Alsancak Yakup, Kan Hasan, Gürbüz Ahmet Seyfettin, Aydın Nergiz, Kaleli Muhammed Fatih
Necmettin Erbakan University, Konya, Turkey.
Safranbolu State Hospital, Karabuk, Turkey.
Egypt Heart J. 2025 May 20;77(1):47. doi: 10.1186/s43044-025-00646-y.
Heart valve diseases affect over 100 million people globally, with mitral regurgitation being the most common in developed countries. Bioprosthetic heart valves, frequently used for replacement, typically last 10-15 years before degeneration. Repeat open-heart surgery for valve replacement poses high risks, especially in older or high-risk patients. Following the success of transcatheter aortic valve replacement, transcatheter mitral valve-in-valve replacement has emerged as a less invasive alternative for patients deemed inoperable due to high surgical risks.
We report the case of a 69-year-old male with a history of mitral bioprosthetic valve replacement and thoracic radiotherapy who presented with shortness of breath and NYHA class 3 functional capacity. Echocardiography revealed bioprosthetic valve dysfunction with a mean gradient of 13 mmHg and pulmonary artery pressure of 70 mmHg. Given his high surgical risk (The Society of Thoracic Surgeons score 10.9%, EuroScore2 9.8%) and prior thoracic radiotherapy, a transcatheter valve-in-valve procedure was planned. A 29 mm MyVal valve was successfully implanted via a transseptal approach, resulting in complete resolution of mitral regurgitation and a mean gradient of 3 mmHg post-procedure. The patient was discharged without complications and reported improved functional capacity (NYHA class 1) at follow-up.
This case highlights the successful application of transcatheter valve-in-valve replacement for a patient with bioprosthetic mitral valve dysfunction who was at high surgical risk. The procedure, performed using a transseptal approach with a 29 mm MyVal valve, resulted in significant symptomatic and hemodynamic improvement with no complications. The patient's functional capacity improved dramatically, and follow-up imaging confirmed the effective functioning of the new valve. This case supports the viability of transcatheter techniques as a preferred alternative for inoperable patients with mitral valve dysfunction, contributing valuable insights to the growing field of minimally invasive cardiac interventions. As technology advances, transcatheter solutions are expected to offer safer and more effective treatments for bioprosthetic valve failures.
心脏瓣膜疾病影响着全球超过1亿人,在发达国家,二尖瓣反流最为常见。常用于置换的生物人工心脏瓣膜通常在退变前可持续使用10至15年。再次进行心脏直视手术置换瓣膜风险很高,尤其是在老年或高危患者中。继经导管主动脉瓣置换术取得成功后,经导管二尖瓣瓣中瓣置换术已成为因手术风险高而被认为无法手术的患者的一种侵入性较小的替代方案。
我们报告了一例69岁男性患者,有二尖瓣生物人工瓣膜置换和胸部放疗史,出现呼吸急促,纽约心脏协会(NYHA)心功能分级为3级。超声心动图显示生物人工瓣膜功能障碍,平均压差为13 mmHg,肺动脉压为70 mmHg。鉴于其手术风险高(胸外科医师协会评分10.9%,欧洲心脏手术风险评估系统2评分9.8%)以及既往胸部放疗史,计划进行经导管瓣中瓣手术。通过经房间隔途径成功植入一枚29 mm的MyVal瓣膜,术后二尖瓣反流完全消失,平均压差为3 mmHg。患者出院时无并发症,随访时报告心功能分级改善(NYHA 1级)。
本病例突出了经导管瓣中瓣置换术在一名具有高手术风险的生物人工二尖瓣功能障碍患者中的成功应用。该手术采用经房间隔途径并使用29 mm的MyVal瓣膜,显著改善了症状和血流动力学,且无并发症。患者的心功能显著改善,随访影像学检查证实新瓣膜功能有效。本病例支持经导管技术作为二尖瓣功能障碍无法手术患者的首选替代方案的可行性,为微创心脏介入这一不断发展的领域提供了有价值的见解。随着技术进步,经导管解决方案有望为生物人工瓣膜功能衰竭提供更安全、有效的治疗。