Skip to main content

Advertisement

Log in

Assessment of aortic valve tract dynamics using automatic tracking of 3D transesophageal echocardiographic images

  • Original Paper
  • Published:
The International Journal of Cardiovascular Imaging Aims and scope Submit manuscript

Abstract

The assessment of aortic valve (AV) morphology is paramount for planning transcatheter AV implantation (TAVI). Nowadays, pre-TAVI sizing is routinely performed at one cardiac phase only, usually at mid-systole. Nonetheless, the AV is a dynamic structure that undergoes changes in size and shape throughout the cardiac cycle, which may be relevant for prosthesis selection. Thus, the aim of this study was to present and evaluate a novel software tool enabling the automatic sizing of the AV dynamically in three-dimensional (3D) transesophageal echocardiography (TEE) images. Forty-two patients who underwent preoperative 3D-TEE images were retrospectively analyzed using the software. Dynamic measurements were automatically extracted at four levels, including the aortic annulus. These measures were used to assess the software’s ability to accurately and reproducibly quantify the conformational changes of the aortic root and were validated against automated sizing measurements independently extracted at distinct time points. The software extracted physiological dynamic measurements in less than 2 min, that were shown to be accurate (error 2.2 ± 26.3 mm2 and 0.0 ± 2.53 mm for annular area and perimeter, respectively) and highly reproducible (0.85 ± 6.18 and 0.65 ± 7.90 mm2 of intra- and interobserver variability, respectively, in annular area). Using the maximum or minimum measured values rather than mid-systolic ones for device sizing resulted in a potential change of recommended size in 7% and 60% of the cases, respectively. The presented software tool allows a fast, automatic and reproducible dynamic assessment of the AV morphology from 3D-TEE images, with the extracted measures influencing the device selection depending on the cardiac moment used to perform its sizing. This novel tool may thus ease and potentially increase the observer’s confidence during prosthesis’ size selection at the preoperative TAVI planning.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. Osnabrugge RL, Mylotte D, Head SJ, Van Mieghem NM, Nkomo VT, LeReun CM, Bogers AJ, Piazza N, Kappetein AP (2013) Aortic stenosis in the elderly: disease prevalence and number of candidates for transcatheter aortic valve replacement: a meta-analysis and modeling study. J Am Coll Cardiol 62(11):1002–1012

    Article  Google Scholar 

  2. Leon MB, Smith CR, Mack M, Miller DC, Moses JW, Svensson LG, Tuzcu EM, Webb JG, Fontana GP, Makkar RR (2010) Transcatheter aortic-valve implantation for aortic stenosis in patients who cannot undergo surgery. N Engl J Med 363(17):1597–1607

    Article  CAS  Google Scholar 

  3. Nishimura RA, Otto CM, Bonow RO, Carabello BA, Erwin JP, Guyton RA, O’Gara PT, Ruiz CE, Skubas NJ, Sorajja P (2014) 2014 AHA/ACC guideline for the management of patients with valvular heart disease. Circulation 129(23):521–643

    Google Scholar 

  4. Vahanian A, Alfieri O, Andreotti F, Antunes MJ, Barón-Esquivias G, Baumgartner H, Borger MA, Carrel TP, De Bonis M, Evangelista A (2012) Guidelines on the management of valvular heart disease (version 2012). Eur Heart J 33(19):2451–2496

    Article  PubMed  Google Scholar 

  5. Leon MB, Smith CR, Mack MJ, Makkar RR, Svensson LG, Kodali SK, Thourani VH, Tuzcu EM, Miller DC, Herrmann HC (2016) Transcatheter or surgical aortic-valve replacement in intermediate-risk patients. N Engl J Med 374(17):1609–1620

    Article  CAS  Google Scholar 

  6. Min JK, Berman DS, Leipsic J (2013) Multimodality imaging for transcatheter aortic valve replacement. Springer Science & Business Media, Berlin

    Google Scholar 

  7. Zamorano J, Gonçalves A, Lancellotti P, Andersen KA, González-Gómez A, Monaghan M, Brochet E, Wunderlich N, Gafoor S, Gillam LD (2016) The use of imaging in new transcatheter interventions: an EACVI review paper. Eur Heart J Cardiovasc Imaging 17(8):835–835af

    Article  PubMed  Google Scholar 

  8. Bloomfield GS, Gillam LD, Hahn RT, Kapadia S, Leipsic J, Lerakis S, Tuzcu M, Douglas PS (2012) A practical guide to multimodality imaging of transcatheter aortic valve replacement. JACC Cardiovasc Imaging 5(4):441–455

