throbber
Journal of Medical Engineering & Technology, Vol. 32, No. 6, November/December 2008, 479–484
`
`Assessment of heart rate variability derived from finger-tip
`photoplethysmography as compared to electrocardiography
`
`N. SELVARAJ{, A. JARYAL{, J. SANTHOSHx, K. K. DEEPAK{ and S. ANAND*{
`
`{Centre for Biomedical Engineering, Indian Institute of Technology-Delhi, New Delhi 110 016, India
`{Department of Physiology, All India Institute of Medical Sciences, New Delhi 110 029, India
`xComputer Services Centre, Indian Institute of Technology-Delhi, New Delhi 110 016, India
`
`Heart rate variability (HRV) is traditionally derived from RR interval time series of
`electrocardiography (ECG). Photoplethysmography (PPG) also reflects the cardiac
`rhythm since the mechanical activity of the heart is coupled to its electrical activity. Thus,
`theoretically, PPG can be used for determining the interval between successive heartbeats
`and heart rate variability. However, the PPG wave lags behind the ECG signal by the
`time required for transmission of pulse wave. In this study, finger-tip PPG and standard
`lead II ECG were recorded for five minutes from 10 healthy subjects at rest. The results
`showed a high correlation (median¼ 0.97) between the ECG-derived RR intervals and
`PPG-derived peak-to-peak (PP) intervals. PP variability was accurate (0.1 ms) as
`compared to RR variability. The time domain, frequency domain and Poincare´ plot
`HRV parameters computed using RR interval method and PP interval method showed
`no significant differences (p 5 0.05). The error analysis also showed insignificant
`differences between the HRV indices obtained by the two methods. Bland-Altman
`analysis showed high degree of agreement between the two methods for all the
`parameters of HRV. Thus, HRV can also be reliably estimated from the PPG based PP
`interval method.
`
`Keywords: Photoplethysmography; Electrocardiography; Heart rate variability
`
`1. Introduction
`
`Heart rate variability (HRV) analysis is a common practice
`for assessment of the cardiovascular autonomic nervous
`system. The oscillations present in the beat-to-beat pacing
`intervals of heart rate are of clinical relevance for both
`diagnostic and prognostic purposes as they are directly
`influenced by the sympathetic and parasympathetic systems
`[1]. Traditionally, time and frequency domain and non-
`linear methods have been used to interpret the physiolo-
`gical
`information embedded in the HRV signal. The
`classical spectral analysis of the HRV signal, generally
`determined from the sequences of successive inter-beat
`RR intervals of the ECG signal, enables separation of
`power distribution in different frequency bands. The low
`
`*Corresponding author. Email: snandaa@gmail.com
`
`frequency (LF) band corresponds mainly to sympathetic
`activity, whereas the high frequency (HF) band is related to
`respiratory sinus arrhythmia mediated by parasympathetic
`activity. The LF/HF ratio and LF and HF band powers are
`good indicators for the assessment of alterations in the
`nervous system behavior [1,2].
`Photoplethysmography (PPG) is a noninvasive optical
`technique for monitoring beat-to-beat
`relative blood
`volume changes in the microvascular bed of peripheral
`tissues. The PPG pulsatile waveform reflects the fluctuations
`in finger blood volume and vasculature characteristics. The
`autonomic influences on spontaneous fluctuations in finger
`blood volume have been assessed by spectral analysis of the
`PPG signal [3,4]. The PPG waveform characteristics such as
`amplitude, baseline and cycle period are useful for the study
`
`Journal of Medical Engineering & Technology
`ISSN 0309-1902 print/ISSN 1464-522X online ª 2008 Informa Healthcare USA, Inc.
`http://www.tandf.co.uk/journals
`DOI: 10.1080/03091900701781317
`
`J Med Eng Technol Downloaded from informahealthcare.com by University of Guelph on 08/26/13
`
`For personal use only.
`
`APPLE 1014
`
`1
`
`

