Skip to main content

A novel approach to determine aortic valve area with phase-contrast cardiovascular magnetic resonance

Abstract

Background

Transthoracic echocardiography (TTE) is the diagnostic routine standard for assessing aortic stenosis (AS). However, its inaccuracies in determining stroke volume (SV) and aortic valve area (AVA) call for a more precise and dependable method. Phase-contrast cardiovascular magnetic resonance imaging (PC-CMR) is a promising tool to push these boundaries. Thus, the aim of this study was to validate a novel approach based on PC-CMR against the gold-standard of invasive determination of AVA in AS compared to TTE.

Methods

A total of 50 patients with moderate or severe AS underwent TTE, cardiac catheterization and CMR. AVA via PC-CMR was determined by plotting momentary flow across the valve against flow-velocity. SV by CMR was measured directly via PC-CMR and volumetrically using cine-images. Invasive SV and AVA were determined via Fick-principle and Gorlin-formula, respectively. TTE yielded SV and AVA using continuity equation. Gradients were calculated via the modified Bernoulli-equation.

Results

SV by PC-CMR (85 ± 31 ml) correlated strongly (r: 0.73, p < 0.001) with cine-CMR (85 ± 19 ml) without significant bias (lower and upper limits of agreement (LLoA and ULoA): − 41 ml and 44 ml, p = 0.83). In PC-CMR, mean pressure gradient correlated significantly with invasive determination (r: 0.36, p = 0.011). Mean AVA, as determined by PC-CMR during systole (0.78 ± 0.25 cm2), correlated moderately (r: 0.54, p < 0.001) with invasive AVA (0.70 ± 0.23 cm2), resulting in a small bias of 0.08 cm2 (LLoA and ULoA: − 0.36 cm2 and 0.55 cm2, p = 0.017). Inter-methodically, AVA by TTE (0.81 ± 0.23 cm2) compared to invasive determination showed similar correlations (r: 0.58, p < 0.001 with a bias of 0.11 cm2, LLoA and ULoA: − 0.30 and 0.52, p < 0.001) to PC-CMR. Intra- and interobserver reproducibility were excellent for AVA (intraclass-correlation-coefficients of 0.939 and 0.827, respectively).

Conclusions

Our novel approach using continuous determination of flow-volumes and velocities with PC-CMR enables simple AVA measurement with no bias to invasive assessment. This approach highlights non-invasive AS grading through CMR, especially when TTE findings are inconclusive.

Background

Aortic stenosis (AS) is regarded the most common valvular heart disease in the Western world, with an estimated prevalence of 3% in patients aged ≥ 75 years [1]. Its hemodynamic severity is best characterized by the transaortic maximum velocity, when transaortic volume flow-rates are normal. However, in patients with low transvalvular flow-rates due to either left ventricular (LV) systolic dysfunction or due to a small hypertrophied LV, diagnostic and management challenges differ from AS patients with high gradient and velocity [2]. Although cardiac catheterization with invasive hemodynamic evaluation was historically the gold-standard for diagnosis of severe valvular heart disease [3], nowadays, due to the risks of invasive measurement and advances in noninvasive methods, transthoracic echocardiography (TTE) is considered the first-choice imaging modality to diagnose and classify AS [4]. However, in recent years, cardiovascular magnetic resonance imaging (CMR) has emerged to be a useful tool in characterizing valvular heart disease, and a good and reliable alternative to invasive techniques such as cardiac catheterization and transesophageal echocardiography (TEE) [5]. The equivalence of valve area measurements in TEE and CMR has recently been shown in a meta-analysis by Woldendorp et al., providing aortic valve area (AVA) measurements with virtually no bias [6]. Compared to TTE, most studies showed a slight overestimation of both AVA and stroke volume index (SVI) using CMR, but stated good correlation and concordance [7,8,9]. Regarding prognostic and therapeutic impact, precise grading of AS severity is absolutely necessary. However, CMR and especially phase-contrast-CMR (PC-CMR) are still used far below their capabilities in AS, and comparison to cardiac catheterization is still lacking. As one main application field of PC-CMR lies in the quantification of flow-volumes and flow-velocities, we deduced that AVA values could be directly determined by calculating the ratio of these two parameters. Thus, determination of AVA would be possible at each moment of the cardiac cycle. Nevertheless, a comparable formula has not yet been assessed in AS, just like PC-CMR studies in AS are still scarce goods. The aims of our study were, therefore, as follows: (1) to compare stroke volumes (SV) as determined by PC-CMR to the ‘gold-standard’ cine-CMR; (2) to determine pressure gradients across the aortic valve (AV) via PC-CMR; and (3) to validate a novel approach of determining AVA by comparing it to the ‘gold-standard’ cardiac catheterization (Fig. 1).

Fig. 1
figure 1

Several approaches to determine aortic valve area, with phase-contrast-cardiovascular magnetic resonance (CMR) yielding solid values comparable to invasive measurement. (Illustration created using biorender.com)

Methods

Study population

The study population consisted of 50 consecutive patients with moderate (n = 6) or severe (n = 44) AS that were referred for further investigation; a flowchart of participant in- and exclusion is shown in Fig. 2. Patients were enrolled in a prospective clinical research study at the University Clinic for Cardiology and Angiology Innsbruck, Austria. All patients underwent cardiac catheterization, TTE and CMR. Twenty-four patients had low-flow states as determined by TTE. We excluded patients younger than 18 years of age and those with arrhythmias during CMR scans, contraindications for cardiac catheterization or CMR and patients with prior rheumatic or infectious heart disease. Prior to study inclusion, written informed consent was given by all participants. The study was designed and conducted in compliance with the Declaration of Helsinki and received approval by the local research ethics committee.

