Harada Atsushi, Shimojima Naoki, Shimotakahara Akihiro, Azuma Saya, Ishizuka Yoshiaki, Tomita Hirofumi, Hirobe Seiichi
Department of Surgery, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan.
J Thorac Dis. 2019 Dec;11(12):5474-5479. doi: 10.21037/jtd.2019.11.31.
Congenital tracheal stenosis (CTS) is a rare and life-threatening disease in children. Although pulmonary artery sling (PA sling) complicated by CTS sometimes occurs, there are few reports detailing the management of CTS with PA sling. The purpose of this retrospective study was to determine the appropriate indications for surgical intervention for CTS complicated by PA sling.
We evaluated 42 patients (19 males and 23 females) with the median age of 9.9±3.3 months (range, 5-34 months) with CTS complicated by PA sling who were treated at our hospital between 2005 and 2018. Twenty-eight patients received both a slide tracheoplasty and PA re-implantation, and 14 patients were managed conservatively for CTS. Among the latter, nine patients received PA re-implantation only, and five were managed conservatively without any surgery. We determined the surgical indications by retrospectively comparing the DLR value [tracheal diameter (mm)/stenotic length ratio], history of ventilator respiration, mortality rate, and post-operative course of patients at a single institution.
The cut-off value for the DLR was determined to be 5.9 (sensitivity: 0.929, specificity: 0.714) by using the ROC curve (AUC 0.89, P<0.05).
A DLR value under 5.9 may serve as a new surgical indication for CTS complicated by PA sling.
先天性气管狭窄(CTS)是一种在儿童中罕见且危及生命的疾病。尽管有时会出现合并CTS的肺动脉吊带(PA吊带),但很少有报告详细说明合并PA吊带的CTS的治疗方法。这项回顾性研究的目的是确定合并PA吊带的CTS手术干预的合适指征。
我们评估了2005年至2018年期间在我院接受治疗的42例合并PA吊带的CTS患者(19例男性和23例女性),中位年龄为9.9±3.3个月(范围5 - 34个月)。28例患者接受了气管成形术和PA重新植入术,14例患者对CTS进行了保守治疗。在后者中,9例患者仅接受了PA重新植入术,5例患者未进行任何手术,采取了保守治疗。我们通过回顾性比较单个机构中患者的DLR值[气管直径(mm)/狭窄长度比]、机械通气史、死亡率和术后病程来确定手术指征。
通过ROC曲线(AUC 0.89,P<0.05)确定DLR的临界值为5.9(敏感性:0.929,特异性:0.714)。
DLR值低于5.9可能作为合并PA吊带的CTS的新手术指征。