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Proceeding Paper

Using Smart Wearables to Monitor Cardiac Ejection †

by
Aristide Mathieu
,
Peter H. Charlton
*,‡ and
Jordi Alastruey
Department of Biomedical Engineering, School of Biomedical Engineering and Imaging Sciences, King’s College London, King’s Health Partners, St Thomas’ Hospital, London SE1 7EH, UK
*
Author to whom correspondence should be addressed.
Presented at the 5th International Electronic Conference on Sensors and Applications, 15–30 November 2018; Available online: https://ecsa-5.sciforum.net.
These authors contributed equally to this work.
Proceedings 2019, 4(1), 48; https://doi.org/10.3390/ecsa-5-05744
Published: 14 November 2018
(This article belongs to the Proceedings of 5th International Electronic Conference on Sensors and Applications)

Abstract

:
An individual’s cardiovascular state is a crucial aspect of a healthy life. However, it is not routinely assessed outside the clinical setting. Smart wearables use photoplethysmography (PPG) to monitor the arterial pulse wave (PW) and estimate heart rate. The PPG PW is strongly influenced by the ejection of blood from the heart, providing an opportunity to monitor cardiac parameters using smart wearables. The aim of this study was to investigate the feasibility of monitoring left ventricular ejection time (LVET) and left ventricular contractility (LVC) from the PPG PW at the wrist. PPG PWs were simulated under a range of cardiovascular conditions using a numerical model of PW propagation. LVET and LVC were estimated from the first and second derivatives of the PPG PWs and compared to reference values extracted from the blood pressure PW at the aortic root. There was strong agreement between the estimated and reference values of LVET, indicating that it may be feasible to assess LVET from PPG signals, including those acquired by smart watches. The correlations between the estimated and reference values of LVC were less strong, indicating that further work is required to assess contractility robustly using smart wearables. This study demonstrated the feasibility of assessing LVET using smart wearables that could allow individuals to monitor their cardiovascular state on a daily basis.

1. Introduction

Wearable sensors routinely acquire a photoplethysmogram (PPG) signal, which is a measure of the arterial pulse wave (PW) [1]. Fitness bands and smart watches, such as the Samsung Gear, Apple Watch and Fitbit Charge devices, use the PPG for heart rate monitoring [2]. In addition, research is being conducted into estimating arterial blood oxygen saturation from PPG signals acquired by smart wearables, in the same manner as clinical pulse oximeters [3]. However, the PPG PW contains a wealth of additional information on the state of the heart which is not currently exploited.
Photoplethysmography is the optical measurement of arterial blood volume changes in a tissue bed. Smart wearables usually obtain the PPG at the wrist by illuminating the skin with an LED and measuring the level of reflected light. A pulsatile signal consisting of PWs is produced as the arterial blood volume increases and decreases with each heart beat, as shown in Figure 1a. The PPG PW, shown in Figure 1b, has been found to be closely related to the arterial blood pressure (BP) PW, and the two signals have been related by a transfer function [4]. Consequently, it has been proposed that the methods used to estimate cardiac properties from the BP signal could be adapted for use with the PPG signal. However, there are challenges in extracting information from a PPG, including: (1) The shape of the PW changes as it propagates from the heart to the periphery, meaning that information may be distorted or lost. (2) High-frequency content is attenuated in the PPG, making it more difficult to identify features on the PPG PW than the BP PW. In this study we focus on estimating two cardiac parameters from the PPG: Left ventricular ejection time (LVET) and left ventricular contractility (LVC).
LVET is the time period of blood flowing through the aortic valve. LVET is influenced by several cardiac factors, including heart rate, stroke volume, preload, afterload and inotropic drugs [5]. Consequently, LVET is a valuable clinical parameter when monitoring the effects of drugs and diseases [5]. Techniques have been previously proposed for estimating LVET from BP [6,7,8] and PPG [9,10,11] PWs. LVET estimates derived from the BP PW have been found to perform well, whilst those derived from the PPG were found to be less accurate but still useful for detecting intra-subject changes in LVET [9]. If LVET could be reliably estimated from smart wearables then it would have utility for monitoring both health and fitness. However, at present it is not clear whether LVET could be accurately estimated from the peripheral PPG signals acquired by smart wearables, or whether accuracy would be improved by measuring BP signals in smart wearables.
Left ventricular contractility (LVC) is the strength of the contractile force generated by the heart [13]. Whilst it is difficult to assess in vivo, it can be quantified as the maximal rate of intraventricular pressure rise during systole [14]. Drugs can affect LVC, and consequently measurements of LVC can be valuable for assessing the safety of new drugs. It has been proposed that LVC could be assessed from the carotid BP signal [15]. However, to our knowledge no research has investigated whether LVC could be accurately assessed from PPG signals acquired by smart wearables.
The aim of this pilot study was to investigate whether LVET and LVC could be accurately estimated from peripheral PPG signals. Simultaneous BP and PPG PWs were simulated at the aortic root, wrist and carotid artery using a numerical model of pulse wave propagation. LVET and LVC values were estimated from PPG and BP PWs at the wrist and carotid artery, and compared to reference values obtained from the aortic root.

