El niño con estridor persistente / The child with persistent stridor

El estridor es un ruido respiratorio anormal generado por obstrucción o colapso de la vía aérea laringotraqueal, de manera aguda o de evolución crónica. Existen distintas causas tanto congénitas como adquiridas capaces de producir dificultad respiratoria, que puede llegar a ser grave y con potencial riesgo vital. El diagnóstico clínico del paciente con estridor persistente debe ser complementado con un estudio endoscópico de la vía aérea y en ocasiones con imágenes, para intentar determinar el o los sitios comprometidos y posibles malformaciones asociadas. La indicación de tratamiento debe ser individualizada, considerando el estado general del paciente, las etiologías responsables, el im pacto sobre la respiración y la deglución, el pronóstico y la capacidad técnica del equipo tratante, entre otras. Las alternativas pueden incluir observación, medidas no farmacológicas, medicamentos locales o sistémicos, procedimientos endoscópicos, cirugías abiertas, o bien la instalación de una traqueostomía de manera temporal o como manejo definitivo. El objetivo de esta revisión es entregar un adecuado conocimiento de la fisiopatología y la etiopatogenia del estridor pediátrico persistente, fundamental para el correcto manejo de estos pacientes complejos, que debiera realizarse idealmente en un contexto multidisciplinario.

Stridor is an abnormal respiratory sound caused by obstruction or collapse of the laryngotracheal airway, either acutely or chronically. There are different causes, both congenital and acquired, that can produce shortness of breath which may be severe and potentially life-threatening. The clini cal diagnosis must be complemented with an endoscopic airway assessment and sometimes with imaging, to try to determine the areas involved and possible associated malformations. Treatment should be individualized, considering the patient's overall condition, stridor etiology, its impact on breathing and swallowing, prognosis, and technical capacity of the managing team, among others. Alternatives may include observation, non-pharmacological measures, local or systemic medications, endoscopic and open surgeries, or a temporary or long-term tracheostomy. A thorough understan ding of the pathophysiology and etiopathogenesis of persistent pediatric stridor is essential for the correct management of these complex patients, ideally in a multidisciplinary manner.

Pediatric airway reconstruction: results after implementation of an airway team in Brazil / Reconstrução de vias aéreas pediátricas: resultados após a implantação de uma equipe de vias aéreas no Brasil

Abstract Introduction Since development of pediatric intensive care units, children have increasingly and appropriately been treated for complex surgical conditions such as laryngotracheal stenosis. Building coordinated airway teams to achieve acceptable results is still a challenge. Objective To describe patient demographics and surgical outcomes during the first 8 years of a pediatric airway reconstruction team. Methods Retrospective chart review of children submitted to open airway reconstruction in a tertiary university healthcare facility during the first eight years of an airway team formation. Results In the past 8 years 43 children underwent 52 open airway reconstructions. The median age at surgery was 4.1 years of age. Over half of the children (55.8%) had at least one comorbidity and over 80% presented Grade III and Grade IV subglottic stenosis. Other airway anomalies occurred in 34.8% of the cases. Surgeries performed were: partial and extended cricotracheal resections in 50% and laryngotracheoplasty with anterior and/or posterior grafts in 50%. Postoperative dilatation was needed in 34.15% of the patients. Total decannulation rate in this population during the 8-year period was 86% with 72% being decannulated after the first procedure. Average follow-up was 13.6 months. Initial grade of stenosis was predictive of success for the first surgery (p = 0.0085), 7 children were submitted to salvage surgeries. Children with comorbidities had 2.5 greater odds (95% CI 1.2-4.9, p = 0.0067) of unsuccessful surgery. Age at first surgery and presence of other airway anomalies were not significantly associated with success. Conclusions The overall success rate was 86%. Failures were associated with higher grades of stenosis and presence of comorbidities, but not with patient age or concomitant airway anomalies.

Resumo Introdução: Com o desenvolvimento de unidades de terapia intensiva pediátrica, o tratamento de crianças para situações cirúrgicas complexas, como a estenose laringotraqueal, tem sido cada vez mais adequado. Montar equipes coordenadas de via aérea para alcançar resultados aceitáveis ainda é um desafio. Objetivo: Descrever os dados demográficos e os resultados cirúrgicos dos pacientes durante os primeiros oito anos de uma equipe de reconstrução de via aérea pediátrica. Método: Revisão retrospectiva de prontuários de crianças submetidas à reconstrução aberta de via aérea em uma unidade de saúde universitária de nível terciário durante os primeiros oito anos de desenvolvimento de uma equipe de vias aéreas. Resultados: Nos últimos 8 anos, 43 crianças foram submetidas a 52 reconstruções abertas de vias aéreas. A mediana de idade na cirurgia foi de 4,1 anos. Mais da metade das crianças (55,8%) apresentavam pelo menos uma comorbidade e mais de 80% apresentavam estenose subglótica Grau III e Grau IV. Outras anomalias das vias aéreas ocorreram em 34,8% dos casos. As cirurgias feitas foram: ressecções cricotraqueais parciais e estendidas em 50% e laringotraqueoplastia com enxertos anterior e/ou posterior em 50%. A dilatação pós-operatória foi necessária em 34,15% dos pacientes. A taxa de decanulação total nesta população durante o período de 8 anos foi de 86%, com 72% dos pacientes decanulados após o primeiro procedimento. O seguimento médio foi de 13,6 meses. O grau inicial de estenose foi preditivo de sucesso para a primeira cirurgia (p = 0,0085), 7 crianças foram submetidas a cirurgias de resgate. Crianças com comorbidades apresentaram uma probabilidade 2,5 vezes maior (IC95% 1,2-4,9, p = 0,0067) de cirurgias sem sucesso. A idade na primeira cirurgia e a presença de outras anomalias das vias aéreas não foram significantemente associadas ao sucesso. Conclusões: A taxa global de sucesso foi de 86%. As falhas foram associadas a graus maiores de estenose e a presença de comorbidades, mas não com a idade do paciente ou anomalias concomitantes das vias aéreas.

