Pub Date : 2024-01-01DOI: 10.1016/j.imu.2024.101558
Maarja Pajusalu, Kerli Mooses, Marek Oja, Sirli Tamm, Markus Haug, Raivo Kolde
Background and objectives
With the proliferation of real-world or observational health data, there is increasing interest in studying treatment trajectories. The real-life treatment trajectories can be complex, and one has to simplify the patterns to draw any conclusions; however, oversimplification will cause the loss of essential details. Thus, the visualization challenge is to strike a balance between the two extremes.
Methods
We have implemented the observation of treatment trajectories starting from cohort definitions in cooperation with medical specialists, data processing, and then generating the interactive visualizations and detailed data tables derived from input data within an open-source R package as a Shiny dashboard. The created R package called TrajectoryViz (https://github.com/HealthInformaticsUT/TrajectoryViz) enables reproducible visual analysis and visual content generation for various data investigations and explanations.
Results
We illustrate the use of the tool by assessing the sequence of events present within the data of cervical cancer prevention pathways, as well as the proportions of timely follow-up procedure events.
Conclusion
Building a toolset to access, manage, and analyze observational health data enables more accessible visual analysis of complicated data, adding time dimension to otherwise simplified event sequences that make up trajectories.
背景和目的随着真实世界或观察性健康数据的激增,人们对治疗轨迹的研究越来越感兴趣。现实生活中的治疗轨迹可能很复杂,人们必须简化其模式才能得出结论;但是,过度简化又会导致基本细节的丢失。因此,可视化的挑战在于如何在这两个极端之间取得平衡。方法我们与医学专家合作,从队列定义、数据处理开始,对治疗轨迹进行观察,然后在一个开源的 R 软件包中以 Shiny dashboard 的形式生成从输入数据中提取的交互式可视化和详细数据表。创建的 R 软件包名为 TrajectoryViz (https://github.com/HealthInformaticsUT/TrajectoryViz),可以为各种数据调查和解释提供可重复的可视化分析和可视化内容生成。结果我们通过评估宫颈癌预防路径数据中存在的事件序列以及及时随访程序事件的比例,说明了该工具的使用情况。结论建立一个工具集来访问、管理和分析观察性健康数据,可以更方便地对复杂数据进行可视化分析,为构成轨迹的简化事件序列增加时间维度。
{"title":"TrajectoryViz: Interactive visualization of treatment trajectories","authors":"Maarja Pajusalu, Kerli Mooses, Marek Oja, Sirli Tamm, Markus Haug, Raivo Kolde","doi":"10.1016/j.imu.2024.101558","DOIUrl":"10.1016/j.imu.2024.101558","url":null,"abstract":"<div><h3>Background and objectives</h3><p>With the proliferation of real-world or observational health data, there is increasing interest in studying treatment trajectories. The real-life treatment trajectories can be complex, and one has to simplify the patterns to draw any conclusions; however, oversimplification will cause the loss of essential details. Thus, the visualization challenge is to strike a balance between the two extremes.</p></div><div><h3>Methods</h3><p>We have implemented the observation of treatment trajectories starting from cohort definitions in cooperation with medical specialists, data processing, and then generating the interactive visualizations and detailed data tables derived from input data within an open-source R package as a Shiny dashboard. The created R package called TrajectoryViz (<span><span>https://github.com/HealthInformaticsUT/TrajectoryViz</span><svg><path></path></svg></span>) enables reproducible visual analysis and visual content generation for various data investigations and explanations.</p></div><div><h3>Results</h3><p>We illustrate the use of the tool by assessing the sequence of events present within the data of cervical cancer prevention pathways, as well as the proportions of timely follow-up procedure events.</p></div><div><h3>Conclusion</h3><p>Building a toolset to access, manage, and analyze observational health data enables more accessible visual analysis of complicated data, adding time dimension to otherwise simplified event sequences that make up trajectories.</p></div>","PeriodicalId":13953,"journal":{"name":"Informatics in Medicine Unlocked","volume":"49 ","pages":"Article 101558"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S235291482400114X/pdfft?md5=0894191c372d2fc40671b6cd74491d0e&pid=1-s2.0-S235291482400114X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141728678","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}
Tricuspid regurgitation (TR) is one of the most common forms of valvular heart diseases. The morphological information of the tricuspid valve annulus (TVA) is critical in treatment planning for TR. It is necessary to extract the TVA from medical images to obtain that information, however this task is difficult and time-consuming to perform manually. In this paper, we propose a method to automatically extract and measure the TVA from computed tomography (CT) images.