    Article  Google Scholar 

  9. Hamdan A, Guetta V, Konen E, Goitein O, Segev A, Raanani E, Spiegelstein D, Hay I, Di Segni E, Eldar M (2012) Deformation dynamics and mechanical properties of the aortic annulus by 4-dimensional computed tomography: insights into the functional anatomy of the aortic valve complex and implications for transcatheter aortic valve therapy. J Am Coll Cardiol 59(2):119–127

    Article  PubMed  Google Scholar 

  10. Suchá D, Tuncay V, Prakken NH, Leiner T, van Ooijen PM, Oudkerk M, Budde RP (2015) Does the aortic annulus undergo conformational change throughout the cardiac cycle? A systematic review. Eur Heart J Cardiovasc Imaging 16(12):1307–1317

    PubMed  Google Scholar 

  11. Murphy DT, Blanke P, Alaamri S, Naoum C, Rubinshtein R, Pache G, Precious B, Berger A, Raju R, Dvir D (2016) Dynamism of the aortic annulus: effect of diastolic versus systolic CT annular measurements on device selection in transcatheter aortic valve replacement (TAVR). J Cardiovasc Comput Tomogr 10(1):37–43

    Article  PubMed  Google Scholar 

  12. Blanke P, Russe M, Leipsic J, Reinöhl J, Ebersberger U, Suranyi P, Siepe M, Pache G, Langer M, Schoepf UJ (2012) Conformational pulsatile changes of the aortic annulus: impact on prosthesis sizing by computed tomography for transcatheter aortic valve replacement. JACC Cardiovasc Interv 5(9):984–994

    Article  PubMed  Google Scholar 

  13. von Aspern K, Foldyna B, Etz C, Hoyer A, Girrbach F, Holzhey D, Lücke C, Grothoff M, Linke A, Mohr F (2015) Effective diameter of the aortic annulus prior to transcatheter aortic valve implantation: influence of area-based versus perimeter-based calculation. Int J Cardiovasc Imaging 31(1):163–169

    Article  Google Scholar 

  14. Mehrotra P, Flynn AW, Jansen K, Tan TC, Mak G, Julien HM, Zeng X, Picard MH, Passeri JJ, Hung J (2015) Differential left ventricular outflow tract remodeling and dynamics in aortic stenosis. J Am Soc Echocardiogr 28(11):1259–1266

    Article  PubMed  Google Scholar 

  15. Bersvendsen J, Beitnes JO, Urheim S, Aakhus S, Samset E (2014) Automatic measurement of aortic annulus diameter in 3-dimensional transoesophageal echocardiography. BMC Med Imaging 14(1):31

    Article  PubMed  PubMed Central  Google Scholar 

  16. Ionasec RI, Voigt I, Georgescu B, Wang Y, Houle H, Vega-Higuera F, Navab N, Comaniciu D (2010) Patient-specific modeling and quantification of the aortic and mitral valves from 4-D cardiac CT and TEE. IEEE Trans Med Imaging 29(9):1636–1651

    Article  PubMed  Google Scholar 

  17. Veronesi F, Corsi C, Mor-Avi V, Sugeng L, Wienert L, Lang R, Lamberti C (2009) Quantification of aortic valve stenosis using transesophageal real-time 3D echocardiographic images. In: Computers in Cardiology 2009. IEEE. pp 37–40

  18. Barbosa D, Heyde B, Dietenbeck T, Friboulet D, D’hooge J, Bernard O (2013) Fast left ventricle tracking in 3D echocardiographic data using anatomical affine optical flow. In: Functional Imaging and Modeling of the Heart (FIMH2013). pp 191–199

  19. Queirós S, Barbosa D, Heyde B, Morais P, Vilaça JL, Friboulet D, Bernard O, D’hooge J (2014) Fast automatic myocardial segmentation in 4D cine CMR datasets. Med Image Anal 18(7):1115–1131

    Article  PubMed  Google Scholar 

  20. Queirós S, Vilaça JL, Morais P, Fonseca JC, D’hooge J, Barbosa D (2017) Fast left ventricle tracking using localized anatomical affine optical flow. Int J Numer Methods Biomed Eng 33(11):e2871. https://doi.org/10.1002/cnm.2871

    Article  Google Scholar 

  21. Queirós S, Morais P, Dubois C, Voigt J-U, Fehske W, Kuhn A, Achenbach T, Fonseca JC, Vilaça JL, D’hooge J (2018) Validation of a novel software tool for automatic aortic annulus sizing in 3D transesophageal echocardiographic images. J Am Soc Echocardiogr 31(4):515–525.e515

