Aortic valve bypass (AVB) has been shown to be a viable solution for patients with severe aortic stenosis (AS). Under this circumstance, the left ventricle (LV) has a double outlet. The objective was to develop a mathematical model capable of evaluating the hemodynamic performance following the AVB surgery. A mathematical model that captures the interaction between LV, AS, arterial system, and AVB was developed. This model uses a limited number of parameters that all can be non-invasively measured using patient data. The model was validated using in vivo data from the literature. The model was used to determine the effect of different AVB and AS configurations on flow proportion and pressure of the aortic valve and the AVB. Results showed that the AVB leads to a significant reduction in transvalvular pressure gradient. The percentage of flow through the AVB can range from 55.47% to 69.43% following AVB with a severe AS. LV stroke work was also significantly reduced following the AVB surgery and reached a value of around 1.2 J for several AS severities. Findings of this study suggest: 1) the AVB leads to a significant reduction in transvalvular pressure gradients; 2) flow distribution between the AS and the AVB is significantly affected by the conduit valve size; 3) the AVB leads to a significant reduction in LV stroke work; and 4) hemodynamic performance variations can be estimated using the model.
Citation: Benevento E, Djebbari A, Keshavarz-Motamed Z, Cecere R, Kadem L (2015) Hemodynamic Changes following Aortic Valve Bypass: A Mathematical Approach. PLoS ONE 10(4): e0123000. https://doi.org/10.1371/journal.pone.0123000
Academic Editor: Alberto Aliseda, University of Washington, UNITED STATES
Received: May 25, 2014; Accepted: February 26, 2015; Published: April 16, 2015
Copyright: © 2015 Benevento et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper.
Funding: The work was supported by Fonds de recherche du Québec – Nature et technologies, 176048 (ZKM). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Aortic stenosis (AS) is the most common valvular disease in the elderly population. Untreated symptomatic AS is associated with a poor prognosis and significant morbidity. Aortic valve replacement (AVR) is currently the standard of care for reducing the left ventricular overload and improving the quality of life of patients . However, a significant proportion of patients (around 30% to 60%) are not referred to AVR because they fall within the category of high-risk patients [2,3,4]. This is typically because of comorbidities, severely calcified aorta (porcelain aorta) or narrow LVOT (<18 mm) . Transcatheter aortic valve replacement (TAVI) has recently emerged as a good option for such inoperable patients. However, TAVI might also be not feasible in all inoperable patients, such as those with porcelain aorta, bicuspid aortic valve, ostial encroachment or small LVOT, leaving a sub-population of ‘no-option’ patients [6,7]. Furthermore, TAVI and AVR appear to have similar major stroke rates at 30 days and 1 year (p = 0.20 and p = 0.07, respectively). However, when strokes and transient ischemic events are considered, AVR showed significantly better results compared to TAVI both at 30 days and 1 year (p = 0.04) . As a consequence, some investigators suggested the use of aortic valve bypass (AVB) as an alternative to TAVI or for patients with contraindications to both AVR and TAVI [9,10,11].
In AVB, also called apico-aortic bypass, the AS and the aorta are never manipulated and a second outflow tract for blood flow during systolic phase is created by inserting a valved conduit at the level of the left ventricle apex. This leads to a double outlet ventricle . The outflow conduit is connected to the descending thoracic aorta. The advantages of this approach are: 1) the calcified aortic valve and the aorta are never manipulated; 2) it is less subjected to patient-prosthesis mismatch; 3) there is no risk of damage to the ascending aorta or obstruction of the coronary arteries; 4) it potentially leads to less risks of stroke compared to the AVR.
In AVB, several combinations of conduit size and conduit valve size can be used. An important clinical parameter to predict is the proportion of blood flow crossing the native stenotic valve vs. the bypass conduit. In addition, previous studies [13,14,15] showed that this flow distribution can be clinically determined using magnetic resonance imaging. Another important parameter to evaluate is the left ventricle stroke work, representing the work of the left ventricle during each heart beat, before and following the AVB surgery.
The objective of this study was to develop a mathematical model that can predict the variation in hemodynamic parameters (mainly transvalvular pressure gradients; flow distribution between the native aortic valve and the conduit) and left ventricle load following the aortic valve bypass surgery. The challenge was to develop a model solely based on non-invasive patient data, characteristics of the conduit (its diameter) and the hemodynamic performance of the conduit valve (its effective orifice area). We validated the model using existing clinical data and we provided results allowing a better understanding of the expected hemodynamic outcomes following the AVB surgery.