`

`480
`
`N. Selvaraj et al.
`
`of autonomic control of the peripheral vascular tone [5 – 8].
`As the pulse period of blood volume pulse is directly related
`to the cardiac activity,
`the physiological
`information
`derived from RR intervals of ECG can also be derived
`from the pulse period of PPG (figure 1). The PP interval
`variability of the PPG signal was proven to be reasonably
`accurate compared to RR interval variability of ECG
`signal with high correlation [9,10]. The authors suggested
`the possibility of determining HRV parameters using PPG
`technique. Selvaraj et al. [11] and Bolanas et al. [12] have
`supported the same idea.
`Electrical activity of the heart (ECG) is followed by
`spread of the pulsatile wave of blood to the periphery. The
`pulse travel time shows very minor (a few milliseconds)
`beat-to-beat fluctuations [13 – 15], such that heartbeat
`intervals derived from ECG and PPG are very similar but
`they are not exactly the same. Such small variations in the
`heartbeat interval between the two methods do not appear
`to be significant in the time domain analysis but may
`potentially and significantly affect the frequency domain
`and nonlinear analysis of HRV. This issue has not been
`addressed in previous studies. In the present study, a
`comprehensive and systematic analysis of PPG based HRV
`as compared to ECG based HRV has been conducted to
`demonstrate the feasibility and reliability of deriving all the
`traditional HRV parameters from the PPG based method.
`
`2. Materials and methods
`
`Ten healthy subjects (age 21 – 28 years, nine males and one
`female) with no history of cardiovascular diseases and
`hypertension were included in this study. The experimental
`
`Figure 1. The RR interval (RRI) and PP interval (PPI)
`representing cardiac beat-to-beat interval extracted from
`the simultaneously recorded ECG and PPG signals
`respectively.
`
`protocol was explained to the subjects and written consent
`was obtained. The protocol was approved by the institu-
`tional ethics committee, All India Institute of Medical
`Sciences, New Delhi, India. The experiments were con-
`ducted at Autonomic Function Laboratory, All India
`Institute of Medical Sciences, New Delhi, India. The
`subjects were given a resting period of 15 minutes prior
`to the study.
`
`2.1. Experimental set-up
`
`The photoplethysmograph transducer TSD200 (BIOPAC
`Systems, Inc., CA, USA), a reflectance type sensor pri-
`marily designed for finger attachment, consisted of a
`matched infrared emitter of wavelength 860 + 6 nm and a
`photo diode to detect variation in infrared reflectance
`resulting from blood flow variation. This transducer was
`strapped on to the right middle finger of the subject and
`connected to the PPG amplifier (PPG100C) through a
`shielded cable to record the blood volume pulse (BVP)
`waveform with band-pass cut-off frequencies of 0.05 –
`10 Hz and gain of 100. Disposable Ag-AgCl electrodes
`were used to record standard lead II ECG signal. An
`ECG amplifier (ECG100C) was used to amplify the ECG
`signal with band-pass cut-off frequencies of 0.05 – 35 Hz
`and gain of 1000. The MP 150 (BIOPAC Systems), a
`computer-based data acquisition system with software
`1
`3.8.2, was used to acquire the standard
`AcqKnowledge
`lead II ECG and PPG data simultaneously at a sampling
`rate of 1 kHz. The data were recorded for a duration of
`five minutes under relaxed supine condition. The signal
`processing techniques were implemented offline with
`1
`7.0 (The Mathworks, Natick, MA, USA).
`Matlab
`
`2.2. Data analysis
`
`The recorded ECG and PPG signals were extracted
`separately. The short-term recordings were free of ectopic
`beats, missing data and noise. The R wave peaks of the
`ECG signal were identified and an RR tachogram
`representing heartbeat
`intervals was constructed. The
`following HRV measures were computed from the RR
`tachogram.
`
`1. Time domain HRV measures: mean normal-to-normal
`(NN) interval, mean HR, standard deviation of NN
`interval (SDNN), the square root of the mean squared
`differences of
`successive NN intervals
`(RMSSD),
`standard deviation of differences between adjacent
`NN interval (SDSD), the number of interval differences
`of successive NN intervals greater than 50 ms (NN50)
`and the proportion derived by dividing NN50 by the
`total number of NN intervals (pNN50).
`2. Frequency domain measures:
`total band power,
`normalized very low frequency (VLF), low frequency
`
`J Med Eng Technol Downloaded from informahealthcare.com by University of Guelph on 08/26/13
`
`For personal use only.
`
`2
`
`