    Article  PubMed  Google Scholar 

  22. Heyde B, Barbosa D, Claus P, Maes F, D’hooge J (2013) Three-dimensional cardiac motion estimation based on non-rigid image registration using a novel transformation model adapted to the heart. In: Statistical atlases and computational models of the heart. Imaging and modelling challenges. Springer. pp 142–150

  23. Kasel AM, Cassese S, Bleiziffer S, Amaki M, Hahn RT, Kastrati A, Sengupta PP (2013) Standardized imaging for aortic annular sizing: implications for transcatheter valve selection. JACC Cardiovasc Imaging 6(2):249–262

    Article  PubMed  Google Scholar 

  24. Kenny C, Monaghan M (2015) How to assess aortic annular size before transcatheter aortic valve implantation (TAVI): the role of echocardiography compared with other imaging modalities. Heart 101(9):727–736. https://doi.org/10.1136/heartjnl-2013-304689

    Article  PubMed  Google Scholar 

  25. Bland JM, Altman D (1986) Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 327(8476):307–310

    Article  Google Scholar 

  26. Piazza N, de Jaegere P, Schultz C, Becker AE, Serruys PW, Anderson RH (2008) Anatomy of the aortic valvar complex and its implications for transcatheter implantation of the aortic valve. Circ Cardiovasc Interv 1(1):74–81

    Article  PubMed  Google Scholar 

  27. Elattar MA, Vink LW, van Mourik MS, Baan J Jr, Planken RN, Marquering HA (2017) Dynamics of the aortic annulus in 4D CT angiography for transcatheter aortic valve implantation patients. PLoS ONE 12(9):e0184133

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Looi J-L, Lee AP-W, Fang F, Hsiung MC, Sun J-P, Yin W-H, Wei J, Tsai S-K, Wan S, Wong RH (2015) Abnormal mitral–aortic intervalvular coupling in mitral valve diseases: a study using real-time three-dimensional transesophageal echocardiography. Clin Res Cardiol 104(10):831–842

    Article  PubMed  Google Scholar 

  29. Caballero L, Saura D, Oliva-Sandoval MJ, González-Carrillo J, Espinosa MD, García-Navarro M, Valdés M, Lancellotti P, de la Morena G (2017) Three-dimensional morphology of the left ventricular outflow tract: impact on grading aortic stenosis severity. J Am Soc Echocardiogr 30(1):28–35

    Article  PubMed  Google Scholar 

  30. Khamooshian A, Amador Y, Hai T, Jeganathan J, Saraf M, Mahmood E, Matyal R, Khabbaz KR, Mariani M, Mahmood F (2017) Dynamic three-dimensional geometry of the aortic valve apparatus—a feasibility study. J Cardiothorac Vasc Anesth 31(4):1290–1300

    Article  PubMed  Google Scholar 

  31. Tsang W, Veronesi F, Sugeng L, Weinert L, Takeuchi M, Jeevanandam V, Lang RM (2013) Mitral valve dynamics in severe aortic stenosis before and after aortic valve replacement. J Am Soc Echocardiogr 26(6):606–614

    Article  PubMed  Google Scholar 

  32. Queirós S, Papachristidis A, Barbosa D, Theodoropoulos KC, Fonseca JC, Monaghan MJ, Vilaça JL, D’ hooge J (2016) Aortic valve tract segmentation from 3D-TEE using shape-based B-spline explicit active surfaces. IEEE Trans Med Imaging 35(9):2015–2025. https://doi.org/10.1109/TMI.2016.2544199

    Article  PubMed  Google Scholar 

  33. Prihadi EA, van Rosendael PJ, Vollema EM, Bax JJ, Delgado V, Marsan NA (2018) Feasibility, accuracy, and reproducibility of aortic annular and root sizing for transcatheter aortic valve replacement using novel automated three-dimensional echocardiographic software: comparison with multi–detector row computed tomography. J Am Soc Echocardiogr 31(4):505–514.e503

    Article  PubMed  Google Scholar 

  34. Doddamani S, Bello R, Friedman MA, Banerjee A, Bowers JH, Kim B, Vennalaganti PR, Ostfeld RJ, Gordon GM, Malhotra D (2007) Demonstration of left ventricular outflow tract eccentricity by real time 3D echocardiography: implications for the determination of aortic valve area. Echocardiography 24(8):860–866

    Article  PubMed  Google Scholar 

  35. Flachskampf FA, Wouters PF, Edvardsen T, Evangelista A, Habib G, Hoffman P, Hoffmann R, Lancellotti P, Pepi M, Imaging EAoC (2014) Recommendations for transoesophageal echocardiography: EACVI update 2014. Eur Heart J Cardiovasc Imaging 15(4):353–365

