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Diagnostics, Volume 12, Issue 6 (June 2022) – 211 articles

Cover Story (view full-size image): Poststroke thalamic pain (PS-TP) has often been a challenge to improving the rehabilitation outcomes and quality of life after a stroke; however, in the majority of PS-TP it is difficult to manage the pain and hypersensitivity. Central imbalance, central disinhibition, central sensitization, other thalamic adaptative changes, and local inflammatory responses are possible pathogeneses for it. Several drugs and non-invasive as well as minimally invasive interventions such as transcranial magnetic or direct current brain stimulations, vestibular caloric stimulation, and epidural motor cortex stimulation are recommended first for PS-TP. Invasive interventions including deep brain stimulation and other neurosurgical interventions can also be recommended for incurable PS-TP. View this paper
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7 pages, 832 KiB  
Brief Report
Performance of Whole Blood Stimulation Assays for the Quantification of SARS-CoV-2 Specific T-Cell Response: A Cross-Sectional Study
by Federica Bergami, Francesca Arena, Eleonora Francesca Pattonieri, Marilena Gregorini, Federica Meloni, Massimo Abelli, Elena Ticozzelli, Giorgia Testa, Daniele Lilleri, Irene Cassaniti and Fausto Baldanti
Diagnostics 2022, 12(6), 1509; https://doi.org/10.3390/diagnostics12061509 - 20 Jun 2022
Cited by 3 | Viewed by 2259
Abstract
Since the identification of the new severe acute respiratory syndrome virus 2 (SARS-CoV-2), a huge effort in terms of diagnostic strategies has been deployed. To date, serological assays represent a valuable tool for the identification of recovered COVID-19 patients and for the monitoring [...] Read more.
Since the identification of the new severe acute respiratory syndrome virus 2 (SARS-CoV-2), a huge effort in terms of diagnostic strategies has been deployed. To date, serological assays represent a valuable tool for the identification of recovered COVID-19 patients and for the monitoring of immune response elicited by vaccination. However, the role of T-cell response should be better clarified and simple and easy to perform assays should be routinely introduced. The main aim of this study was to compare a home-made assay for whole blood stimulation with a standardized ELISpot assay design in our laboratory for the assessment of spike-specific T-cell response in vaccinated subjects. Even if a good correlation between the assays was reported, a higher percentage of responder subjects was reported for immunocompromised subjects with ELISpot assay (56%) than home-made whole blood stimulation assay (33%). Additionally, three commercial assays were compared with our home-made assay, reporting a good agreement in terms of both positive and negative results. Full article
(This article belongs to the Section Diagnostic Microbiology and Infectious Disease)
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<p>Correlation between HM-WB IGRA (IFNγ pg/mL) and ELISpot assay in HCWs (<b>A</b>) and ICs (<b>B</b>). Each dot represents a single sample; r and <span class="html-italic">p</span> value are given in the graph. HCWs: healthcare workers; ICs: immunocompromised subjects.</p>
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<p>Distribution of SFU/million PBMC based on the IFNγ production measured by HM-WB IGRA is shown in HCWs (<b>A</b>) and ICs (<b>B</b>). Subjects were divided into three groups based on the level of IFNγ measured by HM-WB IGRA: negative (&lt;10 pg/mL), positive at low/medium level (ranging from 10 to 100 pg/mL) and positive at high level (&gt;100 pg/mL). Median SFU/million PBMC were measured in all the three groups and the p value for each comparison is given.</p>
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<p>Comparison of home-made WB stimulation assay with Covi-FERON (<b>A</b>), Quant-T-Cell (<b>B</b>) and QuantiFERON SARS-CoV-2 (<b>C</b>) tests. Correlation was determined using Spearman correlation test and r and p value were given for each comparison.</p>
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24 pages, 428 KiB  
Review
False Negative Results in Cervical Cancer Screening—Risks, Reasons and Implications for Clinical Practice and Public Health
by Anna Macios and Andrzej Nowakowski
Diagnostics 2022, 12(6), 1508; https://doi.org/10.3390/diagnostics12061508 - 20 Jun 2022
Cited by 8 | Viewed by 4558
Abstract
False negative (FN) results in cervical cancer (CC) screening pose serious risks to women. We present a comprehensive literature review on the risks and reasons of obtaining the FN results of primary CC screening tests and triage methods and discuss their clinical and [...] Read more.
False negative (FN) results in cervical cancer (CC) screening pose serious risks to women. We present a comprehensive literature review on the risks and reasons of obtaining the FN results of primary CC screening tests and triage methods and discuss their clinical and public health impact and implications. Misinterpretation or true lack of abnormalities on a slide are the reasons of FN results in cytology and p16/Ki-67 dual-staining. For high-risk human papillomavirus (HPV) molecular tests, those include: truly non-HPV-associated tumors, lesions driven by low-risk HPV types, and clearance of HPV genetic material before sampling. Imprecise disease threshold definition lead to FN results in visual inspection with acetic acid. Lesions with a discrete colposcopic appearance are a source of FN in colposcopic procedures. For FAM19A4 and hsa-miR124-2 genes methylation, those may originate from borderline methylation levels. Histological misinterpretation, sampling, and laboratory errors also play a role in all types of CC screening, as well as reproducibility issue, especially in methods based on human-eye evaluation. Primary HPV-based screening combined with high quality-assured immunocytochemical and molecular triage methods seem to be an optimal approach. Colposcopy with histological evaluation remains the gold standard for diagnosis but requires quality protocols and assurance measures. Full article
(This article belongs to the Section Pathology and Molecular Diagnostics)
23 pages, 1670 KiB  
Review
Hodgkin Lymphoma: Biology and Differential Diagnostic Problem
by Taishi Takahara, Akira Satou, Toyonori Tsuzuki and Shigeo Nakamura
Diagnostics 2022, 12(6), 1507; https://doi.org/10.3390/diagnostics12061507 - 20 Jun 2022
Cited by 4 | Viewed by 4740
Abstract
Hodgkin lymphomas (HLs) are lymphoid neoplasms that are morphologically defined as being composed of dysplastic cells, namely, Hodgkin and Reed–Sternberg cells, in a reactive inflammatory background. The biological nature of HLs has long been unclear; however, our understanding of HL-related genetics and tumor [...] Read more.
Hodgkin lymphomas (HLs) are lymphoid neoplasms that are morphologically defined as being composed of dysplastic cells, namely, Hodgkin and Reed–Sternberg cells, in a reactive inflammatory background. The biological nature of HLs has long been unclear; however, our understanding of HL-related genetics and tumor microenvironment interactions is rapidly expanding. For example, cell surface overexpression of programmed cell death 1 ligand 1 (CD274/PD-L1) is now considered a defining feature of an HL subset, and targeting such immune checkpoint molecules is a promising therapeutic option. Still, HLs comprise multiple disease subtypes, and some HL features may overlap with its morphological mimics, posing challenging diagnostic and therapeutic problems. In this review, we summarize the recent advances in understanding the biology of HLs, and discuss approaches to differentiating HL and its mimics. Full article
(This article belongs to the Special Issue Diagnostic Pathology of Lymphomas and Lymphoproliferative Disorders)
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<p>Histological and immunohistochemical features of nodular sclerosis classical Hodgkin lymphoma (NSCHL). (<b>A</b>) Cellular nodules are separated by collagen bundles. (<b>B</b>) Sclerotic thickening of the lymph node capsule is shown. (<b>C</b>) Neoplastic cells that are binucleated with a “mirror-image” appearance, called “Reed–Stenberg cells”. (<b>D</b>) Neoplastic cells with a lacuna-like space around the cytoplasm, called “lacunar cells”. (<b>E</b>–<b>H</b>) Neoplastic cells expressing CD30 and PD-L1 (assessed using clone SP142), lacking CD20 expression, and with very weak PAX5 expression.</p>
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<p>Histological features of mixed cellularity classical Hodgkin lymphoma (MCCHL). (<b>A</b>) Granuloma formation by histiocyte aggregation is observed in the background. (<b>B</b>) Neoplastic cells are scattered against a background rich in histiocytes and lymphocytes. (<b>C</b>) Neoplastic cells with highlighted Epstein–Barr virus RNA through in situ hybridization (EBER-ISH).</p>
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<p>Histological and immunohistochemical features of nodular lymphocyte-predominant HL (NLPHL). (<b>A</b>) Vague nodular architecture is observed. (<b>B</b>) Scattered neoplastic cells feature polylobated (popcorn-like) nuclei, and are called lymphocyte-predominant (LP) cells. (<b>C</b>) LP cells show strong PAX5 expression. (<b>D</b>) LP cells lack PD-L1 expression (assessed using clone SP142). (<b>E</b>) LP cells are ringed by PD-1-positive “rosetting” T lymphocytes.</p>
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<p>Images of the disease entities of classic Hodgkin lymphoma subtypes and its mimics. EBV = Epstein-Barr virus; AITL = angioimmunoblastic T-cell lymphoma; NSCHL = nodular sclerosis classic Hodgkin lymphoma; LRCHL = lymphocyte-rich classic Hodgkin lymphoma; MCCHL = mixed cellularity classic Hodgkin lymphoma; NLPHL = nodular lymphocyte-predominant Hodgkin lymphoma; DLBCL = diffuse large B-cell lymphoma; EBVMCU = EBV-positive mucocutaneous ulcer; MTX = methotrexate; LPD = lymphoproliferative disorder; PMBL = primary mediastinal large B-cell lymphoma; GZL = B-cell lymphoma unclassifiable, with features intermediate between DLBCL and CHL/Gray zone lymphoma; TCRBCL = T-cell/histiocyte-rich large B-cell lymphoma; a-DLBCL = anaplastic variant of DLBCL; SLBCL = sinusoidal large B-cell lymphoma; FDCS = follicular dendritic cell sarcoma.</p>
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10 pages, 431 KiB  
Article
Cone Beam Computerized Tomographic Analysis of Collum Angle of the Maxillary Central Incisors in Different Types of Malocclusion: Comparative Assessment in Saudi, Jordan and Egypt Subpopulation
by Rakhi Issrani, Namdeo Prabhu, Sunitha Siddanna, Sarah Hatab Alanazi, Mohammad Khursheed Alam, Manay Srinivas Munisekhar, May Othman Hamza, Reham Fawzi Dawood Shabanah and Rasha Saleh Ali Gadh
Diagnostics 2022, 12(6), 1506; https://doi.org/10.3390/diagnostics12061506 - 20 Jun 2022
Cited by 2 | Viewed by 1984
Abstract
Background: The collum angle (CA) is an extremely significant for patients who are undergoing orthodontic, dental implant restoration, prosthodontic and periodontic treatments. Aim and Objectives: To determine and compare the mean CA for maxillary central incisor in different types of malocclusion utilizing 3D [...] Read more.
Background: The collum angle (CA) is an extremely significant for patients who are undergoing orthodontic, dental implant restoration, prosthodontic and periodontic treatments. Aim and Objectives: To determine and compare the mean CA for maxillary central incisor in different types of malocclusion utilizing 3D Cone Beam Computerized Tomography (CBCT) images. The additional objectives were to determine and compare the mean CA for maxillary central incisor based upon the demographic characteristics among Saudi, Jordan and Egypt subpopulation and to test for significant differences in the CA of maxillary central incisor with different molar malocclusions. Methodology: A total of 400 CBCT images were included from the radiology archive at the College of Dentistry, Jouf University (Sakaka, Saudi Arabia). The CBCT images were divided into four groups based upon molar classifications. The selected records were used for the measurement of CA of maxillary central incisor using the measurement tool built into 3D:OnDemand software. Statistical analysis was done using independent t test and ANOVA to examine the differences between gender and races. Results: The mean CA for Class II div 2 exhibited significantly higher crown-root variation as compared other groups (p < 0.0001). Males sample showed greater value of CA for each group as compared to the females and this difference was statistically significant for all the groups other than for Class I (p < 0.05). The post hoc pairwise comparisons between the races showed statistically insignificant findings (p > 0.05). Significant difference was found on pairwise comparisons among different malocclusion groups other than for group Class I/Class II div 1 (p < 0.05). Conclusion: The CA of Class II div 2 group was the greatest as compared to other malocclusion groups. Males sample showed greater value of CA for each group as compared to the females and this difference was statistically significant for all the groups other than for Class I. Statistically insignificant difference was noted for the mean CA among different races whereas significant difference was found on pairwise comparisons among different malocclusion groups other than for group Class I/Class II div 1. Full article
(This article belongs to the Special Issue Advances in Orthodontic Diagnosis and Treatment)
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<p>Use of the 3D:OnDemand software to locate the specific points of median sagittal sections for maxillary anterior teeth and to measure crown to root angle.</p>
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14 pages, 1545 KiB  
Article
COVID-19 Underreporting in Brazil among Patients with Severe Acute Respiratory Syndrome during the Pandemic: An Ecological Study
by Tainá Momesso Lima, Camila Vantini Capasso Palamim, Vitória Franchini Melani, Matheus Ferreira Mendes, Letícia Rojina Pereira and Fernando Augusto Lima Marson
Diagnostics 2022, 12(6), 1505; https://doi.org/10.3390/diagnostics12061505 - 20 Jun 2022
Cited by 8 | Viewed by 1976
Abstract
Underreporting of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection is a global problem and might hamper Coronavirus Disease (COVID-19) epidemiological control. Taking this into consideration, we estimated possible SARS-CoV-2 infection underreporting in Brazil among patients with severe acute respiratory syndrome (SARS). An [...] Read more.
Underreporting of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection is a global problem and might hamper Coronavirus Disease (COVID-19) epidemiological control. Taking this into consideration, we estimated possible SARS-CoV-2 infection underreporting in Brazil among patients with severe acute respiratory syndrome (SARS). An ecological study using a descriptive analysis of the SARS report was carried out based on data supplied by the Influenza Epidemiological Surveillance Information (SIVEP)-Flu (in Brazilian Portuguese, Sistema de Vigilância Epidemiológica da Gripe) in the period between January 2015 and March 2021. The number of SARS cases and related deaths after infection by SARS-CoV-2 or Influenzae was described. The estimation of underreporting was evaluated considering the relative increase in the number of cases with undefined etiological agent comparing 2020 to 2015–2019; and descriptive analysis was carried out including data from January–March/2021. In our data, SARS-CoV-2 infection and the presence of SARS with undefined etiological agent were associated with the higher number of cases and deaths from SARS in 2020/2021. SARS upsurge was six times over that expected in 2020, according to SARS seasonality in previous years (2015–2019). The lowest possible underdiagnosis rate was observed in the age group < 2 y.o. and individuals over 30 y.o., with ~50%; while in the age groups 10–19 and 20–29 y.o., the rates were 200–250% and 100%, respectively. For the remaining age groups (2–5 and 5–9 y.o.) underreporting was over 550%, except for female individuals in the age group 2–5 y.o., in which a ~500% rate was found. Our study described that the SARS-CoV-2 infection underreporting rate in Brazil in SARS patients is alarming and presents different indices, mainly associated with the patients’ age groups. Our results, mainly the underreporting index according to sex and age, should be evaluated with caution. Full article
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<p>Severe Acute Respiratory Syndrome (SARS) overview in Brazil during the study period (January 2015 to March 2021). (<b>A</b>) SARS cases regardless of the etiological factor. (<b>B</b>) Evolution in the number of SARS cases resulting from Influenzae. (<b>C</b>) Evolution in the number of SARS cases with undefined etiological agent. (<b>D</b>) Evolution in the number of Coronavirus Disease (COVID-19) cases in 2020–2021.The data presented in this figure demonstrate SARS evolution according to Brazilian geopolitical regions. In <a href="#diagnostics-12-01505-f001" class="html-fig">Figure 1</a>A–C, the description of the epidemiological weeks from Jan 2015 to Mar 2021 is observed. In <a href="#diagnostics-12-01505-f001" class="html-fig">Figure 1</a>D, epidemiological weeks from Jan 2020 to Mar 2021 are described.</p>
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<p>Death from severe acute respiratory syndrome (SARS) overview in Brazil during the study period (January 2015 to March 2021). (<b>A</b>) Deaths from SARS regardless of etiological factor. (<b>B</b>) Evolution in the number of deaths from SARS resulting from Influenzae. (<b>C</b>) Evolution in the number of deaths from SARS with undefined etiological agent. (<b>D</b>) Evolution in the number of deaths from Coronavirus Disease (COVID-19) in 2020–2021. The data presented demonstrate the SARS evolution according to Brazilian geopolitical regions. In <a href="#diagnostics-12-01505-f001" class="html-fig">Figure 1</a>A–C, the description of the epidemiological weeks from Jan 2015 to Mar 2021 is presented. In <a href="#diagnostics-12-01505-f001" class="html-fig">Figure 1</a>D, the epidemiological weeks from Jan 2020 to Mar h2021 are described.</p>
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<p>Number of cases (<b>A</b>) and deaths (<b>B</b>) from severe acute respiratory syndrome (SARS) due to the Coronavirus Disease (COVID-19) pandemic development, according to the etiological agent, in the period from January 2015 to March 2021.</p>
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<p>Number of cases in absolute value of possible Coronavirus Disease (COVID-19) underdiagnosis according to sex (female and male) and age groups (years old, y.o.: &lt;2; 2–4; 5–9; 10–19; 20–29; 30–39; 40–49; 50–59; and +60) (<b>A</b>) and according to age only (<b>B</b>). The analysis included only data from 2020.</p>
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<p>Relative number comparing the number of severe acute respiratory syndrome (SARS) cases with Coronavirus Disease (COVID-19) underdiagnosis and the number of COVID-19 cases per patients’ sex and age group. The data are presented according to sex and age (<b>A</b>) and according to age only (<b>B</b>). The analysis included only data from 2020.</p>
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<p>Odds ratio (OR) and 95% confidence interval (95% CI) for the association between patients with severe acute respiratory syndrome (SARS) due to undefined etiological agent compared with patients with SARS due to Coronavirus Disease (COVID-19) or Influenzae virus infection regarding sex and age. Ref, reference.</p>
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23 pages, 1561 KiB  
Article
Predicting Visual Acuity in Patients Treated for AMD
by Beatrice-Andreea Marginean, Adrian Groza, George Muntean and Simona Delia Nicoara
Diagnostics 2022, 12(6), 1504; https://doi.org/10.3390/diagnostics12061504 - 20 Jun 2022
Cited by 1 | Viewed by 2376
Abstract
The leading diagnostic tool in modern ophthalmology, Optical Coherence Tomography (OCT), is not yet able to establish the evolution of retinal diseases. Our task is to forecast the progression of retinal diseases by means of machine learning technologies. The aim is to help [...] Read more.
