| Literature DB >> 32104555 |
Jiang Shao1, Ping Shi1, Sijung Hu2, Yang Liu3, Hongliu Yu1.
Abstract
Continuous blood pressure (BP) monitoring has a significant meaning for the prevention and early diagnosis of cardiovascular disease. However, under different calibration methods, it is difficult to determine which model is better for estimating BP. This study was firstly designed to reveal a better BP estimation model by evaluating and optimizing different BP models under a justified and uniform criterion, i.e., the advanced point-to-point pairing method (PTP). Here, the physical trial in this study caused the BP increase largely. In addition, the PPG and ECG signals were collected while the cuff bps were measured for each subject. The validation was conducted on four popular vascular elasticity (VE) models (MK-EE, L-MK, MK-BH, and dMK-BH) and one representative elastic tube (ET) model, i.e., M-M. The results revealed that the VE models except for L-MK outperformed the ET model. The linear L-MK as a VE model had the largest estimated error, and the nonlinear M-M model had a weaker correlation between the estimated BP and the cuff BP than MK-EE, MK-BH, and dMK-BH models. Further, in contrast to L-MK, the dMK-BH model had the strongest correlation and the smallest difference between the estimated BP and the cuff BP including systolic blood pressure (SBP) and diastolic blood pressure (DBP) than others. In this study, the simple MK-EE model showed the best similarity to the dMK-BH model. There were no significant changes between MK-EE and dMK-BH models. These findings indicated that the nonlinear MK-EE model with low estimated error and simple mathematical expression was a good choice for application in wearable sensor devices for cuff-less BP monitoring compared to others.Entities:
Mesh:
Year: 2020 PMID: 32104555 PMCID: PMC7035551 DOI: 10.1155/2020/1078251
Source DB: PubMed Journal: J Healthc Eng ISSN: 2040-2295 Impact factor: 2.682
Figure 1The relationships between the BP estimation models.
Summary of mathematical models to calculate BP from PAT.
| Models | SBP | DBP | Category and mechanism (linear or nonlinear) | |
|---|---|---|---|---|
| MK-EE [ |
|
| Nonlinear | Vascular elasticity (VE) models |
| L-MK [ |
|
| Linear | |
| MK-BH [ | SBP0 − (2/( | SBP − PP0 | Nonlinear | |
| dMK-BH [ | DBP+PP0 | MBP0+(2/ | Nonlinear | |
| M-M [ |
|
| Nonlinear | Elastic tube (ET) model |
Note. γ denoted a vascular information parameter which might be altered with age and the development of cardiovascular diseases. For the healthy subjects, it was set as 0.031 mm·Hg−1 [9]. PP0=SBP0 − DBP0, MBP0=(1/3)SBP0+(2/3)DBP0. SBP0, DBP0, PP0 could be determined at the beginning of monitoring by calibration using an additional cuff-type BP monitor device (see Subsection 3.2). a, b, a′, b′(i=1, 2, 3); c, c′ were the corresponding function coefficients. i was the subscript, and for their calibration method, see Subsection 3.2.
Figure 2Example of PAT delineation.
Characteristics of the subjects.
| Selection factor | Number |
|---|---|
| Total number (M, F) | 12 (9, 3) |
| Age (years) | 25.3 ± 4.1 |
| Height (cm) | 168.5 ± 7.4 |
| Body mass (kg) | 60.4 ± 9.4 |
| BMI (kg/m2) | 21.2 ± 2.1 |
| SBP (mm·Hg) | 118.37 ± 12.95 |
| DBP (mm·Hg) | 69.40 ± 8.79 |
Figure 3Illustration of the experimental design and the data collection procedure.
Figure 4The advanced PTP method for the BP monitoring system.
The correlations between BPest and BPcuf.
| Models | SBPest vs. SBPcuf | DBPest vs. DBPcuf |
|---|---|---|
| MK-EE |
|
|
| L-MK | 0.5537 | 0.6831 |
| MK-BH | 0.8131 | 0.7653 |
| dMK-BH |
|
|
| M-M | 0.8329 | 0.7350 |
Figure 5Box plots of dispersion degree comparison during different estimation methods in (a), (b) and (c) (d). Box and whisker plots: box, first and third quartiles; horizontal line, median; whiskers, the furthest point that lies no more than 1.5 times the interquartile range from the median. Note: each point represented an independent subject (estimated error). The dotted blue line represented the median value for dMK-BH (the strongest correlation, see Table 3). “††” indicated the BP estimation model with the strongest correlation.
Quantitative comparison of the SSE and RMSE for the subject with the largest BP range.
| Indexes | SBP | DBP | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| MK-EE | L-MK | MK-BH | dMK-BH | M-M | MK-EE | L-MK | MK-BH | dMK-BH | M-M | |
| SSE | 306.51 |
| 890.08 | 283.65 | 798.00 | 262.50 |
| 256.71 | 264.53 | 428.14 |
| RMSE | 3.5737 | 21.628 | 6.0899 | 3.4379 | 5.7663 | 3.3072 | 10.206 | 3.2705 | 3.3200 | 4.2236 |
|
| 22.593 |
| 9.2495 | 951.70 | 16.500 | 27.954 |
| 513.98 | 35.204 | 9.4641 |
Note. CV, a standardized measure of dispersion of a probability distribution or frequency distribution, denoted the coefficient of variation.
Figure 6The five BP-PAT function curves of the subject with the largest BP range: (a) SBP trend in general. (b) SBP trend in the experiment. (c) DBP trend in general. (d) DBP trend in experiment.
The estimated BP errors in different BP models.
| Models | Systolic blood pressure (SBP) | Diastolic blood pressure (DBP) | ||
|---|---|---|---|---|
| Mean ± SD (mm·Hg) | MAD (mm·Hg) | Mean ± SD (mm·Hg) | MAD (mm·Hg) | |
|
|
|
|
|
|
| L-MK |
|
|
|
|
| MK-BH | 0.11 ± 7.53 | 5.48 | −2.10 ± 5.69 | 4.69 |
|
|
|
|
|
|
| M-M | 1.11 ± 7.51 | 5.57 | −0.23 ± 6.47 | 5.13 |
| ANSI/AAMI | |mean| ≤ 5 mm·Hg | ≤7 mm·Hg | |mean| ≤ 5 mm·Hg | ≤7 mm·Hg |
| SP10 standard | |SD| ≤ 8 mm·Hg | |SD| ≤ 8 mm·Hg | ||
Figure 7Scatter plot of differences among the five models. Note: significant differences between different PAT models were identified as follows: p < 0.05, p < 0.01, p < 0.001, and p < 0.0001. “†”indicates the recommended BP estimation model.
Figure 8Sensitivity analysis with regard to γ for the dMK-BH model. Note: the curves with MAD and γ were based on De Boor algorithm [35] to the real-time interpolation for SBP and DBP in all subjects.