A schematic diagram of the lumped parameter model is presented in Fig 1. The code developed by Keshavarz-Motamed et al. [16,17] was modified to simulate the AVB. This model includes four different sub-models: 1) left ventricle (LV) model; 2) AS model; 3) systemic circulation model; and 4) AVB model. All parameters used in the lumped parameter model are listed in Table 1.
(A) Electrical representation, (B) schematic representation of the lumped parameter model used to simulate left-sided heart in presence of aortic stenosis and/or apico-aortic conduit (please see Table 1 for all other parameters used in the lumped parameter model).
Heart function was described by time varying elastance as the following: (1) where PLV(t), V(t) and V0 are the LV pressure, the LV volume and the unloaded volume , respectively. The amplitude of E(t) was normalized with respect to maximal elastance Emax, giving EN(tN) = E(t)/Emax. Time was then normalized with respect to the time to attain peak elastance, TEmax (tN = t/TEmax). Note that normalized time-varying elastance curves EN(tN) have similar shapes in the normal human hearts with various inotropic situations or for diseased human hearts despite the existence of differences with regard to etiology of cardiovascular diseases [18,19].(2)
This normalized curve, represented as a Fourier series , can be described mathematically. Thus, when EN(tN) is given, the relation between PLV(t) and V(t) for any ventricle is determined. The ventricle is filled by a normalized physiological mitral flow waveform adjusted for the total required stroke volume, in this study 75 ml [16,17].
Aortic Stenosis Model
The AS was modeled using the analytical formulation for the net pressure gradient (TPGnet) across the stenotic valve during LV ejection introduced by Garcia et al.  This formulation expresses the instantaneous net pressure gradient across the AS as a function of the instantaneous flow rate and the energy loss coefficient.(3)
and (4) Where ELCo, EOA, A, ρ and Q are the valvular energy loss coefficient, the effective orifice area, ascending aorta cross sectional area, the fluid density and the transvalvular flow rate, respectively. ELCo, introduced by Garcia et al. , representing the ‘recovered EOA’, denotes valve effective orifice area adjusted for the area of the aorta at the level of sinotubular junction. Therefore, variable aortic valve resistance (Rav) and constant aortic valve inductance (Lav) (Fig 1) in the lumped parameter model are and , respectively (Eq 3).
Aortic Valve Bypass Model
In a normal heart, total blood flow ejected by the LV, after crossing the aortic valve, is redirected towards the upper-body. However, after the AVB surgery, a portion of the blood flow ejected by the LV goes towards the AS and the other portion towards the descending aorta through the bypass conduit. To take this into account in the model, a branch is placed in parallel to the AS (Fig 1). This branch simulates the flow bypassing the AS. Since, no formulation has been developed to express the net instantaneous pressure gradient through a conduit valve yet, we elected to use the same formulation as the one used for modeling the stenotic valve (Eq 3). Therefore, this branch includes a constant resistance for conduit tube (RAVB) (Table 1) plus a time-varying resistance (), and an inductance () which together represent the net pressure gradient induced by the conduit valve (Eq 3). The EOA of the conduit valve was determined as follows: for a specific bioprosthetic valve size (between 19 and 29 mm), the reported EOAs of all the manufacturers listed in Pibarot et al.  were averaged. Yet a 17 mm valve can also be used for AVB surgery in adult patients. Therefore, the EOA for a conduit valve of 17 mm was extrapolated from the data reported in Pibarot et al .
Here, we provide a succinct description, see Keshavarz-Motamed et al. [16,17] for more details. The lumped model illustrated in Fig 1 was analyzed numerically by creating and solving a system of ordinary differential equations in Matlab Simscape (MathWorks, Inc). Fourier series representation of experimental normalized elastance curve for human adults introduced by Senzaki et al.  was used to generate a signal as an input into the main program. Simulation started at the onset of isovolumic contraction. The left ventricle volume V(t) was calculated using the left ventricle pressure PLV and elastance values using Eq 1. The left ventricle is filled by a normalized physiological mitral flow waveform adjusted for the total required stroke volume. The left ventricle flow rate subsequently was calculated as the time derivative of the left ventricle volume. After few initial cycles, solution converged. Matlab’s “ode23t” trapezoidal rule variable-step solver was used to solve system of differential equations with the initial time step of 0.1 milliseconds. The convergence residual criterion was set to 10–5. All initial values including voltages and currents of capacitors and inductors were set to zero.