The leading diagnostic tool in modern ophthalmology, Optical Coherence Tomography (OCT), is not yet able to establish the evolution of retinal diseases. Our task is to forecast the progression of retinal diseases by means of machine learning technologies. The aim is to help the ophthalmologist to determine when early treatment is needed in order to prevent severe vision impairment or even blindness. The acquired data are made up of sequences of visits from multiple patients with age-related macular degeneration (AMD), which, if not treated at the appropriate time, may result in irreversible blindness. The dataset contains 94 patients with AMD and there are 161 eyes included with more than one medical examination. We used various techniques from machine learning (linear regression, gradient boosting, random forest and extremely randomised trees, bidirectional recurrent neural network, LSTM network, GRU network) to handle technical challenges such as how to learn from small-sized time series, how to handle different time intervals between visits, and how to learn from different numbers of visits for each patient (1–5 visits). For predicting the visual acuity, we performed several experiments with different features. First, by considering only previous measured visual acuity, the best accuracy of 0.96 was obtained based on a linear regression. Second, by considering numerical OCT features such as previous thickness and volume values in all retinal zones, the LSTM network reached the highest score (R2=0.99). Third, by considering the fundus scan images represented as embeddings obtained from the convolutional autoencoder, the accuracy was increased for all algorithms. The best forecasting results for visual acuity depend on the number of visits and features used for predictions, i.e., 0.99 for LSTM based on three visits (monthly resampled series) based on numerical OCT values, fundus images, and previous visual acuities. Full article
(This article belongs to the Special Issue Artificial Intelligence in Clinical Medical Imaging Analysis)
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<p>The third visit, i.e., follow-up (#2), of a patient, right eye only. The right column shows that the values are computed on all of the layers of the retina: between the top layer (i.e., ILM) and the bottom layer (i.e., Bruch’s membrane—BM). The middle column shows nine values for the retinal thickness (black color), and nine values for the retinal volume (red color).</p>
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<p>The 9 zones analysed in the retina (<math display="inline"><semantics> <msub> <mi>C</mi> <mn>0</mn> </msub> </semantics></math> is the fovea).</p>
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<p>Cumulative explained variance: 99% of the data are represented with 12,000 components.</p>
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<p>Cumulative explained variance: 80% of the data are represented with 250 components.</p>
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<p>Gradient boosting machine showing how much the numerical OCT features influence the prediction of visual acuity. The case with prediction timestep as a features appears on the left. The case with 1-month resampling appears on the right.</p>
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<p>The proposed LSTM architecture.</p>
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<p>Autoencoder training and validation plot.</p>
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<p>Examples of OCT scan reconstruction and noise filtering using the convolutional autoencoder.</p>
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<p>Confusion matrix results for the disease evolution classification using gradient boosting classifier. Label 0 represents a good disease evolution, while 1 stands for a poor evolution. The matrix column represents the actual label.</p>
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<p>Average cross-validated <math display="inline"><semantics> <msup> <mi>R</mi> <mn>2</mn> </msup> </semantics></math> scores when predicting future visual acuity only from previous visual acuity data.</p>
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<p>Average <math display="inline"><semantics> <msup> <mi>R</mi> <mn>2</mn> </msup> </semantics></math> scores when predicting future visual acuity from all numerical OCT data.</p>
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<p>Comparison of feature selection methods’ performance when predicting future visual acuity from all OCT data. Average cross-validated R<math display="inline"><semantics> <msup> <mrow/> <mn>2</mn> </msup> </semantics></math> scores for all neural networks were computed.</p>
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<p>Actual vs. predicted VA values for the best model (LSTM with <math display="inline"><semantics> <mrow> <msup> <mi>R</mi> <mn>2</mn> </msup> <mo>=</mo> <mn>0.98</mn> </mrow> </semantics></math>, for three previous visits). The second figure shows that the actual and predicted visual acuities are highly correlated (<math display="inline"><semantics> <mrow> <mi>r</mi> <mo>=</mo> <mn>0.993</mn> </mrow> </semantics></math>).</p>
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<p>Actual vs. predicted VA values for the best model using all data (LSTM with <math display="inline"><semantics> <mrow> <msup> <mi>R</mi> <mn>2</mn> </msup> <mo>=</mo> <mn>0.99</mn> </mrow> </semantics></math>, for three previous visits). The second figure shows that the actual and predicted visual acuities are highly correlated (<math display="inline"><semantics> <mrow> <mi>r</mi> <mo>=</mo> <mn>0.994</mn> </mrow> </semantics></math>).</p>
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<p>Comparison of feature selection methods’ performance when predicting future visual acuities from all OCT data. Average cross-validated <math display="inline"><semantics> <msup> <mi>R</mi> <mn>2</mn> </msup> </semantics></math> scores for all neural networks were computed.</p>
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18 pages, 2167 KiB  
Review
COVID-19 Diagnosis: A Comprehensive Review of the RT-qPCR Method for Detection of SARS-CoV-2
by Debashis Dutta, Sarah Naiyer, Sabanaz Mansuri, Neeraj Soni, Vandana Singh, Khalid Hussain Bhat, Nishant Singh, Gunjan Arora and M. Shahid Mansuri
Diagnostics 2022, 12(6), 1503; https://doi.org/10.3390/diagnostics12061503 - 20 Jun 2022
Cited by 45 | Viewed by 9092
Abstract
The world is grappling with the coronavirus disease 2019 (COVID-19) pandemic, the causative agent of which is severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). COVID-19 symptoms are similar to the common cold, including fever, sore throat, cough, muscle and chest pain, brain fog, [...] Read more.
The world is grappling with the coronavirus disease 2019 (COVID-19) pandemic, the causative agent of which is severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). COVID-19 symptoms are similar to the common cold, including fever, sore throat, cough, muscle and chest pain, brain fog, dyspnoea, anosmia, ageusia, and headache. The manifestation of the disease can vary from being asymptomatic to severe life-threatening conditions warranting hospitalization and ventilation support. Furthermore, the emergence of mutecated variants of concern (VOCs) is paramount to the devastating effect of the pandemic. This highly contagious virus and its emergent variants challenge the available advanced viral diagnostic methods for high-accuracy testing with faster result yields. This review is to shed light on the natural history, pathology, molecular biology, and efficient diagnostic methods of COVID-19, detecting SARS-CoV-2 in collected samples. We reviewed the gold standard RT-qPCR method for COVID-19 diagnosis to confer a better understanding and application to combat the COVID-19 pandemic. This comprehensive review may further develop awareness about the management of the COVID-19 pandemic. Full article
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<p>Structure of SARS-CoV-2. The figure was created with <a href="http://Biorender.com" target="_blank">Biorender.com</a> on 8 June 2022.</p>
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<p>Overview of COVID-19 symptoms and SARS-CoV-2 detection methods for COVID-19 diagnosis. This figure was created with <a href="http://Biorender.com" target="_blank">Biorender.com</a> on 6 June 2022.</p>
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<p>Schematic representation of COVID-19 diagnostic test using RT-PCR. This figure was created with <a href="http://Biorender.com" target="_blank">Biorender.com</a> on 18 May 2022.</p>
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<p>Mechanism of fluorescent probe-based real-time PCR (qPCR) for COVID-19 diagnosis. Figure was created with <a href="http://Biorender.com" target="_blank">Biorender.com</a> on 20 May 2022.</p>
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14 pages, 7500 KiB  
Article
MCRS1 Expression Regulates Tumor Activity and Affects Survival Probability of Patients with Gastric Cancer
by Liang-Han Wang, Chih-Chun Chang, Chiao-Yin Cheng, Yao-Jen Liang, Dee Pei, Jen-Tang Sun and Yen-Lin Chen
Diagnostics 2022, 12(6), 1502; https://doi.org/10.3390/diagnostics12061502 - 20 Jun 2022
Viewed by 2092
Abstract
Gastric cancer is the fifth most common cancer worldwide and the third most common cause of cancer-related deaths. Surgery remains the first-choice treatment. Chemotherapy is considered in the middle and advanced stages, but has limited success. Microspherule protein 1 (MCRS1, also known as [...] Read more.
Gastric cancer is the fifth most common cancer worldwide and the third most common cause of cancer-related deaths. Surgery remains the first-choice treatment. Chemotherapy is considered in the middle and advanced stages, but has limited success. Microspherule protein 1 (MCRS1, also known as MSP58) is a protein originally identified in the nucleus and cytoplasm that is involved in the cell cycle. High expression of MCRS1 increases tumor growth, invasiveness, and metastasis. The mechanistic relationships between MCSR1 and proliferation, apoptosis, angiogenesis, and epithelial–mesenchymal transition (EMT) remain to be elucidated. We clarified these relationships using immunostaining of tumor tissues and normal tissues from patients with gastric cancer. High MCRS1 expression in gastric cancer positively correlated with Ki-67, Caspase3, CD31, Fibronectin, pAKT, and pAMPK. The hazard ratio of high MCRS1 expression was 2.44 times that of low MCRS1 expression, negatively impacting patient survival. Full article
(This article belongs to the Special Issue Advances in the Detection and Screening of Gastric Cancer)
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<p>Differences in H-score of MCRS1 according to different categories. (<b>A</b>) Age; (<b>B</b>) Gender; (<b>C</b>) Tissue type; (<b>D</b>) Degree of differentiation; (<b>E</b>) Disease stage. *** <span class="html-italic">p</span>-value &lt; 0.001.</p>
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<p>Kaplan–Meier plot of MCRS1. (<b>A</b>) The green line indicates low MCRS1 expression (N = 159). The red line indicates high expression of MCRS1 (N = 22). (<span class="html-italic">p</span>-value = 0.004) (<b>B</b>) Mortality at 12 months, 19 months, 57 months, and 81 months.</p>
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<p>Comparison of different expression levels of MCRS1 in gastric tumor tissues.</p>
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<p>Immunostaining images of high or low expression levels of MCRS1 and related tumorigenic proteins. (1–8) Low MCRS1 expression levels. (9–16) High MCRS1 expression levels.</p>
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15 pages, 7468 KiB  
Article
Different Lung Parenchyma Quantification Using Dissimilar Segmentation Software: A Multi-Center Study for COVID-19 Patients
by Camilla Risoli, Marco Nicolò, Davide Colombi, Marco Moia, Fausto Rapacioli, Pietro Anselmi, Emanuele Michieletti, Roberta Ambrosini, Marco Di Terlizzi, Luigi Grazioli, Cristian Colmo, Angelo Di Naro, Matteo Pio Natale, Alessandro Tombolesi, Altin Adraman, Domenico Tuttolomondo, Cosimo Costantino, Elisa Vetti and Chiara Martini
Diagnostics 2022, 12(6), 1501; https://doi.org/10.3390/diagnostics12061501 - 20 Jun 2022
Cited by 12 | Viewed by 3168
Abstract
Background: Chest Computed Tomography (CT) imaging has played a central role in the diagnosis of interstitial pneumonia in patients affected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and can be used to obtain the extent of lung involvement in COVID-19 pneumonia patients [...] Read more.
Background: Chest Computed Tomography (CT) imaging has played a central role in the diagnosis of interstitial pneumonia in patients affected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and can be used to obtain the extent of lung involvement in COVID-19 pneumonia patients either qualitatively, via visual inspection, or quantitatively, via AI-based software. This study aims to compare the qualitative/quantitative pathological lung extension data on COVID-19 patients. Secondly, the quantitative data obtained were compared to verify their concordance since they were derived from three different lung segmentation software. Methods: This double-center study includes a total of 120 COVID-19 patients (60 from each center) with positive reverse-transcription polymerase chain reaction (RT-PCR) who underwent a chest CT scan from November 2020 to February 2021. CT scans were analyzed retrospectively and independently in each center. Specifically, CT images were examined manually by two different and experienced radiologists for each center, providing the qualitative extent score of lung involvement, whereas the quantitative analysis was performed by one trained radiographer for each center using three different software: 3DSlicer, CT Lung Density Analysis, and CT Pulmo 3D. Results: The agreement between radiologists for visual estimation of pneumonia at CT can be defined as good (ICC 0.79, 95% CI 0.73–0.84). The statistical tests show that 3DSlicer overestimates the measures assessed; however, ICC index returns a value of 0.92 (CI 0.90–0.94), indicating excellent reliability within the three software employed. ICC was also performed between each single software and the median of the visual score provided by the radiologists. This statistical analysis underlines that the best agreement is between 3D Slicer “LungCTAnalyzer” and the median of the visual score (0.75 with a CI 0.67–82 and with a median value of 22% of disease extension for the software and 25% for the visual values). Conclusions: This study provides for the first time a direct comparison between the actual gold standard, which is represented by the qualitative information described by radiologists, and novel quantitative AI-based techniques, here represented by three different commonly used lung segmentation software, underlying the importance of these specific values that in the future could be implemented as consistent prognostic and clinical course parameters. Full article
(This article belongs to the Special Issue Advances in Cardiopulmonary Imaging)
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<p>Lung segmentation provided by 3DSlicer. In the first stripe, two graphics concerning the extensions of different densities are shown. In the second stripe, there are three representations of the lung segmentation as provided by the 3DSlicer software, in axial, sagittal, and coronal multiplanar reconstructions.</p>
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<p>The 3DSlicer manual tool (“<span class="html-italic">Segment Editor</span>”) accomplished the unsatisfactory segmentation. In this section, the user can perform a manual segmentation using the colors listed on the left board.</p>
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<p>LungCTAnalyzer and the thresholds used. Here is an example of the analysis pursued. It was quantified that the “emphysematous”, “inflated”, “infiltrated”, and “collapsed” lung parenchyma were affected, and also their respective percentages were calculated.</p>
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<p>CT Lung Density Analysis. This image shows: (<b>a</b>) parenchyma contouring; (<b>b</b>) lesion display; (<b>c</b>) manual editing; (<b>d</b>) final result with a volumetric rendering.</p>
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<p>CT Lung Density Analysis: histogram of attenuation areas. The red area represents the low attenuation area [−990; −750 HU]; the yellow one represents the medium attenuation area [−750; 660 HU]; and the blue area shows the high attenuation area [−660; 0 HU].</p>
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<p>CT Pulmo 3D: thresholds and volumes. This figure shows the HU thresholds and relative volumes per lobe.</p>
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<p>CT Pulmo 3D: graphic of HU thresholds. This graphic represents the HU thresholds and their relative frequencies.</p>
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<p>CT Pulmo 3D: lung contouring. This figure shows the lung parenchyma lesions counted; the different colors employed suggest different HU sub-ranges.</p>
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<p>The descriptive statistics from the radiologists’ measurements. The agreement between radiologists for visual estimation of pneumonia from CT was good, as shown in this box, plot scheme (ICC 0.79, 95% CI 0.73–0.84). Only one radiologist esteemed a higher visual score (considered as the median). ICC = Intraclass Correlation Coefficient, CI = Confidence Interval.</p>
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<p>Statistical description of the three software. This box plot scheme shows that 3DSlicer delivers a higher value in the median of the measures assessed.</p>
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<p>Bland–Altman graphics demonstrate the trend of the values assessed. For the software “LungCTAnalyzer”, the results lie in a range between 36.7 and −8.6 with an SD of ±1.96. For the Canon software, the results filled the space between 34.8 and −12.5 with an SD of ±1.96; for the Siemens software, instead, the values were positioned between 36.8 and −13.6 with the same SD of ±1.96. Finally, the “Parenchyma Analysis” outcomes were placed between 26.3 and −20.6 with an SD of ±1.96. SD = Standard Deviation.</p>
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13 pages, 1219 KiB  
Article
Cardiac Rehabilitation and Mortality Risk Reduction in Peripheral Artery Disease at 6-Month Outcome
by Razvan Anghel, Cristina Andreea Adam, Ovidiu Mitu, Dragos Traian Marius Marcu, Viviana Onofrei, Mihai Roca, Alexandru Dan Costache, Radu Stefan Miftode, Grigore Tinica and Florin Mitu
Diagnostics 2022, 12(6), 1500; https://doi.org/10.3390/diagnostics12061500 - 20 Jun 2022
Cited by 5 | Viewed by 2395
Abstract
The management of patients with peripheral artery disease (PAD) is integrative and multidisciplinary, in which cardiac rehabilitation (CR) plays a prognostic role in terms of functional status, quality of life, and long-term impact on morbidity and mortality. We conducted a prospective cohort study [...] Read more.
