Rockefeller Toby, Shahanavaz Shabana, Zajarias Alan, Balzer David
Department of Pediatrics, Division of Cardiology, Washington University School of Medicine.
Cardiovascular Division, Washington University School of Medicine.
Catheter Cardiovasc Interv. 2016 Jul;88(1):E28-33. doi: 10.1002/ccd.26480. Epub 2016 Mar 4.
Pulmonary valve replacement (PVR) is indicated in patients with significant pulmonary regurgitation (PR), stenosis (PS), or mixed pulmonary valve disease. While once an exclusively surgical procedure, many patients can undergo transcatheter PVR (TPVR) with excellent early outcomes (Haas et al. 2013, Clin. Res. Cardiol. Off. J. German Cardiac Soc. 102:119-128; Kenny et al. 2011, J. Am. Coll. Cardiol. 58:2248-2256; Cheatham et al. Circulation 2015, 131:1960-1970). The available transcatheter options continue to expand, but the majority of cases performed in the United States involve the use of FDA approved Melody valve (Medtronic; Minneapolis, MN) or the SAPIEN (Edwards Lifesciences; Irvine, CA) family of valves. The SAPIEN 3 valve (S3) recently received FDA approval for transcatheter aortic valve replacement. We report the first S3 implantation in the pulmonary position for treatment of chronic pulmonary regurgitation and progressive right ventricular dilation in an 18 year old male with repaired Tetralogy of Fallot. © 2016 Wiley Periodicals, Inc.
对于患有严重肺动脉反流(PR)、狭窄(PS)或混合性肺动脉瓣疾病的患者,需进行肺动脉瓣置换术(PVR)。虽然肺动脉瓣置换术曾经完全是一种外科手术,但现在许多患者可以接受经导管肺动脉瓣置换术(TPVR),且早期效果良好(哈斯等人,2013年,《临床研究心脏病学》,德国心脏病学会会刊102:119 - 128;肯尼等人,2011年,《美国心脏病学会杂志》58:2248 - 2256;切atham等人,《循环》2015年,131:1960 - 1970)。可用的经导管瓣膜选择在不断增加,但在美国进行的大多数病例使用的是美国食品药品监督管理局(FDA)批准的Melody瓣膜(美敦力公司;明尼阿波利斯,明尼苏达州)或SAPIEN瓣膜系列(爱德华兹生命科学公司;尔湾,加利福尼亚州)。SAPIEN 3瓣膜(S3)最近获得了FDA批准用于经导管主动脉瓣置换术。我们报告了首例将S3瓣膜植入肺动脉位置,用于治疗一名18岁法洛四联症修补术后男性的慢性肺动脉反流和进行性右心室扩张。© 2016威利期刊公司