Fig. 2
figure 2

Flowchart of included and excluded participants. CMR cardiovascular magnetic resonance imaging, PC-CMR phase-contrast CMR, TTE transthoracic echocardiography

Cardiovascular magnetic resonance

All CMR scans were performed on a 1.5 T clinical CMR scanner (MAGNETOM Avantofit; Siemens Healthineers AG, Erlangen, Germany) 16 days (IQR 1–30) after cardiac catheterization. High-resolution cine-images in long- and short axis covering the LV (10–12 slices) were acquired using a balanced steady state free precession (bSSFP) sequence with retrospective electrocardiographic (ECG) gating (slice thickness: 8 mm, interslice gap: 2 mm, echo time: 1.19 ms, repetition time: 2.83 ms, 22 lines per segments, temporal frame duration: 62.26 ms, frame rate: 25 frames per second, flip angle: 70°, field of view: 380 × 310 mm, matrix: 320 × 260, voxel size: 2.6 × 1.8 × 8.0 mm3, parallel imaging mode: GRAPPA (generalized autocalibrating partial parallel acquisition) with acceleration factor 2). To quantify blood flow across the aortic valve via PC-CMR, a modified free-breathing, velocity-encoded phase-contrast-protocol with a spatial resolution of 1.3 × 1.3 × 8 mm was applied without through-plane correction for cardiac motion. Velocity encoding ranged from 300 to 800 cm/s, with 500 cm/s being used most often (n = 25). Retrospective ECG-triggering with 20 (n = 1), 50 (n = 42) or 128 (n = 7) phases per cardiac cycle was applied. Repetition time was 13.56 ms, echo time was 2.62 ms. The mean heart rate (HR) during PC-CMR measurements was 68 ± 13 beats per minute, resulting in a mean reconstructed temporal resolution of 17 ms. One (n = 11), two (n = 2), three (n = 16) or five (n = 21) slices were set perpendicular to the aortic root to measure through-plane flow.

cvi42 software (Circle Cardiovascular Imaging, Calgary, Alberta, Canada) was used for post-processing analyses with semi-automatic detection of LV endo- and epicardial borders. Papillary muscles were excluded from LV myocardial mass (LVM) and included in the LV volume. Myocardial mass, end-diastolic volume (EDV) and end-systolic volume (ESV) were then divided by the body surface area (BSA) [m2] to obtain indexed values (LVMI, EDVI and ESVI, respectively). To calculate BSA, the Du Bois formula was used [10]. In 4 patients, the obtained cine-image stacks were not suitable for volumetric measurements.

If available, for our PC-CMR measurements, the uppermost layer that still included the AV during systole was used, which was chosen in synopsis with three-chamber cine-stacks, shown in Fig. 3.

Fig. 3
figure 3

Cine-3-Chamber CMR (left end-diastolic, right end-systolic) and phase-contrast-CMR (end-systolic, middle) in the displayed layer of the aortic valve of a patient with severe aortic stenosis

Using cvi42 software (Circle Cardiovascular Imaging), we computed the momentary flow-volume rate and momentary peak velocity at each measuring point (Fig. 4); measuring range for peak velocity was defined as the single “fastest” pixel without using neighbouring pixels. Contours of the AV orifice area were drawn manually on all images of the chosen slice, and flow [ml/s] throughout the cardiac cycle was measured using velocity values of the corresponding velocity-encoded images. LV-SV was defined as forward blood flow through the AV over the cardiac cycle minus reverse blood flow in the same layer. HR was determined from the mean RR interval of cine-stacks and PC-CMR, respectively. SVI was calculated by dividing SV by BSA. In 12 patients (24%), a phase unwrapping algorithm was used to salvage datasets with obvious velocity aliasing.

Fig. 4
figure 4

Calculation of aortic valve area (AVA) with simultaneous measurement of flow-volumes and flow-velocities across the aortic valve. According to the formula given above AVA can be calculated continuously over the whole cardiac cycle.The graph shows an example of 50 phases across the cardiac cycle of a patient with a mean AVA of 0.92 cm2 and a stroke volume of 44 ml by PC-CMR. AVA aortic valve area, PC-CMR phase-contrast cardiovascular magnetic resonance imaging

Pressure gradients were calculated according to the modified Bernoulli-equation [11]; for mean pressure gradient (MPG), mean velocity over the whole systolic phase was used; for peak pressure gradient (PPG), the peak velocity was used.

In PC-CMR, AVA was calculated according to Eq. 1, in order to obtain a momentary AVA for every moment of the cardiac cycle. Finally, AVA during systole was calculated as mean AVA over the whole systolic cycle.

$${{AVA}}\left( {{{cm}}^{2} } \right) = {\raise0.7ex\hbox{${{{Flow}}\;{{Rate}}\left( {\frac{{{{ml}}}}{{{s}}}} \right)}$} \!\mathord{\left/ {\vphantom {{{{Flow}}\;{{Rate}}\left( {\frac{{{{ml}}}}{{{s}}}} \right)} {{{Peak}}\;{{Velocity}}\left( {\frac{{{{cm}}}}{{{s}}}} \right)}}}\right.\kern-\nulldelimiterspace} \!\lower0.7ex\hbox{${{{Peak}}\;{{Velocity}}\left( {\frac{{{{cm}}}}{{{s}}}} \right)}$}}$$
(1)

To perform planimetry of the AVA, three cine images were acquired orthogonal to the aortic root (slice thickness: 5 mm, no interslice gap). The slice, which exactly recorded the valve opening was used for planimetry of the anatomical AVA.

Additionally, we used the Hakki-formula to compute AVA. This equation represents a simplified version of the Gorlin-formula, calculated as the ratio of cardiac output (CO) and the square root of MPG [12, 13].