Methods
Our proposed method coarsely crops CT images to the region surrounding the tricuspid valve based on the right atrium and the right ventricle regions. The cropped CT images are input to a stacked hourglass network with loss function integrating the mean squared error loss, the focal loss and the shape-aware weighted Hausdorff distance loss to extract 36 landmarks on the TVA. The extraction accuracy of TVA landmarks was evaluated by five-fold cross validation using 120 CT images with manually annotated TVA landmarks. In addition, measurements of TVA morphology based on automatically extracted TVA and those based on manually annotated TVA were calculated and compared using the same measurement algorithm which provides a means to automatically generate seven measurements based on TVA landmarks.
Results
Our proposed method extracted TVA inside the right heart in all CT images without any processing interruption. The mean processing time was 27.09 ± 8.65 s, and the Chamfer distance and Hausdorff distance were 2.07 ± 0.53 and 4.09 ± 1.29, respectively. The mean absolute error between the measurements based on automatically extracted TVA and those based on manually annotated TVA was less than 4 mm, which is less than the typical device size interval for surgical prosthetic valve rings in current use, for measurement items related to distance. For all seven measurement items, significant correlations (r = 0.51–0.99, p < 0.0071) were shown between the measurements based on automatically extracted TVA and those based on manually annotated TVA.
Conclusions
Our proposed method was able to automatically extract and measure the TVA. This method is expected to reduce the time and effort required by physicians in treatment planning for TR.
{"title":"Automatic tricuspid valve annulus extraction and measurement from computed tomography images","authors":"Gakuto Aoyama , Zhexin Zhou , Longfei Zhao , Shun Zhao , Keitaro Kawashima , James V. Chapman , Masahiko Asami , Yui Nozaki , Shinichiro Fujimoto , Takuya Sakaguchi","doi":"10.1016/j.imu.2024.101577","DOIUrl":"10.1016/j.imu.2024.101577","url":null,"abstract":"<div><h3>Background and objective</h3><p>Tricuspid regurgitation (TR) is one of the most common forms of valvular heart diseases. The morphological information of the tricuspid valve annulus (TVA) is critical in treatment planning for TR. It is necessary to extract the TVA from medical images to obtain that information, however this task is difficult and time-consuming to perform manually. In this paper, we propose a method to automatically extract and measure the TVA from computed tomography (CT) images.</p></div><div><h3>Methods</h3><p>Our proposed method coarsely crops CT images to the region surrounding the tricuspid valve based on the right atrium and the right ventricle regions. The cropped CT images are input to a stacked hourglass network with loss function integrating the mean squared error loss, the focal loss and the shape-aware weighted Hausdorff distance loss to extract 36 landmarks on the TVA. The extraction accuracy of TVA landmarks was evaluated by five-fold cross validation using 120 CT images with manually annotated TVA landmarks. In addition, measurements of TVA morphology based on automatically extracted TVA and those based on manually annotated TVA were calculated and compared using the same measurement algorithm which provides a means to automatically generate seven measurements based on TVA landmarks.</p></div><div><h3>Results</h3><p>Our proposed method extracted TVA inside the right heart in all CT images without any processing interruption. The mean processing time was 27.09 ± 8.65 s, and the Chamfer distance and Hausdorff distance were 2.07 ± 0.53 and 4.09 ± 1.29, respectively. The mean absolute error between the measurements based on automatically extracted TVA and those based on manually annotated TVA was less than 4 mm, which is less than the typical device size interval for surgical prosthetic valve rings in current use, for measurement items related to distance. For all seven measurement items, significant correlations (<em>r</em> = 0.51–0.99, <em>p</em> < 0.0071) were shown between the measurements based on automatically extracted TVA and those based on manually annotated TVA.</p></div><div><h3>Conclusions</h3><p>Our proposed method was able to automatically extract and measure the TVA. This method is expected to reduce the time and effort required by physicians in treatment planning for TR.</p></div>","PeriodicalId":13953,"journal":{"name":"Informatics in Medicine Unlocked","volume":"50 ","pages":"Article 101577"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2352914824001333/pdfft?md5=b7839b2fa5e3a7bce93db530a02e4724&pid=1-s2.0-S2352914824001333-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142122271","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}
