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首页> 外文期刊>Frontiers in Cardiovascular Medicine >Transcatheter Valve-in-Valve Procedures for Bioprosthetic Valve Dysfunction in Patients With Rheumatic vs. Non-Rheumatic Valvular Heart Disease
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Transcatheter Valve-in-Valve Procedures for Bioprosthetic Valve Dysfunction in Patients With Rheumatic vs. Non-Rheumatic Valvular Heart Disease

机译:转膜表阀内瓣膜内瓣膜术治疗患者的生物抑制阀功能障碍与非风湿性瓣膜心脏病

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Background: Bioprosthetic heart valve has limited durability and lower long-term performance especially in rheumatic heart disease (RHD) patients that are often subject to multiple redo operations. Minimally invasive procedures, such as transcatheter valve-in-valve (ViV) implantation, may offer an attractive alternative, although data is lacking. The aim of this study was to evaluate the baseline characteristics and clinical outcomes in rheumatic vs. non-rheumatic patients undergoing ViV procedures for severe bioprosthetic valve dysfunction. Methods: Single center, prospective study, including consecutive patients undergoing transcatheter ViV implantation in aortic, mitral and tricuspid position, from May 2015 to September 2020. RHD was defined according to clinical history, previous echocardiographic and surgical findings. Results: Among 106 patients included, 69 had rheumatic etiology and 37 were non-rheumatic. Rheumatic patients had higher incidence of female sex (73.9 vs. 43.2%, respectively; p = 0.004), atrial fibrillation (82.6 vs. 45.9%, respectively; p 0.001), and 2 or more prior surgeries (68.1 vs. 32.4%, respectively; p = 0.001). Although, device success was similar between groups (75.4 vs. 89.2% in rheumatic vs. non-rheumatic, respectively; p = 0.148), there was a trend toward higher 30-day mortality rates in the rheumatic patients (21.7 vs. 5.4%, respectively; p = 0.057). Still, at median follow-up of 20.7 [5.1–30.4] months, cumulative mortality was similar between both groups ( p = 0.779). Conclusion: Transcatheter ViV implantation is an acceptable alternative to redo operations in the treatment of patients with RHD and severe bioprosthetic valve dysfunction. Despite similar device success rates, rheumatic patients present higher 30-day mortality rates with good mid-term clinical outcomes. Future studies with a larger number of patients and follow-up are still warranted, to firmly conclude on the role transcatheter ViV procedures in the RHD population.
机译:背景:生物假体心脏瓣膜具有有限的耐久性和较低的长期性能,尤其是往往受到多重重做操作的风湿性心脏病(RHD)患者。尽管缺乏数据,但微创手术,例如经电截管阀内(VIV)植入,可以提供有吸引力的替代方案。本研究的目的是评估风湿性患者的基线特征和临床结果,进行VIV程序的严重生物假体瓣膜功能障碍。方法:单中心,前瞻性研究,包括在2015年5月至9月20日至9月20日期间在主动脉,二尖瓣和三尖球位置进行经截瘫VIV植入的连续患者。根据临床历史,先前的超声心动图和外科调查结果,RHD定义。结果:包括106名患者,69例风湿病因,37例是非风湿性的。风湿患者的母性发病率较高(分别为43.9%; P = 0.004),心房颤动(分别为82.6与45.9%; P <0.001),以及2个或更多的先前手术(68.1与32.4 %,分别; p = 0.001)。虽然,在群体之间的成功相似(流动性与非风湿性的75.4 vs.89.2%; P = 0.148),风湿患者中的30天死亡率呈现出趋势(21.7 vs.5.4%分别; p = 0.057)。尽管如此,在20.7 [5.1-30.4]月份的中位随访,两组之间的累积死亡率相似(P = 0.779)。结论:经截管VIV植入是一种可接受的选择,用于治疗RHD患者和严重的生物假瓣功能障碍。尽管有类似的设备成功率,风湿患者患有较高的30天死亡率,中期临床结果良好。仍然有保证患者和随访的未来研究仍然保证,在RHD人口中的角度转会VIV程序中坚定地结束。

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