Traqueomalacia pediátrica / Pediatric tracheomalacia

RESUMEN La malacia de la vía aérea central puede afectar la tráquea y/o los bronquios, haciéndola susceptible al colapso de sus paredes durante el ciclo respiratorio. Puede clasificarse como primaria o secundaria y clínicamente se manifiesta por síntomas respiratorios recurrentes o persistentes (especialmente en espiración), infecciones recurrentes y en casos severos, episodios de hipoventilación con cianosis. El diagnóstico se establece mediante broncoscopía flexible o rígida. Los estudios de imágenes se consideran complementarios, siendo especialmente útiles en casos de duda diagnóstica, estudio de causas secundarias o para la planificación preoperatoria. Su tratamiento depende de distintos factores como la severidad de los síntomas, su etiología, ubicación y extensión. En casos leves, una observación activa y tratamiento médico en espera de la resolución espontánea en los primeros 2 años, suelen ser suficientes. En casos moderados, la ventilación a presión positiva podría ser de utilidad. En casos severos está indicado el tratamiento quirúrgico, mediante distintas técnicas que buscan dar soporte a la estructura traqueobronquial debilitada, incluyendo traqueostomía, suspensiones directas (traqueopexias) o indirectas (aortopexia), tutores externos o stents intraluminales. En este articulo se revisarán las principales causas y tratamientos disponibles para la traqueomalacia pediátrica. Ya que su diagnóstico y manejo son complejos, es fundamental el trabajo de equipos médicos multidisciplinarios familiarizados con esta patología.

ABSTRACT Central airway malacia can affect the trachea and/or the main bronchi, making their walls susceptible to collapse during the respiratory cycle. It can be classified as primary or secondary, and clinically presents with recurrent or persistent respiratory symptoms (especially on expiration), recurrent infections and in severe cases, episodes of hypoventilation with cyanosis. The diagnosis is established by flexible or rigid bronchoscopy; imaging studies are considered as complementary, especially in cases of unclear diagnosis, secondary causes or for preoperative planning. Treatment depends on different factors such as the severity of the symptoms, their etiology, location and extension. In mild cases, active observation and medical treatment waiting for spontaneous resolution may be enough, which usually occurs in the first 2 years of age. In moderate cases, positive pressure ventilation could be useful. In severe cases, surgical treatment is indicated. Different techniques aiming to provide support to the weakened tracheobronchial structures are available, including tracheostomy, direct (tracheopexies) or indirect suspensions (aortopexy), external splints and intraluminal stents. In this article we present the main etiologies and available treatments for pediatric tracheomalacia. Given that diagnosis and management of these patients is complex, the work of multidisciplinary teams familiar with this pathology is of paramount importance.

Complicaciones de traqueostomía en pacientes pediátricos: revisión de la literatura / Complications of tracheostomy in pediatric patients: literature review

RESUMEN Las indicaciones de traqueostomía en niños han cambiado considerablemente en los últimos años, así como el perfil epidemiológico de los pacientes y la morbimortalidad de este procedimiento. Las complicaciones de este procedimiento pueden ser clasificadas en intraoperatorias, inmediatas y tardías. La mortalidad global en pacientes pediátricos llevados a traqueostomía oscila entre el 13% y 19%. Sin embargo, menos del 5% es directamente atribuible a la cirugía. La presente revisión abarcará las complicaciones más frecuentes asociadas a traqueostomía pediátrica con recomendaciones en su prevención y manejo.

ABSTRACT Indications of tracheostomy in children have changed considerably in recent years, as well as the epidemiological profile of patients, and morbidity and mortality related to this procedure. Complications of pediatric tracheostomy can be classified into intraoperative, immediate and late. Overall mortality in pediatric patients with tracheostomy ranges from 13% to 19%. However, less than 5% is directly attributable to tracheostomy. This review will cover the most frequent complications associated with pediatric tracheostomy with recommendations for its prevention and management.

Prevention and treatment of laryngotracheal stenosis after tracheal intubation or tracheotomy in children / 国际儿科学杂志

In pediatric emergency,we often encounter laryngotracheal stenosis after tracheal intubation and tracheotomy. For acute cannulation injury,mitomycin C and other drugs can be tried. And for laryngotracheal stenosis with mature scar,surgery is the main treatment. Children with mild illness can be treated by endoscopic balloon dilatation and laser surgery,with less injury and faster recovery,but with a certain recurrence rate. Most of the children with severe stenosis need to be treated with open surgery such as laryngotracheal reconstruction, slideplasty,partial cricotracheal resection and so on. To prevent complications caused by tracheal intubation and tracheotomy,the appropriate size of tube should be selected,and intermittent discharging is required during intu-bation. If the tracheal intubation is needed for longer than 7 days,tracheotomy should be performed as soon as possible.