Extraction of heart rate variability from smartphone photoplethysmograms

Rong-Chao Peng, Xiao-Lin Zhou, Wan-Hua Lin, Yuan-Ting Zhang, Rong-Chao Peng, Xiao-Lin Zhou, Wan-Hua Lin, Yuan-Ting Zhang

Abstract

Heart rate variability (HRV) is a useful clinical tool for autonomic function assessment and cardiovascular diseases diagnosis. It is traditionally calculated from a dedicated medical electrocardiograph (ECG). In this paper, we demonstrate that HRV can also be extracted from photoplethysmograms (PPG) obtained by the camera of a smartphone. Sixteen HRV parameters, including time-domain, frequency-domain, and nonlinear parameters, were calculated from PPG captured by a smartphone for 30 healthy subjects and were compared with those derived from ECG. The statistical results showed that 14 parameters (AVNN, SDNN, CV, RMSSD, SDSD, TP, VLF, LF, HF, LF/HF, nLF, nHF, SD1, and SD2) from PPG were highly correlated (r > 0.7, P < 0.001) with those from ECG, and 7 parameters (AVNN, TP, VLF, LF, HF, nLF, and nHF) from PPG were in good agreement with those from ECG within the acceptable limits. In addition, five different algorithms to detect the characteristic points of PPG wave were also investigated: peak point (PP), valley point (VP), maximum first derivative (M1D), maximum second derivative (M2D), and tangent intersection (TI). The results showed that M2D and TI algorithms had the best performance. These results suggest that the smartphone might be used for HRV measurement.

Figures

Figure 1
Figure 1
An example of outlier removal. (a) A raw smartphone photoplethysmogram with abrupt change. (b) The difference of the signal in panel (a). The circle shows the location of the outlier. (c) The outlier was removed and replaced with a new value using cubic spline interpolation. (d) The new smartphone photoplethysmogram without abrupt change.
Figure 2
Figure 2
Illustration of five characteristic points including A, the peak point; B, the valley point; C, the maximum first derivative; D, the maximum second derivative; and E, the tangent intersection.
Figure 3
Figure 3
Comparison of HRV derived from the smartphone and the electrocardiograph for one subject. (a) R-to-R intervals (RRI) derived from the electrocardiogram. (b)–(f) Pulse-to-pulse intervals (PPI) derived from the smartphone photoplethysmogram, using the characteristic points determined by (b) peak point, (c) valley point, (d) maximum first derivative, (e) maximum second derivative, and (f) tangent intersection.
Figure 4
Figure 4
Bland-Altman plots of HRV parameters derived from the smartphone and the electrocardiograph. For each plot, the horizontal axis represents the mean of HRV parameters derived from smartphone and electrocardiograph, while the vertical axis represents the difference between HRV parameters derived from smartphone and electrocardiograph. The five columns correspond to five different algorithms: PP, peak point; VP, valley point; M1D, maximum first derivative; M2D, maximum second derivative; and TI, tangent intersection. LF, low frequency power; HF, high frequency power; LF/HF, ratio of LF to HF; nLF, normalized LF = LF/(TP − VLF); and nHF, normalized HF = HF/(TP − VLF).

