Previous studies have suggested that concomitant mitral regurgitation (MR) is a risk factor for acute transcatheter aortic valve implantation (TAVI) failure, but may improve afterwards. Aim of this study was to assess the prevalence, clinical meaning and modifications of MR in patients undergoing TAVI.
Methods
In a retrospective, two-center (Potenza-San Carlo and Roma- San Camillo) study, from January 2010 to June 2014 we enrolled 165 consecutive patients (age =80 ± 5 years, 74 males, Ejection Fraction 51 ± 9 %) referred for TAVI with either Medtronic Core-ReValving System (in 114 patients, 69 %) or balloon-expandable Edwards SAPIEN/SAPIEN XT (in 51 patients, 31 %). All patients underwent TTE and TEE assessment of MR (from 1, mild to 4 = severe according to ESC latest guidelines) with core lab reading by a single observer blinded to patient identity and status. Assessment was performed at baseline (24 h prior to intervention) and at 1, 6, 12 and 24 months.
Results
Mild-to-Moderate MR (grade 1–2) was present in 137 patients and Moderate-to-Severe MR (grade 3–4) was present in 28 patients. No significant differences were seen comparing perioperative mortality and morbidity between the two groups. In the group of preoperative MR grade 3–4 the mean decrease from MR pre-TAVI to MR at 1 month post-TAVI was 0.464 (p < 0.0001) and this improvement was persistent at 6 months (p < 0.0001) and at 12 months (p < 0.0001), with partial benefit loss at 1 and 2 years. The mean difference from Left Atrial volume post-TAVI at 1 month was 16.5 ml (p < 0.0001) and this improvement was persistent at 12 months 12.12 ml (p < 0.0001).
Conclusions
TAVI effectively treats the aortic valve but as a beneficial by product also ameliorates concomitant MR. The presence of moderate-to-severe MR does not increase the acute risk of failure of TAVI. In successful procedures, the MR improves immediately and persistently.
Hinweise
Competing interests
All Authors have not competing interests (financial and non-financial competing interests).
Authors’ contributions
MFC participated in the design of the study, in the data collect, performed exams, coordinated and helped to draft the manuscript. ED participated in the design of the study, in the data collect, performed exams, helped to draft the manuscript. PI participated in the design of the study, in the data collect, performed exams, helped to draft the manuscript. AM participated in the design of the study, in the data collect, performed exams, helped to draft the manuscript. VS participated in the design of the study, in the data collect, performed exams, helped to draft the manuscript. RV performed invasive procedures. RF performed invasive procedures. GC performed statistical analysis. NM participated in the design of the study, in the data collect, helped to draft the manuscript. EP participated in the design of the study, coordinated and helped to draft the manuscript. GD performed invasive procedures. All authors read and approved the final manuscript.
Background
Mitral regurgitation (MR) is a common finding in patients with aortic stenosis (AS). At the time of aortic valve replacement (AVR) up to two thirds of patients with AS have varying degrees of MR [1]. Most published studies on valvular heart disease have focused on either regurgitant or stenotic single valve disease. Data on multi-valve disease are scarce. As result, North American and European guidelines offer limited insight with respect to management of multivalve disease. Those recommendations that are made are largely based on small studies or on expert consensus opinion (Grade C).
A decrease in MR severity is common following isolated AVR [2‐4]. Early improvement might result from acute reverse left ventricular (LV), including a reduction in LV end-diastolic volume and a decrease in mitral tethering forces [5, 6].
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Transcatheter valve therapies are a feasible alternative to conventional open-heart surgery in many patients with valvular disease. For AS, transcatheter aortic valve implantation (TAVI) is the standard of care in inoperable patients and an alternative to SVAR in high-surgical risk patients [7‐13]. However , TAVI is still a relatively novel technology, and short and long term morbidity and mortality after TAVI remain significant [14]. There is substantial interest in the identification and modification of factors influencing morbidity and mortality after TAVI.