Echocardiography

All patients underwent a comprehensive TTE examination in our tertiary echo lab, including assessment of the AV by measuring SV, pressure gradients and AVA via the continuity equation and LV ejection fraction (LVEF) by the Simpson method. Patients were then divided into two groups according to their flow status—group 1 had low-flow states with a SVI ≤ 35 ml/m2, group 2 had normal-flow states with a SVI > 35 ml/m2.

Cardiac catheterization

All patients were referred to left and right heart catheterization. A 7-French Swan-Ganz-catheter was routinely used for hemodynamic measurements. LV end-systolic and end-diastolic pressures were recorded. CO was determined according to Fick principle [14], SV was calculated according to Eq. 2.

$$SV \left({\rm ml}\right)=\left. Cardiac Output \left(\frac{l}{\mathrm{min}}\right) \right/ heart rate \left(\frac{1}{\mathrm{min}}\right)*1000$$
(2)

Indexing SV by the BSA yielded SVI. AV gradients were assessed by simultaneous measurement of LV and aortic pressures by a double-lumen-catheter placed in the LV and the aortic root. Invasive MPG was calculated via the area under these pressure curves and the peak‐to‐peak gradient pressure by the difference between LV end-systolic and systolic arterial pressure. Systolic and diastolic arterial pressure were measured invasively. AVA was then calculated using the Gorlin-formula (Eq. 3).

$$AVA\left( {cm^{2} } \right) = \frac{{{{\left( {Cardiac\;Output \left( {\frac{l}{\min }} \right)*1000} \right)} \mathord{\left/ {\vphantom {{\left( {Cardiac\;Output \left( {\frac{l}{\min }} \right)*1000} \right)} {\left( {systolic ejection period \left( \frac{s}{beat} \right)*heart rate\left( {\frac{1}{\min }} \right)} \right)}}} \right. \kern-\nulldelimiterspace} {\left( {systolic ejection period \left( \frac{s}{beat} \right)*heart rate\left( {\frac{1}{\min }} \right)} \right)}}}}{{44.5*\sqrt {mean pressure gradient \left( {mmHg} \right)} }}$$
(3)

In a small subgroup of 17 patients, SV and AVA were additionally determined via thermodilution. None of our patients underwent AV intervention during the study period.

Statistical analysis

SPSS (version 26.0; Statistical Package for the Social Sciences, International Business Machines, Inc., Armonk, New York, USA) was used for statistical analyses. Kolmogorov–Smirnov-test was applied to test for normal distribution. All results for continuous variables are expressed as means ± standard deviation (SD) if normal distribution was given, or as medians with interquartile range if not. A p-value < 0.05 was considered as statistically significant. To evaluate the agreement between two methods, Pearson correlation as well as Bland–Altman analysis were used; limits of agreement (LoA) were defined as mean difference plus (upper LoA, ULoA) or minus (lower LoA, LLoA) 1.96 × SD. Bias was defined as mean difference between methods. Pearson’s correlation was interpreted as negligible (< 0.2), low (0.2–0.39), moderate (0.4–0.59), strong (0.6–0.79) and very strong (≥ 0.8) [15]. Receiver operating characteristic (ROC) analysis was performed to assess the discriminative power of CMR in discriminating between moderate and severe AS. Area under the curve (AUC) values were interpreted according to Rice and Harris [16]. Dichotomization of AVA via CMR was performed by using the Youden-index and, regarding its impact on therapeutic decision-making, the cut-off with highest specificity was used. Intra- and interobserver variability were evaluated by two observers blinded to each other’s results in all study participants, using a two-way mixed-effects model with intraclass correlation coefficients (ICC).

Results

Baseline patient characteristics

Mean age of the overall cohort was 71 ± 9 years, 42% (n = 21) were female. All patients underwent CMR 28 days (IQR 15–62) after TTE and 16 days (IQR 1–31) after cardiac catheterization. During these intervals, no patient showed clinical signs of deterioration or complained of an increase in symptom intensity or frequency. In 5 patients (10%), blood pressure medication was initiated or adapted before CMR was performed. Thirty-one patients (62%) had tricuspid AV, 19 (38%) had bicuspid AV. Thirty patients (60%) had aortic regurgitation in TTE, of whom 19 had first-degree and 11 had second-degree regurgitation. The baseline patient characteristics are summarized in Table 1. Patients were then split into two groups according to their flow state in TTE (group 1 with low-flow, n = 24; group 2 with normal-flow, n = 26). Results of echocardiography, cardiac catheterization and CMR according to different flow states are displayed in Table 2. AVA measures by the respective modality are shown in Fig. 5 according to flow and gradient states. Key results of correlation values and intermethodical biases are listed in the following paragraphs, details are listed in Table 3, corresponding Bland–Altman plots are shown in the Additional file 1.

Table 1 Baseline patient characteristics
Table 2 TTE, invasive and CMR measurements
Fig. 5
figure 5

AVA by the respective modality classified according to flow and gradient states. Panel A AVA by TTE. Panel B Invasive AVA. Panel C AVA by PC-CMR. AVA aortic valve area, HG high gradient, LF low-flow, LG low gradient, NF normal-flow, PC-CMR phase-contrast-cardiovascular magnetic resonance, TTE transthoracic echocardiography

Table 3 Correlation values and intermethodical biases

Stroke volume

SV by PC-CMR (85 ± 31 ml) correlated strongly with volumetric measurements in cine-images (85 ± 19 ml; r: 0.73, p < 0.001) and with invasive determination according to Fick principle (57 ± 13 ml; r: 0.70, p < 0.001). Scatter plot and Bland–Altman-analysis are shown in Fig. 6, panel A.

