories: 10-second bins (6 bins), 20-second bins (3 bins), 30-second bins (2 bins), and RPMs in each sub-session (1 minute, 1 bin). Then, the mean difference of each category (iBikE, tachometer) was calculated for each sub-session. Finally, mean and standard deviation (SD) of the calculated mean differences were reported for all individuals. We saw decreasing trend in both mean and SD from 10 second to 1 minute measurement. For BLE iBikE system, minimum mean RPM difference was $0.2 pm 0.3$ in one-minute sub-session with medium speed. This number was $0.21 pm 0.21$ in one-minute sub-session with slow speed for Wi-Fi iBikE system. Thus, testing confirmed high accuracy of our interfaces.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"6 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131325493","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
TcT: Temporal and channel Transformer for EEG-based Emotion Recognition 基于脑电图的情感识别的时间和通道转换器
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00072
Yanling Liu, Yueying Zhou, Daoqiang Zhang
In recent years, Electroencephalogram (EEG)-based emotion recognition has developed rapidly and gained increasing attention in the field of brain-computer interface. Relevant studies in the neuroscience domain have shown that various emotional states may activate differently in brain regions and time points. Though the EEG signals have the characteristics of high temporal resolution and strong global correlation, the low signal-to-noise ratio and much redundant information bring challenges to the fast emotion recognition. To cope with the above problem, we propose a Temporal and channel Transformer (TcT) model for emotion recognition, which is directly applied to the raw preprocessed EEG data. In the model, we propose a TcT self-attention mechanism that simultaneously captures temporal and channel dependencies. The sliding window weight sharing strategy is designed to gradually refine the features from coarse time granularity, and reduce the complexity of the attention calculation. The original signal is passed between layers through the residual structure to integrate the features of different layers. We conduct experiments on the DEAP database to verify the effectiveness of the proposed model. The results show that the model achieves better classification performance in less time and with fewer resources than state-of-the-art methods.
近年来,基于脑电图(EEG)的情绪识别技术发展迅速,在脑机接口领域受到越来越多的关注。神经科学领域的相关研究表明,不同的情绪状态在大脑区域和时间点的激活可能不同。虽然脑电信号具有高时间分辨率和强全局相关性的特点,但其低信噪比和大量冗余信息给快速情绪识别带来了挑战。为了解决上述问题,我们提出了一种用于情绪识别的时间和通道变换(TcT)模型,该模型直接应用于原始预处理的脑电数据。在模型中,我们提出了一种同时捕获时间和通道依赖性的TcT自注意机制。滑动窗口权值共享策略旨在从粗时间粒度逐步细化特征,降低注意力计算的复杂度。原始信号通过残差结构在层与层之间传递,以整合不同层的特征。我们在DEAP数据库上进行了实验,以验证所提出模型的有效性。结果表明,该模型在更短的时间和更少的资源下获得了比现有方法更好的分类性能。
{"title":"TcT: Temporal and channel Transformer for EEG-based Emotion Recognition","authors":"Yanling Liu, Yueying Zhou, Daoqiang Zhang","doi":"10.1109/CBMS55023.2022.00072","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00072","url":null,"abstract":"In recent years, Electroencephalogram (EEG)-based emotion recognition has developed rapidly and gained increasing attention in the field of brain-computer interface. Relevant studies in the neuroscience domain have shown that various emotional states may activate differently in brain regions and time points. Though the EEG signals have the characteristics of high temporal resolution and strong global correlation, the low signal-to-noise ratio and much redundant information bring challenges to the fast emotion recognition. To cope with the above problem, we propose a Temporal and channel Transformer (TcT) model for emotion recognition, which is directly applied to the raw preprocessed EEG data. In the model, we propose a TcT self-attention mechanism that simultaneously captures temporal and channel dependencies. The sliding window weight sharing strategy is designed to gradually refine the features from coarse time granularity, and reduce the complexity of the attention calculation. The original signal is passed between layers through the residual structure to integrate the features of different layers. We conduct experiments on the DEAP database to verify the effectiveness of the proposed model. The results show that the model achieves better classification performance in less time and with fewer resources than state-of-the-art methods.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"20 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122197822","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: 1
Graph-based Regional Feature Enhancing for Abdominal Multi-Organ Segmentation in CT 基于图的腹部多脏器CT区域特征增强
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00029
Zefan Yang, Yi Wang
Automatic segmentation of abdominal organs in CT is of essential importance for radiation therapy and image-guided surgery. However, the development of such automatic solutions remains challenging due to complicated structures and low tissue contrast in abdominal CT images. To address these issues, we propose a novel deep neural network equipped with an edge detection (ED) module and a graph-based regional feature enhancing (GRFE) module for better organ segmentation, by enhancing the long-range representation power of regional features. Specifically, the proposed ED module learns an edge representation by leveraging both fine-grained and structural information. The edge representation is then fused with the segmentation features to provide constraint guidance for better prediction. Our GRFE module propagates features to capture contextual information via graphic voxel-by-voxel connections. The GRFE module leverages the edge representation to highlight the features of boundaries to build strong contextual dependencies between the features of organs' boundaries and central areas. We evaluate the efficacy of the proposed network on two challenging abdominal multi-organ datasets. Experimental results demonstrate that our network outperforms several state-of-the-art methods. The code is publicly available at https://github.com/zefanyang/organseg_dags.
