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1 the animals with stents placed distal to the pulmonary valve.
2 lmonic stenosis, pulmonic atresia and absent pulmonary valve.
3 identified as that due to the absence of the pulmonary valve.
4 n the endograft at the level of the original pulmonary valve.
5 re piglets (n = 14) were used for PHT of the pulmonary valve.
6 th or without the need of replacement of the pulmonary valve.
7 transcatheter placement of stents across the pulmonary valve.
8 n's syndrome patients or those with unusable pulmonary valves.
9 part of the heart containing the aortic and pulmonary valves.
10 tissue and isolated interstitial cells, than pulmonary valves.
11 rs frequently in aortic valves but rarely in pulmonary valves.
12 ctin-positive VICs in neonatal aortic versus pulmonary valves.
13 s, we isolated clonal populations from human pulmonary valves.
14 ineered valves reminiscent of that in native pulmonary valves.
15 urgitation severity was discordant for seven pulmonary valves, 22 mitral valves, and 21 tricuspid val
16 e mitral and aortic but not the tricuspid or pulmonary valves, accompanied by inflammatory cell infil
17 nary atresia with ventricular septal defect, pulmonary valve agenesis, aortopulmonary window, and dou
19 RVCO calculated from blood flow through the pulmonary valve and from QDA and QP was good (r = .97, P
21 ly resect the right posterior leaflet of the pulmonary valve and replace it with an engineered valve
22 such as transcatheter perforation of atretic pulmonary valves and endovascular stenting for coarctati
24 l technique, transcatheter implantation of a pulmonary valve, and outlines how real-time MRI in the n
25 rvention for failing implanted bioprosthetic pulmonary valves, and considers a new approach to determ
27 ons had a significantly higher occurrence of pulmonary valve atresia (P = 0.001) compared with cases
28 between air pollution and CHDs (specifically pulmonary valve atresia/stenosis, tetralogy of Fallot [T
29 s and diminutive pulmonary arteries, initial pulmonary valve balloon dilation increases the annulus Z
30 for 10 such patients undergoing preoperative pulmonary valve balloon dilation, among other transcathe
32 atients with RVOT conduits and bioprosthetic pulmonary valves by providing sustained symptomatic and
38 peptide inhibitor reduced VEGF-induced human pulmonary valve endothelial cell proliferation, indicati
39 GF stimulates NFATc1 nuclear import in human pulmonary valve endothelial cells by a calcineurin-depen
40 monstrate that activation of NFATc1 in human pulmonary valve endothelial cells is specific to vascula
41 ted and translocated to the nucleus in human pulmonary valve endothelial cells to gain a better under
42 t is an emerging therapy intended to restore pulmonary valve function in patients with right ventricu
47 of the novel Medtronic Harmony transcatheter pulmonary valve (hTPV) and to assess its effect on pulmo
48 ressure gradient acutely after transcatheter pulmonary valve implantation (39 versus 10 mm Hg; P<0.00
49 d pulmonary regurgitation (PR), percutaneous pulmonary valve implantation (PPVI) aims to preserve RV
54 iological effects of BMS versus percutaneous pulmonary valve implantation (PPVI) using an x-ray/magne
59 e Melody device (Medtronic) for percutaneous pulmonary valve implantation experience stent fractures
60 f patients who underwent Melody percutaneous pulmonary valve implantation experienced subsequent BSI,
65 outcomes of patients in whom a percutaneous pulmonary valve implantation was performed using the fol
66 All patients who benefit from percutaneous pulmonary valve implantation with a folded Melody valve
67 w the combined experience with transcatheter pulmonary valve implantation within BPVs from 8 centers
71 scular nitinol stents were placed across the pulmonary valve in 6 young pigs to induce pulmonary regu
72 valve was affected in all 8 patients (73%), pulmonary valve in 7 (64%), and left sided valves in 4 (
75 rated that TVR with the Melody transcatheter pulmonary valve in properly selected patients is safe, e
76 ment patch, but this causes issues including pulmonary valve insufficiency and progressive right vent
77 aortic valve interstitial cells (AVICs) and pulmonary valve interstitial cells (PVICs) differ in exp
78 is, with selective absence of the aortic and pulmonary valves, leading to death in utero from congest
79 lymer construct was implanted to replace one pulmonary valve leaflet in the same juvenile animal from
82 rm effectiveness of the Melody transcatheter pulmonary valve (Medtronic, Inc., Minneapolis, Minnesota
83 n the survival with the originally implanted pulmonary valve (Melody group, 80%; SPVR group, 73%; P=0
85 he potential to guide stent placement in the pulmonary valve or artery and to evaluate flow volume wi
86 circulation due to severe stenosis involving pulmonary valves or arteries or due to pulmonary atresia
87 tetralogy of Fallot (cTOF) often results in pulmonary valve pathology and right ventricular (RV) dys
89 124 patients; in the other 12, transcatheter pulmonary valve placement was not attempted because of t
91 In all animals, the TEL persisted in the pulmonary valve position after 8 to 10 weeks, and all po
