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Anterior Tracheal Suspension for Tracheobronchomalacia in Infants and Children

机译:婴幼儿气管支气管软化前气管悬吊术

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Statistical AnalysisBronchogramSurgical ProcedureResultsComplications and Notable EventsSevere tracheobronchomalacia significantly complicates the postoperative course of infants and children with congenital heart disease, tracheoesophageal fistula, and tracheal stenosis. We have found that traditional approaches, including aortopexy, have been inconsistent in preventing acute life threatening events (ALTEs). In order to directly support the anterior tracheal wall, we have adopted the use of direct anterior tracheal suspension (ATS).MethodsTwenty-one children, median age 5 months (35 days to 11 years) and weight 5.0 (2.3 to 28.0) kg have undergone anterior tracheal suspension for severe tracheobronchomalacia through median sternotomy; 15 for inability to ventilate despite mechanical respiratory support,?3 for intermittent ALTEs without mechanical respiratory?support, and 3 for recurrent respiratory admissions. Nine procedures were performed as isolated ATS and 12 procedures were combined with at least 1 of the following: repair of ventricular septal defect; vascular ring; atrioventricular canal; tracheal reconstruction or arterial-pexy. Level of respiratory support was graded at preoperative (preop), discharge, and follow-up, and respiratory clinical status was graded at preop and follow-up. Median follow-up was 30.0 months (2.0 to 57.0 months).ResultsThere was no mortality. Both level of respiratory support and the clinical status improved at all time points studied compared with preoperative score (p < 0.001) after ATS. Whether ATS was performed in isolation or combined with other procedures did not impact these findings.ConclusionsAnterior tracheal suspension is feasible and appears effective in dramatically improving respiratory clinical status. Tracheal suspension is applicable to a wide range of anatomic variants. Additional study is needed to characterize long-term functional outcomes.CTSNet classification:15Tracheomalacia is a disorder of the large airways, primarily found in infants, which results in a spectrum of respiratory symptoms ranging from chronic cough to life threatening apnea with cyanosis and airway?obstruction (ie, acute life threatening events, ALTEs) [
机译:统计分析支气管镜手术结果结果并发症和重要事件严重气管支气管软化症使患有先天性心脏病,气管食管瘘和气管狭窄的婴幼儿的术后病程明显复杂化。我们已经发现,包括动脉粥样硬化在内的传统方法在预防急性威胁生命的事件(ALTE)中一直不一致。为了直接支撑气管前壁,我们采用了直接气管前悬架(ATS)方法.21名年龄中位数为5个月(35天至11岁),体重5.0(2.3至28.0)公斤的儿童通过正中胸骨切开术对严重气管支气管软化症进行气管前悬吊; 15表示尽管有机械呼吸支持仍无法通气; 3表示无机械呼吸支持的间歇性ALTE; 3表示复发性呼吸道入院。作为隔离的ATS进行了9道手术,并将12道手术与以下至少一种结合:修复室间隔缺损;血管环房室管;气管重建或肺动脉狭窄。在术前(术前),出院和随访中对呼吸支持水平进行分级,在术前和随访中对呼吸系统临床状况进行分级。中位随访时间为30.0个月(2.0至57.0个月)。结果无死亡。与ATS术后术前评分(p <0.001)相比,研究的所有时间点呼吸支持水平和临床状况均得到改善。无论是单独进行ATS还是与其他程序结合使用都不会影响这些发现。结论气管前悬挂是可行的,并且在显着改善呼吸道临床状况方面似乎有效。气管悬架适用于多种解剖学变异。 CTSNet分类:15气管软化症是一种大型气道疾病,主要存在于婴儿中,导致一系列呼吸道症状,从慢性咳嗽到威胁生命的呼吸暂停伴紫和气道?阻塞(例如,威胁生命的紧急事件,ALTE)[

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