| Literature DB >> 31388564 |
Mohamed Elgendi1,2,3, Richard Fletcher4,5, Yongbo Liang1, Newton Howard6,7, Nigel H Lovell8, Derek Abbott9,10, Kenneth Lim2,3, Rabab Ward1.
Abstract
The measurement of blood pressure (BP) is critical to the treatment and management of many medical conditions. High blood pressure is associated with many chronic disease conditions, and is a major source of mortality and morbidity around the world. For outpatient care as well as general health monitoring, there is great interest in being able to accurately and frequently measure BP outside of a clinical setting, using mobile or wearable devices. One possible solution is photoplethysmography (PPG), which is most commonly used in pulse oximetry in clinical settings for measuring oxygen saturation. PPG technology is becoming more readily available, inexpensive, convenient, and easily integrated into portable devices. Recent advances include the development of smartphones and wearable devices that collect pulse oximeter signals. In this article, we review (i) the state-of-the-art and the literature related to PPG signals collected by pulse oximeters, (ii) various theoretical approaches that have been adopted in PPG BP measurement studies, and (iii) the potential of PPG measurement devices as a wearable application. Past studies on changes in PPG signals and BP are highlighted, and the correlation between PPG signals and BP are discussed. We also review the combined use of features extracted from PPG and other physiological signals in estimating BP. Although the technology is not yet mature, it is anticipated that in the near future, accurate, continuous BP measurements may be available from mobile and wearable devices given their vast potential.Entities:
Keywords: Data integration; Diagnostic markers; Electrocardiography - EKG; Predictive markers; Statistical methods
Year: 2019 PMID: 31388564 PMCID: PMC6594942 DOI: 10.1038/s41746-019-0136-7
Source DB: PubMed Journal: NPJ Digit Med ISSN: 2398-6352
Fig. 1Key features of blood pressure estimation using PPG and other physiological signals. (i) Using PPG signal and its derivative, (ii) using ECG and PPG signals, (iii) using BCG signals and PPG signals, and (iv) using PCG and PPG signals. Here, PPG photoplethysmogram, APG acceleration photoplethysmogram, BCG ballistocardiogram, PCG phonocardiogram, STT slope transit time, PTT pulse transit time, PEP pre-ejection period, PAT pulse arrival time, TD time interval between the J peak in the BCG signal and the systolic peak in the PPG signal, VTT vascular time interval between the first heart sound S1 and the systolic peak in the PPG signal, S1 first heart sound, S2 second heart sound
Fig. 2Difference between pulse arrival time (PAT) and pulse transit time (PTT). The PAT is defined as the time taken from the pulse waveform to traverse from the heart to a distal site. The PTT is defined as the period from relatively proximal site (e.g., arm) to a distal site (e.g., finger) or between two distal sites (e.g., figure and toe)
A comparison between different wearable blood pressure estimation studies and devices
| Year | Author | Wearable type | Sensors | Transmission mode | # Subjects |
| |
|---|---|---|---|---|---|---|---|
| 2019 | Redha et al.[ | Wristband | PPG | N/R | Feature set | 0.69 | |
| 2017 | Holz et al.[ | Eyeglass frame and finger probe | PPG | N/R | PTT | 0.64–0.84 | |
| 2017 | Zhang et al.[ | Armband | ECG and PPG | USB cable | PAT | N/R | |
| 2016 | Plante et al.[ | Mobile phone (camera + microphone) | Heart sound and PPG | N/R | VTT | ≈0.4 | |