Fig. 6
figure 6

Panel A Scatter plot and Bland–Altman-diagram of SVI via cine-CMR and PC-CMR. Panel B Scatter plot and Bland–Altman-diagram of AVA invasively and via PC-CMR. AVA aortic valve area, CMR cardiovascular magnetic resonance imaging, PC-CMR phase-contrast-cardiovascular magnetic resonance imaging, SVI stroke volume index

In TTE, SV had moderate correlation to cine-volumetry (r: 0.50, p < 0.001) and to invasive data (r: 0.48, p = 0.001) according to continuity equation (71 ± 21 ml).

SV determined via thermodilution also strongly correlated with SV measured according to Fick principle, with the former providing higher values. With regard to thermodilution, SV correlated moderately with PC-CMR and moderately but non-significantly with TTE (see Table 3).

ROC-analysis of PC-CMR-derived SVI to distinguish low and normal flow was not significant (AUC 0.651; p = 0.056).

Pressure gradients

Mean and peak gradients by PC-CMR (22 ± 10 mmHg and 64 ± 29 mmHg, respectively) correlated low with invasive measurements (41 ± 19 mmHg and 48 ± 27 mmHg, respectively). PPG by PC-CMR had low correlation with TTE (58 ± 25 mmHg). MPG by TTE (37 ± 17 mmHg) correlated strongly with cardiac catheterization, as did PPG by TTE (58 ± 25 mmHg). Correlation values and biases are listed in detail in Table 3.

Aortic valve area

In PC-CMR, mean AVA during systole (0.78 ± 0.25 cm2) showed good correlation (r: 0.54, p < 0.001) with a bias of 0.08cm2 (p = 0.017) compared to invasively determined AVA according to the Fick principle (0.70 ± 0.23 cm2). Scatter plot and Bland–Altman-analysis are presented in Fig. 6, panel B.

In TTE, mean AVA as measured by the continuity equation (0.84 ± 0.23 cm2) correlated moderately (r: 0.58, p < 0.001, bias: 0.11 cm2, p < 0.001) to invasive measurement. AVA by TTE correlated low with AVA measured by PC-CMR (0.366, p = 0.009, bias: 0.03 cm2, p = 0.41).

Invasively determined AVA values (i.e. Fick principle and thermodilution) correlated strongly with each other, with thermodilution providing higher values. AVA determined via thermodilution showed a good agreement with AVA measured by PC-CMR over the whole systolic cycle and by TTE. A detailed list of correlation values and biases is shown in Table 3.

Defining the invasively measured AVA by the Fick principle as threshold value between moderate and severe AS, ROC-analysis revealed an AUC-value of 0.81 for AVA determined by PC-CMR. Dichotomization of AVA by PC-CMR at a cut-off value of 0.82 cm2 (Youden-index) yielded a specificity of 100% (i.e. all moderate AS were classified correctly) and a sensitivity of 67% (i.e. two-thirds of severe AS were classified correctly). At a cut-off value of 1 cm2, specificity was 50% and sensitivity 87%.

In TTE, ROC-Analysis showed an AUC of 0.815, with a cut-off at 1.05 cm2 (Youden-index) yielding a specificity and sensitivity of 89% and 75%, respectively.

Cine-planimetry yielded AVA values that weakly correlated with invasive determination (planimetric AVA: 0.97 ± 0.37 cm2; r: 0.35, p = 0.013, bias: − 0.28 cm2, p < 0.001) and AVA by PC-CMR (r: 0.32, p = 0.022, bias: 0.20 cm2, p < 0.001).

AVA computed via the Hakki formula (0.76 ± 0.30 cm2) showed moderate correlation (r: 0.42, p = 0.002) and a bias of 0.06 cm2 (p = 0.15) compared to invasive determination, and a very strong correlation (r: 0.86, p < 0.001) with a bias of 0.02 cm2 (p = 0.35) compared to our PC-CMR method.

Intra and interobserver variabilty

Intra- and interobserver reproducibility of PC-CMR derived measures were excellent for SV (ICC of 0.955 [95%CI 0.921–0.974] and 0.970 [95%CI 0.947–0.983], respectively) as well as for PPG (ICC of 0.918 [95%CI 0.855–0.953] and 0.892 [95%CI 0.811–0.939], respectively) and for AVA (ICC of 0.939 [95%CI 0.892–0.965] and 0.827 [95%CI 0.696–0.902], respectively). Scatter and Bland–Altman plots are shown in the Additional file 1: Figs. S1 (Intraobserver) and S2 (Interobserver).

Discussion

To the best of our knowledge, the utilization of our novel approach simultaneously represents the first-ever study to compare PC-CMR with invasively derived measurements in AS. The main study finding can be summarized as follows: PC-CMR is able to compute AVA values via an innovative technique by plotting momentary flow across the valve against flow-velocity that are very similar to invasive determination with a negligible bias. Therefore, these results clearly argue for the capability of our novel method using PC-CMR to assess AS in a solid and reliable manner compared to the complex gold-standard of invasive determination.

Stroke volume

Computation of SV in PC-CMR compared to the gold-standard cine-CMR yielded a strong correlation with no bias. This is in line with previous data of our and other study groups, reporting a strong agreement between these two modalities in healthy subjects and in patients with myocardial infarction, respectively [17, 18]. SV by PC-CMR also showed good correlation with invasive determination, however revealing a clear bias to the invasively measured SV according to the Fick-principle. In contrast, a recent study by Po et al. described a good correlation between PC-CMR and invasive determination of SV applying right heart catheterization in pulmonary hypertension, displaying a bias of 4 ml [19]. Similarly, Mauritz et al. investigated the correlation between SV by PC-CMR in the aorta and via right heart catheterization in pulmonary hypertension, which showed a good agreement with a bias of only 1 ml, albeit in a relatively small cohort [20]. In AS patients, however, no comparable study has been conducted so far. Anyway, due to the altered flow patterns in AS, a structured comparison between a flow-dependent (PC-CMR) and flow-independent (cine) method seems desirable. In our study, cine-CMR served as gold-standard for quantifying SV, so the underestimation of invasive measurements could be due to the complex hemodynamic findings in this disease entity.