Verification of the Lumped Parameter Model using in vivo Published Data
Verification of the model was done based on the study reported by Stauffer et al.  for different configurations of the AVB: 1) conduit size (diameter): 18 mm, conduit valve size (diameter): 19 mm; 2) conduit size: 20 mm, conduit valve size: 21 mm; and 3) conduit size: 22 mm, conduit valve size: 23 mm. Postoperative flow assessments using magnetic resonance imaging for these configurations show that 65% of the outflow is conducted from the LV apex to the conduit, while only 35% crosses the AS . The blood flow proportion through a severe AS with two different severities (EOAs: 0.61 cm2 and 0.7 cm2) and different configurations of conduit were calculated using the lumped parameter model developed in this study and compared to the flow proportion from in vivo data. Data resulting from our mathematical simulations were consistent with Stauffer et al. findings (range of errors: 0.11% to 8.46%) (see Table 2) .
Pre-AVB Surgery: Simulation in the Presence of a Severe AS
Fig 2 shows the LV and aortic waveforms simulated using the current model for: 1) a healthy aortic valve (no AS: EOA = 4 cm2); 2) severe AS with EOA of 0.7 cm2. As expected, the presence of a severe AS induces very large transvalvular pressure gradients: TPGmax = 99 mmHg; TPGmean = 52 mmHg. The results for an EOA of 0.7 cm2 are displayed because this EOA corresponds to the median value reported in the study of Lund et al.  for patients with AVB.
Post- AVB Surgery: Simulation in the Presence of AS and AVB
Fig 3a and 3b show the computed LV and aortic waveforms after the AVB surgery for the AS with an EOA of 0.7 cm2. Here the results for an AVB with a conduit valve size of 19 mm and two different conduit sizes (18 mm and 26 mm) are displayed. The AVB induced a significant reduction in LV peak pressure and TPGs that can be reduced down from 99 mmHg (Fig 2b) to 28/25 mmHg (Fig 3a and 3b) for TPGmax and from 52 mmHg (Fig 2b) to 17/15 mmHg (Fig 3a and 3b) for TPGmean. Moreover, Fig 3 shows the calculated flow rate distribution between the AS and the AVB. A LV with an AVB with a conduit valve size of 19 mm and a conduit size of 18 mm is expected to eject 36.57% of the total flow rate through the AS and 63.43% through the bypass. Now, if a conduit size of 26 mm is used with the same conduit valve size, flow distribution changes slightly: 40.45% through the AS and 59.55% through the AVB.
(A) Severe AS (EOA = 0.7 cm2) & AVB (conduit valve size: 19 mm, conduit size: 18mm), (B) severe AS (EOA = 0.7 cm2) & AVB (conduit valve size: 19 mm, conduit size: 26mm). Stroke volume, heart rate and cardiac output are 75 ml, 70 beats/min and 5.2 l/min, respectively.
Flow Distribution after AVB
Table 2 represents the flow distribution between the AVB and the aortic valve predicted using the lumped parameter model for EOA = 0.7 cm2. Here several possible combinations of conduit valve size and conduit size are considered. For an AS with EOA = 0.7 cm2, the percentage of the total flow crossing the aortic valve ranges from 30.57% to 44.53% (mean value: 36%).
Left Ventricle Stroke Work after AVB
Fig 4 shows the reduction in LV stroke work following the AVB surgery. The LV has to develop a stroke work of 1.82 J in order to overcome the overload imposed by a severe AS with an EOA of 0.7 cm2 (Fig 4a). Now with an AVB with a conduit valve size of 19 mm and a conduit size of 18 mm, the LV stroke work is significantly reduced to 1.19 J (-0.63 J; -34%) (Fig 4b). A larger conduit size of 26 mm leads to small variations in LV stroke work compared to a 18 mm conduit (1.21 J vs.1.19 J).
(A) Pre-AVB surgery for a severe AS (EOA = 0.7 cm2), (B) post-AVB surgery with a conduit valve size of 19 mm and a conduit size of 18mm, (C) LV stroke work variations with and without AVB for different AS severities. The values are averaged over the all configurations for AVB in terms of conduit and valves sizes simulated in this study.
