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1.
IEEE J Biomed Health Inform ; 27(6): 2818-2828, 2023 06.
Artigo em Inglês | MEDLINE | ID: mdl-37028019

RESUMO

The automatic classification of electrocardiogram (ECG) signals has played an important role in cardiovascular diseases diagnosis and prediction. With recent advancements in deep neural networks (DNNs), particularly Convolutional Neural Networks (CNNs), learning deep features automatically from the original data is becoming an effective and widespread approach in a variety of intelligent tasks including biomedical and health informatics. However, most of the existing approaches are trained on either 1D CNNs or 2D CNNs, and they suffer from the limitations of random phenomena (i.e. random initial weights). Furthermore, the ability to train such DNNs in a supervised manner in healthcare is often limited due to the scarcity of labeled training data. To address the problems of weight initialization and limited annotated data, in this work, we leverage recent self-supervised learning technique, namely, contrastive learning, and present supervised contrastive learning (sCL). Different from existing self-supervised contrastive learning approaches, which often generate false negatives because of random selection of negative anchors, our contrastive learning makes use of labeled data to pull the same class closer together and push different classes far apart to avoid potential false negatives. Furthermore, unlike other kinds of signals (e.g. speech, image, video), ECG signal is sensitive to changes, and inappropriate transformation could directly affect diagnosis results. To deal with this issue, we present two semantic transformations, i.e. semantic split-join and semantic weighted peaks noise smoothing. The proposed deep neural network sCL-ST with supervised contrastive learning and semantic transformations is trained as an end-to-end framework for the multi-label classification of 12-lead ECGs. Our sCL-ST network contains two sub-networks i.e. pre-text task and down-stream task. Our experimental results have been evaluated on 12-lead PhysioNet 2020 dataset and shown that our proposed network outperforms the state-of-the-art existing approaches.


Assuntos
Informática Médica , Semântica , Humanos , Eletrocardiografia , Arritmias Cardíacas/diagnóstico , Redes Neurais de Computação
2.
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22283391

RESUMO

BackgroundSleep disturbance is common following hospitalisation both for COVID-19 and other causes. The clinical associations are poorly understood, despite it altering pathophysiology in other scenarios. We, therefore, investigated whether sleep disturbance is associated with dyspnoea along with relevant mediation pathways. MethodsSleep parameters were assessed in a prospective cohort of patients (n=2,468) hospitalised for COVID-19 in the United Kingdom in 39 centres using both subjective and device-based measures. Results were compared to a matched UK biobank cohort and associations were evaluated using multivariable linear regression. Findings64% (456/714) of participants reported poor sleep quality; 56% felt their sleep quality had deteriorated for at least 1-year following hospitalisation. Compared to the matched cohort, both sleep regularity (44.5 vs 59.2, p<0.001) and sleep efficiency (85.4% vs 88.5%, p<0.001) were lower whilst sleep period duration was longer (8.25h vs 7.32h, p<0.001). Overall sleep quality (effect estimate 4.2 (3.0-5.5)), deterioration in sleep quality following hospitalisation (effect estimate 3.2 (2.0-4.5)), and sleep regularity (effect estimate 5.9 (3.7-8.1)) were associated with both dyspnoea and impaired lung function (FEV1 and FVC). Depending on the sleep metric, anxiety mediated 13-42% of the effect of sleep disturbance on dyspnoea and muscle weakness mediated 29-43% of this effect. InterpretationSleep disturbance is associated with dyspnoea, anxiety and muscle weakness following COVID-19 hospitalisation. It could have similar effects for other causes of hospitalisation where sleep disturbance is prevalent. FundingUK Research and Innovation, National Institute for Health Research, and Engineering and Physical Sciences Research Council.

3.
Preprint em Inglês | medRxiv | ID: ppmedrxiv-21249540

RESUMO

Patients with influenza and SARS-CoV2/Coronavirus disease 2019 (COVID-19) infections have different clinical course and outcomes. We developed and validated a supervised machine learning pipeline to distinguish the two viral infections using the available vital signs and demographic dataset from the first hospital/emergency room encounters of 3,883 patients who had confirmed diagnoses of influenza A/B, COVID-19 or negative laboratory test results. The models were able to achieve an area under the receiver operating characteristic curve (ROC AUC) of at least 97% using our multiclass classifier. The predictive models were externally validated on 15,697 encounters in 3,125 patients available on TrinetX database that contains patient-level data from different healthcare organizations. The influenza vs. COVID-19-positive model had an AUC of 98%, and 92% on the internal and external test sets, respectively. Our study illustrates the potentials of machine-learning models for accurately distinguishing the two viral infections. The code is made available at https://github.com/ynaveena/COVID-19-vs-Influenza and may be have utility as a frontline diagnostic tool to aid healthcare workers in triaging patients once the two viral infections start cocirculating in the communities.

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