Recently, Chakravarty et al. [14], have reported that moderate-severe MR is present in 20 % to 30 % of patients who underwent TAVI and constitutes a significant coexisting valvular heart disease burden [15‐21]. In this meta-analysis, the severity of MR improved after TAVI in 61 ± 6.0 % of patients, but baseline moderate-severe MR and significant residual MR after TAVI are associated with an increase in mortality after TAVI and represent an important group to target with medical or transcatheter therapies in the future [14]. Therefore the aim of this retrospective, observational, two-center study was to evaluate the improvement of mitral regurgitation in patients undergoing TAVI with concomitant MR.
Methods
Study design and patient population
From January 2010 to June 2014, 165 consecutive patients affected by severe aortic stenosis underwent TAVI either using Medtronic Core-ReValving System (in 114 patients, 69 %) or using balloon-expandable Edwards SAPIEN/SAPIEN XT (in 51 patients, 31 %) at Potenza-San Carlo Hospital and Roma-San Camillo Hospital.
All patients were evaluated for TAVI by the local heart team, which included a clinical cardiologist, an interventional cardiologist, a cardiac surgeon, and a cardiac anesthesiologist. The evaluation of the heart team led to the indication for TAVI after careful assessment of all the clinical/anatomic conditions determining a higher risk of mortality/morbidity after surgery. In all patients scheduled for TAVI who gave written consent for the procedure follow-up was scheduled at 1, 6, 12 and 24 months. Patients were followed up by means of outpatient clinics and regular contact with clinical cardiologist. At any follow-up time all patients are underwent a clinical exam and echocardiographic study.
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To define the events in the follow-up we referred to the current standard for definition of the events in TAVI represented by VARC-2 criteria [22].
Device and procedure
Arterial access (femoral,radial), percutaneous puncture, or surgical exposure was also determined
on the basis of the panel of preoperative imaging tests, which included in all cases both angiography and computed tomography scan. After the procedure, all patients were managed in an intensive care unit or coronary care unit for at least one day.
Data collection and definitions
Transthoracic and TEE echocardiography was performed before TAVI, after TAVI, and at 1, 6, 12 and 24 months by a senior cardiologist. MR severity was graded as no/mild (0/1), moderate (2), moderate-severe(3) or severe (4), [23]. Mitral annular calcification, prolapse and thickening was reported according to the guidelines [23]. MR type has been classified as organic (primary) or functional (secondary). Organic MR is attributable to intrinsic valvular disease, whereas functional MR is caused by regional or global left ventricle (LV) remodeling without structural abnormalities of the valve apparatus. A medical record reporting a fatality was available in 13 patients (7.9 %); echocardiographic follow-up was available in 152 patients. Basal characteristic of overall population are shown in Table 1.
Table 1
Basal characteristic of overall population according to MR grade groups
Categorical variables were presented as absolute numbers and percentages and compared using chi-square test. Continuous variables were presented as mean ± standard deviation and were compared using t-test.
For echocardiographic data, a two way analysis for repeated measures (between the two groups and among different times) was performed using the Linear Mixed Model; individual comparison between groups for each parameter at different times was carried using unpaired t-test with post-hoc Bonferroni correction.
Kaplan and Meier curves were used to calculate the survival probability. Cox proportional hazard model was instead used to perform univariate analysis of mortality. Since only a single factor (female sex) was found to have a p value ≤ 0.10, multivariate analysis could not be carried.
All P values reported are 2 sided, and a value of P < 0.05 was considered significant. All data were processed with the Statistical Package for Social Sciences, version 21 (SPSS, Chicago, IL).
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Results
Moderate-Severe MR (Grade 3–4) at the time of the procedure was present in 28 pts (17 %).
Mild-Moderate MR (Grade 1–2) was present in 137 pts (83 %).
Patients with concomitant grade 3–4 MR appear quite different from patients with grade 1–2 MR.
