Five-year follow-up after percutaneous pulmonary valve implantation using the Venus P-valve system for patients with pulmonary regurgitation and an enlarged native right ventricular outflow tract

被引:3
|
作者
Jin, Qinchun [1 ,2 ]
Long, Yuliang [1 ,2 ]
Zhang, Gejun [3 ]
Pan, Xin [4 ]
Chen, Mao [5 ]
Feng, Yuan [5 ]
Liu, Jinfen [6 ]
Yu, Shiqiang [7 ]
Pan, Wenzhi [1 ,2 ,8 ]
Zhou, Daxin [1 ,2 ,8 ]
Ge, Junbo [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Fuwai Hosp, Dept Cardiol, Beijing, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Shanghai Inst Cardiovasc Dis, Dept Cardiol, Shanghai, Peoples R China
[3] Natl Clin Res Ctr Intervent Med, Shanghai, Peoples R China
[4] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Cardiol, Shanghai, Peoples R China
[5] Sichuan Univ, West China Hosp, Dept Cardiol, Chengdu, Sichuan, Peoples R China
[6] Shanghai Jiao Tong Univ, Shanghai Childrens Med Ctr, Sch Med, Shanghai, Peoples R China
[7] Air Force Med Univ, Affiliated Hosp 1, Dept Cardiol, Xian, Peoples R China
[8] Fudan Univ, Zhongshan Hosp, Shanghai Inst Cardiovasc Dis, Dept Cardiol, 180 Fenglin Rd, Shanghai 200032, Peoples R China
关键词
clinical trials; pulmonary regurgitation; transcatheter; EARLY CLINICAL-EXPERIENCE; REPLACEMENT; OUTCOMES; MELODY; STENT;
D O I
10.1002/ccd.30916
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Percutaneous pulmonary valve implantation (PPVI) with the self-expandable Venus P-valve system is a promising treatment for patients with pulmonary regurgitation (PR) and a native right ventricular outflow tract (RVOT). However, limited data is available regarding its midterm outcomes. This study assessed the midterm clinical and echocardiographic outcomes following Venus P-valve implantation. Methods: From 2013 to 2018, 55 patients with moderate or severe PR after surgical RVOT repair with a transannular or RVOT patch were consecutively enrolled from six hospitals in China. Five-year clinical and echocardiographic outcomes were collected and evaluated. The primary endpoint was a freedom from all-cause mortality and reintervention. Results: At 5 years, the primary endpoint was met for 96% of patients, corresponding to a freedom from all-cause mortality of 96% (95% confidence interval [CI]: 86%-99%) and freedom from reintervention of 98% (95% CI: 87%-100%). Endocarditis was reported in five patients (four patients within 1 year and one patient at 5 years) following PPVI. Transpulmonary gradient and stent orifice diameter remained stable compared to at discharge (p > 0.05). No paravalvular leak was reported while only 1 patient gradually increased to moderate PR during follow-up. Significant improvement of RV diameter and LVEF (p < 0.001) sustained over the 5-year follow-up, in consistent with remarked improved New York Heart Association (NYHA) functional class (p < 0.001). Conclusion: The 5-year results of the China VenusP Study demonstrated the midterm benefits of Venus P-valve implantation in the management of patients with severe PR with an enlarged native RVOT by providing sustained symptomatic and hemodynamic improvement.
引用
收藏
页码:359 / 366
页数:8
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