Oshima Y, Yamaguchi M, Ohashi H, Yoshimura N, Tanaka T, Oka S, Ogawa K, Nishijima E, Tsugawa C
Kobe Children's Hospital, Japan.
Jpn J Thorac Cardiovasc Surg. 1998 Apr;46(4):347-53. doi: 10.1007/BF03217754.
Between 1984 and 1996 five infants underwent surgical repair of pulmonary artery sling associated with severe congenital tracheal stenosis. All infants had symptoms of severe respiratory distress and three of them required ventilator support preoperatively ages ranged from 2 to 11 months (mean age 6 months). Complete tracheal rings were present in all patients as an associated lesion and right upper lobe tracheal bronchus in 3 patients. The length of tracheal stenosis ranged from 18 to 45 mm (median 40 mm). Three had associated intracardiac anomalies (Scimitar syndrome (1), VSD (1), double-outlet right ventricle with VSD (1), double-outlet right ventricle with pulmonary hypertension (1)). Surgical intervention was carried out through a right thoracotomy (1) or median sternotomy (4). Cardiopulmonary bypass (CPB) was used in 3 patients and extracorporeal membrane oxgenator (ECMO). In 1. All infants had reimplantation of the left pulmonary artery into the main pulmonary artery left anterior to the trachea. Four patients underwent simultaneous tracheoplasty using costal cartilage grafts and one had complete resection of obstructed trachea between the right upper lobe tracheal bronchus and carina. The length of resected trachea was about 30% of the entire length of the trachea. Three infants underwent simultaneous intracardiac repair. There was no hospital death. All were weaned from ventilatory support and extubated on 1 to 16 months (mean 4, 5 months) postoperatively. AS an additional procedure, aortopexy, removal of granulation tissue or balloon dilatation of the trachea were carried out in one patient each following tracheoplasty using cartilage grafts. There was one late death at 1 year postoperatively. Three of 4 survivors are doing well with no stridor. We adonostridor. We adovocate 1) early aggressive primary repair of pulmonary artery sling with tracheal stenosis, 2) concomitant repair of tracheal lesion and intracardiac anomalies whenever possible, 3) application of CPB or ECMO to avoid cumbersome intubation technique, and 4) utmost effort to perform tracheal resection and end-to-end anastomosis.
1984年至1996年间,5例患有与严重先天性气管狭窄相关的肺动脉吊带的婴儿接受了手术修复。所有婴儿均有严重呼吸窘迫症状,其中3例术前需要呼吸机支持,年龄在2至11个月之间(平均年龄6个月)。所有患者均存在完整气管环这一相关病变,3例患者有右上叶气管支气管。气管狭窄长度为18至45毫米(中位数40毫米)。3例伴有心内畸形(弯刀综合征(1例)、室间隔缺损(1例)、室间隔缺损合并右心室双出口(1例)、肺动脉高压合并右心室双出口(1例))。手术干预通过右胸切口(1例)或正中胸骨切开术(4例)进行。3例患者使用了体外循环(CPB),1例使用了体外膜肺氧合(ECMO)。所有婴儿均将左肺动脉重新植入气管前方左侧的主肺动脉。4例患者同时使用肋软骨移植进行气管成形术,1例患者对右上叶气管支气管与隆突之间的阻塞气管进行了完整切除。切除气管的长度约为气管全长的30%。3例婴儿同时进行了心内修复。无住院死亡病例。所有患者均在术后1至16个月(平均4.5个月)撤机并拔管。作为一项额外操作,在使用软骨移植进行气管成形术后,分别有1例患者进行了主动脉固定术、肉芽组织清除术或气管球囊扩张术。术后1年有1例晚期死亡。4名幸存者中有3名情况良好,无喘鸣。我们提倡:1)对伴有气管狭窄的肺动脉吊带进行早期积极的一期修复;2)尽可能同时修复气管病变和心内畸形;3)应用CPB或ECMO以避免繁琐的插管技术;4)尽最大努力进行气管切除和端端吻合术。