Ou-Yang Wen-Bin, Li Shou-Jun, Xie Yong-Quan, Hu Sheng-Shou, Wang Shou-Zheng, Zhang Feng-Wen, Guo Gai-Li, Liu Yao, Pang Kun-Jing, Pan Xiang-Bin
Department of Cardiovascular Surgery, National Center for Cardiovascular Disease, China & Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Department of Cardiovascular Surgery, National Center for Cardiovascular Disease, China & Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Ann Thorac Surg. 2018 Jan;105(1):175-180. doi: 10.1016/j.athoracsur.2017.05.069. Epub 2017 Sep 28.
Surgical or percutaneous interventional treatment of severe congenital aortic valve stenosis (CAS) in early infancy remains challenging. This single-center, retrospective study analyzed midterm outcomes of a hybrid balloon valvuloplasty procedure through the ascending aorta by way of median sternotomy, including cases with improved technique.
Included were 45 consecutive infants (aged <90 days) with CAS and selected for biventricular repair who underwent hybrid balloon valvuloplasty in a hybrid or ordinary operating room from October 2010 to March 2016. Patients were assessed at 1, 3, 6, and 12 months and yearly thereafter.
Hybrid balloon valvuloplasty was successful in all patients, with the last 8 treated in an ordinary operating room under only echocardiography guidance with a new sheath. Thirty-two patients were successfully rescued from low heart rate or left ventricular systolic dysfunction, or both, by cardiac massage under direct visualization; none required cardiopulmonary bypass. The degree of new aortic insufficiency was mild in 7 patients and changed from mild to moderate in 1 patient. Aortic valve pressure gradient decreased from 70.6 ± 17.5 mm Hg preoperatively to 15.2 ± 4.2 mm Hg immediately postoperatively (p < 0.001). Fluoroscopy time was 4.8 ± 2.3 minutes. At a median of 32.1 months (range, 1 to 68 months) follow-up, all patients were alive and healthy. Aortic valve pressure gradient remained low (19.1 ± 5.2 mm Hg). Left ventricular ejection fraction increased from 0.515 ± 0.134 (range, 0.21 to 0.70) preoperatively to 0.633 ± 0.035 (range, 0.58 to 0.75; p < 0.001). No aortic insufficiency developed, and no patient required reintervention.
For infants with severe CAS, hybrid balloon valvuloplasty through the ascending aorta by way of a median sternotomy appears efficacious and safe up to midterm follow-up.
婴儿早期严重先天性主动脉瓣狭窄(CAS)的手术或经皮介入治疗仍然具有挑战性。这项单中心回顾性研究分析了通过正中胸骨切开术经升主动脉进行的杂交球囊瓣膜成形术的中期结果,包括技术改进的病例。
纳入2010年10月至2016年3月期间在杂交手术室或普通手术室接受杂交球囊瓣膜成形术的45例连续的CAS婴儿(年龄<90天),这些婴儿被选进行双心室修复。在1、3、6和12个月时对患者进行评估,此后每年评估一次。
杂交球囊瓣膜成形术在所有患者中均成功,最后8例在仅超声心动图引导下使用新鞘管在普通手术室进行治疗。32例患者通过直视下心脏按摩成功从低心率或左心室收缩功能障碍或两者中获救;无一例需要体外循环。7例患者新出现的主动脉瓣关闭不全程度为轻度,1例患者从轻度变为中度。主动脉瓣压力阶差术前为70.6±17.5mmHg,术后即刻降至15.2±4.2mmHg(p<0.001)。透视时间为4.8±2.3分钟。在中位随访32.1个月(范围1至68个月)时,所有患者均存活且健康。主动脉瓣压力阶差仍较低(19.1±5.2mmHg)。左心室射血分数从术前的0.515±0.134(范围0.21至0.70)增加到0.633±0.035(范围0.58至0.75;p<0.001)。未出现主动脉瓣关闭不全,无一例患者需要再次干预。
对于患有严重CAS的婴儿,经正中胸骨切开术经升主动脉进行杂交球囊瓣膜成形术在中期随访时似乎有效且安全。