2. Materials and Methods

2.1. Dataset

The dataset used in this study was adapted from the database of simulated PWs presented in [16], which is publicly available [17]. This database was generated by simulating PWs using a numerical model of pulse wave propagation. The cardiac and arterial model parameters were varied within healthy ranges to produce PWs representative of 3,325 virtual healthy adult subjects. BP PWs at the aortic root and radial, brachial and carotid arteries were extracted from the database for this study. PPG PWs were estimated from the BP PWs using the transfer function reported in Reference [4] and implemented in [18]. PPG estimates were made at the wrist, representing those which would be measured from smart watches and fitness bands, and at the carotid artery, representing those which would be measured when using a smartphone camera on the surface of the neck to capture PWs.

2.2. Estimating LVET and LVC from Radial BP and PPG Waves

LVET and LVC were estimated from each of the radial BP and PPG waves using similar pulse wave analysis techniques to those reported in Reference [18]. The techniques are illustrated in Figure 1b. LVET was calculated as the time between the pulse onset and the “e” wave on the second derivative of the PW, since this is indicative of the time of aortic valve closure at the end of cardiac ejection [19]. This was performed by firstly filtering PWs to eliminate non-physiological, high-frequency content (using a low pass filter with a −3 dB cut-off at 35 Hz). Secondly, the first and second derivatives of PWs were calculated using a Savitsky–Golay filter. Thirdly, the “e” wave was identified as the maximum of the second derivative in a search region bounded by the systolic peak and 60% of the PW duration. LVC was calculated as the maximum value of the first derivative of the PW. For the BP PW it was measured in units of mmHg/s. For the PPG PW it was measured in au/s, where au represented arbitrary units (since the PPG is unitless).

2.3. Statistical Analysis

A fixed reference value for LVET of 310 ms was used, as this was not varied in the original database [16]. Errors between estimated and reference LVET values were calculated by subtracting the reference from estimated values. Reference values for LVC were obtained from aortic BP PWs using the same approach as for radial BP waves. The strength of the correlation between estimated and reference LVCs was assessed using the coefficient of determination R2, the square of Pearson’s correlation coefficient. Results were compared between PPG and BP PWs to determine whether it could be beneficial to include BP PW monitoring more widely in smart wearables.

3. Results and Discussion

3.1. Comparing PPG and BP Waves

Figure 2 shows examples of the PPG and BP PWs used in the analysis. The two PWs had different shapes, indicating that pulse wave analysis techniques which have been originally used with the BP PW may not be suitable for use with the PPG. Specifically, the BP PW contained more high-frequency features, such as a dicrotic notch on the downslope. These features were largely attenuated in the PPG PW. Consequently, it may be more difficult to estimate LVET from a PPG, as it relies on precise identification of the end of systole, which is indicated by the dicrotic notch.

3.2. Estimating Left Ventricular Ejection Time (LVET)

The results of estimating LVET at the wrist from the PPG and BP PWs are shown in Figure 3. The estimated LVETs were higher than the reference values, as shown by the positive errors in Figure 3a,b. If this bias was found to be consistent in future studies, then one could obtain more accurate estimates by simply subtracting the bias from estimated values. The errors ranged between 10 and 20 ms (i.e., 3% and 6%). Since typical values for LVET are approximately 295 ± 24 ms [6], these errors may be sufficiently small to allow for inter-subject comparisons and subject-specific risk stratification. There was little difference between the errors obtained when using the PPG and BP PWs, as shown in Figure 3c. This indicates that there would be no advantage to using the BP PW compared to the PPG PW. Therefore, the existing PPG hardware in smart wearables may be sufficient for obtaining clinically useful values of LVET.

