Department of Biomedical Engineering, University of California, 2420 Engineering Hall, Irvine, CA, 92697-2730, USA.
Children Hospital of Orange County, Orange, CA, USA.
Ann Biomed Eng. 2023 Nov;51(11):2384-2392. doi: 10.1007/s10439-023-03328-5. Epub 2023 Aug 5.
A common feature of congenital heart disease is the presence of right ventricular outflow tract (RVOT) obstruction that can range from mild to severe and can lead to atresia of the pulmonary valve, in extreme conditions. RVOT abnormalities can frequently be corrected surgically or via interventional means. However, most of these patients will ultimately develop pulmonary valve insufficiency and eventual right ventricular dilation, which will require a pulmonary valve replacement at some point in their life to mitigate the detrimental effects of pulmonary valve regurgitation (PVR) on the right ventricle (RV). The evolution from the studies done by Philip Bonhoeffer to implant a pulmonary valve via transcatheter means, have provided a bedrock for transcatheter pulmonary valve replacement (TPVR). Yet, several areas of unmet need for a demographic of patients still exist. Here, we discuss the clinical unmet needs in children under 20 Kg and expand the use of hybrid and other TPVR approaches along with the current indications and contraindications for pulmonary valve replacement. The constraints and limitations from commercially available pulmonary valves will be discussed from a clinical standpoint. Finally, we explore the use of hybrid and periventricular delivery of transcatheter pulmonary valves in younger patients.
先天性心脏病的一个共同特征是存在右心室流出道(RVOT)阻塞,其严重程度不一,可导致肺动脉瓣闭锁,在极端情况下。RVOT 异常通常可以通过手术或介入手段进行矫正。然而,这些患者中的大多数最终会发展为肺动脉瓣关闭不全,并最终导致右心室扩张,这将需要在其生命中的某个时刻进行肺动脉瓣置换,以减轻肺动脉瓣反流(PVR)对右心室(RV)的不利影响。从菲利普·邦霍弗(Philip Bonhoeffer)进行的研究到通过经导管手段植入肺动脉瓣的演变,为经导管肺动脉瓣置换(TPVR)提供了基础。然而,对于一部分患者群体,仍然存在一些未满足的临床需求。在这里,我们讨论了体重低于 20 公斤的儿童的临床未满足需求,并扩展了使用杂交和其他 TPVR 方法的范围,以及肺动脉瓣置换的当前适应证和禁忌证。将从临床角度讨论商业上可用的肺动脉瓣的限制和局限性。最后,我们探讨了在年轻患者中使用杂交和经心尖输送经导管肺动脉瓣。