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1 s on the basis of valve position (aortic vs. mitral valve).
2 f a single clip at the A2-P2 segments of the mitral valve.
3 enerative process in the fibrous base of the mitral valve.
4 ed immediately after release obstructing the mitral valve.
5 sophageal echocardiography evaluation of the mitral valve.
6 ed myxomatous changes in the leaflets of the mitral valve.
7 ct through rotating reversal flow around the mitral valve.
8 phied septum and the anterior leaflet of the mitral valve.
9 in 11 myxomatous and 11 nonmyxomatous human mitral valves.
13 success 30 days after implantation using the Mitral Valve Academic Research Consortium definitions.
16 relation of the 3-dimensional morphology of mitral valve and degree of mitral regurgitation (MR) in
17 t of cardiac development but, along with the mitral valve and trabeculae, their developmental traject
19 two scales (nanometer and micrometer), using mitral valve anterior leaflet (MVAL) tissues as the repr
21 heter aortic valve replacement (TAVR) on the mitral valve apparatus and factors influencing the reduc
23 oportional to their regression coefficients: mitral valve area </=1 cm(2) (2), maximum leaflets displ
25 that experimental tethering alone increases mitral valve area in association with endothelial-to-mes
28 in the 1990s structural abnormalities of the mitral valve became appreciated as contributing to SAM p
29 r descending coronary artery calcifications, mitral valve calcifications, descending aorta calcificat
30 ds, and outcomes of transcatheter aortic and mitral valve catheter-based valve procedures in the Unit
31 in those who received mechanical prosthetic mitral valves compared with those who received bioprosth
32 othesized that percutaneous plication of the mitral valve could reduce left ventricular outflow tract
33 Pathological processes underlying myxomatous mitral valve degeneration (MMVD) remain poorly understoo
38 with increased repair rates of degenerative mitral valve disease (adjusted odds ratio [OR]: 1.13 for
42 ial tissues from the patients with rheumatic mitral valve disease in either sinus rhythm or persisten
43 he value of robotically assisted surgery for mitral valve disease is questioned because the high cost
45 also develop aortic root aneurism and aorto-mitral valve disease that can be fatal depending on the
47 t outcomes in patients with heart failure or mitral valve disease, but their impact on outcomes in pa
48 AC, a risk factor for clinically significant mitral valve disease, suggesting a causal association.
53 sociation between KCN and allergic rhinitis, mitral valve disorder, aortic aneurysm, or depression (P
54 The impact of reduced IPMD shortening on mitral valve (dys)function was confirmed in swine and in
55 hyperlipidemia presented with no symptoms of mitral valve dysfunction and had no abnormalities on phy
56 Coming to a conclusion, bearing in mind no mitral valve dysfunction at that time, patient was offer
58 emiautomatically placed in the region of the mitral valve, factor analysis, and a hybrid method that
59 ase category, younger age, and morphological mitral valve features were risk factors for an unfavorab
60 bryos had increased crypt presence, abnormal mitral valve formation and alterations in the compaction
61 remodeling and more effectively restored the mitral valve geometric configuration in ischemic MR, whi
62 ing in the interpapillary muscle distance on mitral valve geometry and function in ischemic heart dis
65 contraction, lateral shortening of the IPMD, mitral valve geometry, and severity of mitral regurgitat
67 or myxoid degeneration, billowing or floppy mitral valve) have appeared, 2 virtually constant histol
68 mpared with those who received bioprosthetic mitral valves; however, the incidence of reoperation was
69 cribe the first-in-man series of transapical mitral valve implantation for mitral regurgitation with
76 rgitation being considered for transcatheter mitral valve implantation who had undergone cardiac CT a
77 e of mechanical prosthetic and bioprosthetic mitral valves in patients aged 50 to 69 years matched by
78 features of operatively excised portions of mitral valves in patients with mitral valve prolapse (MV
79 ents who underwent mitral valve-in-valve and mitral valve-in-ring procedures were high risk, with an
82 n zebrafish, cultured cells and, notably, in mitral valve interstitial cells (MVICs) obtained during
85 Staphylococcus aureus as a cause (HR 2.47), mitral valve involvement (HR 1.29), and anticoagulant th
87 ombination with 3 other parameters: anterior mitral valve leaflet elongation (beta=2.1; 95% CI, 1.7-3
88 of crypts (particularly multiple), anterior mitral valve leaflet elongation, abnormal trabeculae, an
89 ickness, morphology, left atrial volume, and mitral valve leaflet lengths (all P=non-significant).
