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1 lesion with moderate/severe pulmonary valve regurgitation).
2 ting grade III/IV restrictive DD with mitral regurgitation.
3 e thrombosis, and management of paravalvular regurgitation.
4 valve system in patients with severe mitral regurgitation.
5 ngoing clinical trials for functional mitral regurgitation.
6 r FQs increase the risk of aortic and mitral regurgitation.
7 sertions, or moderate or severe paravalvular regurgitation.
8 ular dilation and dysfunction, and tricuspid regurgitation.
9 aiming to treat patients with severe mitral regurgitation.
10 h heart failure and 3 to 4+ secondary mitral regurgitation.
11 valve repair system, for reducing tricuspid regurgitation.
12 branch block morphology, without significant regurgitation.
13 art failure and symptomatic secondary mitral regurgitation.
14 m, and aortic valve focal thickening and any regurgitation.
15 ystolic or diastolic dysfunction, and aortic regurgitation.
16 in Yorkshire swine by inducing severe mitral regurgitation.
17 lung disease, dialysis, and severe tricuspid regurgitation.
18 rum is associated with higher risk of mitral regurgitation.
19 positioning and reduction of residual aortic regurgitation.
20 to improve the lives of patients with mitral regurgitation.
21 with MitraClip in patients with mitral valve regurgitation.
22 d replacement in patients with native mitral regurgitation.
23 re was no residual moderate or severe aortic regurgitation.
24 tion, adverse hemodynamics, or transvalvular regurgitation.
25 of progressive RV dysfunction and tricuspid regurgitation.
26 less severe and subclinical cases of mitral regurgitation.
27 underestimation of Rvol(VALVE) in severe MV regurgitation.
28 s receiving SE-THV: >= moderate paravalvular regurgitation (15.5% versus 8.3%; relative risk, 1.90 [9
29 d 9 others (1.3%) had new moderate or severe regurgitation 2 grades higher than pre-implantation, for
30 d persistence of GERD symptoms (heartburn or regurgitation 2 or more days in past week) among partici
31 igher incidence of moderate or severe aortic regurgitation (3.5% vs. 0.5%) and pacemaker implantation
33 %]) and moderate or severe prosthetic aortic regurgitation (34 [9%] vs ten [3%]) were more common in
34 VR patients had moderate/severe total aortic regurgitation (8.2% vs. 0.0%, p<0.001) and a new pacemak
36 patients with HF and severe secondary mitral regurgitation, a short-term change in disease-specific h
37 y valves have been used to treat stenosis or regurgitation after prior surgical tricuspid valve (TV)
38 tly, moderate or severe mitral and tricuspid regurgitation also decreased (33.7% vs. 8.6% [p < 0.0001
39 d, 28,655 (0.52%) were diagnosed with mitral regurgitation and a further 1,262 (0.02%) were diagnosed
42 ssociated with a higher risk of paravalvular regurgitation and higher in-hospital and 2-year mortalit
43 ng reduced simulation-predicted paravalvular regurgitation and markers of conduction disturbance.
47 001) and after further adjustment for mitral regurgitation and pacemaker/defibrillator (HR: 0.35; 95%
48 ocardiography variables (including tricuspid regurgitation and pulmonary regurgitation) and invasive
49 such as the transvalvular flow rate, closure regurgitation and the orifice area, while the difference
51 luding tricuspid regurgitation and pulmonary regurgitation) and invasive central venous pressure, sys
52 mild MV regurgitation, nine had moderate MV regurgitation, and 11 had severe MV regurgitation, as di
53 female sex, lower ejection fraction, mitral regurgitation, and atrial fibrillation (all P<0.0001).
54 air in patients with severe secondary mitral regurgitation, and implantable cardiac defibrillators in
55 tenosis populations, in patients with aortic regurgitation, and in patients with bicuspid aortic valv
56 ring ventricular systole resulting in mitral regurgitation, and it is associated with sudden cardiac
57 radients, no cases of moderate-severe aortic regurgitation, and none-trace residual aortic regurgitat
58 e, previous acute HF, grade III or IV aortic regurgitation, and pulmonary hypertension both at discha
59 aortic stenosis, moderate and severe aortic regurgitation, and uncorrected coarctation of the aorta.