96 cedures, 1,375 PDA procedures, 270 "typical" pulmonary valve procedures, 305 aortic valve procedures,
97 Off-label use of transcatheter aortic and pulmonary valve prostheses for tricuspid valve-in-valve
99 were to determine the growth pattern of the pulmonary valve (PV) annulus and right heart structures
100 ates the contribution of infundibular versus pulmonary valve (PV) dysfunction on right ventricular (R
105 edictive scores for specific gestations were pulmonary valve (PV) z-score (<23 weeks), median TV z-sc
106 haracteristically affects tricuspid (TV) and pulmonary valves (PV), and TV replacement is helpful in
107 the rest had none/trace; 1 patient had mild pulmonary valve regurgitation and the remainder had none
108 was designed for treatment of postoperative pulmonary valve regurgitation in patients with repaired
121 ts with repaired tetralogy of Fallot require pulmonary valve replacement (PVR), but the evaluation fo
122 Electrophysiological studies (EPS) before pulmonary valve replacement (PVR), the most common reint
130 ed data focused on outcomes of transcatheter pulmonary valve replacement (TPVR) with either a Sapien
131 have been reported early after transcatheter pulmonary valve replacement (TPVR) with the Harmony valv
134 impactful adverse events after transcatheter pulmonary valve replacement (TPVR), but there is limited
135 dable valves are effective for transcatheter pulmonary valve replacement but linked to higher transie
137 tricuspid valve replacement in all patients, pulmonary valve replacement in 3 and valvectomy in 7, mi
138 y offer an alternative for standard surgical pulmonary valve replacement in dilated right ventricular
139 balloon-expandable valves for transcatheter pulmonary valve replacement in dysfunctional right ventr
140 V) offer a promising alternative to surgical pulmonary valve replacement in patients with a large pat
141 w tracts, permitting lower risk, nonsurgical pulmonary valve replacement in previously prohibitive an
143 cular dilation and dysfunction necessitating pulmonary valve replacement is uncommon in long-term fol
144 icant PR with RV dilation, optimal timing of pulmonary valve replacement remains uncertain, although
145 ongenital heart disease (CHD), transcatheter pulmonary valve replacement represents a transformative
147 rapies, including transcatheter and surgical pulmonary valve replacement strategies, as well as manag
149 for 145 patients who underwent transcatheter pulmonary valve replacement with Edwards SAPIEN 3 (ES3)
150 ents in patients who underwent transcatheter pulmonary valve replacement with the Harmony TPV25 devic
152 e remodeling (QRS fragmentation and previous pulmonary valve replacement) (+2.7%; 95% confidence inte
153 0%), 0.9% (0.2%-1.6%), and 3.8% (0.0%-8.4%); pulmonary valve replacement, 0.4% (0.0%-0.8%), 1.3% (0.2
154 ctors and risk mitigating strategies such as pulmonary valve replacement, ablative strategies, and us
155 underwent mitral and tricuspid valve repair, pulmonary valve replacement, and a maze procedure (the l
156 al choices such as transcatheter or surgical pulmonary valve replacement, discusses criteria and opti
158 erienced infective endocarditis; 11 required pulmonary valve replacement, with a lower incidence for
164 mean number of cardiovascular interventions, pulmonary valve replacements (PVRs), and cardiovascular
165 lves (TEHVs) was evaluated up to 24 weeks as pulmonary valve replacements (transapical access) in she
166 ry resistance, pulmonary arterial elastance, pulmonary valve resistance and systemic arterial elastan
167 oplasty is considered first-line therapy for pulmonary valve stenosis and generally results in succes
168 The most prominent cardiac defects in NS are pulmonary valve stenosis and hypertrophic cardiomyopathy
169 alvuloplasty for the treatment of aortic and pulmonary valve stenosis was first described nearly 40 y
170 r septal defects, atrial septal defects, and pulmonary valve stenosis) occurred in 2.0 per 1000 birth
171 graphic abnormalities, ocular hypertelorism, pulmonary valve stenosis, abnormal genitalia, retardatio
172 r septal defect, pulmonary artery anomalies, pulmonary valve stenosis, hydrocephalus) with trends in
176 mmon atrioventricular canal (n = 17), absent pulmonary valve syndrome (n = 24) and aortopulmonary win
178 the animal with the stent placed across the pulmonary valve, the pulmonary regurgitant fraction was
179 1.3% (0.2%-2.4%), and 8.0% (1.2%-14.8%); and pulmonary valve thrombosis, 0.4% (0.0%-0.9%), 0.7% (0.0%
180 rger valves (P = .009), and four experienced pulmonary valve thrombosis, including one who died and t
182 imary outcome was freedom from transcatheter pulmonary valve (TPV) dysfunction (freedom from reoperat
193 he aortic arch, dysgenesis of the aortic and pulmonary valves, ventricular septal defects, and other
194 y bypass, the right posterior leaflet of the pulmonary valve was completely resected and replaced wit
195 ore hemodynamic and 3D ultrasonic study, the pulmonary valve was excised from 6 sheep (31 to 59 kg) t
198 tflow tract (RVOT) conduits or bioprosthetic pulmonary valves, while preserving RV function and reduc
199 The CAM-based monocusp offered a competent pulmonary valve with regurgitation of 4.6 +/- 0.9% and a