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  • Open Access

    ARTICLE

    AutoRhythmAI: A Hybrid Machine and Deep Learning Approach for Automated Diagnosis of Arrhythmias

    S. Jayanthi*, S. Prasanna Devi

    CMC-Computers, Materials & Continua, Vol.78, No.2, pp. 2137-2158, 2024, DOI:10.32604/cmc.2024.045975

    Abstract In healthcare, the persistent challenge of arrhythmias, a leading cause of global mortality, has sparked extensive research into the automation of detection using machine learning (ML) algorithms. However, traditional ML and AutoML approaches have revealed their limitations, notably regarding feature generalization and automation efficiency. This glaring research gap has motivated the development of AutoRhythmAI, an innovative solution that integrates both machine and deep learning to revolutionize the diagnosis of arrhythmias. Our approach encompasses two distinct pipelines tailored for binary-class and multi-class arrhythmia detection, effectively bridging the gap between data preprocessing and model selection. To validate our system, we have rigorously… More >

  • Open Access

    CASE REPORT

    Life Threatening Broad QRS Tachycardia in an Infant with Conduction Disorder and SCN5A Mutation

    Elio Caruso1,*, Silvia Farruggio1, Alfredo Di Pino1, Paolo Guccione1, Mohammadrafie Khorgami2

    Congenital Heart Disease, Vol.17, No.5, pp. 551-556, 2022, DOI:10.32604/chd.2022.023711

    Abstract We present the case of an infant admitted to our department for a rapid broad complex tachycardia and cardiovascular collapse. The patient was submitted to genetic testing because of a conduction defect at baseline ECG and family history of gene mutation. A new SCN5A gene mutation variant was found leading to diagnosis of sodium-channel dysfunction arrhythmia. More > Graphic Abstract

    Life Threatening Broad QRS Tachycardia in an Infant with Conduction Disorder and <i>SCN5A</i> Mutation

  • Open Access

    ARTICLE

    Automatic Heart Disease Detection by Classification of Ventricular Arrhythmias on ECG Using Machine Learning

    Khalid Mahmood Aamir1, Muhammad Ramzan1,2, Saima Skinadar1, Hikmat Ullah Khan3, Usman Tariq4, Hyunsoo Lee5, Yunyoung Nam5,*, Muhammad Attique Khan6

    CMC-Computers, Materials & Continua, Vol.71, No.1, pp. 17-33, 2022, DOI:10.32604/cmc.2022.018613

    Abstract This paper focuses on detecting diseased signals and arrhythmias classification into two classes: ventricular tachycardia and premature ventricular contraction. The sole purpose of the signal detection is used to determine if a signal has been collected from a healthy or sick person. The proposed research approach presents a mathematical model for the signal detector based on calculating the instantaneous frequency (IF). Once a signal taken from a patient is detected, then the classifier takes that signal as input and classifies the target disease by predicting the class label. While applying the classifier, templates are designed separately for ventricular tachycardia and… More >

  • Open Access

    ARTICLE

    3D Non-Fluoroscopic Cryoablation of Right-Sided Accessory Pathways in Children: Monocentric Study and Literature Review

    Fabrizio Drago*, Irma Battipaglia, Pietro Paolo Tamborrino, Luigina Porco, Camilla Calvieri, Mario Salvatore Russo, Vincenzo Pazzano, Romolo Remoli, Massimo Stefano Silvetti

    Congenital Heart Disease, Vol.16, No.6, pp. 561-572, 2021, DOI:10.32604/CHD.2021.016623

    Abstract Background: Cryoablation of accessory pathways (APs) is effective and very safe in children, as previously reported by our group. The aim of this retrospective study was to evaluate the current efficacy of 3D non-fluoroscopic cryoablation of right sided APs in children, comparing results obtained with the Ensite VelocityTM and the more recent Ensite PrecisionTM 3D mapping systems. Methods and Results: From January 2016 to December 2019, 102 pediatric patients [mean age 12.5 ± 2.8, 62 males (61% of total cohort)] with right APs underwent 3D non-fluoroscopic transcatheter cryoablation at our Institution. Fifteen (14.7%) patients had previously undergone catheter ablation. Acute… More >

  • Open Access

    CASE REPORT

    Arrhythmias in Common Arterial Trunk (CAT): Uncommon Atrial Tachycardia in CAT with Anomalous Pulmonary Venous Connection and Re-entry Atrial Tachycardia in CAT with HIV Seropositive Mother

    Elio Caruso1, Silvia Farruggio1,*, Davide Calvaruso1, Corrado Di Mambro1, David Angel Ortiz Ruiz1, Salvatore Agati1, Rafie Khoargami2

    Congenital Heart Disease, Vol.16, No.4, pp. 417-425, 2021, DOI:10.32604/CHD.2021.015808

    Abstract We show a brief report of two common arterial trunk cases (CAT) with different arrhythmias and discuss anatomy, clinical and diagnostic management. The burden of volume and pressure overload of this cardiac malformation may predispose to different types of arrhythmia before and after surgical repair. Because of labile hemodynamic state in this group of patients, prompt diagnosis of any arrhythmia is mandatory as the devastating factor on prognosis. The first patient with a diagnosis of CAT Type II Collett and Edwards (CE) had a particular history with HIV seropositive mother assuming antiretroviral therapy during pregnancy, who presented hyperbilirubinemia and liver… More >

  • Open Access

    REVIEW

    Fetal Bradyarrhythmias: Etiopathogenesis, Diagnosis and Treatment: Between Literature Review and Experience of a Tertiary Center