Fig 4c shows the reduction in LV stroke work following the AVB surgery for several AS severities (EOA range: 0.55 cm2 to 0.75 cm2). LV stroke work values corresponding to the AVB for each AS severity were averaged over all configurations of conduit valve size and conduit size tested in this study. For all AS severities, the AVB contributed to a significant reduction in the LV stroke work. The LV stroke work values reached following the AVB surgery are not significantly affected by the selected conduit valve size/conduit size configurations for the AVB and reached a value around 1.2 J. This value remains however higher than normal LV stroke work values (1.03 J).
We have introduced a lumped-parameter method which captures the interaction between left ventricle, AS, arterial system, and AVB. This method only needs few non-invasively measured quantities described as follows: 1) total stroke volume; 2) EOA of the aortic valve and aortic cross sectional area (A); (3) EOA of the conduit valve and conduit area. All the above mentioned parameters can easily be measured in patients non-invasively [17,22]. The key findings of this study are the followings: 1) the AVB leads to a significant reduction in transvalvular pressure gradient; 2) the conduit valve size, compared to the conduit size, has more effect on flow distribution between the AS and the AVB; 3) The flow distribution between the AS and the AVB can be predicted mathematically using non-invasive patient data; 4) the AVB leads to a significant reduction in LV stroke work.
AVB is not a new technique, the first reference to AVB was in 1910  and in 1995 , used in animals. This was also followed by its implantation in human by Templeton in 1962 (unpublished work). However, as its development was in the same period of prosthetic heart valves, the success of the AVR reduced temporarily the interests in the AVB. But, with the expected increasing number of high-risk patients with severe symptomatic AS and contraindication to the AVR (due to comorbidities, calcified aorta or narrow LVOT), alternative strategies have to be developed or revived.
TAVI seems to be a very attractive option for such inoperable patients. However, TAVI may be complicated if performed in patients with calcified aorta (expect for the apical approach), ostial encroachment or bicuspid valve. In a recent study, Garcia et al.  showed that around 25% of patients with AS have a bicuspid valve. As a consequence, there will always exist a sub-population of ‘no-option’ patients. For such patients, the AVB, using the new developed device by Correx Inc., can be an interesting option for such patients since the aortic valve and the aorta remain undisturbed. As a consequence, this limits significantly the risks of stroke and thromboembolism [10,26]. Furthermore, since the prosthetic valve is located inside the conduit, it is not subjected to prosthesis-patient mismatch restrictions .
In this study, we showed that the AVB leads to a significant reduction in TPG. It should be mentioned however that the reduction in the TPG can mainly be attributed to the significant reduction in the flow rate crossing the aortic valve following the AVB surgery.
This flow distribution is a major determinant of the residual transvalvular pressure gradient through the native aortic valve following AVB. To determine this ratio, the model developed in this study needs only non-invasive parameters that are routinely measured in daily clinical practice and the EOA of the bioprosthetic valve in the conduit (listed in Pibarot and Dumesnil ). The results, using the current model, show that the flow through the conduit may represent between 55.47% and 72.1% of the total flow rate depending on the EOA of the AS, the EOA of the conduit valve and the size of the conduit. The most important determinant of the flow distribution is the conduit valve size (in this study: R = 0.84, p<0.01). The results obtained in this study are consistent with previous in vivo and in silico studies [6,10,26].
Another significant result found in this study is that the AVB significantly reduces the LV stroke work. The expected post-operative LV stroke work is appeared to be quite independent from the selected AVB configurations. Interestingly, it has been hypothesized that the AVB might provide better overall hemodynamic performance since the net effective orifice area should be the summation of the effective orifice area of the stenotic aortic valve plus the effective orifice area of the bioprosthetic valve included in the conduit . Our results show that the LV stroke work values obtained following the AVB surgery are statistically significantly higher than those expected by simply adding up the conduit valve EOA and the aortic valve EOA (1.19±0.03 J vs. 1.10±0.05 J, p<0.001). However, the differences appear not to be clinically significant.
Since no formulation has been developed to express the net instantaneous pressure gradient through a conduit valve yet, we elected to use the same formulation as the one used for modeling the aortic valve. In order to assess the validity of this formulation, data resulting from our mathematical simulations were compared with in vivo findings (Stauffer et al. ), resulted to good agreements between them (range of errors: 0.11% to 8.46%). However, more in vivo and in vivo studies are still required to determine further the validity of the equation mainly for large conduit valve sizes.