91 fts (28% versus 8%; P=0.02), longer anterior mitral valve leaflets (23.5+/-3.0 versus 19.7+/-3.1 mm;
92 onship of left ventricular (LV) flow and the mitral valve leaflets (MVL) on 3-chamber vector flow map
93 oint of a line connecting the origins of the mitral valve leaflets at end systole and end diastole.
94 ium, biatrial enlargement, thickening of the mitral valve leaflets, and interatrial septum and mild p
95 er vector flow mapping frames, and performed mitral valve measurements on 2-dimensional frames in pat
98 omyopathy (HCM) and mild septal hypertrophy, mitral valve (MV) abnormalities may play an important ro
99 al septal hypertrophy, we sought to identify mitral valve (MV) and papillary muscle (PM) abnormalitie
100 The acute effect of MitraClip procedure on mitral valve (MV) annular geometry and its relation to f
104 roups based on cardiovascular comorbidities: mitral valve (MV) disease without coronary artery diseas
105 y-three patients (20%) underwent concomitant mitral valve (MV) intervention (repair, n=29; replacemen
106 ever, LV size is an important determinant of mitral valve (MV) leaflet tethering before and after rep
108 R, due to underlying degenerative/structural mitral valve (MV) pathology, and secondary (functional)
110 ical outcomes and durability of percutaneous mitral valve (MV) repair with the MitraClip device compa
118 ts the following manifestations: a prolapsed mitral valve, myopia, aortic root enlargement, and skele
119 ence between peak twisting and untwisting at mitral valve opening (%untwMVO) using speckle-tracking e
120 nction and maximum left atrium volume before mitral valve opening, and as such contains no added info
128 the potential effectiveness of percutaneous mitral valve plication as a therapy for patients with sy
129 nitial experience suggests that percutaneous mitral valve plication may be effective for symptom reli
131 s study was to investigate the prevalence of mitral valve prolapse (MVP) and its association with ven
145 07-0.23), 0.12 (95% CI, 0.04-0.20) excluding mitral valve prolapse, and 0.44 (95% CI, 0.15-0.73) for
146 higher rates of scoliosis, pectus excavatum, mitral valve prolapse, and mutations in the CFTR gene.
151 er, transapical delivery of a self-expanding mitral valve prosthesis and were examined in a prospecti
152 method and by two 3D quantification methods (mitral valve quantification software and 3D quantificati
153 edian MVAs by the pressure half-time method, mitral valve quantification software, and 3D quantificat
155 n of TMVR in lower-risk patients with severe mitral valve regurgitation (Evaluation of the Safety and
157 s to the development of clinically important mitral valve regurgitation and mitral valve stenosis.
159 MVP and suggests new mechanisms involved in mitral valve regurgitation, the most common indication f
161 luded coronary artery bypass grafting (13%), mitral valve repair (7%), and partial/complete arch repl
164 However, the results with transcatheter mitral valve repair (TMVR) in prohibitive-risk DMR patie
166 e devices currently available, transcatheter mitral valve repair (TMVr) remains challenging in comple
170 dge-to-edge technique using the percutaneous mitral valve repair device in an ex vivo pulsatile model
172 etween 1991 and 2010, patients who underwent mitral valve repair for primary mitral regurgitation wer
174 h a mean (SD) age of 57 (11) years underwent mitral valve repair for regurgitation from posterior lea
175 98.8% complete follow-up) underwent robotic mitral valve repair for severe nonischemic degenerative
176 the commercial experience with transcatheter mitral valve repair for the treatment of mitral regurgit
177 predict postoperative LVD and outcome after mitral valve repair in patients with primary mitral regu
180 ted that recurrent MR following degenerative mitral valve repair is associated with adverse left vent
181 elderly patients with mitral regurgitation, mitral valve repair is associated with superior early an
182 gs demonstrate that commercial transcatheter mitral valve repair is being performed in the United Sta
184 ural costs, robotically assisted surgery for mitral valve repair offers the clinical benefit of least
185 nterval, 0.51-0.62; P<0.0001), and CABG plus mitral valve repair or replacement (adjusted hazard rati
190 nnual mitral volumes of >50 and degenerative mitral valve repair rates of >70%, compared with surgeon
193 itral regurgitation (MR) were treated with a mitral valve repair system (MVRS) via small left thoraco
194 me in which patients underwent transcatheter mitral valve repair using the Edwards PASCAL TMVr system
196 cic Surgeons predicted risk of mortality for mitral valve repair was 4.8% (2.1-9.0) and 6.8% (2.9-10.
