Open-access Different acquisition systems for heart rate variability analysis may lead to diverse outcomes

Abstract

Heart rate variability (HRV) is a relevant physiological variable for the estimation of cardiac autonomic function. Although the gold standard for HRV registration is the electrocardiogram (ECG), several applications (APPs) have been increasingly developed. The evaluation carried out by these devices must be compatible with ECG standards. The aim of this study was to compare the data obtained simultaneously with ECG and APP with chest heart rate transmitters. Fifty-six healthy individuals (28 men and 28 women) were evaluated at rest through a short simultaneous HRV measurement with both devices. Data from both acquisition systems were analyzed separately using their own analysis software and exported and analyzed using a validated software. Signal recordings were compatible between the two acquisition systems (Pearson r=0.99; P<0.0001). Although a high correlation was found for the HRV variables obtained in the time domain (Spearman r=0.99; P<0.0001), the correlation decreased in the frequency domain (Pearson r=0.85; P<0.0001) when two software programs were used. Comparison of the averages of spectral analysis parameters also showed differences when HRV data were analyzed separately in each device for low-frequency (LF) and high-frequency (HF) bands. Although the portability of these mobile devices allows for optimal HRV evaluation, the direct analysis obtained from these devices must be carefully evaluated with respect to frequency domain parameters.

Heart rate variability; Spectral analyses; ECG


Introduction

Heart rate variability (HRV) reflects oscillation in the intervals between consecutive heartbeats or RR intervals (distance between two successive R-waves) (1). HRV evaluation can provide extensive information regarding the autonomic modulation of cardiac function (2,3). Previous reports have demonstrated that HRV measurements and analysis are valuable tools for risk stratification and may predict the development of cardiovascular diseases (4- 6) and metabolic disorders such as diabetes (7,8) and obesity (9,10). The applicability of HRV evaluation has also been demonstrated in neurology (11), anesthesia, and surgery (12). Furthermore, the use of HRV has expanded into the field of exercise physiology to assess the adaptability of the cardiovascular system to physical activity programs (3,13).

The advantage of being a noninvasive and easy-to-run test has encouraged studies of HRV, its application, and development (14- 16). Since the establishment of guidelines for the use of HRV by the European Society of Cardiology and the North American Society of Electrophysiology (1), this technique has been increasingly applied, with a focus on the standardization of evaluation protocols and determination of reference values for the parameters obtained in the HRV analysis (17,18). Electrocardiogram (ECG) is the gold standard for recording RR intervals for subsequent HRV studies (18). However, owing to innovative technological advances, devices with greater portability, lower cost, easier operation, and increased accessibility have recently emerged as new tools for HRV recordings and analysis (19,20). The use of these devices, such as chest heart rate monitors (HRM), despite optimizing HRV evaluation, raises issues regarding the reliability and accuracy of the generated data. Although the reproducibility of HRV devices has been evaluated in different situations (21- 23), whether their performance is equivalent to the gold standard remains controversial. In some validation studies, mobile devices synchronized with the transmitters are used only for signal acquisition (22,24,25). In these studies, HRV analysis is often performed by an external software. Therefore, the aim of this study was to further highlight the compatibility and reliability of these analyses by comparing HRV data obtained by two different recording methods (chest HRM and ECG) and analyzed using two different softwares. We evaluated the accuracy of signal recording using chest HRM and the reliability of data processing of a smartphone application (APP). Our findings confirmed that chest HRM can be used for recording purposes, but the analysis performed by the APP should be considered with caution, especially with regard to spectral analysis.

Material and Methods

Design and participants

In this cross-sectional study, each participant attended an experimental session to simultaneously record their heart electrical activity using ECG and chest HRM. The study was conducted in accordance with the ethical guidelines of the 1975 Declaration of Helsinki, as reflected in a priori approval by the institutional Ethics and Research Committee of the Federal University of Paraiba, Brazil (Protocol No. 2.303.755). Written informed consent was obtained from all volunteers before their participation. Fifty-nine healthy volunteers aged 18-50 years were recruited. Exclusion criteria were anatomic variations, use of artificial pacemakers, thoracic injuries, or other conditions that would interfere with the correct positioning of the elastic belt or ECG electrodes. The final evaluation included 56 participants (28 men and 28 women).