AVB is a viable solution for patients with AS and contraindications to both AVR and TAVI. AVB leads to a double outlet LV. In this study, we have shown by using mathematical modelling that AVB leads to a significant reduction in pressure gradient across the AS and LV stroke work. Furthermore, the results show that the flow distribution (through AS vs. AVB) can be predicted mathematically and its main determinant is conduit valve size. Finally, AVB leads a significant reduction in LV stroke work whatever is the configuration of conduit valve size and conduit size. Finally, the positive hemodynamic results obtained in this study following AVB may suggest a need for a randomized trial comparing TAVI and AVB.
Dr. Zahra Keshavarz-Motamed is supported by the Fonds de Recherche du Québec-Santé (FRSQ) and Natural Sciences and Engineering Research Council of Canada (NSERC).
Conceived and designed the experiments: ZKM LK RC. Performed the experiments: EB AD ZKM. Analyzed the data: EB AD. Contributed reagents/materials/analysis tools: LK ZKM. Wrote the paper: EB ZKM LK. Interpreted the data: EB AD ZKM LK RC.
- 1. Asimakopoulos G, Edwards MB, Taylor KM. Aortic valve replacement in patients 80 years of age and older: survival and cause of death based on 1100 cases. Collective results from the UK Heart Valve Registry. Circulation 1997;96: 3403–3408. pmid:9396434
- 2. Charlson E, Legedza AT, Hamel MB. Decision-making and outcomes in severe symptomatic aortic stenosis. J Heart Valve Dis. 2006;15: 312–321. pmid:16784066
- 3. Rosengart TK, Feldman T, Borger MA, Vassiliades TA Jr, Gillinov AM, Hoercher KJ, et al. Percutaneous and minimally invasive valve procedures: a scientific statement from the American Heart Association Council on Cardiovascular Surgery and Anesthesia, Council on Clinical Cardiology, Functional Genomics and Translational Biology Interdisciplinary Working Group, and Quality of Care and Outcomes Research Interdisciplinary Working Group. Circulation 2008;117: 1750–1767. pmid:18332270
- 4. Varadarajan P, Kapoor N, Bansal RC, Pai RG. Survival in elderly patients with severe aortic stenosis is dramatically improved by aortic valve replacement: Results from a cohort of 277 patients aged > or = 80 years. Eur J Cardiothorac Surg. 2006;30: 722–727. pmid:16950629
- 5. Lund JT, Jensen MB, Arendrup H, Ihlemann N. Aortic valve bypass: experience from Denmark. Interact CardioVasc Thorac Surg. 2013;17: 79–83. pmid:23529752
- 6. Vliek CJ, Balaras E, Li S, Lin JY, Young CA, DeFilippi CR, et al. Early and midterm hemodynamics after aortic valve bypass (apicoaortic conduit) surgery. Ann Thorac Surg. 2010;90: 136–143. pmid:20609764
- 7. Wijesinghe N, Ye J, Rodes-Cabau J, Cheung A, Velianou JL, Natarajan MK, et al. Transcatheter aortic valve implantation in patients with bicuspid aortic valve stenosis. JACC Cardiovasc Interv. 2010;3: 1122–1125. pmid:21087746
- 8. Palacios I. Transcatheter aortic valve implantation: the interventionist vision. Circulation 2012;125: 3233–3236. pmid:22733338
- 9. Cooley D, Lopez RM, Absi TS. Apicoaortic conduit for left ventricular outflow tract obstruction: revisited. Ann Thorac Surg. 2000;69: 1511–1514. pmid:10881832
- 10. Gammie JS, Krowsoski LS, Brown JM, Odonkor PN, Young CA, Santos MJ, et al. Aortic valve bypass surgery: midterm clinical outcomes in a high-risk aortic stenosis population. Circulation 2008;118: 1460–1466. pmid:18794389
- 11. Reuthebuch O, Fassl J, Brown J, Grapow M, Eckstein F. Early experiences and in-hospital results with a novel off-pump apico-aortic conduit. Interact CardioVasc Thorac Surg. 2013;16: 482–487. pmid:23307931
- 12. Shanebrook JR, Levine ML. Hemodynamics of left ventricular apex-aortic valved conduits Cardiovasc Dis. 1979;6: 425–438. pmid:15216295
- 13. Kotani S, Hattori K, Kato Y, Shibata T. Thrombus in the distal aortic arch after apicoaortic conduit for severe aortic stenosis. Interact Cardiovasc Thorac Surg. 2010;10: 486–488. pmid:20007638
- 14. Stauffer CE, Jeudy J, Ghoreishi M, Vliek C, Young C, Griffith B, et al. Magnetic resonance investigation of blood flow after aortic valve bypass (apicoaortic conduit). The Ann Thorac Surg. 2011;92: 1332–1337. pmid:21958780
- 15. To A, Karuppasamy K, Roselli E, Flamm S. Comprehensive Post-Operative Assessment of Apico-Aortic conduit for Aortic Stenosis with Cardiac Magnetic Resonance Imaging. J Am Coll Cardiol. 2011;58: 0735–1097.