    Elio Caruso*, Silvia Farruggio, Salvatore Agati, Corrado Di Mambro

    Congenital Heart Disease, Vol.16, No.4, pp. 309-331, 2021, DOI:10.32604/CHD.2021.015470

    Abstract Fetal arrhythmias reach up around 10% of the total third-level perinatal cardiology references. Sustained bradycardia is defined as a baseline fetal heart rate (FHR) of less than 110 bpm sustained for at least 10 min. The overall incidence of malignant fetal bradyarrhythmias, such as complete atrioventricular block (AVB) and channellopathies, is relatively rare, 1:5000 pregnancies, but represents a serious emergency for the gynecologist, neonatologists, and pediatric cardiologists. Fetal complete AVB is strongly associated with maternal connective tissue disease, but it can be also associated with congenital heart disease and usually with a poorer prognosis with high risk of fetal hydrops… More >

  • Open Access

    ARTICLE

    Arrhythmia burden and related outcomes in Eisenmenger syndrome

    Shankar Baskar1, Philippa Horne2, Samantha Fitzsimmons3, Philip R. Khoury1, Joseph Vettukattill4, Koichiro Niwa5, Teiji Agaki6, Mark Spence7, Hisanori Sakazaki8, Gruschen Veldtman1

    Congenital Heart Disease, Vol.12, No.4, pp. 512-519, 2017, DOI:10.1111/chd.12481

    Abstract Background: Patients with Eisenmenger syndrome have a shorter lifespan than the general population. A significant proportion develop arrhythmia and some, sudden death.
    Objective: The aims of this study were to characterize the frequency, type and effects of arrhythmias in adult patients with Eisenmenger’s syndrome and to identify risk factors for arrhythmias.
    Methods: This retrospective study included patients aged ≥18 years of age with Eisenmenger’s syndrome from three institutions. Arrhythmias were noted from electrocardiograms and Holter study reviews.
    Results: A total of 167 patients, 96 females, 63 males (gender not available in 9 patients) were included in this study. The mean… More >

  • Open Access

    ARTICLE

    Analysis of adults with congenital heart disease presenting to pediatric emergency departments with arrhythmias

    Shaun Mohan1, Brady S. Moffett2, Wilson Lam2, Caridad de la Uz2, Christina Miyake2, Santiago O. Valdes2, Jeffrey J. Kim2

    Congenital Heart Disease, Vol.12, No.4, pp. 507-511, 2017, DOI:10.1111/chd.12478

    Abstract Objective: As survivors of congenital heart disease (CHD) continue to age, healthcare utilization by this population has increased. It is unknown how often these patients utilize the emergency department (ED) at children’s hospitals and how arrhythmias play a role in their utilization of care.
    Design: Using a retrospective cohort design, the Pediatric Hospital Information System (PHIS) database was investigated and we studied adults (≥18 years) with CHD (ACHD) who presented to pediatric EDs from 2004 to 2014.
    Setting: Tertiary care pediatric hospitals.
    Results: Of the 6310 encounters to pediatric EDs, 1594 (25%) were for arrhythmias. The median age was 21… More >

  • Open Access

    ARTICLE

    Anticoagulation practices in adults with congenital heart disease and atrial arrhythmias in Switzerland

    Ketina Arslani1*, Lukas Notz1*, Marzena Zurek1, Matthias Greutmann2, Markus Schwerzmann3, Judith Bouchardy4, Reto Engel5, Christine Attenhofer Jost6, Daniel Tobler1

    Congenital Heart Disease, Vol.13, No.5, pp. 678-684, 2018, DOI:10.1111/chd.12627

    Abstract Background: In adults with congenital heart disease (CHD) and atrial arrhythmias, recommendations for thromboprophylaxis are vague and evidence is lacking. We aimed to identify factors that influence decision-making in daily practice.
    Methods: From the Swiss Adult Congenital HEart disease Registry (SACHER) we identified 241 patients with either atrial fibrillation (Afib) or atrial flutter/intraatrial reentrant tachycardia (Aflut/ IART). The mode of anticoagulation was reviewed. Logistic regression models were used to assess factors that were associated with oral anticoagulation therapy.
    Results: Compared with patients with Aflut/IART, patients with Afib were older (51 ± 16.1 vs 37 ± 16 years, P < .001)… More >

  • Open Access

    ARTICLE

    The incidence of arrhythmias during exercise stress tests among children with Kawasaki disease: A single-center case series

    Varun Aggarwal1,2, Kristen Sexson-Tejtal1, Wilson Lam1, Santiago O. Valdes1, Caridad M. de la Uz1, Jeffrey J. Kim1, Christina Y. Miyake1

    Congenital Heart Disease, Vol.14, No.6, pp. 1032-1036, 2019, DOI:10.1111/chd.12864

    Abstract Objective: Based on 2017 guidelines, participation in competitive sports with prior history of Kawasaki Disease (KD) requires those with coronary artery aneurysms (CAA) z score ≥ 5 to undergo evaluation for evidence of inducible ischemia or arrhythmias. The use of exercise stress testing (EST) to evaluate arrhythmias among KD patients has never been reported. This retrospective single-center case series study sought to describe the presence of inducible arrhythmias during EST in KD patients with or without CAA.
    Methods: Single-center retrospective review of medical records of patients diagnosed with KD between 1989-2015 at Texas Children’s Hospital, Houston, Texas who underwent EST… More >

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