Causas de estridor congénito / Causes of congenital stridor

INTRODUCTION. Airway abnormalities are rare but potentially fatal. Stridor is a res-piratory noise with greater predominance in the inspiratory phase. OBJECTIVE. To evaluate the etiology of stridor, determine its comorbidities and mortality. MATERIALS AND METHODS. Retrospective cross-sectional study. Population of 110 and sample of 33 data from the Medical Records of neonatal or infant patients who presented stri-dor at the Carlos Andrade Marín Specialties Hospital of Quito-Ecuador, from january 2009 to december 2020. RESULTS. The 51,51% (17; 33) of cases were men. The age of the first consultation for stridor was within the first month in 18,00% (6; 33) and 40,00% (13; 33) at 3 months. The most frequent congenital laryngeal patholo-gy was: laryngomalacia 81,82% (27; 33), followed by subglottic stenosis 9,09% (3; 33), bilateral chordal paralysis 6,06% (2; 33) and tracheal stenosis 3,03% (1; 33). The 51,51% (17; 33) presented comorbidities of causes: neurological, pulmonary and genetic among the main ones. Mortality was 18,20% (6; 33) related to the severity of comorbidities, except one secondary to tracheal stenosis. CONCLUSION. Laryn-gomalacia and subglottic stenosis were the predominant pathologies with congenital stridor. The comorbidities that occurred were neurological, pulmonary, genetic and caused mortality within 90 days after diagnosis.

INTRODUCCIÓN. Las anomalías de la vía aérea son poco frecuentes, pero potencialmente mortales. El estridor es un ruido respiratorio con mayor predominio en la fase inspiratoria. OBJETIVO. Evaluar la etiología del estridor, determinar sus comorbilidades y la mortalidad. MATERIALES Y MÉTODOS. Estudio transversal retrospectivo. Población de 110 y muestra de 33 datos de Historias Clínicas de pacientes neonatos o lactantes que presentaron estridor en el Hospital de Especialidades Carlos Andrade Marín de Quito - Ecuador, de enero 2009 a diciembre 2020. RESULTADOS. El 51,51% (17; 33) de casos fueron hombres. La edad de la primera consulta por estridor fue dentro del primer mes en el 18,00% (6; 33) y del 40,00% (13; 33) a los 3 meses. La patología congénita laríngea más frecuente fue: laringomalacia 81,82% (27; 33), seguida de estenosis subglótica 9,09% (3; 33), parálisis cordal bila-teral 6,06% (2; 33) y estenosis traqueal 3,03% (1; 33). El 51,51% (17; 33) presentaron comorbilidades de causas: neurológica, pulmonar y genética entre las principales. La mortalidad fue 18,20% (6; 33) relacionada con la severidad de las comorbilidades, excepto una secundaria a estenosis traqueal. CONCLUSIÓN. La laringomalacia y la estenosis subglótica fueron las patologías que predominaron con estridor congénito. Las comorbilidades que se presentaron fueron neurológica, pulmonar, genética y causaron mortalidad dentro de los 90 días posteriores al diagnóstico.

Indicaciones y resultados de la supraglotoplastia en pacientes pediátricos en la Fundación Hospital de la Misericordia en Bogotá, Colombia, una ciudad a 2 600 metros sobre el nivel del mar, del año 2017-2018 / Indications and results of supraglottoplasty in pediatric patients at Fundación Hospital de la Misericordia in Bogotá, Colombia, a city at 2,600 meters above sea level, years 2017-2018