HRV recordings

HRV measurements were performed at the Human Physiology Laboratory, Department of Physiology and Pathology, Health Sciences Center at the Federal University of Paraiba, Brazil. Initially, age, body mass, height, body mass index (BMI), and systolic and diastolic blood pressures using the auscultatory method were recorded. Participants also answered a short questionnaire regarding their level of physical activity. Recordings were performed during the day, at least 24 h after any physical exercise. All tests were performed with the participant at rest and in the supine position. A short-term recording was carried out for 10 min, and the participant was told to remain silent and breathe normally at tidal volume. The ECG 26T-LTS model (ADinstruments®, Australia) was used, and the recordings were made with the 5-electrode configuration using Labchart® data acquisition software (ADinstruments®, version 8.1.6). The ECG was set to a sampling rate of 1 kHz and a range of 2 mV using a digital filter of 50 Hz (low pass). Simultaneously, a smartphone (iPhone, model 5S, IOS system version 11.3.1, Apple Inc., USA) was used to record the RR intervals on an APP (HRV Expert by Cardiomood®, version 1.6, Russia) through wireless transmission. An elastic belt of adjustable size was positioned comfortably around the participant's chest and a transmission device (Polar® model H7, Polar Electro, Finland; 5 kHz transmission system coded with Owncode®, Polar Electro) was attached on the front at the level of the xiphoid process of the sternum. The RR intervals obtained using Cardiomood® were exported to the manufacturer's web platform and ECG data were exported to Labchart. Both sets of data were also analyzed directly by each systems' programs.

Recordings were made for 10 min. The first 5 min were considered the stabilization period and discarded, and the last 5 min of each recording were used for comparison purposes. Both devices were handled together, and the recordings were performed simultaneously. Data obtained by both systems were separately analyzed on each device's analysis software and exported and analyzed with Kubios HRV standard software version 3.0.2 (Biomedical Signal and Medical Imaging Analysis group, Department of Applied Physics, University of Kuopio, Finland) (Figure 1). In this software, frequency domain analysis was conducted using a fast Fourier transformation (FFT) and threshold medium, and the interpolation of the series was performed by cubic spline. The frequency values were set to 3 hz.

Figure 1
Illustration of the research strategy. Blue flowchart: Division between data acquisition and data processing/analysis process; Grey flowchart: Data acquisition by the attached chest device (heart rate monitors - HRM) with analysis in the mobile phone application (APP); Yellow flowchart: Data acquisition by the coupled electrocardiogram (ECG) with analysis in the ECG software; Green flowchart: Data acquisition by coupled ECG and chest device with analysis with a validated common external/alternative software.

The HRV evaluation included the following parameters in the time domain: standard deviation between the duration of RR intervals (SDNN, ms) and root mean square differences of successive RR intervals (RMSSD, ms). We also evaluated the following variables in the frequency domain: low-frequency band (LF, from 0.04 to 0.15 Hz) and high-frequency band (HF, from 0.15 to 0.40 Hz). The power of each spectral component was calculated using normalized units (nu). Normalization was performed by dividing the power of each band by the total power, from which the very low frequency (VLF, 0.0033-0.04 Hz) band value was subtracted and the result was then multiplied by 100 (26).

Statistical analysis

Data were subjected to the Shapiro-Wilk normality test and then evaluated using Pearson or Spearman correlation tests as appropriate. For mean comparison, the unpaired t-test was used. Geometric means (back-transformed means of the log-transformed data) were calculated for the time domain variables. The agreement between methods for every derived HRV parameter was assessed using Bland-Altman technique (27). Further, paired t-test was used to test significant differences between parameters derived from the two methods. Linear regression analyses were applied to assess biases of proportionality adopting the average values of each software's measures as independent variables and the differences between both measures as dependent variables. Data are reported as means±SD for the profile variables of volunteers and as means and 95% confidence intervals for HRV parameters. The significance level was set at P<0.05.

Results

The general characteristics of the 56 participants are presented in Table 1. The profile of the participants revealed that the study population consisted of young, eutrophic, and normotensive adults. Additionally, most individuals reported doing physical activity (33.8% regularly and 35.4% irregularly), while 30.8% did not perform physical exercises. Notably, data from the two devices were similar. Correlation analysis of the RR intervals showed that the records obtained with the two systems had a high level of correlation (r=0.99, P<0.0001, Figure 2).

