Cardiology, ASST Spedali Civili, Department of Medical and Surgical Specialities, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Cardiology, ASST Spedali Civili, Department of Medical and Surgical Specialities, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Am J Cardiol. 2024 May 15;219:60-70. doi: 10.1016/j.amjcard.2024.01.028. Epub 2024 Feb 23.
Evidence regarding gender-related differences in response to transcatheter aortic valve implantation according to the valve type is lacking. This study aimed to evaluate the impact of gender on the treatment effect of Evolut PRO/PRO+ (PRO) or SAPIEN 3 Ultra (ULTRA) devices on clinical outcomes. The Comparative Analysis of Evolut PRO vs SAPIEN 3 Ultra Valves for Transfemoral Transcatheter Aortic Valve Implantation (OPERA-TAVI) is a multicenter, multinational registry including patients who underwent the latest-iteration PRO or ULTRA implantation. Overall, 1,174 of 1,897 patients were matched based on valve type and compared according to gender, whereas 470 men and 630 women were matched and compared according to valve type. The 30-day and 1-year outcomes were evaluated. In the PRO and ULTRA groups, men had a higher co-morbidity burden, whereas women had smaller aortic root. The 30-day (device success [DS], early safety outcome, permanent pacemaker implantation, patient-prosthesis mismatch, paravalvular regurgitation, bleedings, vascular complications, and all-cause death) and 1-year outcomes (all-cause death, stroke, and heart failure hospitalization) did not differ according to gender in both valve groups. However, the male gender decreased the likelihood of 30-day DS with ULTRA versus PRO (p for interaction = 0.047). A higher risk of 30-day permanent pacemaker implantation and 1-year stroke and a lower risk of patient-prosthesis mismatch was observed in PRO versus ULTRA, regardless of gender. In conclusion, gender did not modify the treatment effect of PRO versus ULTRA on clinical outcomes, except for 30-day DS, which was decreased in men (vs women) who received ULTRA (vs PRO).
关于根据瓣膜类型评估经导管主动脉瓣植入术反应中性别差异的证据尚缺乏。本研究旨在评估性别对 Evolut PRO/PRO+(PRO)或 SAPIEN 3 Ultra(ULTRA)器械治疗效果的影响,以评估经股动脉入路行经导管主动脉瓣置换术的临床结局。经导管主动脉瓣置换术 Evolut PRO 与 SAPIEN 3 Ultra 瓣膜的比较分析(OPERA-TAVI)是一项多中心、多国注册研究,纳入了接受最新一代 PRO 或 ULTRA 植入术的患者。共有 1897 例患者中的 1174 例根据瓣膜类型进行了匹配,并根据性别进行了比较,其中 470 例男性和 630 例女性根据瓣膜类型进行了匹配和比较。评估了 30 天和 1 年的结局。在 PRO 和 ULTRA 组中,男性合并症负担更高,而女性主动脉根部更小。30 天(器械成功率[DS]、早期安全性结局、永久性起搏器植入、患者-瓣膜不匹配、瓣周漏、出血、血管并发症和全因死亡)和 1 年(全因死亡、卒中和心力衰竭住院)结局在两组瓣膜中均未因性别而不同。然而,与 PRO 相比,男性接受 ULTRA 治疗时 30 天 DS 的可能性降低(交互作用 p 值=0.047)。PRO 与 ULTRA 相比,无论性别如何,30 天永久性起搏器植入和 1 年卒中和患者-瓣膜不匹配的风险更高,而 1 年心力衰竭住院的风险更低。总之,性别并未改变 PRO 与 ULTRA 对临床结局的治疗效果,除了 30 天 DS,男性(与女性相比)接受 ULTRA(与 PRO 相比)时降低。