La causa más común de estridor en población pediátrica es la laringomalacia. En trabajos publicados a nivel del mar se ha descrito una incidencia del 70% en pacientes con estridor. Materiales y Métodos: Realizamos un estudio retrospectivo de corte transversal de la cohorte de pacientes operados de supraglotoplastía en un hospital pediátrico de cuarto nivel en una ciudad localizada a 2600 mts de altitud entre el año 2017 - 2018. Resultados: Fueron intervenidos 44 pacientes, el 55% de los pacientes eran mujeres, con una mediana de edad de 11 meses (RIQ 11 días ­ 6 años), el 4,5% fueron diagnosticados con laringomalacia Tipo I, Tipo II 43%, 2,2% Tipo III y mixtas 29,5% según la clasificación de Olmey. La indicación quirúrgica se debió a falla del medro en 8 pacientes, Síndrome sibilante con riesgo inminente de falla respirato Trabajos ria en 17, episodio breve resuelto inexplicado (BRUE) de alto riesgo en 3 y apnea del sueño de predominio obstructivo 20 pacientes. De los 20 pacientes con síndrome de apnea del sueño se obtuvo el resultado del polisomnograma en 18 pacientes donde el promedio de Índice de apnea hipopnea fue de 30,5 con una desaturación de oxígeno máxima (Nadir) del 70%. Con respecto a la intervención quirúrgica se realizó supraglotoplastia tipo I en 5 pacientes, tipo II en 30, y en 9 tipo III. el 95% de los pacientes presentaban alguna comorbilidad y el 25% de los pacientes tenían diagnóstico de anomalías craneofaciales. En 9 pacientes con síndrome de apnea hipopnea del sueño se obtuvo un polisomnograma postoperatorio con un promedio de Índice de apnea hipopnea de 15 con un nadhir del 82,8%. Conclusión: Al analizar los datos obtenidos encontramos que los pacientes operados en altura por esta condición presentan una menor incidencia de resolución completa del SAHs, pero presentan mejoría de los síntomas durante el sueño, y la saturación de oxigeno mínima, independientemente del índice de apnea hipopnea residual

The most common cause of stridor in pediatric population is laryngomalacia. In papers published at sea level it has been describe an incidence of 70% in patients with stridor. We conducted a cross-sectional study of the cohort of patients that had undergo supraglotoplasty surgery in a fourth level pediatric hospital in a city located at an altitude of 2600 meter between 2017 - 2018. 44 patients were intervened, 4.5% of whom were diagnosed with type I laryngomalacia, 43% type II, 2.2% type III, 29.5% has more tan one type this according to Oley´s classification. The surgical indication was due to growing failure in 8 patient, inminent risk to respiratory failure in 17, high risk BRUE in 3 and severe sleep apnea in 20. Type I supraglotoplasty was performed in 5 patients , type II in 30 and in 9 type III. In 14 patients it was performed and additional procedure as dilatation of subglottic stenosis, amigdalectomy and tongue base resection. 95% of the patients had a comorbidity and 25% had a diagnosis of craniofacial anomalies. Conclusión: When analyzing the data obtained we found that patients operated at height for laryngomalacia, have a lower incidence of complete resolution of OSA, but show improvement of symptoms during sleep and minimal oxygen saturation, regardless of the residual hypopnea apnea index. The authors recommend pediatric otolaryngologists to take this difference into account when adressing a patient with laryngomalacia and other comorbidities.

Kyste valléculaire de l'enfant : à propos de 3 cas

Le kyste valléculaire est une pathologie rare. Il est responsable de détresse respiratoire avec stridor et de décès chez le nouveau-né et le nourrisson. La nasofibroscopie est un outil performant pour le diagnostic.Nous rapportons 3 cas de kystes de la vallécule chez un nouveau-né et deux nourrissons. La détresse respiratoire et le stridor ont été les symptômes rencontrés.La nasofibroscopie a permis le diagnostic. Les deux nourrissons ont bénéficié d'une marsupialisation par voie trans-orale. Le troisième patient est décédé avantla prise en charge

A case of FLNA gene mutation with respiratory insufficiency and periventricular heterotopia

Filamin A is an actin-binding protein and, in humans, is encoded by FLNA gene in the long arm of X chromosome. Filamin A plays a role in the formation of cytoskeleton by crosslinking actin filaments in cytoplasm. FLNA mutations affect cytoskeletal regulatory processes and cellular migrating abnormalities that result in periventricular heterotopia. A 5-month-old girl was hospitalized because of breathing difficulty and was diagnosed as having periventricular heterotopia with laryngomalacia, cricopharyngeal incoordination, pulmonary hypertension, and chronic lung disease. A genetic test was performed to find the cause of periventricular heterotopia, and FLNA gene mutation (c.5998+1G>A) was confirmed for the first time in Korea. After discharge, she developed respiratory failure due to a viral infection at 8 months of her age. In spite of management with mechanical ventilation, she died of pneumothorax and pulmonary hemorrhage. Herein, we report a case of FLNA gene mutation who presented with periventricular nodular heterotopia with respiratory insufficiency.

