Nielsen Per Hostrup, Hjortdal Vibeke, Modrau Ivy Susanne, Jensen Henrik, Kimose Hans-Henrik, Terp Kim, Poulsen Steen Hvitfelt, Smerup Morten, Nielsen Sten Lyager
Department of Cardiothoracic and Vascular Surgery, Aarhus University Hospital, Aarhus, Denmark
Department of Cardiothoracic and Vascular Surgery, Aarhus University Hospital, Aarhus, Denmark.
Eur J Cardiothorac Surg. 2016 Jun;49(6):1705-10. doi: 10.1093/ejcts/ezv432. Epub 2016 Mar 16.
This study compares the durability and risk of reoperation in patients undergoing aortic valve replacement (AVR) with either a Mitroflow or a Carpentier-Edwards (CE) pericardial bioprosthesis. Since AVR with bioprosthetic valves has increased progressively in recent years as compared to mechanical valves, especially in patients aged 60-70 years, there has been renewed interest in the long-term durability of current pericardial bioprostheses.
We compared 440 AVR with Mitroflow valves with 1953 AVR with CE pericardial valves implanted from 1999 to 2014 with regard to reoperation, reoperation for structural valve deterioration (SVD) and all-cause mortality.
Ten-year freedom from explant of any cause was higher for CE Perimount (98 ± 0.7%) than for Mitroflow (95 ± 1.4%, P < 0.01). Reasons for explant for CE Perimount were SVD (n = 2), endocarditis (n = 8) and paraprosthetic leak (n = 10). The reasons for explant for Mitroflow were SVD (n = 11), endocarditis (n = 3) SVD and pericarditis (n = 1) and paraprosthetic leak (n = 2). Ten-year freedom from explant due to SVD was higher for CE Perimount (100%) than for Mitroflow (96%) (P < 0.01). In small aortic annuli (bioprosthesis size 19-21 mm), freedom from SVD at 10 years for CE Perimount and Mitroflow was 100 versus 96%, respectively. By multivariate analysis, it was found that bioprosthesis size was not a risk factor for SVD. The choice of valve type could not be demonstrated to influence long-term survival.
The Mitroflow pericardial bioprosthesis provides less than optimal mid- and long-term durability compared with the CE Perimount pericardial valve, especially for small aortic diameter implants (19 and 21 mm). This study hereby confirms the existence of a real risk of valvular deterioration of the Mitroflow valve that might compromise the prognosis of the patients.
本研究比较接受主动脉瓣置换术(AVR)的患者使用 Mitroflow 或 Carpentier-Edwards(CE)心包生物瓣膜后的耐用性和再次手术风险。近年来,与机械瓣膜相比,生物瓣膜置换主动脉瓣手术逐渐增多,尤其是在 60 - 70 岁的患者中,人们对当前心包生物瓣膜的长期耐用性重新产生了兴趣。
我们比较了 1999 年至 2014 年间植入 Mitroflow 瓣膜的 440 例 AVR 患者与植入 CE 心包瓣膜的 1953 例 AVR 患者的再次手术情况、因结构性瓣膜退变(SVD)进行的再次手术情况以及全因死亡率。
CE Perimount 瓣膜 10 年无任何原因取出率(98 ± 0.7%)高于 Mitroflow 瓣膜(95 ± 1.4%,P < 0.01)。CE Perimount 瓣膜取出的原因包括 SVD(n = 2)、心内膜炎(n = 8)和人工瓣膜旁漏(n = 10)。Mitroflow 瓣膜取出的原因包括 SVD(n = 11)、心内膜炎(n = 3)、SVD 和心包炎(n = 1)以及人工瓣膜旁漏(n = 2)。CE Perimount 瓣膜因 SVD 的 10 年无取出率(100%)高于 Mitroflow 瓣膜(96%)(P < 0.01)。在小主动脉瓣环(生物瓣膜尺寸 19 - 21mm)中,CE Perimount 和 Mitroflow 瓣膜 10 年无 SVD 率分别为 100%和 96%。多因素分析发现,生物瓣膜尺寸不是 SVD 的危险因素。瓣膜类型的选择未被证明会影响长期生存率。
与 CE Perimount 心包瓣膜相比,Mitroflow 心包生物瓣膜的中长期耐用性欠佳,尤其是对于小主动脉直径植入物(19 和 21mm)。本研究证实 Mitroflow 瓣膜确实存在瓣膜退变风险,这可能会影响患者的预后。