Cardiac arrhythmias, characterized by irregular heartbeats, are difficult to diagnose in real-world scenarios. Machine learning has advanced arrhythmia detection; however, the optimal number of heartbeats for precise classification remains understudied. This study addresses this using machine learning while assessing the performance of arrhythmia detection across inter-patient and intra-patient conditions. Furthermore, the performance-resource trade-offs are evaluated for practical deployment in mobile health (mHealth) applications. Beat-wise segmentation and resampling techniques were utilized for preprocessing electrocardiography (ECG) signals to ensure consistent input lengths. A 1-D convolutional neural network was used to classify the eight multi-labeled arrhythmias. The dataset comprised real-world ECG recordings from the HiCardi wireless device alongside data from the MIT-BIH Arrhythmia database. Model performance was assessed through fivefold cross-validation under both inter-patient and intra-patient conditions. The proposed model demonstrated peak accuracy at four beats under inter-patient conditions, with minimal improvements beyond this point. This configuration achieved a balance between performance (94.82% accuracy) and resource consumption (training time: 72.27 s per epoch; prediction time: 155 μs per segment). Real-world simulations validated the feasibility of real-time arrhythmia detection for approximately 5000 patients. Utilizing four heartbeats as the input size for arrhythmia classification results in a trade-off between accuracy and computational efficiency. This discovery has significant implications for real-time wearable ECG devices, where both performance and resource constraints are crucial considerations. This insight is expected to serve as a valuable reference for enhancing the design and implementation of arrhythmia detection systems for scalable and efficient mHealth applications.
Cardiovascular disease is a major global health concern, with early detection being critical. This study assesses the effectiveness of a portable ECG device, based on Internet of Medical Things (IoMT) technology, for remote cardiovascular monitoring during daily activities. We conducted a clinical trial involving 2000 participants who wore the HiCardi device while engaging in hiking activities. The device monitored their ECG, heart rate, respiration, and body temperature in real-time. If an abnormal signal was detected while a physician was remotely monitoring the ECG at the IoMT monitoring center, he notified the clinical research coordinator (CRC) at the empirical research site, and the CRC advised the participant to visit a hospital. Follow-up calls were made to determine compliance and outcomes. Of the 2000 participants, 318 showed abnormal signals, and 182 were advised to visit a hospital. The follow-up revealed that 139 (76.37%) responded, and 30 (21.58% of those who responded) sought further medical examination. Most visits (80.00%) occurred within one month. Diagnostic approaches included ECG (56.67%), ECG and ultrasound (20.00%), ultrasound alone (16.67%), ECG and X-ray (3.33%), and general treatment (3.33%). Seven participants (23.33% of those who visited) were diagnosed with cardiovascular disease, including conditions such as arrhythmia, atrial fibrillation, and stent requirements. The portable ECG device using the patch-type electrocardiograph detected abnormal cardiovascular signals, leading to timely diagnoses and interventions, demonstrating its potential for broad applications in preventative healthcare.
Background: In this study, we explored the potential of predicting dysglycemia in patients who need to continuously manage blood glucose levels using a non-invasive method via electrocardiography (ECG). Methods: The data were collected from patients with diabetes, and heart rate variability (HRV) features were extracted via ECG processing. A residual block-based one-dimensional convolution neural network model was used to predict dysglycemia. Results: The dysglycemia prediction results at each time point, including at the time of blood glucose measurement, 15 min prior to measurement, and 30 min prior to measurement, exhibited no significant differences compared with the blood glucose measurement values. This result confirmed that the proposed artificial intelligence model for dysglycemia prediction performed well at each time point. Additionally, to determine the optimal number of features required for predicting dysglycemia, 77 HRV features were individually eliminated in the order of decreasing importance with respect to the prediction accuracy; the optimal number of features for the model to predict dysglycemia was determined to be 12. The dysglycemia prediction results obtained 30 min prior to measurement, which exhibited the highest prediction range in this study, were as follows: accuracy = 90.5, sensitivity = 87.52, specificity = 92.74, and precision = 89.86. Conclusions: Furthermore, we determined that no significant differences exist in the blood glucose prediction results reported in previous studies, wherein various vital signs and blood glucose values were used as model inputs, and the results obtained in this study, wherein only ECG data were used to predict dysglycemia.