TTE assessed SV showed a lower bias, but also less correlation when compared to invasive SV data. Corresponding to several previous studies [9, 18, 21], TTE-assessed SV mostly showed a good agreement to PC-CMR derived SV. Barone-Rochette et al. showed good correlation between SVi by PC-CMR and by TTE; additionally, in that study, PC-CMR was able to confirm low-flow states diagnosed via TTE [9].

In our subgroup analysis with invasively assessed SV via thermodilution, PC-CMR showed good correlation and a distinctly smaller bias, whilst TTE presented a bias of 20 ml and no significant correlation. The discrepancy in SV according to Fick principle compared to thermodilution is in line with selected studies made in patients with pulmonary hypertension, proclaiming no interchangeability between these two measurements, with one of them explicitly recommending thermodilution [22, 23]. Kresoja et al. showed, that especially in elderly patients, SV by the Fick method provided large individual errors, whilst thermodilution served as gold-standard in that study [24]. Anyway, the patients undergoing thermodilution in our study provided good results that sorted well with PC-CMR and cine-CMR measurements; nonetheless, the cohort undergoing thermodilution in our study is quite small, so no general statements can be made.

ROC-analysis of PC-CMR-derived SVI was not significant. However, as was shown by Chin et al., TTE is quite prone to underestimate SV [25], which is why a CMR-based classification seems even more desirable. What is more, a graduated or continual classification of flow-states based on CMR would represent a promising approach and a sensible alternative to the quite arbitrary defined 35 ml/m2-threshold. Though, further studies to assess this classification are needed.

Pressure gradients

In our study, MPG and PPG gradients by PC-CMR showed low correlation to their invasive counterparts, with mean biases of 19 (MPG) and 16 (PPG) mmHg, respectively. In line with our study, in 2003 Caruthers et al. used the modified Bernoulli equation to compute pressure gradients in AS by PC-CMR, yielding a strong correlation compared to TTE, but without quantifying any absolute biases [26]. This discrepancy in correlation values could be due to the waiver of using neighbouring pixels in our study, detecting only the single fastest pixel to compute momentary peak velocity, thus leading to an overestimation of PPG. As opposed to this, MPG was significantly underestimated in our study; a possible explanation could be the general underestimation of peak jet velocity by CMR due to its lower temporal resolution in contrast to ultrasound [5]. A distinct underestimation of MPG between TTE and PC-CMR was also described by Defrance et al., which was even 25 mmHg in a mixed patient cohort and 16 mmHg in AS patients, although higher correlation levels were reported [27]. Sirin et al. described an underestimation of PPG of 12 mmHg in PC-CMR compared to TTE in a small cohort of pediatric AS patients [28]. These divergences could be due to the narrow range of invasive MPG (95% Confidence Interval (CI) 36–46 mmHg) and PPG (95%CI 40–55 mmHg) in our study as opposed to the above-mentioned studies. Moreover, the distinct underestimation of MPG in PC-CMR compared to TTE has been described previously by Garcia et al., grounding this finding (by analogy to ultrasound) on energy loss in AS and on pressure recovery [29,30,31].

Aortic valve area

Our main finding was that AVA determined by PC-CMR showed a good compatibility with invasively measured AVA, displaying only a small bias. However, the correlation values yielded in our study still have some room for improvement. The lack of a definite gold-standard in the assessment of AS could be a major reason, implying the possible presence of factors hampering the accuracy of cardiac catheterization (i.e. pressure recovery effects) or TTE (i.e. misalignment of Doppler beam with flow direction) without having an effect on CMR [8, 27]. PC-CMR provided an abundance of methods to determine AVA, but measuring the mean AVA over the whole systolic cycle appears to be the most objectifiable and easiest one, simultaneously yielding the best results. We used cardiac catheterization and calculation of AVA by using the Gorlin-formula as gold-standard to determine AVA. However, the use of this equation to estimate AVA is associated with several pitfalls, as it is directly related to cardiac output, blood viscosity, and turbulent flow. What is more, invasive measurement of the AVA is associated with a substantial risk of cerebral embolism [32]. In 2016, Wong et al. provided a review of 12 papers regarding the comparison between TTE and CMR assessment of AVA in AS, concluding that CMR does not succumb TTE, whilst showing better inter- and intraobserver reliability and greater specificity and sensitivity [33]. Nevertheless, the studies being investigated in that review calculated AVA in CMR very heterogeneously by using either continuity equation [8, 26, 27, 34], cine-planimetry [7, 9, 35, 36], the Hakki formula [27] or planimetry in magnitude images [34]. A fifth approach previously published is planimetry in PC-CMR images, suggesting a better correlation of that method to TEE than cine-planimetry [37]. In our present study, AVA was additionally computed via the Hakki formula and via cine-planimetry, but both methods showed lower correlation and at best a similar bias compared to invasive measurement than our primarily used approach, with both being rather prone to errors.