Table 1
Characteristics of the healthy individuals (28 men and 28 women) evaluated for heart rate variability simultaneously using smartphone application and electrocardiogram.

Figure 2
Correlation between RR intervals obtained simultaneously during a 5-min period by electrocardiogram (ECG) and by mobile phone application (APP). The data are shown as averages of each interval [number of XY pairs=404]. Pearson's correlation was performed with 95% confidence interval (0.99 to 0.99).

The SDNN values ranged from 23.2 to 95.5 milliseconds and RMSSD values from 14.2 to 116.5 milliseconds. Our findings demonstrated diverse HRV within the population studied. Despite the apparent HRV heterogeneity, the correlation between the simultaneous recordings by the devices was very strong (r=0.99 and P<0.0001). This pattern was maintained when analyses were performed separately in each software, as well as when using a common external software.

The variables in the frequency domain were also studied (Figure 3). As observed for the parameters in the time domain, the average HF and LF bands also maintained a high level of correlation when analyzed using the same software (r=0.99 and P<0.0001). However, when the evaluation was performed separately in each software, considerable dispersion was observed and the correlation levels for both LF and HF decreased (r=0.86 and 0.85, respectively). Inter-device reliability for LF and HF bands was evaluated using Bland-Altman plots (Figure 4) and showed differences in the analysis methods for obtaining these parameters (Table 2). The linear regression results for proportionality bias in absolute differences and average values (LF and HF nu) between APP, ECG, and external analyzes can be viewed in Table 3. The mean values of each variable were compared in addition to the correlation analyses (Table 4). Consistently, a significant difference was found between the parameters in the frequency domain (LF and HF) when the analysis was performed using different softwares. There was no difference between means in the time domain.

Figure 3
Correlation between the frequency domain variables [low and high frequency (LF and HF)] separately calculated by each software [application (APP) and electrocardiogram (ECG)]. Data are reported as means of each registry [n=56]. Pearson's correlation was performed and the 95% confidence intervals were LF=(0.78 to 0.91) and HF=(0.76 to 0.91). nu: normalized units.
Figure 4
Bland-Altman agreement analysis between electrocardiogram (ECG), smartphone application (APP), and external software measurements of the frequency domain bands (low and high frequency - LF and HF). Solid lines indicate average differences and dotted lines refer to 95% limits of agreement (±1.96*SD). nu: normalized units.
Table 2
Parameters analyzed by the Bland-Altman technique.
Table 3
Linear regression for proportionality bias in absolute differences and average values (LF and HF nu) between APP, ECG, and external analyses.
Table 4
Comparison of the heart rate variability parameters obtained separately with a smartphone application (chest HRM) and electrocardiogram (ECG) and analyzed with a common or different analysis software.

Discussion

With the advancement of HRV analysis, different devices have been developed and tested, with portable transmission devices being found to be reliable (28- 30). The HRV analyses of the various applications under development must be tested and proven to be equally reliable. However, the reliability of the records obtained using mobile devices and their potential applicability in clinical evaluation and scientific research remains controversial. In the present study, we compared HRV data obtained using chest HRM with data obtained with the gold standard (ECG). Herein, the signal quality obtained with the chest HRM was found to be reliable, but the data processing by the APP software was not reliable and should be used with caution.

Although the profile of the participants examined in this study revealed that the sample cohort was composed of young, eutrophic, and normotensive adults, our primary aim was not to evaluate the HRV of these participants in relation to their own health status, age, or gender, but instead to compare HRV analyses obtained using two different recording methods, regardless of possible individual differences between participants. Based on the wide spectrum of the obtained HRV recordings, the comparison can be valid for any group of participants with high or low variability. Furthermore, the mean values obtained in this study are in agreement with the reference values of other studies (18,31,32).

