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首页> 外文期刊>The Internet Journal of Thoracic and Cardiovascular Surgery >Valve-sparing reconstruction of a congenital bicuspid aortic valve with severe calcified aortic stenosis
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Valve-sparing reconstruction of a congenital bicuspid aortic valve with severe calcified aortic stenosis

机译:先天性双尖瓣主动脉瓣严重瓣钙化狭窄的保瓣重建

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Bicuspid aortic valve is now known to be the most common congenital lesion affecting the human heart. Bicuspid aortic valve is well known to cause calcified aortic stenosis. Valve-sparing reconstruction in cases of bicuspid valves, represents a promising alternative to prosthetic valve replacement. Reconstruction of the bicuspid valve is feasible with good results by the technique of valve repair.In this study we present our valve-sparing reconstruction technique of a congenital bicuspid aortic valve with severe calcified aortic stenosis. Introduction The bicuspid aortic valve affects 1 to 2% of the population and may be complicated by aortic stenosis (1). Aortic valve replacement is the standard procedure in patients with aortic valve pathology. Currently, isolated reconstruction of a regurgitant bicuspid aortic valve can be performed with adequate early results (2). Although long-term results for both biological and mechanical heart valves could be improved, a valve-sparing operation has several advantages especially in young patients (3). In patients with a bicuspid aortic valve, the aortic valvular pathology can be corrected by the valve reconstruction. Case Presentation Our case was a 10-year-old boy. After his birth he was suffering from intermittent cyanosis of the extremities and the lips. Transthoracic echocardiography revealed a bicuspid aortic valve with severe stenosis where the peak pressure gradient was measured as 60 mm Hg. Left ventricular end-diastolic and end-systolic diameters were measured as 44 and 23 mm, respectively. No aortic regurgitation was identified. Ejection fraction was measured as 83%. Cardiac catheterization revealed no additional pathology. Our patient was taken to the operating room with these findings. Following a median sternotomy,pericardium was opened longitudinally. After heparinization, extra-corporeal circulation was established between the venae cavae and the ascending aorta. A cross clamp was placed on aorta and by antegrade intermittent isothermic blood cardioplegia from aortic root,cardiac arrest was established.Hypothermia was moderate (29oc). Standard aortotomy was made. Aortic valve was bicuspid, thickened and calcific in structure. Additionally, the commissures were adhered (Figure 1).
机译:现在已知双尖瓣主动脉瓣膜是影响人心脏的最常见的先天性病变。众所周知,二尖瓣主动脉瓣会引起钙化的主动脉瓣狭窄。在二尖瓣的情况下,保留瓣膜的重建代表了人工瓣膜置换的有希望的替代方案。通过瓣膜修复技术重建二尖瓣是可行的,并取得了良好的效果。在这项研究中,我们提出了一种先天性双尖瓣主动脉瓣严重钙化性主动脉瓣狭窄的保留瓣膜的重建技术。简介双尖瓣主动脉瓣占总人口的1%至2%,可能因主动脉瓣狭窄而复杂化(1)。主动脉瓣置换术是患有主动脉瓣病理的患者的标准程序。目前,可以对反流性双尖瓣主动脉瓣进行孤立的重建,并获得足够的早期结果(2)。尽管可以改善生物和机械心脏瓣膜的长期效果,但保留瓣膜的手术具有许多优势,尤其是在年轻患者中(3)。在患有二尖瓣主动脉瓣的患者中,可以通过瓣膜重建来纠正主动脉瓣膜病变。案例介绍我们的案例是一个10岁的男孩。他出生后患上了四肢和嘴唇的间歇性紫cyan。经胸超声心动图检查发现双尖瓣主动脉瓣狭窄严重,其峰值压力梯度为60 mm Hg。左心室舒张末期和收缩末期直径分别测量为44和23 mm。没有发现主动脉瓣关闭不全。射血分数测得为83%。心脏导管检查未发现其他病理。这些发现将我们的患者带到手术室。正中胸骨切开术后,将心包膜纵向打开。肝素化后,在静脉腔和升主动脉之间建立体外循环。将一个交叉钳夹在主动脉上,并从主动脉根部顺行间歇性等温血液性停跳,建立心脏骤停。低体温症为中度(29oc)。进行标准的主动脉切开术。主动脉瓣二尖瓣,增厚,钙化。另外,连合处也被粘住(图1)。

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