Wen-Bin Ou-Yang1, Shakeel Qureshi2, Jun-Bo Ge3, Sheng-Shou Hu1, Shou-Jun Li1, Ke-Ming Yang1, Ge-Jun Zhang1, Da-Xin Zhou3, Mao Chen4, Shou-Zheng Wang1, Feng-Wen Zhang1, Xiang-Bin Pan5. 1. Department of Structural Heart Disease, National Center for Cardiovascular Disease, China & Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China. 2. Department of Paediatric Cardiology, Evelina London Children's Hospital, London, United Kingdom. 3. Department of Cardiology, Shanghai Zhongshan Hospital, Fudan University, Shanghai, China. 4. Department of Cardiology, West China Hospital, Sichuan University, Chengdu, Sichuan, China. 5. Department of Structural Heart Disease, National Center for Cardiovascular Disease, China & Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China. Electronic address: panxiangbin@fuwaihospital.org.
Abstract
BACKGROUND: A percutaneous approach for pulmonary valve replacement (PVR) is a feasible alternative to surgical PVR in selected patients with severe pulmonary regurgitation after repair of tetralogy of Fallot. However, large right ventricular outflow tract (RVOT, diameter>25mm) remains challenging. METHODS: This retrospective multicenter study enrolled consecutive patients with large RVOT who underwent percutaneous PVR (Venus P-valve; n=35) or surgical PVR (homograft valve; n=30) between May 2014 and April 2017. Patients were followed up at 1, 3, 6 and 12 months, and yearly thereafter. Main study outcomes were pulmonary valve function and right ventricular function at discharge and midterm follow-up. RESULTS: PVR was successful in all patients. Percutaneous compared with surgical PVR group had: similarly distributed baseline characteristics; shorter hospitalization, intensive care unit stay, and endotracheal intubation duration; lower cost; lower pulmonary valve gradient before discharge; and lower pulmonary valve regurgitant grade (mean difference: -0.63; 95% CI:-1.11 to -0.20, p=0.022), pulmonary valve gradient (mean difference:-5.7 mmHg; 95% CI:-9.4 to -2.2 mmHg, p=0.005), and right ventricular end-diastolic volume index (mean difference:-9.5 ml/m2; 95% CI:-16.9 to -3.1 ml/m2, p=0.022); and greater right ventricular ejection fraction (mean difference:5.4%; 95% CI:2.4 to 8.3%, p=0.002) at median 36 months follow-up, without deaths in either group. CONCLUSIONS: Percutaneous PVR using Venus P-valve appeared to be a safe, efficacious and minimally invasive alternative to surgical PVR in selected patients with large RVOT yielding better right ventricular and pulmonary valve function at midterm follow-up.
BACKGROUND: A percutaneous approach for pulmonary valve replacement (PVR) is a feasible alternative to surgical PVR in selected patients with severe pulmonary regurgitation after repair of tetralogy of Fallot. However, large right ventricular outflow tract (RVOT, diameter>25mm) remains challenging. METHODS: This retrospective multicenter study enrolled consecutive patients with large RVOT who underwent percutaneous PVR (Venus P-valve; n=35) or surgical PVR (homograft valve; n=30) between May 2014 and April 2017. Patients were followed up at 1, 3, 6 and 12 months, and yearly thereafter. Main study outcomes were pulmonary valve function and right ventricular function at discharge and midterm follow-up. RESULTS: PVR was successful in all patients. Percutaneous compared with surgical PVR group had: similarly distributed baseline characteristics; shorter hospitalization, intensive care unit stay, and endotracheal intubation duration; lower cost; lower pulmonary valve gradient before discharge; and lower pulmonary valve regurgitant grade (mean difference: -0.63; 95% CI:-1.11 to -0.20, p=0.022), pulmonary valve gradient (mean difference:-5.7 mmHg; 95% CI:-9.4 to -2.2 mmHg, p=0.005), and right ventricular end-diastolic volume index (mean difference:-9.5 ml/m2; 95% CI:-16.9 to -3.1 ml/m2, p=0.022); and greater right ventricular ejection fraction (mean difference:5.4%; 95% CI:2.4 to 8.3%, p=0.002) at median 36 months follow-up, without deaths in either group. CONCLUSIONS: Percutaneous PVR using Venus P-valve appeared to be a safe, efficacious and minimally invasive alternative to surgical PVR in selected patients with large RVOT yielding better right ventricular and pulmonary valve function at midterm follow-up.