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42. Feuchtner GM, Stolzmann P, Dichtl W, Schertler T, Bonatti J, Scheffel H, et al. Multislice computed tomography in infective endocarditis: comparison with transesophageal echocardiography and intraoperative fi ndings. J Am Coll Cardiol. 2009;53(5): 436–44.
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© Springer International Publishing 2016 M.J. Budoff, J.S. Shinbane (eds.), Cardiac CT Imaging: Diagnosis of Cardiovascular Disease, DOI 10.1007/978-3-319-28219-0_15
Transcatheter Aortic Valve Implantation (TAVI)
Chesnal Dey Arepalli , Christopher Naoum , Philipp Blanke , and Jonathon A. Leipsic
Abstract
Computerized tomography (CT) plays a pivotal role in selection of patients’, appropriate device size and pre-procedural guidance in successful outcome of transcatheter aortic valve implantation (TAVI). CT based vascular and non-vascular evaluation and integration of relevant measurements into TAVI work up has been shown to reduce morbidity and mortal­ity. Post-procedural device assessment and complications could also be reliably evaluated with CT. Utilization of CT is not just confi ned to TAVI but it is also increasingly being used for any transcatheter valvular assessment.
Keywords
AS – Aortic Stenosis • AVC – Aortic Valvular Calcifi cations • AA – Aortic Annulus • SOV – Sinus of Valsalva • Coronary Artery Ostium • PAR – Paravalvular Regurgitation • CT – Computerized tomography • TTE – Transthoracic Echocardiography • TEE – Transesophageal Echocardiography • TAVI – Transcatheter Aortic Valve Implantation
Introduction
Transcatheter aortic valve implantation (TAVI) is an alterna­tive treatment option for symptomatic severe aortic stenosis (AS) patients who are deemed inoperable or at high risk for surgical aortic valve replacement (AVR). TAVI as the name suggests is a procedure where in a bio-prosthetic device is implanted without removing the diseased valve via a trans­catheter approach.
The most common cause for AS is age related progressive calcifi cation of a normal aortic valve (Fig. 15.1a–c ) [ 1 , 2 ]. Additionally, congenital causes like bicuspid aortic valve or infl ammatory conditions like rheumatic heart disease are also common causes of AS [ 1 ]. The prevalence of senile AS is increasing as the mean age of Western societies is increas­ing [ 3 , 4 ]. Current data has documented the prevalence of AS in the elderly population (age ≥ 75 years) as 12.4 % and severe AS is 3.4 % [ 3 ]. Although senile or degenerative aor- tic stenosis occurs primarily in the elderly population, with mean age of 65–70 years, congenital bicuspid aortic valve (BAV) with signifi cant aortic stenosis tends to occur slightly earlier between 15 and 65 years of age (Fig. 15.1d ) [ 5 , 6 ]. In one study it was observed that BAV was the commonest cause of AS between the ages of 60 and 75 years (59 % of cases) and those aged less than 60 years, BAV was a caus­ative factor in 40 % [ 7 ]. BAV AS were found to require AVR 5 years before than those with a tricuspid valve [ 8 ].
Importantly, the natural clinical progression of symp­tomatic AS is rapid and associated with a poor clinical
C. D. Arepalli , MBBS, DNB • C. Naoum , MBBS, FRACP Department of Radiology , St Paul’s Hospital UBC , Vancouver , BC , Canada
P. Blanke , MD Department of Medicine , St Paul’s Hospital UBC , Vancouver , BC , Canada
J. A. Leipsic , MD, FRCPC, FSCCT (
*)
Department of Radiology , St. Paul’s Hospital , Room P2214 – 2nd Floor Providence Building 1081 Burrard Street , Vancouver , BC V6Z 1Y6 , Canada e-mail: jleipsic@providencehealth.bc.ca
1 5
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outcome with an average time of death shown to be within 5 years after onset of angina, 3 years after onset of syn­cope and within 1–2 years after onset of heart failure symptoms [ 9 ].