| 2016 | Seeberg et al.[ | Chest belt | ECG and PPG | Bluetooth | PTT | −0.56 | |
| 2016 | Griggs et al.[ | Bicep- and wrist-worn device | ECG and PPG | Radio frequency | PAT | −0.7 | |
| 2016 | Zheng et al.[ | Armband | ECG and PPG | Bluetooth | PAT | N/R | |
| 2015 | Munnoch and Jiang[ | Handheld | ECG and PPG | Bluetooth | PAT | N/R | |
| 2014 | Jung et al.[ | Finger probe and chest pad | ECG and PPG | Bluetooth | N/R | PAT | N/R |
| 2014 | Thomas et al.[ | Wrist watch | ECG and PPG | Bluetooth | N/R | PAT | −0.55 |
| 2012 | Miao et al.[ | Portable device | ECG and PPG | Bluetooth | N/R | N/R | N/R |
| 2009 | Guo et al.[ | Wrist watch and finger probe | ECG and PPG | ZigBee | N/R | PAT | N/R |
| 2008 | Pandian et al.[ | Vest-worn device | ECG and PPG | Radio frequency | PAT | N/R |
r Pearson’s correlation coefficient, f PPG-based feature(s), N/R not reported, n1 number of healthy subjects, n2 number of hypertensive subjects, PAT pulse arrival time, PTT pulse transit time, VTT vascular transit time
Fig. 3Filter impact on PPG morphology. The left figure shows the impulse response difference between the Butterworth (red line) and ChebyshevII (black line) filters. The right figure shows the Butterworth bandpass filtered (red line) and the ChebyshevII bandpass (black line) filtered PPG signals of the raw PPG signal (blue line). It is clear that the ChebyshevII filter is able to emphasize the difference between the systolic and diastolic waves, compared to the Butterworth filter.[6] PPG photoplethysmogram, dB Decibel, GHz Gigahertz
Fig. 4Pulse arrival time in different hypertension stages. PAT pulse arrival time, ECG electrocardiogram, ABP arterial blood pressure, PPG photoplethysmogram
A summary of computing model and performance of the BP estimation
| Year | Features | Model/Method | BP confidence interval in mmHg | # Subjects | Ref. | |
|---|---|---|---|---|---|---|
| 2019 | 10 features | N/R |
[ | |||
| 2019 | PAT | BP = ( | N/R |
[ | ||
| 2019 | N/R | Partial least-squares regression | CIs = −0.2.3 ± 18 |
[ | ||
| 2018 | PPG signal | N/R | Deep learning | N/R |
[ | |
| 2016 | PPG signal | N/R | Neural networks | CIs = 2.3 ± 2.9, CId = 1.9 ± 2.5 | N/R |
[ |
| 2015 | PAT, AI, LASI, IPA | N/R | Support vector machines | CIs = 12.3 ± 18.5, CId = 6.4 ± 8.5 | N/R |
[ |
| 2014 | PAT | BP = ( | CIs = 5.8 ± N/R, CId = 5.15 ± N/R |
[ | ||
| 2014 | PAT | N/R | BP = ( | CIs = 0.1 ± 2.5, CId = 1.3 ± 7.4 |
[ | |
| 2013 | 4 features | N/R | Neural networks | CIs = 5.2 ± 5.0, CId = 2.9 ± 2.9 | N/R |
[ |
| 2013 | 21 features | N/R | Neural networks | CIs = 3.8 ± 3.5, CId = 2.2 ± 2.1 | N/R |
[ |
| 2013 | N/R | N/R | Neural networks | CIs = −2.9 ± 19.4, CId = −3.7 ± 8.7 |
[ | |
| 2013 | PAT | BP = ( | CIs = 0.81 ± 5.48, CId = 0.34 ± 2.94 |
[ | ||
| 2013 | PAT, HR | N/R | BP = ( | CIs = 1.8 ± N/R, CId = 1.57 ± N/R |
[ | |
| 2010 | PTT | BP = ( | CIs = N/R, CId = N/R | N/R |
[ | |
| 2010 | PAT, HR, TDB | N/R | BP = | CIs = −0.002 ± 5.9, CId = −0.02 ± 4.7 |
[ | |
| 2004 | PAT | N/R | BP = ( | CIs = 0.08 ± 11.3, CId = N/R |
[ |
PAT pulse arrival transit time, PTT pulse transit time, HR heart rate, TDB arterial stiffness index, AI augmentation index, LASI large artery stiffness index, IPA inflection point area ratio, β0, β1 and β2 regression coefficients, N/R not reported, n1 number of healthy subjects, nx number of unhealthy subjects
CIs and CId are the confidence interval (mean ± standard deviation) for the estimated systolic pressure and diastolic pressure, respectively. Here, rs is the correlation coefficient for the systolic pressure while rd is correlation coefficient for the diastolic pressure