Pub Date : 2024-01-01DOI: 10.1016/j.imu.2024.101462
Zulqarnain Baqar , Sk Injamamul Islam , Gunjan Das , Sarower Mahfuj , Foysal Ahammad
Acinetobacter baumannii is widely recognized as a human opportunistic pathogen in nosocomial infections. The proliferation of multidrug-resistant strains of A. baumannii has presented an array of difficulties for clinical anti-infective therapies and diagnostic procedures, owing to the existence of numerous variations. The development of therapy utilizing CRISPR/Cas9 for treatment and diagnosis necessitates an in-depth study of potential off-target consequences. The objective of this work is to assess potential off-target effects associated with a single guide RNA (sgRNA) designed to identify several variants present in A. baumannii. The current investigation involved the identification of Cas12 nuclease-specific protospacer adjacent motif (PAM) and downstream target sequences. This was achieved by utilizing computational tools and software to analyze conserved sections of the A. baumannii siderophore protein gene. Further, the in-silico expression vector was created with the SnapGene software. A total of 24 potential off-target sequences were identified in these sequences with 100% query identity with 96 different A. baumannii strains. In addition, a target-specific oligonucleotide single-guide RNA (sgRNA) template was synthesized by appending an additional nucleotide 'G' to the 5′ end. This research uses A. baumannii as an example of a problem that affects all treatments and diagnosis procedures to illustrate the significance of screening off-targets in different variants of a pathogen. Our findings may impact the safety and effectiveness of CRISPR/Cas9, which may have wider implications for additional targets that are currently being used therapeutically.
{"title":"Development and design of CRISPR-based diagnostic for Acinetobacter baumannii by employing off-target gene editing of sgRNA","authors":"Zulqarnain Baqar , Sk Injamamul Islam , Gunjan Das , Sarower Mahfuj , Foysal Ahammad","doi":"10.1016/j.imu.2024.101462","DOIUrl":"https://doi.org/10.1016/j.imu.2024.101462","url":null,"abstract":"<div><p><em>Acinetobacter baumannii</em> is widely recognized as a human opportunistic pathogen in nosocomial infections. The proliferation of multidrug-resistant strains of <em>A. baumannii</em> has presented an array of difficulties for clinical anti-infective therapies and diagnostic procedures, owing to the existence of numerous variations. The development of therapy utilizing CRISPR/Cas9 for treatment and diagnosis necessitates an in-depth study of potential off-target consequences. The objective of this work is to assess potential off-target effects associated with a single guide RNA (sgRNA) designed to identify several variants present in <em>A. baumannii</em>. The current investigation involved the identification of Cas12 nuclease-specific protospacer adjacent motif (PAM) and downstream target sequences. This was achieved by utilizing computational tools and software to analyze conserved sections of the <em>A. baumannii</em> siderophore protein gene. Further, the <em>in-silico</em> expression vector was created with the SnapGene software. A total of 24 potential off-target sequences were identified in these sequences with 100% query identity with 96 different <em>A. baumannii</em> strains. In addition, a target-specific oligonucleotide single-guide RNA (sgRNA) template was synthesized by appending an additional nucleotide 'G' to the 5′ end. This research uses <em>A. baumannii</em> as an example of a problem that affects all treatments and diagnosis procedures to illustrate the significance of screening off-targets in different variants of a pathogen. Our findings may impact the safety and effectiveness of CRISPR/Cas9, which may have wider implications for additional targets that are currently being used therapeutically.</p></div>","PeriodicalId":13953,"journal":{"name":"Informatics in Medicine Unlocked","volume":"46 ","pages":"Article 101462"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2352914824000182/pdfft?md5=eb4876167a9018484ca7e27ab10f59bc&pid=1-s2.0-S2352914824000182-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139985242","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}
Pub Date : 2024-01-01DOI: 10.1016/j.imu.2024.101518
Gadiel J. Marira , Esther G. Kimaro , Elingarami Sauli
Background
There is limited information on burden of hepatitis B infection in the Western zone of Tanzania. In this study, we analyzed a dataset from blood donors to determine Hepatitis B virus (HBV) seroprevalence and related socio-demographic factors among blood donors in the Western regions of Tanzania.
