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2 of patients in the United States undergoing transcatheter and surgical aortic valve replacement for
3 namic in the first year after self-expanding transcatheter and surgical aortic valve replacement, but
4 this study was to compare the durability of transcatheter and surgical bioprosthetic aortic valves u
5 history of this finding, differences between transcatheter and surgical valves, and its association w
6 r catheter-delivered valve implantation (eg, transcatheter aortic and mitral valve replacements) was
10 The SURTAVI trial (Surgical Replacement and Transcatheter Aortic Implantation) compared TAVR using a
16 intermediate coronary stenoses treated with transcatheter aortic valve implantation (TAVI) were incl
19 The multicenter Transfusion Requirements in Transcatheter Aortic Valve Implantation (TRITAVI) regist
20 l Evolution and Ventricular Remodeling After Transcatheter Aortic Valve Implantation [RASTAVI]; NCT03
21 ES <20 but were still considered appropriate transcatheter aortic valve implantation candidates by th
23 try is to capture the sizing ratios used for transcatheter aortic valve implantation in BAV and analy
25 with BAV along with available pre- and post-transcatheter aortic valve implantation multidetector co
26 f SAPIEN 3 transcatheter heart valve treated transcatheter aortic valve implantation patients had a l
27 luded 353 consecutive patients who underwent transcatheter aortic valve implantation using new-genera
28 dent predictor of CSA in patients undergoing transcatheter aortic valve implantation without preexist
30 alves and General Versus Local Anesthesia in Transcatheter Aortic Valve Implantation) trial is a mult
31 l Evolution and Ventricular Remodeling After Transcatheter Aortic Valve Implantation) trial is an ong
35 riable adjustment for age, sex, and surgical/transcatheter aortic valve replacement (as time-dependen
36 low-surgical-risk aortic stenosis to undergo transcatheter aortic valve replacement (n = 221) or surg
37 t of evidence supports the widespread use of transcatheter aortic valve replacement (TAVR) among pati
39 , left ventricular assist device (LVAD), and transcatheter aortic valve replacement (TAVR) are expens
41 However, data on the risk of IE following transcatheter aortic valve replacement (TAVR) are sparse
42 ollected data on 276,316 patients undergoing transcatheter aortic valve replacement (TAVR) at sites i
45 manage cardiac conduction disturbances after transcatheter aortic valve replacement (TAVR) has been e
48 stenosis between 2008 and 2017, when use of transcatheter aortic valve replacement (TAVR) in older a
49 al studies have demonstrated the benefits of transcatheter aortic valve replacement (TAVR) in patient
51 A patient-specific computer simulation of transcatheter aortic valve replacement (TAVR) in tricusp
54 Recent clinical trial results showed that transcatheter aortic valve replacement (TAVR) is noninfe
58 se of this study was to assess the effect of transcatheter aortic valve replacement (TAVR) on hospita
60 tomographic imaging 30 days and 1 year after transcatheter aortic valve replacement (TAVR) or surgery
62 t intermediate surgical risk, treatment with transcatheter aortic valve replacement (TAVR) or surgica
63 lity at 1 year is similar after transfemoral transcatheter aortic valve replacement (TAVR) or surgica
64 zation and then randomized to treatment with transcatheter aortic valve replacement (TAVR) or surgica
65 k patients with severe aortic stenosis given transcatheter aortic valve replacement (TAVR) or surgica
66 The optimal antithrombotic treatment after transcatheter aortic valve replacement (TAVR) remains a
67 is (AS) at low surgical risk, treatment with transcatheter aortic valve replacement (TAVR) results in
70 ration approved expanding the indication for transcatheter aortic valve replacement (TAVR) to low-ris
71 ntervention (NOTION) was designed to compare transcatheter aortic valve replacement (TAVR) to surgica
74 arce data exist on coronary events following transcatheter aortic valve replacement (TAVR), and no st
75 s (THVs) may cause coronary occlusion during transcatheter aortic valve replacement (TAVR)-in-TAVR an
93 nts were compared across treatment arms (eg, transcatheter aortic valve replacement [TAVR] versus sur
94 ening (HALT) in low-risk patients undergoing transcatheter aortic valve replacement and assessed 1-ye
95 cific differences in older adults undergoing transcatheter aortic valve replacement and draws attenti
96 ortality and acute kidney injury early after transcatheter aortic valve replacement and is an indepen
97 ears old with an indication for transfemoral transcatheter aortic valve replacement as agreed by the
98 ramipril or control groups after successful transcatheter aortic valve replacement at 14 centers in
100 ding complications were commonly reported in transcatheter aortic valve replacement clinical trials.
