Unilateral lingual nerve and hypoglossal nerve injury caused by a novel laryngeal mask airway: a case report

Abstract Cranial nerve injury by a laryngeal mask airway is rare but a serious complication. The nerve injuries must be prevented during the intubation using a laryngeal mask airway. We report a female patient who complained of tongue numbness, slurred speech, and slight difficulty in swallowing solid food after a hand surgery. She was then diagnosed with unilateral lingual nerve and hypoglossal nerve injuries. Extreme head rotation, relatively small oral cavity, and wide rigid composition at the lower part of the novel laryngeal mask probably resulted in cranial nerve injury.

Clinical evaluation of the use of laryngeal tube versus laryngeal mask airway for out-of-hospital cardiac arrest by paramedics in Singapore

INTRODUCTION@#It remains unclear which advanced airway device has better placement success and fewer adverse events in out-of-hospital cardiac arrests (OHCAs). This study aimed to evaluate the efficacy of the VBM laryngeal tube (LT) against the laryngeal mask airway (LMA) in OHCAs managed by emergency ambulances in Singapore.@*METHODS@#This was a real-world, prospective, cluster-randomised crossover study. All OHCA patients above 13 years of age who were suitable for resuscitation were randomised to receive either LT or LMA. The primary outcome was placement success. Per-protocol analysis was performed, and the association between outcomes and airway device group was compared using multivariate binomial logistic regression analysis.@*RESULTS@#Of 965 patients with OHCAs from March 2016 to January 2018, 905 met the inclusion criteria, of whom 502 (55.5%) were randomised to receive LT while 403 (44.5%) were randomised to receive LMA. Only 174 patients in the LT group actually received the device owing to noncompliance. Placement success rate for LT was lower than for LMA (adjusted odds ratio [OR] 0.52, 95% confidence interval [CI] 0.31-0.90). Complications were more likely when using LT (OR 2.82,0 95% CI 1.64-4.86). Adjusted OR for prehospital return of spontaneous circulation (ROSC) was similar in both groups. A modified intention-to-treat analysis showed similar outcomes to the per-protocol analysis between the groups.@*CONCLUSION@#LT was associated with poorer placement success and higher complication rates than LMA. The likelihood of prehospital ROSC was similar between the two groups. Familiarity bias and a low compliance rate to LT were the main limitations of this study.

Time comparison of artificial airway establishment in operating room and on slope using endotracheal intubation and laryngeal mask / 北京大学学报(医学版)

OBJECTIVE@#To compare the completion time of endotracheal intubation and laryngeal mask implantation in operating room and on slope of ski resort, and to discuss the optimal method of estab-lishing artificial airway on slope of ski resort.@*METHODS@#The simulator was placed with the head under the feet on slope of ski resort. The artificial airway was established by tracheal intubation assisted by video laryngoscope (endotracheal intubation group) and laryngeal mask placement (laryngeal mask group) respectively by an anesthesiologist who wore full set of ski suits, helmets, goggles, gloves and ski boots. Each method was repeated 5 times, and the operation time of artificial airway establishment was recorded. While the simulated human was placed flat on the operating table in an operating room of a hospital, and the artificial airway was established by the same anesthesiologist using the same methods. Time was recorded and repeated for 5 times. The completion time of endotracheal intubation and laryngeal mask placement in the operating room and on the ski slope were compared.@*RESULTS@#The operating time of tracheal intubation in the operating room was longer than that of laryngeal mask placement [(79.8±10.4) s vs. (53.4±2.7) s, P=0.005], and the operating time of endotracheal intubation on the ski slope was longer than that of laryngeal mask placement [(209.2±32.7) s vs. (72.2±3.1) s, P=0.001]. The time of endotracheal intubation group on the slope of the ski resort was longer than that in the opera-ting room(t=-7.851, P=0.001). The time of laryngeal mask group on the slope was longer than that in the operating room (t=-19.391, P < 0.001).@*CONCLUSION@#On ski slope, both of tracheal intubation assisted by video laryngoscope and laryngeal mask placement can quickly complete the establishment of artificial airway, but the time required is longer than that in the operating room. The time of laryngeal mask placement to establish artificial airway is shorter than that of tracheal intubation assisted video laryngoscope, which may have a certain advantage in ski rescue.