`

`Heart rate variability using photoplethysmography
`
`481
`
`(LF) and high frequency (HF) band powers and LF/
`HF ratio.
`3. Poincare´ plot measures: short-term HRV (SD1), long-
`term HRV (SD2) and SD ratio (SD1/SD2).
`
`In frequency domain analysis, the series of RR intervals
`was cubic interpolated and re-sampled at 4 Hz [2], as RR
`intervals were non-uniformly spaced according to the
`heartbeat intervals. The DC component of the HRV signal
`was removed and then the power spectrum was obtained
`using discrete Fourier transform (DFT). The HRV power
`spectrum was divided into three bands: VLF (0.003 –
`0.04 Hz), LF (0.04 – 0.15 Hz) and HF (0.15 – 0.4 Hz) to
`evaluate the sympathetic and parasympathetic activities of
`the ANS [1]. The Poincare´ plot, one of the most accepted
`techniques of nonlinear HRV analysis, is a diagram which
`plots each RR interval against the previous interval. The
`standard deviations of the distances of the HR intervals to
`the lines y¼ x and y¼ 7xþ 2 6 mean (RR intervals) were
`quantified as SD1 and SD2 respectively [16].
`The systolic peaks of the PPG signal were identified and
`a PP tachogram was constructed from the time difference
`between successive systolic peak instances of PPG signal.
`The time domain and frequency domain and Poincare´ plot
`parameters were obtained for PP tachogram by the above
`mentioned procedures used for ECG based HRV analysis.
`The Pearson correlation coefficient was determined to
`correlate the beat-to-beat changes of RR interval and PP
`interval derived from ECG and PPG respectively.
`The absolute difference (actual error) between the values
`of each HRV parameter derived by two methods was
`calculated for each individual. Then, the overall actual
`error for each parameter was calculated as mean + SD
`from the group of 10 subjects. The agreement between two
`methods for every derived HRV parameter was assessed
`using Bland-Altman technique by GraphPad Prism version
`4.00 for Windows (GraphPad Software, USA). Further,
`paired t-test was used to test any significant difference
`between each parameter derived from two methods.
`
`3. Results
`
`Figures 2 – 5 show the HRV parameters derived from ECG
`and PPG based methods for a representative subject (male,
`22 years). A high correlation (0.998) was found between
`beat-to-beat RR intervals and PP intervals (figure 2).
`Figure 3 shows a good match between PP tachogram
`and RR tachogram. Similarly, the HRV power spectrum
`(figure 4) and Poincare´ plot (figure 5) were well matched
`between the two methods.
`For 10 subjects, the mean correlation between RR and
`PP intervals was 0.87 + 0.19 with median of 0.97. Table 1
`shows the various HRV parameters derived by the two
`methods. The mean NN interval derived from PP
`error *0.1 ms
`variability was accurate with actual
`
`Figure 2. The Pearson correlation coefficient between beat-
`to-beat changes of ECG-derived RR intervals and PPG-
`derived PP intervals for a representative male subject of
`age 22.
`
`Figure 3. Comparison of tachograms derived from RR
`intervals (RRI) of ECG signal (top) and PP intervals (PPI)
`of PPG (bottom) represented in figure 1 after cubic
`interpolation at 4 Hz. The PP variability matched RR
`variability all along the time scale.
`
`compared to RR variability. The error analysis also showed
`insignificant differences between all
`the HRV indices
`obtained by the two methods. More over, all the HRV
`parameters showed no significant difference (p 5 0.05)
`between the two methods.
`The degree of agreement between two methods was
`assessed using Bland-Altman analysis (figure 6). The Bland-
`Altman plot showed the mean difference of NN interval,
`LF/HF ratio and SD ratio as 70.02 ms, 70.02 and
`0.02 respectively and their corresponding 95% limits of
`
`J Med Eng Technol Downloaded from informahealthcare.com by University of Guelph on 08/26/13
`
`For personal use only.
`
`3
`
`