101 with aortic stenosis undergoing transfemoral transcatheter aortic valve replacement comparing CS vers
102 nt the pathophysiological mechanisms of post-transcatheter aortic valve replacement complications and
103 ropensity-matched patients who had undergone transcatheter aortic valve replacement for aortic stenos
104 adequately assess the efficacy and safety of transcatheter aortic valve replacement for bicuspid aort
105 y Registry, we evaluated patients undergoing transcatheter aortic valve replacement from November 1,
106 valves (THVs) on individual end points after transcatheter aortic valve replacement has been conducte
108 nd 2017, the rate of 30-day stroke following transcatheter aortic valve replacement in a US registry
109 l High Risk) and SURTAVI trials (Surgical or Transcatheter Aortic Valve Replacement in Intermediate-R
111 tients with nonvalvular atrial fibrillation; transcatheter aortic valve replacement in patients with
113 52 medical centres experienced in performing transcatheter aortic valve replacement in the USA and Au
114 risk of patients with AS and concomitant CA, transcatheter aortic valve replacement may be preferred
117 ive surgical risk, the estimated benefits of transcatheter aortic valve replacement on survival and h
119 imal antithrombotic regimen after successful transcatheter aortic valve replacement remains unclear,
121 ts with large and extra-large aortic annuli, transcatheter aortic valve replacement using 29-mm Sapie
122 Placement of Aortic Transcatheter Valves) of transcatheter aortic valve replacement versus standard c
123 the 2-year rates of clinical events between transcatheter aortic valve replacement versus surgical a
126 transthoracic echocardiography pre- and post-transcatheter aortic valve replacement were considered e
127 c stenosis and large aortic annuli underwent transcatheter aortic valve replacement with 29-mm Sapien
128 risk cohort, and vascular access method, to transcatheter aortic valve replacement with the first ge
129 ibility, preliminary safety, and efficacy of transcatheter aortic valve replacement with the HLT Meri
132 mized trials have compared bioprostheses for transcatheter aortic valve replacement, and no trials ha
134 arteriotomies created by current generation transcatheter aortic valve replacement, percutaneous end
135 icenter investigation in patients undergoing transcatheter aortic valve replacement, percutaneous end
136 osure devices have limitations when used for transcatheter aortic valve replacement, percutaneous end
137 astolic parameters is well established after transcatheter aortic valve replacement, the role of Tei
138 with aortic stenosis undergoing transfemoral transcatheter aortic valve replacement, use of CS compar
139 a large proportion of patients treated with transcatheter aortic valve replacement, yet there remain
156 ctively included patients after transfemoral transcatheter aortic valve replacement; propensity score
158 of the self-expanding intra-annular Portico transcatheter aortic valve system (Abbott Structural Hea
159 controlled trial (the Portico Re-sheathable Transcatheter Aortic Valve System US Investigational Dev
160 on alone or with an antiplatelet agent after transcatheter aortic-valve implantation (TAVI) have not
161 on bleeding and thromboembolic events after transcatheter aortic-valve implantation (TAVI) in patien
162 ith surgery, major outcomes are similar with transcatheter aortic-valve replacement (TAVR) and surgic
163 comes and bioprosthetic-valve function after transcatheter aortic-valve replacement (TAVR) as compare
166 coagulation can reduce these phenomena after transcatheter aortic-valve replacement (TAVR) is not kno
167 aban can prevent thromboembolic events after transcatheter aortic-valve replacement (TAVR) is unclear
172 temic and surgical treatments, radiotherapy, transcatheter arterial therapies, and portal vein revasc
174 early clinical case series, a novel therapy, transcatheter bariatric embolotherapy (TBE) of the left
175 have established the proof-of-principle that transcatheter bariatric embolotherapy of the left gastri
176 ical leaflet thrombosis was more frequent in transcatheter compared with surgical valves at 30 days,
184 35.8% in the surgical group and 48.3% in the transcatheter group (hazard ratio, 1.38; 95% CI, 1.12-1.
185 ve and to determine whether patient-specific transcatheter heart valve (THV) sizing and positioning m
186 eatment with the balloon-expandable SAPIEN 3 transcatheter heart valve and underwent CA with or witho
188 The Safety and Effectiveness of the SAPIEN 3 Transcatheter Heart Valve in Low-Risk Patients With Aort
189 valvular heart disease for many decades, but transcatheter heart valve therapy has revolutionized the
190 s real-world setting, two-thirds of SAPIEN 3 transcatheter heart valve treated transcatheter aortic v
194 the self-expanding Evolut PRO or Evolut PRO+ transcatheter heart valves (THVs) may cause coronary occ
195 oon expandable (BE) with self expanding (SE) transcatheter heart valves (THVs) on individual end poin
196 theter mitral valve replacement using aortic transcatheter heart valves has recently become an altern
197 on self-expandable versus balloon-expandable transcatheter heart valves in bicuspid aortic stenosis a
198 ce of balloon-expandable and self-expandable transcatheter heart valves in the treatment of bicuspid
200 espite the tremendous technical evolution of transcatheter heart valves, to date, the clinically avai
202 gnificant proportion of lesions treated with transcatheter interventions in the coronary arteries, mo
203 t to prevent LVOT obstruction (LAMPOON) is a transcatheter mimic of surgical chord-sparing leaflet re
206 418 patients >65 years of age who underwent transcatheter mitral valve repair (MitraClip) for severe
208 ulmonary hypertension influences outcomes of transcatheter mitral valve repair (TMVr) in patients wit
209 with Functional Mitral Regurgitation) trial, transcatheter mitral valve repair (TMVr) led to reduced
210 mitral regurgitation, patients treated with transcatheter mitral valve repair (TMVr) through leaflet
211 r severe secondary mitral regurgitation with transcatheter mitral valve repair (TMVr) using the Mitra
212 s have demonstrated health status benefit of transcatheter mitral valve repair (TMVr) with MitraClip
213 egurgitation) demonstrated that edge-to-edge transcatheter mitral valve repair (TMVr) with the MitraC
214 With Functional Mitral Regurgitation) trial, transcatheter mitral valve repair (TMVr) with the MitraC
215 procedure, one-sixth of patients undergoing transcatheter mitral valve repair had AKI, linked to dev
216 patients with interventricular dyssynchrony, transcatheter mitral valve repair in patients with sever
217 idence on benefit-risk tradeoffs relevant to transcatheter mitral valve repair versus medical therapy
220 structures (eg, cardiac resynchronization or transcatheter mitral valve repair), but they may derive
222 ts include SGLT2 inhibitors, vericiguat, and transcatheter mitral valve repair, all of which incremen
226 he feasibility of a percutaneous transseptal transcatheter mitral valve replacement (TMVR) system.
