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Clinical and echocardiographic results of the Kalangos biodegradable tricuspid ring for moderate and severe functional tricuspid regurgitation treatment

机译:Kalangos可生物降解三尖瓣环治疗中度和重度三尖瓣反流的临床和超声心动图结果

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Introduction: The Kalangos Biodegradable Tricuspid Ring (Kalangos Biodegradable Tricuspid Ring®, Bioring SA, Lonay, Switzerland) is a biodegradable prothesis in the treatment of functional tricuspid regurgitation (FTR). In this study, we aimed to determine the clinical and echocardiographic results of this prosthesis for moderate and severe FTR treatment and compare this technique with the results of semicircular DeVega annuloplasty. Materials and methods: From January 2005 through January 2010 we retrospectively studied the data on 64 consecutive patients underwent annuloplasty procedures for FTR treatment. The patients were assigned to 2 groups: (1) Kalangos BTR annuloplasty was performed in 32 patients, and (2) Semicircular DeVega annuloplasty was performed in the 32 patients. All patients were evaluated clinically and by echocardiography preoperatively, at the end of the 1st week, 3rd and 6th month following surgery. Results: No complications related to the prosthesis or the procedures within the follow-up period were recorded. At the follow-up period, systolic pulmonary arterial pressure and tricuspid valve area diameter were found to be significantly lower than the preoperative values in both groups (p < 0.0001). At the follow-up period residual tricuspid regurgitation and the Tei index (Myocardial performance index) was significantly lower in group 1 compared to group 2 (p < 0.05). Three-quarters of the annuloplasty ring had degraded in the postoperative 6-months period. Discussion: We conclude that Kalangos BTR is an efficient and safe prosthesis with easy implantation technique for FTR treatment, with encouraging midterm results.
机译:简介:Kalangos可生物降解三尖瓣环(Kalangos可生物降解三尖瓣环®,Bioring SA,瑞士洛纳)是一种可生物降解的假体,用于治疗功能性三尖瓣关闭不全(FTR)。在这项研究中,我们旨在确定该假体用于中度和重度FTR治疗的临床和超声心动图结果,并将该技术与半圆形DeVega瓣环成形术的结果进行比较。材料和方法:自2005年1月至2010年1月,我们回顾性研究了64例接受瓣膜成形术治疗FTR的连续患者。将患者分为2组:(1)32例进行了Kalangos BTR瓣环成形术,(2)32例进行了半圆形DeVega瓣膜成形术。在手术后第1周,第3个月和第6个月结束时对所有患者进行临床和术前超声心动图检查。结果:在随访期内未发现与假体或手术相关的并发症。在随访期,发现两组的收缩期肺动脉压和三尖瓣面积直径均明显低于术前值(p< 0.0001)。在随访期,与第2组相比,第1组的残余三尖瓣关闭不全和Tei指数(心肌性能指数)明显更低(p< 0.05)。在术后6个月内,四分之三的瓣环成形术环已退化。讨论:我们得出的结论是,Kalangos BTR是一种有效且安全的假体,采用易于植入的技术进行FTR治疗,具有令人鼓舞的中期效果。

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