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2 enrolled in the RESOLVE study (Assessment of Transcatheter and Surgical Aortic Bioprosthetic Valve Dy
3 alve thrombosis have been reported with both transcatheter and surgical aortic valve bioprostheses.
4 ug Administration-approved studies comparing transcatheter and surgical aortic valve replacement with
5 ent characteristics, trends, and outcomes of transcatheter aortic and mitral valve catheter-based val
7 he mid- to long-term cognitive trajectory of transcatheter aortic valve (TAVR) recipients are scarce.
15 (ASARVI) is still a major limiting factor in transcatheter aortic valve implantation and affects the
16 ventricular (RV) function and outcomes after transcatheter aortic valve implantation has not previous
17 ectiveness claims supporting the adoption of transcatheter aortic valve implantation in intermediate-
18 selected patients experiencing ASARVI after transcatheter aortic valve implantation is feasible, saf
21 liac occlusive disease undergoing subclavian transcatheter aortic valve implantation to avoid acute l
30 occurrence of paravalvular regurgitation and transcatheter aortic valve prosthesis failure seems to b
32 base who were recorded as having undergone a transcatheter aortic valve replacement (n = 3223), an en
33 s in a cohort of 8039 patients who underwent transcatheter aortic valve replacement (November 2011-Ju
35 nts with severe aortic stenosis undergoing a transcatheter aortic valve replacement (TAVR) and the ef
38 sociated with PAD in a population undergoing transcatheter aortic valve replacement (TAVR) are unknow
48 ited data exist about safety and efficacy of transcatheter aortic valve replacement (TAVR) in patient
53 Residual aortic regurgitation (AR) following transcatheter aortic valve replacement (TAVR) is associa
54 t increased risk for surgery, self-expanding transcatheter aortic valve replacement (TAVR) is associa
61 t intermediate surgical risk, treatment with transcatheter aortic valve replacement (TAVR) or surgica
62 he potential for functional recovery after a transcatheter aortic valve replacement (TAVR) or surgica
63 ferential impact of sex has been observed in transcatheter aortic valve replacement (TAVR) outcomes f
64 phic outcomes of patients who underwent redo transcatheter aortic valve replacement (TAVR) procedures
65 permanent pacemaker implantation (PPI) after transcatheter aortic valve replacement (TAVR) remains co
67 atients at high risk for poor outcomes after transcatheter aortic valve replacement (TAVR) to help gu
70 clinical and device performance outcomes of transcatheter aortic valve replacement (TAVR) with a nex
71 ents with severe aortic valve stenosis after transcatheter aortic valve replacement (TAVR) with a sel
72 ssociated with increased mortality following transcatheter aortic valve replacement (TAVR) with first
76 nscaval access may enable fully percutaneous transcatheter aortic valve replacement (TAVR) without th
78 In patients with aortic stenosis undergoing transcatheter aortic valve replacement (TAVR), studies h
89 ion abnormalities are a common finding after transcatheter aortic valve replacement and often result
90 and procedural evolution, support the use of transcatheter aortic valve replacement as the preferred
91 We identified 42 189 patients who underwent transcatheter aortic valve replacement between the years
95 valence and treatment distribution including transcatheter aortic valve replacement eligibility in lo
96 ients with CoreValve, Evolut R, and SAPIEN 3 transcatheter aortic valve replacement enrolled in the R
97 Placement of Aortic Transcatheter Valves) of transcatheter aortic valve replacement for high-risk (HR
102 cance of early LVEF recovery after CoreValve transcatheter aortic valve replacement have not been des
103 nosis, with over 25% patients presenting for transcatheter aortic valve replacement having chronic ki
104 d to the unique requirements of transfemoral transcatheter aortic valve replacement in contemporary p
105 (MR) angiography for vascular mapping before transcatheter aortic valve replacement in patients with
107 lied to 3491 consecutive patients undergoing transcatheter aortic valve replacement in Switzerland be
109 th baseline and discharge ECGs who underwent transcatheter aortic valve replacement in the Placement
114 e maturity of THV technology, variability in transcatheter aortic valve replacement practice, end poi
115 ed Risk of Mortality [PROM]) of 7% to 6% and transcatheter aortic valve replacement PROM (TVT PROM) o
116 al neurological events rates associated with transcatheter aortic valve replacement raised concerns t
117 ARC (Valve Academic Research Consortium) for transcatheter aortic valve replacement set the standard
118 0-day outcomes with the low-profile SAPIEN 3 transcatheter aortic valve replacement system demonstrat