199 ry determination who underwent transcatheter mitral valve repair with the MitraClip device in multice
200 tery bypass graft, aortic valve replacement, mitral valve repair) using an interrupted time series mo
210 l per square meter of body-surface area with mitral-valve repair and 60.6+/-39.0 ml per square meter
211 at 12 months between patients who underwent mitral-valve repair and those who underwent mitral-valve
212 gurgitation undergoing CABG, the addition of mitral-valve repair did not lead to significant differen
213 bypass grafting (CABG) alone with CABG plus mitral-valve repair in patients with moderate ischemic m
214 hemic mitral regurgitation to undergo either mitral-valve repair or chordal-sparing replacement in or
218 chemic mitral regurgitation, the addition of mitral-valve repair to CABG did not result in a higher d
220 derate regurgitation, the benefits of adding mitral-valve repair to coronary-artery bypass grafting (
225 % in the CABG-alone group (hazard ratio with mitral-valve repair, 0.90; 95% confidence interval, 0.38
226 Limited data exist regarding transcatheter mitral valve replacement (TMVR) for patients with failed
230 e are scarce data available on transcatheter mitral valve replacement (TMVR), and these have been lim
232 50-69 years) who underwent primary, isolated mitral valve replacement in New York State hospitals fro
233 mong patients aged 50 to 69 years undergoing mitral valve replacement in New York State, there was no
235 though these findings suggest bioprosthetic mitral valve replacement may be a reasonable alternative
237 , 0.90 (0.86-0.93) compared to dysfunctional mitral valve replacement or repair, 0.78 (0.70-0.90), P
238 t, 0.78 (0.73-0.87), P < .001, as did normal mitral valve replacement or repair, 0.90 (0.86-0.93) com
239 85 (74-96) seconds compared to dysfunctional mitral valve replacement or repair, 143 (128-192) second
240 ement, 36 patients with normally functioning mitral valve replacement or repair, 19 patients with dys
241 , P < .001, and also in normally functioning mitral valve replacement or repair, 85 (74-96) seconds c
242 nt or repair, 19 patients with dysfunctional mitral valve replacement or repair, and 31 patients with
243 ormance of the Twelve Intrepid Transcatheter Mitral Valve Replacement System in High Risk Patients wi
252 air and 60.6+/-39.0 ml per square meter with mitral-valve replacement (mean changes from baseline, -9
253 il 70 years of age among patients undergoing mitral-valve replacement and until 55 years of age among
254 zed trial comparing mitral-valve repair with mitral-valve replacement in patients with severe ischemi
255 nderwent primary aortic-valve replacement or mitral-valve replacement with a mechanical or biologic p
257 increased substantially for aortic-valve and mitral-valve replacement, from 11.5% to 51.6% for aortic
261 e replacements and in 14 of 19 dysfunctional mitral valve replacements or repairs (P < .001 for both)
262 tic valve replacements and in 2 of 36 normal mitral valve replacements or repairs but were abnormal i
264 Left-sided structures, namely aortic and mitral valve sizes and left ventricular volume, were sig
268 ventricular ejection fraction, who underwent mitral valve surgery (92% repair) at our center between
269 re associated with higher mortality, whereas mitral valve surgery (HR: 0.82) was associated with impr
270 mitral regurgitation in the 24 hours before mitral valve surgery and 13 age- and sex-matched healthy
271 and revascularization when appropriate, and mitral valve surgery and transcatheter interventions.
272 on, surgical ventricular reconstruction, and mitral valve surgery in this high-risk patient populatio
275 the most common valvular heart disease, and mitral valve surgery is the gold standard therapy for se
276 re to recognize the importance of FTR during mitral valve surgery may result in inferior early and la
278 Prophylactic aortic root replacement and mitral valve surgery were rare during childhood versus a
279 ad electrophysiological studies for AT after mitral valve surgery, 20 patients had prior superior tra
280 rty-eight patients subsequently had isolated mitral valve surgery, and 26 of these had an additional
282 ventricular ejection fraction who underwent mitral valve surgery, brain natriuretic peptide and LV-G
284 ricular (LV) ejection fraction who underwent mitral valve surgery, we sought to discover whether base
291 addition of atrial fibrillation ablation to mitral-valve surgery significantly increased the rate of
292 persistent atrial fibrillation who required mitral-valve surgery to undergo either surgical ablation
294 (Early Feasibility Study of the Tendyne Mitral Valve System [Global Feasibility Study]; NCT02321
295 ed for morphofunctional abnormalities of the mitral valve that could explain a regional mechanical my
297 though systolic anterior motion (SAM) of the mitral valve was discovered as the cause of LV outflow t
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