Material and methods
This was a cross-sectional retrospective hospital-based study, in which data were retrieved from the blood donor dataset at the Zonal Blood Transfusion Center. The analyzed information from the dataset included reported Transfusion Transmissible Infections (TTIs), which included Hepatitis B, donor demographics, donor status, donor type, donation place, and the year of donation. The analyzed data was retrieved within five years from January 2018 to December 2022. Rates of hepatitis B surface antigen (HBsAg) were determined and univariate and multivariate analyses were conducted to determine the association between infection and demographic risk factors.
Results
A total of 9604 retrospective blood donors were screened. Majority 8963 (93.3 %) were men, and most of them were under 45 years (89.6 %). Overall, HBsAg seroprevalence was 6.9 % (661), with Katavi (7.8 %) being relatively higher in the studied three regions. The highest HBsAg seroprevalence of 8.2 % (199) was found in the age group ranging from 35 to 44 years. Moreover, 2 (9.5 %) polygamists and 15 (17.1 %) car drivers had relatively high seroprevalence. Results from the multivariate analysis indicated that, car drivers (OR 5.44, 95 % CI; 2.43–12.20, p < 0.001), and first-time donors (OR 5.19, 95 % CI 2.56 = 10.52, P < 0.001), were highly associated with increased chance of getting hepatitis B infection.
Conclusion
The findings from this study indicated that, there was high seroprevalence of HBV infection in the Western regions of Tanzania during the studied time period. These findings call for more advocacy on HBV immunization for all groups of persons found at high risk for HBV infection.
{"title":"Seroprevalence of hepatitis B infection among blood donors in Western zone of Tanzania","authors":"Gadiel J. Marira , Esther G. Kimaro , Elingarami Sauli","doi":"10.1016/j.imu.2024.101518","DOIUrl":"https://doi.org/10.1016/j.imu.2024.101518","url":null,"abstract":"<div><h3>Background</h3><p>There is limited information on burden of hepatitis B infection in the Western zone of Tanzania. In this study, we analyzed a dataset from blood donors to determine Hepatitis B virus (HBV) seroprevalence and related socio-demographic factors among blood donors in the Western regions of Tanzania.</p></div><div><h3>Material and methods</h3><p>This was a cross-sectional retrospective hospital-based study, in which data were retrieved from the blood donor dataset at the Zonal Blood Transfusion Center. The analyzed information from the dataset included reported Transfusion Transmissible Infections (TTIs), which included Hepatitis B, donor demographics, donor status, donor type, donation place, and the year of donation. The analyzed data was retrieved within five years from January 2018 to December 2022. Rates of hepatitis B surface antigen (HBsAg) were determined and univariate and multivariate analyses were conducted to determine the association between infection and demographic risk factors.</p></div><div><h3>Results</h3><p>A total of 9604 retrospective blood donors were screened. Majority 8963 (93.3 %) were men, and most of them were under 45 years (89.6 %). Overall, HBsAg seroprevalence was 6.9 % (661), with Katavi (7.8 %) being relatively higher in the studied three regions. The highest HBsAg seroprevalence of 8.2 % (199) was found in the age group ranging from 35 to 44 years. Moreover, 2 (9.5 %) polygamists and 15 (17.1 %) car drivers had relatively high seroprevalence. Results from the multivariate analysis indicated that, car drivers (OR 5.44, 95 % CI; 2.43–12.20, p < 0.001), and first-time donors (OR 5.19, 95 % CI 2.56 = 10.52, P < 0.001), were highly associated with increased chance of getting hepatitis B infection.</p></div><div><h3>Conclusion</h3><p>The findings from this study indicated that, there was high seroprevalence of HBV infection in the Western regions of Tanzania during the studied time period. These findings call for more advocacy on HBV immunization for all groups of persons found at high risk for HBV infection.</p></div>","PeriodicalId":13953,"journal":{"name":"Informatics in Medicine Unlocked","volume":"48 ","pages":"Article 101518"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2352914824000741/pdfft?md5=c03e612e78897f41dc7c5ebd90ddc9c2&pid=1-s2.0-S2352914824000741-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140900965","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}
Liver hepatocellular carcinoma (LIHC) is considered one of the primary contributors to cancer-related mortality on a global scale. The identification of new biomarkers is of utmost importance due to the fact that patients with LIHC are frequently detected at advanced stages, leading to an increased mortality rate. The study utilized TCGA-LIHC gene expression datasets to identify biomarkers and to address the complexity of datasets. A combination of feature selection (FS) techniques was used, and the performance of this strategy was assessed using ten machine learning classifiers. The findings were integrated, revealing biomarkers identified through at least five FS techniques. Through our proposed approach, we identified 55 potential biomarkers for LIHC. The Gaussian Naive Bayes Classifier (AUC = 0.99) was found to be the most effective classifier, achieving 98.67% accuracy when utilizing the 55 identified biomarkers in the test dataset. Additionally, we conducted differential gene expression, survival analysis, and enrichment