Until the advent of TAVI, the sole effective treatment option for symptomatic AS was surgical AVR. Medical treat­ment alone had very poor prognosis with a mortality rate of 50 % at 2 years. Unfortunately, many patients with severe symptomatic AS are denied this surgery owing to associated
co-morbidities in the elderly population that make surgical risk prohibitive [ 3 , 10 ].
TAVI is a new alternate therapy that has been shown through many registries, meta-analyses, and a number of randomized trials to be an effective therapy for severe symp­tomatic AS who were deemed inoperable and high risk sur­gical patients [ 11 , 12 ]. TAVI was fi rst pioneered by Cribier et al. in 2002 through transvenous transeptal approach [ 13 ]. However, over the past decade, alternative procedures have
a
cd
b
Fig. 15.1 Aortic valvular calcifi cation (AVC). AVC of varying degrees – ( a ) mild, ( b ) moderate, ( c ) severe, ( d ) Bicuspid aortic valve (BAV) with calcifi cation. Note the asymmetry of the cusps
with a larger non-coronary cusp and raphae between the right and the left coronary cusps in keeping with a Type 1 A Bicuspid Valve
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been developed and at present retrograde transarterial trans­femoral path, fi rst described by Webb and colleagues in 2005, is the most favored approach.
As opposed to surgical AVR where it is possible to directly visualize and measure the size of the aortic root; TAVI relies indirectly on imaging measurements before implantation. Based on these measurements; device selection and the pro­cedural approach are planned. Pre-procedural imaging plays a critical role in ensuring the success of the procedure and also to minimize the peri and post-procedural complications.
Imaging Modalities
Historically, TAVI imaging was reliant on measurements derived form 2-dimensional echocardiography and invasive angiography. However, multidetector computed tomography (MDCT) has grown to become an essential tool for the assessment of aortic root/annulus, evaluation of thoracic and abdominal aorta and ilio-femoral vessels. Moreover, MDCT is being used to predict optimal co-planar projection angles for device deployment.
Current state of the art CT scanners acquire data volu­metrically with isotropic spatial and high temporal resolu­tion. Post processing of data provide multiplanar and curved planar reformations (MPR and CPR), volume rendered tech­nique images (VRT), minimum and maximum intensity pro­jections (MIP
min
and MIP
max
respectively) which are essential to accurately size the aortic annulus, aortic root and other vascular access sites. Integration of CT data into sizing algo­rithms and work fl ow has consistently demonstrated signifi ­cant reduction in the incidence of paravalvular and vascular complications [ 1416 ]. Thus CT has become an accepted integral part in the overall work fl ow of TAVI patients. Of late, CT has also been shown to play an important additional role in valve in valve procedures.
The role of MDCT for valvular intervention can be
broadly discussed under three headings:
(a) Pre-procedural, (b) Peri-procedural and (c) Post procedural.
Although the focus of this chapter is on pre-procedural role of CT; it is equally pertinent to understand the peri and post procedural complications as they play an important role in understanding the dynamics of TAVI and thus indirectly infl uence the pre-procedural work up.
Before one can proceed with CT based ‘Sizing of the aor­tic annulus’ and procedural planning in the work up of TAVI patients, it is important to understand the complex aortic valve and root anatomy. Knowledge of the 3 dimensional (3 D) complex aortic root geometry and consideration of
various anatomical measurements are critical in the determi­nation of patient eligibility, bioprosthesis size, procedural planning and to anticipate procedural complications.
A n a t o m y
Aortic Root
The Aortic root is a further extension of the left ventricular outfl ow tract (LVOT). As a result, the LVOT should be con­sidered an anatomical segment between the left ventricle and ascending aorta.
As the aortic root is a complex dynamic structure; under­standing the morphology and kinesis of the aortic root sub­components helps in better appreciation of interplay of different sub-components with each other and also with adjacent struc­tures. This not only helps in procedural success but also has the potential in refi nement of the bio-prosthesis devices.
