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(Hypertension. 2005;46:244.)
© 2005 American Heart Association, Inc.
Fifth International Workshop on Structure and Function of Large Arteries |
From the Department of Internal Medicine, Nephrology Section (F.V., R.V.), Ghent University Hospital; and the Hydraulics Laboratory (P.S., P.V.), Department of Civil Engineering, and the Heymans Institute of Pharmacology (S.H., L.M.V.B.), Ghent University, Ghent, Belgium.
Correspondence to Francis Verbeke, University Hospital Ghent, Department of Internal Medicine, Nephrology Section, De Pintelaan 185, B-9000 Ghent, Belgium. E-mail francis.verbeke{at}UGent.be
| Abstract |
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Key Words: pulse blood pressure blood pressure determination arterial pressure
| Introduction |
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Methods have been developed to measure central blood pressure. One method has been proposed by Kelly and Fitchett.9 It makes use of calibration on pressure waveforms obtained at superficial arteries with applanation tonometry. This method assumes that mean arterial pressure (MAP) minus diastolic blood pressure is constant throughout the large artery tree9 and has been found accurate.10 Alternatively, radial-to-aorta pressure transfer can be used to mathematically transform radial artery (RA) waveforms into central aorta waveforms. A population-based radial-to-aorta transfer function is used in the SphygmoCor device (AtCor Medical Pty Ltd, Sydney, Australia). The advantage of this technique is the ease to perform applanation tonometry at the RA. Although this transfer function has been validated,11 the accuracy of central aortic PP obtained with the SphygmoCor has been largely debated.1219 The debate focused mainly on the validity of the transfer function but ignored a second possible source of error in the advocated SphygmoCor procedure: calibration of the RA wave with brachial instead of radial blood pressure values.
We hypothesize that both the generalized transfer function and the use of BA blood pressure values as surrogate of RA blood pressure contribute to the presumed erroneous assessment of central PP by SphygmoCor. The present study investigates this hypothesis as well as the relative contribution of the 2 procedures. The validated calibration method proposed by Kelly and Fitchett is used as reference method.
| Materials and Methods |
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Measurements and Derived Parameters
BA blood pressure was measured with a validated20 oscillometric device (Omron HEM-705CP; Omron Healthcare Europe), and the mean of the 3 stable (coefficient of variation <5%) consecutive measurements was subsequently used. MAP was estimated from the numeric integral of the BA pressure wave over time measured with applanation tonometry, calibrated with the systolic and diastolic BA blood pressure. PP (PPBA) was defined as the difference between systolic and diastolic blood pressure.
Arterial pressure waves were recorded at the BA, RA, and common CA using applanation tonometry. For both the calibration method and the SphygmoCor, the same applanation tonometer was used (Millar SPT-301B probe; Millar Instruments, Houston, Tex). For the calibration method, a dedicated homemade data acquisition system was used consisting of a hardware set-up (NI SC 2345; National Instruments, Houston, Tex) connected to a personal computer and post-processing software written in Matlab 6.0 (The Mathworks). This device allowed to calculate an average waveform over a defined time period (Figure 2).
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Aortic PP was assessed in several ways: (1) PPAORTF was calculated according to the advocated SphygmoCor procedure, using a population based generalized radial-to-aorta transfer function with RA waveform calibration on BA blood pressure; (2) PPAORTFimp also used the radial-to-aorta transfer function, but RA waveform calibration was performed on RA pressures; and (3) PPAOCTF was obtained from CA waveforms, calibrated on the carotid pressures obtained with the calibration method, and using the carotid-to-aorta transfer function in the SphygmoCor. PPCACAL was used as primary estimate of aortic pressure (reference method) and PPAOCTF as secondary estimate.
PP amplification between different arterial sites was expressed as the absolute difference between PPs at each site and in percent amplification. For example, PP amplification from brachial-to-RA (PPamplBARA) was calculated as follows: absolute PPamplBARA=PPRACALPPBA and in percent PPamplBARA=(PPRACAL/PPBA1)* 100.
Statistics
Demographic data are presented as numbers or means±SD. BlandAltman plots were used to evaluate the agreement between estimates of the same parameter; the mean difference between estimates reflects systematic bias and the SD of the differences [between estimates reflects], the level of agreement.21 Reproducibility was assessed by calculating the coefficients of variation. Differences in PP were examined by paired-samples t tests or Wilcoxon signed ranks tests for normal or not normal distributed variables, respectively. The effect of age, gender, height, body mass index, smoking status, PPamplBARA, MAP, and BA PP on the differences in aortic PP between radial-to-aorta transfer function and reference method was assessed using multiple linear regression analysis. P<0.05 was considered significant. Statistical analysis was performed using SPSS 11.0.1 for Windows (SPSS Inc).
| Results |
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PPAORTF was always lower than the aortic PP obtained with any of the 2 candidate reference methods (PPCACAL, PPAOCTF). The difference with PPCACAL is shown in Figure 3a. The use of brachial instead of RA pressures to calibrate the radial pressure wave resulted in an underestimation of mean arterial pressure by 3.2±1.8 mm Hg. Calibration of the RA wave with RA pressures instead of BA pressures resulted in an increase of estimated central PP from 33.0±6.8 mm Hg (PPAORTF) to 37.1±8.2 mm Hg (PPAORTFimp). At the same time, the difference with the candidate reference methods decreased with 4 mm Hg (9.7 to 5.7 mm Hg when compared with PPCACAL; 7.1 to 3.1 mm Hg when compared with PPAOCTF) but remained statistically significant (Table 2). The difference with PPCACAL is shown in Figure 3b.