The RR intervals and HRV parameters in the time and frequency domains were compared and correlated. First, we evaluated the quality of the signal generated by the chest HRM. This was possible because of a simple strategy: the recordings of RR intervals obtained with each device (chest HRM and ECG) were exported and processed by the same external software, previously validated for HRV analysis (29). The original tachogram obtained using the two different systems showed a high similarity between the tracings over time. Consequently, the correlation between the obtained RR intervals was high. This finding suggested that the recording and signal transmission of RR intervals were equivalent in both acquisition systems. Because the tachogram is a graphical representation of instantaneous RR intervals obtained over time, it can be assumed that both devices detect the same variations between RR intervals. A study using the same chest HRM suggested that the mobile approach could modify the signal during pre-processing (33). Based on the present findings, we believe that the quality of the signal is sufficiently reliable, once a consistent match was found between the data obtained with the two devices when analyzed using the same software (both in time and frequency domains). Of note, the compatibility between data from the two devices was consistent despite the diverse range of individual values for each parameter in the correlation line (indicating various levels of HRV among participants). The records obtained using chest HRM or ECG were equivalent for participants with higher or lower HRV parameters.

The second phase of the study involved data processing using the APP's or the ECG's own analysis software. A decrease in the correlation values of the parameters in the frequency domain (LF and HF) was found between the devices used. A recent comparative study (24) demonstrated excellent compatibility between the smartphone APP and the ECG. In addition, agreement was observed for all parameters in the time domain, frequency domain, and nonlinear indices. However, in that study, the devices were used only as signal recorders and the obtained data were compared a single analysis software. In the current study, we demonstrated that the data obtained by the two methods are only consistent for the time domain parameters (we did not evaluate non-linear parameters). The frequency domain parameters (HF and LF) obtained by the ECG and by the APP, without interference from other programs, showed significant variations. Thus, portability of the APP method was attested only for time-domain analyses and not for frequency-domain analyses.

As expected, a high level of correlation was found between RR intervals and consequently between the parameters in the time domain obtained with the two methods. This compatibility occurred regardless of the software used for analyses (common/single software or obtained by each device's software) because, as mentioned, they are calculated from a set of identical RR intervals. However, the weak correlation between the frequency domain parameters analyzed within each device indicated that data processing for spectral analysis may differ between the devices. Considering the Bland-Altman plot, it can be inferred that there is a difference between the analysis methods (non-concordant models). However, the analyses performed with the external software had a greater similarity. This observation is reinforced by the proximity of the mean plot line to zero on the difference axis, but also by the widening of the limits of agreement when the methods are compared. The Kubios® software (external software used to analyze the data from the ECG and the mobile device) uses Welch's periodogram and provides results analyzed by the autoregressive method. For comparison, the results obtained by Welch's periodogram (FFT spectrum) were used. Welch's periodogram is not suitable for 24-h spectral analysis because it uses an FFT width of 256 s, which does not reflect the HRV of the full period (34). However, in the current study, a short registration period was used, which does not result in any loss in the analysis capacity of this periodogram. The company Labchart® (ECG software) certifies that the software uses the Lomb periodogram for spectral analysis. The Lomb-Scargle periodogram is a spectral estimation technique appropriate for time series with irregular samples using the original data (35), and this signal treatment provides a spectral estimate of HRV with less noise. However, we could not obtain information about the data processing used in the Cardiomood® software. Sometimes, softwares on mobile devices are real “black boxes” and do not provide details about the analysis/parameters used for data processing. Thus, the post-processing signal management may be a cause of disparities, as equivalent HRV signals result in different values for frequency domain parameters (33). This may contribute to the tendency to assign advantages of time-domain parameters over frequency-domain parameters in HRV interpretation (36).

The technological advancement for accessing biomedical signals seems to be a very promising field, and the portability offered by various devices has shown considerable potential. It would be an important development for clinical practice, especially in health systems focused on primary care, if the arsenal of diagnostic tools adapted to mobile applications (thus making assessment more accessible and portable) would have a high and reliable level of accuracy to enable better quality of preventive follow-up at home.

Regarding HRV, our data suggested that the chest HRM and the smartphone APP can acquire the signal correctly compared to the gold standard [ECG]. However, the APP apparently did not reproduce the HRV analysis identically to the ECG in the frequency domain, although it is fully compatible with the variables in the time domain. Considering the conditions under which the measurements were performed and the manner in which the data were processed, chest HRM can be recommended for data recording purposes. The evaluation of variables in the time domain using the APP is compatible with the results obtained using the gold standard and can be viewed as reliable. However, for a more complete analysis of HRV parameters, including the variables in the frequency domain, data processing of RR intervals obtained using chest HRM should be performed by a recognized external HRV analysis software.

