scholarly journals A Hybrid Method Based on LSTM and Optimized SVM for Diagnosis of Novel Coronavirus (COVID-19)

2021 ◽  
Vol 38 (4) ◽  
pp. 1061-1069
Author(s):  
Jamal Mhawesh Challab ◽  
Farhad Mardukhi

The coronavirus disease of 2019 (COVID-19), a unique Coronavirus strain, has created a chaotic situation, negatively impacting the number of deaths and people's lives globally. The daily increase in COVID-19 instances is due to a lack of and restricted availability of detection techniques for determining the disease's presence. Therefore, detecting positive results as soon as feasible is important to preventing the spread of this epidemic and treating infected people as soon as possible. As a result of these constraints, the demand for clinical decision-making systems based on predictive algorithms has increased. The article describes a recurrent neural network (RNN) for identifying Coronavirus (COVID-19) and tries to improve the detection method. Different machine learning methodologies, such as Support Vector Machines (SVMs), were used to create a detection system with a deep learning algorithm called Long Short Term Memory (LSTM). The research describes a method for detecting COVID-19 in tagged CT images of patients. Various common picture features, such as central moments, Gabor wavelets, and GLCM-related features, are discussed. Ant colony optimization-ant lion optimization (ACO-ALO) is used to select optimum subsets of SVM parameters. The results show that SVM parameters such as penalty and kernel parameters have a positive effect on SVM model correctness and complexity. Besides, the findings revealed that the proposed method may be employed as a system of aid to diagnose COVID-19 disease. The findings uncover that the suggested strategy has promising behavior in terms of increasing classification accuracies as well as optimal feature selection. Promisingly, the presented strategy can be regarded as a useful clinical decision-making tool for clinicians.

2019 ◽  
Vol 6 (Supplement_2) ◽  
pp. S273-S274
Author(s):  
Lorne W Walker ◽  
Andrew J Nowalk ◽  
Shyam Visweswaran

Abstract Background Deciding whether to attempt salvage of an infected central venous catheter (CVC) can be challenging. While line removal is the definitive treatment for central-line associated bloodstream infection (CLABSI), salvage may be attempted with systemic antibiotics and antibiotic lock therapy (ALT). Weighing risk and benefit of CVC salvage is limited by uncertainty in the future viability of salvaged CVCs. If a CVC is likely to require subsequent removal (e.g., due to recurrent infection) salvage may not be beneficial, whereas discarding a viable CVC is also not desirable. Here we describe a machine learning approach to predicting outcomes in CVC salvage. Methods Episodes of pediatric CLABSI cleared with ALT were identified by retrospective record review between January 1, 2008 and December 31, 2018 and were defined by a single positive central blood culture of a known pathogen or two matching cultures of a possible contaminant. Clearance was defined as 48-hours of negative cultures and relapse was defined as a matching positive blood culture after clearance. Predictive models [logistic regression (LR), random forest (RF), support vector machine (SVM) and an ensemble combining the three] were used to predict recurrence-free CVC retention (RFCR) at various time points using a training and test set approach. Results Overall, 712 instances CLABSI cleared with ALT were identified. Demographic and microbiological data are summarized in Tables 1 and 2. Few (8%) instances recurred in the first 28 days. 58% recurred at any time within the study period. Rates of RFCR were 75%, 43%, 22% and 10% at 28, 91, 182 and 365 days. Machine learning (ML) models varied in their ability to predict RFCR (Table 3). RF models performed best overall, although no model performed well at 91 days. Conclusion ML models provide an opportunity to augment clinical decision making by learning patterns from data. In this case, estimating the likelihood of useful line retention in the future could help guide informed decisions on salvage vs. removal of infected CVCs. Limitations include the heterogeneity of clinical data and the use of an outcome capturing both clinical decision making (line removal) and infection recurrence. With further model development and prospective validation, practical machine learning models may prove useful to clinicians. Disclosures All authors: No reported disclosures.


Author(s):  
Rawan AlSaad ◽  
Qutaibah Malluhi ◽  
Ibrahim Janahi ◽  
Sabri Boughorbel

Abstract Background Predictive modeling with longitudinal electronic health record (EHR) data offers great promise for accelerating personalized medicine and better informs clinical decision-making. Recently, deep learning models have achieved state-of-the-art performance for many healthcare prediction tasks. However, deep models lack interpretability, which is integral to successful decision-making and can lead to better patient care. In this paper, we build upon the contextual decomposition (CD) method, an algorithm for producing importance scores from long short-term memory networks (LSTMs). We extend the method to bidirectional LSTMs (BiLSTMs) and use it in the context of predicting future clinical outcomes using patients’ EHR historical visits. Methods We use a real EHR dataset comprising 11071 patients, to evaluate and compare CD interpretations from LSTM and BiLSTM models. First, we train LSTM and BiLSTM models for the task of predicting which pre-school children with respiratory system-related complications will have asthma at school-age. After that, we conduct quantitative and qualitative analysis to evaluate the CD interpretations produced by the contextual decomposition of the trained models. In addition, we develop an interactive visualization to demonstrate the utility of CD scores in explaining predicted outcomes. Results Our experimental evaluation demonstrate that whenever a clear visit-level pattern exists, the models learn that pattern and the contextual decomposition can appropriately attribute the prediction to the correct pattern. In addition, the results confirm that the CD scores agree to a large extent with the importance scores generated using logistic regression coefficients. Our main insight was that rather than interpreting the attribution of individual visits to the predicted outcome, we could instead attribute a model’s prediction to a group of visits. Conclusion We presented a quantitative and qualitative evidence that CD interpretations can explain patient-specific predictions using CD attributions of individual visits or a group of visits.