In comparison to TTE, AVA values obtained by PC-CMR showed only a weak correlation, with PC-CMR demonstrating a lower bias in comparison to the gold-standard of cardiac catheterization. While many studies comparing TTE to CMR in AS reported an overestimation of AVA in CMR [6], our results are in line with a study comparing the continuity equation in TTE to PC-CMR [27], possibly indicating that TTE measurements in AS generally tend to slightly overestimate AVA in AS compared to PC-CMR. One of the major reasons for this finding could be the more exact detection of flow-velocity in PC-CMR, as it is less prone to miss the true peak velocity.

Competing with our PC-CMR approach, Reant et al. described a good concordance between planimetric measurement of AVA in cine-images, direct planimetry in TEE and invasive determination via cardiac catheterization, but a significant bias for TTE [36]. Another study provided evidence for a good concordance between TTE and CMR in a cohort of 31 patients, using continuity equation in both modalities to determine AVA. However, this group described a compensation of an underestimated LV outflow tract area for an overestimated velocity time integral in TTE measurements [8], which appears to be an unstable base for solid calculations. In comparison, our approach of determining AVA via plotting momentary flow-volume across the valve against flow-velocity is an easy-to-apply method that provided stable results with a bearable bias compared to invasive measurement.

In addition to the excellent intra- and interobserver reproducibility shown in our study, the superior interstudy reproducibility of CMR compared to TTE was demonstrated in a study by Grothues et al. [38].

In our subgroup undergoing thermodilution, AVA measured by this method yielded a better correlation and a smaller bias compared to AVA by PC-CMR as opposed to Fick principle. There are hardly any data available comparing these two invasive methods of determining AVA, but by analogy to the determination of SV, higher values of SV in thermodilution lead to larger AVA measures. As mentioned before, this subgroup is too small to justify general statements and studies investigating it on a larger cohort are lacking. However, by tendency, AVA measured via thermodilution appears to be a more stable parameter than AVA calculated via the Fick principle.

Limitations

Firstly, all of the patients in our study had moderate to severe AS, which makes translation of our results on patients without AS or with only mild AS uncertain. However, it can be assumed that a narrow AV does not have a major impact on the accuracy of PC-CMR, as has already been suggested by Defrance et al. [27]. Another important limitation of this study is the lack of a uniform CMR protocol, leading to PC-CMR measurements in different planes above the AV. Possibly, layer positioning has an unneglectable impact on flow and velocity measurements. Our study group is currently working on further standardization of this. Furthermore, in cardiac catheterization, thermodilution was only performed in a small subset (n = 17) of patients. Another issue is the partially quite long interval between the different examinations. However, according to a study by Nistri et al., mean progression of jet velocity in AS is 0.26 m/s/year [39], which is why this point may not be a major concern in our study. Lastly, in 5 patients, blood pressure medication was changed before CMR scan, which might influence flow dynamics over the AV and furthermore could have an impact on the comparability and objectivity between diagnostic modalities.

Conclusion

This study introduces a simple and easy-to-use approach to determine AVA in patients with moderate to severe AS via PC-CMR. AVA measurement by continuous determination of flow-volumes and velocities as well as SV determination yielded by PC-CMR were in good agreement with invasive measurement. Thus,

PC-CMR represents a useful tool in diagnosing and characterizing AS that provides a non-invasive alternative to TTE, especially when findings are inconclusive.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

AS:

Aortic stenosis

AUC:

Area under the curve

AV:

Aortic valve

AVA:

Aortic valve area

BSA:

Body surface Area

bSSFP:

Balanced steady state free precession

CI:

Confidence interval

CMR:

Cardiovascular magnetic resonance imaging

CO:

Cardiac output

ECG:

Electrocardiogram

EDV:

End-diastolic volume

EDVI:

End-diastolic volume index

ESV:

End-systolic volume

ESVI:

End-systolic volume index

HR:

Heart rate

ICC:

Intraclass correlation coefficient

IQR:

Interquartile range

LLoA:

Lower limit of agreement

LoA:

Limit of agreement

LV:

Left ventricle/left ventricular

LVEF:

Left ventricular ejection fraction

LVM:

Left ventricular mass

LVMI:

Left ventricular mass index

MPG:

Mean pressure gradient

PC-CMR:

Phase-contrast cardiovascular magnetic resonance

PPG:

Peak pressure gradient

ROC:

Receiver operating characteristics

SD:

Standard deviation

SV:

Stroke volume

SVI:

Stroke volume index

TEE:

Transesophageal echocardiography

TTE:

Transthoracic echocardiography

ULoA:

Upper limit of agreement

References

  1. Maganti K, Rigolin V, Sarano M, Bonow R. Valvular heart disease: diagnosis and management. Mayo Clin Proc. 2010;85(5):483–500.

    Article  Google Scholar 

  2. Nishimura R, Otto C, Bonow R, Carabello B, Erwin J, Guyton R. 2014 AHA/ACC guideline for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Thorac Cardiovasc Surg. 2014;148(1):e1–132.

    Article  Google Scholar 

  3. Nishimura R, Carabello B. Hemodynamics in the cardiac catheterization laboratory of the 21st century. Circulation. 2012;125:2138–50.

    Article  Google Scholar 

  4. Baumgartner H, Falk V, Bax J, De Bonis M, Hamm C, Holm P, et al. ESC/EACTS Guidelines for the management of valvular heart disease. Eur Heart J. 2017;38(36):2739–91.

    Article  Google Scholar 

  5. Bohbot Y, Renard C, Manrique A, Levy F, Maréchaux S, Gerber B, et al. Usefulness of cardiac magnetic resonance imaging in aortic stenosis. Circ Cardiovasc Imaging. 2020;13(5):e010356.

  6. Woldendorp K, Bannon P, Grieve S. Evaluation of aortic stenosis using cardiovascular magnetic resonance: a systematic review & meta-analysis. J Cardiovasc Magn Reson. 2020;22(1):45.