    Article  PubMed  Google Scholar 

  36. Papachristidis A, Papitsas M, Roper D, Wang Y, Dworakowski R, Byrne J, Wendler O, MacCarthy P, Monaghan MJ (2017) Three-dimensional measurement of aortic annulus dimensions using area or circumference for transcatheter aortic valve replacement valve sizing: does it make a difference? J Am Soc Echocardiogr 30(9):871–878

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

This work was funded by projects “NORTE-01-0145-FEDER-000013” and “NORTE-01-0145-FEDER-024300”, supported by Northern Portugal Regional Operational Programme (Norte2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (FEDER). This work has also been funded by FEDER funds, through Competitiveness Factors Operational Programme (COMPETE), and by national funds, through the FCT—Fundação para a Ciência e Tecnologia, under the scope of the project POCI-01-0145-FEDER-007038. The authors also acknowledge support from FCT and the European Social Found, through Programa Operacional Capital Humano (POCH), in the scope of the PhD grant SFRH/BD/93443/2013 (S. Queirós). The authors would also like to thank Judith Simons (St. Vinzenz-Hospital, Cologne, Germany) and Mahvish T. Elahi (KU Leuven, Leuven, Belgium) for their technical assistance in collecting all patient/image data.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sandro Queirós.

Ethics declarations

Conflict of interest

The authors declare no conflict of interest.

Additional information

Publisher's Note

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

Electronic supplementary material

Appendices

Appendix A

To better understand the AoA dynamics (potentially relevant for TAVI prosthesis sizing), Fig. 6 presents the average area/perimeter throughout the cardiac cycle over all subjects, as well as the relative area/perimeter change over time using the value at the end-diastole phase (last frame; ED) as reference. The average (and SD) eccentricity index (EI) was also calculated [34], and its relative change with respect to the ED phase is also depicted. Note that an EI of 0 represents a perfect circle, with higher EI indicating an elliptical geometry. Moreover, Fig. 7 illustrates the distribution of the temporal phase (as a percentage of the cardiac cycle duration) in which the maximum and minimum area and perimeter values were detected for the entire study population. Note that both first and last moments of the cycle correspond to the ED phase, with the average MS time point defined by the observer (used in the segmentation stage and set as the starting point for the tracking) also shown. Note also that, in the study population, the end-systolic (ES) moment occurred at a median ~ 53% of the R–R interval.

Overall, both area and perimeter (Fig. 6a–e) were larger in systole and lower in diastole, which is in agreement with previous reports that used independent delineation-based analyses in multidetector row computed tomography or 3D-TEE images [9, 12, 27, 28]. These results demonstrate the adequacy of the proposed software in extracting physiological and clinically-relevant measurements. Moreover, from the computed eccentricity index (Fig. 6c, f), one observed a more circular annular shape during systole, being more oval in diastole, which is also in accordance to the known dynamic conformational changes of the AoA throughout the cardiac cycle [10, 14, 27].

Fig. 6
figure 6

Average a area, b perimeter, and c eccentricity index (EI) values measured across the cardiac cycle at the aortic annulus (AoA). Relative change of d area, e perimeter, and f EI values with respect to the end-diastole (last frame; 100% R–R interval). The vertical bars indicate the standard deviation of the measures across the entire study population. To obtain a temporal correspondence between frames of all measurement curves, the first and last frames of all sequences were aligned, and the curves’ values linearly interpolated over time

Fig. 7
figure 7

Histogram of the temporal phase (as %R–R) at which the a maximum and b minimum area, and c maximum and d minimum perimeter were measured at the aortic annulus (AoA). The red dashed line represents the average mid-systolic phase (as %R–R) used by the observer to start the analyses (i.e. segmentation stage) across the study population. All measurement curves were temporally aligned as described in Fig. 6

The fact that the exact phase of maximum and minimum area/perimeter (Fig. 7) varied across the study population also corroborates the relevance of extracting these measures from multiple time points for an accurate prosthesis selection during preoperative TAVI planning, rather than from a single frame. Indeed, the phase of maximum size occurred, in median, at 20% of the R–R interval (area: 18.8%R–R, IQR [14.8, 27.0]; perimeter: 19.3%R–R, IQR [14.8 31.0]), as reported in Blanke et al. [12], which means that early systolic measures are slightly larger than those obtained at the mid-systolic phase, i.e. the indicated measurement phase in current guidelines [35]. In its turn, the phase of minimum size was, in median, at 80% the R–R interval (area: 81.7%R–R, IQR [63.0 92.9]; perimeter: 80.0%R–R, IQR [65.2, 92.5]), which is slightly later than the reported in a previous study [12]. This is partly related to a few cases in which the minimum value was found to be the ED frame (the last one in the sequence), which may be associated to some inaccuracy of the tracking algorithm given its distance from the mid-systolic reference frame and thus cumulated error. This result might be improved if one minimizes the number of propagation steps, as reported in Queirós et al. [19]. However, this type of strategies can only be applied to sequences with a complete cycle.