`

`482
`
`N. Selvaraj et al.
`
`Figure 4. The comparison of discrete Fourier transform
`based HRV power spectra of RR (top) and PP (bottom)
`tachograms represented in figure 2. The frequency char-
`acteristics of RR and PP tachograms were found to be
`similar.
`
`agreement were 70.41 to 0.38 ms, 70.12 to 0.09 ms and
`70.04 to 0.07 ms, respectively. Similarly, high degree of
`agreement was found for all the parameters derived by two
`methods of HRV analysis.
`
`4. Discussion
`
`The results clearly demonstrate an excellent correspon-
`dence between the HRV parameters derived by ECG and
`PPG based methods. A high correlation was found between
`the beat-to-beat RR interval and PP intervals. This is in
`agreement with Teng and Zhang [9] and Johnson and
`Mendelson [10], who reported similar correlations between
`heart rate intervals derived from ECG and PPG. However,
`the authors did not derive and compare HRV parameters
`from the PPG signal with the ECG method. In the present
`study, a complete HRV analysis as recommended by the
`task force has been performed and the comparison of
`derived HRV measures showed insignificant actual errors
`between the two methods. Further, the Bland-Altman
`technique demonstrated good agreement between the two
`methods.
`The PP intervals were calculated from systolic peak of
`PPG waveform. Teng and Zhang [9] used similar method to
`compute the PP interval. Nitzan et al. [5] and Bolanos et al.
`[12] used end-diastolic point and dicrotic notch, respec-
`tively, of the PPG waveform to compute the pulse period.
`From our point of view, changes in the baseline can
`potentially affect the identification of end-diastolic point
`and dicrotic notch may not be sharply demarcated in all the
`subjects. Therefore, a method based on identification of
`systolic peak is practical and accurate, as shown in the
`results.
`
`Figure 5. The Poincare´ plot of RR intervals (a) and PP
`intervals (b) represented in figure 1. SD1 and SD2 are
`referred to short term and long term HRV respectively.
`
`Table 1. The comparison of time domain, frequency domain
`and Poincare´ plot parameters derived from ECG and PPG for
`group of subjects (n¼ 10) using error analysis.
`
`Parameters
`
`ECG
`
`PPG
`
`Actual error
`
`Time domain
`Mean NN (ms)
`SDNN (ms)
`RMSSD (ms)
`SDSD (ms)
`NN50 (count)
`
`Frequency domain
`LF nu*
`HF nu
`LF/HF ratio
`
`Poincare´ plot
`SD1 (ms)
`SD2 (ms)
`SD ratio
`
`800.0 + 94.7
`52.0 + 15.8
`49.0 + 25.0
`49.1 + 25.0
`45.1 + 24.5
`
`800.0 + 94.7
`52.4 + 15.4
`50.3 + 23.1
`50.4 + 23.1
`46.2 + 24.1
`
`44.72 + 13.17
`55.28 + 13.17
`0.92 + 0.54
`
`44.39 + 12.43
`55.61 + 12.43
`0.90 + 0.51
`
`34.7 + 17.7
`64.4 + 16.3
`0.51 + 0.15
`
`35.6 + 16.4
`64.6 + 16.1
`0.53 + 0.13
`
`*nu—normalized unit; all the values are mean + SD.
`
`0.1 + 0.1
`0.9 + 0.5
`2.4 + 1.4
`2.4 + 1.4
`3.9 + 2.4
`
`1.93 + 2.02
`1.93 + 2.02
`0.04 + 0.04
`
`1.7 + 1.0
`1.1 + 0.8
`0.03 + 0.02
`
`J Med Eng Technol Downloaded from informahealthcare.com by University of Guelph on 08/26/13
`
`For personal use only.
`
`4
`
`