    Article  Google Scholar 

  7. Kupfahl C, Honold M, Meinhardt G, Vogelsberg H, Wagner A, Mahrholdt H, et al. Evaluation of aortic stenosis by cardiovascular magnetic resonance imaging: comparison with established routine clinical techniques. Heart. 2004;90(8):893–901.

    CAS  Article  Google Scholar 

  8. Garcia J, Kadem L, Larose E, Clavel M, Pibarot P. Comparison between cardiovascular magnetic resonance and transthoracic Doppler echocardiography for the estimation of effective orifice area in aortic stenosis. J Cardiovasc Magn Reson. 2011;13(1):25.

    Article  Google Scholar 

  9. Barone-Rochette G, Piérard S, Seldrum S, de Meester de Ravenstein C, Melchior J, Maes F, et al. Aortic valve area, stroke volume, left ventricular hypertrophy, remodeling, and fibrosis in aortic stenosis assessed by cardiac magnetic resonance imaging: comparison between high and low gradient and normal and low flow aortic stenosis. Circ Cardiovasc Imaging. 2013;6(6):1009–17.

  10. Du Bois D, Du Bois E. A formula to estimate the approximate surface area if height and weight be known. Nutrition. 1989;5(5):303–11.

    PubMed  Google Scholar 

  11. Hatle L, Angelsen B, Tromsdal A. Non-invasive assessment of aortic stenosis by Doppler ultrasound. Br Heart J. 1980;43(3):284–92.

    CAS  Article  Google Scholar 

  12. Hakki AH, Iskandrian AS, Bemis CE, Kimbiris D, Mintz GS, Segal BL, et al. A simplified valve formula for the calculation of stenotic cardiac valve areas. Circulation. 1981;63(5):1050–5.

    CAS  Article  Google Scholar 

  13. Puymirat E, Chassaing S, Trinquart L, Barbey C, Chaudeurge A, Bar O, et al. Hakki’s formula for measurement of aortic valve area by magnetic resonance imaging. Am J Cardiol. 2010;106(2):249–54.

    Article  Google Scholar 

  14. Shapiro E. Adolf Fick–forgotten genius of cardiology. Am J Cardiol. 1972;30(6):662–5.

    CAS  Article  Google Scholar 

  15. Kowang T, Long C, Rasli A. Innovation management and performance framework for research university in Malaysia. Int Educ Stud. 2015;8:32–45.

    Article  Google Scholar 

  16. Rice M, Harris G. Comparing effect sizes in follow-up studies: ROC Area, Cohen’s d, and r. Law Hum Behav. 2005;29(6):615–20.

    Article  Google Scholar 

  17. Klug G, Reinstadler SJ, Feistritzer HJ, Kremser C, Schwaiger JP, Reindl M, et al. Cardiac index after acute ST-segment elevation myocardial infarction measured with phase-contrast cardiac magnetic resonance imaging. Eur Radiol. 2016;26(7):1999–2008.

    Article  Google Scholar 

  18. Guzzetti E, Capoulade R, Tastet L, Garcia J, Le Ven F, Arsenault M, et al. Estimation of stroke volume and aortic valve area in patients with aortic stenosis: a comparison of echocardiography versus cardiovascular magnetic resonance. J Am Soc Echocardiogr. 2020;33(8):953–63 e5.

  19. Po J, Tong M, Meeran T, Potluri A, Raina A, Doyle M, et al. Quantification of cardiac output with phase contrast magnetic resonance imaging in patients with pulmonary hypertension. J Clin Imaging Sci. 2020;10:26.

    Article  Google Scholar 

  20. Mauritz G, Marcus J, Boonstra A, Postmus P, Westerhof N, Vonk-Noordegraaf A. Non-invasive stroke volume assessment in patients with pulmonary arterial hypertension: left-sided data mandatory. J Cardiovasc Magn Reson. 2008;10(1):51.

    Article  Google Scholar 

  21. da Silveira JS, Smyke M, Rich AV, Liu Y, Jin N, Scandling D, et al. Quantification of aortic stenosis diagnostic parameters: comparison of fast 3 direction and 1 direction phase contrast CMR and transthoracic echocardiography. J Cardiovasc Magn Reson. 2017;19(1):35.

    Article  Google Scholar 

  22. Fares W, Blanchard S, Stouffer G, Chang P, Rosamond W, Ford H, et al. Thermodilution and Fick cardiac outputs differ: impact on pulmonary hypertension evaluation. Can Respir J. 2012;19(4):261–6.

    Article  Google Scholar 

  23. Alkhodair A, Tsang M, Cairns J, Swiston J, Levy R, Lee L, et al. Comparison of thermodilution and indirect Fick cardiac outputs in pulmonary hypertension. Int J Cardiol. 2018;258:228–31.

    Article  Google Scholar 

  24. Kresoja K, Faragli A, Abawi D, Paul O, Pieske B, Post H, et al. Thermodilution vs estimated Fick cardiac output measurement in an elderly cohort of patients: a single-centre experience. PLoS ONE. 2019;14(12):e0226561.

  25. Chin CW, Khaw HJ, Luo E, Tan S, White AC, Newby DE, et al. Echocardiography underestimates stroke volume and aortic valve area: implications for patients with small-area low-gradient aortic stenosis. Can J Cardiol. 2014;30(9):1064–72.

    Article  Google Scholar 

  26. Caruthers S, Lin S, Brown P, Watkins M, Williams T, Lehr K, et al. Practical value of cardiac magnetic resonance imaging for clinical quantification of aortic valve stenosis: comparison with echocardiography. Circulation. 2003;108(18):2236–43.