For completeness sake, Fig. 8 presents the measurements’ variation across the cardiac cycle for the other three studied levels. Despite the similar trends in relative changes across the cycle for both area and perimeter (larger values in systole and smaller ones in diastole), a distinct magnitude of relative change was obtained over time for each level. Indeed, the LVOT and aortic annulus presented larger relative changes in area and perimeter across the cycle when compared to both SoV and STJ levels (Table 2), with the difference between maximum and minimum measured values being statistically different for all levels. This has been reported for the aortic annulus in several previous studies [9, 11,12,13, 30], although the exact amount of change or its significance varied between populations (e.g., with or without aortic stenosis) and between studies (as described in the recent review on the subject in Suchá et al. [10]). Similar findings have also been described for the LVOT [14, 31]. Of note, when splitting the study population on the basis of the calcification severity (none/mild vs. moderate/severe cases; Table 1), no significant differences were observed for the measures’ relative changes at any of the studied levels (Appendix B).

Fig. 8
figure 8

Average ac area, df perimeter, and gi eccentricity index (EI) values measured across the cardiac cycle at the left ventricular outflow tract (LVOT), sinuses of Valsalva (SoV) and sinotubular junction (STJ), respectively. Relative change of jl area, mo perimeter, and pr EI values with respect to the end-diastole (last frame, 100% R–R interval). The vertical bars indicate the standard deviation of the measures across the study population. To obtain a temporal correspondence between frames, the first and last frames of all sequences were aligned, and the curves’ values linearly interpolated over time

Interestingly, the observed relative changes were lower for perimeter, when compared to the area. Such observation has been previously reported for the aortic annulus [12, 13], and has led to the suggestion of using perimeter-based values to size the TAVI prosthesis [36]. Note that this lower relative change for perimeter is not only associated to the relative change in AoA size (i.e. mathematically, these two quantities vary in different proportions with respect to the radius), but is particularly associated to the change in the AoA shape itself (see the changes in EI across the cycle in Fig. 6c, f), making the perimeter more robust (i.e. less variable) to differences throughout the cardiac cycle.

With respect to the EI (Figs. 6c, f, 8g–i, p–r), the AV tract presented a more circular geometry at the SoV and STJ levels, when compared to either AoA or LVOT planes. Moreover, the relative change of EI was significantly larger at the LVOT level (in a paired t-test against the other levels), which is in agreement with previous studies [14, 29]. In contrast, both SoV and STJ had smaller relative changes in EI across the cycle (in paired t-tests against both LVOT and AoA levels). Their larger area/perimeter values in systole can be mostly associated to an increase in size due to higher systolic than diastolic pressures. Note that, between them, the STJ presented a tendency for a lower relative change in area/perimeter values (Table 2; Fig. 8), which might be explained by the lower elasticity of this anatomical ring [26].

Appendix B

Table 4 presents the average (and standard deviation) of the maximum/minimum area and perimeter measured during the cardiac cycle, and associated absolute and relative differences, for the four studied levels, when splitting the study population on the basis of the calcification severity (none/mild vs. moderate/severe). Note that the calcification score (none, mild, moderate or severe grade) was visually determined by an experienced cardiologist using a preoperative MDCT scan at the time of TAVI planning and was retrospectively gathered for this study. Overall, despite the slightly different maximum/minimum values for some levels (namely LVOT, SoV and STJ), no statistically significant difference was found between groups for the measures’ relative changes (in a two-tailed unpaired t-test, with Welch’s correction). This result suggests that, for our study population, no differences exist in terms of magnitude of conformational changes between patients with lower (none/mild group) or higher (moderate/severe) amount of calcium.

Table 4 Maximum/minimum dimensions, and associated absolute and relative changes, for the four studied levels when dividing the study population based on the calcification score into “none/mild” and “moderate/severe” groups

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Queirós, S., Morais, P., Fehske, W. et al. Assessment of aortic valve tract dynamics using automatic tracking of 3D transesophageal echocardiographic images. Int J Cardiovasc Imaging 35, 881–895 (2019). https://doi.org/10.1007/s10554-019-01532-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10554-019-01532-w

Keywords

Navigation