60 roublesome esophageal symptoms of heartburn, regurgitation, and/or chest pain and inadequate PPI resp
63 re, or more than mild intraprosthetic aortic regurgitation (AR) either new or worsening from 3 months
64 2152 patients (41.2% of native VHD), aortic regurgitation (AR) in 279 (5.3%), mitral stenosis (MS) i
67 The percentage of moderate or severe aortic regurgitation (AR) was low and not statistically differe
71 outcomes after surgical treatment of mitral regurgitation are worse if intervention occurs after det
72 fficient, 0.91), more than mild paravalvular regurgitation (area under the receiver operating charact
73 tricular dysfunction, atrioventricular valve regurgitation, arrhythmia, protein-losing enteropathy, a
74 erate MV regurgitation, and 11 had severe MV regurgitation, as diagnosed by using semiquantitative ec
75 d left atrial pressure and stiffness, mitral regurgitation, as well as features of metabolic syndrome
76 3.9%; P=0.01), and moderate or severe aortic regurgitation at 30 days (10% versus 3%; P=0.002) were s
77 sociated with more moderate or severe aortic regurgitation at 30 days and cardiac death at 30 days an
78 ease, heart failure, aortic stenosis, mitral regurgitation, atrial fibrillation, ischemic stroke, per
79 on the basis of the severity of aortic valve regurgitation (AVR) and aortic valve stenosis (AVS).
80 erable over replacement for rheumatic mitral regurgitation but is not available to the vast majority
82 recent percutaneous approach to treat mitral regurgitation by placement of MC in the center of the mi
88 serositis and severe mitral and aortic valve regurgitation, controlled with adalimumab, tacrolimus, a
90 eart Failure Patients With Functional Mitral Regurgitation) demonstrated that edge-to-edge transcathe
91 artery pressure assessed from the tricuspid regurgitation derived maximal pressure gradient added to
92 ow-up intervals for TTE assessment of mitral regurgitation, despite risk-adjustment for patient varia
93 lation (AF) complicating degenerative mitral regurgitation (DMR) a debated indication for surgery.
94 largement is frequent in degenerative mitral regurgitation (DMR), but its link to outcomes remains un
97 ic; however, symptoms may include heartburn, regurgitation, dysphagia, nausea, or vague epigastric pa
98 subgroups of patients with functional mitral regurgitation (eg, disproportionate versus proportionate
100 lower-risk patients with severe mitral valve regurgitation (Evaluation of the Safety and Performance
101 te of moderate-to-severe paravalvular aortic regurgitation (Evolut R/PRO 10.5% versus Sapien 3 4.2%,
102 f chordae tendineae is used, a lower closure regurgitation flow is observed compared to that of a lin
103 167 (14%) had AR + MR (9% functional mitral regurgitation [FMR] [84% nonischemic] and 5% organic mit
106 l valve repair (MitraClip) for severe mitral regurgitation from 2007 to 2013 as part of the EVEREST I
107 h heart failure and 3 to 4+ secondary mitral regurgitation from the perspective of the US healthcare
108 the treatment of severe functional tricuspid regurgitation (FTR) due to the awareness of its poor out
110 as 7 mm Hg, most patients (96.7%) had mitral regurgitation grade <=1 (+) and were in New York Heart A
114 acement therapy, severe preimplant tricuspid regurgitation, history of cardiac surgery, and concomita
115 ; 95% CI: 1.5 to 5.4; p < 0.001), and mitral regurgitation (HR: 5.0; 95% CI: 1.5 to 17.1; p = 0.01).
117 evice removal was recurrence of heartburn or regurgitation in 5 patients (46%), followed by dysphagia
118 .002) and regurgitation or combined stenosis-regurgitation in 62 (83.8%) and 86 (62.3%) (p = 0.028),
119 ic regurgitation (none-trace and mild aortic regurgitation in 76% and 24% of patients, respectively).
120 s the most common cause of primary tricuspid regurgitation in adults with congenital heart disease, b
122 managed patients with >= moderate tricuspid regurgitation in Europe and North America (n = 1,179) we
123 , weekly, monthly, and overall prevalence of regurgitation in Iranian population was 4.00% (95%CI: 1.
124 r treatment of postoperative pulmonary valve regurgitation in patients with repaired right ventricula
128 Despite the anatomical complexity of mitral regurgitation in the patients in this compassionate use
129 tients with significant functional tricuspid regurgitation, in comparison with tricuspid annular plan
130 e percentage of moderate or severe tricuspid regurgitation increased from baseline to 1 year in SAVR
133 Patients were enrolled in the MIDA (Mitral Regurgitation International Database) registry, which re
139 n of the papillary muscles, the magnitude of regurgitation is greater than that predicted by LV volum
140 ults show that the risk of aortic and mitral regurgitation is highest with current use followed by re
141 c (TTE) surveillance of patients with mitral regurgitation is indicated to avoid adverse ventricular
142 ejection fraction, and isolated pure aortic regurgitation is now under investigation in clinical tri
143 udy, we demonstrate that Ag released upon DC regurgitation is sufficient to efficiently induce early
144 disproportionate versus proportionate mitral regurgitation) is key to the success of new devices.