3.3. Estimating Left Ventricular Contractility (LVC)

The results of estimating LVC from the PPG at the wrist are shown in Figure 4c, and for comparison results are also shown for the carotid artery (Figure 4a) and brachial artery (Figure 4b). The correlation of PPG-derived LVC values at the wrist was too low to be clinically useful (R2 = 0.03). This indicates that further work is required to obtain useful assessments of LVC at the wrist. However, the strength of the correlation was higher at arterial sites closer to the heart (carotid and brachial sites). In particular, the correlation of R2 = 0.41 at the carotid artery may be strong enough to provide useful assessments of LVC. Such assessments could potentially be performed using an imaging PPG signal acquired using a smartphone at the neck.

3.4. Limitations and Future Work

The main limitation of this pilot study was that it used simulated signals. This had the benefits of ensuring that reference parameter values were known precisely, without measurement error, and allowing the performance of techniques for estimating LVET and LVC to be assessed across a wide range of cardiovascular conditions. A second limitation was the use of a fixed value for LVET. The study indicated that further work is required to develop techniques to estimate LVC. In addition, the PPG signals routinely acquired by wearable sensors may be sufficient to assess LVET, without the need to acquire BP signals, which are more difficult to acquire from wearables.
Future studies should assess the performance of the technique for estimating LVET from smart wearables in vivo. Initial validation should be performed in controlled laboratory settings, where it is easier to acquire reference measurements. The technique could then be assessed in daily living, where less-precise reference measurements could be acquired to validate the technique. If validated, then this approach would allow LVET to be continuously monitored in daily life, improving health monitoring. It would also allow for large-scale research studies to be conducted into the utility of LVET for clinical decision making and diagnosis in various types of cardiovascular diseases, including aortic valve disease, left ventricular failure, stenosis and aortic regurgitation [20].

3.5. Implications

The inclusion of PPG sensors in smart wearables provides opportunity to monitor cardiovascular states unobtrusively in daily life. Photoplethysmography was first reported in the 1930s [21], and began being widely used in clinical practice in the 1980s with the proliferation of pulse oximeters for measuring arterial blood oxygen saturation [22]. The ability to unobtrusively measure oxygen saturation was deemed so revolutionary that it became considered the fifth vital sign [23]. Despite its routine use in clinical practice, the full utility of the PPG signal has not yet been exploited. A wide range of applications have been investigated in the research setting, including assessing arterial stiffness, respiratory rate, microcirculation, venous function and blood pressure [24], as well as the possibility of assessing LVET and LVC, which has been investigated in this study. It may be that the widespread use of PPG sensors in smart wearables provides sufficient incentive to translate more of these potential applications into routine practice.

4. Conclusions

The main finding of this pilot study was that LVET could be estimated from PPG signals at the wrist with sufficient precision for use in some settings. Clinical studies are warranted to determine whether this approach could be used to estimate LVET precisely from wrist-worn smart wearables. LVC could not be estimated precisely from the wrist using the trialed technique. Further development of pulse wave analysis techniques may improve the performance of LVC estimates, although this study indicates that they are likely to perform better when obtained from signals acquired at the neck, such as imaging PPG signals.

Funding

This research was funded by the British Heart Foundation, grant number [PG/15/104/31913]. It was additionally supported by the Wellcome/EPSRC Centre for Medical Engineering at King’s College London, grant number [WT 203148/Z/16/Z]. The views expressed are those of the authors and not necessarily those of the British Heart Foundation, Wellcome Trust or EPSRC.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses or interpretation of data; in the writing of the manuscript or in the decision to publish the results.
Data Access Statement: The data used in this research are publicly available at http://haemod.uk/. Further information about the data and conditions of access can be found by emailing [email protected].