Acknowledgments

The authors thank Dr. V.J.B. Martins for the statistical analysis. C.M. Balarini and V.A. Braga received financial support from the National Council for the Development of Science and Technology (CNPq, 429767/2016-1 and 472133/2013-6304718/2011-4, respectively) and Paraiba State Research Foundation (FAPESQ, ID: 007/2019 FAPESQ-PB-MCT/CNPq).

References

  • 1 Camm AJ, Malik M, Bigger J, Breithardt G, Cerutti S, Cohen R, et al. Heart rate variability: standards of measurement, physiological interpretation and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Circulation 1996; 93: 1043-1065, doi: 10.1161/01.CIR.93.5.1043.
    » https://doi.org/10.1161/01.CIR.93.5.1043
  • 2 Lahiri MK, Kannankeril PJ, Goldberger JJ. Assessment of autonomic function in cardiovascular disease. J Am Coll Cardiol 2008; 51: 1725-1733, doi: 10.1016/j.jacc.2008.01.038.
    » https://doi.org/10.1016/j.jacc.2008.01.038
  • 3 Dong JG. The role of heart rate variability in sports physiology. Exp Ther Med 2016; 11: 1531-1536, doi: 10.3892/etm.2016.3104.
    » https://doi.org/10.3892/etm.2016.3104
  • 4 Terathongkum S, Pickler RH. Relationships among heart rate variability, hypertension, and relaxation techniques. J Vasc Nurs 2004; 22: 78-82, doi: 10.1016/j.jvn.2004.06.003.
    » https://doi.org/10.1016/j.jvn.2004.06.003
  • 5 Karas M, Larochelle P, LeBlanc RA, Dubé B, Nadeau R, de Champlain J. Attenuation of autonomic nervous system functions in hypertensive patients at rest and during orthostatic stimulation. J Clin Hypertens (Greenwich) 2008; 10: 97-104, doi: 10.1111/j.1751-7176.2008.07324.x.
    » https://doi.org/10.1111/j.1751-7176.2008.07324.x
  • 6 Melillo P, Izzo R, Orrico A, Scala P, Attanasio M, Mirra M, et al. Automatic prediction of cardiovascular and cerebrovascular events using heart rate variability analysis. PloS One 2015; 10: e0118504, doi: 10.1371/journal.pone.0118504.
    » https://doi.org/10.1371/journal.pone.0118504
  • 7 Carnethon MR, Golden SH, Folsom AR, Haskell W, Liao D. Prospective investigation of autonomic nervous system function and the development of type 2 diabetes: the atherosclerosis risk in communities. Circulation 2003; 107: 2190-2195, doi: 10.1161/01.CIR.0000066324.74807.95.
    » https://doi.org/10.1161/01.CIR.0000066324.74807.95
  • 8 Anaruma CP, Ferreira Jr M, Sponton CH, Delbin MA, Zanesco A. Heart rate variability and plasma biomarkers in patients with type 1 diabetes mellitus: effect of a bout of aerobic exercise. Diabetes Res Clin Pract 2016; 111: 19-27, doi: 10.1016/j.diabres.2015.10.025.
    » https://doi.org/10.1016/j.diabres.2015.10.025
  • 9 Molfino A, Fiorentini A, Tubani L, Martuscelli M, Fanelli FR, Laviano A. Body mass index is related to autonomic nervous system activity as measured by heart rate variability. Eur J Clin Nutr 2009; 63: 1263-1265, doi: 10.1038/ejcn.2009.35.
    » https://doi.org/10.1038/ejcn.2009.35
  • 10 Rodríguez‐Colón SM, Bixler EO, Li X, Vgontzas AN, Liao D. Obesity is associated with impaired cardiac autonomic modulation in children. Int J Pediatr Obes 2011; 6: 128-134, doi: 10.3109/17477166.2010.490265.
    » https://doi.org/10.3109/17477166.2010.490265
  • 11 Sharif H, Millar PJ, Incognito AV, Ditor DS. Non-invasive electrocardiographic assessments of cardiac autonomic modulation in individuals with spinal cord injury. Spinal Cord 2016; 54: 166-171, doi: 10.1038/sc.2015.207.
    » https://doi.org/10.1038/sc.2015.207