145 hickening, excessive leaflet tip motion, and regurgitation jet length >=2 cm, and aortic valve focal
146 d stiffness associations with ECV, tricuspid regurgitation jet velocity (TRV) and exercise abnormalit
147 +/- 0.61 cm(2) and 1.51 +/- 0.57 cm(2); and regurgitation <=mild in 91% and 91%, respectively.
151 long-term association between SBP and mitral regurgitation (mediator-adjusted HR 1.22; CI 1.20, 1.25;
152 oup had more frequent post-procedural mitral regurgitation moderate or higher (19.4% vs. 6.8%; p = 0.
153 ction fraction, worse post-procedural mitral regurgitation, moderate or severe lung disease, dialysis
156 gation has been described for primary mitral regurgitation (MR) caused by mitral valve prolapse.
157 tive for patients with severe primary mitral regurgitation (MR) considered at high or prohibitive sur
159 r has become the standard therapy for mitral regurgitation (MR) due to degenerative diseases, but inf
160 , mitral stenosis (MS) in 234 (4.5%), mitral regurgitation (MR) in 1114 (21.3%, primary in 746 and se
161 tinct pathways can lead to functional mitral regurgitation (MR) in patients with chronic heart failur
165 ve repair (TMVr) for the treatment of mitral regurgitation (MR) is a complex procedure that requires
170 symptomatic HF and 3+ to 4+ secondary mitral regurgitation (MR) on maximally-tolerated medical therap
171 Etiology, mechanisms, and survival of mitral regurgitation (MR) plus hemodynamically-significant chro
174 s of AKI in patients with significant mitral regurgitation (MR) undergoing transcatheter valve repair
175 ive patients with severe degenerative mitral regurgitation (MR) were treated with a mitral valve repa
176 restimated in patients with secondary mitral regurgitation (MR) when using LV ejection fraction (EF).
177 ents with either primary or secondary mitral regurgitation (MR) who were at high or prohibitive surgi
181 Patients with moderate or greater triscuspid regurgitation, New York Heart Association class II or hi
183 g) and the absence of moderate-severe aortic regurgitation (none-trace and mild aortic regurgitation
187 nts, resulting in procedural residual mitral regurgitation of grade 2+ or less in 22 (96%) patients.
192 in 12 (16.2%) and 51 (37.0%) (p = 0.002) and regurgitation or combined stenosis-regurgitation in 62 (
193 d by recurrent and troublesome heartburn and regurgitation or GERD-specific complications and affects
195 58 (8.5%) had moderate or greater pulmonary regurgitation or maximum Doppler gradients >40 mm Hg.
196 ulmonary hypertension, severity of tricuspid regurgitation, or individual mitral regurgitation charac
197 ocedure, moderate or severe prosthetic valve regurgitation, or prosthetic valve stenosis within 30 da
200 ntricular valve failure (moderate or greater regurgitation, or valve operation) is a risk factor for
201 (p < 0.001), moderate-to-severe paravalvular regurgitation (p = 0.002), and 30-day mortality (p = 0.0
203 -severe (3+) or severe (4+) secondary mitral regurgitation, patients treated with transcatheter mitra
204 We mapped their nesting sites and collected regurgitation pellets to recover lemming mandibles, whic
205 dural characteristics (residual mitral valve regurgitation, periprocedural bleeding), site volume, an
208 y greater than 2.82 m/s as well as tricuspid regurgitation pressure gradient greater than 32 mm Hg pr
209 indings at discharge (grade III or IV aortic regurgitation, pulmonary hypertension) identified patien
210 severity of coronary artery disease, mitral regurgitation, pulmonary hypertension, right ventricular
211 Moderate/severe and even mild paravalvular regurgitation (PVR) are associated with increased mortal
212 enables more accurate 4D flow MRI-derived MV regurgitation quantification than valve tracking in term
213 2 patients) or severe (6 patients) tricuspid regurgitation recorded at either initial or repeat ablat
214 ith hospital mortality of 2% and with mitral regurgitation reduced to grade </=2 in 87% of patients (
216 tients enrolled in the TRI-REPAIR (TrIcuspid Regurgitation RePAIr With CaRdioband Transcatheter Syste
217 s 69%; P=0.003), and in patients with mitral regurgitation, reproducibility was improved with higher
218 amic abnormalities (more than mild tricuspid regurgitation, residual ventricular septal defect) reduc
219 for severe, moderate, mild, and trace mitral regurgitation, respectively, with 20% of providers deeme
220 ll other symptom scores including heartburn, regurgitation, respiratory symptoms, and pain scores rem
221 e COAPT trial with 3+ or 4+ secondary mitral regurgitation, selected using strict echocardiographic c
222 lve, moderate aortic stenosis, severe mitral regurgitation, severe aortic regurgitation, or subaortic
223 ficacy endpoint was a reduction in tricuspid regurgitation severity by at least one grade at 30 days
224 algorithm was implemented for grading mitral regurgitation severity during the screening process.
