Real-Time Arrhythmia Detection Using Hybrid Convolutional Neural Networks.

Background Accurate detection of arrhythmic events in the intensive care units (ICU) is of paramount significance in providing timely care. However, traditional ICU monitors generate a high rate of false alarms causing alarm fatigue. In this work, we develop an algorithm to improve life threatening arrhythmia detection in the ICUs using a deep learning approach. Methods and Results This study involves a total of 953 independent life-threatening arrhythmia alarms generated from the ICU bedside monitors of 410 patients. Specifically, we used the ECG (4 channels), arterial blood pressure, and photoplethysmograph signals to accurately detect the onset and offset of various arrhythmias, without prior knowledge of the alarm type. We used a hybrid convolutional neural network based classifier that fuses traditional handcrafted features with features automatically learned using convolutional neural networks. Further, the proposed architecture remains flexible to be adapted to various arrhythmic conditions as well as multiple physiological signals. Our hybrid- convolutional neural network approach achieved superior performance compared with methods which only used convolutional neural network. We evaluated our algorithm using 5-fold cross-validation for 5 times and obtained an accuracy of 87.5%±0.5%, and a score of 81%±0.9%. Independent evaluation of our algorithm on the publicly available PhysioNet 2015 Challenge database resulted in overall classification accuracy and score of 93.9% and 84.3%, respectively, indicating its efficacy and generalizability. Conclusions Our method accurately detects multiple arrhythmic conditions. Suitable translation of our algorithm may significantly improve the quality of care in ICUs by reducing the burden of false alarms.

Real-time machine learning-based intensive care unit alarm classification without prior knowledge of the underlying rhythm.

AIMS: This work attempts to develop a standalone heart rhythm alerting system for the intensive care unit (ICU), where life-threatening arrhythmias have to be identified/alerted more precisely and more instantaneously (i.e. with lower latency) than existing bedside monitors. METHODS AND RESULTS: We use the dataset from the PhysioNet 2015 Challenge, which contains records that led to true and false arrhythmic alarms in the ICU. These records have been re-annotated as one of eight classes, namely (i) asystole, (ii) extreme bradycardia, (iii) extreme tachycardia, (iv) ventricular fibrillation (VF), (v) ventricular tachycardia (VT), (vi) normal sinus rhythm, (vii) sinus tachycardia, and (viii) noise/artefacts. Arrhythmia-specific features and features that measure the signal quality were extracted from all the records. To improve VF detection, an improved, over an existing, single-lead R-wave detection was developed that takes into account the R-waves detected in all electrocardiographic (ECG) leads. To avoid false R-wave detection due to pacing spikes, ECG signals were filtered with a low pass filter prior to R-wave detection, while the raw signals were used for feature extraction. Random forest was used as the classifier, and 10-time five-fold cross-validation, resulted in a macro-average sensitivity of 81.54%. CONCLUSIONS: In conclusion, comparing with the bedside monitors used in the PhysioNet 2015 competition, we find that our method achieves higher positive predictive values for asystole, extreme bradycardia, VT, and VF; furthermore, our method is able to alert the presence of arrhythmia instantaneously, i.e. up to 4 s earlier.

Transfer Learning for Molecular Cancer Classification Using Deep Neural Networks.

The emergence of deep learning has impacted numerous machine learning based applications and research. The reason for its success lies in two main advantages: 1) it provides the ability to learn very complex non-linear relationships between features and 2) it allows one to leverage information from unlabeled data that does not belong to the problem being handled. This paper presents a transfer learning procedure for cancer classification, which uses feature selection and normalization techniques in conjunction with s sparse auto-encoders on gene expression data. While classifying any two tumor types, data of other tumor types were used in unsupervised manner to improve the feature representation. The performance of our algorithm was tested on 36 two-class benchmark datasets from the GEMLeR repository. On performing statistical tests, it is clearly ascertained that our algorithm statistically outperforms several generally used cancer classification approaches. The deep learning based molecular disease classification can be used to guide decisions made on the diagnosis and treatment of diseases, and therefore may have important applications in precision medicine.