[Treatment strategy of congenital tracheal stenosis associated with non-vascular ring cardiac malformations]

Zhonghua Wai Ke Za Zhi. 2023 Dec 1;62(1):66-71. doi: 10.3760/cma.j.cn112139-20230410-00154. Online ahead of print.
[Article in Chinese]

Abstract

Objective: To examine the treatment strategy of congenital tracheal stenosis associated with non-vascular ring cardiac malformations. Methods: This is a retrospective case series. Clinic data from 24 children with tracheal stenosis who underwent surgical treatment in the Department of Cardiac Surgery, Children's Hospital Affiliated to Shandong University from February 2017 to March 2023 were retrospectively collected. There were 16 males and 8 females, aged (M(IQR)) 6.5 (19.6) months (range: 2.2 to 66.3 months) and weighted 5.95 (4.76) kg (range: 3.2 to 20.0 kg). All patients had obvious respiratory symptoms. Eighteen patients underwent cardiac malformation correction and tracheoplasty at the same time (simultaneous group). Six patients in the staged operation group were treated with cardiac malformation correction in the first stage operation and tracheoplasty in the second stage operation due to missed diagnosis or delayed diagnosis of tracheal stenosis or no condition for tracheoplasty. Slide tracheoplasty was used to correct tracheal stenosis in both groups. The recovery of the children was followed. Wilcoxon sign rank test was used for comparison between the two groups. Results: There was no death during the perioperative period and hospitalization. In the simultaneous group, 1 case with delayed chest closure underwent bedside chest closure after 52 hours, 2 cases were intubated again after operation, and 1 case was implanted with an endotracheal stent. The duration of mechanical ventilation was 40.5 (39.6) hours (range: 19.0 to 438.8 hours). In the staged group, there was 1 case of re-intubation after operation, combined with left vocal cord paralysis and respiratory multidrug-resistant bacterial infection (Acinetobacter baumanii). One patient underwent 3 times of bronchoscopic balloon dilatation of the right middle bronchus, and heart rate returned to normal range. The duration of mechanical ventilation was 19.0 (21.4) hours (range: 17.1 to 96.7 hours). During follow-up, a patient in the simultaneous group was prone to respiratory infection and had good exercise tolerance, 1 patient in the staged group still had sputum stridor in the throat 3 months after the operation, and symptoms improved significantly 6 months after the operation. The other children didn't have obvious respiratory symptoms. Conclusions: The diagnosis of tracheal stenosis may be delayed or missed when tracheal stenosis is complicated by non-vascular ring cardiac malformations. One-stage correction of tracheal stenosis and cardiac malformation can achieve a good outcome.

目的: 探讨先天性气管狭窄合并非血管环类心脏畸形的手术治疗策略。 方法: 本研究为回顾性病例系列研究。回顾性收集2017年2月至2023年3月于山东大学附属儿童医院心脏外科接受手术治疗气管狭窄的24例患儿资料。男16例,女8例;年龄[M(IQR)]6.5(19.6)个月(范围:2.2~66.3个月),体重5.95(4.76)kg(范围:3.2~20.0 kg)。全组病例均存在明显呼吸道症状。其中同期行心脏畸形矫治及气管成形术(同期组,18例);因一期手术前漏诊、延迟诊断气管狭窄或不存在气管成形术条件,一期手术仅行心脏畸形矫治,二期手术行气管成形(分期组,6例)。气管狭窄矫治均采用Slide气管成形术。随访患儿恢复情况。组间比较采用Wilcoxon符号秩检验。 结果: 全部病例无手术死亡,无住院期间死亡。同期组1例延迟关胸患儿于52 h后行床旁关胸手术,2例术后再次行气管插管,1例行气管内支架植入;呼吸机辅助通气时间40.5(39.6)h(范围:19.0~438.8 h)。分期组1例术后再次插管,合并左侧声带麻痹、呼吸道多重耐药菌感染(鲍曼不动杆菌);1例支气管镜下球囊扩张右中间支气管3次,心率恢复至正常范围;呼吸机辅助通气时间19.0(21.4)h(范围:17.1~96.7 h)。两组呼吸机辅助时间的差异无统计学意义(Z=-1.363,P=0.173)。随访中同期组1例易患上呼吸道感染,活动耐力可,分期组1例术后3个月仍存在喉中痰鸣,术后6个月症状明显改善;其余患儿无明显呼吸道症状。 结论: 当气管狭窄合并非血管环类心脏畸形时,可能会出现延迟或遗漏诊断气管狭窄。同期矫治气管狭窄和心脏畸形可取得较好效果。.

Publication types

  • English Abstract