Unbehaun Axel, Kelm Marcus, Miera Oliver, Kempfert Joerg
Department of Cardiothoracic and Vascular Surgery, German Heart Center Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.
DZHK (German Centre for Cardiovascular Research), Partner Site Berlin, Potsdamer Straße 58, 10785 Berlin, Germany.
Eur Heart J Case Rep. 2021 Feb 16;5(2):ytab034. doi: 10.1093/ehjcr/ytab034. eCollection 2021 Feb.
Left ventricular non-compaction cardiomyopathy (LVNC) has been reported in association with almost all types of congenital heart valve disease. The presence of LVNC-related ventricular dysfunction increases the perioperative risk in these patients. The advantages of transcatheter treatment modalities outweigh those of surgical strategies, as they avoid cardioplegic arrest and myocardial trauma. To our knowledge, there have been no reports on transcatheter treatment of pure aortic regurgitation in patients with a bicuspid aortic valve (BAV) and concomitant LVNC.
In this article, we present the case of a 13-year-old boy with a regurgitant BAV and concomitant LVNC who presented with end-stage heart failure and severe pulmonary hypertension. As a bridge to definitive therapy, the patient underwent an uneventful transcatheter aortic valve implantation (TAVI) using a 26-mm balloon-expandable prosthesis. Device success without paravalvular regurgitation was achieved. At 17 months of follow-up, a steady reduction in pulmonary arterial pressure, persistent normalization of systolic left ventricular function and a tremendous improvement in the patient's physical resilience was observed. The initially considered heart-lung transplantation was avoided and will not be necessary.
To the best of our knowledge, this is the first case performed with TAVI for BAV regurgitation in the context of LVNC. With technical modifications and appropriate planning, TAVI in paediatric patients with a non-calcified BAV is feasible. Different imaging modalities revealed an intriguing relationship between aortic regurgitation and morphological signs of a left ventricular non-compaction myocardium.
据报道,左心室心肌致密化不全心肌病(LVNC)与几乎所有类型的先天性心脏瓣膜病相关。LVNC相关的心室功能障碍会增加这些患者的围手术期风险。经导管治疗方式的优势超过手术策略,因为它们避免了心脏停搏和心肌创伤。据我们所知,尚无关于经导管治疗二叶式主动脉瓣(BAV)合并LVNC患者单纯主动脉瓣反流的报道。
在本文中,我们介绍了一名13岁男孩的病例,他患有反流性BAV并伴有LVNC,出现终末期心力衰竭和严重肺动脉高压。作为确定性治疗的桥梁,患者使用26毫米球囊扩张式假体顺利进行了经导管主动脉瓣植入术(TAVI)。实现了装置成功且无瓣周反流。在随访的17个月中,观察到肺动脉压稳步下降,左心室收缩功能持续正常化,患者的身体恢复能力有了极大改善。最初考虑的心肺移植得以避免,且不再必要。
据我们所知,这是首例在LVNC背景下对BAV反流进行TAVI治疗的病例。通过技术改进和适当规划,对非钙化BAV的儿科患者进行TAVI是可行的。不同的成像方式揭示了主动脉瓣反流与左心室心肌致密化不全形态学征象之间的有趣关系。