Estridor persistente / Persistent stridor

Stridor is a musical, often high-pitched sound produced by a rapid, turbulent flow of air through a narrowed segment of the large airways. The cause of stridor can be located anywhere in the extrathoracic airway (nose, pharynx, larynx, and trachea) or the intrathoracic airway (tracheobronchial tree). Stridor may be acute (caused by inflammation/infection or foreign body inhalation) or chronic. It may be congenital or acquired. Various congenital and acquired disorders prevail in neonates, infants, children, and adolescents, and need to be distinguished. Medical history and age of the child, together with physical examination, often allow a presumptive diagnosis. Further tests may be necessary to establish a definite diagnosis, and flexible airway endoscopy is the diagnostic procedure of choice in most circumstances

Estridor es un sonido musical, de alta frecuencia, generado por el paso de un flujo de aire turbulento en zonas con calibre disminuido de la vía aérea de mayor tamaño.La causa del estridor puede estar localizado en cualquier lugar de la vía aérea extratorácica (nariz, faringe, laringe y tráquea) o la vía aérea intratorácica (árbol traqueobronquial). El estridor puede ser agudo (causado por inflamación/infección o aspiración de cuerpos extraños) o crónica. Puede ser congénita o adquirida. Varios trastornos congénitos y adquiridos prevalecen en neonatos, lactantes, niños y adolescentes, y tienen que ser distinguidos. La historia clínica, edad del niño y examen físico a menudo permiten un diagnóstico presuntivo. Puede requerirse mayor estudio para establecer un diagnóstico definitivo, y la endoscopia flexible de la vía aérea es el procedimiento diagnóstico de elección en la mayoría de las circunstancias

Laringomalacia en pacientes con síndrome de apnea obstructiva del sueño: Reporte de casos / Laryngomalacia in patients with obstructive sleep apnea syndrome: Case report

Introducción: El síndrome de apnea obstructiva del sueño, es una patología frecuente en nuestro medio y ha cobrado gran interés por su asociación a otras enfermedades. El colapso laríngeo es causa frecuente de no mejoría (persistencia de índice de apnea-hipopnea residual elevado) tras el manejo de otros niveles de la vía aérea. Objetivo: Realizar una descripción sociodemográfica y clínica de una serie de pacientes con laringomalacia y síndrome de apnea obstructiva del sueño. Diseño: Estudio de serie de casos. Métodos: Se realiza un reporte de casos de una serie de pacientes manejados en el Hospital Militar Central y Clínica Universitaria Hospital San Rafael de Bogotá, con síndrome de apnea obstructiva del sueño y laringomalacia a quienes se les realizó supraglotoplastia, entre los años 2015 - 2017. Resultados: Se incluyeron 11 pacientes con edad promedio de 6.8 años. El diagnóstico se realizó mediante somnoendoscopia. El tipo más frecuente de laringomalacia fue tipo III en 7 pacientes (63.6%), seguido de laringomalacia tipo II en 4 casos (36.3%). 6 de los pacientes (54.5%) presentaban un trastorno genético y/o neurológico asociado. La mayoría de los pacientes mejoraron su sintomatología durante el sueño, aunque 2 no presentaron un resultado favorable tras el procedimiento quirúrgico. Conclusiones: Los resultados de este estudio sugieren una relación entre laringomalacia y SAHOS en la edad pediátrica.