Patients with Moderate-Severe MR (Grade 3–4) had a lower LV function compared with patients with Mild-Moderate MR (Grade 1–2) (39.8 ± 7.5 % versus 53.2 ± 7.9 %; p < 0.0001), a lower trans-aortic Mean gradient (39.5 ± 10.5 mmHg versus 45.8 ± 7.2 mmHg; p = 0.002) and a lower trans-aortic Peak gradient (63.8 ± 20.8 mmHg versus 77.9 ± 15.7 mmHg; p < 0.0001).
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In patients with grade 3–4 MR, the aetiology of mitral valve disease is predominantly functional (75 %) as also confirmed by the significantly lower incidence of structural changes of the mitral leaflets (Calcifications 7.1 % and Thickening 17.9 %).
Although preoperative characteristics are different, there aren’t statistically significant differences, as shown in Table 2, regarding mortality at 30 days between two groups (3 patients, 2.1 % for MR grade 1–2 group and 0 patients, 0 % for MR grade 3–4 group; p = 0.99) and incidence of peri-procedure complications: bleeding (4 patients, 2.9 % for MR grade 1–2 group and 2 patients, 7.1 % for MR grade 3–4 group; p = 0.26); neurological complications (7 patients, 5.1 % for MR grade 1–2 group and 0 patients, 0 % for MR grade 3–4 group; p = 0.60).
Table 2
Post operative results, according to MR grade groups
All
Preoperative MR
Preoperative MR
p value
Grade 3–4
Grade 1–2
Patients
165
28
137
30 days mortality
3 (1.8 %)
0
3 (2.1 %)
0.99
Bleeding
6 (3.6 %)
2 (7.1 %)
4 (2.9 %)
0.26
Neurological complications
7 (4.2 %)
0
7 (5.1 %)
0.60
Analysis of echocardiographic parameters
In the overall population, MR score went from 2.1 ± 0.6 to 1.6 ± 0.8 (p < 0.001) at the end of follow-up. Figure 1 depicts the comparison between the two study groups regarding the degree of MR before and following TAVI up to two years: two way repeated analysis showed a significant difference on the degree of MR between the groups (F = 573.1; p < 0.001) and across the different times (F = 72.3; p < 0.0001). For the group with preoperative MR grade 1–2 no significant difference was noted comparing the degree of preoperative MR with any of the postoperative timeframes.
Fig. 1
Different value of degree of mitral regurgitation at 0, 6, 12 and 24 months of follow-up in the two groups
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In the group with preoperative MR grade 3–4 the mean decrease from MR pre-TAVI to MR at 1 month post-TAVI was 0.464 (p < 0.0001) and this improvement was persistent at 6 months (p < 0.0001), 12 months (p < 0.0001) and 24 months (p < 0.0001), with partial benefit loss at 1 and 2 years (Fig. 1).
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Figure 2 depicts the comparison between the two study groups regarding the degree of Vena Contracta (VC) before and following TAVI up to two years: two way repeated analysis showed a significant difference on the degree of VC between the groups (F = 431.0; p < 0.001) and across the different times (F = 6.4; p = 0.0005). For the group with preoperative MR grade 1–2 no significant difference was noted comparing the degree of preoperative VC with any of the postoperative timeframes.
Fig. 2
Different value of MR Vena Contracta (VC) at 0, 6, 12 and 24 months of follow-up in the two groups
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In the group with preoperative MR grade 3–4 the mean decrease from VC pre-TAVI to VC at 1 month post-TAVI was 4.1 mm (p < 0.0001) and this improvement was persistent at 6 months , 14.4 mm (p < 0.0001), 12 months (p < 0.0001) and 24 months (p < 0.0001), (Fig. 2).
Figure 3 depicts the comparison between the two study groups regarding the degree of EROA before and following TAVI up to two years: two way repeated analysis showed a significant difference on the degree of EROA between the groups (F = 477.5; p < 0.001) and across the different times (F = 8.9; p < 0.0001). For the group with preoperative MR grade 1–2 no significant difference was noted comparing the degree of preoperative EROA with any of the postoperative timeframes.