References

    1. Pomeranz B., Macaulay R. J., Caudill M. A., et al. Assessment of autonomic function in humans by heart rate spectral analysis. The American Journal of Physiology. 1985;248(1):H151–H153.
    1. Camm A. J., Malik M., Bigger J. T., et al. Heart rate variability: standards of measurement, physiological interpretation, and clinical use. Circulation. 1996;93:1043–1065.
    1. Charlot K., Cornolo J., Brugniaux J. V., Richalet J. P., Pichon A. Interchangeability between heart rate and photoplethysmography variabilities during sympathetic stimulations. Physiological Measurement. 2009;30(12):1357–1369. doi: 10.1088/0967-3334/30/12/005.
    1. Gil E., Orini M., Bailón R., Vergara J. M., Mainardi L., Laguna P. Photoplethysmography pulse rate variability as a surrogate measurement of heart rate variability during non-stationary conditions. Physiological Measurement. 2010;31(9):1271–1290. doi: 10.1088/0967-3334/31/9/015.
    1. Lu S., Zhao H., Ju K., et al. Can photoplethysmography variability serve as an alternative approach to obtain heart rate variability information? Journal of Clinical Monitoring and Computing. 2008;22(1):23–29. doi: 10.1007/s10877-007-9103-y.
    1. McKinley P. S., Shapiro P. A., Bagiella E., et al. Deriving heart period variability from blood pressure waveforms. Journal of Applied Physiology. 2003;95(4):1431–1438.
    1. Suhrbier A., Heringer R., Walther T., Malberg H., Wessel N. Comparison of three methods for beat-to-beat-interval extraction from continuous blood pressure and electrocardiogram with respect to heart rate variability analysis. Biomedizinische Technik. 2006;51(2):70–76. doi: 10.1515/BMT.2006.013.
    1. Kristiansen N. K., Fleischer J., Jensen M. S., Andersen K. S., Nygaard H. Design and evaluation of a handheld impedance plethysmograph for measuring heart rate variability. Medical and Biological Engineering and Computing. 2005;43(4):516–521. doi: 10.1007/BF02344734.
    1. Treo E. F., Herrera M. C., Valentinuzzi M. E. Algorithm for identifying and separating beats from arterial pulse records. BioMedical Engineering OnLine. 2005;4, article 48 doi: 10.1186/1475-925x-4-48.
    1. Shin J. H., Hwang S. H., Chang M. H., Park K. S. Heart rate variability analysis using a ballistocardiogram during Valsalva manoeuvre and post exercise. Physiological Measurement. 2011;32(8):1239–1264. doi: 10.1088/0967-3334/32/8/015.
    1. Morbiducci U., Scalise L., De Melis M., Grigioni M. Optical vibrocardiography: a novel tool for the optical monitoring of cardiac activity. Annals of Biomedical Engineering. 2007;35(1):45–58. doi: 10.1007/s10439-006-9202-9.
    1. Lu G., Yang F., Tian Y., Jing X., Wang J. Contact-free measurement of heart rate variability via a microwave sensor. Sensors. 2009;9(12):9572–9581. doi: 10.3390/s91209572.
    1. Poh M.-Z., McDuff D. J., Picard R. W. Advancements in noncontact, multiparameter physiological measurements using a webcam. IEEE Transactions on Biomedical Engineering. 2011;58(1):7–11. doi: 10.1109/TBME.2010.2086456.
    1. Sun Y., Hu S., Azorin-Peris V., Kalawsky R., Greenwald S. Noncontact imaging photoplethysmography to effectively access pulse rate variability. Journal of Biomedical Optics. 2013;18(6) doi: 10.1117/1.jbo.18.6.061205.61205
    1. Istepanian R. S. H., Jovanov E., Zhang Y. T. Introduction to the special section on m-Health: beyond seamless mobility and global wireless health-care connectivity. IEEE Transactions on Information Technology in Biomedicine. 2004;8(4):405–414. doi: 10.1109/titb.2004.840019.
    1. Boulos M. N. K., Wheeler S., Tavares C., Jones R. How smartphones are changing the face of mobile and participatory healthcare: an overview, with example from eCAALYX. BioMedical Engineering OnLine. 2011;10, article 24 doi: 10.1186/1475-925x-10-24.
    1. Jonathan E., Leahy M. Investigating a smartphone imaging unit for photoplethysmography. Physiological Measurement. 2010;31(11):N79–N83. doi: 10.1088/0967-3334/31/11/N01.