analysis for all the identified biomarkers. Subsequently, Lasso-penalized Cox regression further refined the identified biomarkers to thirteen. Out of thirteen genes, we singled out B4GALNT1 because of its statistical significance in differential expression analysis and increasing importance across various cancer types, including LIHC. We carried out comprehensive bioinformatics and molecular dynamics simulation studies along with other structural analysis of B4GALNT1 in LIHC. In LIHC, six mutations (P64Q, S131F, A311S, R340Q, D478H, and P507Q) have been predicted to be probably damaging by evaluating in-silico prediction algorithms. In comparison to the wild type, the B4GALNT1 variations, specifically P64Q and S131F, demonstrate increased stability. However, these mutations lead to decreased atomic fluctuations, indicating a rigid protein structure. Again, mutations like A311S and P507Q induce increased flexibility, highlighting their structural impact on B4GALNT1. The study demonstrated the combination of various feature selection methods effectively reveals new biomarkers, thereby directly impacting their biological significance. Furthermore, our findings indicate a link between increased B4GALNT1 expression in individuals with liver cancer and a poorer prognosis, highlighting its potential as a promising therapeutic target.
{"title":"Elucidating B4GALNT1 as potential biomarker in hepatocellular carcinoma using machine learning models and mutational dynamics explored through MD simulation","authors":"Rohit Kumar Verma , Kiran Bharat Lokhande , Prashant Kumar Srivastava , Ashutosh Singh","doi":"10.1016/j.imu.2024.101514","DOIUrl":"https://doi.org/10.1016/j.imu.2024.101514","url":null,"abstract":"<div><p>Liver hepatocellular carcinoma (LIHC) is considered one of the primary contributors to cancer-related mortality on a global scale. The identification of new biomarkers is of utmost importance due to the fact that patients with LIHC are frequently detected at advanced stages, leading to an increased mortality rate. The study utilized TCGA-LIHC gene expression datasets to identify biomarkers and to address the complexity of datasets. A combination of feature selection (FS) techniques was used, and the performance of this strategy was assessed using ten machine learning classifiers. The findings were integrated, revealing biomarkers identified through at least five FS techniques. Through our proposed approach, we identified 55 potential biomarkers for LIHC. The Gaussian Naive Bayes Classifier (AUC = 0.99) was found to be the most effective classifier, achieving 98.67% accuracy when utilizing the 55 identified biomarkers in the test dataset. Additionally, we conducted differential gene expression, survival analysis, and enrichment analysis for all the identified biomarkers. Subsequently, Lasso-penalized Cox regression further refined the identified biomarkers to thirteen. Out of thirteen genes, we singled out B4GALNT1 because of its statistical significance in differential expression analysis and increasing importance across various cancer types, including LIHC. We carried out comprehensive bioinformatics and molecular dynamics simulation studies along with other structural analysis of B4GALNT1 in LIHC. In LIHC, six mutations (P64Q, S131F, A311S, R340Q, D478H, and P507Q) have been predicted to be probably damaging by evaluating in-silico prediction algorithms. In comparison to the wild type, the B4GALNT1 variations, specifically P64Q and S131F, demonstrate increased stability. However, these mutations lead to decreased atomic fluctuations, indicating a rigid protein structure. Again, mutations like A311S and P507Q induce increased flexibility, highlighting their structural impact on B4GALNT1. The study demonstrated the combination of various feature selection methods effectively reveals new biomarkers, thereby directly impacting their biological significance. Furthermore, our findings indicate a link between increased B4GALNT1 expression in individuals with liver cancer and a poorer prognosis, highlighting its potential as a promising therapeutic target.</p></div>","PeriodicalId":13953,"journal":{"name":"Informatics in Medicine Unlocked","volume":"48 ","pages":"Article 101514"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2352914824000704/pdfft?md5=fc03e97d776921a1dbf9039b163e1a45&pid=1-s2.0-S2352914824000704-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140900979","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}
Pub Date : 2024-01-01DOI: 10.1016/j.imu.2024.101466
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Pub Date : 2024-01-01DOI: 10.1016/j.imu.2024.101481
Anthoula Lazaris , Migmar Tsamchoe , Susan Kaplan , Peter Metrakos , Nathan Hayes
The current study applies a new artificial intelligence (AI) method, ALiX, which is based on interval arithmetic, to analyze and interpret biological data for a clinical problem: identification of biomarkers for cancer diagnosis. The key unique and important feature of this study is that ALiX provides an explanation to our clinical hypothesis in the form of a list of ranked protein biomarkers that identifies which biomarkers are the most significant drivers of the predicted outcome, a capability that is not currently available in other AI methods. Based on the significant drivers, this study identifies a machine learning model and solution for stratifying cancer patients into subtypes that will predict response to treatment.
