Roemers Rosa, Kluin Jolanda, de Heer Frederiek, Arrigoni Sara, Bökenkamp Regina, van Melle Joost, Ebels Tjark, Hazekamp Mark
1 Department of Cardiothoracic Surgery, Leiden University Center, Leiden, the Netherlands.
2 Department of Cardiothoracic Surgery, Academic Medical Center, Amsterdam, the Netherlands.
World J Pediatr Congenit Heart Surg. 2018 Mar;9(2):131-138. doi: 10.1177/2150135117745004.
Supravalvar aortic stenosis (SVAS) is a rare congenital anomaly. The "single-patch technique," "'two sinus augmentation with an inverted Y-patch" (both nonsymmetrical corrections), "three-patch technique," and the "slide aortoplasty" (both symmetrical corrections) are the techniques implemented by the majority of surgeons for the correction of SVAS. In the few studies that compared these techniques, no technique was shown to be superior over another. The aim of the present study is to review the 52-year experience with the surgical correction of SVAS in two of four congenital cardiothoracic surgical centers in the Netherlands.
We retrospectively reviewed all patient files of those who underwent an operation to correct their SVAS, between 1962 and 2014 in our centers. Patients were divided according to their operating technique. These groups were compared using the end points freedom from reoperation and mortality.
A total of 49 patients were included, 23 (46.9%) patients in the nonsymmetrical group and 26 (53.1%) patients in the symmetrical group. Survival after 20 years in the nonsymmetrical group was 80% (standard error [SE]: 0.091) and in the symmetrical group was 85% (SE: 0.085; P = .163). Freedom from reoperation after 20 years in the nonsymmetrical group was 88% (SE: 0.079) and in the symmetrical group was 71% (SE: 0.107; P = 0.313).
In this patient group, there is no significant difference in survival and freedom from reoperation between the different surgical techniques for SVAS repair. Compared to the survival in the general population, the survival of SVAS patients is remarkably low. Apparently, SVAS is not a benign disease and probably patients should be followed more closely for the rest of their lives.
瓣上主动脉狭窄(SVAS)是一种罕见的先天性异常。“单片技术”、“倒Y形补片双窦扩大术”(均为非对称矫正)、“三片技术”以及“滑动主动脉成形术”(均为对称矫正)是大多数外科医生用于矫正SVAS的技术。在少数比较这些技术的研究中,没有一种技术被证明优于另一种。本研究的目的是回顾荷兰四个先天性心胸外科中心中的两个中心在52年里对SVAS进行手术矫正的经验。
我们回顾性分析了1962年至2014年间在我们中心接受SVAS矫正手术患者的所有病历。根据手术技术对患者进行分组。使用再次手术自由度和死亡率这些终点指标对这些组进行比较。
共纳入49例患者,非对称组23例(46.9%),对称组26例(53.1%)。非对称组20年后的生存率为80%(标准误[SE]:0.091),对称组为85%(SE:0.085;P = 0.163)。非对称组20年后再次手术自由度为88%(SE:0.079),对称组为71%(SE:0.107;P = 0.313)。
在该患者群体中,不同手术技术矫正SVAS后的生存率和再次手术自由度没有显著差异。与一般人群的生存率相比,SVAS患者的生存率显著较低。显然,SVAS不是一种良性疾病,可能患者在余生应接受更密切的随访。