Sleep staging is critical for investigating sleep quality and detecting disorders. Polysomnography (PSG) remains the gold standard, but is costly and impractical for routine monitoring. This study evaluates the feasibility of a patch-type wearable device using single-lead electrocardiography (ECG) and impedance pneumography (IPG) for multi-stage sleep classification. Data from 92 patients were collected using a wearable ECG-IPG device. Preprocessing entailed bandpass filtering, segmentation into 5-min windows with 30-s overlaps, and feature extraction in time, frequency, and nonlinear domains. Three classification methods were tested and validated using 5-fold patient-independent cross-validation across 2-class (Wake, Sleep), 3-class (Wake, rapid eye movement (REM), and Non-REM), and 4-class (Wake, REM, N1, and N2) tasks. The combined approach achieved the highest accuracy in the 2-class task (accuracy: 83.6%, area under the receiver operating characteristic (AUROC): 86.0%). For 3- and 4-class tasks, feature-based methods outperformed the others, with the RCNN achieving the best F1-score (0.618 in 3-class and 0.552 in 4-class). Modality analysis revealed that IPG + R-R interval (RRI) + motion sensors provided the highest performance, with IPG and RRI identified as the most effective in sleep staging. Feature reduction using maximum relevance and minimum redundancy (mRMR) identified the top 15 features that retained 99% of the performance of the full feature set while reducing the training time by 73%. These findings highlight the feasibility of a portable ECG-IPG system for sleep staging, balancing accuracy and computational efficiency. The proposed approach has the potential to enable continuous sleep monitoring and personalized health management in real-world applications.
Accurate cardiac output (CO) measurement is vital for hemodynamic management; however, it usually requires invasive monitoring, which limits its continuous and out-of-hospital use. Wearable sensors integrated with deep learning offer a noninvasive alternative. This study developed and validated a lightweight deep learning model using wearable electrocardiography (ECG) and photoplethysmography (PPG) signals to predict CO and examined whether cardiac index-based normalization (Cardiac Index (CI) = CO/body surface area) improves performance. Twenty-seven patients who underwent cardiac surgery and had pulmonary artery catheters were prospectively enrolled. Single-lead ECG (HiCardi+ chest patch) and finger PPG (WristOx2 3150) were recorded simultaneously and processed through an ECG–PPG fusion network with cross-modal interaction. Three models were trained as follows: (1) CI prediction, (2) direct CO prediction, and (3) indirect CO prediction. The total number of CO = predicted CI × body surface area. Reference values were derived from thermodilution. The CI model achieved the best performance, and the indirect CO model showed significant reductions in error/agreement metrics (MAE/RMSE/bias; p < 0.0001), while correlation-based metrics are reported descriptively without implying statistical significance. The Pearson correlation coefficient (PCC) and percentage error (PE) for the indirect CO estimates (PCC = 0.904; PE = 23.75%). The indirect CO estimates met the predefined PE < 30% agreement benchmark for method-comparison; this is not a universal clinical standard. These results demonstrate that wearable ECG–PPG fusion deep learning can achieve accurate, noninvasive CO estimation and that CI-based normalization enhances model agreement with pulmonary artery catheter measurements, supporting continuous catheter-free hemodynamic monitoring.
Cardiovascular disease is a major global health concern, with early detection being critical. This study assesses the effectiveness of the portable ECG device, based on Internet of Medical Things (IoMT) technology, for remote cardiovascular monitoring during daily activities. We conducted a clinical trial involving 2,000 participants who wore the HiCardi device while engaging in hiking activities. The device monitored their ECG, heart rate, respiration, and body temperature in real-time. If an abnormal signal was detected while a physician was remotely monitoring the ECG at the IoMT monitoring center, he notified the clinical research coordinator (CRC) at the empirical research site, and the CRC advised the participant to visit a hospital. Follow-up calls were made to determine compliance and outcomes. Of the 2,000 participants, 318 showed abnormal signals, and 182 were advised to visit a hospital. Follow-up revealed that 139 (76.37%) responded, and 30 (21.58% of those who responded) sought further medical examination. Most visits (80.00%) occurred within one month. Diagnostic approaches included ECG (56.67%), ECG and ultrasound (20.00%), ultrasound alone (16.67%), ECG and X-ray (3.33%), and general treatment (3.33%). Seven participants (23.33% of those who visited) were diagnosed with cardiovascular disease, including conditions such as arrhythmia, atrial fibrillation, and stent requirements. The portable ECG device using the patch-type electrocardiograph detected abnormal cardiovascular signals, leading to timely diagnoses and interventions, demonstrating its potential for broad application in preventative health care.