Introduction: Obstructive sleep apnea syndrome is a frequent disease in our region and due to its association with other diseases its importance is high. Larynx´s collapse is a frequent cause of non-improvement (persistence of residual apnea-hypopnea index) after treatment of other obstructive areas inside the airway. Objective: To perform a sociodemographic and clinical description of a series of patients with laryngomalacia and obstructive sleep apnea syndrome. Design: Case series. Materials and methods: We present a report of patients managed at the Hospital Militar Central and University Hospital "Clínica San Rafael" of Bogotá, with obstructive sleep apnea and laryngomalacia syndrome who underwent supraglotoplasty between the years 2015 - 2017. Results: Eleven patients with an average age of 6.8 years were included. The diagnosis was made by somnoendoscopy. The most frequent type of laryngomalacia was type III in 7 patients (63.6%), followed by type II in 4 cases (36.3%). 6 of the patients (54.5%) presented an associated genetic and/or neurological disorder. Most of the patients improved their symptoms during sleep, although some did not show a favorable result after the surgical procedure. Conclusions: The study results suggest a relationship between laryngomalacia and OSAS in children.

Classification and Management in Patients with Laryngomalacia

Laryngomalacia is the most common congenital anomaly that causes inspiratory stridor and airway obstruction in the newborn. Symptoms begin to appear after weeks of age, become worse at 4-8 months, improve between 8-12 months, and usually heal naturally at 12-18 months. Despite these common natural processes, the symptoms of the disease can be very diverse and, in severe cases, require surgical treatment. The diagnosis can be made by suspicion of clinical symptoms and direct observation of the larynx with the spontaneous breathing of the child. Typical laryngeal features include omega-shaped epiglottis, retroflexed epiglottis, short aryepiglottic fold, poor visualization of the vocal folds, and edema of the posterior glottis, including inspiratory supra-arytenoid tissue prolapse. In this review, we discuss the classification and treatment based on symptoms and laryngoscopic findings in patients with laryngomalacia.

Supraglotoplastía láser en laringomalacia severa / Laser supraglottoplasty for severe laryngomalacia

Introducción: La laringomalacia es la causa más frecuente de estridor en lactantes, representando el 60%-70% de los defectos congénitos laríngeos. Entre 10%-20% de estos pacientes puede requerir tratamiento quirúrgico. Objetivo: Revisar las manifestaciones clínicas y los resultados de las supragloto-plastías en laringomalacia severa en nuestro hospital durante 2015. Material y método: Estudio descriptivo retrospectivo mediante revisión de fichas clínicas de pacientes sometidos a supraglotoplastía en el Hospital Guillermo Grant Benavente de Concepción en 2015. Resultados: Se intervinieron 11 pacientes siendo el promedio de edad, al momento de la cirugía, de 7,3 meses. Todos los pacientes tenían dificultad para alimentarse y el 45% además cianosis con la alimentación y el llanto, desaturaciones y pausas respiratorias. Cuatro casos portaban anomalías congénitas asociadas y el 73% presentó lesiones concomitantes de vía aérea, principalmente estenosis subglótica (64%). Los tipos morfológicos observados de laringomalacia fueron los tipos I y II con 27% y 73%, respectivamente. La tasa de éxito quirúrgico fue de 91%, sin necesidad de revisiones y no se presentaron complicaciones relacionadas al procedimiento. Conclusiones: La supraglotoplastía con láser es una técnica segura y efectiva para el tratamiento de laringomalacia severa. Los pacientes con laringomalacia severa debiesen ser sometidos a una revisión completa de vía aérea para evaluar otras comorbilidades.

Introduction: Laryngomalacia is the most common cause of stridor in infants, accounting for 60%-70% of laryngeal congenital defects. Between 10% to 20% of these patients may require surgical treatment. Aim: To review the clinical manifestations and outcomes of supraglottoplasties in severe laryngomalacia at our hospital during 2015. Material and method: Retrospective medical record review of children that underwent CO2 laser supraglottoplasty at Hospital Guillermo Grant Benavente in Concepcion during 2015. Results: Eleven patients were included in this study, the average age at the time of surgery was 7.3 months. All the patients had stridor associated with feeding difficulty and 45% of them also had cyanosis with feeding and crying, desaturations and respiratory pauses. Four cases had associated congenital anomalies and 73% of the patients had airway comorbidity, mostly subglottic stenosis (64%). All of ourpatients had types I and II laryngomalacia with 27% and 73%, respectively. The success rate of surgery was 91%, no patients required a revision supraglottoplasty and there were no complications related to the procedure. Conclusions: CO2 laser supraglottoplasty proved to be a safe and effective treatment for severe laryngomalacia. Patients with severe laryngomalacia should undergo a full airway revision under general anesthesia to assess airway comorbidity.