120 of intraoperative implanted to a theoretical transcatheter aortic valve replacement valve size result
122 an aortic annulus area <400 mm(2) undergoing transcatheter aortic valve replacement with either a sel
123 afety profile with low clinical event rates, transcatheter aortic valve replacement with the ACURATE
125 echanical interventions for aortic stenosis (transcatheter aortic valve replacement) may alter the ri
126 tients with normally functioning surgical or transcatheter aortic valve replacement, 24 patients with
127 In patients with renal impairment undergoing transcatheter aortic valve replacement, FE MR angiograph
129 multicenter, non-US cohort of patients with transcatheter aortic valve replacement, the validation o
130 To exclude patients who may have undergone transcatheter aortic valve replacement, we conducted a s
148 bclinical leaflet thrombosis in surgical and transcatheter aortic valves and the effect of novel oral
149 ic stenosis, survival rates are similar with transcatheter aortic-valve replacement (TAVR) and surgic
152 ho require aortic valve replacement, but the transcatheter approach is established for high-risk pati
157 selective angiography, which was followed by transcatheter arterial embolization (TAE) of the BAA and
158 circulating angiogenesis factors after bland transcatheter arterial embolization (TAE), a purely isch
164 tested the feasibility and safety of a novel transcatheter device and assessed its early performance
165 ticenter, early feasibility study of a novel transcatheter device to plicate the tricuspid annulus (T
166 COUT trial confirmed the safety of the novel transcatheter device, which reduced TA and EROA, increas
168 ssment of valve morphology and function, and transcatheter devices typically require intraprocedural
169 discuss imaging requirements for the current transcatheter devices under development for the treatmen
170 oints reflecting safety and effectiveness of transcatheter devices, and defining single and composite
172 This experimental work demonstrated that the transcatheter edge-to-edge repair technique is a feasibl
173 ution of imaging abnormalities, and elevated transcatheter gradients with anticoagulation or surgical
174 ACURATE neo, n=129) or a balloon-expandable transcatheter heart valve (Edwards SAPIEN 3, n=117).
175 lve replacement with either a self-expanding transcatheter heart valve (Symetis ACURATE neo, n=129) o
176 traditionally requires stricter criteria for transcatheter heart valve (THV) approval, including rand
178 hy is useful for determining the appropriate transcatheter heart valve (THV) size in patients with se
179 TAVR) with a next-generation, self-expanding transcatheter heart valve (THV) system in patients with
180 c echocardiographic follow-up, the advent of transcatheter heart valve (THV) technologies coupled wit
181 al implications, and predisposing factors of transcatheter heart valve (THV) thrombosis following tra
183 udy of the Edwards CENTERA-EU Self-Expanding Transcatheter Heart Valve [CENTERA-2]; NCT02458560).
184 eir consecutive experience with the SAPIEN 3 transcatheter heart valve, dependent on patient consent,
185 ational registry of the latest generation of transcatheter heart valve, the SAPIEN 3 (Edwards Lifesci
191 This large, core laboratory-based study of transcatheter heart valves revealed excellent durability
193 Cirrhosis was induced in swine by means of transcatheter infusion of ethanol and iodized oil into t
195 In nonrandomized, open-label studies, a transcatheter interatrial shunt device (IASD, Corvia Med
197 cle, we give the rationale for a therapeutic transcatheter interatrial shunt device in HFpEF, and we
198 ding was common among patients who underwent transcatheter intervention using large-bore catheters an
200 antages in the evaluation of new devices and transcatheter interventions in chronic heart failure and
201 Bleeding complications after percutaneous transcatheter interventions that used large-bore cathete
205 e, we provide an updated overview of current transcatheter left atrial appendage closure devices and
211 evaluations will help to define the role of transcatheter mitral therapy as a potentially exciting n
213 ore biomechanically appropriate to determine transcatheter mitral valve implantation size and eligibi
215 re mitral regurgitation being considered for transcatheter mitral valve implantation who had undergon
217 hors examined the commercial experience with transcatheter mitral valve repair for the treatment of m
218 Our findings demonstrate that commercial transcatheter mitral valve repair is being performed in
219 te use programme in which patients underwent transcatheter mitral valve repair using the Edwards PASC
227 afety and Performance of the Twelve Intrepid Transcatheter Mitral Valve Replacement System in High Ri
228 equired to determine the long-term impact of transcatheter MV repair in this patient population.