References

  1. Zhang, Z.; Pi, Z.; Liu, B. TROIKA: A general framework for heart rate monitoring using wrist-type photoplethysmographic signals during intensive physical exercise. IEEE Trans. Biomed. Eng. 2015, 62, 522–531. [Google Scholar] [CrossRef] [PubMed]
  2. Wallen, M.P.; Gomersall, S.R.; Keating, S.E.; Wisløff, U.; Coombes, J.S. Accuracy of heart rate watches: Implications for weight management. PLoS ONE 2016, 11, 1–9. [Google Scholar] [CrossRef] [PubMed]
  3. Jarchi, D.; Salvi, D.; Velardo, C.; Mahdi, A.; Tarassenko, L.; Clifton, D.A. Estimation of HRV and SpO2 from wrist-worn commercial sensors for clinical settings. In Proceedings of the IEEE 15th International Conference on Wearable and Implantable Body Sensor Networks (BSN), Las Vegas, NV, USA, 4–7 March 2018; pp. 144–147. [Google Scholar]
  4. Millasseau, S.C.; Guigui, F.G.; Kelly, R.P.; Prasad, K.; Cockcroft, J.R.; Ritter, J.M.; Chowienczyk, P.J. Noninvasive assessment of the digital volume pulse. Comparison with the peripheral pressure pulse. Hypertension 2000, 36, 952–956. [Google Scholar] [CrossRef] [PubMed]
  5. Hassan, S.; Turner, P. Systolic time intervals: A review of the method in the non-invasive investigation of cardiac function in health, disease and clinical pharmacology. Postgrad. Med. J. 1983, 59, 423–434. [Google Scholar] [CrossRef] [PubMed]
  6. Gerstenblith, G.; Frederiksen, J.; Yin, F.; Fortuin, N.; Lakatta, E.; Weisfeldt, M. Echocardiographic assessment of a normal aging population. Circulation 1977, 56, 273–278. [Google Scholar] [CrossRef] [PubMed]
  7. Van de Werf, F.; Piessens, J.; Kesteloot, H.; De Geest, H. A comparison of systolic time intervals derived from the central aortic pressure and from the external carotid pulse tracing. Circulation 1975, 51, 310–316. [Google Scholar] [CrossRef] [PubMed]
  8. Martin, C.E.; Shaver, J.A.; Thompson, M.E.; Reddy, S.P.; Leonard, J.J. Direct correlation of external systolic time intervals with internal indices of left ventricular function in man. Circulation 1971, 44, 419–431. [Google Scholar] [CrossRef] [PubMed]
  9. Chan, G.S.H.; Middleton, P.M.; Celler, B.G.; Wang, L.; Lovell, N.H. Automatic detection of left ventricular ejection time from a finger photoplethysmographic pulse oximetry waveform: Comparison with Doppler aortic measurement. Physiol. Meas. 2007, 28, 439–452. [Google Scholar] [CrossRef] [PubMed]
  10. Von Wowern, E.; Östling, G.; Nilsson, P.M.; Olofsson, P. Digital photoplethysmography for assessment of arterial stiffness: Repeatability and comparison with applanation tonometry. PLoS ONE 2015, 10, 1–19. [Google Scholar] [CrossRef] [PubMed]
  11. Blažek, R.B.; Lee, C. Multi-resolution linear model comparison for detection of dicrotic notch and peak in blood volume pulse signals. In Analysis of Biomedical Signals and Images; Brno University of Technology: Brno, Czech Republic, 2010; pp. 378–386. [Google Scholar]
  12. Charlton, P.H.; Bonnici, T.; Tarassenko, L.; Clifton, D.A.; Beale, R.; Watkinson, P.J. An assessment of algorithms to estimate respiratory rate from the electrocardiogram and photoplethysmogram. Physiol. Meas. 2016, 37, 610–626. [Google Scholar] [CrossRef] [PubMed]
  13. Wijayasiri, L.; Rhodes, A.; Cecconi, M. Cardiac contractility. In Encyclopedia of Intensive Care Medicine; Vincent, J.-L., Hall, J.B., Eds.; Springer: Berlin/Heidelberg, Germany, 2012; pp. 46–462. ISBN 978-3-642-00417-9. [Google Scholar]
  14. Mason, D.T.; Braunwald, E.; Covell, J.W.; Sonnenblick, E.H.; Ross, J. Assessment of cardiac contractility. The relation between the rate of pressure rise and ventricular pressure during isovolumic systole. Circulation 1971, 44, 47–58. [Google Scholar] [CrossRef] [PubMed]
  15. Ifuku, H.; Taniguchi, K.; Matsumoto, H. Noninvasive assessment of cardiac contractility by using (dP/dt)/P of carotid artery pulses during exercise. Eur. J. Appl. Physiol. Occup. Physiol. 1994, 69, 244–249. [Google Scholar] [CrossRef] [PubMed]
  16. Willemet, M.; Chowienczyk, P.; Alastruey, J. A database of virtual healthy subjects to assess the accuracy of foot-to-foot pulse wave velocities for estimation of aortic stiffness. Am. J. Physiol. Hear. Circ. Physiol. 2015, 309, H663–H675. [Google Scholar] [CrossRef] [PubMed]