`

`Heart rate variability using photoplethysmography
`
`483
`
`lag time is called the pulse
`tissue. This
`peripheral
`transit time (PTT). The PTT shows beat-to-beat fluctua-
`tions [13 – 15] and thus it can potentially introduce errors in
`the estimation of pulse period and HRV parameters by
`PPG method. The present results show that the errors are
`negligible in all the HRV parameters of the PPG method
`during resting conditions.
`Methods other than ECG and PPG have also been used
`to derive HRV parameters. McKinley et al.
`[17] and
`Giardino et al.
`[18] used the arterial blood pressure
`waveform to compute HRV parameters and found it to be
`reliable. PPG is a simple and highly cost-effective method
`and it is not subjected to electrical interference and drying
`and dropping-off of electrodes. Hence, it can be used for
`long-term recordings with minimal discomfort to patients.
`Apart from HRV estimation, PPG has been shown to be of
`clinical utility in measurement of oxygen saturation, cardiac
`output, arterial compliance, endothelial functions, etc. [19].
`Although the ECG based method is the gold standard for
`estimation of HRV, the PPG based method can also be
`employed for HRV estimation when it is in use for other
`applications with patients as single recording procedure.
`In conclusion, PPG waveforms can easily be recorded
`from finger and digitized to compute reliable estimates of
`HRV. The correspondence between the ECG and PPG
`derived HRV parameters suggests that PPG based method
`can be used for estimation of short term HRV and long term
`monitoring of patients for diagnostic and prognostic
`purposes.
`
`References
`
`[1] Task Force of the European Society of Cardiology and The North
`American Society of Pacing and Electrophysiology, 1996, Heart rate
`variability—Standards of measurement, physiological interpretation
`and clinical use. European Heart Journal, 17, 354 – 381.
`[2] Carvalho, J.L.A., Rocha, A.F., Junqueira, L.F. Jr, Neto, J.S., Santos, I.
`and Nascimento, F.A.O., 2003, A tool for time-frequency analysis of
`heart rate variability. Proceedings of the 25th Annual International Con-
`ference of the IEEE EMBS, Cancun, Mexico, Sept 17 – 21, 2574 – 2577.
`[3] Bernadi, L., Radaelli, A., Solda, P.L., Coats, A.J., Reeder, M.,
`Calciati, A., Garrard, C.S. and Sleight, P., 1996, Autonomic control of
`skin microvessels: assessment by power spectrum of photoplethysmo-
`graphic waves. Clinical Science (London), 90, 345 – 355.
`[4] Murthy, V.S., Ramamoorthy, S., Srinivasan, N., Rajagopal, S. and
`Rao, M.M., 2001, Analysis of photoplethysmographic signals of
`the 23rd Annual EMBS
`cardiovascular patients. Proceedings of
`International Conference, Istanbul, Turkey, Oct 25 – 28, 2204 – 2207.
`[5] Nitzan, M., Babchenko, A., Khanokh, B. and Landau, D., 1998, The
`variability of the photoplethysmographic signal—a potential method
`for the evaluation of the autonomic nervous system. Physiological
`Measurement, 19, 93 – 102.
`[6] Khanokh, B., Slovik, Y., Landau and D., Nitzan, M., 2004,
`Sympathetically induced spontaneous fluctuations of
`the photo-
`plethysmographic signal. Medical & Biological Engineering & Comput-
`ing, 42, 80 – 85.
`[7] Tanaka, G. and Sawada, Y., 2003, Examination of normalized pulse
`volume-blood volume relationship: toward a more valid estimation of
`the finger sympathetic tone. International Journal of Psychophysiology,
`48, 293 – 306.
`
`Figure 6. Bland-Altman agreement analysis between ECG
`and PPG methods showed higher agreement of HRV
`parameters: heart rate interval (a), LF/HF ratio (b) and SD
`ratio (c). Solid lines indicate mean difference and dotted
`lines refer to boundaries of 95% limits of agreement.
`
`The PPG pulse is generated due to contractility of the
`heart and flow of blood from the heart to the peripheral
`tissue. Thus, the PPG waveform lags behind the R wave of
`ECG by a time period required for the mechanical activity
`of the heart and time required for transit of blood to the
`
`J Med Eng Technol Downloaded from informahealthcare.com by University of Guelph on 08/26/13
`
`For personal use only.
`
`5
`
`