232 In this historical comparison study, the transcatheter pacemaker met the prespecified safety and
233 ective multicenter study without controls, a transcatheter pacemaker was implanted in patients who ha
235 ptal aneurysm or large interatrial shunt, to transcatheter PFO closure plus long-term antiplatelet th
236 of these disease states, minimally invasive transcatheter portal venous interventions have been deve
239 implantation of the novel Medtronic Harmony transcatheter pulmonary valve (hTPV) and to assess its e
240 peak conduit pressure gradient acutely after transcatheter pulmonary valve implantation (39 versus 10
247 ational study, the safety and feasibility of transcatheter repair of chronic severe TR with the Mitra
248 atheter left valve interventions, developing transcatheter solutions for functional TR has gained gre
256 XT valve or SAVR in the Placement of Aortic Transcatheter Valve 2 Trial and were followed up for 2 y
257 s with Food and Drug Administration-approved transcatheter valve devices performed in the United Stat
260 ombosis of bioprosthetic aortic valves after transcatheter valve replacement (TAVR) and surgical aort
262 ar aortic regurgitation after self-expanding transcatheter valve replacement without an increase in c
264 2 patients who underwent TAVR as part of the Transcatheter Valve Therapies Registry, we examined rate
265 acic Surgeons/American College of Cardiology Transcatheter Valve Therapy (STS/ACC TVT) Registry.
266 urgeons (STS)/American College of Cardiology Transcatheter Valve Therapy (TVT) Registry captures all
267 acic Surgeons/American College of Cardiology Transcatheter Valve Therapy (TVT) Registry from November
269 acic Surgeons/American College of Cardiology Transcatheter Valve Therapy Registry (November 2011 to O
273 conducted at 395 hospitals submitting to the Transcatheter Valve Therapy Registry from 2011 through 2
274 S AND Using the Society of Thoracic Surgeons/Transcatheter Valve Therapy Registry linked to Medicare
275 racic Surgery/American College of Cardiology Transcatheter Valve Therapy Registry on patients commerc
276 acic Surgeons/American College of Cardiology Transcatheter Valve Therapy Registry was used to charact
277 acic Surgeons/American College of Cardiology Transcatheter Valve Therapy Registry were used for in-ho
283 VR, with prior right bundle-branch block and transcatheter valve type and implantation depth being th
284 ater body mass index, and the use of a 23-mm transcatheter valve were associated with higher rates of
285 in the PARTNER I trial (Placement of Aortic Transcatheter Valve) who had systolic blood pressure (SB
289 patients enrolled in the Placement of Aortic Transcatheter Valves (PARTNER) 1 Trial with successful T
290 d analysis of PVR in the Placement of Aortic Transcatheter Valves (PARTNER) II SAPIEN 3 trial, conduc
291 nalysis of data from the Placement of Aortic Transcatheter Valves (PARTNER) randomized clinical trial
293 either balloon-expandable or self-expanding transcatheter valves and results in reduced residual tra
294 There is anecdotal experience with use of transcatheter valves by either a catheter-based approach
295 on-expandable (n=8) or self-expanding (n=12) transcatheter valves in Mitroflow, Carpentier-Edwards Pe
296 discrimination as in the Placement of Aortic Transcatheter Valves Trial cohorts (c-indexes, 0.637 to
297 the multicenter PARTNER (Placement of Aortic Transcatheter Valves) 2 VIV trial and continued access r
298 e initial PARTNER trial (Placement of Aortic Transcatheter Valves) of transcatheter aortic valve repl
300 VR in the PARTNER trial (Placement of Aortic Transcatheter Valves; as-treated), including the continu
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