Fig. 3
Different value of MR EROA at 0, 6, 12 and 24 months of follow-up in the two groups
×
In the group with preoperative MR grade 3–4 the mean decrease from EROA pre-TAVI to EROA at 1 month post-TAVI was 3.42 mm2 (p < 0.0001) and this improvement was persistent at 6 months (p < 0.0001), 12 months (p < 0.0001) and 24 months (p < 0.0001), (Fig. 3).
Figure 4 depicts the comparison between the two study groups regarding the degree of Regurgitant fraction (RF) before and following TAVI up to two years: two way repeated analysis showed a significant difference on the degree of RF between the groups (F = 285.2; p < 0.001) and across the different times (F = 68.3; p < 0.0001). For the group with preoperative MR grade 1–2 no significant difference was noted comparing the degree of preoperative RF with any of the postoperative timeframes.
Fig. 4
Different value of MR Regurgitant Fraction (RF) at 0, 6, 12 and 24 months of follow-up in the two groups
×
In the group with preoperative MR grade 3–4 the mean decrease from RF pre-TAVI to RF at 1 month post-TAVI was 7.5 % (p < 0.0001) and this improvement was persistent at 6 months (p < 0.0001), 12 months (p < 0.0001) and 24 months (p < 0.0001), (Fig. 4).
Figure 5 depicts the comparison between the two study groups regarding the degree of Regurgitant volume (RV) before and following TAVI up to two years: two way repeated analysis showed a significant difference on the degree of RV between the groups (F = 284.4; p < 0.001) and across the different times (F = 35.9; p < 0.0001). For the group with preoperative MR grade 1–2 no significant difference was noted comparing the degree of preoperative RV with any of the postoperative timeframes.
Fig. 5
Different value of MR Regurgitant Volume (RV) at 0, 6, 12 and 24 months of follow-up in the two groups
×
In the group with preoperative MR grade 3–4 the mean decrease from RV pre-TAVI to RV at 1 month post-TAVI was 6.2 (p < 0.0001) and this improvement was persistent at 6 months (p < 0.0001), 12 months (p < 0.0001) and 24 months (p < 0.0001), (Fig. 5).
Figure 6 depicts the comparison between the two study groups regarding the Left atrial volume (LA) of MR before and following TAVI up to two years: two way repeated analysis showed a significant difference on the degree of LA between the groups (F = 103.4; p < 0.001) and across the different times (F = 33.7; p < 0.0001). For the group with preoperative MR grade 1–2 no significant difference was noted comparing the degree of preoperative LA with any of the postoperative timeframes.
Fig. 6
Different value of Left Atrial Volume (ml) at 0, 6, 12 and 24 months of follow-up in the two groups
×
In the group with preoperative LA grade 3–4 the mean decrease from LA pre-TAVI to MR at 1 month post-TAVI was 16.5 (p < 0.0001) and this improvement was persistent at 6 months (p < 0.0001), 12 months (p < 0.0001) and 24 months (p < 0.0001), (Fig. 6).
Follow-up survival
The mean follow-up was 1.1 ± 0.6 years and all patients (100 %) completed at the follow-up.
Figure 7 shows the 2 years survival curve for both groups: 6 months of 94.5 ± 1.8 %, at 12 months of 90.9 ± 2.5 % and 24 months of 90.0 ± 2.5 %. The follow up mortality (10 patients, 6.0 %) occurred exclusively in the grade 1–2 MR group. Cox hazard model showed that the only predictive factor of follow-up mortality was female sex (HR:11.5, 95 % CI:1.4-85.2, p = 0.02).