- 16. Keshavarz-Motamed Z, Garcia J, Pibarot P, Larose E, Kadem L. Modeling the impact of concomitant aortic stenosis and coarctation of the aorta on left ventricular workload. J Biomech. 2011;44: 2817–25. pmid:21955730
- 17. Keshavarz-Motamed Z, Garcia J, Gaillard E, Capoulade R, LeVen F, Cloutier G, et al. Non-invasive determination of left ventricular workload in patients with aortic stenosis using magnetic resonance imaging and Doppler echocardiography. PLoS ONE 2014;9: e86793. pmid:24489786
- 18. Suga H, Sagawa K, Shoukas AA. Load independence of the instantaneous pressure-volume ratio of the canine left ventricle and effects of epinephrine and heart rate on the ratio. Circulation Research 1973;32: 314–322. pmid:4691336
- 19. Senzaki H, Chen CH, Kass DA. Single-beat estimation of end-systolic pressure-volume relation in humans. A new method with the potential for noninvasive application. Circulation 1996;94: 2497–2506. pmid:8921794
- 20. Garcia D, Pibarot P, Durand LG. Analytical modeling of the instantaneous pressure gradient across the aortic valve. J Biomech. 2005;38: 1303–1311. pmid:15863115
- 21. Pibarot P, Dumesnil JG. Prosthetic heart valves: selection of the optimal prosthesis and long-term management. Circulation 2009;119: 1034–1048. pmid:19237674
- 22. Zoghbi WA, Chambers JB, Dumesnil JG, Foster E, Gottdiener JS, Grayburn PA, et al. Recommendations for evaluation of prosthetic valves with echocardiography and doppler ultrasound: a report From the American Society of Echocardiography's Guidelines and Standards Committee and the Task Force on Prosthetic Valves, developed in conjunction with American College of Cardiology Cardiovascular Imaging Committee; Cardiac Imaging Committee of the American Heart Association; European Association of Echocardiography; European Society of Cardiology; Japanese Society of Echocardiography; Canadian Society of Echocardiography; American College of Cardiology Foundation; American Heart Association; European Association of Echocardiography; European Society of Cardiology; Japanese Society of Echocardiography; Canadian Society of Echocardiography. J Am Soc Echocardiogr. 2009;22: 975–1014. pmid:19733789
- 23. Carrel A. On the Experimental Surgery of the Thoracic Aorta and Heart. Ann Surg. 1910;52: 83–95. pmid:17862563
- 24. Sarnoff SJ, Donovan TJ, Case RB. The surgical relief of aortic stenosis by means of apical-aortic valvular anastomosis. Circulation 1995;11: 564–575.
- 25. Garcia J, Kadem L, Larose E, Clavel MA, Pibarot P. Comparison between cardiovascular magnetic resonance and transthoracic doppler echocardiography for the estimation of effective orifice area in aortic stenosis. JCMR. 2011;13: 25. pmid:22029838
- 26. Balaras E, Cha KS, Griffith BP, Gammie JS. Treatment of aortic stenosis with aortic valve bypass (apicoaortic conduit) surgery: an assessment using computational modeling. Thorac Cardiovasc Surg. 2009;137: 680–687. pmid:19258088
- 27. Elmistekawy E, Lapierre H, Mesana T, Ruel M. Apico-Aortic Conduit for severe aortic stenosis: Technique, applications, and systematic review. Journal of the Saudi Heart Association 2010;22: 187–194. pmid:23960619