    1. Jonathan E., Leahy M. J. Cellular phone-based photoplethysmographic imaging. Journal of Biophotonics. 2011;4(5):293–296. doi: 10.1002/jbio.201000050.
    1. Scully C. G., Lee J., Meyer J., et al. Physiological parameter monitoring from optical recordings with a mobile phone. IEEE Transactions on Biomedical Engineering. 2012;59(2):303–306. doi: 10.1109/tbme.2011.2163157.
    1. Gregoski M. J., Mueller M., Vertegel A., et al. Development and validation of a smartphone heart rate acquisition application for health promotion and wellness telehealth applications. International Journal of Telemedicine and Applications. 2012;2012:7. doi: 10.1155/2012/696324.696324
    1. Matsumura K., Yamakoshi T. iPhysioMeter: a new approach for measuring heart rate and normalized pulse volume using only a smartphone. Behavior Research Methods. 2013;45(4):1272–1278. doi: 10.3758/s13428-012-0312-z.
    1. Chandrasekaran V., Dantu R., Jonnada S., Thiyagaraja S., Subbu K. P. Cuffless differential blood pressure estimation using smart phones. IEEE Transactions on Biomedical Engineering. 2013;60(4):1080–1089. doi: 10.1109/TBME.2012.2211078.
    1. Allen J. Photoplethysmography and its application in clinical physiological measurement. Physiological Measurement. 2007;28(3):R1–R39. doi: 10.1088/0967-3334/28/3/r01.
    1. Zhang X.-Y., Zhang Y.-T. The effect of local mild cold exposure on pulse transit time. Physiological Measurement. 2006;27(7):649–660. doi: 10.1007/s00376-006-0649-2.
    1. Chiu Y. C., Arand P. W., Shroff S. G., Feldman T., Carroll J. D. Determination of pulse wave velocities with computerized algorithms. American Heart Journal. 1991;121(5):1460–1470. doi: 10.1016/0002-8703(91)90153-9.
    1. Pan J., Tompkins W. J. A real-time QRS detection algorithm. IEEE Transactions on Biomedical Engineering. 1985;32(3):230–236.
    1. Bland J. M., Altman D. G. Statistical methods for assessing agreement between two methods of clinical measurement. The Lancet. 1986;1(8476):307–310.
    1. Schäfer A., Vagedes J. How accurate is pulse rate variability as an estimate of heart rate variability? A review on studies comparing photoplethysmographic technology with an electrocardiogram. International Journal of Cardiology. 2013;166(1):15–29. doi: 10.1016/j.ijcard.2012.03.119.
    1. Posada-Quintero H. F., Delisle-Rodríguez D., Cuadra-Sanz M. B., de la Vara-Prieto R. R. F. Evaluation of pulse rate variability obtained by the pulse onsets of the photoplethysmographic signal. Physiological Measurement. 2013;34(2):179–187. doi: 10.1088/0967-3334/34/2/179.
    1. Wong J.-S., Lu W.-A., Wu K.-T., Liu M., Chen G.-Y., Kuo C.-D. A comparative study of pulse rate variability and heart rate variability in healthy subjects. Journal of Clinical Monitoring and Computing. 2012;26(2):107–114. doi: 10.1007/s10877-012-9340-6.
    1. Bolkhovsky J. B., Scully C. G., Chon K. H. Statistical analysis of heart rate and heart rate variability monitoring through the use of smart phone cameras. Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society; 2012; pp. 1610–1613.
    1. Lee C. T., Wei L. Y. Spectrum analysis of human pulse. IEEE Transactions on Biomedical Engineering. 1983;30(6):348–352.
    1. Verkruysse W., Svaasand L. O., Nelson J. S. Remote plethysmographic imaging using ambient light. Optics Express. 2008;16(26):21434–21445. doi: 10.1364/OE.16.021434.
    1. Grimaldi D., Kurylyak Y., Lamonaca F., Nastro A. Photoplethysmography detection by smartphone's videocamera. Proceedings of the 6th IEEE International Conference on Intelligent Data Acquisition and Advanced Computing Systems: Technology and Applications (IDAACS '11); September 2011; Prague, Czech Republic. pp. 488–491.
    1. Hayes M. J., Smith P. R. Artifact reduction in photoplethysmography. Applied Optics. 1998;37(31):7437–7446. doi: 10.1364/AO.37.007437.
    1. Kim B. S., Yoo S. K. Motion artifact reduction in photoplethysmography using independent component analysis. IEEE Transactions on Biomedical Engineering. 2006;53(3):566–568. doi: 10.1109/TBME.2005.869784.

Source: PubMed

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