Fig. 7
2 years survival curve for both group
×
Discussion
Compared with patients with mild baseline MR, those with moderate or severe MR have a worse baseline clinical characteristics (Low EF, Dilated LV), but post-procedural mortality and morbidity are similar in two groups. In fact, in patients with moderate or severe baseline MR, the MR severity improves in post procedural follow-up by overall echo-indices (vena contracta, Regurgitant volume, Regurgitant fraction) : in 24 months follow-up the post procedural values are lower than pre-procedural status.
The presence of 2 different devices might add complexity to the interpretation of the scenario. It has been postulated that differences in the structure of the 2 devices (Core Valve and Sapien) may imply a different risk of mitral valve dysfunction; in other words, the longer nitinol frame of the Core Valve could mechanically interfere with the anterior leaflet of the mitral apparatus, especially in the presence of a low implantation [24]. Our data actually rule out this phenomenon because the incidence of worsened MR was quite low and no difference was observed in the low implantation rate between those with and those without a worsened MR. Similarly there are no differences, in our population, between organic and functional MR.
About follow-up survival, our data showed that female sex was the only predictive factor of mortality. This is not surprising since 12 out 13 deaths were females.
Few and contrasting results have been reported in the literature in terms of the prognostic significance and magnitude of MR changes following TAVI. A sub-analysis of the PARTNER trial [25] reported that preoperative moderate or severe MR (mostly moderate) was associated with increased two-year mortality after surgical AVR, but not after TAVI, suggesting that TAVI may be a reasonable option in selected high-risk patients with combined aortic and mitral valve disease. As with the PARTNER sub-analysis, D’Onofrio et al. [26] found that moderate or severe MR did not appear to be a significant risk factor for in-hospital mortality after TAVI. In contrast, Toggweiler et al. [27] found that moderate or severe MR in patients undergoing TAVI was associated with a higher early, but not late, mortality rate.
The results of our study are consistent with the previous literature. Recently a meta-analysis of 8 studies involving 8927 patients [14] evaluating the impact of MR on outcomes after TAVI found that (a) significant MR at baseline is associated with increased mortality after TAVI; (b) the cause of MR (functional or degenerative) or the type of transcatheter heart valve (Edwards valve or CoreValve) does not affect mor- tality after TAVI; (c) MR severity improves in up to 2/3 of patients after TAVI; and (d) moderate-severe residual MR is associated with increased mortality after TAVI.
The mechanism of improvement in MR severity is clearly multifactorial [17]. The improved aortic valve performance, with the subsequent reduction of the afterload, is conceivably expected to reduce the pathological retrograde flow through the mitral valve. It can also be presumed that the resolution of aortic stenosis may facilitate the achievement of a better hemodynamic balance by reducing the neurohormonal activation caused by the heart failure status. The treatment of the aortic stenosis may also contribute to the restoration of the proper geometry of the LV contraction, which may in turn contribute to improved function of the mitral valve apparatus, in particular when the concomitant MR is a functional type.
Conclusions
TAVI effectively treats the aortic valve but as a beneficial by product also ameliorates concomitant MR. The presence of moderate-to-severe MR does not increase the acute risk of failure of TAVI. In successful procedures, the MR improves immediately and persistently.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
Competing interests
All Authors have not competing interests (financial and non-financial competing interests).
Authors’ contributions
MFC participated in the design of the study, in the data collect, performed exams, coordinated and helped to draft the manuscript. ED participated in the design of the study, in the data collect, performed exams, helped to draft the manuscript. PI participated in the design of the study, in the data collect, performed exams, helped to draft the manuscript. AM participated in the design of the study, in the data collect, performed exams, helped to draft the manuscript. VS participated in the design of the study, in the data collect, performed exams, helped to draft the manuscript. RV performed invasive procedures. RF performed invasive procedures. GC performed statistical analysis. NM participated in the design of the study, in the data collect, helped to draft the manuscript. EP participated in the design of the study, coordinated and helped to draft the manuscript. GD performed invasive procedures. All authors read and approved the final manuscript.
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