  • 12 Naraghi L, Peev MP, Esteve R, Chang Y, Berger DL, Thayer SP, et al. The influence of anesthesia on heart rate complexity during elective and urgent surgery in 128 patients. J Crit Care 2015; 30: 145-149, doi: 10.1016/j.jcrc.2014.08.008.
    » https://doi.org/10.1016/j.jcrc.2014.08.008
  • 13 da Silva CC, Pereira LM, Cardoso JR, Moore JP, Nakamura FY. The effect of physical training on heart rate variability in healthy children: a systematic review with meta-analysis. Pediatr Exerc Sci 2014; 26: 147-158, doi: 10.1123/pes.2013-0063.
    » https://doi.org/10.1123/pes.2013-0063
  • 14 Buccelletti E, Gilardi E, Scaini E, Galiuto L, Persiani R, Biondi A, et al. Heart rate variability and myocardial infarction: systematic literature review and metanalysis. Eur Rev Med Pharmacol Sci 2009; 13: 299-307.
  • 15 Tannus LR, Sperandei S, Montenegro Jr RM, Carvalho VR, Pedrosa HC, Félix MT, et al. Reproducibility of methods used for the assessment of autonomous nervous system's function. Auton Neurosci 2013; 177: 275-279, doi: 10.1016/j.autneu.2013.05.444.
    » https://doi.org/10.1016/j.autneu.2013.05.444
  • 16 Makovac E, Thayer JF, Ottaviani C. A meta-analysis of non-invasive brain stimulation and autonomic functioning: implications for brain-heart pathways to cardiovascular disease. Neurosci Biobehav Rev 2017; 74: 330-341, doi: 10.1016/j.neubiorev.2016.05.001.
    » https://doi.org/10.1016/j.neubiorev.2016.05.001
  • 17 Antelmi I, de Paula RS, Shinzato AR, Peres CA, Mansur AJ, Grupi CJ. Influence of age, gender, body mass index, and functional capacity on heart rate variability in a cohort of subjects without heart disease. Am J Cardiol 2004; 93: 381-385, doi: 10.1016/j.amjcard.2003.09.065.
    » https://doi.org/10.1016/j.amjcard.2003.09.065
  • 18 Sammito S, Böckelmann I. Reference values for time-and frequency-domain heart rate variability measures. Heart Rhythm 2016; 13: 1309-1316, doi: 10.1016/j.hrthm.2016.02.006.
    » https://doi.org/10.1016/j.hrthm.2016.02.006
  • 19 Radespiel-Tröger M, Rauh R, Mahlke C, Gottschalk T, Mück-Weymann M. Agreement of two different methods for measurement of heart rate variability. Clin Auton Res 2003; 13: 99-102, doi: 10.1007/s10286-003-0085-7.
    » https://doi.org/10.1007/s10286-003-0085-7
  • 20 Plews DJ, Scott B, Altini M, Wood M, Kilding AE, Laursen PB. Comparison of heart rate variability recording with smart phone photoplethysmographic, polar H7 chest strap and electrocardiogram methods. Int J Sports Physiol Perform 2017; 12: 1324-1328, doi: 10.1123/ijspp.2016-0668.
    » https://doi.org/10.1123/ijspp.2016-0668
  • 21 Naranjo-Hernandez D, Roa LM, Reina-Tosina J, Barbarov-Rostan G, Galdamez-Cruz O. Smart device for the determination of heart rate variability in real time. J Sensors 2017; 2017.
  • 22 Braga LM, Prado GF, Umeda IIK, Kawauchi TS, Taboada AMF, Azevedo RS, et al. Reproducibility for heart rate variability analysis during 6-min walk test in patients with heart failure and agreement between devices. PLoS One 2016; 11: e0167407, doi: 10.1371/journal.pone.0167407.
    » https://doi.org/10.1371/journal.pone.0167407
  • 23 Flatt AA, Esco MR. Validity of the ithlete (TM) smart phone application for determining ultra-short-term heart rate variability. J Hum Kinet 2013; 39: 85-92, doi: 10.2478/hukin-2013-0071.
    » https://doi.org/10.2478/hukin-2013-0071
  • 24 Pereira RA, Alves JLB, Silva JHC, Costa MS, Silva AS. Validity of a smartphone application and chest strap for recording RR intervals at rest in athletes. Int J Sports Physiol Perform 2020; 15: 896-899, doi: 10.1123/ijspp.2019-0406.