228 this study was to evaluate the potential for transcatheter mitral valve replacement in patients with
231 leaflet (LAMPOON) is an effective adjunct to transcatheter mitral valve replacement that prevents lef
237 ular and valvular heart disease are invasive transcatheter procedures or surgeries that do not fully
243 imited published data focused on outcomes of transcatheter pulmonary valve replacement (TPVR) with ei
244 tral valve anatomy, an update on the current transcatheter repair and replacement therapies, as well
245 able heart valve prostheses for surgical and transcatheter replacement have considerable limitations.
252 port the 6-month safety and performance of a transcatheter tricuspid valve reconstruction system in t
253 fectiveness of TriClip, a minimally invasive transcatheter tricuspid valve repair system, for reducin
254 termediate-term valve-related outcomes after transcatheter tricuspid valve replacement (TTVR), includ
260 ctancy was <0.10 between TAVR and SAVR until transcatheter valve prosthesis failure time was 70% shor
262 tive capacity of potential tissue engineered transcatheter valve scaffolds (1) acellular porcine peri
263 s (STS)/American College of Cardiology (ACC) Transcatheter Valve Therapies Registry from June 2015 to
264 acic Surgeons/American College of Cardiology Transcatheter Valve Therapies Registry from November 9,
265 S)/American College of Cardiology (ACC) TVT (Transcatheter Valve Therapies) registry, 3,053 (4.2%) pa
266 acic Surgeons/American College of Cardiology Transcatheter Valve Therapy Registry (November 2011 thro
268 acic Surgeons/American College of Cardiology Transcatheter Valve Therapy registry were analyzed with
270 acic Surgeons-American College of Cardiology Transcatheter Valve Therapy Registry) from 2011 to 2019
271 acic Surgeons/American College of Cardiology Transcatheter Valve Therapy Registry, we evaluated patie
274 Surgeons/American College of Cardiology TVT (Transcatheter Valve Therapy) registry with linkage to Me
276 s, and they were treated successfully with a transcatheter valve-in-valve procedure (Melody TPV).
277 (The PARTNER II Trial: Placement of AoRTic TraNscathetER Valves - PII A [PARTNERII A]; NCT01314313;
281 22128; PARTNER II Trial: Placement of AoRTic TraNscathetER Valves II - High Risk and Nested Registry
282 (The PARTNER II Trial: Placement of Aortic Transcatheter Valves II - PARTNER II - Nested Registry 3
283 3; The PARTNER II Trial: Placement of AoRTic TraNscathetER Valves II - PARTNER II - PARTNERII - S3 In
284 (The PARTNER II Trial: Placement of AoRTic TraNscathetER Valves II - PARTNER II - PARTNERII - S3 In
286 ing TAVR in the PARTNER (Placement of Aortic Transcatheter Valves) 1, 2, and PARTNER 2 S3 trials betw
287 ograms from the PARTNER (Placement of Aortic Transcatheter Valves) 2 SAPIEN 3 registry were analyzed
288 the multicenter PARTNER (Placement of Aortic Transcatheter Valves) 2 valve-in-valve and continued acc
290 the PARTNER 2 trial (The Placement of Aortic Transcatheter Valves) and registry the outcomes after ao
291 ved TAVR in the PARTNER (Placement of Aortic Transcatheter Valves) I, II, and S3 trials or registries
292 om the PARTNER 1B trial (Placement of Aortic Transcatheter Valves) of transcatheter aortic valve repl
293 The PARTNER 3 trial (Placement of Aortic Transcatheter Valves) randomized 1000 patients with seve
296 ed superiority (PARTNER [Placement of Aortic Transcatheter Valves] 3) or noninferiority (Evolut Low R
299 rcise test and echocardiography 1 day before transcatheter VSD closure and 6 months after interventio