The management of patients with peripheral artery disease (PAD) is integrative and multidisciplinary, in which cardiac rehabilitation (CR) plays a prognostic role in terms of functional status, quality of life, and long-term impact on morbidity and mortality. We conducted a prospective cohort study on 97 patients with PAD admitted to a single tertiary referral center. Based on a prognostic index developed to stratify long-term mortality risk in PAD patients, we divided the cohort into two groups: low and low-intermediate risk group (45 cases) and high-intermediate and high risk group (52 cases). We analyzed demographics, clinical parameters, and paraclinical parameters in the two groups, as well as factors associated with cardiological reassessment prior to the established deadline of 6 months. Obesity (p = 0.048), renal dysfunction (p < 0.001), dyslipidemia (p < 0.001), tobacco use (p = 0.048), and diabetes mellitus (p < 0.001) are comorbidities with long-term prognostic value. Low-density lipoprotein cholesterol (p = 0.002), triglycerides (p = 0.032), fasting glucose (p = 0.011), peak oxygen uptake (p = 0.005), pain-free walking distance (p = 0.011), maximum walking time (p < 0.001), and maximum walking distance (p = 0.002) influence the outcome of PAD patients by being factors associated with clinical improvement at the 6-month follow-up. PAD patients benefit from enrollment in CR programs, improvement of clinical signs, lipid and carbohydrate profile, and weight loss and maintenance of blood pressure profile within normal limits, as well as increased exercise capacity being therapeutic targets. Full article
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<p>Flow chart of the studied group (IC: intermittent claudication; ABI: ankle-brachial index; PAD: peripheral artery disease).</p>
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<p>Risk index for 10-year mortality rates in patients with PAD (adapted after [<a href="#B11-diagnostics-12-01500" class="html-bibr">11</a>]).</p>
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<p>The receiver operating characteristic curve of factors associated with specialist reassessment before the 6-month assessment period.</p>
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9 pages, 1575 KiB  
Article
Optics and Utility of Low-Cost Smartphone-Based Portable Digital Fundus Camera System for Screening of Retinal Diseases
by K. V. Chalam, Joud Chamchikh and Suzie Gasparian
Diagnostics 2022, 12(6), 1499; https://doi.org/10.3390/diagnostics12061499 - 20 Jun 2022
Cited by 10 | Viewed by 3782
Abstract
Purpose: To describe optical principles and utility of inexpensive, portable, non-contact digital smartphone-based camera for the acquisition of fundus photographs for the evaluation of retinal disorders. Methods: The digital camera has a high-quality glass 25 D condensing lens attached to a 21.4-megapixel smartphone [...] Read more.
Purpose: To describe optical principles and utility of inexpensive, portable, non-contact digital smartphone-based camera for the acquisition of fundus photographs for the evaluation of retinal disorders. Methods: The digital camera has a high-quality glass 25 D condensing lens attached to a 21.4-megapixel smartphone camera. The white-emitting LED light of the smartphone at low illumination levels is used to visualize the fundus and limit source reflection. The camera captures a high-definition fundus (5344 × 4016) image on a complementary metal oxide semiconductor (CMO) with an area of 6.3 mm × 4.5 mm. The auto-acquisition mode of the device facilitates the quick capture of the image from continuous video streaming in a fraction of a second. Results: This new smartphone-based camera provides high-resolution digital images of the retina (50° telescopic view) in patients at a fraction of the cost (USD 1000) of established, non-transportable, office-based fundus photography systems. Conclusions: The portable user-friendly smartphone-based digital camera is a useful alternative for the acquisition of fundus photographs and provides a tool for screening retinal diseases in various clinical settings such as primary care clinics or emergency rooms. The ease of acquisition of photographs from a continuously streaming video of fundus obviates the need for a skilled photographer. Full article
(This article belongs to the Section Biomedical Optics)
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<p>Schematic Drawing Illustrating the Viewing System of the smartphone Retinal Imager. The digital camera has a 25D condensing lens attached to a 21.4-megapixel camera with a built-in lens complex. The smart phone camera’s flash provides the internal light source with a real image created between the 25D lens and smartphone.</p>
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<p>Housing and optical principles of smartphone retinal imager. The 25D condensing lens sits approximately 4.8 cm from the eye at the farthest end of the 18 cm metal tube, which is attached to the smartphone. The smartphone-based fundus camera allows for creation of an inverted, real aerial image approximately 6.6 cm from the condensing lens.</p>
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<p>The smart phone lens complex has approximately 6.5 mm total track of lens with about 5.067 mm effective focal length and image height of 3.96 mm. The smart phone image is captured on the CMO chip.</p>
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<p>Smartphone Retinal Imager in Operation. Volk iNview Retinal Imager in use, stabilized on a patient’s forehead owing to the BIO lens-like end tube structure allowing for fundus photography to be obtained in any clinical setting without need of a slit lamp or specialized equipment.</p>
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<p>Side-by-side Comparison of Fundus Photography Utilizing the traditional fundus camera (Optos California) and Smartphone Retinal Imager. (<b>a</b>). Normal fundus photograph of a left eye using the Optos fundus camera (<b>b</b>). Normal fundus photograph of the same left eye using the smartphone retinal Imager (<b>c</b>). Fundus photograph of the right eye demonstrating diabetic retinopathy with macular edema taken using the Optos fundus camera (<b>d</b>). Fundus photograph of the same right eye demonstrating diabetic retinopathy with macular edema taken with the smartphone retinal Imager (<b>e</b>). Fundus photograph of the left eye demonstrating central retinal artery occlusion taken using the Optos fundus camera (<b>f</b>). Fundus photograph of the same left eye demonstrating central retinal artery occlusion taken with the smartphone retinal Imager (<b>g</b>). Fundus photograph of the left eye demonstrating bull’s eye maculopathy secondary to hydroxychloroquine use taken using the Optos fundus camera (<b>h</b>). Fundus photograph of the same left eye demonstrating bull’s eye maculopathy secondary to hydroxychloroquine use taken with the smartphone retinal Imager.</p>
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10 pages, 4319 KiB  
Article
Monitoring Protein Denaturation of Egg White Using Passive Microwave Radiometry (MWR)
by Igor Goryanin, Lev Ovchinnikov, Sergey Vesnin and Yuri Ivanov
Diagnostics 2022, 12(6), 1498; https://doi.org/10.3390/diagnostics12061498 - 19 Jun 2022
Cited by 1 | Viewed by 2031
Abstract
Passive microwave radiometry (MWR) is a measurement technique based on the detection of passive radiation in the microwave spectrum of different objects. When in equilibrium, this radiation is known to be proportional to the thermodynamic temperature of an emitting body. We hypothesize that [...] Read more.
Passive microwave radiometry (MWR) is a measurement technique based on the detection of passive radiation in the microwave spectrum of different objects. When in equilibrium, this radiation is known to be proportional to the thermodynamic temperature of an emitting body. We hypothesize that living systems feature other mechanisms of emission that are based on protein unfolding and water rotational transitions. To understand the nature of these emissions, microwave radiometry was used in several in vitro experiments. In our study, we performed pilot measurements of microwave emissions from egg whites during denaturation induced by ethanol. Egg whites comprise 10% proteins, such as albumins, mucoproteins, and globulins. We observed a novel phenomenon: microwave emissions changed without a corresponding change in the water’s thermodynamic temperature. We also found striking differences between microwave emissions and thermodynamic temperature kinetics. Therefore, we hypothesize that these two processes are unrelated, contrary to what was thought before. It is known that some pathologies such as stroke or brain trauma feature increased microwave emissions. We hypothesize that this phenomenon originates from protein denaturation and is not related to the thermodynamic temperature. As such, our findings could explain the reason for the increase in microwave emissions after trauma and post mortem for the first time. These findings could be used for the development of novel diagnostics methods. The MWR method is inexpensive and does not require fluorescent or radioactive labels. It can be used in different areas of basic and applied pharmaceutical research, including in kinetics studies in biomedicine. Full article
(This article belongs to the Section Point-of-Care Diagnostics and Devices)
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<p>The experimental setup and volume of measurement. A probe is immersed into a liquid. The averaging volume is 28 mm in width (denoted <math display="inline"><semantics> <mrow> <msub> <mi>W</mi> <mi>x</mi> </msub> </mrow> </semantics></math>) and approximately 30 mm in depth (denoted <math display="inline"><semantics> <mrow> <msub> <mi>W</mi> <mi>z</mi> </msub> </mrow> </semantics></math>). Microwave emissions from the liquid are measured.</p>
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<p>RTMM device with USB connector.</p>
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<p>Time dependences were obtained using MWR Dynamics software (MMWR LTD). Step 1. Add egg whites; Step 2. Immerse probe and IR thermometer in the cup; Step 3. Add ethanol 96%; Step 4. Stir; Step 5. Remove probe.</p>
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<p>Microwave emissions (brightness) temperature of the egg white during ethanol-induced denaturation. Black line denotes experimentally observed temperature; red line denotes approximation (slope). Different panel figures refer to results from repeated experiments.</p>
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<p>Thermodynamic temperature during alcohol-induced denaturation. Black solid line denotes experimentally observed brightness temperature; orange line denotes approximation (slope).</p>
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<p>Microwave emissions (brightness temperature) when adding tap water (30 mL) to egg white at Time 0.</p>
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<p>Microwave emissions (brightness temperature) when adding ethanol to tap water during control experiment with no egg white. Black solid line denotes experimental observations. Orange line denotes approximation (slope).</p>
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<p>Microwave emissions (brightness temperature) when adding ethanol to tap water during control experiment with no egg white. Black solid line denotes experimental observations. Orange line denotes approximation (slope).</p>
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7 pages, 6233 KiB  
Interesting Images
A Case of Hepatic Immunoglobulin G4-Related Disease Presenting as an Inflammatory Pseudotumor and Sclerosing Cholangitis
by Se Young Jang, Young Seok Han, Sang Yub Lee, Ja Ryung Han, Young Oh Kweon, Won Young Tak, Soo Young Park, Yu Rim Lee, Hun Kyu Ryeom, Jung Guen Cha, Jihoon Hong and Yoo Na Kang
Diagnostics 2022, 12(6), 1497; https://doi.org/10.3390/diagnostics12061497 - 19 Jun 2022
Cited by 3 | Viewed by 1857
Abstract
An inflammatory pseudotumor is a benign disease characterized by tumor-like lesions consisting of inflammatory cells including plasma cells and fibrous tissue. Recently, some inflammatory pseudotumor cases proved to be a form of Immunoglobulin G4-related disease (IgG4-RD). This novel clinical entity, recognized as a [...] Read more.
An inflammatory pseudotumor is a benign disease characterized by tumor-like lesions consisting of inflammatory cells including plasma cells and fibrous tissue. Recently, some inflammatory pseudotumor cases proved to be a form of Immunoglobulin G4-related disease (IgG4-RD). This novel clinical entity, recognized as a fibroinflammatory condition, is characterized by lymphoplasmacytic infiltration with a predominance of IgG4-positive plasma cells, storiform fibrosis, and often elevated serum IgG4 concentrations. We report a case of IgG4-RD in the form of an inflammatory pseudotumor in the liver with combined sclerosing cholangitis. We recommend that for diagnosing IgG4-RD accurately, it is important to obtain adequate tissue samples and follow-up the lesion in clinical practice. Full article
(This article belongs to the Special Issue Advancements on Diagnostic and Management of Liver Disease)
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<p>Before (<b>A</b>,<b>B</b>) and 1 month (<b>C</b>,<b>D</b>) after laparoscopic cholecystectomy. Multiple, focal bile duct dilation is shown (<b>A</b>,<b>B</b>). The newly developed low density mass overlays in segment 6 and 7 (<b>C</b>,<b>D</b>).</p>
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<p>Arterial phase (<b>A</b>), portal phase (<b>B</b>), and delayed phase (<b>C</b>) of axial CT scan shows a poorly enhancing low density mass with right upstream bile duct dilatation.</p>
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<p>Serial portal phase CT scan (<b>A</b>–<b>C</b>) shows aggravated right intrahepatic duct dilatation and newly appeared low density nodules in the liver segment 6 (<b>C</b>, black arrows). Main low density mass (<b>A</b>–<b>C</b>, white arrows) size was not changed. Percutaneous biliary drainage was performed via right posterior bile duct. Catheter passage to the downstream was not possible for the tight biliary stricture at biliary confluence (<b>D</b>).</p>
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<p>The mass on segment 7 has increased in size and the inner cystic area has newly developed (<b>A</b>). Before the hepatic resection, CT scan of portal phase demonstrates stationary state of biliary dilatation (<b>B</b>–<b>D</b>, white arrows).</p>
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<p>An ill-defined, pale tan to yellow, slightly firm and solid mass is seen, measuring 6.5 × 4.6 × 4.2 cm in maximum dimensions in the right lobe of the liver (<b>A</b>). Diffuse lymphoplasmacytic infiltrate with lymphoid aggregates in the fibrotic background. Obliterative phlebitis is also seen (arrow) (<b>B</b>, Hematoxylin &amp; eosin stain, ×100). The bile duct is surrounded by a dense lymphoplasmacytic infiltrate with a feature of luminal narrowing. Storiform fibrosis is found in a background. (<b>C</b>, Hematoxylin &amp; eosin stain, ×100). An immunohistochemical stain for IgG4 shows a diffuse increase in IgG4+ plasma cells (<b>D</b>, IgG4 immunohistochemistry, ×100). The IgG4: IgG ratio is greater than 40% (<b>Box D</b>, IgG immunohistochemistry, ×200).</p>
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22 pages, 11590 KiB  
Article
Explainable Machine Learning-Based Risk Prediction Model for In-Hospital Mortality after Continuous Renal Replacement Therapy Initiation
by Pei-Shan Hung, Pei-Ru Lin, Hsin-Hui Hsu, Yi-Chen Huang, Shin-Hwar Wu and Chew-Teng Kor
Diagnostics 2022, 12(6), 1496; https://doi.org/10.3390/diagnostics12061496 - 19 Jun 2022
Cited by 8 | Viewed by 2548
Abstract
In this study, we established an explainable and personalized risk prediction model for in-hospital mortality after continuous renal replacement therapy (CRRT) initiation. This retrospective cohort study was conducted at Changhua Christian Hospital (CCH). A total of 2932 consecutive intensive care unit patients receiving [...] Read more.