{"title":"Predictive biomarker discovery in cancer using a unique AI model based on set theory","authors":"Anthoula Lazaris , Migmar Tsamchoe , Susan Kaplan , Peter Metrakos , Nathan Hayes","doi":"10.1016/j.imu.2024.101481","DOIUrl":"https://doi.org/10.1016/j.imu.2024.101481","url":null,"abstract":"<div><p>The current study applies a new artificial intelligence (AI) method, ALiX, which is based on interval arithmetic, to analyze and interpret biological data for a clinical problem: identification of biomarkers for cancer diagnosis. The key unique and important feature of this study is that ALiX provides an explanation to our clinical hypothesis in the form of a list of ranked protein biomarkers that identifies which biomarkers are the most significant drivers of the predicted outcome, a capability that is not currently available in other AI methods. Based on the significant drivers, this study identifies a machine learning model and solution for stratifying cancer patients into subtypes that will predict response to treatment.</p></div>","PeriodicalId":13953,"journal":{"name":"Informatics in Medicine Unlocked","volume":"46 ","pages":"Article 101481"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2352914824000376/pdfft?md5=326258b16e753fc14ca4736843412893&pid=1-s2.0-S2352914824000376-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140195904","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}
The International Classification of Diseases 11th revision (ICD-11) serves a wide extent of uses and provides detailed information on the range, causes, and effects of human disease and death through the reported and coded data.
Objective
Concerning the ICD-11 classification system, the present study was conducted to implement the ICD-11 and evaluate coding productivity in medical coders following a 1-month training program.
Methods
An observational study was conducted in two general hospitals. During the four months from August to November, twelve trained coders coded 1,909 inpatient records. The timing of medical record reading and diagnostic coding with ICD-10 and ICD-11 was documented separately in minutes as a self-report. The trend of coding productivity changes was analyzed to evaluate productivity in the first months of ICD-11 implementation.
Results
For record this research, 1475 medical records were included. The overall productivity loss was 42.24 % in the first three months after ICD-11 use. Productivity at the end of the fourth month was slightly better than baseline ICD-10 coding. Trauma cases required more coding time as more details should be coded for post-coordination.
Conclusion
Regarding the comprehensive documentation of medical records and the completeness of the details needed for coding with ICD-11 along with the instruction of the principles of ICD-11 coding rules and convention, the time required for coding can be significantly reduced when transitioning to the ICD-11 coding system. It can be hoped that after the four months of training and mentoring the coders, the coding speed will return to the baseline.
