首页> 外文期刊>Arquivos brasileiros de cardiologia. >Implante Percutaneo Transeptal de Bioprótese em Disfun??o de Prótese Valvar Cirúrgica Mitral – Experiência Multicêntrica Brasileira
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Implante Percutaneo Transeptal de Bioprótese em Disfun??o de Prótese Valvar Cirúrgica Mitral – Experiência Multicêntrica Brasileira

机译:二尖瓣手术瓣膜假体功能障碍的生物化植入生物化植入物 - 巴西多中心体验

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Background Percutaneous intervention in patients with bioprosthetic mitral valve dysfunction is an alternative to conventional surgical treatment. Objectives To report the first Brazilian experience with transseptal transcatheter bioprosthetic mitral valve-in-valve implantation (transseptal-TMVIV). Methods Patients with surgical bioprosthetic dysfunction submitted to transseptal-TMVIV in 12 Brazilian hospitals were included. The significance level adopted was p0.05. Results From June/2016 to February/2019, 17 patients underwent transseptal-TMVIV. Their median age was 77 years (IQR,70-82) and median Society of Thoracic Surgeons predicted risk of mortality (STS-PROM) score was 8.7% (IQR,7.2-17.8). All patients had limiting symptoms of heart failure (FC≥III) and 5 (29.4%) had undergone more than one previous thoracotomy. Transseptal-TMVIV was successful in all patients. Echocardiographic assessment showed a significant reduction in mean mitral valve gradient (pre-intervention, 12±3.8 mmHg; post-intervention, 5.3±2.6 mmHg; p0.001), in addition to an increase in mitral valve area (pre-intervention, 1.06±0.59 cm2; post-intervention, 2.18±0.36 cm2; p0.001) sustained for 30 days. There was a significant and immediate reduction in the pulmonary artery systolic pressure, with an additional reduction in 30 days (pre-intervention, 68.9±16.4 mmHg; post-intervention, 57.7±16.5 mmHg; 30 days, 50.9±18.7 mmHg; p0.001). During follow-up (median, 162 days; IQR, 102-411), significant clinical improvement (FC≤II) was observed in 87.5% of the patients. One patient (5.9%) had left ventricular outflow tract (LVOT) obstruction and died right after the procedure, and another died at 161 days of follow-up. Conclusion The first Brazilian experience with transseptal-TMVIV shows the safety and effectivity of the new technique. The LVOT obstruction is a potentially fatal complication, reinforcing the importance of patients’ selection and of procedural planning. (Arq Bras Cardiol.
机译:背景技术生物假体二尖瓣功能障碍患者的经皮干预是常规手术治疗的替代品。目的举报第一个巴西对纵向转膜转截管生物原因二尖瓣内瓣膜植入(Transseptal-TMVIV)的体验。方法包括提交患有手术生物假体功能障碍的患者在12位巴西医院中提交给Transseptal-TMVIV。采用的显着性水平为P <0.05。结果六月/ 2016年至2019年2月/ 2019年,17例患者接受了Transseptal-TMVIV。他们的中位数年龄为77岁(IQR,70-82),胸外科医生的中位数会预测死亡率的风险(STS-PROM)得分为8.7%(IQR,7.2-17.8)。所有患者都限制了心力衰竭(FC≥III)的症状,5(29.4%)经历了超过一个以前的胸廓切开术。 Transseptal-TMVIV在所有患者中都是成功的。超声心动图评估显示平均二尖瓣梯度的显着降低(预干预,12±3.8mmHg;干预后,5.3±2.6mmHg; P <0.001),除了二尖瓣区(预介入,1.06 ±0.59 cm2;干预后,2.18±0.36 cm2; p <0.001)持续30天。肺动脉收缩压有显着和立即降低,额外减少30天(预干预,68.9±16.4 mmHg;干预后,57.7±16.5mmHg; 30天,50.9±18.7 mmHg; P < 0.001)。在随访期间(中位数,162天; IQR,102-411),在87.5%的患者中观察到显着的临床改善(FC≤II)。一名患者(5.9%)左心室流出道(LVOT)梗阻并在程序后立即死亡,另一个在161天的随访中死亡。结论Transseptal-TMViv的第一个巴西体验显示了新技术的安全性和有效性。液体梗阻是一种潜在的致命并发症,加强了患者选择和程序规划的重要性。 (ARQ BRAS Cardiol。

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