Actualización en el abordaje de la vía respiratoria del paciente obeso / Update on the approach to the obese patient respiratory tract

RESUMEN El manejo de la vía respiratoria es uno de los aspectos más importantes en Anestesia. Entre el 50 y 70 % de los paros cardiacos durante la anestesia general obedecen a dificultades en la intubación. Los pacientes obesos tienen un 30 % más de probabilidades de presentar intubación difícil con respecto a pacientes normopesos. También desarrollan desaturación de oxígeno más rápido, lo que aumenta el riesgo de complicaciones. Teniendo en cuenta lo anterior, se decidió realizar este trabajo, con el objetivo de actualizar sobre el uso de los métodos para el abordaje de la vía respiratoria en dichos pacientes. Se mostraron los criterios y resultados de investigaciones de autores sobre el tema. Se concluye que, a pesar de que el método más utilizado para abordar la vía aérea en obesos es la intubación orotraqueal con visión directa, se debe considerar el uso de máscara laríngea de intubación, fibroscopio flexible y videolaringoscopios, sobre todo en personas superobesas (AU).

ABSTRACT The respiratory tract management is one of the most important topics in anesthesia. Between 50 and 70 % of the heart arrests occurring during general anesthesia are due to intubation difficulties. Obese patients are 30 % more likely of presenting difficult intubation with respect to normal weight patients. They also develop oxygen desaturation faster, increasing the complication risk. Taking into consideration the above reasons, the authors decided to write this article, with the aim of updating on the methods to approach the respiratory tract in those patients. The authors' criteria and research outcomes on the theme are showed. It was concluded that even though the most used method to approach the airway in obese patients is the orotracheal intubation with direct vision, the use of a laryngeal intubation mask, flexible fiberscope and video laryngoscopes should be considered, especially in superobese patients (AU).

Craneotomía en el paciente despierto / Awake craniotomy

Introducción: La craneotomía con el paciente despierto es útil para lograr resecciones cerebrales amplias de lesiones de áreas elocuentes. Objetivo: Presentar un caso al que se le realizó la técnica dormido- despierto. Método: Se realizó la inducción de la anestesia con propofol/fentanilo/rocuronio y se colocó una mascarilla laríngea. Después del bloqueo de escalpe se mantuvo la infusión de propofol/fentanilo y lidocaína hasta que se realizó la craneotomía. Se disminuyó la velocidad de infusión y se mantuvo de esta manera hasta finalizada la intervención. Resultados: Se logró el despertar del paciente a los 13 minutos de reducida la infusión. Se mantuvo buena estabilidad hemodinámica, sin depresión respiratoria ni otras complicaciones. El paciente se mantuvo colaborador, respondió preguntas y movilizó sus extremidades. No presentó complicaciones posoperatorias. Discusión: Dentro de las técnicas anestésicas utilizadas en el mundo la dormido- despierto-dormido es la más popular; sin embargo, constituye una alternativa no dormir nuevamente al paciente ni reinstrumentar la vía respiratoria. Los medicamentos más empleados son el propofol/remifentanilo, aunque la comparación con otros opioides no arrojan diferencias significativas; aunque sí supone un beneficio adicional la dexmedetomidina. Conclusiones: La craneotomía con el paciente despierto es posible de realizar en el entorno hospitalario siempre que exista un equipo multidisciplinario que consensue las mejores acciones médicas para el paciente(AU)

Introduction: Awake craniotomy is useful to achieve wide brain resections of lesions in eloquent areas. Objective: To present the case of a patient who was operated on with the asleep-awake-asleep technique. Method: Anesthesia was induced with propofol-fentanyl-rocuronium and a laryngeal mask was placed. After scalp block, the propofol-fentanyl and lidocaine infusion was maintained until craniotomy was performed. The infusion rate was decreased and remained this way until the end of the intervention. Results: The patient was awakened thirteen minutes after the infusion was reduced. Good hemodynamic stability was maintained, without respiratory depression or other complications. The patient remained collaborative, answered questions, and mobilized his limbs. He had no postoperative complications. Discussion: Among the anesthetic techniques used in the world, asleep-awake-asleep is the most popular. However, it is an alternative not to put the patient back to sleep or re-instrument the airway. The most commonly used drugs are propofol-remifentanil, although the comparison with other opioids does not show significant differences, except for dexmedetomidine, which does represent an additional benefit. Conclusions: Awake craniotomy is possible to be performed in the hospital setting as long as there is a multidisciplinary team that agrees on the best medical actions for the patient(AU)

Dispositivos supraglóticos con acceso gástrico en colecistectomía laparoscópica / Supraglottic Devices with Gastric Access in Laparoscopic Cholecystectomy