An Evaluation Protocol of the Upper Airway for Pediatric Patients with Stridor or Extubation Failure / 대한이비인후과학회지

BACKGROUND AND OBJECTIVES: Adequate evaluation of the upper airway is critical in the management of pediatric patients with stridor or extubation failure. For this purpose, we designed an evaluation protocol of the upper airway for these patients, in collaboration with Dept. of Pediatrics, Intensive care team and Anesthesiology. Here we present the clinical results of our evaluation protocol and provide information about the etiology and management of the upper airway problems. SUBJECTS AND METHOD: Clinical data of 380 pediatric patients (M:F=231:149) having airway evaluation for their problems (stridor or extubation failure) were retrospectively analyzed. Among them, patients of age less than 3 months ranked first (30.0%). Comorbidities of pulmonary diseases (30.8%) and cardiovascular diseases (29.5%) were found. The pre and post-evaluation diagnosis, management and prognosis were evaluated and the usefulness of an airway evaluation protocol was discussed. RESULTS: Frequent pre-evaluation diagnoses were subglottic stenosis (55.2%), laryngomalacia (12.6%) and tracheal stenosis (9.2%) and these were changed to subglottic stenosis (44.5%), laryngomalacia (9.7%), tracheal stenosis (6.6%) and no abnormality (14.5%). Particularly, 50% of pre-diagnosis laryngomalacia, 25% of subglottic stenosis and 37% of tracheal stenosis were corrected to other causes by airway evaluation. The procedures were exam only (41.6%), endoscopic dilatation (20.8%) and tracheostomy (17.9%). In 190 out of 380 (50.0%), extubation was successful, but 151 patients (39.7%) had tracheostomy tube. CONCLUSION: Adequate evaluation of the upper airway in pediatric patients with stridor or extubation failure can facilitate the diagnosis and management of their problems.

A Case of Aryepiglottoplasty under Conventional Ventilation in Congenital Laryngomalacia Patient / 대한이비인후과학회지

Laryngomalacia is reported as the most common cause of congenital laryngeal stridor. Despite its benign and self-limited aspects, 10% of all cases require intervention. However, endolaryngeal surgery in neonates makes great demands on the anesthesiologist and the surgeon because of the narrowness of the airways. This case report will present a surgical management of severe laryngomalacia in a newborn using the combination carbon dioxide laser and cold instrument to surgically divide the aryepiglottic fold under conventional ventilation.

Oropharyngeal 24-Hour pH Monitoring in Children With Airway-Related Problems

OBJECTIVES: Diagnosis and clinical presentation of pediatric laryngopharyngeal reflux (LPR) is still controversial. The aims of this work were to study the possibility of performing 24-hour oropharyngeal pH monitoring for children in the outpatient clinic setup and to explore the results of this test in correlation to airway-related problems. METHODS: In this descriptive qualitative study, 26 children suffering from airway-related problems were included. Oropharyngeal 24-hour pH monitoring was performed for all subjects in the outpatient clinic setting. The distribution of airway diagnoses among the study group was studied versus the results of the pH monitoring. RESULTS: There were 16 males and 10 females participated in the study with a mean age of 6.88 (SD, ±5.77) years. Thirty-five percent of the patients were under the age of 3 years (range, 11 months to 3 years). Eight-five percent of the patients tolerated the pH probe insertion and completed 24-hour of pH recording. Laryngomalacia and subglottic stenosis (SGS) were more frequently reported in the positive LPR patients (77%). CONCLUSION: Oropharyngeal 24-hour pH monitoring can be conducted for children in the outpatient setup even in young age children below 3 years old. Among the positive LPR group, SGS and laryngomalacia were the most commonly reported airway findings.

