Fathallah Mouhammad, Krasuski Richard A
Duke University Hospital, 2301 Erwin Road, Durham, NC, 27710, USA.
Curr Cardiol Rep. 2017 Sep 16;19(11):108. doi: 10.1007/s11886-017-0922-2.
Our review is intended to provide readers with an overview of disease processes involving the pulmonic valve, highlighting recent outcome studies and guideline-based recommendations; with focus on the two most common interventions for treating pulmonic valve disease, balloon pulmonary valvuloplasty and pulmonic valve replacement.
The main long-term sequelae of balloon pulmonary valvuloplasty, the gold standard treatment for pulmonic stenosis, remain pulmonic regurgitation and valvular restenosis. The balloon:annulus ratio is a major contributor to both, with high ratios resulting in greater degrees of regurgitation, and small ratios increasing risk for restenosis. Recent studies suggest that a ratio of approximately 1.2 may provide the most optimal results. Pulmonic valve replacement is currently the procedure of choice for patients with severe pulmonic regurgitation and hemodynamic sequelae or symptoms, yet it remains uncertain how it impacts long-term survival. Transcatheter pulmonic valve replacement is a rapidly evolving field and recent outcome studies suggest short and mid-term results at least equivalent to surgery. The Melody valve® was FDA approved for failing pulmonary surgical conduits in 2010 and for failing bioprosthetic surgical pulmonic valves in 2017 and has been extensively studied, whereas the Sapien XT valve®, offering larger diameters, was approved for failing pulmonary conduits in 2016 and has been less extensively studied. Patients with pulmonic valve disease deserve lifelong surveillance for complications. Transcatheter pulmonic valve replacement is a novel and attractive therapeutic option, but is currently only FDA approved for patients with failing pulmonary conduits or dysfunctional surgical bioprosthetic valves. New advances will undoubtedly increase the utilization of this rapidly expanding technology.
我们的综述旨在为读者提供涉及肺动脉瓣疾病过程的概述,重点介绍近期的结局研究和基于指南的建议;重点关注治疗肺动脉瓣疾病的两种最常见干预措施,即球囊肺动脉瓣成形术和肺动脉瓣置换术。
球囊肺动脉瓣成形术是肺动脉狭窄的金标准治疗方法,其主要长期后遗症仍是肺动脉瓣反流和瓣膜再狭窄。球囊与瓣环比值是这两者的主要影响因素,高比值会导致更大程度的反流,而小比值会增加再狭窄风险。近期研究表明,约1.2的比值可能会带来最理想的结果。肺动脉瓣置换术目前是重度肺动脉瓣反流及血流动力学后遗症或症状患者的首选治疗方法,但它对长期生存率的影响仍不确定。经导管肺动脉瓣置换术是一个快速发展的领域,近期的结局研究表明其短期和中期结果至少与手术相当。Melody瓣膜于2010年获美国食品药品监督管理局(FDA)批准用于治疗失败的肺动脉外科管道,2017年获批用于治疗失败的生物假体外科肺动脉瓣,并且已得到广泛研究;而直径更大的Sapien XT瓣膜于2016年获批用于治疗失败的肺动脉管道,其研究较少。肺动脉瓣疾病患者应接受终身并发症监测。经导管肺动脉瓣置换术是一种新颖且有吸引力的治疗选择,但目前仅获FDA批准用于肺动脉管道功能衰竭或外科生物假体瓣膜功能障碍的患者。新进展无疑将增加这种快速发展技术的应用。