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Innovative Pulse Monitoring: Exploring Auscultation-Based Diagnostic Technique

Published: 06 February 2025 Publication History

Abstract

Pulse Rate Variability (PRV) refers to the slight variations in the time between each pulse beat. These variations reflect the effect of the autonomic nervous system on the heart rate. This makes PRV a valuable tool to assess cardiovascular health. This study presents an acoustic system using an electret condenser microphone to measure variations in the pulse cycles. The system extracts the signals from the radial artery, having minimal external electronic or interference noise. Signal processing techniques are applied to the acquired waveform to extract useful features. Signals were obtained from two groups of participants – 14 diabetic and 16 healthy age-matched control (AMC) groups, respectively. Various PRV measures were evaluated. It was observed that the PRV indexes of the diabetic group were significantly lower than those of the AMC group. Further acquisition of more data sets could be applied to train a machine learning model to classify and predict the signal waveforms in cardiovascular diseases like diabetes.

1 Introduction

Pulse is generated by the contraction and relaxation of blood vessels during cardiac activity. This causes a dilatation of the vessels, which reflects as a pulse pressure in the upper layer of the skin above the blood vessel.
Electrocardiogram (ECG) is the common way to evaluate the functioning of the heart. It reflects the cardiac functions but is limited to the electrical activity of the heart. Radial pulse wave analysis provides a comprehensive characterisation of cardiovascular function, including changes in the properties of the blood vessels, autonomous nervous system, and respiration. Hence, the utilisation of radial pulse waves serves as an indicator of heart activity. There are various techniques used for signal acquisition, namely tonometry [1]–[3], photoplethysmography (PPG) [4]–[6], ultrasound manometry [7]-[8] and tactile pressure sensors [9]-[10]. These strategies are employed based on the application of the obtained signals. PPG is used to measure blood volume changes, and its measurement is affected by the light intensity of the external environment. Ultrasonic measurement is generally used to measure radial blood flow velocity.
Most of the current methodologies employ piezoelectric sensors, which have certain drawbacks. When the sensor touches the radial artery, it interacts with soft tissues such as tendons and skin tension. The sensor captures the arterial axial tension forces and the muscular radial pulse, which causes skin and soft tissues to deform. This deformation introduces unwanted signals, affecting the accuracy of the pulse measurement [11].
Heart Rate Variability (HRV) results from the impact of the autonomous regulation of the heartbeat. In recent years, Pulse Rate Variability (PRV) has been used as a surrogate for HRV, and studies have shown a high correlation between PRV and HRV when measurements are taken at rest [12]. A non-invasive way to look at cardiac autonomic regulation is to measure the PRV. It facilitates the observation of the cardiorespiratory control system and the evaluation of alterations in the sympathetic and parasympathetic divisions of the autonomic nervous system (ANS). PRV refers to the variation in the time intervals between consecutive pulse beats. It measures the ANS functioning and the interactions between the heart and the brain [13].
The current study presents an electronic system based on an acoustic sensor designed to detect the subtle vibrations at the radial artery and measure the pulse variations during cardiac activity. Additionally, this system addresses the shortcomings of the existing one. Moreover, it focuses on the usability of pulse wave signals to evaluate PRV and its impact on diabetic participants.

2 Materials and Methods

2.1 Pulse auscultation system

The proposed system comprises three main components: the sensing transmitter consisting of acoustic sensors; the signal conditioning unit (noise filter circuits and signal amplification circuits); and the waveform display and storage unit.
The device for capturing pulse signals includes an electret condenser microphone, including a pre-polarized diaphragm. The pulse signal acquisition design uses an electret condenser microphone with a sensitivity of -51 dB ± 4 dB, an impedance of 2.2 k \(\Omega\) and a signal-to-noise ratio (SNR) of 45 dB. Electret microphones exhibit excellent sensitivity and exceptional signal-to-noise ratio, producing remarkable fidelity. The condenser microphone provides enhanced sensitivity with precise output. A 10 k \(\Omega\) pull-up resistor is incorporated to bias the microphone, along with a high-pass filter featuring a cutoff frequency of 0.16 Hz. The high-pass filter comprises a 10 µF DC blocking capacitor and a 100 k \(\Omega\) resistor. Figure 1(a) shows the schematic of the designed circuit, and Figure 1(b) shows the PCB layout diagram. This circuit exhibits low power consumption at 8 mA, allowing for the use of standard batteries as the power supply, hence mitigating interference from conventional 50 Hz/60 Hz AC power. Figure 1(c) shows the measurement site and the setup of the microphone sensor module, circuit assembly, and DC power supply. The initial wrist line serves as the horizontal axis, while the vertical axis is decided by manually sensing the pulse (marked as (a) and (b), respectively in Figure 1(c)).
The input signal is transmitted to the hardware unit, where a filter is developed to remove unwanted signals, primarily noise. The sensor was positioned at the radial artery for signal capture during experimental validation. The specifications of the sensor technology are as follows: Capacitance can be determined if the geometries of the conductors and the dielectric properties of the insulator are known. As sound waves enter the microphone's diaphragm, the separation between the two components alters due to the diaphragm's oscillations. The alteration in distance induces an electric potential that creates a current through resistors, leading to a reduction in voltage. The alteration in the spacing distance between the capacitor plates induces voltage generation. The creation of pulse waves induces vibrations in the form of acoustic waves that penetrate the diaphragm, resulting in alterations in the space between the two plates due to variations and vibrations. The acoustic signals are then set up to be converted to electrical signals later.
Figure 1
Schematic diagram of the circuit consisting primarily of a RC and an amplifier
(a)