{"title":"A study on initial productivity trend in the transition of the ICD-10 to ICD-11 morbidity coding in Iran","authors":"Zahra Azadmanjir , Abbas Sheikhtaheri , Javad Zarei , Reza Golpira , Hooman Bakhshandeh , Akram Vahedi , Nasim Hashemi","doi":"10.1016/j.imu.2023.101440","DOIUrl":"https://doi.org/10.1016/j.imu.2023.101440","url":null,"abstract":"<div><h3>Background</h3><p>The International Classification of Diseases 11th revision (ICD-11) serves a wide extent of uses and provides detailed information on the range, causes, and effects of human disease and death through the reported and coded data.</p></div><div><h3>Objective</h3><p>Concerning the ICD-11 classification system, the present study was conducted to implement the ICD-11 and evaluate coding productivity in medical coders following a 1-month training program.</p></div><div><h3>Methods</h3><p>An observational study was conducted in two general hospitals. During the four months from August to November, twelve trained coders coded 1,909 inpatient records. The timing of medical record reading and diagnostic coding with ICD-10 and ICD-11 was documented separately in minutes as a self-report. The trend of coding productivity changes was analyzed to evaluate productivity in the first months of ICD-11 implementation.</p></div><div><h3>Results</h3><p>For record this research, 1475 medical records were included. The overall productivity loss was 42.24 % in the first three months after ICD-11 use. Productivity at the end of the fourth month was slightly better than baseline ICD-10 coding. Trauma cases required more coding time as more details should be coded for post-coordination.</p></div><div><h3>Conclusion</h3><p>Regarding the comprehensive documentation of medical records and the completeness of the details needed for coding with ICD-11 along with the instruction of the principles of ICD-11 coding rules and convention, the time required for coding can be significantly reduced when transitioning to the ICD-11 coding system. It can be hoped that after the four months of training and mentoring the coders, the coding speed will return to the baseline.</p></div>","PeriodicalId":13953,"journal":{"name":"Informatics in Medicine Unlocked","volume":"44 ","pages":"Article 101440"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2352914823002861/pdfft?md5=a39ecb63d77f410943dc5f8c0a4d868d&pid=1-s2.0-S2352914823002861-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139108904","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}
Pub Date : 2024-01-01DOI: 10.1016/j.imu.2024.101470
Erick Mutwiri Kirimi , Grace Gakii Muthuri , Cyrus Gitonga Ngari , Stephen Karanja
Numerous prevention intervention strategies have been developed to curtail the spread of pulmonary tuberculosis to susceptible populations. However, pulmonary tuberculosis continues to claim many lives worldwide. In this paper, a deterministic mathematical model incorporating an asymptomatic infectious population, considering vaccine efficacy, and vaccination rate, has been formulated. The model includes asymptomatic infectious individuals since they spread infections incessantly to susceptible populations without being noticed, thus contributing to the high transmission rate. Sensitivity and numerical analysis have been conducted to investigate the impact of varying vaccine efficacy and vaccination rates on the transmission of pulmonary tuberculosis infections from the asymptomatic infectious population. The sensitivity and numerical results show that an increase in vaccine efficacy reduces the asymptomatic infectious population and subsequently lowers the transmission rate of infections. Moreover, an increase in vaccine efficacy was shown to reduce the control reproduction number due to asymptomatic infectious individuals, thereby decreasing the transmission of pulmonary tuberculosis to susceptible populations. Further results indicate that an increase in vaccination rate reduces the control reproduction number due to asymptomatic infectious individuals, consequently lowering the rate of infection transmission. These findings emphasize the need to develop a vaccine of higher efficacy to reduce infection transmission to susceptible populations by the asymptomatic infectious individuals. Additionally, the results underscore the importance of increasing vaccination rates to eradicate pulmonary tuberculosis from the population.
