Cardiovascular Department, Cliniche Humanitas Gavazzeni, Bergamo, Italy.
Division of Robotic and Minimally Invasive Cardiac Surgery, Cliniche Humanitas Gavazzeni, Bergamo, Italy.
Scand Cardiovasc J. 2022 Dec;56(1):79-84. doi: 10.1080/14017431.2022.2071460.
. The safety and effectiveness of the Trifecta GT bioprosthesis (introduced in 2016) in less invasive aortic valve replacement are scarcely investigated. Our aim was to evaluate the immediate and initial follow-up results of this device in the context of less invasive surgery. We discuss patient-specific strategies for the selection of the surgical approach. A retrospective review of 133 patients undergoing AVR with the Trifecta GT through three less invasive accesses (UMS, Upper ministernotomy; RMS, Reversed ministernotomy; RAMT, Right anterior minithoracotomy) was performed. In-hospital, follow-up and hemodynamic performance (PPM, Patient-prosthesis mismatch) data were collected. Among patients, 79% received UMS, 11% RMS and 10% RAMT. Selection of approach was based on preoperative anatomical analysis (CT-scan) and planned concomitant procedures. There was no operative mortality, no valve-related adverse events. There were 36 concomitant procedures. No significant intergroup differences occurred in cardiopulmonary bypass, aortic clamp, mechanical ventilation time, ICU stay and average bleeding. There were two cases of moderate PPM (1.5%) and no instances of severe PPM; there were no significant (≥2/4) perivalvular leaks. Average mean gradient at discharge was 8 ± 3 mmHg. At follow-up (average: 2.5 ± 0.9 years, 100% complete, 315 patient years) there was no mortality and no valve-related adverse event. Hemodynamic performance was maintained at follow-up. The optimal device for less invasive AVR needs to be individualized, as well as the selection of the surgical approach. The use of the Trifecta GT bioprosthesis appears to be reproductible whatever less invasive approach is employed, with confirmed excellent hemodynamic performance.
. 2016 年推出的 Trifecta GT 生物瓣在微创主动脉瓣置换术中的安全性和有效性鲜有研究。我们旨在评估该器械在微创外科背景下的即刻和初始随访结果。我们讨论了针对手术入路选择的个体化策略。 我们回顾性分析了 133 例接受 Trifecta GT 经三种微创入路(UMS,胸骨上段小切口;RMS,反向胸骨下段小切口;RAMT,右前小开胸)行主动脉瓣置换术的患者。收集了围手术期、随访和血流动力学性能(PPM,患者-假体不匹配)数据。 患者中 79%接受 UMS,11%接受 RMS,10%接受 RAMT。入路选择基于术前解剖分析(CT 扫描)和计划的合并手术。无手术死亡,无瓣膜相关不良事件。有 36 例合并手术。体外循环、主动脉阻断、机械通气时间、重症监护病房停留时间和平均出血量无显著组间差异。有 2 例中度 PPM(1.5%),无重度 PPM(≥2/4);无明显瓣周漏(≥2/4)。出院时平均平均梯度为 8 ± 3 mmHg。随访时(平均 2.5 ± 0.9 年,100%完整,315 患者年)无死亡,无瓣膜相关不良事件。血流动力学性能在随访时得以维持。 微创主动脉瓣置换术的最佳器械需要个体化,手术入路的选择也是如此。使用 Trifecta GT 生物瓣,无论采用何种微创入路,似乎都具有可重复性,且证实具有出色的血流动力学性能。