Estridores laríngeos supraglóticos / Supraglottic laryngeal stridors / Estridores laríngeos supraglóticos

Toda obstrucción de la vía aérea se expresa por un estridor que será diferente según la localización de la obstrucción. El estridor es un ruido ocasionado por el pasaje de aire en forma turbulenta a través de una vía aérea con calibre disminuido. Cuando la obstrucción se ubica por encima de las cuerdas vocales el estridor será inspiratorio. Describimos diferentes patologías de la laringe supraglótica, congénitas y adquiridas, que presentan estridor en algún momento de su evolución.

An obstructed airway causes stridor. Stridor willbe different depending on the location of the obstruction. Stridor is a noise caused by the passage ofturbulent air through a diminished airway caliber. If the obstruction occurs above the vocal cords, itwill be inspiratory. We describe different pathologies of the supraglotticlarynx, both congenital and acquired, producingstridor at some moment of their evolution.

Uma via aérea obstruída provoca estridor. Estridor será diferente dependendo da localização da obstrução. Estridor é um ruído causado pela passagemdo ar turbulento através de uma diminuição do calibre das vias aéreas. Nós descrevemos diferentes patologias da laringe supraglótica, tanto congênitas e adquiridas, que apresentam stridor em algum momento de sua evolução.

Congenital laryngeal anomalies / Anomalias congênitas da laringe

Introduction: It is essential for clinicians to understand issues relevant to the airway management of infants and to be cognizant of the fact that infants with congenital laryngeal anomalies are at particular risk for an unstable airway. Objectives: To familiarize clinicians with issues relevant to the airway management of infants and to present a succinct description of the diagnosis and management of an array of congenital laryngeal anomalies. Methods: Revision article, in which the main aspects concerning airway management of infants will be analyzed. Conclusions: It is critical for clinicians to understand issues relevant to the airway management of infants. .

Introdução: As anomalias congênitas da laringe estão em risco de uma via aérea instável, sendo essencial que o clínico tenha uma boa compreensão dos problemas relevantes para o manuseio das vias aéreas de bebês. Objetivos: Familiarizar os clínicos com os problemas relevantes para o manuseio das vias aéreas de bebês e apresentar uma descrição sucinta do diagnóstico e tratamento de uma série de anomalias congênitas da laringe. Método: Artigo de revisão, no qual serão tratados os principais aspectos relacionados ao manuseio das vias aéreas de bebês. Conclusões: É essencial que o clínico tenha um bom conhecimento dos problemas relevantes ao manuseio das vias aéreas de bebês. .

Tratamento cirurgico da laringomalacia grave: estudo retrospectivo de 11 casos / Surgical treatment of severe laryngomalacia: a retrospective study of 11 case

A laringomalácia é a anomalia congênita da laringe mais frequente, sendo responsável por cerca de 60% a 75% dos casos de estridor congênito. Apesar de seu curso benigno e autolimitado, 10% dos casos necessitam de intervenção. Atualmente, as supraglotoplastias são consideradas o tratamento padrão da laringomalácia grave. OBJETIVO: Descrever a experiência adquirida pelos autores no tratamento cirúrgico dos pacientes com laringomalácia grave. Metodologia: Estudo retrospectivo. MÉTODO: Os prontuários de 11 casos consecutivos de laringomalácia grave, submetidos ao tratamento cirúrgico entre 2003 e 2012, foram analisados quanto à idade, gênero, sintomas, doenças associadas, técnica cirúrgica adotada, tempo de extubação, complicações cirúrgicas, tempo de internação e evolução clínica. RESULTADOS: Dos 11 casos de laringomalácia grave, seis pacientes (54,5%) foram operados com o uso do laser de CO2 e em cinco pacientes (45,5%) foram realizadas a técnica a frio. Apenas um paciente (9,1%) necessitou reabordagem cirúrgica. Não foram observados casos de complicações cirúrgicas. Todos os pacientes apresentaram melhora clínica importante. CONCLUSÃO: A supraglotoplastia mostrou-se um procedimento eficaz e seguro no tratamento da laringomalácia grave. .