In this study, we established an explainable and personalized risk prediction model for in-hospital mortality after continuous renal replacement therapy (CRRT) initiation. This retrospective cohort study was conducted at Changhua Christian Hospital (CCH). A total of 2932 consecutive intensive care unit patients receiving CRRT between 1 January 2010, and 30 April 2021, were identified from the CCH Clinical Research Database and were included in this study. The recursive feature elimination method with 10-fold cross-validation was used and repeated five times to select the optimal subset of features for the development of machine learning (ML) models to predict in-hospital mortality after CRRT initiation. An explainable approach based on ML and the SHapley Additive exPlanation (SHAP) and a local explanation method were used to evaluate the risk of in-hospital mortality and help clinicians understand the results of ML models. The extreme gradient boosting and gradient boosting machine models exhibited a higher discrimination ability (area under curve [AUC] = 0.806, 95% CI = 0.770–0.843 and AUC = 0.823, 95% CI = 0.788–0.858, respectively). The SHAP model revealed that the Acute Physiology and Chronic Health Evaluation II score, albumin level, and the timing of CRRT initiation were the most crucial features, followed by age, potassium and creatinine levels, SPO2, mean arterial pressure, international normalized ratio, and vasopressor support use. ML models combined with SHAP and local interpretation can provide the visual interpretation of individual risk predictions, which can help clinicians understand the effect of critical features and make informed decisions for preventing in-hospital deaths. Full article
(This article belongs to the Special Issue Diagnostic Modalities in Critical Care)
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<p>Flow chart of study patients.</p>
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<p>Study framework and feature engineering.</p>
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<p>Receiver operation characteristic curves of the models for predicting in-hospital mortality.</p>
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<p>The raincloud plot of in-hospital mortality predicted score in machine learning methods. (<b>a</b>) GBM, XGB and random forest, (<b>b</b>) SVM with radial kernel, SVM with polynomial kernel, and SVM with sigmoid kernel.</p>
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<p>The raincloud plot of in-hospital mortality predicted score in machine learning methods. (<b>a</b>) GBM, XGB and random forest, (<b>b</b>) SVM with radial kernel, SVM with polynomial kernel, and SVM with sigmoid kernel.</p>
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<p>Calibration of machine learning models for predicting in-hospital mortality with calibration belts. (<b>a</b>) GBM, (<b>b</b>) XGB, (<b>c</b>) random forest, (<b>d</b>) SVM with radial kernel, (<b>e</b>) SVM with polynomial kernel, and (<b>f</b>) SVM with sigmoid kernel.</p>
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<p>Calibration of machine learning models for predicting in-hospital mortality with calibration belts. (<b>a</b>) GBM, (<b>b</b>) XGB, (<b>c</b>) random forest, (<b>d</b>) SVM with radial kernel, (<b>e</b>) SVM with polynomial kernel, and (<b>f</b>) SVM with sigmoid kernel.</p>
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<p>The Kaplan–Meier curve for predicting the 28-day and 90-day mortality. (<b>a</b>) 28-day mortality, (<b>b</b>) 90-day mortality.</p>
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<p>Summary SHapley Additive exPlanations (SHAP) plot. (<b>a</b>) Global feature importance in final XGBoost model output. (<b>b</b>) Relationship between features and in-hospital mortality in XGBoost model. Diversion on <span class="html-italic">x</span>-axis represents effect on model output, with colors used to represent low (yellow) to high (purple) value of predictors.</p>
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<p>Summary SHapley Additive exPlanations (SHAP) plot. (<b>a</b>) Global feature importance in final XGBoost model output. (<b>b</b>) Relationship between features and in-hospital mortality in XGBoost model. Diversion on <span class="html-italic">x</span>-axis represents effect on model output, with colors used to represent low (yellow) to high (purple) value of predictors.</p>
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<p>Local explanation plots for individuals with various in-hospital mortality statuses and XGB model predictions. (<b>a</b>) In-hospital death and AI predicted in-hospital death; (<b>b</b>) non-in-hospital death and AI predicted non-in-hospital death; (<b>c</b>) in-hospital death but AI predicted non-in-hospital death; (<b>d</b>) non-in-hospital death but AI predicted in-hospital death. Green and red bars correspond to the contribution of the features to the prediction. Green represents a negative value, which decreases the predicted value; red represents a positive value, which increases the predicted value. <span class="html-italic">X</span>-axis represents model prediction value; <span class="html-italic">y</span>-axis lists the features and their observed values.</p>
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<p>Local explanation plots for individuals with various in-hospital mortality statuses and XGB model predictions. (<b>a</b>) In-hospital death and AI predicted in-hospital death; (<b>b</b>) non-in-hospital death and AI predicted non-in-hospital death; (<b>c</b>) in-hospital death but AI predicted non-in-hospital death; (<b>d</b>) non-in-hospital death but AI predicted in-hospital death. Green and red bars correspond to the contribution of the features to the prediction. Green represents a negative value, which decreases the predicted value; red represents a positive value, which increases the predicted value. <span class="html-italic">X</span>-axis represents model prediction value; <span class="html-italic">y</span>-axis lists the features and their observed values.</p>
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<p>Summary SHapley Additive exPlanations (SHAP) plot. (<b>a</b>) Global feature importance in final GBM model output. (<b>b</b>) Relationship between features and in-hospital mortality in GBM model. Diversion on <span class="html-italic">x</span>-axis represents effect on model output, with colors used to represent low (yellow) to high (purple) value of predictors.</p>
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<p>Local explanation plots for individuals with various in-hospital mortality statuses and GBM model predictions. (<b>a</b>) In-hospital death and AI predicted in-hospital death; (<b>b</b>) non-in-hospital death and AI predicted non-in-hospital death; (<b>c</b>) in-hospital death but AI predicted non-in-hospital death; (<b>d</b>) non-in-hospital death but AI predicted in-hospital death.</p>
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<p>Local explanation plots for individuals with various in-hospital mortality statuses and GBM model predictions. (<b>a</b>) In-hospital death and AI predicted in-hospital death; (<b>b</b>) non-in-hospital death and AI predicted non-in-hospital death; (<b>c</b>) in-hospital death but AI predicted non-in-hospital death; (<b>d</b>) non-in-hospital death but AI predicted in-hospital death.</p>
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<p>Summary SHapley Additive exPlanations (SHAP) plot. (<b>a</b>) Global feature importance in final random forest model output. (<b>b</b>) Relationship between features and in-hospital mortality in random forest model. Diversion on <span class="html-italic">x</span>-axis represents effect on model output, with colors used to represent low (yellow) to high (purple) value of predictors.</p>
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<p>Summary SHapley Additive exPlanations (SHAP) plot. (<b>a</b>) Global feature importance in final random forest model output. (<b>b</b>) Relationship between features and in-hospital mortality in random forest model. Diversion on <span class="html-italic">x</span>-axis represents effect on model output, with colors used to represent low (yellow) to high (purple) value of predictors.</p>
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<p>Local explanation plots for individuals with various in-hospital mortality statuses and random forest model predictions. (<b>a</b>) In-hospital death and AI predicted in-hospital death; (<b>b</b>) non-in-hospital death and AI predicted non-in-hospital death; (<b>c</b>) in-hospital death but AI predicted non-in-hospital death; (<b>d</b>) non-in-hospital death but AI predicted in-hospital death.</p>
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<p>Local explanation plots for individuals with various in-hospital mortality statuses and random forest model predictions. (<b>a</b>) In-hospital death and AI predicted in-hospital death; (<b>b</b>) non-in-hospital death and AI predicted non-in-hospital death; (<b>c</b>) in-hospital death but AI predicted non-in-hospital death; (<b>d</b>) non-in-hospital death but AI predicted in-hospital death.</p>
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17 pages, 740 KiB  
Article
Diagnostic Coding Intensity among a Pneumonia Inpatient Cohort Using a Risk-Adjustment Model and Claims Data: A U.S. Population-Based Study
by Ruchi Mishra, Himadri Verma, Venkata Bhargavi Aynala, Paul R. Arredondo, John Martin, Michael Korvink and Laura H. Gunn
Diagnostics 2022, 12(6), 1495; https://doi.org/10.3390/diagnostics12061495 - 19 Jun 2022
Cited by 5 | Viewed by 2319
Abstract
Hospital payments depend on the Medicare Severity Diagnosis-Related Group’s estimated cost and the set of diagnoses identified during inpatient stays. However, over-coding and under-coding diagnoses can occur for different reasons, leading to financial and clinical consequences. We provide a novel approach to measure [...] Read more.
Hospital payments depend on the Medicare Severity Diagnosis-Related Group’s estimated cost and the set of diagnoses identified during inpatient stays. However, over-coding and under-coding diagnoses can occur for different reasons, leading to financial and clinical consequences. We provide a novel approach to measure diagnostic coding intensity, built on commonly available administrative claims data, and demonstrated through a 2019 pneumonia acute inpatient cohort (N = 182,666). A Poisson additive model (PAM) is proposed to model risk-adjusted additional coded diagnoses. Excess coding intensity per patient visit was estimated as the difference between the observed and PAM-based expected counts of secondary diagnoses upon risk adjustment by patient-level characteristics. Incidence rate ratios were extracted for patient-level characteristics and further adjustments were explored by facility-level characteristics to account for facility and geographical differences. Facility-level factors contribute substantially to explain the remaining variability in excess diagnostic coding, even upon adjusting for patient-level risk factors. This approach can provide hospitals and stakeholders with a tool to identify outlying facilities that may experience substantial differences in processes and procedures compared to peers or general industry standards. The approach does not rely on the availability of clinical information or disease-specific markers, is generalizable to other patient cohorts, and can be expanded to use other sources of information, when available. Full article
(This article belongs to the Special Issue Advances in the Diagnosis of Pneumonia)
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<p>Effect plot illustrating excess coding intensity by admission month (<b>a</b>), and effect plot of excess coding intensity estimates for a stratum of hospitals with the same values (modal categories for each variable) for all facility-level characteristics (<b>b</b>).</p>
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<p>Average adjusted excess coding intensity (AECI) by U.S. Census Bureau regional division within each quarter in 2019.</p>
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<p>Histogram of the unexplained variability in excess coding intensity (represented by the AECI metric) averaged by facility.</p>
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37 pages, 73340 KiB  
Review
Role of Echocardiography in the Diagnosis and Interventional Management of Atrial Septal Defects
by P. Syamasundar Rao
Diagnostics 2022, 12(6), 1494; https://doi.org/10.3390/diagnostics12061494 - 18 Jun 2022
Cited by 5 | Viewed by 9000
Abstract
This review centers on the usefulness of echo-Doppler studies in the diagnosis of ostium secundum atrial septal defects (ASDs) and in their management, both in children and adults. Transthoracic echocardiography can easily identify the secundum ASDs and also differentiate secundum ASDs from other [...] Read more.
This review centers on the usefulness of echo-Doppler studies in the diagnosis of ostium secundum atrial septal defects (ASDs) and in their management, both in children and adults. Transthoracic echocardiography can easily identify the secundum ASDs and also differentiate secundum ASDs from other kinds of ASDs, such as ostium primum ASD, sinus venosus ASD and coronary sinus ASD, as well as patent foramen ovale. Preliminary selection of patients for device occlusion can be made by transthoracic echocardiograms while final selection is based on transesophageal (TEE) or intracardiac (ICE) echocardiographic studies with optional balloon sizing of ASDs. TEE and ICE are extremely valuable in guiding device implantation and in evaluating the position of the device following its implantation. Echo-Doppler evaluation during follow-up is also useful in documenting improvements in ventricular size and function, in assessing the device position, in detecting residual shunts, and in identifying rare device-related complications. Examples of echo images under each section are presented. The reasons why echo-Doppler is very valuable in diagnosing and managing ASDs are extensively discussed. Full article
(This article belongs to the Special Issue Diagnosis and Management of Congenital Heart Disease)
Show Figures

Figure 1

Figure 1
<p>Echo images from apical four chamber (<b>A</b>) and precordial short axis (<b>B</b>,<b>C</b>) projections of a child with an atrial septal defect (ASD) demonstrating dilation of the right atrium (RA), right ventricle (RV) (<b>A</b>) and pulmonary arteries (<b>B</b>,<b>C</b>). LA, left atrium; LV, left ventricle; LPA, left pulmonary artery; MPA, main pulmonary artery; RPA, right pulmonary artery.</p>
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<p>M-mode echocardiogram of a patient with a diagnosis of an atrial septal defect (ASD). It demonstrates dilation of the right ventricle (RV) and paradoxical movement of the interventricular septum in the M-mode recording (2D-derived) in parasternal short axis projection (see lower insert). Normally the ventricular septum functions as a part of the left ventricle (LV); in large ASDs, the septum functions as a part of RV and moves in opposite direction, i.e., paradoxical, also described as “diastolic septal flattening”. The findings are very typical indirect signs of an ASD. A, B, and C stand for measurements of the end-diastolic RV, end-diastolic LV, and end-systolic LV, in that order. The dimensions are shown top left. Modified from Reference [<a href="#B1-diagnostics-12-01494" class="html-bibr">1</a>].</p>
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<p>2D echocardiogram (<b>A</b>) and color flow imaging (<b>B</b>) in subcostal long-axis view, demonstrating an atrial septal defect (ASD) (arrow in (<b>A</b>)) with a left-to-right shunt (arrow in (<b>B</b>)). Left atrium (LA) and right atrium (RA) are marked. Reproduced from Reference [<a href="#B6-diagnostics-12-01494" class="html-bibr">6</a>].</p>
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<p>2D echocardiogram (<b>A</b>) and color flow imaging (<b>B</b>) in subcostal short-axis view, demonstrating an atrial septal defect (ASD) (arrow in (<b>A</b>)) with a left-to-right shunt (arrow in (<b>B</b>)). Left atrium (LA) and right atrium (RA) are shown. Reproduced from Reference [<a href="#B6-diagnostics-12-01494" class="html-bibr">6</a>].</p>
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<p>Selected video frame demonstrating flow across an atrial septal defect (ASD) by pulsed Doppler by placing the sample volume on the right side of the ASD (top insert).</p>
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<p>Echo images from subcostal long-axis views of an atrial septum illustrating fenestrated atrial septal defect. Fenestration 1 (F1) (<b>A</b>) is much larger and is a somewhat different projection of the atrial septum (<b>B</b>). Left-to-right shunts across both fenestrations is shown in (<b>C</b>). F2, fenestration 2; LA, left atrium; RA, right atrium.</p>
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<p>Two-dimensional subcostal long (<b>A</b>,<b>B</b>) and short (<b>C</b>,<b>D</b>) -axis projections from a transthoracic echo study illustrating an atrial septal defect (ASD) (<b>A</b>,<b>C</b>). Color flow imaging (<b>B</b>,<b>D</b>) demonstrates left-to-right shunt. IVC, Inferior vena cava; LA, left atrium; RA, right atrium; SVC, superior vena cava. Reproduced from Reference [<a href="#B7-diagnostics-12-01494" class="html-bibr">7</a>].</p>
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<p>Echo images from modified subcostal four-chambered views illustrating an ostium primum atrial septal defect (PASD) (<b>A</b>) with shunting left-to-right (arrow in (<b>B</b>)). Left atrium (LA), left ventricle (LV), right atrium (RA), and right ventricle (RV) are labeled.</p>
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<p>2D (<b>A</b>) and color flow (<b>B</b>) images from subcostal views demonstrating a sinus venosus atrial septal defect (SVASD) in 2D (<b>A</b>) (arrow) with a shunt (Sh) from left to right (arrow in (<b>B</b>)). Left atrium (LA) and right atrium (RA) are marked. Modified from Reference [<a href="#B6-diagnostics-12-01494" class="html-bibr">6</a>].</p>
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<p>2D (<b>A</b>) and color flow (<b>B</b>–<b>D</b>) images from subcostal short-axis views of the atrial septum, illustrating a patent foramen ovale (PFO) (arrow in (<b>A</b>)) with a left-to-right shunt (thin arrows in (<b>B</b>–<b>D</b>)). Note the overlapping of the septum primum over the septum secundum in (<b>A</b>), suggesting that this atrial defect is a PFO. DAo, descending aorta; LA, left atrium; RA, right atrium; SVC, superior vena cava. Reproduced from Reference [<a href="#B6-diagnostics-12-01494" class="html-bibr">6</a>].</p>
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<p>Two-dimensional transthoracic echocardiograms to illustrate the atrial septal rims in multiple views. The apical four-chamber (<b>a</b>), subcostal long-axis (<b>b</b>), parasternal short-axis (<b>c</b>), and subcostal short-axis (<b>d</b>) projections are shown. The unfilled arrowheads point to the ASD. Adequate-sized septal rims are seen in each image. This child is deemed to be a suitable candidate for percutaneous device occlusion. Ao, Aorta; LA, left atrium; LV, left ventricle; RA, right atrium; RV, right ventricle. Reproduced from Reference [<a href="#B25-diagnostics-12-01494" class="html-bibr">25</a>].</p>
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<p>Two-dimensional echocardiograms of atrial septal defects (ASDs) in three different patients to illustrate deficient atrial septal margins. In (<b>a</b>) superior and inferior rims are small, in (<b>b</b>) the inferior septal rim is deficient, and in (<b>c</b>) the superior rim is tiny; the rims are shown with arrowheads. These ASDs are considered unsuitable for transcatheter device occlusion, because the rims of the ASD are inadequate for the device to achieve a good grasp on the atrial septum. LA, left atrium; LV, left ventricle: RA, right atrium; RV, right ventricle. Reproduced from Reference [<a href="#B26-diagnostics-12-01494" class="html-bibr">26</a>].</p>
