Sai Sadahiro, Konishi Akinobu, Sato Mitsuru, Matsuo Satoshi, Nitta Megumi
Department of Cardiovascular Surgery, Miyagi Children׳s Hospital, Sendai, Japan.
Department of Cardiovascular Surgery, Miyagi Children׳s Hospital, Sendai, Japan.
Semin Thorac Cardiovasc Surg. 2015 Autumn;27(3):321-5. doi: 10.1053/j.semtcvs.2015.08.004. Epub 2015 Aug 20.
Early surgical intervention is required for sudden onset, severe mitral regurgitation (MR) due to chordal rupture in infants with normal development younger than 1 year. The condition has been recognized as idiopathic. However, the surgical options in children are limited because of their size and somatic growth. We sought to examine the efficacy of mitral valve plasty by artificial chordal reconstruction for these infants in mid-to-long term. From August 2005 through June 2012, 8 consecutive patients aged 1-7 months underwent mitral valve plasty by chordal reconstruction using expanded polytetrafluoroethylene sutures for MR, owing to leaflet prolapse. The geometric parameters of the diameter of the mitral annulus (D1), the long axis of the left ventricular (LV) chamber (D2), and the length of the papillary muscle including the reconstructed chordae (D3) were measured, as well as MR grade (0-4) and LV end-diastolic dimension, at each time point. The parameters were compared with those in the control group that included Kawasaki disease patients without cardiac lesions and healthy children (n = 51). Mean follow-up period was 5.8 (2.8-9.6) years. Freedom from reoperation was 100%. MR grades were 3.9 ± 0.4 preoperatively, 2.4 ± 0.9 at discharge, and 1.4 ± 0.6 at the latest. Postoperative MR was improved within 1 year in 5 of 6 patients who had grade 2 or higher regurgitation. LV end-diastolic dimensions were 109% (% of normal), 113%, and 107% at discharge, 3, and 5 years, respectively. Geometric configuration indicated by the D1/D2 ratio did not significantly change with time. The length of the papillary muscle including reconstructed chordae (D3) strongly correlated with body surface area (r(2) = 0.65), which seemed to be equivalent to that in the control group. In conclusion, postoperative mitral valve function and geometry was preserved. This procedure with a low morbidity should be an option for pediatric patients with acute severe MR.
对于1岁以下发育正常的婴儿因腱索断裂导致的突发严重二尖瓣反流(MR),需要早期手术干预。这种情况被认为是特发性的。然而,由于儿童的体型和身体生长,其手术选择有限。我们试图从中长期研究人工腱索重建二尖瓣成形术对这些婴儿的疗效。从2005年8月至2012年6月,8例年龄在1 - 7个月的连续患者因瓣叶脱垂,使用膨体聚四氟乙烯缝线进行腱索重建二尖瓣成形术治疗MR。在每个时间点测量二尖瓣环直径(D1)、左心室(LV)腔长轴(D2)、包括重建腱索的乳头肌长度(D3)等几何参数,以及MR分级(0 - 4级)和LV舒张末期内径。将这些参数与包括无心脏病变的川崎病患者和健康儿童的对照组(n = 51)进行比较。平均随访期为5.8(2.8 - 9.6)年。再次手术率为100%。术前MR分级为3.9±0.4,出院时为2.4±0.9,最近一次为1.4±0.6。6例术前MR分级为2级或更高的患者中,5例在术后1年内MR得到改善。出院时、3年和5年时LV舒张末期内径分别为正常的109%、113%和107%。由D1/D2比值表示的几何构型随时间无显著变化。包括重建腱索的乳头肌长度(D3)与体表面积密切相关(r² = 0.65),这似乎与对照组相当。总之,术后二尖瓣功能和几何形态得以保留。这种发病率低的手术方法应是急性严重MR儿科患者的一种选择。