Aortic root sub-components include aortic annulus (AA), aortic sinus and the valvular leafl ets, the coronary ostia and the sinotubular junction.
Aortic Annulus
Broadly, two terms defi ne the aortic annulus – (a) anatomic annulus and (b) virtual basal ring. The Anatomical Aortic annulus is more of a histological demarcation that is defi ned as a fi brous structure that attaches the aortic root to the left ventricle. It consists of three coronets like structures that support the valvular leafl ets. The Virtual basal annulus is defi ned by nadir (lowest depth) plane of each of the coronets and it corresponds to the aortic-ventricular junction.
Although the term annulus suggests a circular shape, with the use of 3-D MDCT imaging , it has been found to be fairly consistently to be of a non-circular geometry with often elliptical and sometimes oval shaped confi guration [ 17 , 18 ].
It has been also observed that there are considerable variations in shape, size and direction of the annulus dur­ing the cardiac cycle (Fig. 15.2 ). These are infl uenced by deformation, stretch, compliance of the aortic root as well as left ventricular geometry, mitral valve anatomy and pathology [ 19 , 20 ]. Further, Nakai et al. [ 21 ] showed that there is cranial displacement of aortic annulus during early systole and in diastole whereas in rest of the systole and in isovolumetric relaxation there is caudal displacement. It has been observed in multiple studies, that the aortic annu­lus measurements in cohorts without and with aortic steno­sis show largest size (area) and diameter in systole and smallest measurements during diastole due to cyclical changes [ 2226 ].
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Imaging Modalities and Aortic Annulus Assessment
Strengths and Limitations of Echocardiography and MDCT
Accurate and reproducible pre-operative measurements of annulus are of paramount importance that helps in patient selection, device selection and size for TAVI procedure and also forecasting the outcome of the geometrical confi gura­tion of aortic annulus-prosthesis after implantation. In addition, better understanding of the aortic root complex and precise measurements would help in predicting and mitigating peri and post procedural complications.
Owing to the complex 3D aortic root geometry, measure­ments in a single plane have been shown to lead to both under or overestimation (depending upon the plane used) and have therefore been shown to be limited value for TAVI sizing. Two dimensional (2D) measurements as provided by transthoracic echocardiography (TTE) and transesophageal
echocardiography (TEE) are routinely used. In fact, the cur­rent TAVI device sizes provided by vendors are based on 2D echocardiography measurements. However, it was noted in several studies that echocardiography measurements under­estimated the true aortic annular size and were smaller in size when compared to MDCT.
In a meta-analysis, MDCT aortic annulus diameter mea­surements on coronal view were 25.3 ± 0.52 mm which were larger than sagittal view measurements by MDCT (22.7 ± 0.37 mm), TTE (22.6 ± 0.28 mm), and TEE (23.1 ± 0.32 mm) [ 27 ]. In a study by Mizia-Stec at el, the mean aortic annulus diameter on TTE was 24 ± 3.6 mm, 26 ± 4.2 mm using TEE, and 26.9 ± 3.2 mm on MDCT ( P = 0.04 vs. TTE) [ 28 ]. Messika-Zeitoun and colleagues [ 29 ] observed larger differences between CT and TTE (1.22 ± 1.3 mm) or TEE (1.52 ± 1.1 mm) than the difference between TTE and TEE (0.6 ± 0.8 mm; and p < 0.0001, respec­tively p = 0.03).