Laryngomalacia is the most frequent congenital abnormality of the larynx, accounting for approximately 60-75% of congenital stridor cases. Despite its benign and self-limited aspects, 10% of cases require intervention. Currently, supraglottoplasty is considered the standard treatment of severe laryngomalacia. OBJECTIVE: To describe the experience of the authors in the surgical treatment of patients with severe laryngomalacia. Methodology: A retrospective study. METHOD: The medical records of 11 consecutive cases of severe laryngomalacia who underwent surgical treatment between 2003 and 2012 were analyzed for age, gender, symptoms, associated diseases, surgical technique employed, extubation time, surgical complications, length of hospital stay and clinical outcome. RESULTS: Of the 11 cases of severe laryngomalacia, six patients (54.5%) were operated with the use of CO2 laser and five patients (45.5%) were submitted to the cold technique. Only 1 patient (9.1%) required surgical reintervention. There were no cases of surgical complications. All patients had clinical improvement. CONCLUSION: Supraglottoplasty proved to be effective and safe in the treatment of severe laryngomalacia. .

Supraglotoplastía asistida con microdebridador en pacientes con síndrome de Pierre Robin y laringomalacia severa / Assisted endoscopic microdebrider supraglottoplasty in patients with Pierre Robin syndrome and severe laryngomalacia

Se presenta el caso de una paciente recién nacida de término portadora de un síndrome de Pierre Robin asociada a laringomalacia severa que requirió resolución quirúrgica para estabilización de su vía aérea superior Se presenta la experiencia clínica en el uso de microdebridador para realización de supraglotoplastía como una novedosa alternativa en el tratamiento quirúrgico de este tipo de pacientes y se realiza revisión de la literatura respecto de esta técnica.

Pierre Robin syndrome is a triad formed by micrognathia, and cleft palate glossoptosis. His association with laryngomalacia is not set however determining the coexistence of these two diseases and their severity is of utmost importance as they condition the prognosis of a patient with Pierre Robin syndrome. Currently one of the surgical techniques used in patients with severe laryngomalacia, is assisted endoscopic microdebrider supraglottoplasty. In the ENT unit of the Hospital Luis Calvo Mackenna, this procedure is being implemented in order to give our patients a safe and effective treatment option for their pathology.

CO2 laser supraglottoplasty for infantile laryngomalacia / 中华耳鼻咽喉头颈外科杂志

<p><b>OBJECTIVE</b>To evaluate the feasibility and safety of CO2 laser supraglottoplasty for severe laryngomalacia in infants.</p><p><b>METHODS</b>From January 2009 to December 2011, 32 infants with severe laryngomalacia were confirmed by electronic laryngoscope and clinical assessment in Shenzhen Children's Hospital. According to the choice made by the parents, 16 children accepted CO2 laser supraglottoplasty (group 1), the others were treated conservatively (group 2). The beginning observation point T0 was defined as the age on the first medicine taking day or the age of surgery. T1, T3, T6 were defined as 1, 3, 6 months following T0. Clinical symptoms included stridor, dyspnea, aspiration, and respiratory infections. The body weight, PSG reports, laryngoscope findings, cure rates of the two groups were compared.</p><p><b>RESULTS</b>The anatomical abnormalities were corrected surgically, and the symptoms ,such as stridor, dyspnea, and aspiration improved rapidly after the operation. The cure rates was higher in group 1 than in group 2 on T1, T3, T6 stage. There were statistically significant differences(χ(2) were 13.9, 28.1, 24.6 respectively; all P < 0.01). Children in group 1 gained weight better than in group 2. There was a statistically significant difference in Z scores median on T1, T3, T6 stage (z score were -0.848, -2.940, -4.110; P < 0.05, or P < 0.01 respectively). The lowest oxygen saturation in group 1 improved one month after the surgery (from average 0.686 ± 0.106 to 0.901 ± 0.041). There was a statistically significant difference (t = -7.876, P = 0.001). Complications included adhesion (1 case) and temporary new-onset aspiration (1 case).</p><p><b>CONCLUSIONS</b>The CO2 laser supraglottoplasty can resolve severe laryngomalacia symptoms including stridor, dyspnea and aspiration. It can reduce the frequency of respiratory infections, and contribute to weight gaining. The CO2 laser supraglottoplasty is effective, of high security and with rare complications.</p>

Surgical management for severe congenital laryngomalacia: 16 consecutive cases / 临床耳鼻咽喉头颈外科杂志