{"title":"Modeling the effects of vaccine efficacy and rate of vaccination on the transmission of pulmonary tuberculosis","authors":"Erick Mutwiri Kirimi , Grace Gakii Muthuri , Cyrus Gitonga Ngari , Stephen Karanja","doi":"10.1016/j.imu.2024.101470","DOIUrl":"https://doi.org/10.1016/j.imu.2024.101470","url":null,"abstract":"<div><p>Numerous prevention intervention strategies have been developed to curtail the spread of pulmonary tuberculosis to susceptible populations. However, pulmonary tuberculosis continues to claim many lives worldwide. In this paper, a deterministic mathematical model incorporating an asymptomatic infectious population, considering vaccine efficacy, and vaccination rate, has been formulated. The model includes asymptomatic infectious individuals since they spread infections incessantly to susceptible populations without being noticed, thus contributing to the high transmission rate. Sensitivity and numerical analysis have been conducted to investigate the impact of varying vaccine efficacy and vaccination rates on the transmission of pulmonary tuberculosis infections from the asymptomatic infectious population. The sensitivity and numerical results show that an increase in vaccine efficacy reduces the asymptomatic infectious population and subsequently lowers the transmission rate of infections. Moreover, an increase in vaccine efficacy was shown to reduce the control reproduction number due to asymptomatic infectious individuals, thereby decreasing the transmission of pulmonary tuberculosis to susceptible populations. Further results indicate that an increase in vaccination rate reduces the control reproduction number due to asymptomatic infectious individuals, consequently lowering the rate of infection transmission. These findings emphasize the need to develop a vaccine of higher efficacy to reduce infection transmission to susceptible populations by the asymptomatic infectious individuals. Additionally, the results underscore the importance of increasing vaccination rates to eradicate pulmonary tuberculosis from the population.</p></div>","PeriodicalId":13953,"journal":{"name":"Informatics in Medicine Unlocked","volume":"46 ","pages":"Article 101470"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2352914824000261/pdfft?md5=59cfb545aaf72bd46c326b9ee9518880&pid=1-s2.0-S2352914824000261-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140181382","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}
In intensity-modulated radiation therapy (IMRT) techniques, although the dose conformity increases, the out-of-field doses would not decrease. This study aimed to assess the dose error calculated by the treatment planning system (TPS) in the out-of-field regions using the dynamic IMRT (D-IMRT) method in nasopharyngeal cancer (NPC) patients.
Methods
The out-of-field doses were measured for the chiasm and parotid organs using the D-IMRT technique (6 MV energy) with Monaco TPS. Computed tomography (CT) images of 10 NPC patients (54–77 years, mean: 61.6 ± 12.2 years) were considered and countered using 7-field and 11-field methods. The OCTAVIUS 4D phantom was utilized for dose assessment.
Results
According to the OCTAVIUS measurements, the Monaco TPS dose errors ranged from −58.8 to 105.5%. The average dose error for optic chiasm and parotid organs was −25% and 8.5%, respectively, with several cases falling within tolerance (±5%).
Conclusion
There were considerable dose calculation errors by Monaco TPS for organs located in out-of-field regions (optic chiasm and parotid) during IMRT for NPC patients. Therefore, accurate dose estimation in the out-of-field regions should be considered in clinical practices.
{"title":"Dose measurement of optic chiasm and parotid organs using OCTAVIUS 4D phantom: a dynamic IMRT method for nasopharyngeal cancer treatment","authors":"Laya Karimkhani , Elham Saeedzadeh , Dariush Sardari , Seied Rabi Mahdavi","doi":"10.1016/j.imu.2024.101479","DOIUrl":"https://doi.org/10.1016/j.imu.2024.101479","url":null,"abstract":"<div><h3>Introduction</h3><p>In intensity-modulated radiation therapy (IMRT) techniques, although the dose conformity increases, the out-of-field doses would not decrease. This study aimed to assess the dose error calculated by the treatment planning system (TPS) in the out-of-field regions using the dynamic IMRT (D-IMRT) method in nasopharyngeal cancer (NPC) patients.</p></div><div><h3>Methods</h3><p>The out-of-field doses were measured for the chiasm and parotid organs using the D-IMRT technique (6 MV energy) with Monaco TPS. Computed tomography (CT) images of 10 NPC patients (54–77 years, mean: 61.6 ± 12.2 years) were considered and countered using 7-field and 11-field methods. The OCTAVIUS 4D phantom was utilized for dose assessment.</p></div><div><h3>Results</h3><p>According to the OCTAVIUS measurements, the Monaco TPS dose errors ranged from −58.8 to 105.5%. The average dose error for optic chiasm and parotid organs was −25% and 8.5%, respectively, with several cases falling within tolerance (±5%).</p></div><div><h3>Conclusion</h3><p>There were considerable dose calculation errors by Monaco TPS for organs located in out-of-field regions (optic chiasm and parotid) during IMRT for NPC patients. Therefore, accurate dose estimation in the out-of-field regions should be considered in clinical practices.</p></div>","PeriodicalId":13953,"journal":{"name":"Informatics in Medicine Unlocked","volume":"46 ","pages":"Article 101479"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2352914824000352/pdfft?md5=b9aec1cd6136252ad6eb04c8bd722b45&pid=1-s2.0-S2352914824000352-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140188054","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}