Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2012 Oct 30:38:62.
doi: 10.1186/1824-7288-38-62.

Aortopexy for the treatment of tracheomalacia in children: review of the literature

Affiliations
Review

Aortopexy for the treatment of tracheomalacia in children: review of the literature

Michele Torre et al. Ital J Pediatr. .

Abstract

Severe tracheomalacia presents a significant challenge for Paediatricians, Intensivists, Respiratory Physicians, Otolaryngologists and Paediatric Surgeons. The treatment of tracheomacia remains controversial, but aortopexy is considered by most to be one of the best options. We conducted a review of the English literature relating to aortopexy.Among 125 papers, 40 have been included in this review. Among 758 patients (62% males) affected with tracheomalacia, 581 underwent aortopexy. Associated co-morbidities were reported in 659 patients. The most frequent association was with oesophageal atresia (44%), vascular ring or large vessel anomalies (18%) and innominate artery compression (16%); in 9% tracheomalacia was idiopathic. The symptoms reported were various, but the most important indication for aortopexy was an acute life-threatening event (ALTE), observed in 43% of patients. The main preoperative investigation was bronchoscopy. Surgical approach was through a left anterior thoracotomy in 72% of patients, while median approach was chosen in 14% and in 1.3% a thoracoscopic aortopexy was performed. At follow-up (median 47 months) more than 80% of the patients improved significantly, but 8% showed no improvement, 4% had a worsening of their symptoms and 6% died. Complications were observed in 15% of patients, in 1% a redo aortopexy was deemed necessary.In our review, we found a lack of general consensus about symptom description and evaluation, indications for surgery, though ALTE and bronchoscopy were considered by all an absolute indication to aortopexy and the gold standard for the diagnosis of tracheomalacia, respectively. Differences were reported also in surgical approaches and technical details, so that the same term "aortopexy" was used to describe different types of procedures. Whatever approach or technique was used, the efficacy of aortopexy was reported as high in the majority of cases (more than 80%). A subgroup of patients particularly delicate is represented by those with associated gastro-esophageal reflux, in whom a fundoplication should be performed. Other treatments of tracheomalacia, particularly tracheal stenting, were associated with a higher rate of failure, severe morbidity and mortality.

PubMed Disclaimer

References

    1. Masters IB, Chang AB. Interventions for primary (intrinsic) tracheomalacia in children. Cochrane Database Syst Rev. 2005;4:CD005304. doi: 10.1002/14651858.CD005304.pub2. - DOI - PubMed
    1. Brawn WJ, Huddart SN. Tracheoaortopexy via midline sternotomy in tracheomalacia. J Pediatr Surg. 1991;26:660–662. doi: 10.1016/0022-3468(91)90004-D. - DOI - PubMed
    1. Kiely EM, Spitz L, Bereton R. Management of tracheomalacia by aortopexy. Pediatr Surg Int. 1987;2:13–15.
    1. Van der Zee DC, Bax NM. Thoracoscopic tracheoaortopexia for the treatment of life-threatening events in tracheomalacia. Surg Endosc. 2007;21:2024–2025. doi: 10.1007/s00464-007-9250-8. - DOI - PubMed
    1. Gardella C, Girosi D, Rossi GA, Silvestri M, Tomà P, Bava G, Sacco O. Tracheal compression by aberrant innominate artery: clinical presentations in infants and children, indications for surgical correction by aortopexy, and short- and long-term outcome. J Pediatr Surg. 2010;45:564–573. doi: 10.1016/j.jpedsurg.2009.04.028. - DOI - PubMed

LinkOut - more resources