OBJECTIVE@#Laryngomalacia is the most common cause for stridor in neonate and infant. Our study aims at assessing the outcome of surgical management in patients diagnosed by fibrolaryngoscope as congenital Laryngomalacia.@*METHOD@#Retrospective study of 16 patients undergoing surgery for severe laryngomalacia. The patients' symptoms, associated medical conditions and surgical management were recorded.@*RESULT@#Stridor and feeding difficulty were observed in 16 patients on admission, while dyspnea was found in 11 patients. Medical co-morbidities exist in 14 cases. The mean age of surgery was 23 weeks, 15 patients had follow-up records for 24 months. Fourteen cases underwent supraglortoplasty. Tracheotomy was performed on the other 2 cases complicated with tracheomalacia. Nine cases showed full recovery of stridor 48 hours post-supraglottoplasty, and 7 were free of feeding difficulties. In the 6 months follow-up, complete or partial relief was achieved in all main symptoms and signs.@*CONCLUSION@#Supraglottoplasty is effective in relieving stridor and feeding difficulty as well as respiratory insufficiency, which makes it a first line option for managing severe laryngomalacia.

Tratamento cirúrgico de laringomalácia: casuística de hospital pediátrico terciário / Laryngomalacia surgery: a series from a tertiary pediatric hospital

Laringomalácia é o colapso supraglótico durante a inspiração; é responsável por até 75% dos casos de estridor em crianças de até 30 meses. O achado característico é estridor inspiratório; até 20% dos pacientes apresentam quadros graves, sendo necessária intervenção cirúrgica. A supraglotoplastia é o procedimento de escolha e se considera a presença de comorbidades como o maior fator prognóstico para o sucesso da cirurgia. OBJETIVOS: Descrever a casuística de hospital pediátrico terciário, índices de sucesso e analisando fatores prognósticos cirúrgicos. MÉTODO: Estudo de coorte retrospectivo. Incluídos 20 pacientes submetidos à supraglotoplastia no período de julho de 2007 a maio de 2011. RESULTADOS: Dos 20 pacientes, 13 (65%) eram do sexo masculino; a média de idade no procedimento foi de 6,32 meses. Na endoscopia, 12 apresentavam associações de tipos de laringomalácia, 40% apresentavam faringomalácia associada e três apresentavam também traqueomalácia. Treze crianças apresentavam laringomalácia isolada e sete pacientes apresentavam doença do refluxo gastroesofágico. Quinze (75%) pacientes foram submetidos à ressecção de pregas ariepiglóticas. Após o procedimento, 11 pacientes ficaram assintomáticos e dois necessitaram traqueostomia. A presença de comorbidades foi a variável preditora de desfecho desfavorável pós-operatório (p = 0,034). CONCLUSÃO: A supraglotoplastia é um procedimento seguro para tratamento de laringomalácia em casos selecionados.

Laryngomalacia is the condition responsible for 75% of the cases of stridor in children aged up to 30 months, in which there is supraglottic collapse during inhalation. Inspiratory stridor is a characteristic telltale. As many as 20% of the patients are severely affected and require surgery. Supraglottoplasty is the procedure of choice and the presence of comorbidities is the most relevant prognostic factor for surgery success. OBJECTIVE: To describe a series in a tertiary pediatric hospital, its success rates, and surgery prognostic factors. METHOD: This retrospective cohort study enrolled 20 patients submitted to supraglottoplasty between July 2007 and May 2011. RESULTS: Thirteen (65%) patients were males; mean age at the time of the procedure was 6.32 months. Endoscopic examination showed that 12 subjects had combined forms of laryngomalacia, 40% had associated pharyngomalacia, and three also had tracheomalacia. Thirteen subjects had isolated laryngomalacia and seven had gastroesophageal reflux disease. Fifteen (75%) patients underwent aryepiglottic fold resection. After the procedure, eleven patients were asymptomatic and two required tracheostomy. Presence of comorbidities was the strongest predictor of unfavorable postoperative outcome (p = 0.034). CONCLUSION: Supraglottoplasty is a safe therapeutical procedure for select patients with laryngomalacia.