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<p>Line drawings of the atrial septum along with the atrial septal defect (ASD) in multiple echo projections, namely, subcostal long axis (<b>A</b>), subcostal short axis (<b>B</b>), and apical four chamber (<b>C</b>), illustrating the methods of measurement of sizes of the defect, length of the atrial septum (LAS), and inferior (IR) and superior (SR) rims of the ASD. Left atrium (LA), left ventricle (LV), right atrium (RA), right pulmonary artery (RPA), and right ventricle (RV), and superior vena cava (SVC) are marked. Replicated from Reference [<a href="#B27-diagnostics-12-01494" class="html-bibr">27</a>].</p>
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<p>Transesophageal echocardiographic examination demonstrating an atrial septal defect (ASD) in long-axis (<b>A</b>,<b>B</b>), bi-caval (<b>C</b>), and short-axis (<b>D</b>) views. Shunt across the ASD is shown by color flow imaging (<b>B</b>). Note the very small aortic (anterio-superior) rim (AR) in (<b>D</b>). A good-sized superior vena caval (SVC) rim is seen in (<b>C</b>). Aorta (Ao), inferior vena cava (IVC), left atrium (LA), and right atrium (RA) are marked. Reproduced from Reference [<a href="#B6-diagnostics-12-01494" class="html-bibr">6</a>].</p>
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<p>Transesophageal echocardiographic (TEE) images of an atrial septal defect (ASD) in a short-axis projection. An extremely small retro-aortic (RAR) (anterio-superior) rim in (<b>A</b>) is seen. Left-to-right (L to R) shunt through the atrial defect by color Doppler is shown in (<b>B</b>). Ao, aorta; LA, left atrium; RA, right atrium.</p>
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<p>Transesophageal echocardiographic (TEE) study of the atrial septum in short-axis (<b>A</b>) and four-chamber (<b>B</b>) views demonstrating an atrial septal defect (ASD). Small retro-aortic and mitral rims are seen. Ao, aorta; LA, left atrium; LV, left ventricle; RV, right ventricle.</p>
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<p>Transesophageal echocardiographic (TEE) study of an atrial septal defect demonstrating adequate-sized inferior vena caval (IVC) (<b>A</b>) and superior vena caval (SVC) (<b>B</b>) rims.</p>
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<p>Transesophageal echocardiographic study of an atrial septal defect (ASD) in a four-chamber view demonstrating an ASD (arrow) with shunting left to right. The insert shows dimensions of superior rim (1), ASD (2), and inferior rim (3) in that order. LA, left atrium; RA, right atrium. Reproduced from Reference [<a href="#B3-diagnostics-12-01494" class="html-bibr">3</a>].</p>
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<p>Transesophageal echocardiographic study of a fenestrated atrial septal defect in short projection demonstrating left-to-right shunt across a fenestrated atrial defect (arrows). LA, Left atrium; RA, right atrium. Reproduced from Reference [<a href="#B4-diagnostics-12-01494" class="html-bibr">4</a>].</p>
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<p>Transesophageal echocardiographic studies of the atrial septum demonstrating aortic (ARim), mitral (MRim), superior vena caval (SVC Rim), and inferior vena caval (IVC Rim) rims in sort-axis (<b>A</b>) four-chamber (<b>B</b>), and bi-caval (<b>C</b>,<b>D</b>) views, respectively. Aorta (Ao), atrial septal defect (ASD), inferior vena cava (IVC), left atrium (LA), left ventricle (LV), right atrium (RA), right ventricle (RV), and superior vena cava (SVC) are labeled.</p>
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<p>Selected video frames from transthoracic 2D and color Doppler echo demonstrating: (<b>a</b>) a shunt across the atrial septal defect (ASD) (filled arrow), (<b>b</b>) balloon sizing (unfilled arrow) of the ASD, and (<b>c</b>) the device in place (filled arrowhead) without residual shunting. LA, left atrium; RA, right atrium. Reproduced from Reference [<a href="#B45-diagnostics-12-01494" class="html-bibr">45</a>].</p>
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<p>Plot is drawn demonstrating the correlation of the calculated diameter of the atrial septal defect (ASD) by the equation ([1.05 × echo diameter in mm] + 5.49) with the balloon-sized ASD diameter. Statistically important (<span class="html-italic">p</span> &lt; 0.001) relationship with an r value of 0.9 was found. Modified from Reference [<a href="#B47-diagnostics-12-01494" class="html-bibr">47</a>].</p>
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<p>Trans-esophageal echocardiogram demonstrating static balloon sizing of an atrial defect. Waist (W) of the balloon is seen, which measures the size of the ASD. LA, left atrium; RA, right atrium. Reproduced from Reference [<a href="#B4-diagnostics-12-01494" class="html-bibr">4</a>].</p>
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<p>Transesophageal echocardiogram demonstrating static sizing balloon. Note waisting of a sizing balloon (arrow in both (<b>A</b>,<b>B</b>)). Note that there is no evidence for any shunt in (<b>B</b>).</p>
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<p>Transesophageal echo of the atrial septal defect, demonstrating the thin margin (arrow) of the atrial septal defect (<b>A</b>) which is not included (<b>B</b>) in the measurement of the size of the defect. LA, left atrium; RA, right atrium. Reproduced from Reference [<a href="#B6-diagnostics-12-01494" class="html-bibr">6</a>].</p>
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<p>Precordial echo frames from apical four-chamber views of the atria during the deployment of a buttoned device (unfilled arrowheads) to occlude an atrial septal defect (ASD). The occlude component of the device is in the left atrium (LA) and frames (<b>a</b>–<b>d</b>) demonstrate the occluder being slowly withdrawn towards the ASD to close the atrial defect. The filled arrowheads points to the loading wire attached to the occluder. LV, left ventricle; RA, right atrium; RV, right ventricle. Reproduced from Reference [<a href="#B25-diagnostics-12-01494" class="html-bibr">25</a>].</p>
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<p>Transesophageal echocardiographic images during the delivery of an Amplatzer Septal Occluder. (<b>A</b>). The left atrial disc (LA Disc) (thick arrow) was delivered into the left atrium (LA). (<b>B</b>). Both the LA and right atrial (RA) discs (thick arrows) were delivered across the atrial septal defect. It is clearly seen that the aortic rim (AR) (thin arrow in (<b>B</b>)) is sandwiched in-between the LA Disc and RA Disc. Ao, aorta. Reproduced from Reference [<a href="#B7-diagnostics-12-01494" class="html-bibr">7</a>].</p>
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<p>Transesophageal echocardiographic images during the delivery of an Amplatzer Septal Occluder in a different patient. (<b>A</b>). The left atrial disc (LA Disc) (thick arrow) was delivered into the left atrium (LA). (<b>B</b>). Both the LA and right atrial (RA) discs (thick arrows) were delivered across the atrial septal defect. Again, note the thin arrows pointing to the sandwiching of the septal rims between the LA and RA discs. The labeling notations are those used in <a href="#diagnostics-12-01494-f027" class="html-fig">Figure 27</a>. Reproduced from Reference [<a href="#B7-diagnostics-12-01494" class="html-bibr">7</a>].</p>
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<p>Transesophageal echocardiographic images after the deployment of an Amplatzer Septal Occluder to close an atrial defect, illustrating the location of both the left atrial (LA) and right atrial (RA) discs in four-chamber (<b>A</b>), bi-caval (<b>B</b>) and long-axis (<b>C</b>) projections. It is important to ensure that the septal rims of the atrial defect (thin arrows) are sandwiched in-between the LA and RA discs. LV, left ventricle; RV, right ventricle; SVC, superior vena cava. Replicated from Reference [<a href="#B7-diagnostics-12-01494" class="html-bibr">7</a>].</p>
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<p>Intracardiac echocardiographic (ICE) images secured during Gore HELEX device deployment to occlude an atrial septal defect (ASD) illustrating the position of the device components. (<b>A</b>) The left atrial disc (LA Disc) is in the left atrium (LA). (<b>B</b>) The right atrial disc (RA Disc) is in the right atrium. (<b>C</b>) The LA and RA discs are on either side of the atrial septum after detachment of device delivery catheter (DC) from the device. Note that the margins of the ASD (thin arrows) are sandwiched in-between LA and RA discs. Replicated from Reference [<a href="#B7-diagnostics-12-01494" class="html-bibr">7</a>].</p>
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<p>Transesophageal echocardiographic pictures of the fenestrated atrial septal defect by two-dimensional (2D) (<b>A</b>) and color Doppler (<b>B</b>) imaging. Note the fenestrations (F1 and F2) within the atrial septum in (<b>A</b>) and shunting from the left atrium (LA) to the right atrium (RA) in (<b>B</b>). Replicated from Reference [<a href="#B7-diagnostics-12-01494" class="html-bibr">7</a>].</p>
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<p>Transesophageal echocardiographic images showing three fenestrations by color Doppler in echocardiographic views (<b>A</b>,<b>B</b>) different than shown in <a href="#diagnostics-12-01494-f031" class="html-fig">Figure 31</a>. LA, left atrium; RA, right atrium; SVC, superior vena cava. Reproduced from Reference [<a href="#B7-diagnostics-12-01494" class="html-bibr">7</a>].</p>
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<p>Transesophageal echocardiographic images after the implantation of an Amplatzer Cribriform Device (CD) illustrating the location of right (RA) and left (LA) atrial discs across the atrial septal defect (ASD) (<b>A</b>). On color Doppler imaging (<b>B</b>), there is no residual shunt (<b>B</b>) in a child who had a fenestrated ASD demonstrated in <a href="#diagnostics-12-01494-f031" class="html-fig">Figure 31</a> and <a href="#diagnostics-12-01494-f032" class="html-fig">Figure 32</a>. Ao, aorta; LA, left atrium; RA, right atrium. Reproduced from Reference [<a href="#B6-diagnostics-12-01494" class="html-bibr">6</a>].</p>
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<p>Transesophageal echocardiographic images of the GORE<sup>®</sup> CARDIOFORM ASD Occluder device after its deployment in two different projections. In the short-axis view (<b>A</b>), the aortic rim (AR) (arrow in (<b>A</b>)) is visualized sandwiched in-between the right and left atrial discs. In the bi-caval view (<b>B</b>) note that there was a little splaying of the upper part of the right atrial disc (RAD). Ao, aorta; LA, left atrium; RA, right atrium; SVC, superior vena cava. Reproduced from reference [<a href="#B37-diagnostics-12-01494" class="html-bibr">37</a>].</p>
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<p>Three-dimensional reconstruction of transesophageal echocardiographic study showing GORE<sup>®</sup> CARDIOFORM ASD Occluder (GCO) from the right atrial aspect, demonstrating its good position without impinging on the aortic root.</p>
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<p>Changes in the end-diastolic diameters of the right ventricle (<b>left panel</b>) and left ventricle (<b>right panel</b>) following percutaneous occlusion of atrial defects are demonstrated in the above bar graph. The panel on the left illustrates decreased (<span class="html-italic">p</span> &lt; 0.01) size of the right ventricle shortly after occlusion (POST) of the atrial septal defect (ASD). At follow-up (FU), there was a further, but not statistically significant (<span class="html-italic">p</span> &gt; 0.1), reduction in the end-diastolic measurements of the right ventricle. The panel on the right shows no statistically important alteration (<span class="html-italic">p</span> &gt; 05) in the left ventricular dimension either immediately following atrial defect occlusion or during follow-up. The mean + SD (standard deviation) is shown for each measurement. N, number of patients; POST, on the day after ASD occlusion; PRE, before ASD occlusion. Reproduced from Reference [<a href="#B60-diagnostics-12-01494" class="html-bibr">60</a>].</p>
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<p>Changes in the inter-ventricular septal motion following percutaneous occlusion of atrial defects are demonstrated in the above graph. Before atrial septal defect (ASD) occlusion (PRE), the inter-ventricular septal motion is either flat or paradoxical in most subjects. Shortly following atrial defect closure (POST), the inter-ventricular septal motion has normalized in all except a single patient. During follow-up (FU), the inter-ventricular septal motion is normal in the entire patient cohort. Reproduced from Reference [<a href="#B60-diagnostics-12-01494" class="html-bibr">60</a>].</p>
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<p>Enhancement of myocardial performance indices (MPI) of right ventricle (RV) and left ventricle (LV) after occlusion of atrial septal defects (ASDs) is illustrated in the above bar diagram. PRE, prior to ASD occlusion; POST, three months following ASD occlusion. Created from the information of Salehian O, et al., JACC, 2005;45:499–504 [<a href="#B61-diagnostics-12-01494" class="html-bibr">61</a>]. Reproduced from Reference [<a href="#B51-diagnostics-12-01494" class="html-bibr">51</a>].</p>
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<p>Echocardiographic images from subcostal projections demonstrating an atrial septal defect (ASD) (unfilled arrow) with adequate septal margins before (<b>a</b>) and shortly after (<b>b</b>) device (filled arrow) deployment. Residual shunt was not seen by color flow Doppler (not shown). LA, left atrium; RA, right atrium. Replicated from Reference [<a href="#B62-diagnostics-12-01494" class="html-bibr">62</a>].</p>
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<p>Echocardiographic images from subcostal projections of an atrial septal defect (ASD) (arrow in (<b>a</b>)) before occlusion (<b>a</b>) with a buttoned device and several hours (<b>b</b>) and three months (<b>c</b>) following device deployment. The big arrows in both (<b>b</b>) and (<b>c</b>) identify the occluder component (O) on the left-atrial (LA) side of the atrial septum and the small arrows points out the counter-occluder (Co) on end on the right-atrial (RA) side of the atrial septum. LV, left ventricle. Replicated from Reference [<a href="#B26-diagnostics-12-01494" class="html-bibr">26</a>].</p>
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<p>Selected video frames from subcostal (<b>A</b>,<b>E</b>,<b>F</b>) and apical four-chamber (<b>B</b>–<b>D</b>) transthoracic echo views of the atrial septum, demonstrating GORE<sup>®</sup> CARDIOFORM ASD Occluder device across the atrial septal defect three months after the device implantation. Good location of the device (DEVICE) without residual left-to-right shunt (<b>C</b>,<b>F</b>) is shown. LA, left atrium; LV, left ventricle; RA, right atrium.</p>
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<p>Two-dimensional echocardiographic images in the subcostal projections of the atrial septal defect (ASD) in long-axis views before (<b>a</b>), shortly following (<b>b</b>), and at one (<b>c</b>), six (<b>d</b>), twelve (<b>e</b>), and twenty-four (<b>f</b>) months after ASD occlusion demonstrating the outcome of percutaneous occlusion of an atrial defect with buttoned device. Stable position of the device (D) on the atrial septum (<b>b</b>–<b>e</b>) is seen. Twenty-four months later (<b>f</b>), the device components look to be incorporated into the atrial septal tissue. On pulsed and color Doppler studies simultaneous with 2D examination, no residual shunt was seen (not shown). LA, left atrium; RA, right atrium. Replicated from Reference [<a href="#B60-diagnostics-12-01494" class="html-bibr">60</a>].</p>
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<p>Echocardiographic images from subcostal long (<b>A</b>,<b>B</b>) and short (<b>C</b>,<b>D</b>) -axis transthoracic study of the atrial septum, illustrating Amplatzer Septal Occluder (ASO) closing an atrial defect three years after the device implantation; note good position of the ASO device (<b>A</b>–<b>D</b>) without residual shunt (<b>B</b>,<b>D</b>). Left atrium (LA), right atrium (RA), and superior vena cava (SVC) are labeled.</p>
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<p>Echocardiographic images from apical four-chamber projections of an atrial septal defect (ASD) illustrating an ASD with a shunt from the left (LA) to the right (RA) atrium before (<b>a</b>) and 3 months after (<b>b</b>) deployment of a buttoned device. No residual shunt is observed in b. Black arrow in (<b>b</b>) shows the occluder (O) on the LA side of the atrial septum while a white arrow displays counter-occluder (CO) end on the RA side of the atrial septum. Left ventricle (LV) and right ventricle (RV) are labeled. Replicated from Reference [<a href="#B26-diagnostics-12-01494" class="html-bibr">26</a>].</p>
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<p>Transthoracic subcostal echocardiographic images of the atrial septum with color Doppler imaging demonstrating the device (unfilled arrow heads) across atrial septal defects in two different patients (<b>a</b>,<b>b</b>) with residual shunts (filled arrowheads). LA, left atrium; RA, right atrium. Reproduced from Reference [<a href="#B4-diagnostics-12-01494" class="html-bibr">4</a>].</p>
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<p>Rates of resolution of residual atrial shunts following occlusion of atrial defects with fourth-generation buttoned devices. The percentage of subjects with residual shunts was calculated as a ratio of the patients with residual shunts divided by the number of subjects examined at that specific follow-up duration. Note the gradual decline in the percentage of patients with residual shunts. mo, month; yr, year. Reproduced from Reference [<a href="#B65-diagnostics-12-01494" class="html-bibr">65</a>].</p>
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<p>The relation between the diameters of atrial defects and sizes of the Amplatzer device among patients who showed no evidence of perforation (Trial), and those with perforation (Erosion) are shown in this bar diagram. The diameter (Dia) of the atrial septal defect (ASD) was identical in both the described groups (left most panel). However, the balloon-stretched diameter (Stretch), diameter of the device (Dev size), and the ratio of device to atrial defect (Ratio) were larger (2nd, 3rd, and 4th panels) in patients who had perforation than those who did not have perforation (graph was created from the data published in References [<a href="#B71-diagnostics-12-01494" class="html-bibr">71</a>,<a href="#B72-diagnostics-12-01494" class="html-bibr">72</a>]). Based on this information, it was suggested that Amplatzer devices no bigger than 1.5 × the atrial defect diameter should be utilized. Replicated from Reference [<a href="#B51-diagnostics-12-01494" class="html-bibr">51</a>].</p>
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21 pages, 32993 KiB  
Article
MixPatch: A New Method for Training Histopathology Image Classifiers
by Youngjin Park, Mujin Kim, Murtaza Ashraf, Young Sin Ko and Mun Yong Yi
Diagnostics 2022, 12(6), 1493; https://doi.org/10.3390/diagnostics12061493 - 18 Jun 2022
Cited by 2 | Viewed by 2905
Abstract
CNN-based image processing has been actively applied to histopathological analysis to detect and classify cancerous tumors automatically. However, CNN-based classifiers generally predict a label with overconfidence, which becomes a serious problem in the medical domain. The objective of this study is to propose [...] Read more.