    Article  Google Scholar 

  27. Defrance C, Bollache E, Kachenoura N, Perdrix L, Hrynchyshyn N, Bruguière E, et al. Evaluation of aortic valve stenosis using cardiovascular magnetic resonance: comparison of an original semiautomated analysis of phase-contrast cardiovascular magnetic resonance with Doppler echocardiography. Circ Cardiovasc Imaging. 2012;5(5):604–12.

    Article  Google Scholar 

  28. Sirin S, Nassenstein K, Neudorf U, Jensen C, Mikat C, Schlosser T. Quantification of congenital aortic valve stenosis in pediatric patients: comparison between cardiac magnetic resonance imaging and transthoracic echocardiography. Pediatr Cardiol. 2014;35(5):771–7.

    Article  Google Scholar 

  29. Garcia J, Capoulade R, Le Ven F, Gaillard E, Kadem L, Pibarot P, et al. Discrepancies between cardiovascular magnetic resonance and Doppler echocardiography in the measurement of transvalvular gradient in aortic stenosis: the effect of flow vorticity. J Cardiovasc Magn Reson. 2013;15:84.

    Article  Google Scholar 

  30. Garcia D, Pibarot P, Dumesnil JG, Sakr F, Durand LG. Assessment of aortic valve stenosis severity: a new index based on the energy loss concept. Circulation. 2000;101(7):765–71.

    CAS  Article  Google Scholar 

  31. Bahlmann E, Cramariuc D, Gerdts E, Gohlke-Baerwolf C, Nienaber CA, Eriksen E, et al. Impact of pressure recovery on echocardiographic assessment of asymptomatic aortic stenosis: a SEAS substudy. JACC Cardiovasc Imaging. 2010;3(6):555–62.

    Article  Google Scholar 

  32. Omran H, Schmidt H, Hackenbroch M, Illien S, Bernhardt P, von der Recke G, et al. Silent and apparent cerebral embolism after retrograde catheterisation of the aortic valve in valvular stenosis: a prospective, randomised study. Lancet. 2003;361(9365):1241–6.

    Article  Google Scholar 

  33. Wong S, Spina R, Toemoe S, Dhital K. Is cardiac magnetic resonance imaging as accurate as echocardiography in the assessment of aortic valve stenosis? Interact Cardiovasc Thorac Surg. 2016;22(4):480–6.

    Article  Google Scholar 

  34. Speiser U, Quick S, Haas D, Youssef A, Waessnig N, Ibrahim K, et al. 3-T magnetic resonance for determination of aortic valve area: a comparison to echocardiography. Scand Cardiovasc J. 2014;48(3):176–83.

    Article  Google Scholar 

  35. Debl K, Djavidani B, Seitz J, Nitz W, Schmid F, Muders F, et al. Planimetry of aortic valve area in aortic stenosis by magnetic resonance imaging. Invest Radiol. 2005;40(10):631–6.

    Article  Google Scholar 

  36. Reant P, Lederlin M, Lafitte S, Serri K, Montaudon M, Corneloup O, et al. Absolute assessment of aortic valve stenosis by planimetry using cardiovascular magnetic resonance imaging: comparison with transesophageal echocardiography, transthoracic echocardiography, and cardiac catheterisation. Eur J Radiol. 2006;59(2):276–83.

    Article  Google Scholar 

  37. Abe H, Iguchi N, Utanohara Y, Takada K, Hen Y, Machida H, et al. Planimetry of the orifice area in aortic valve stenosis using phase-contrast cardiac magnetic resonance imaging. Int Heart J. 2018;59(1):77–80.

    Article  Google Scholar 

  38. Grothues F, Smith GC, Moon JC, Bellenger NG, Collins P, Klein HU, et al. Comparison of interstudy reproducibility of cardiovascular magnetic resonance with two-dimensional echocardiography in normal subjects and in patients with heart failure or left ventricular hypertrophy. Am J Cardiol. 2002;90(1):29–34.

    Article  Google Scholar 

  39. Nistri S, Faggiano P, Olivotto I, Papesso B, Bordonali T, Vescovo G, et al. Hemodynamic progression and outcome of asymptomatic aortic stenosis in primary care. Am J Cardiol. 2012;109(5):718–23.

    Article  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

None.

Author information

Affiliations

Authors

Contributions

We hereby confirm that all listed authors contributed to this work in terms of (a) conception, design, analysis or interpretation of data; (b) manuscript drafting and revising. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Gert Klug.

Ethics declarations

Ethics approval and consent to participate

Prior to study inclusion, written informed consent was given by all participants. The study received approval by the research ethics committee of the Medical University of Innsbruck.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Figure S1. Intraobserver Variability. Scatter and Bland-Altman plots of stroke volume (Panel A) and aortic valve area (Panel B). AVA: aortic valve area, SV: stroke volume. Figure S2. Interobserver Variability. Scatter and Bland-Altman plots of stroke volume (Panel A) and aortic valve area (Panel B). AVA: aortic valve area, Obs: observer, SV: stroke volume. Figure S3. Bland-Altman plots of SV and AVA between different modalities. AVA: aortic valve area, PC-CMR: phase-contrast-cardiovascular magnetic resonance imaging, SV: stroke volume, TTE: transthoracic echocardiography.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Troger, F., Lechner, I., Reindl, M. et al. A novel approach to determine aortic valve area with phase-contrast cardiovascular magnetic resonance. J Cardiovasc Magn Reson 24, 7 (2022). https://doi.org/10.1186/s12968-021-00838-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12968-021-00838-w

Keywords

  • Aortic stenosis
  • Cardiac magnetic resonance imaging
  • Phase-contrast-CMR
  • Valvular heart disease