| Literature DB >> 28546862 |
Anurag Singh1, Samarendra Dandapat1.
Abstract
In recent years, compressed sensing (CS) has emerged as an effective alternative to conventional wavelet based data compression techniques. This is due to its simple and energy-efficient data reduction procedure, which makes it suitable for resource-constrained wireless body area network (WBAN)-enabled electrocardiogram (ECG) telemonitoring applications. Both spatial and temporal correlations exist simultaneously in multi-channel ECG (MECG) signals. Exploitation of both types of correlations is very important in CS-based ECG telemonitoring systems for better performance. However, most of the existing CS-based works exploit either of the correlations, which results in a suboptimal performance. In this work, within a CS framework, the authors propose to exploit both types of correlations simultaneously using a sparse Bayesian learning-based approach. A spatiotemporal sparse model is employed for joint compression/reconstruction of MECG signals. Discrete wavelets transform domain block sparsity of MECG signals is exploited for simultaneous reconstruction of all the channels. Performance evaluations using Physikalisch-Technische Bundesanstalt MECG diagnostic database show a significant gain in the diagnostic reconstruction quality of the MECG signals compared with the state-of-the art techniques at reduced number of measurements. Low measurement requirement may lead to significant savings in the energy-cost of the existing CS-based WBAN systems.Entities:
Keywords: Bayes methods; MECG signals; Physikalisch-Technische Bundesanstalt MECG diagnostic database; WBAN; block sparsity-based joint compressed sensing recovery; body area networks; correlation methods; data compression; data reduction; discrete wavelet transforms; discrete wavelets transform; electrocardiography; energy-efficient data reduction; learning (artificial intelligence); medical signal processing; multichannel ECG signals; patient monitoring; resource-constrained wireless body area network; signal reconstruction; sparse Bayesian learning; spatial correlations; spatiotemporal phenomena; spatiotemporal sparse model; telemedicine; telemonitoring; temporal correlations
Year: 2017 PMID: 28546862 PMCID: PMC5437710 DOI: 10.1049/htl.2016.0049
Source DB: PubMed Journal: Healthc Technol Lett ISSN: 2053-3713
Fig. 1Spatiotemporal correlation structures in MECG signals. ECG signals from three different channels/leads of dataset s0146lrem exhibiting anterior myocardial infarction are shown in a, b and c. Encircled heart beats indicate the spatially and temporally correlated information across the channels and within the channel
Fig. 2Variation of amplitudes of wavelet coefficients in various subbands (cA7, cD7-cD1) of eight fundamental ECG channels
Fig. 3Best K-term joint sparse approximation of MECG signals in wavelet domain. Indices of non-zero wavelet coefficients are represented by blue dots
Fig. 4Signal reconstruction quality of the MECG signals taken from PTB dataset s0008rem exhibiting BBB using the proposed approach. Original signals from channels I, aVL, and V1 are shown in (a), (d), (g), and the corresponding recovered signals at are depicted in (b), (e), (h). Reconstruction error is shown in plots (c), (f), (i). Diagnostic features are encircled and indicated by arrows
a Lead I original signal
b Lead I reconstructed signal
c Reconstruction error
d Lead aVL original signal
e Lead aVL reconstructed signal
f Reconstruction error
g Lead V1 original signal
h Lead V1 reconstructed signal
i Reconstruction error
Fig. 5Reconstruction results of the proposed method for ECG signals from data record 419 of VFDB database exhibiting VF at . Arrows indicate the points of distortion in the reconstructed signals
Fig. 6Average joint PRD variation with the number of measurements
Average PRD values with standard deviations in different leads of ECG signals from normal and different pathological classes of PTB database at number of measurements, M = 120. Average PRD is calculated over all the datasets of a particular class in the PTB database
| Pathological classes | No. of datasets | PRD value in different ECG channels | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Lead I | Lead II | V1 | V2 | V3 | V4 | V5 | V6 | ||
| Healthy control | 52 | ||||||||
| Myocardial infarction | 148 | ||||||||
| Hypertrophy | 7 | ||||||||
| Bundle branch block | 15 | ||||||||
Fig. 7Boxplot showing the variation of PRD values of different datasets of PTB database at different CR values
MOS error (in %) in different types of ECG signals
| ECG features | BBB | HC | HP | MI | PVC | VF |
|---|---|---|---|---|---|---|
| P wave | 8.57 | 17.14 | 17.28 | 17.14 | 21.42 | – |
| Q wave | – | – | – | 15.71 | – | – |
| QRS complex | 7.85 | 10 | 7 | 17.14 | 14.28 | – |
| QRS duration | 8.28 | – | 7.14 | – | – | – |
| ST segment | 9 | 14.28 | 10.46 | 15.71 | 17.14 | – |
| T wave | 13.14 | 12.85 | 8.15 | 10.76 | 12.85 | – |
| RSr′ complex | 7 | – | – | – | – | – |
| Slurred S wave | 8.42 | – | – | – | – | – |
| PVC beat 1 | – | – | – | – | 12.85 | – |
| PVC beat 2 | – | – | – | – | 12.85 | – |
| VF waves | – | – | – | – | – | 14.28 |
| Overall ECG signal | 8.89 | 13.5 | 10 | 15.29 | 15.23 | 14.28 |
Performance comparison table
| Techniques | Distortion metrics | CR(M) | Correlation type | Database | |
|---|---|---|---|---|---|
| PRD | 2.15 | 6.58 | spatiotemporal | MIT-BIH ( | |
| QS | 3.06 | ||||
| WEDD | 1.13 | ||||
| MMB-IHT [ | PRD | 3.74 | 6.4 | temporal | |
| QS | 1.71 | ||||
| PRD | 1.67 | 192 | spatiotemporal | ||
| WLM [ | PRD | 3.64 | 192 | temporal | |
| PRD | 4.68 | 73.3% | spatiotemporal | PTB ( | |
| WEDD | 3.61 | ||||
| JCS [ | PRD | 9.00 | 72.7% | spatial | |
| WMNM [ | PRD | 5.5 | 73.4% | spatial | |
| PWMNM [ | PRD | 3.3 | 73.9% | spatial | |
Fig. 8Output distortions variation with number of 1 s in each column of sensing matrix