Early experiences with the integration of CT not only documented differences in annular measurements between
Fig. 15.2 Dynamic nature of Aortic Annulus over the course of cardiac cycle (75–25 %) ( a – f ) and corresponding measurements ( g – l ). Note the variation in the shape and size of the aortic annulus from diastole (65–75 %) through systole (25–35 %). Measurement of aortic annulus is usually performed in systole. The Geometrical
shape of the aortic annulus changes from elliptical in diastole (75 %) to near circular in systole (25 %). The perimeter size increased from 74 to 79 mm (~5 mm difference – ~6 %) variation, whereas area size increased from 4.24 to 4.84 cm
2
(~0.6 cm 2 differ-
ence – ~variation of 13 %)
abc
def
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MDCT and echocardiography but also differences in poten­tial sizing recommendations. Koos et al. evaluated the impact of 3D imaging methods (Cardiac magnetic reso­nance – CMR and dual source CT – DSCT) versus 2D TEE methods on TAVI selection [ 30 ]. In their cohort of 58 patients, different measurements would have changed TAVI strategy in 22–24 % patients. DSCT coronal measurements when compared to 2D TEE would have changed strategy in 16 patients. Further in 14/16 of those patients, the prosthe­sis size would have been larger and in the rest of the two, it was too large to implant. In a related similar study of 45 patients comparing 2D TTE and TEE and MSCT measure­ments, Messika-Zeitoun et al. observed that a decision based on MSCT would have modifi ed TAVI strategy in 40–42 % [ 29 ].
The limitations of 2-D imaging largely refl ect the complex almost uniformly non-circular confi guration of the annulus. It is not that 2-D diameters derived from echocardiography or MSCT are inaccurate but it is simply a geometrical reality that the complex morphology of a non-circular structure can­not be accurately characterized with a single 2-D measure­ment. The growing appreciation of the limitations of 2-D imaging has driven and increased focus on the utilization of
3D modalities in measurement of aortic root including aortic annulus and left ventricular outfl ow tract.
Ng et al. evaluated 2D circular, 3D circular and 3D pla­nimetered annular and LVOT areas by TEE and compared with MSCT planimetered areas [ 23 ]. In their cohort, the mean annular area by MSCT planimetry was 4.65 ± 0.82 cm 2 whereas by 2D TEE circular (3.89 ± 0.74 cm 2 , P < 0.001), 3D TEE circular (4.06 ± 0.79 cm 2 , P < 0.001), and 3D TEE pla­nimetered annular areas (4.22 ± 0.77 cm 2 , P < 0.001). They observed 3D TEE derived planimetered annular areas had the narrowest limits of agreement and least bias when com­pared to MDCT. Although the circular geometric assump­tions made by 2D and 3D circular measurements were overcome by 3D TEE; Ng et al. observed 3D TEE when compared to MDCT still underestimated annular areas by up to 10 %.
MSCT has also been shown to be highly discriminatory of those patients that historically experienced paravalvular regurgitations owing to undersizing secondary to device siz­ing on the basis of 2-dimensional echocardiography. Willson and colleagues noted that the annular area in particular on MDCT was highly discriminatory of PAR [ 31 ]. This was important knowledge as it has been well established the
ghi
jkl
Fig. 15.2 (continued)
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paravalvular regurgitation is associated with increased mor­bidity and mortality [ 2830 , 32 , 33 ].
Building upon this retrospective knowledge multiple groups have shown that the integration of MDCT in device selection allows for the reduction in the burden of PAR. Jilaihawi et al, prospective integration of CT guided algorithm reduced worse than mild paravalvular regurgita­tion (PAR) from 21.9 to 7.5 % when compared to 2D TEE [ 24 ]. Building upon this single center data Binder et al. in a prospective, multicenter controlled trial, evaluated the effects of the integration of an area based sizing algorithm on the clinical outcomes post TAVI [ 34 ]. With a non-randomized trial design half of the subjects (n = 133) underwent TAVI with the integration of MDCT measurements and sizing recommendations and the other half underwent TAVI without the integration of MDCT. They observed more than mild PAR (primary endpoint) was present in 5.3 % (7 of 133) of the MDCT group and in 12.8 % (17 of 133) in the control group (p = 0.032). The combined secondary endpoint (com­posite of in-hospital death, aortic annulus rupture, and severe PAR) occurred in 3.8 % (5 of 133) of the MDCT group and in 11.3 % (15 of 133) of the control group (p = 0.02). Finally the recently published large multicenter high risk CoreValve (Medtronic, Minneapolis, MN) trial showed excellent clini­cal outcomes as compared to surgical aortic valve replace­ment with the THV selection supported almost exclusively by MDCT perimeter measurements [ 35 ].