PCB layout diagram of the circuit
(b)
Microphone device measurement set-up showing the location on the wrist (radial artery) where the waveform signals are acquired
(c)
Figure 1 (a) Schematic diagram of the circuit (b) PCB layout diagram of the circuit (c) Measurement set-up
ADInstruments’ Power Lab (8/35) digitiser with 16-bit accuracy was used to convert the analog signals into discrete values. The data acquisition system aims to collect, store, and analyse data. The first input signal usually manifests as an analog voltage that undergoes continuous variations in amplitude over time. Signal conditioning involves amplifying and filtering the voltage when it enters the Power Lab via the input connections. The analog voltage is periodically sampled following signal conditioning. The signals were acquired at a sampling frequency of 1kHz. The visualisation and analysis of the acquired signal was done using MATLAB (MathWorks). Once the signal is acquired, preprocessing of the signal is done. A low pass filter of 40 Hz was applied to remove any high-frequency noise from the signal.

2.2 Measurement Methodology

A total of 30 volunteers participated in the study, including 14 diabetic and 16 age-matched control (AMC) participants. The participants were asked to refrain from intense physical activity for a minimum of two hours prior to the measurement. All the participants were asked to relax in a sitting position while maintaining the hand at the level of the heart before recording the pulse. During data acquisition, the participants were requested to maintain a stable and comfortable hand position. Written informed consent was obtained from all the participants before starting the measurements. Pulse waveform data was recorded for each participant over 2 minutes.
Two cohorts of participants were compared utilising distinct PRV measurements. The PRV was assessed using time-domain, frequency-domain, and non-linear metrics to compare the differences between the two groups of participants. Various time-domain measures like Average PP, Median PP, SDPP, RMSSD, where Average PP is the average of the time difference between two successive peaks, median PP is the median of the time difference between two consecutive peaks, SDPP is the measure that represents the standard deviation of all PP intervals over a given period of time. It reflects the total variability in the pulse rate and provides an estimate of the overall PRV. RMSSD calculates the square root of the mean of the squared differences between successive PP intervals. It measures short-term variability and is primarily influenced by parasympathetic (vagal) activity. pPP50 refers to the percentage of successive PP intervals that differ by more than 50 ms. It provides a measure of the short-term variability relative to the total variability. Frequency-domain measures estimating the power spectrum of the PP interval time series, such as very low frequency (VLF) 0.0033-0.04 Hz, low frequency (LF) 0.04-0.15 Hz, and high frequency (HF) 0.15-0.40 Hz, were also measured. Poincare plots were used for non-linear PRV analysis and time and frequency-domain analysis. It shows the beat-to-beat pulse rate change as a scatter plot of each PP interval versus the previous one. It assesses the overall variability and the short-term (SD1) and long-term (SD2) components of PRV, which can provide insights into the autonomic nervous system's regulation of the heart.

