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A Modified Technique for Transcatheter Pulmonary Valve Implantation of SAPIEN 3 Valves in Large Right Ventricular Outflow Tract: A Matched Comparison Study
被引:2
|作者:
Houeijeh, Ali
[1
,2
]
Karsenty, Clement
[1
,3
]
Combes, Nicolas
[1
,4
]
Batteux, Clement
[1
,5
]
Lecerf, Florence
[1
,5
]
Remy, Frederic
[1
]
Valdeolmillos, Estibaliz
[1
,5
]
Petit, Jerome
[1
]
Hascoet, Sebastien
[1
,5
]
机构:
[1] Univ Paris Saclay, Hop Marie Lannelongue, Ctr Reference Cardiopathies Congenitales Complexes, Fac Med,Grp Hosp Paris St Joseph,BME Lab, F-92350 Le Plessis Robinson, France
[2] Lille II Univ, Lille Univ Hosp, Pediat Cardiol Unit, Lab EA4489, F-59000 Lille, France
[3] Univ Toulouse, Hop Enfants, Cardiol Pediat & Congenitale, CHU Toulouse, F-31300 Toulouse, France
[4] Clin Pasteur, F-31300 Toulouse, France
[5] Univ Paris Saclay, Inserm, UMRS1180, F-92296 Le Plessis Robinson, France
关键词:
pulmonary valve;
infective endocarditis;
melody;
SAPIEN;
congenital heart disease;
VENUS P-VALVE;
HEART-VALVE;
PERCUTANEOUS IMPLANTATION;
EARLY OUTCOMES;
REPLACEMENT;
CONDUIT;
REGURGITATION;
FEASIBILITY;
DYSFUNCTION;
EXPERIENCE;
D O I:
10.3390/jcm12247656
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Introduction: Percutaneous pulmonary valve implantation (PPVI) with a SAPIEN 3 valve is effective for treating treat right ventricle outflow (RVOT) dysfunction. A modified technique was developed without prestenting using a protective valve delivery method. We aimed to compare the procedural results of the modified technique group (MTG) to those of patients in a conventional technique group (CTG). Methods: We designed a matched before-after study. All consecutive PPVI with SAPIEN 3 performed in the MTG over 9 months were matched, based on the RVOT type and size, to consecutive procedures performed previously with SAPIEN 3. Results: A total of 54 patients were included, equally distributed in the two groups. The sizes of the SAPIEN 3 valves were 23 mm (n = 9), 26 mm (n = 9), 29 mm (n = 36). The two groups were similar regarding demographic data, RVOT type, and pre-procedure hemodynamics. PPVI was performed in a single procedure in all patients of the MTG, whereas six (22.2%) patients of the CTG group underwent prestenting as a first step and valve implantation later (p = 0.02). The procedures were successful in all cases. Stent embolization was reported in two patients (7.4%) in the CTG, which were impacted in pulmonary arteries. In one case (3.7%), in the MTG, an unstable 29 mm SAPIEN 3 valve was stabilized with two stents and additional valve-in-valve implantation. The hemodynamics results were good in all cases, without significant differences between the two groups. The procedures' durations and fluoroscopy times were significantly reduced in the MTG (48.1 versus 82.6 min, p < 0.0001; 15.2 versus 29.8 min, p = 0.0002). During follow-up, neither stent fracture nor valve dysfunction was noticed in either group. Conclusion: PPVI without prestenting and with a protective delivery method of the SAPIEN 3 valve significantly reduces the procedure's complexity, the duration, and the irradiation while maintaining excellent hemodynamics results in selected cases.
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