Slide tracheoplasty outcomes in children with congenital pulmonary malformations

Michael A. DeMarcantonio, Catherine K. Hart, Christina J. Yang, Meredith Tabangin, Michael J. Rutter, Roosevelt Bryant, Peter B. Manning, Alessandro de Alarcón

Research output: Contribution to journalArticlepeer-review

27 Scopus citations


Objectives/Hypothesis: Evaluate and compare surgical outcomes of slide tracheoplasty for the treatment of congenital tracheal stenosis in children with and without pulmonary malformations. Study Design: Retrospective chart review at a tertiary care pediatric medical center. Methods: We identified patients with tracheal stenosis who underwent slide tracheoplasty from 2001 to 2014, and a subset of these patients who were diagnosed with congenital pulmonary malformations. Hospital course and preoperative and postoperative complications were recorded. Results: One hundred thirty patients (18 with pulmonary malformations, 112 with normal pulmonary anatomy) were included. Pulmonary malformations included unilateral pulmonary agenesis (61%) and hypoplasia (39%). Children with pulmonary malformations had a greater median age compared to their normal lung anatomy counterparts. Preoperatively, patients with pulmonary malformations more frequently required preoperative mechanical ventilation (55.6% vs. 21.3%, P =.007), extracorporeal membrane oxygenation (ECMO) (11% vs. 0.9%, P =.05), and tracheostomy (22.2% vs. 3.6%, P =.01). Postoperatively, patients with pulmonary malformations more frequently required mechanical ventilation >48 hours (78% vs. 37%, P =.005) and ECMO use (11% vs. 0.9%, P =.05). Pulmonary malformation patients and children with normal anatomy did not differ in terms of postoperative tracheostomy (16.7% vs. 4.4%, P >.05), dehiscence (6% vs. 0%, P >.05%), restenosis (11% vs. 6%, P >.05) or postoperative figure 8 deformity (6% vs. 3%, P >.05). Mortality, however, was significantly increased (22.2% vs. 3.6%, P =.01) in children with pulmonary malformations. Conclusions: Although slide tracheoplasty can be successfully performed in patients with abnormal pulmonary anatomy, surgeons and families should anticipate a more difficult postoperative course, with possible associated prolonged mechanical ventilation, ECMO use, and higher mortality than in children with tracheal stenosis alone. Level of Evidence: 4. Laryngoscope, 127:1283–1287, 2017.

Original languageEnglish (US)
Pages (from-to)1283-1287
Number of pages5
Issue number6
StatePublished - Jun 2017


  • Slide tracheoplasty
  • complete tracheal rings
  • pulmonary agenesis
  • pulmonary hypoplasia
  • tracheal stenosis

ASJC Scopus subject areas

  • Otorhinolaryngology


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