CT对腹部器官的自动分割对放射治疗和影像引导手术具有重要意义。然而,由于腹部CT图像结构复杂和组织对比度低,这种自动解决方案的发展仍然具有挑战性。为了解决这些问题,我们提出了一种新的深度神经网络,该网络配备了边缘检测(ED)模块和基于图的区域特征增强(GRFE)模块,通过增强区域特征的远程表示能力来实现更好的器官分割。具体来说,所提出的ED模块通过利用细粒度和结构信息来学习边缘表示。然后将边缘表示与分割特征融合,为更好的预测提供约束指导。我们的GRFE模块通过逐体素的图形连接传播特征以捕获上下文信息。GRFE模块利用边缘表示来突出边界的特征,从而在器官边界和中心区域的特征之间建立强大的上下文依赖性。我们评估了所提出的网络在两个具有挑战性的腹部多器官数据集上的有效性。实验结果表明,我们的网络优于几种最先进的方法。该代码可在https://github.com/zefanyang/organseg_dags上公开获得。
{"title":"Graph-based Regional Feature Enhancing for Abdominal Multi-Organ Segmentation in CT","authors":"Zefan Yang, Yi Wang","doi":"10.1109/CBMS55023.2022.00029","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00029","url":null,"abstract":"Automatic segmentation of abdominal organs in CT is of essential importance for radiation therapy and image-guided surgery. However, the development of such automatic solutions remains challenging due to complicated structures and low tissue contrast in abdominal CT images. To address these issues, we propose a novel deep neural network equipped with an edge detection (ED) module and a graph-based regional feature enhancing (GRFE) module for better organ segmentation, by enhancing the long-range representation power of regional features. Specifically, the proposed ED module learns an edge representation by leveraging both fine-grained and structural information. The edge representation is then fused with the segmentation features to provide constraint guidance for better prediction. Our GRFE module propagates features to capture contextual information via graphic voxel-by-voxel connections. The GRFE module leverages the edge representation to highlight the features of boundaries to build strong contextual dependencies between the features of organs' boundaries and central areas. We evaluate the efficacy of the proposed network on two challenging abdominal multi-organ datasets. Experimental results demonstrate that our network outperforms several state-of-the-art methods. The code is publicly available at https://github.com/zefanyang/organseg_dags.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"14 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114039866","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
Dual Fusion Mass Detector for Mammogram Mass Detection 双融合质量检测器用于乳房x光片质量检测
Pub Date : 2022-07-01 DOI: 10.1109/CBMS55023.2022.00033
Shuo Liu, Zhihui Lai, Heng Kong, Linlin Shen
Mammogram mass detection is a difficult task due to the mass character of the tiny area, fuzzy boundary, and occlusion. To address these problems, this paper proposes a novel detection network for mammogram mass detection. Firstly, we propose a novel feature fusion structure and Small Target Attention Module (STAM) to improve the model's ability to detect small masses. Secondly, Results-oriented Loss (ROL) is adopted to obtain better model performance. Finally, Incremental Positive Selection (IPS) is used to divide positive and negative anchors. The scarcity of breast mammogram images for training aggravates the difficulty of mass detection. Thus, we open our collected dataset, which contains 1456 mammogram images from 400 patients. Since the model includes a double feature fusion structure, the proposed network is named Dual Fusion Mass Detector (DFMD). Experiment results show that DFMD is robust to various variations on scale, blurry and occlusion.
乳房x线肿块检测是一项困难的任务,因为肿块的特点是面积小,边界模糊,遮挡。为了解决这些问题,本文提出了一种新的乳房x线肿块检测网络。首先,我们提出了一种新的特征融合结构和小目标注意模块(STAM),以提高模型对小质量的检测能力。其次,采用结果导向损失(Results-oriented Loss, ROL)来获得更好的模型性能。最后,使用增量正向选择(IPS)来划分正锚和负锚。用于训练的乳房x光图像的稀缺性加剧了大规模检测的困难。因此,我们打开收集到的数据集,其中包含来自400名患者的1456张乳房x线照片。由于该模型包含双特征融合结构,因此将该网络命名为双融合质量检测器(DFMD)。实验结果表明,DFMD对各种尺度、模糊和遮挡变化都具有鲁棒性。
{"title":"Dual Fusion Mass Detector for Mammogram Mass Detection","authors":"Shuo Liu, Zhihui Lai, Heng Kong, Linlin Shen","doi":"10.1109/CBMS55023.2022.00033","DOIUrl":"https://doi.org/10.1109/CBMS55023.2022.00033","url":null,"abstract":"Mammogram mass detection is a difficult task due to the mass character of the tiny area, fuzzy boundary, and occlusion. To address these problems, this paper proposes a novel detection network for mammogram mass detection. Firstly, we propose a novel feature fusion structure and Small Target Attention Module (STAM) to improve the model's ability to detect small masses. Secondly, Results-oriented Loss (ROL) is adopted to obtain better model performance. Finally, Incremental Positive Selection (IPS) is used to divide positive and negative anchors. The scarcity of breast mammogram images for training aggravates the difficulty of mass detection. Thus, we open our collected dataset, which contains 1456 mammogram images from 400 patients. Since the model includes a double feature fusion structure, the proposed network is named Dual Fusion Mass Detector (DFMD). Experiment results show that DFMD is robust to various variations on scale, blurry and occlusion.","PeriodicalId":218475,"journal":{"name":"2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)","volume":"27 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114822570","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
期刊
2022 IEEE 35th International Symposium on Computer-Based Medical Systems (CBMS)
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