CNN-based image processing has been actively applied to histopathological analysis to detect and classify cancerous tumors automatically. However, CNN-based classifiers generally predict a label with overconfidence, which becomes a serious problem in the medical domain. The objective of this study is to propose a new training method, called MixPatch, designed to improve a CNN-based classifier by specifically addressing the prediction uncertainty problem and examine its effectiveness in improving diagnosis performance in the context of histopathological image analysis. MixPatch generates and uses a new sub-training dataset, which consists of mixed-patches and their predefined ground-truth labels, for every single mini-batch. Mixed-patches are generated using a small size of clean patches confirmed by pathologists while their ground-truth labels are defined using a proportion-based soft labeling method. Our results obtained using a large histopathological image dataset shows that the proposed method performs better and alleviates overconfidence more effectively than any other method examined in the study. More specifically, our model showed 97.06% accuracy, an increase of 1.6% to 12.18%, while achieving 0.76% of expected calibration error, a decrease of 0.6% to 6.3%, over the other models. By specifically considering the mixed-region variation characteristics of histopathology images, MixPatch augments the extant mixed image methods for medical image analysis in which prediction uncertainty is a crucial issue. The proposed method provides a new way to systematically alleviate the overconfidence problem of CNN-based classifiers and improve their prediction accuracy, contributing toward more calibrated and reliable histopathology image analysis. Full article
(This article belongs to the Special Issue Artificial Intelligence in Pathological Image Analysis)
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<p>Baseline vs. MixPatch. A single WSI generates multiple patches. The process of tiling creates certain case patches and uncertain case patches. Most parts of a certain patch are covered by a single label, but those of an uncertain patch are mixed. The baseline methods are overconfident, even for uncertain patches and incorrect outputs. The proposed method, MixPatch, overcomes these problems by explicitly incorporating the mixed-region variations in histopathological images into the training process.</p>
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<p>The overall process of the proposed method. In the existing methods, the patch-level classifier is trained using a CNN model and a cleaned patch dataset, <math display="inline"><semantics> <mrow> <msub> <mi>D</mi> <mrow> <mi>o</mi> <mi>r</mi> <mi>i</mi> <mi>g</mi> <mi>i</mi> <mi>n</mi> <mi>a</mi> <mi>l</mi> </mrow> </msub> </mrow> </semantics></math>, which pathologists previously confirmed. The proposed method, MixPatch, additionally uses a new subtraining dataset, which consists of image <math display="inline"><semantics> <mrow> <msub> <mi>x</mi> <mrow> <mi>m</mi> <mi>i</mi> <mi>x</mi> <mi>e</mi> <mi>d</mi> </mrow> </msub> </mrow> </semantics></math> and label <math display="inline"><semantics> <mrow> <msub> <mi>y</mi> <mrow> <mi>m</mi> <mi>i</mi> <mi>x</mi> <mi>e</mi> <mi>d</mi> </mrow> </msub> </mrow> </semantics></math>. <math display="inline"><semantics> <mrow> <msub> <mi>x</mi> <mrow> <mi>m</mi> <mi>i</mi> <mi>x</mi> <mi>e</mi> <mi>d</mi> </mrow> </msub> </mrow> </semantics></math> is built by combining randomly selected images from the minipatch dataset. <math display="inline"><semantics> <mrow> <msub> <mi>y</mi> <mrow> <mi>m</mi> <mi>i</mi> <mi>x</mi> <mi>e</mi> <mi>d</mi> </mrow> </msub> </mrow> </semantics></math> is defined according to the ratio of abnormal mini-patches. In the figure, a minibatch is a randomly built mix of samples from <math display="inline"><semantics> <mrow> <msub> <mi>D</mi> <mrow> <mi>o</mi> <mi>r</mi> <mi>i</mi> <mi>g</mi> <mi>i</mi> <mi>n</mi> <mi>a</mi> <mi>l</mi> </mrow> </msub> </mrow> </semantics></math> and samples from <math display="inline"><semantics> <mrow> <msub> <mi>D</mi> <mrow> <mi>m</mi> <mi>i</mi> <mi>x</mi> <mi>e</mi> <mi>d</mi> <mo>−</mo> <mi>p</mi> <mi>a</mi> <mi>t</mi> <mi>c</mi> <mi>h</mi> </mrow> </msub> </mrow> </semantics></math>.</p>
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<p>ROC curve for the different methods.</p>
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<p>Integrated reliability diagram for patch-level classifiers trained using each method.</p>
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<p>The Grad-Cam [<a href="#B62-diagnostics-12-01493" class="html-bibr">62</a>] visualization examples for uncertain patch images.</p>
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11 pages, 287 KiB  
Review
The Continuum of Invasive Techniques for the Assessment of Intermediate Coronary Lesions
by Nicoleta-Monica Popa-Fotea, Alexandru Scafa-Udriste and Maria Dorobantu
Diagnostics 2022, 12(6), 1492; https://doi.org/10.3390/diagnostics12061492 - 18 Jun 2022
Viewed by 1936
Abstract
Ischemic heart disease is one of the most important causes of mortality and morbidity worldwide. Revascularization of coronary stenosis inducing ischemia, either by percutaneous or surgical intervention, significantly reduces major adverse cardiovascular events and improves quality of life. However, in cases of intermediate [...] Read more.
Ischemic heart disease is one of the most important causes of mortality and morbidity worldwide. Revascularization of coronary stenosis inducing ischemia, either by percutaneous or surgical intervention, significantly reduces major adverse cardiovascular events and improves quality of life. However, in cases of intermediate lesions, classified by a diameter stenosis between 50 and 90% by European guidelines and 40–70% in American counterparts with no clear evidence of ischemia, the indication of revascularization and impact is determined using various methods that altogether comprehensively evaluate the lesions. This review will discuss the various techniques to assess intermediate stenoses, highlighting indications and advantages, but also drawbacks. Fractional flow rate (FFR) and instantaneous wave-free ratio (iFR) are the gold standard for the functional evaluation of intermediate lesions, but there are clinical circumstances in which these pressure-wire-derived indices are not accurate. Complementary invasive investigations, mainly intravascular ultrasound and/or optical coherence tomography, offer parameters that can be correlated with FFR/iFR and additional insights into the morphology of the plaque guiding the eventual percutaneous intervention in terms of length and size of stents, thus improving the outcomes of the procedure. The development of artificial intelligence and machine learning with advanced algorithms of prediction will offer multiple scenarios for treatment, allowing real-time selection of the best strategy for revascularization. Full article
(This article belongs to the Section Pathology and Molecular Diagnostics)
21 pages, 3238 KiB  
Review
Machine Learning of Raman Spectroscopy Data for Classifying Cancers: A Review of the Recent Literature
by Nathan Blake, Riana Gaifulina, Lewis D. Griffin, Ian M. Bell and Geraint M. H. Thomas
Diagnostics 2022, 12(6), 1491; https://doi.org/10.3390/diagnostics12061491 - 17 Jun 2022
Cited by 24 | Viewed by 4138
Abstract
Raman Spectroscopy has long been anticipated to augment clinical decision making, such as classifying oncological samples. Unfortunately, the complexity of Raman data has thus far inhibited their routine use in clinical settings. Traditional machine learning models have been used to help exploit this [...] Read more.
Raman Spectroscopy has long been anticipated to augment clinical decision making, such as classifying oncological samples. Unfortunately, the complexity of Raman data has thus far inhibited their routine use in clinical settings. Traditional machine learning models have been used to help exploit this information, but recent advances in deep learning have the potential to improve the field. However, there are a number of potential pitfalls with both traditional and deep learning models. We conduct a literature review to ascertain the recent machine learning methods used to classify cancers using Raman spectral data. We find that while deep learning models are popular, and ostensibly outperform traditional learning models, there are many methodological considerations which may be leading to an over-estimation of performance; primarily, small sample sizes which compound sub-optimal choices regarding sampling and validation strategies. Amongst several recommendations is a call to collate large benchmark Raman datasets, similar to those that have helped transform digital pathology, which researchers can use to develop and refine deep learning models. Full article
(This article belongs to the Special Issue Advances of Raman Spectroscopy in Medical Applications)
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<p>Literature search strategy: PRISMA flowchart of the literature selection process. <span class="html-italic">n</span> = number of studies.</p>
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<p>Validation strategy used in the reviewed literature. Some studies used more than one strategy.</p>
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<p>Spectra versus patient data splitting: note how the test set when split by spectra includes some spectra from all the patients contained in the train set.</p>
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23 pages, 1559 KiB  
Systematic Review
Systematic Review on Post-Mortem Protein Alterations: Analysis of Experimental Models and Evaluation of Potential Biomarkers of Time of Death
by Matteo Antonio Sacco, Fabrizio Cordasco, Carmen Scalise, Pietrantonio Ricci and Isabella Aquila
Diagnostics 2022, 12(6), 1490; https://doi.org/10.3390/diagnostics12061490 - 17 Jun 2022
Cited by 9 | Viewed by 2534
Abstract
Estimating the post-mortem interval (PMI) is a very complex issue due to numerous variables that may affect the calculation. Several authors have investigated the quantitative and qualitative variations of protein expression on post-mortem biological samples in certain time intervals, both in animals and [...] Read more.
Estimating the post-mortem interval (PMI) is a very complex issue due to numerous variables that may affect the calculation. Several authors have investigated the quantitative and qualitative variations of protein expression on post-mortem biological samples in certain time intervals, both in animals and in humans. However, the literature data are very numerous and often inhomogeneous, with different models, tissues and proteins evaluated, such that the practical application of these methods is limited to date. The aim of this paper was to offer an organic view of the state of the art about post-mortem protein alterations for the calculation of PMI through the analysis of the various experimental models proposed. The purpose was to investigate the validity of some proteins as “molecular clocks” candidates, focusing on the evidence obtained in the early, intermediate and late post-mortem interval. This study demonstrates how the study of post-mortem protein alterations may be useful for estimating the PMI, although there are still technical limits, especially in the experimental models performed on humans. We suggest a protocol to homogenize the study of future experimental models, with a view to the next concrete application of these methods also at the crime scene. Full article
(This article belongs to the Section Pathology and Molecular Diagnostics)
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<p>Algorithm followed for the selection of papers on PubMed and SCOPUS databases.</p>
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<p>Overall frequency of tissue analysis examined in the studies selected for review (%).</p>
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<p>Overall percentage of studies that evaluated early, intermediate and late PMI.</p>
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<p>Overall frequency of analysis of the methodologies examined in the studies selected for the review (N=number of studies).</p>
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<p>Markers that showed more evidence in the studies selected for review.</p>
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<p>Operating protocol proposed in early PMI (analysis of biological fluids), intermediate PMI (muscle analysis) and late PMI (bone analysis).</p>
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37 pages, 2410 KiB  
Review
A Survey on Deep Learning for Precision Oncology
by Ching-Wei Wang, Muhammad-Adil Khalil and Nabila Puspita Firdi
Diagnostics 2022, 12(6), 1489; https://doi.org/10.3390/diagnostics12061489 - 17 Jun 2022
Cited by 7 | Viewed by 3498
Abstract
Precision oncology, which ensures optimized cancer treatment tailored to the unique biology of a patient’s disease, has rapidly developed and is of great clinical importance. Deep learning has become the main method for precision oncology. This paper summarizes the recent deep-learning approaches relevant [...] Read more.
Precision oncology, which ensures optimized cancer treatment tailored to the unique biology of a patient’s disease, has rapidly developed and is of great clinical importance. Deep learning has become the main method for precision oncology. This paper summarizes the recent deep-learning approaches relevant to precision oncology and reviews over 150 articles within the last six years. First, we survey the deep-learning approaches categorized by various precision oncology tasks, including the estimation of dose distribution for treatment planning, survival analysis and risk estimation after treatment, prediction of treatment response, and patient selection for treatment planning. Secondly, we provide an overview of the studies per anatomical area, including the brain, bladder, breast, bone, cervix, esophagus, gastric, head and neck, kidneys, liver, lung, pancreas, pelvis, prostate, and rectum. Finally, we highlight the challenges and discuss potential solutions for future research directions. Full article
(This article belongs to the Section Machine Learning and Artificial Intelligence in Diagnostics)
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<p>Deep-learning methods commonly used for precision oncology. (<b>a</b>) Convolution Neural Network (CNN), (<b>b</b>) Recurrent Neural Network (RNN), (<b>c</b>) Deep Neural Network (DNN), and (<b>d</b>) Generative Adversarial Network (GAN).</p>
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<p>CNN architectures commonly used for precision oncology. (<b>a</b>) FCN, (<b>b</b>) AlexNet, (<b>c</b>) VGG-16, (<b>d</b>) ResNet-18, (<b>e</b>) U-Net, (<b>f</b>) V-Net, (<b>g</b>) Inception-V3, (<b>h</b>) DenseNet, (<b>i</b>) CapsNet, (<b>j</b>) DeepLab, (<b>k</b>) RP-Net, (<b>l</b>) Dense V-Net, and (<b>m</b>) BibNet.</p>
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<p>Deep learning architectures for dose distribution using (<b>a</b>) ResNet-antiResNet [<a href="#B47-diagnostics-12-01489" class="html-bibr">47</a>], (<b>b</b>) 3D U-ResNet-B [<a href="#B140-diagnostics-12-01489" class="html-bibr">140</a>], (<b>c</b>) 3D dense dilated U-Net [<a href="#B49-diagnostics-12-01489" class="html-bibr">49</a>], and (<b>d</b>) DeepLabV3+ [<a href="#B16-diagnostics-12-01489" class="html-bibr">16</a>].</p>
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<p>The detailed architectures of DL models (<b>a</b>) a CNN [<a href="#B23-diagnostics-12-01489" class="html-bibr">23</a>] and (<b>b</b>) a DeepSurv [<a href="#B52-diagnostics-12-01489" class="html-bibr">52</a>] to predict the overall survival time of glioblastoma and oral cancer patients, respectively. (<b>c</b>) A residual CNN [<a href="#B41-diagnostics-12-01489" class="html-bibr">41</a>] and (<b>d</b>) a SRN [<a href="#B7-diagnostics-12-01489" class="html-bibr">7</a>] to generate the risk score of overall survival and the survival probability of gastric cancer patients. (<b>e</b>) A multi-input CNN [<a href="#B27-diagnostics-12-01489" class="html-bibr">27</a>], (<b>f</b>) a densely connected center cropping CNN (DC3CNN) [<a href="#B82-diagnostics-12-01489" class="html-bibr">82</a>], and (<b>g</b>) a 3D DenseNet [<a href="#B86-diagnostics-12-01489" class="html-bibr">86</a>] to predict the treatment response from breast cancer chemotherapy, colorectal liver metastases chemotherapy, and lung cancer immunotherapy, respectively. (<b>h</b>) A modified FCN [<a href="#B37-diagnostics-12-01489" class="html-bibr">37</a>] to predict HSILs or higher (SQCC) for further treatment suggestion for cervical cancer patients; and (<b>i</b>) a ResNet [<a href="#B42-diagnostics-12-01489" class="html-bibr">42</a>] to guide the patient selection of adjuvant imatinib therapy for gastrointestinal stromal tumor patients.</p>
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12 pages, 710 KiB  
Article
The Impact of SARS-CoV-2 Pandemic on Patients Undergoing Radiation Therapy for Advanced Cervical Cancer at a Romanian Academic Center: A Four-Year Retrospective Analysis
by Alin Popescu, Stelian Pantea, Daniela Radu, Adrian Gluhovschi, Catalin Dumitru, George Dahma, Adelina Geanina Mocanu, Radu Neamtu, Sorin Dema, Codruta Victoria Tigmeanu, Mirela Loredana Grigoras, Silvius Alexandru Pescariu, Hazzaa Aabed and Marius Craina
Diagnostics 2022, 12(6), 1488; https://doi.org/10.3390/diagnostics12061488 - 17 Jun 2022
Viewed by 1869
Abstract
Background and Objectives: Throughout the COVID-19 pandemic, health systems worldwide adapted to support COVID-19 patients while continuing to provide assistance to patients with other potentially fatal illnesses. While patients with cancer may be at an elevated risk of severe COVID-19-related complications, their [...] Read more.