Introducción: El abordaje de la vía aérea del paciente bajo cirugía laparoscópica representa múltiples retos para el anestesiólogo. Objetivo: Evaluar la efectividad y seguridad de tres dispositivos supraglóticos con acceso gástrico en el abordaje de la vía aérea de pacientes bajo colecistectomía laparoscópica. Métodos: Se realizó un estudio cuasiexperimental, prospectivo, longitudinal en el Hospital Universitario "General Calixto García", entre el 2017 y 2019. Se constituyeron tres grupos de 40 pacientes, según dispositivo: máscara laríngea proseal, máscara laríngea supreme y máscara I-gel. Se estudió: tiempo de inserción, número de intentos para colocación, facilidad de inserción de la sonda nasogástrica, presión y suficiencia de sellado orofaríngeo, presión pico con neumoperitoneo y complicaciones. Las variables cualitativas se analizaron con frecuencias absolutas y relativas, y las cuantitativas con medias y desviación estándar. Para la asociación entre variables cualitativas, se utilizó la prueba de chi-cuadrado, y el análisis de varianza para la asociación entre cuantitativas y cualitativas. Se consideró significativo valor de p < 0,05. Resultados: La máscara laríngea supreme se insertó con éxito al primer intento en la mayoría de los pacientes (p = 0,004). La I-gel registró el menor tiempo de inserción (10,05 ± 1,75 seg) y la Supreme mayor facilidad para la sonda nasogástrica (p < 0,001). La mayor presión de sellado fue con la máscara laríngea proseal (30,87 ± 2,60 cmH2O). Las complicaciones fueron pocas y similares con cada uno. Conclusiones: La utilización de dispositivos supraglóticos con acceso gástrico demostró seguridad y efectividad en pacientes intervenidos por colecistectomía laparoscópica(AU)

Introduction: Airway management in the patient undergoing laparoscopic surgery presents multiple challenges for the anesthesiologist. Objective: To assess the effectiveness and safety of three supraglottic devices with gastric access in the airway management in patients undergoing laparoscopic cholecystectomy. Methods: A quasiexperimental, prospective and longitudinal study was carried out, between 2017 and 2019, at General Calixto García University Hospital. Three groups of forty patients were made up, according to the usage of each device: ProSeal laryngeal mask, Supreme laryngeal mask, and I-gel mask. The following variables were studied: insertion time, number of placement attempts, ease of insertion of nasogastric tube, pressure and sufficiency of oropharyngeal sealing, peak pressure with pneumoperitoneum, and complications. Qualitative variables were analyzed with absolute and relative frequencies; and quantitative variables, with means and standard deviation. For the association between qualitative variables, the chi-square test was used, while variance analysis was used for the association between quantitative and qualitative variables. A value of P< 0.05 was considered significant. Results: The Supreme laryngeal mask was successfully inserted on the first attempt in most patients (P=0.004). The I-gel mask had the shortest insertion time (10.05±1.75 seconds), while the Supreme was the easiest for the nasogastric tube (P< 0.001). The highest sealing pressure was obtained with the ProSeal laryngeal mask (30.87±2.60 cmH2O). The complications were few and similar with each device. Conclusions: The use of supraglottic devices with gastric access showed safety and effectiveness in patients who underwent laparoscopic cholecystectomy(AU)

Comparación de máscaras laríngeas (I-gel Fastrach) para realización de intubación endotraqueal guiada con broncofibroscopio flexible / Comparison of I-gel Fastrach laryngeal masks in conducting flexible bronchofiberscope-guided

GOALS: Determine the success rate of guided intubation with a flexible bronchofibroscope (BFC) through supraglottic devices: I-gel or Fastrach, establish the degree of fibroscopic visualization and determine the insertion time of the laryngeal mask airway (LMA) and endotracheal intubation. METHODS: Experimental, prospective, comparative and randomized study of 60 ASA I-II-III patients, older than 18 years, undergoing elective surgeries that required general anesthesia and endotracheal intubation. After anesthetic induction, the assigned LMA was placed and intubation with BFC was performed through it. Both the success of laryngeal mask insertion and intubation were recorded, as well as the time (in seconds) equired for these procedures. The vision of the laryngeal structures was classified according to the Brimacombe Scale. RESULTS: The groups analyzed presented similar general characteristics. Insertion time of he LMA was significantly lower with I-gel than Fastrach (median 12 s vs 16 s. Respectively, p = 0.001). Also, in the intubation time BFC guided through the laryngeal mask, differences in favor of I-gel were found, with a median of 72 s. vs 89 s. (p = 0.001). Regarding the degree of glottic visualization with BFC, no statistically significant differences were found between both groups.CONCLUSIONS: Although both devices had the highest success rate (both in their placement and in intubation through them), with I-gel the intubation was performed quicker.