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In multiple linear regression analysis, the difference between PPAORTF and PPCACAL appeared to be strongly dependent on PPamplBARA and brachial PP, but not on MAP, age, gender, smoking status, height, or body mass index (Table 3). PPamplBARA and brachial PP together explained 69% of the variation (63% for PPamplBARA) between the 2 methods (adjusted R2=0.69, P<0.001).
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| Discussion |
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In the present study, we identified inadequate calibration caused by centrifugal PP amplification and transfer function effects as major source of bias in the estimation of the central PP using the SphygmoCor when compared with PPCACAL, a validated calibration method.10 Because the primary objective was to verify the accuracy of the SphygmoCor procedure as advocated by the manufacturer, we initially compared the PPAORTF with the PPCACAL, which yielded a systematic underestimation of 9.7±4.6 mm Hg by PPAORTF. This systematic bias is lower than the 19.0 to 24.8 mm Hg observed in studies14,34 comparing the PPAORTF with invasively measured central PP, and supports the view of ORourke et al that a large part of the difference found in these studies was caused by the difference between sphygmomanometer and invasive blood pressure values.17
The present study identified a substantial PP amplification between brachial and RA (average 12%), larger than the carotid-to-brachial PP amplification. Because the SphygmoCor procedure advocates the use of brachial instead of RA pressure to calibrate the radial pressure wave, a substantial error is introduced accounting for
4 mm Hg of underestimation. Because PP amplification may vary considerably, the degree of underestimation by using brachial pressure values as a surrogate for RA pressure is unpredictable. The brachial-to-radial PP amplification largely determined the underestimation of aortic PP (estimated by PPCACAL) by the advocated SpygmoCor procedure (PPAORTF). The level of PP was the only additional but less important determinant of this underestimation.
After calibration of the RA pressure wave with RA pressure obtained with the calibration method (PPRACAL) the difference between PPAORTFimp and PPCACAL decreased to 5.7 mm Hg. The question remains whether this residual difference can be attributed to the transfer function itself. We used the PP at the CA obtained with the calibration method PPCACAL as surrogate for PP in the ascending aorta. The important question is whether PPCACAL is a valid surrogate for aortic PP. Although some authors have shown that the PP in the common CA and in the ascending aorta is identical,30 other studies indicate a small difference.10 In a validation study of the calibration method, CA PP was found on average 1.8±5.2 mm Hg higher than ascending aortic PP.10 Another way of obtaining surrogate aortic PP is to calculate aortic pressure from carotid waveforms via a carotid-to-aorta transfer function (PPAOCTF), presuming that the carotid-to-aorta transfer function is valid. This method shows aortic PP to be 2.6 mm Hg lower than at the CA and reduces the residual underestimation of the aortic pressure to 3.1 mm Hg. Thus, depending on the candidate estimate of aortic PP, the residual underestimation is between 3.1 and 5.7 mm Hg. This residual underestimation of aortic pressure may be caused by the generalized population-based transfer function itself, but is larger than the 0.7±4.2 mm Hg found by Pauca et al in an invasive study11 in anesthetized patients.
The present study shows that depending on the candidate estimate of aortic PP used, the average error from the CA PP as surrogate for aortic PP (ranging between 0 and +2.6 mm Hg) is smaller than the average error (ranging between 3.1 and 5.7 mm Hg) from the improved SphygmoCor procedure using RA pressures. This supports the idea that CA pressure can be used as surrogate for central aortic pressure. A drawback of the calibration method and the improved SphygmoCor method is the need for an additional tonometry at the BA as long as reliable RA pressures from noninvasive devices are not available.
This study had some limitations. First, we did not have invasive blood pressure measurements in the present study. However, simultaneous comparison of invasive pressures at different arterial sites, like in the present study, might pose ethical problems, especially in a healthy population. In addition, the reference method had previously been validated against invasive measurements.10 Second, the calibration and SphygmoCor methods were performed consecutively and during this time blood pressure could have changed. To limit this bias, CAL and SphygmoCor procedures were performed in random order and both procedures were calibrated on the same BA blood pressure values. This procedure is presumed to limit systematic bias but cannot avoid variation between methods.
Perspectives
The use of BA pressure as surrogate for RA pressure in the advocated SphygmoCor procedure is an important source of error and should be avoided. This means a real need for an easy and reliable method to measure RA blood pressure noninvasively. Although oscillometric wrist sphygmomanometers have been developed, they do not provide RA pressures, because they have been calibrated on BA pressures. As long as direct accurate noninvasive measurement of RA pressure is not available, the more complex calibration method by Kelly and Fitchett remains advocated. The underestimation of central aortic PP caused by the radial-to-aorta population-based transfer function itself is much less than previously reported by some authors. However, its validity in different situations has not been fully established. Future research should further validate this and other transfer functions. Progress could be made by automation of the calibration method proposed by Kelly and Fitchett and by developing alternative methods for handheld applanation tonometers to obtain arterial pressure waves at different arterial sites.
Received February 11, 2005; first decision February 28, 2005; accepted April 6, 2005.
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