3 Results and Discussions

The preliminary data collection involved analysing pulse signals from diabetic and AMC participants. Figure 2 represents one of the signals acquired from each of the AMC groups (Figure 2 (a)) and diabetic groups (Figure 2 (b)). For representation purposes, signals spanning approximately 4 seconds are shown for each of the five pulse cycles. There are noticeable fluctuations in the amplitudes of the pulse waveform, the ascending and descending slopes, and the systolic and diastolic energies during the contraction and relaxation of the heart.
A pulse cycle typically has these sub-waves. Percussion (P), tidal (T), valley (V), and dicrotic (D) sub-waves. A typical pulse cycle should have discrete sub-waves with specified amplitude and length, indicating proper cardiac and physiological activity. The observations regarding the visual patterns are: A pulse cycle of an AMC participant usually has a prominent primary peak (at P-sub-wave) with a lower amplitude than a participant with diabetes, which could indicate increased arterial stiffness or higher blood pressure in people with diabetes. The time to systolic peak in people with diabetes is less than in AMC participants, which may indicate altered early systolic function in diabetics. Also, an AMC participant has two separate secondary peaks
Figure 2
The waveform pattern of an AMC participant showing the features of the radial arterial pulse waveformThe waveform pattern of a diabetic participant showing the difference in features of the radial arterial pulse waveform from a healthy AMC participant
Figure 2 Different patterns demonstrate the potential of rigorous data analysis algorithms to identify different patterns
Table 1:
   AMCDiabeticp-value
Time-domain measuresSDPP (ms)Mean33.417.2<0.001
SD11.06.7
RMSSD (ms)Mean43.422.0<0.001
SD13.28.0
pPP50 (%)Mean17.57.5<0.001
SD16.83.2
Frequency-domain measuresTotal (ms2)Mean1240.0590.9<0.001
SD1055.0355.0
VLF (ms2)Mean308.8183.50.007
SD221.793.8
LF (ms2)Mean327.6172.1<0.001
SD195.697.7
HF (ms2)Mean550.7258.8<0.001
SD223.2147.7
Non-linear measuresSD1 (ms)Mean30.820.70.007
SD16.511.1
SD2 (ms)Mean42.120.9<0.001
SD15.59.9
Table 1: PRV indexes of the AMC and Diabetic group
showing the presence of T, V, and D-sub waves. The pulse cycle of diabetes behaviour does not contain distinct secondary peaks and has many subtle variations beyond secondary peaks. The above results show that the shape or morphology of the arterial pulse is dynamic, varies significantly between participants, and is directly linked to different pathological conditions. There is an observable difference in the patterns of the pulse waveforms acquired from both groups of participants. PRV highlights the significance of fluctuations in the intervals between beats. This can be of more relevance than the overall heart rate or average values.
Independent sample t-tests were performed on these PRV measures using SPSS statistical software. Except for average PP and Median PP, all the other parameters were statistically significant, having p-values <0.05. It was observed that the diabetic group showed significantly lower PRV indexes than the control group, as shown in Table 1.
Time-domain measures:
SDPP (Standard Deviation of Peak-to-Peak Intervals): Significantly higher in AMC (33.4 ms) compared to diabetics (17.2 ms), indicating more significant overall pulse rate variability in the AMC group.
RMSSD (Root Mean Square of Successive Differences): Much higher in AMC (43.4 ms) than in people with diabetes (22.0 ms), suggesting better short-term variability and parasympathetic activity in healthy controls.
pPP50: Considerably higher in AMC (17.5%) than people with diabetes (7.5%), further supporting better beat-to-beat variability in AMC participants.
Frequency-domain measures:
Total power: Substantially higher in AMC (1240.0 ms²) than people with diabetes (590.9 ms²), indicating overall reduced HRV in people with diabetes.
VLF (Very Low Frequency): Higher in AMC (308.8 ms²) compared to people with diabetes (183.5 ms²).
LF (Low Frequency): Notably higher in AMC (327.6 ms²) than in people with diabetes (172.1 ms²), suggesting reduced sympathetic modulation in people with diabetes.
HF (High Frequency): Markedly higher in AMC (550.7 ms²) compared to people with diabetes (258.8 ms²), indicating reduced parasympathetic activity in diabetics.
Non-linear measures:
SD1: Higher in AMC (30.8 ms) than people with diabetes (20.7 ms), indicating better short-term variability in healthy controls.
SD2: Higher in AMC (42.1 ms) than people with diabetes (20.9 ms), suggesting better long-term variability in healthy controls.
This suggests that people with diabetes have reduced overall pulse rate variability, which may indicate autonomic dysfunction - a common complication of diabetes affecting both sympathetic and parasympathetic nervous system functions. The reduced variability in diabetics could be associated with increased cardiovascular risk and other diabetes-related complications.
These differences can also be ascertained by extracting different time and frequency domain features of the waveforms, such as the amplitude and frequency of the waveforms at significant time instances of P, T, V & D subwaves. After extracting such features, these can be applied to the machine learning model to predict the patterns and classify them into diseases. Analysing larger datasets can strengthen the relationships between pulse parameters and diseases. This information can be used for improved disease characterisation and potential diagnosis.

4 Conclusion

This paper introduces a novel pulse auscultation system for capturing and analysing radial pulse data and extracting features that effectively characterise critical aspects of the physiological signal. The pulse waveform reveals distinct patterns corresponding to different disorders, which is evident from the waveform morphology and the corresponding PRV measures. The initial study on the data sets shows that the PRV indexes of the diabetic group are significantly lower than those of the AMC group. The diabetic group shows consistently lower values across all PRV parameters than the AMC group. However, it's important to acknowledge limitations, particularly the small sample size, which may affect the generalisation of the results. Overall, the pulse characteristics (morphology, amplitude, time intervals) hold promise for disease characterisation and classification through machine learning analysis.

Acknowledgments

The research was conducted at the Biomedical Engineering & Technology Innovation Center (BETIC) at IIT Bombay, with financial support from the RG S&T Commission (Mumbai) and the Department of S&T (New Delhi).

References

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            cover image ACM Other conferences
            ICBBE '24: Proceedings of the 2024 11th International Conference on Biomedical and Bioinformatics Engineering
            November 2024
            284 pages
            ISBN:9798400718274
            DOI:10.1145/3707127

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            Association for Computing Machinery

            New York, NY, United States

            Publication History

            Published: 06 February 2025

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            Author Tags

            1. Keywords— Radial pulse
            2. diabetes classification
            3. pulse rate variability
            4. signal processing

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