    » https://doi.org/10.1123/ijspp.2019-0406
  • 25 Chen YS, Lu WA, Pagaduan JC, Kuo CD. A novel smartphone app for the measurement of ultra-short-term and short-term heart rate variability: validity and reliability study. JMIR Mhealth UHhealth 2020; 8: e18761, doi: 10.2196/18761.
    » https://doi.org/10.2196/18761
  • 26 Achten J, Jeukendrup AE. Heart rate monitoring. Sports Med 2003; 33: 517-538, doi: 10.2165/00007256-200333070-00004.
    » https://doi.org/10.2165/00007256-200333070-00004
  • 27 Bland JM, Altman D. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986; 327: 307-310, doi: 10.1016/S0140-6736(86)90837-8.
    » https://doi.org/10.1016/S0140-6736(86)90837-8
  • 28 Ventola CL. Mobile devices and apps for health care professionals: uses and benefits. P T 2014; 39: 356-364.
  • 29 Tarvainen MP, Niskanen JP, Lipponen JA, Ranta-aho PO, Karjalainen PA. Kubios HRV - Heart rate variability analysis software. Comput Methods Programs Biomed 2014; 113: 210-220, doi: 10.1016/j.cmpb.2013.07.024.
    » https://doi.org/10.1016/j.cmpb.2013.07.024
  • 30 Hernando D, Garatachea N, Almeida R, Casajús JA, Bailón R. Validation of heart rate monitor polar RS800 for heart rate variability analysis during exercise. J Strength Cond Res 2018; 32: 716-725, doi: 10.1519/JSC.0000000000001662.
    » https://doi.org/10.1519/JSC.0000000000001662
  • 31 Corrales MM, Torres BC, Esquivel AG, Salazar MAG, Orellana JN. Normal values of heart rate variability at rest in a young, healthy and active Mexican population. Health 2012; 4: 377, doi: 10.4236/health.2012.47060.
    » https://doi.org/10.4236/health.2012.47060
  • 32 Koenig J, Thayer JF. Sex differences in healthy human heart rate variability: a meta-analysis. Neurosci Biobehav Rev 2016; 64: 288-310, doi: 10.1016/j.neubiorev.2016.03.007.
    » https://doi.org/10.1016/j.neubiorev.2016.03.007
  • 33 Guzik P, Piskorski J, Krauze T, Schneider R, Wesseling KH, Wykretowicz A, et al. Correlations between the Poincare plot and conventional heart rate variability parameters assessed during paced breathing. J Physiol Sci 2007; 57: 63-71, doi: 10.2170/physiolsci.RP005506.
    » https://doi.org/10.2170/physiolsci.RP005506
  • 34 Bauer A, Camm AJ, Cerutti S, Guzik P, Huikuri H, Lombardi F, et al. Reference values of heart rate variability. Heart Rhythm 2017; 14: 302-303, doi: 10.1016/j.hrthm.2016.12.015.
    » https://doi.org/10.1016/j.hrthm.2016.12.015
  • 35 Clifford GD, Tarassenko L. Quantifying errors in spectral estimates of HRV due to beat replacement and resampling. IEEE Trans Biomed Eng 2005; 52: 630-638, doi: 10.1109/TBME.2005.844028.
    » https://doi.org/10.1109/TBME.2005.844028
  • 36 Kuss O, Schumann B, Kluttig A, Greiser KH, Haerting J. Time domain parameters can be estimated with less statistical error than frequency domain parameters in the analysis of heart rate variability. J Electrocardiol 2008; 41: 287-291, doi: 10.1016/j.jelectrocard.2008.02.014.
    » https://doi.org/10.1016/j.jelectrocard.2008.02.014

Publication Dates

  • Publication in this collection
    04 Feb 2022
  • Date of issue
    2022

History

  • Received
    23 July 2021
  • Accepted
    26 Nov 2021
location_on
Associação Brasileira de Divulgação Científica Av. Bandeirantes, 3900, Cep: 14049-900 , Tel: +55 16 3630-2778, +55 16 3315-3173 - Ribeirão Preto - SP - Brazil
E-mail: bjournal@terra.com.br
rss_feed Acompanhe os números deste periódico no seu leitor de RSS
Acessibilidade / Reportar erro