2020 ◽  
Vol 4 (12) ◽  
pp. 1197-1207
Author(s):  
Wanshan Ning ◽  
Shijun Lei ◽  
Jingjing Yang ◽  
Yukun Cao ◽  
Peiran Jiang ◽  
...  

AbstractData from patients with coronavirus disease 2019 (COVID-19) are essential for guiding clinical decision making, for furthering the understanding of this viral disease, and for diagnostic modelling. Here, we describe an open resource containing data from 1,521 patients with pneumonia (including COVID-19 pneumonia) consisting of chest computed tomography (CT) images, 130 clinical features (from a range of biochemical and cellular analyses of blood and urine samples) and laboratory-confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) clinical status. We show the utility of the database for prediction of COVID-19 morbidity and mortality outcomes using a deep learning algorithm trained with data from 1,170 patients and 19,685 manually labelled CT slices. In an independent validation cohort of 351 patients, the algorithm discriminated between negative, mild and severe cases with areas under the receiver operating characteristic curve of 0.944, 0.860 and 0.884, respectively. The open database may have further uses in the diagnosis and management of patients with COVID-19.


2018 ◽  
Vol 09 (01) ◽  
pp. 122-128 ◽  
Author(s):  
B. Jones ◽  
B. South ◽  
Y. Shao ◽  
C.C. Lu ◽  
J. Leng ◽  
...  

Background Identifying pneumonia using diagnosis codes alone may be insufficient for research on clinical decision making. Natural language processing (NLP) may enable the inclusion of cases missed by diagnosis codes. Objectives This article (1) develops a NLP tool that identifies the clinical assertion of pneumonia from physician emergency department (ED) notes, and (2) compares classification methods using diagnosis codes versus NLP against a gold standard of manual chart review to identify patients initially treated for pneumonia. Methods Among a national population of ED visits occurring between 2006 and 2012 across the Veterans Affairs health system, we extracted 811 physician documents containing search terms for pneumonia for training, and 100 random documents for validation. Two reviewers annotated span- and document-level classifications of the clinical assertion of pneumonia. An NLP tool using a support vector machine was trained on the enriched documents. We extracted diagnosis codes assigned in the ED and upon hospital discharge and calculated performance characteristics for diagnosis codes, NLP, and NLP plus diagnosis codes against manual review in training and validation sets. Results Among the training documents, 51% contained clinical assertions of pneumonia; in the validation set, 9% were classified with pneumonia, of which 100% contained pneumonia search terms. After enriching with search terms, the NLP system alone demonstrated a recall/sensitivity of 0.72 (training) and 0.55 (validation), and a precision/positive predictive value (PPV) of 0.89 (training) and 0.71 (validation). ED-assigned diagnostic codes demonstrated lower recall/sensitivity (0.48 and 0.44) but higher precision/PPV (0.95 in training, 1.0 in validation); the NLP system identified more “possible-treated” cases than diagnostic coding. An approach combining NLP and ED-assigned diagnostic coding classification achieved the best performance (sensitivity 0.89 and PPV 0.80). Conclusion System-wide application of NLP to clinical text can increase capture of initial diagnostic hypotheses, an important inclusion when studying diagnosis and clinical decision-making under uncertainty.


Healthcare is major issue and challenge now-a-days for human being in a daily life. Parkinson Disease or P.D is a one of the disorders that affected in the mid of nervous system. Parkinson Disease affected person cannot be act as normal human being. Among the innumerable disease listed so far, the Parkinson disease occupies an alarming position due to its life threaten concern. Early prediction of Parkinson disease from large volume of electronic health records leads to protect various health issues. There are various challenges and issues such as scalability, accuracy, risk factor, time complexity and sparsity in early prediction of Parkinson disease. There are various conventional algorithms have been proposed to solve these issues and challenges and still needs improvement. The present study, systematic predictive analytics using various classification algorithms such as Support Vector Machine (SVM), Random Forest, AdaBoost, Multi-Layer Perceptron (MLP), Naive Bayes, Decision table, J48, Logistic Regression is presented and evaluated using benchmarking Parkinson disease data set which are collected from UCI machine learning repository. The extraction of hidden data present in the dataset is obtained using WEKA environment. The results from the prediction models gives better clinical decision-making support to the doctors in predicting disease earlier and risk level.


2011 ◽  
Vol 20 (4) ◽  
pp. 121-123
Author(s):  
Jeri A. Logemann

Evidence-based practice requires astute clinicians to blend our best clinical judgment with the best available external evidence and the patient's own values and expectations. Sometimes, we value one more than another during clinical decision-making, though it is never wise to do so, and sometimes other factors that we are unaware of produce unanticipated clinical outcomes. Sometimes, we feel very strongly about one clinical method or another, and hopefully that belief is founded in evidence. Some beliefs, however, are not founded in evidence. The sound use of evidence is the best way to navigate the debates within our field of practice.


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