Goncu Tugrul, Alur Ihsan, Gucu Arif, Tenekecioglu Erhan, Toktas Faruk, Kahraman Nail, Vural Hakan, Yavuz Senol
Department of Cardiovascular Surgery, Bursa Yuksek Ihtisas Education and Research Hospital Bursa, Turkey.
Department of Cardiovascular Surgery, Pamukkale University Faculty of Medicine Denizli, Turkey.
Int J Clin Exp Med. 2015 Feb 15;8(2):2839-45. eCollection 2015.
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.
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.
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.
We conclude that Kalangos BTR is an efficient and safe prosthesis with easy implantation technique for FTR treatment, with encouraging midterm results.
卡朗戈斯生物可降解三尖瓣环(卡朗戈斯生物可降解三尖瓣环®,Bioring SA,瑞士洛奈)是一种用于治疗功能性三尖瓣反流(FTR)的生物可降解假体。在本研究中,我们旨在确定该假体治疗中度和重度FTR的临床和超声心动图结果,并将该技术与半圆形德维加瓣环成形术的结果进行比较。
从2005年1月至2010年1月,我们回顾性研究了64例连续接受FTR治疗的瓣环成形术患者的数据。患者分为2组:(1)32例患者接受卡朗戈斯生物可降解三尖瓣环瓣环成形术,(2)32例患者接受半圆形德维加瓣环成形术。所有患者在术前、术后第1周、第3个月和第6个月进行临床评估和超声心动图检查。
随访期间未记录到与假体或手术相关的并发症。在随访期间,两组患者的收缩期肺动脉压和三尖瓣瓣环面积直径均显著低于术前值(p < 0.0001)。随访期间,与第2组相比,第1组的残余三尖瓣反流和Tei指数(心肌性能指数)显著降低(p < 0.05)。术后6个月,四分之三的瓣环成形环已降解。
我们得出结论,卡朗戈斯生物可降解三尖瓣环是一种高效、安全的假体,植入技术简单,用于治疗FTR,中期结果令人鼓舞。