Dynamism of the Aortic Annulus
It is to be noted that aortic annulus is a dynamic structure with variation during systole and diastole phases of the car­diac cycle. The aortic annulus is often elliptical and assumes more circular shape during systole (Fig. 15.2 ). Further, it has been observed that there is increased asymmetrical deforma­tion during diastole which especially affects the right coro­nary cusp portion of the annulus [ 36 ]. The ellipticity index (EI) defi ned as ratio of maximum to minimum diameters substantially decreased from diastole to systole due to sig­nifi cant increase in antero-posterior minor diameter [ 25 ]. Signifi cant changes in area and radius were observed in both non-diseased annulus and stenotic annulus [ 37 ]. This has been attributed to annular reshaping than stretch with corre­sponding increase in systolic area [ 25 ].
Although cross-sectional area (CSA) derived measure­ments varied during cardiac cycle, it was found perimeter based diameter measurements show negligible increase in patients with calcifi ed valves (0.56 ± 0.85 %; p < 0.001) and very small changes in normal subjects (2.2 ± 2.2 %, p = 0.01) [ 25 ]. In another study by Aspern et al., no signifi cant differ- ence was observed with perimeter- derived effective diame­ters (ED) (mean difference: 0.2 ± 0.4; p = 0.07), however,
area derived ED showed a signifi cant mean difference (0.4 ± 0.6 mm; p = 0.009), thus reconfi rming infl uence of the cardiac cycle on aortic annulus area measurements [ 38 ]. It is likely that the diseased valves/tissues leave little scope for stretch and therefore perimeter derived aortic annulus mea­surements are least subjected to variation in cardiac cycle (Fig. 15.2 ). However, it is being noted smoothing algorithms used for perimeter derived measurements are inconsistent across work station platforms and might cause measurement errors. Although area based ED measurements are smaller than perimeter derived ED, both approaches showed good agreement [ 38 ].
Whether perimeter or area is chosen for transcatheter heart valve (THV) selection it is essential to understand the impact that the geometrical variable (area or perimeter derived measurements) may have on the prosthesis size that would be selected. Blanke et al. showed assuming a perfect circle with ellipticity index of 1, with increase in nominal diameter, area increases exponentially whereas perimeter increases proportionally [ 39 ]. Thus, for e.g. 10 % diameter oversizing would translate to 10 % increase in perimeter whereas it would increase area by 21 %. These geometrical truths are essential to understand and of clinical importance when certain degree of annular oversizing is contemplated during TAVI.
In summation, 3D MDCT measurements play a critical role in annular sizing and THV selection. MDCT measure­ments are accurate, reproducible and choice of area or perim­eter derived measurements need to be tailored depending upon the choice of prosthesis devices, allowing for dyna­mism of the aortic annulus and based on the available tools (software) available at the sites.
MDCT Measurement of the Aortic Annulus
Approach to Aortic Annulus Measurement
We recommend using the phase of the cardiac cycle with best image quality and in systolic phases (25–45 %) to allow for consistent assessment of the annulus when it is the largest. Aortic annulus measurements are performed orthogonally in relation to the plane of 3 hinge points on a dedicated work station. Manual multiplanar reformats of the annulus is pre­ferred as it helps in better understanding of the annulus and the annular plane rather than relying on automated tools which should ideally only be used by highly experienced operators. Briefl y, the steps to achieve ‘optimal’ sizing of the aortic annulus are mentioned below (Fig. 15.3 ), however, reader should look into expert consensus documents/recom­mendations for further in-depth information [ 15 , 40 ].
