Abstract

ABSTRACTObjective:To evaluate clinical stability of neurologically impaired children and adolescents with recurrent pneumonia submitted to laryngotracheal separation.Methods:Between October 2002 and June 2015, 92 neurologically impaired children from a reference service, with median age of 68.5 months were submitted to laryngotracheal separation. Data were evaluated and statistical analysis was made by Student's t test and Pearson's χ2 test (significance level adopted of 95%).Results:Fifty-three children were male (57.6%). Forty-six children required admission to intensive care, and 42.4% needed mechanical ventilation. We observed that 90.2% of patients were exclusively fed by gastrostomy and 72.4% of the gastrostomies were performed before the tracheal surgery. Thirteen (14.1%) children had postoperative complications as follows: fistulae (5.4%), bleeding (4.3%), granuloma (2.2%) and stenosis (3.2%). A total of 24 patients had pneumonia in the postoperative period (26.1%), but there was a significant drop in occurrence of this condition after surgery (100% versus 26.1%; p<0.001). Twenty-three patients (25%) died. Postoperative complications were similar when comparing patients who died and those that presented good outcome (16.7% versus 13.2%; p=0.73).Conclusion:When well-indicated, the laryngotracheal separation reduces the incidence of postoperative pulmonary infections, thus improving quality of life and reducing admissions to hospital. Laryngotracheal separation should be indicated as a primary procedure in patients with cerebral palsy and recurrent aspiration pneumonia.

Highlights

  • Chronic pulmonary aspiration is frequently observed in children with chronic non-progressive encephalopathy

  • Laryngotracheal separation should be indicated as a primary procedure in patients with cerebral palsy and recurrent aspiration pneumonia

  • Among the patients who presented with a tracheocutaneous fistula, only one had tracheostomy prior to laryngotracheal separation (LTS)

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Summary

Introduction

Chronic pulmonary aspiration is frequently observed in children with chronic non-progressive encephalopathy. The ideal surgery to treat chronic aspiration, especially in neuropathic children, should completely avoid aspiration, be a single procedure, safely performed in small structures, cause no damage or scars that would avoid larynx growth and integrity, allow phonation and be reversible. Considering all these requirements, the technique preferred by many physicians and used in children, is the laryngotracheal separation (LTS), first described by Lindeman, in 1975, and modified in 1976.(3-5). It is important that the surgery details be fully explained to the family.[3]

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