Percutaneous Implantation of the Edwards SAPIEN Transcatheter Heart Valve for Conduit Failure in the Pulmonary Position Early Phase 1 Results From an International Multicenter Clinical Trial

被引:165
作者
Kenny, Damien
Hijazi, Ziyad M. [1 ]
Kar, Saibal [2 ]
Rhodes, John [3 ]
Mullen, Michael [4 ]
Makkar, Raj [2 ]
Shirali, Girish [5 ]
Fogel, Mark [6 ]
Fahey, John [7 ]
Heitschmidt, Mary G.
Cain, Christopher [8 ]
机构
[1] Rush Univ, Med Ctr, Rush Ctr Congenital & Struct Heart Dis, Chicago, IL 60612 USA
[2] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[3] Duke Family Med Ctr, Durham, NC USA
[4] Heart Hosp, London, England
[5] Med Univ S Carolina, Charleston, SC 29425 USA
[6] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[7] Yale New Haven Med Ctr, New Haven, CT 06504 USA
[8] Edwards Lifesci, Irvine, CA USA
关键词
conduit; pulmonary valve replacement; SAPIEN; stent; transcatheter; AORTIC-VALVE; REPLACEMENT; TETRALOGY; OUTCOMES; FALLOT;
D O I
10.1016/j.jacc.2011.07.040
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The purpose of this study was to evaluate the safety and effectiveness of the Edwards SAPIEN transcatheter heart valve (Edwards Lifesciences LLC, Irvine, California) in the pulmonary position in patients with moderate to severe pulmonary regurgitation with or without stenosis. Background Transcatheter pulmonary valve replacement is evolving, but to date, experience has been limited to the Melody valve (Medtronic Inc., Minneapolis, Minnesota). Methods Eligible patients with dysfunctional right ventricle-to-pulmonary artery conduits were screened if body weight was >= 35 kg and the in situ conduit diameter was >= 16 mm and >= 24 mm. Standardized implantation and follow-up protocols were used. Results Thirty-six patients from 4 centers were recruited between April 2008 and May 2010. Mean body weight was 73.4 +/- 22.9 kg. Successful valve deployment was achieved in 33 of 34 attempts (97.1%). Valve migration occurred in 3 patients, with 2 requiring surgical retrieval; however, 1 patient underwent successful perventricular valve implantation. Further intraprocedure complications included pulmonary hemorrhage (n = 2), ventricular fibrillation (n = 1), and stent migration (n = 1). Pullback gradient across the conduit decreased from 26.8 +/- 18.4 mm Hg to 11.7 +/- 8.0 mm Hg (p < 0.001). The right ventricular/aortic pressure ratio decreased from 0.6 +/- 0.2 to 0.4 +/- 0.1 (p < 0.001). Peak Doppler gradient across the right ventricular outflow tract decreased from 41.9 +/- 27.9 mm Hg to 19.1 +/- 13.3 mm Hg (p < 0.001). At 6-month follow-up, all patients were alive. The number of patients with New York Heart Association functional class I increased from 5 at baseline to 27 at follow-up. Pulmonary regurgitation was <= 2+ in 97% of patients. Freedom from reintervention was 97% with 1 patient undergoing elective placement of a second valve due to conduit-induced distortion of the initial implant. Conclusions Transcatheter pulmonary valve replacement using the Edwards SAPIEN transcatheter heart valve is safe and effective in patients with dysfunctional right ventricle-to-pulmonary artery conduits. (J Am Coll Cardiol 2011;58:2248-56) (C) 2011 by the American College of Cardiology Foundation
引用
收藏
页码:2248 / 2256
页数:9
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