The fi rst step is to lock the orthogonal planes at 90° to each other. The cross hairs in the coronal and sagittal images
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a
d
ghi
ef
bc
Fig. 15.3 Steps to achieve optimal sizing of aortic annulus. Step 1: Volumetric data is loaded onto the workstation and in a standard 3D for­mat ( panel 1 ), the views are transverse ( a ), Coronal ( b ) and sagittal ( c ). The fi rst step is to lock the orthogonal planes at 90° to each other ( a – c ). Step 2: The cross hairs in the coronal and sagittal images are moved to the level of aortic valves and adjusted so that the cross hairs on the transverse plane are positioned at the level of aortic valve ( panel 2 – d – f ). Step 3: Then the cross hairs on the coronal and sagittal views are rotated and adjusted so as to correspond to the aortic annulus plane ( panel 3 ). Now the corresponding views are oblique set of images, for e.g. transverse/coronal/ sagittal oblique ( g – i ). Step 4: The cross hairs on the transverse oblique are rotated either clockwise or anticlockwise ( panel 3 g ) so as to check whether the cross hairs correspond to aortic annular plane i.e. nadir point of the coronary cusps ( panel 4 – j – l ). In this panel views, the cross hairs cuts across the cusp rather than located at the hinge/nadir point ( panel 4 – k ). Step 5: The cross hairs are further adjusted by placing the cross hairs at the aortic annular plane ( panel 5 – m – o ). Once again the cross hair on the transverse oblique view is rotated and again investigated to see the cross
hairs on the rest of the two oblique planes correspond to aortic annulus plane ( panel 6 – p – r ). Any adjustments, if necessary, are made by follow- ing the above steps. Step 6: Once a satisfactory plane is achieved ( panel 7s – u ), it is further confi rmed by toggling the transverse oblique set of images cranially and caudally across the aortic root ( panel 7 – s and panel 8 – v , red arrows ). If a true aortic annular plane has been achieved, then one would observe that the valve hinge points would disappear or appear symmetrically all at once ( panels 7 – su and 8 – vx ). Utmost focus is given so that cross hairs are just touching the nadir points (
panel 7s – u ). If this plane is not achieved, then the coronal ( panel 7 – t ) and sagittal oblique ( panel 7 – u ) planes needs to be further fi ne-tuned so as to achieve desired plane and again cross checked by rotating the cross hairs on the transverse oblique view ( panel 7 – s ). Step 7: Once an optimal view is achieved then the cross hairs are at the true aortic annular plane ( panel 9y , z , A ). Then a ROI trace is made along the circumference of the aortic annulus to calculate the major and minor diameters, mean diameters, area and circumference of the aortic annulus ( panel 9 – y ). Corresponding coronal and sagittal oblique planes are shown ( panel 9 – z , a )
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jkl
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Fig. 15.3 (continued)
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should be moved to the level of aortic valves and adjusted so that the transverse plane is positioned at the level of aortic valve. This would correspond to coronal and sagittal oblique planes respectively. Next the transverse oblique plane is moved up and down across the aortic root so as to visualize the valve hinge points. The valve hinge points should disap­pear or appear symmetrically all at once, if not, coronal and sagittal oblique planes need to be further fi ne-tuned so as to achieve desired plane. Again, the cross hairs are rotated
across the transverse oblique so that to visualize the nadir point of the valves in coronal oblique and sagittal oblique planes. Utmost focus is given so that cross hairs are just touching the nadir points and they disappear equally in all planes. Once this is confi rmed, the specifi c position of aortic annulus in the transverse oblique plane is identifi ed and a ROI trace is made along the circumference of the aortic annulus. Majority of the present day work stations have auto­matic tools that would calculate diameters (D) – Dmin,
s
v
yz
wx
tu
Fig. 15.3 (continued)
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