  17. Haemodynamic Modelling Research Group Home Page. Available online: http://haemod.com (accessed on 4 February 2019).
  18. Charlton, P.H.; Celka, P.; Farukh, B.; Chowienczyk, P.; Alastruey, J. Assessing mental stress from the photoplethysmogram: A numerical study. Physiol. Meas. 2018, 39, 054001. [Google Scholar] [CrossRef] [PubMed]
  19. Blažek, R.B.; Lee, C. Multi-resolution linear model comparison for detection of dicrotic notch and peak in blood volume pulse signals. In Analysis of Biomedical Signals and Images; Brno University of Technology: Brno, Czech Republic, 2010; pp. 378–386. [Google Scholar]
  20. Lewis, R.P.; Rittogers, S.E.; Froester, W.F.; Boudoulas, H. A critical review of the systolic time intervals. Circulation 1977, 56, 146–158. [Google Scholar] [CrossRef] [PubMed]
  21. Allen, J. Photoplethysmography and its application in clinical physiological measurement. Physiol. Meas. 2007, 28, R1–R39. [Google Scholar] [CrossRef] [PubMed]
  22. Jubran, A. Pulse oximetry. Crit. Care 1999, 3, R11–R17. [Google Scholar] [CrossRef] [PubMed]
  23. Neff, T.A. Routine oximetry: A fifth vital sign? Chest 1988, 94, 227. [Google Scholar] [CrossRef] [PubMed]
  24. Elgendi, M. On the analysis of fingertip photoplethysmogram signals. Curr. Cardiol. Rev. 2012, 8, 14–25. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The photoplethysmogram (PPG) signal: (a) A 10 s in vivo recording of the PPG, exhibiting 12.5 pulse waves (PWs), one for each heart beat. (b) The techniques for estimating left ventricular ejection time (LVET) and left ventricular contractility (LVC) from a single PW. au: Arbitrary units. Data from the Vortal dataset [12].
Figure 1. The photoplethysmogram (PPG) signal: (a) A 10 s in vivo recording of the PPG, exhibiting 12.5 pulse waves (PWs), one for each heart beat. (b) The techniques for estimating left ventricular ejection time (LVET) and left ventricular contractility (LVC) from a single PW. au: Arbitrary units. Data from the Vortal dataset [12].
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Figure 2. A comparison of (a) photoplethysmogram (PPG) and (b) blood pressure (BP) pulse waves.
Figure 2. A comparison of (a) photoplethysmogram (PPG) and (b) blood pressure (BP) pulse waves.
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Figure 3. Estimating left ventricular ejection time (LVET) at the wrist: (a) errors when using the photoplethysmogram (PPG) pulse wave (PW); (b) errors when using the blood pressure PW; and (c) a comparison of the errors when using each signal (showing median and lower and upper quartiles).
Figure 3. Estimating left ventricular ejection time (LVET) at the wrist: (a) errors when using the photoplethysmogram (PPG) pulse wave (PW); (b) errors when using the blood pressure PW; and (c) a comparison of the errors when using each signal (showing median and lower and upper quartiles).
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Figure 4. Estimating left ventricular contractility (LVC) from the PPG: the correlation between estimated and reference values at (a) the carotid artery (i.e., neck); (b) the brachial artery (i.e., upper arm); and (c) the radial artery (i.e., wrist). Least-squares lines are shown in red.
Figure 4. Estimating left ventricular contractility (LVC) from the PPG: the correlation between estimated and reference values at (a) the carotid artery (i.e., neck); (b) the brachial artery (i.e., upper arm); and (c) the radial artery (i.e., wrist). Least-squares lines are shown in red.
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MDPI and ACS Style

Mathieu, A.; Charlton, P.H.; Alastruey, J. Using Smart Wearables to Monitor Cardiac Ejection. Proceedings 2019, 4, 48. https://doi.org/10.3390/ecsa-5-05744

AMA Style

Mathieu A, Charlton PH, Alastruey J. Using Smart Wearables to Monitor Cardiac Ejection. Proceedings. 2019; 4(1):48. https://doi.org/10.3390/ecsa-5-05744

Chicago/Turabian Style

Mathieu, Aristide, Peter H. Charlton, and Jordi Alastruey. 2019. "Using Smart Wearables to Monitor Cardiac Ejection" Proceedings 4, no. 1: 48. https://doi.org/10.3390/ecsa-5-05744

APA Style

Mathieu, A., Charlton, P. H., & Alastruey, J. (2019). Using Smart Wearables to Monitor Cardiac Ejection. Proceedings, 4(1), 48. https://doi.org/10.3390/ecsa-5-05744

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