229 tative assessment of severe secondary mitral regurgitation (sMR) reflect the lacking link of the sMR
232 tcomes, mixed data on SMR and primary mitral regurgitation, studies not clearly reporting the outcome
233 valve consistency, particularly in severe MV regurgitation.Supplemental material is available for thi
234 ndred four patients with degenerative mitral regurgitation surgically amenable to either leaflet rese
236 prevalence of all types GERD, heartburn and regurgitation symptoms by removing a study showed that t
237 significantly lower in patients with mitral regurgitation than in healthy control subjects (P < .001
238 ve dysfunction, men had more frequent aortic regurgitation than women (33.8% versus 22.2%, P<0.001),
239 isk Patients with Severe, Symptomatic Mitral Regurgitation - The Twelve Intrepid TMVR Pilot Study; NC
240 eart Failure Patients With Functional Mitral Regurgitation [The COAPT Trial] [COAPT]; NCT01626079).
242 tients with significant functional tricuspid regurgitation, timely detection of right ventricular (RV
243 h heart failure and 3 to 4+ secondary mitral regurgitation, TMVr increases life expectancy and qualit
244 sion and volume index, >= moderate tricuspid regurgitation (TR) (7%, 35%, and 53%, respectively), and
245 rsistent or new moderate or severe tricuspid regurgitation (TR) 20.8%, and new atrial fibrillation (A
246 dical treatment options for severe tricuspid regurgitation (TR) are limited, and additional intervent
247 upright invasive exercise testing, tricuspid regurgitation (TR) Doppler estimates and invasive measur
253 significant (moderate and severe) tricuspid regurgitation (TR), the decision to intervene is influen
255 , 0.89-0.99; P=0.027), and </=mild tricuspid regurgitation (TR; HR, 3.58; 95% CI, 2.04-6.30; P<0.001)
256 eart Failure Patients With Functional Mitral Regurgitation), treatment of heart failure (HF) patients
257 eart Failure Patients with Functional Mitral Regurgitation) trial among patients with heart failure (
258 for Symptomatic Chronic Functional Tricuspid Regurgitation) trial is a prospective, single-arm, multi
259 eart Failure Patients with Functional Mitral Regurgitation) trial, 614 patients with HF with moderate
260 eart Failure Patients with Functional Mitral Regurgitation) trial, transcatheter mitral valve repair
261 eart Failure Patients With Functional Mitral Regurgitation) trial, transcatheter mitral valve repair
263 No correlation was found between pulmonary regurgitation velocities and either mean pulmonary arter
264 ed 19%-35%), E/e' ratio (18%-29%), tricuspid regurgitation velocity (27%-41%), and tricuspid annular
265 mitral E velocity, E/e' ratio, and tricuspid regurgitation velocity; and worse right ventricular func
271 r FTR degree compared with trivial tricuspid regurgitation was independently associated with higher m
279 rate of moderate-severe paravalvular aortic regurgitation was observed in the Evolut R/PRO group at
280 y these proximate causes of secondary mitral regurgitation was only 13% (CI 6.1%, 20%), and accountin
284 alence of >=moderate tricuspid and neoaortic regurgitation was uncommon and did not vary by group or
285 ears]) with significant functional tricuspid regurgitation were divided according to the presence of
286 volume was increased in patients with mitral regurgitation when compared with that in healthy volunte
287 lusions bias related to detectable tricuspid regurgitation, which may limit generalizability of our f
289 imary outcome was incident reports of mitral regurgitation, which were identified from hospital disch
290 r of patients with severe symptomatic mitral regurgitation who are at too high of a risk to undergo o
291 patients with HF and severe secondary mitral regurgitation who remained symptomatic despite maximally
292 d moderate-severe or severe secondary mitral regurgitation who remained symptomatic despite maximally
293 h moderate-severe or severe secondary mitral regurgitation who remained symptomatic despite maximally
294 patients with HF and severe secondary mitral regurgitation who were alive at 1 month, those randomize
295 Among patients with degenerative mitral regurgitation with a flail leaflet referred to mitral su
297 nstable angina, acute endocarditis, valvular regurgitation with impending heart failure), 10 patients
298 s continuously related to the risk of mitral regurgitation with no evidence of a nadir down to 115 mm
299 h moderate-severe or severe secondary mitral regurgitation with transcatheter mitral valve repair (TM
300 Decision Pathway on the Management of Mitral Regurgitation, with some sections updated and others add