`

`484
`
`N. Selvaraj et al.
`
`[8] Gal-on, B., Brown, I. and Nunn, A., 2005, Monitoring and assess-
`ment
`of
`cardiovascular
`regulation
`in
`spinal
`cord
`injured
`patients. Proceedings of
`the IEEE Engineering in Medicine and
`Biology 27th Annual Conference, Shanghai, China, Sept 1 – 4, 6859 –
`6862.
`[9] Teng, X.F. and Zhang, Y.T., 2003, Study on the peak interval
`variability of photoplethysmographic signals. IEEE EMBS Asian –
`Pacific Conference on Biomedical Engineering, Japan, Oct 20 – 22,
`140 – 141.
`[10] Johnston, W. and Mendelson, Y., 2005, Extracting heart rate
`variability from a wearable reflectance pulse oximeter. Proceedings
`of
`the IEEE 31st Annual Northeast Bioengineering Conference,
`Hoboken, NJ, USA, Apr 2 – 3, 157 – 158.
`[11] Selvaraj, N., Santhosh, J. and Anand, S., 2007, Feasibility of
`photoplethysmographic signal for assessment of autonomic response
`using heart rate variability analysis. IFMBE Proceedings (Berlin,
`Heidelberg: Springer), 15, 391 – 395.
`[12] Bolanos, M., Nazeran, H. and Haltiwanger, 2006, Comparison of
`heart rate variability signal features derived from electrocardiography
`and photoplethysmography in healthy individuals. Proceedings of the
`28th IEEE EMBS Annual International Conference, New York, USA,
`Aug 30 – Sept 3, pp. 4289 – 4294.
`
`[13] Drinnan, M.J., Allen, J. and Murray, A., 2001, Relation between heart
`rate and pulse transit time during paced respiration. Physiological
`Measurement, 22, 425 – 432.
`[14] Johansson, A., Ahlstrom, C., Lanne, T. and Ask, P., 2006, Pulse wave
`transit time for monitoring respiration rate. Medical & Biological
`Engineering & Computing, 44, 471 – 478.
`[15] Porta, A., Gasperi, C., Nollo, G., Lucini, D., Pizzinelli, P., Antolini,
`R. and Pagani, M., 2006, Global versus local
`linear beat-to-beat
`analysis of the relationship between arterial pressure and pulse transit
`time during dynamic exercise. Medical & Biological Engineering &
`Computing, 44, 331 – 337.
`[16] Piskorski, J. and Guzik, P., 2005, Filtering Poincare´ plots. Computa-
`tional Methods in Science and Technology, 11, 39 – 48.
`[17] McKinley, P.S., Shapiro, P.A., Bagiella, E., Myers, M.M., Meersman,
`R.E., Grant, I. and Sloan, R.P., 2003, Deriving heart period variability
`from blood pressure waveforms. Journal of Applied Physiology, 95,
`1431 – 1438.
`[18] Giardino, N.D., Lehrer, P.M. and Edelberg, R., 2002, Comparison of
`finger plethysmograph to ECG in the measurement of heart rate
`variability. Psychophysiology, 39, 246 – 253.
`[19] Allen, J., 2007, Photoplethysmography and its application in clinical
`physiological measurement. Physiological Measurement, 28, R1 – R39.
`
`J Med Eng Technol Downloaded from informahealthcare.com by University of Guelph on 08/26/13
`
`For personal use only.
`
`6
`
`

This document is available on Docket Alarm but you must sign up to view it.


Or .

Accessing this document will incur an additional charge of $.

After purchase, you can access this document again without charge.

Accept $ Charge
throbber

Still Working On It

This document is taking longer than usual to download. This can happen if we need to contact the court directly to obtain the document and their servers are running slowly.

Give it another minute or two to complete, and then try the refresh button.

throbber

A few More Minutes ... Still Working

It can take up to 5 minutes for us to download a document if the court servers are running slowly.

Thank you for your continued patience.

This document could not be displayed.

We could not find this document within its docket. Please go back to the docket page and check the link. If that does not work, go back to the docket and refresh it to pull the newest information.

Your account does not support viewing this document.

You need a Paid Account to view this document. Click here to change your account type.

Your account does not support viewing this document.

Set your membership status to view this document.

With a Docket Alarm membership, you'll get a whole lot more, including:

  • Up-to-date information for this case.
  • Email alerts whenever there is an update.
  • Full text search for other cases.
  • Get email alerts whenever a new case matches your search.

Become a Member

One Moment Please

The filing “” is large (MB) and is being downloaded.

Please refresh this page in a few minutes to see if the filing has been downloaded. The filing will also be emailed to you when the download completes.

Your document is on its way!

If you do not receive the document in five minutes, contact support at support@docketalarm.com.

Sealed Document

We are unable to display this document, it may be under a court ordered seal.

If you have proper credentials to access the file, you may proceed directly to the court's system using your government issued username and password.


Access Government Site

We are redirecting you
to a mobile optimized page.





Document Unreadable or Corrupt

Refresh this Document
Go to the Docket

We are unable to display this document.

Refresh this Document
Go to the Docket