Background and Objectives: Throughout the COVID-19 pandemic, health systems worldwide adapted to support COVID-19 patients while continuing to provide assistance to patients with other potentially fatal illnesses. While patients with cancer may be at an elevated risk of severe COVID-19-related complications, their oncologic therapies generally cannot be postponed indefinitely without a negative effect on outcomes. Taking this into account, a thorough examination of the therapy management of various cancers is necessary, such as cervical cancer. Therefore, we aimed to develop a retrospective cohort study to measure the impact of the COVID-19 pandemic on the delivery of cancer care services for women diagnosed with cervical cancer staged IB2-IVA, necessitating chemo- and radiotherapy in Romania, as well as determine the difference in cervical cancer staging between the pandemic and pre-pandemic period. Materials and Methods: Using a multicentric hospital database, we designed a retrospective study to compare the last 24 months of the pre-pandemic period to the first 24 months of the SARS-CoV-2 pandemic to evaluate the variation in the proportion of women diagnosed with cervical cancer and the percentage of inoperable cases requiring chemotherapy and radiotherapy, as well as to detail their clinical presentation and other findings. Results: We observed that the likelihood of cervical cancer patients requiring radiation therapy at a later stage than before the pandemic increased by about 20% during the COVID-19 pandemic. Patients at an advanced FIGO stage of cervical cancer had a 3.39 higher likelihood of disease progression after radiotherapy (CI [2.06–4.21], p-value < 0.001), followed by tumor size at diagnosis with a hazard ratio (HR) of 3.12 (CI [2.24–4.00], p-value < 0.001). The factors related to the COVID-19 pandemic, postponed treatment and missed appointments, were also identified as significant risk factors for cervical cancer progression (HR = 2.51 and HR = 2.24, respectively). Conclusions We predict that there will be a considerable rise in cervical cancer cases over the next several years based on existing data and that expanding screening and treatment capacity will attenuate this with a minimal increase in morbidity and fatality. Full article
(This article belongs to the Special Issue Diagnosis and Management of Gynecological Cancers)
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<p>Graphical comparison of patients with radiotherapy-necessitating cervical cancer (IB2-IVB) before and during the COVID-19 pandemic. Cervical cancer staging is reported by International Federation of Gynecology and Obstetrics (FIGO) staging system.</p>
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<p>Graphical representation of risk factors for disease progression in patients with cervical cancer undergoing radiation therapy. The likelihood of disease progression reported as hazard ratio (HR) and confidence interval.</p>
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7 pages, 251 KiB  
Article
Performance Evaluation of the VITEK2 and Sensititre Systems to Determine Colistin Resistance and MIC for Acinetobacter baumannii
by Hae-Sun Chung, Soo-Kyung Kim, Chorong Hahm and Miae Lee
Diagnostics 2022, 12(6), 1487; https://doi.org/10.3390/diagnostics12061487 - 17 Jun 2022
Cited by 3 | Viewed by 2055
Abstract
Performances of the colistin antimicrobial susceptibility testing (AST) systems of Acinetobacter baumannii vary depending on the manufacturer, and data on colistin-resistant A. baumannii are limited. We evaluated the VITEK2 and Sensititre systems to determine colistin resistance and minimum inhibitory concentration (MIC) for A. [...] Read more.
Performances of the colistin antimicrobial susceptibility testing (AST) systems of Acinetobacter baumannii vary depending on the manufacturer, and data on colistin-resistant A. baumannii are limited. We evaluated the VITEK2 and Sensititre systems to determine colistin resistance and minimum inhibitory concentration (MIC) for A. baumannii isolated from a clinical microbiology laboratory. A total of 213 clinical A. baumannii isolates were tested, including 81 colistin-resistant A. baumannii. ASTs were performed using the VITEK2 and Sensititre systems according to the manufacturer’s instructions. Reference MICs for colistin were determined using the manual broth microdilution method (BMD). The results of the two AST methods were compared with the BMD results. VITEK2 and Sensititre systems showed category agreements of 95.3% and 99.1%, respectively. VITEK2 had a relatively high very major error (VME) rate (9.9%). Sensititre reported higher MICs than the reference method for the susceptible isolates and showed low essential agreement. In conclusion, the automated systems investigated in this study showed good category agreements for colistin AST of A. baumannii. However, VITEK2 had a high VME rate, and Sensititre had differences in MIC results. Colistin AST remains a challenging task in the clinical laboratory. Full article
(This article belongs to the Section Diagnostic Microbiology and Infectious Disease)
13 pages, 995 KiB  
Article
Triglyceride and Glucose Index Predicts Acute Coronary Syndrome in Patients with Antineutrophil Cytoplasmic Antibody-Associated Vasculitis
by Pil Gyu Park, Jung Yoon Pyo, Sung Soo Ahn, Jason Jungsik Song, Yong-Beom Park, Ji Hye Huh and Sang-Won Lee
Diagnostics 2022, 12(6), 1486; https://doi.org/10.3390/diagnostics12061486 - 17 Jun 2022
Cited by 3 | Viewed by 2028
Abstract
This study investigated whether the triglyceride (TG) glucose (TyG) index at diagnosis could predict acute coronary syndrome (ACS) in patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). The medical records of 152 AAV were reviewed. Clinical and laboratory data were collected. The TyG [...] Read more.
This study investigated whether the triglyceride (TG) glucose (TyG) index at diagnosis could predict acute coronary syndrome (ACS) in patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). The medical records of 152 AAV were reviewed. Clinical and laboratory data were collected. The TyG index was calculated by TyG index = Ln (fasting TG (mg/dL) × fasting glucose (mg/dL)/2). The cut-offs of Birmingham vasculitis activity score (BVAS) and the TyG were obtained by the receiver operator characteristic (ROC) curve and the highest tertile (9.011). The mean age was 57.2 years and 32.9% were male. AAV patients with a TyG index ≥ 9.011 exhibited a lower cumulative ACS-free survival rate than those with a TyG index < 9.011. However, a TyG index ≥ 9.011 was not independently associated with ACS in the multivariable Cox analysis. Meanwhile, there might be a close relationship for predicting ACS among the TyG index, metabolic syndrome (MetS), and BVAS. AAV patients with a TyG index ≥ 9.011 exhibited a higher risk for MetS than those with a TyG index < 9.011 (relative risk 2.833). AAV patients with BVAS ≥ 11.5 also exhibited a higher risk for ACS than those with BVAS < 11.5 (relative risk 10.225). Both AAV patients with MetS and those with BVAS ≥11.5 exhibited lower cumulative ACS-free survival rates than those without. The TyG index at AAV diagnosis could estimate the concurrent presence of MetS and predict the occurrence of ACS during follow-up along with high BVAS at diagnosis in patients with AAV. Full article
(This article belongs to the Section Pathology and Molecular Diagnostics)
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<p>Comparison of cumulative survival rates according to the TyG index. Patients were divided into two groups according to the highest tertile of the TyG index (≥9.011). Only the occurrence of ACS significantly differed between AAV patients with a TyG index ≥ 9.011 and those with a TyG index &lt; 9.011 among the five poor prognoses. TyG, triglyceride-glucose; ACS, acute coronary syndrome; AAV, ANCA-associated vasculitis; ANCA, antineutrophil cytoplasmic antibody; ESKD, end-stage renal disease; CVA, cerebrovascular accident.</p>
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<p>TyG index estimating MetS and BVAS anticipating ACS. (<b>A</b>) The cut-off value of the TyG index for the presence of MetS was obtained using the ROC curve and was set as 8.688. (<b>B</b>) AAV patients with a TyG index ≥ 8.688 more often had MetS than those with a TyG index &lt; 8.688. (<b>C</b>) When the cut-off TyG index of 9.011 was applied, AAV patients with a TyG index ≥ 9.011 more frequently had MetS than those with a TyG index &lt; 9.011. (<b>D</b>) The cut-off of BVAS for ACS occurrence was obtained using the ROC curve and was set as 11.5. (<b>E</b>) AAV patients with BVAS ≥ 11.5, exhibited a significantly higher risk for the occurrence of ACS than those with BVAS &lt; 11.5. TyG, triglyceride-glucose; MetS, metabolic syndrome; ROC, receiver operating characteristic; AAV, ANCA-associated vasculitis; ANCA, antineutrophil cytoplasmic antibody; BVAS, Birmingham vasculitis activity score; ACS, acute coronary syndrome.</p>
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<p>Comparison of cumulative survival rates according to MetS and BVAS. AAV patients with MetS exhibited a significantly lower cumulative ACS-free survival rate than those without MetS, and AAV patients with BVAS ≥ 11.5, exhibited a significantly lower cumulative ACS-free survival rate than those with BVAS &lt; 11.5. MetS, metabolic syndrome; BVAS, Birmingham vasculitis activity score; AAV, ANCA-associated vasculitis; ANCA, antineutrophil cytoplasmic antibody; ACS, acute coronary syndrome.</p>
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<p>Overall hypotheses of a mechanism from the TyG index to ACS. Black solid arrow: the results of this study; black dotted arrow: hypothesis with high probability; grey dotted arrow: hypothesis with low probability. AAV, ANCA-associated vasculitis; ANCA, antineutrophil cytoplasmic antibody; TyG, triglyceride-glucose; MetS, metabolic syndrome; BVAS, Birmingham vasculitis activity score; ACS, acute coronary syndrome.</p>
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15 pages, 1579 KiB  
Article
Comparison of Rapid Diagnostic Test, Microscopy, and Polymerase Chain Reaction for the Detection of Plasmodium falciparum Malaria in a Low-Transmission Area, Jazan Region, Southwestern Saudi Arabia
by Aymen M. Madkhali, Ahmad Hassn Ghzwani and Hesham M. Al-Mekhlafi
Diagnostics 2022, 12(6), 1485; https://doi.org/10.3390/diagnostics12061485 - 17 Jun 2022
Cited by 11 | Viewed by 4518
Abstract
This cross-sectional study aimed to assess the performances of a rapid diagnostic test (RDT)—the AllTest Malaria p.f./p.v., microscopy, and nested polymerase chain reaction (PCR) for diagnosing Plasmodium falciparum malaria in 400 febrile patients from a low-transmission region (Jazan) in southwestern Saudi Arabia. Diagnostic [...] Read more.
This cross-sectional study aimed to assess the performances of a rapid diagnostic test (RDT)—the AllTest Malaria p.f./p.v., microscopy, and nested polymerase chain reaction (PCR) for diagnosing Plasmodium falciparum malaria in 400 febrile patients from a low-transmission region (Jazan) in southwestern Saudi Arabia. Diagnostic performance of all three methods was compared using microscopy and nested PCR as reference methods. Overall, 42 (10.5%), 48 (12.0%), and 57 (14.3%) samples were found positive by microscopy, RDT, and PCR, respectively. With PCR as reference method, the RDT showed higher sensitivity (79% vs. 71.9%), similar specificity (99.1% vs. 99.7%), and better NLR (0.20 vs. 0.27) and area under the curve (89.0% vs. 85.8%) than microscopy. The sensitivity of RDT and microscopy decreased as age increased, and false negatives were associated with low parasite density. In addition, the sensitivity of RDT and microscopy was higher in non-Saudi than in Saudi participants. Against microscopy, both RDT and PCR showed high sensitivity (83.3% vs. 97.6%), specificity (96.4% vs. 95.5%), and NPVs (98.0% vs. 99.7%), but reduced PPVs (72.9% vs. 71.9%), respectively. The results showed that the performance of the AllTest Malaria p.f./p.v RDT was better than that of microscopy in diagnosing P. falciparum malaria among febrile patients in the Jazan region when nested PCR was used as the reference. However, further studies are required to assess malaria diagnostic methods among asymptomatic individuals in the region. Full article
(This article belongs to the Special Issue Diagnosis and Management of Malaria)
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<p>Malaria detection results obtained by light microscopy, RDT, and PCR techniques.</p>
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<p>Receiver operating characteristic (ROC) curve analysis of malaria diagnostic techniques. (<b>A</b>) ROC for microscopy and RDT versus PCR as reference method. (<b>B</b>) ROC for PCR and RDT versus microscopy as reference method.</p>
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<p>Sensitivity by parasite density level of the RDT and PCR versus microscopy as gold standard.</p>
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<p>Schematic chart of diagnostic detection limits of microscopy, HRP2-based RDT, and PCR with respect to parasite and HRP2 density. The black line curve represents parasite density and the red dotted curve represents HRP2 gene density. Time scale is in days pre-treatment and in weeks post-treatment. Horizontal lines over the chart represent the detection limits of the three methods respective to parasite and HRP2 densities. The shaded areas represent detectability of parasites by the three methods over time. Reprinted from Wu, L., van den Hoogen, L.L., Slater, H., Walker, P.G., Ghani, A.C., Drakeley, C.J., Okell, L.C. Comparison of diagnostics for the detection of asymptomatic <span class="html-italic">Plasmodium falciparum</span> infections to inform control and elimination strategies. <span class="html-italic">Nature</span> <b>2015</b>, <span class="html-italic">528</span> (7580), S86–S93; Copyright (2015). The article is licensed under the Creative Commons Attribution 4.0 International License.</p>
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28 pages, 9140 KiB  
Article
A New Artificial Intelligence-Based Method for Identifying Mycobacterium Tuberculosis in Ziehl–Neelsen Stain on Tissue
by Sabina Zurac, Cristian Mogodici, Teodor Poncu, Mihai Trăscău, Cristiana Popp, Luciana Nichita, Mirela Cioplea, Bogdan Ceachi, Liana Sticlaru, Alexandra Cioroianu, Mihai Busca, Oana Stefan, Irina Tudor, Andrei Voicu, Daliana Stanescu, Petronel Mustatea, Carmen Dumitru and Alexandra Bastian
Diagnostics 2022, 12(6), 1484; https://doi.org/10.3390/diagnostics12061484 - 17 Jun 2022
Cited by 12 | Viewed by 5550
Abstract
Mycobacteria identification is crucial to diagnose tuberculosis. Since the bacillus is very small, finding it in Ziehl–Neelsen (ZN)-stained slides is a long task requiring significant pathologist’s effort. We developed an automated (AI-based) method of identification of mycobacteria. We prepared a training dataset of [...] Read more.
Mycobacteria identification is crucial to diagnose tuberculosis. Since the bacillus is very small, finding it in Ziehl–Neelsen (ZN)-stained slides is a long task requiring significant pathologist’s effort. We developed an automated (AI-based) method of identification of mycobacteria. We prepared a training dataset of over 260,000 positive and over 700,000,000 negative patches annotated on scans of 510 whole slide images (WSI) of ZN-stained slides (110 positive and 400 negative). Several image augmentation techniques coupled with different custom computer vision architectures were used. WSIs automatic analysis was followed by a report indicating areas more likely to present mycobacteria. Our model performs AI-based diagnosis (the final decision of the diagnosis of WSI belongs to the pathologist). The results were validated internally on a dataset of 286,000 patches and tested in pathology laboratory settings on 60 ZN slides (23 positive and 37 negative). We compared the pathologists’ results obtained by separately evaluating slides and WSIs with the results given by a pathologist aided by automatic analysis of WSIs. Our architecture showed 0.977 area under the receiver operating characteristic curve. The clinical test presented 98.33% accuracy, 95.65% sensitivity, and 100% specificity for the AI-assisted method, outperforming any other AI-based proposed methods for AFB detection. Full article
(This article belongs to the Special Issue Artificial Intelligence in Pathological Image Analysis)
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<p>ROC curve obtained by the model on the validation set.</p>
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<p>Precision-recall curve obtained by the model on the validation set.</p>
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<p>Sensitivity, specificity, F1-score, and MCC of the model computed for various thresholds.</p>
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<p>Patch of 64 × 64 pixels (in green) with a positive score (probability of similarity with positive dataset used for training) of 0.96 due to the presence in the upper left margin of the green square of a red blood cell. Lymph node with toxoplasmosis ZN × 400.</p>
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<p>Patch of 64 × 64 pixels (in green) with a positive score of 0.96 due to the presence in the inferior right margin of the green square of several purple mast cell granules with linear arrangement mimicking an acid-fast bacillus. Hodgkin’s lymphoma, nodular sclerosis variant. ZN × 400.</p>
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<p>Active learning process for iteratively improving the model performance.</p>
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<p>Repartition of the test group according to diagnosis.</p>
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<p>Variation of sensitivity, specificity, accuracy, and precision in correlation to pathologists’ experience. (<b>a</b>) Variation of sensitivity in correlation to pathologists’ experience. (<b>b</b>) Variation of specificity in correlation to pathologists’ experience. (<b>c</b>) Variation of accuracy in correlation to pathologists’ experience. (<b>d</b>) Variation of precision in correlation to pathologists’ experience.</p>
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<p>Variation of sensitivity, specificity, accuracy and precision in correlation to pathologists’ experience of examining whole slide images. (<b>a</b>) Variation of sensitivity in correlation to pathologists’ experience of examining WSIs. (<b>b</b>) Variation of specificity in correlation to pathologists’ experience of examining WSIs. (<b>c</b>) Variation of accuracy in correlation to pathologists’ experience of examining WSIs. (<b>d</b>) Variation of precision in correlation to pathologists’ experience of examining WSIs.</p>
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<p>Paucibacillary lesion identified as positive by 5 of 8 pathologists in 1–32 min (medium of 13.75 min); the time of AI-assisted examination was 15 s (the convincing positive patch—the green square—was the second one).</p>
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<p>Paucibacillary lesion identified as positive by 6 of 8 pathologists in 1–33 min (medium of 12.25 min); the time of AI-assisted examination was 9 s (first patch—green square—was convincingly positive).</p>
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<p>(<b>a</b>) Errors in WSIs evaluation for all the team (qualified pathologists and residents). (<b>b</b>) Errors in WSIs evaluation for qualified pathologists.</p>
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<p>Cat scratch disease. Centrally, one structure reminiscent of AFB but pale blue in color (green oval); however, the color of red blood cells is not appropriate (green stars). Paler than regular in a good Ziehl–Neelsen stain. ZN × 400 as offered by Aperio ImageScope platform; WSI scanned with Aperio GT450, 40× magnification.</p>
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<p>Cat scratch disease. Centrally, several structures look like AFB but pale blue in color (green rectangular area); however, enhancement of the image—black contour window in the lower right corner of the picture (digital magnification offered by Aperio ImageScope software)—shows improper format of the pink structures. ZN × 400 as offered by Aperio ImageScope platform; WSI scanned with Aperio GT450, 40× magnification.</p>
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<p>Tuberculosis. Centrally, two AFBs present (green oval); please note the good quality of the Ziehl–Neelsen stain certified by the pink color of red blood cells. ZN × 400 as offered by Aperio ImageScope platform; WSI scanned with Aperio GT450, 40× magnification.</p>
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<p>Tuberculous epithelioid granulomatous lymphadenitis with extensive caseation. One AFB is present within the center (green circle). Higher resolution is in the right inferior rectangular area (detail: green arrow). ZN × 400 as offered by Aperio ImageScope platform; WSI scanned with Aperio GT450, 40× magnification.</p>
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9 pages, 255 KiB  
Article
First Results of an External Quality Assessment (EQA) Scheme for Molecular, Serological and Antigenic Diagnostic Test for SARS-CoV-2 Detection in Lombardy Region (Northern Italy), 2020–2022
by Fabio Pasotti, Laura Pellegrinelli, Giuseppa Liga, Manuela Rizzetto, Giovanna Azzarà, Simona Da Molin, Oana Livia Lungu, Silvia Greco, Cristina Galli, Laura Bubba, Elena Pariani, Matteo Corradin, Danilo Cereda and Sabrina Buoro
Diagnostics 2022, 12(6), 1483; https://doi.org/10.3390/diagnostics12061483 - 16 Jun 2022
Cited by 5 | Viewed by 1910
Abstract
For diagnosing SARS-CoV-2 infection and for monitoring its spread, the implementation of external quality assessment (EQA) schemes is mandatory to assess and ensure a standard quality according to national and international guidelines. Here, we present the results of the 2020, 2021, 2022 EQA [...] Read more.
For diagnosing SARS-CoV-2 infection and for monitoring its spread, the implementation of external quality assessment (EQA) schemes is mandatory to assess and ensure a standard quality according to national and international guidelines. Here, we present the results of the 2020, 2021, 2022 EQA schemes in Lombardy region for assessing the quality of the diagnostic laboratories involved in SARS-CoV-2 diagnosis. In the framework of the Quality Assurance Programs (QAPs), the routinely EQA schemes are managed by the regional reference centre for diagnostic laboratories quality (RRC-EQA) of the Lombardy region and are carried out by all the diagnostic laboratories. Three EQA programs were organized: (1) EQA of SARS-CoV-2 nucleic acid detection; (2) EQA of anti-SARS-CoV-2-antibody testing; (3) EQA of SARS-CoV-2 direct antigens detection. The percentage of concordance of 1938 molecular tests carried out within the SARS-CoV-2 nucleic acid detection EQA was 97.7%. The overall concordance of 1875 tests carried out within the anti-SARS-CoV-2 antibody EQA was 93.9% (79.6% for IgM). The overall concordance of 1495 tests carried out within the SARS-CoV-2 direct antigens detection EQA was 85% and it was negatively impacted by the results obtained by the analysis of weak positive samples. In conclusion, the EQA schemes for assessing the accuracy of SARS-CoV-2 diagnosis in the Lombardy region highlighted a suitable reproducibility and reliability of diagnostic assays, despite the heterogeneous landscape of SARS-CoV-2 tests and methods. Laboratory testing based on the detection of viral RNA in respiratory samples can be considered the gold standard for SARS-CoV-2 diagnosis. Full article
(This article belongs to the Section Diagnostic Microbiology and Infectious Disease)
41 pages, 25585 KiB  
Article
COVLIAS 2.0-cXAI: Cloud-Based Explainable Deep Learning System for COVID-19 Lesion Localization in Computed Tomography Scans
by Jasjit S. Suri, Sushant Agarwal, Gian Luca Chabert, Alessandro Carriero, Alessio Paschè, Pietro S. C. Danna, Luca Saba, Armin Mehmedović, Gavino Faa, Inder M. Singh, Monika Turk, Paramjit S. Chadha, Amer M. Johri, Narendra N. Khanna, Sophie Mavrogeni, John R. Laird, Gyan Pareek, Martin Miner, David W. Sobel, Antonella Balestrieri, Petros P. Sfikakis, George Tsoulfas, Athanasios D. Protogerou, Durga Prasanna Misra, Vikas Agarwal, George D. Kitas, Jagjit S. Teji, Mustafa Al-Maini, Surinder K. Dhanjil, Andrew Nicolaides, Aditya Sharma, Vijay Rathore, Mostafa Fatemi, Azra Alizad, Pudukode R. Krishnan, Ferenc Nagy, Zoltan Ruzsa, Mostafa M. Fouda, Subbaram Naidu, Klaudija Viskovic and Mannudeep K. Kalraadd Show full author list remove Hide full author list
Diagnostics 2022, 12(6), 1482; https://doi.org/10.3390/diagnostics12061482 - 16 Jun 2022
Cited by 35 | Viewed by 3845
Abstract
Background: The previous COVID-19 lung diagnosis system lacks both scientific validation and the role of explainable artificial intelligence (AI) for understanding lesion localization. This study presents a cloud-based explainable AI, the “COVLIAS 2.0-cXAI” system using four kinds of class activation maps (CAM) models. [...] Read more.
Background: The previous COVID-19 lung diagnosis system lacks both scientific validation and the role of explainable artificial intelligence (AI) for understanding lesion localization. This study presents a cloud-based explainable AI, the “COVLIAS 2.0-cXAI” system using four kinds of class activation maps (CAM) models. Methodology: Our cohort consisted of ~6000 CT slices from two sources (Croatia, 80 COVID-19 patients and Italy, 15 control patients). COVLIAS 2.0-cXAI design consisted of three stages: (i) automated lung segmentation using hybrid deep learning ResNet-UNet model by automatic adjustment of Hounsfield units, hyperparameter optimization, and parallel and distributed training, (ii) classification using three kinds of DenseNet (DN) models (DN-121, DN-169, DN-201), and (iii) validation using four kinds of CAM visualization techniques: gradient-weighted class activation mapping (Grad-CAM), Grad-CAM++, score-weighted CAM (Score-CAM), and FasterScore-CAM. The COVLIAS 2.0-cXAI was validated by three trained senior radiologists for its stability and reliability. The Friedman test was also performed on the scores of the three radiologists. Results: The ResNet-UNet segmentation model resulted in dice similarity of 0.96, Jaccard index of 0.93, a correlation coefficient of 0.99, with a figure-of-merit of 95.99%, while the classifier accuracies for the three DN nets (DN-121, DN-169, and DN-201) were 98%, 98%, and 99% with a loss of ~0.003, ~0.0025, and ~0.002 using 50 epochs, respectively. The mean AUC for all three DN models was 0.99 (p < 0.0001). The COVLIAS 2.0-cXAI showed 80% scans for mean alignment index (MAI) between heatmaps and gold standard, a score of four out of five, establishing the system for clinical settings. Conclusions: The COVLIAS 2.0-cXAI successfully showed a cloud-based explainable AI system for lesion localization in lung CT scans. Full article
(This article belongs to the Section Machine Learning and Artificial Intelligence in Diagnostics)
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<p>COVLIAS 2.0-cXAI system.</p>
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<p>Raw CT slice of COVID-19 patients taken from Croatian data set.</p>
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<p>Raw control CT slice taken from Italian data set.</p>
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<p>(<b>a</b>) DenseNet-121 model. (<b>b</b>) DenseNet-169 model. (<b>c</b>) DenseNet-201 model.</p>
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<p>(<b>a</b>) DenseNet-121 model. (<b>b</b>) DenseNet-169 model. (<b>c</b>) DenseNet-201 model.</p>
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<p>Grad-CAM.</p>
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<p>Grad-CAM++.</p>
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<p>Score-CAM++.</p>
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<p>Heatmap using four CAM techniques using three kinds of DenseNet classifiers on COVID-19 lesion images.</p>
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<p>Heatmap using four CAM techniques and three kinds of DenseNet classifiers on COVID-19 lesion images. The top row is the CT slice for patient 1, and the bottom row is the CT slice for patient 2.</p>
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<p>Heatmap using four CAM techniques using three kinds of DenseNet classifiers on COVID-19 lesion images. The top row is the CT slice for patient 1, and the bottom row is the CT slice for patient 2.</p>
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<p>Heatmap using four CAM techniques using three kinds of DenseNet classifiers on COVID-19 lesion images. The top row is the CT slice for patient 1, and the bottom row is the CT slice for patient 2.</p>
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<p>Heatmap using four CAM techniques using three kinds of DenseNet classifiers on control images. The top row is the CT slice for patient 1, and the bottom row is the CT slice for patient 2.</p>
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<p>Heatmap using four CAM techniques using three kinds of DenseNet classifiers on control images. The top row is the CT slice for patient 1, and the bottom row is the CT slice for patient 2.</p>
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<p>Heatmap using four CAM techniques using three kinds of DenseNet classifiers on control images. The top row is the CT slice for patient 1, and the bottom row is the CT slice for patient 2.</p>
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<p>Overlay of ground truth annotation on heatmap using four CAM techniques on three kinds of DenseNet classifiers for COVID-19 lesion images as part of the performance evaluation.</p>
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<p>Overlay of ground truth annotation on heatmap using four CAM techniques on three kinds of DenseNet classifiers for COVID-19 lesion images as part of the performance evaluation.</p>
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<p>Overlay of ground truth annotation on heatmap using four CAM techniques on three kinds of DenseNet classifiers for COVID-19 lesion images as part of the performance evaluation.</p>
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<p>Bar chart representing the MAI.</p>
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<p>COVLIAS 2.0 cloud-based display of the lesion images using four CAM models.</p>
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<p>COVLIAS 2.0 cloud-based display of the lesion images using four CAM models.</p>
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<p>COVLIAS 2.0 cloud-based display of the lesion images using four CAM models.</p>
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<p>A web-view screenshot.</p>
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<p>ResNet-UNet architecture.</p>
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10 pages, 1393 KiB  
Review
Assessment of Orbital Compartment Pressure: A Comprehensive Review
by Tim J. Enz and Markus Tschopp
Diagnostics 2022, 12(6), 1481; https://doi.org/10.3390/diagnostics12061481 - 16 Jun 2022
Cited by 1 | Viewed by 2261
Abstract
The orbit is a closed compartment defined by the orbital bones and the orbital septum. Some diseases of the orbit and the optic nerve are associated with an increased orbital compartment pressure (OCP), e.g., retrobulbar hemorrhage or thyroid eye disease. Our aim was [...] Read more.
The orbit is a closed compartment defined by the orbital bones and the orbital septum. Some diseases of the orbit and the optic nerve are associated with an increased orbital compartment pressure (OCP), e.g., retrobulbar hemorrhage or thyroid eye disease. Our aim was to review the literature on the different approaches to assess OCP. Historically, an assessment of the tissue resistance provoked by the retropulsion of the eye bulb was the method of choice for estimating OCP, either by digital palpation or with specifically designed devices. We found a total of 20 articles reporting direct OCP measurement in animals, cadavers and humans. In nine studies, OCP was directly measured in humans, of which five used a minimally invasive approach. Two groups used experimental/custom devices, whilst the others applied commercially available devices commonly used for monitoring the compartment syndromes of the limbs. None of the nine articles on direct OCP measurements in humans reported complications. Today, OCP is mainly estimated using clinical findings considered surrogates, e.g., elevated intraocular pressure or proptosis. These diagnostic markers appear to reliably indicate elevated OCP. However, particularly minimally invasive approaches show promises for direct OCP measurements. In the future, more sophisticated, specifically designed equipment might allow for even better and safer measurements and hence facilitate the diagnosis and monitoring of orbital diseases. Full article
(This article belongs to the Special Issue Eye Diseases: Diagnosis and Management)
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<p>Flowchart showing the methodology of the systematic review.</p>
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<p>Timeline of the development of the different methods to measure orbital compartment pressure.</p>
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<p>Overview of the different approaches to assess orbital compartment pressure and the corresponding main conclusions.</p>
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19 pages, 32792 KiB  
Article
Unsupervised Learning Based on Multiple Descriptors for WSIs Diagnosis
by Taimoor Shakeel Sheikh, Jee-Yeon Kim, Jaesool Shim and Migyung Cho
Diagnostics 2022, 12(6), 1480; https://doi.org/10.3390/diagnostics12061480 - 16 Jun 2022
Cited by 6 | Viewed by 2093
Abstract
An automatic pathological diagnosis is a challenging task because histopathological images with different cellular heterogeneity representations are sometimes limited. To overcome this, we investigated how the holistic and local appearance features with limited information can be fused to enhance the analysis performance. We [...] Read more.
An automatic pathological diagnosis is a challenging task because histopathological images with different cellular heterogeneity representations are sometimes limited. To overcome this, we investigated how the holistic and local appearance features with limited information can be fused to enhance the analysis performance. We propose an unsupervised deep learning model for whole-slide image diagnosis, which uses stacked autoencoders simultaneously feeding multiple-image descriptors such as the histogram of oriented gradients and local binary patterns along with the original image to fuse the heterogeneous features. The pre-trained latent vectors are extracted from each autoencoder, and these fused feature representations are utilized for classification. We observed that training with additional descriptors helps the model to overcome the limitations of multiple variants and the intricate cellular structure of histopathology data by various experiments. Our model outperforms existing state-of-the-art approaches by achieving the highest accuracies of 87.2 for ICIAR2018, 94.6 for Dartmouth, and other significant metrics for public benchmark datasets. Our model does not rely on a specific set of pre-trained features based on classifiers to achieve high performance. Unsupervised spaces are learned from the number of independent multiple descriptors and can be used with different variants of classifiers to classify cancer diseases from whole-slide images. Furthermore, we found that the proposed model classifies the types of breast and lung cancer similar to the viewpoint of pathologists by visualization. We also designed our whole-slide image processing toolbox to extract and process the patches from whole-slide images. Full article
(This article belongs to the Section Pathology and Molecular Diagnostics)
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<p>Block diagram of the proposed model. (<b>A</b>) Following segmentation and annotation, image patches are extracted from the tissue regions of the WSIs. (<b>B</b>) Patches are encoded into a set of descriptive feature representations (i.e., RAW, HOG, and LBPs). The representations are further split into two portions, and data augmentation is applied to the set of descriptive representations of the training portion. (<b>C</b>,<b>Left</b>) For unsupervised learning, the set of generated descriptive features is feed into the stacked autoencoders without labels, which embeds the input vectors into a lower-dimensional space. (<b>C</b>,<b>Right</b>) The learned representations are fused together and passed with labels to the classifier with respective labels, which are used to make the final diagnostic prediction and classification.</p>
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<p>Microscopic H&amp;E patched images of four types in the ICIAR2018 dataset.</p>
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<p>Histological images of five types of lung adenocarcinoma in the Dartmouth Lung Cancer dataset.</p>
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<p>Accuracy for multi-class classification on the ICIAR2018 and Dartmouth datasets. Using the different combination of generated representations.</p>
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<p>Confusion matrices for the multi-class classification of ICIAR2018 and Dartmouth datasets. Class labels are according to the abbreviations of <a href="#diagnostics-12-01480-f002" class="html-fig">Figure 2</a> and <a href="#diagnostics-12-01480-f003" class="html-fig">Figure 3</a>.</p>
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<p>Two-dimensional visualization of two different layers using t-SNE [<a href="#B52-diagnostics-12-01480" class="html-bibr">52</a>] for the multi-class classification. Projection of the last fully connected layer. Cross shapes represent test samples. (Best viewed in color).</p>
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<p>Two-dimensional visualization of two different layers using t-SNE [<a href="#B52-diagnostics-12-01480" class="html-bibr">52</a>] for the multi-class classification. Projection of the last fully connected layer. Cross shapes represent test samples. (Best viewed in color).</p>
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<p>AUC (ROC) curves for the multi-class classification of the ICIAR2018 and Dartmouth datasets. Class labels are according to the abbreviations of <a href="#diagnostics-12-01480-f002" class="html-fig">Figure 2</a> and <a href="#diagnostics-12-01480-f003" class="html-fig">Figure 3</a> (Best viewed in color).</p>
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