OBJETIVOS: Determinar la tasa de éxito de intubación guiada con broncofibroscopio flexible (BFC) a través de los dispositivos supraglóticos: I-gel o Fastrach, establecer el grado de visualización fibroscópica y determinar el tiempo de inserción de la máscara laríngea y de intubación endotraqueal. MATERIALES Y MÉTODOS: Estudio experimental, prospectivo, comparativo y aleatorizado de 60 pacientes ASA I- II ­III, mayores de 18 años, sometidos a cirugías electivas que requerían anestesia general e intubación endotraqueal. Luego de la inducción anestésica, se procedió a colocar la máscara laríngea asignada y se realizó la intubación con BFC a través de la misma. Tanto el éxito de inserción de máscara laríngea como de intubación fueron registrados, así como el tiempo (en segundos) requerido para dichos procedimientos. La visión de las estructuras laríngeas fue clasificada de acuerdo a Escala de Brimacombe. RESULTADOS: Los grupos analizados presentaron características generales similares. El tiempo de inserción de la ML fue significativamente menor con I-gel que con Fastrach (medianas: 12 s. vs 16 s. respectivamente, p = 0,001). También en el tiempo de intubación guiada con BFC a través de la máscara laríngea, se encontraron diferencias en favor de I-gel, con una mediana de 72 s. vs 89 s. (p = 0,001). Respecto al grado de visualización glótica con BFC, no se encontraron diferencias estadísticamente significativas entre ambos grupos. CONCLUSIONES: Aunque ambos dispositivos tuvieron la máxima tasa de éxito (tanto en su colocación como en la intubación a través de ellos), con I-gel se realizó la intubación de manera más rápida.

Reporte de caso: Manejo anestésico en un paciente pediátrico con ictiosis más deshidratación grave / Case report: Anesthetic management of an infant patient with ichthyosis plus severe dehydration

INTRODUCTION: Ichthyosis are hereditary disorders of keratinization which are characterized for the presence of hyperkeratosis and/or peeling. This disorder group can put in danger the life of the patient because of the severe alteration of the skin barrier, associated with a severe transdermic loss of water, different grades of hypothermia and a hypernatremic dehydration. OBJECTIVE: Introducing the clinic case of an infant patient with the diagnosis of ichthyosis plus severe dehydration who is scheduled for placement of CVC. CLINICAL CASE: Male infant, 3 months old, with the diagnosis of ichthyosis and severe dehydration, scheduled for placement of CVC. CONCLUSIONS: Due to the urgency of our patient, who presented severe dehydration, an inhaled general anesthesia with sevoflurane and oxygen was decided, without instrumenting the airway which in these patients has the risk of being potentially difficult, from the placement of the face mask itself, until finding lesions within the oral cavity, ventilatory assis- tance should be maintained by the pediatric anesthesiologist, once venous access is achieved, the fluids restitution is performed with loads of 10 to 20 ml/kg of the patient's weight, hyperthermia was controlled with physical means.

INTRODUCCIÓN: Las ictiosis son trastornos hereditarios de la queratinización caracterizadas por la presencia de hiperqueratosis y/o descamación. Este grupo de patologías pueden poner en peligro la vida del paciente debido a la severa alteración de la barrera cutánea, asociada a intensa pérdida transepidérmica de agua, diferentes grados de hipotermia y la deshidratación hipernatrémica. OBJETIVO: Presentar un caso clínico de paciente lactante menor con diagnóstico de ictiosis, cursando un cuadro grave por deshidratación, al que se le instala un CVC. CASO CLÍNICO: Lactante masculino, 3 meses de edad, con diagnóstico de ictiosis y deshidratación grave programado para colocación de CVC. CONCLUSIONES: Debido a la urgencia del paciente quien presentaba un caso de deshidratación severa se decide anestesia general inhalada con sevoflurano y oxígeno, sin instrumentación de la vía área, la cual en estos pacientes tiene el riesgo de ser potencialmente difícil, desde la propia colocación de la mascarilla facial hasta encontrar lesiones dentro de la cavidad oral; se debe mantener la asistencia ventilatoria por el anestesiólogo pediatra, una vez logrado el acceso venoso se procede a la restitución hídrica con cargas de 10 a 20 ml/kg de peso del paciente, el control de la hipertermia fue con medios físicos.

Complicaciones del uso de la Máscara Laríngea en Pacientes Pediátricos. Estudio Multicéntrico / Complications of the use laryngeal mask in Pediatric Patients. Multicenter Study

Introducción: La máscara laríngea es el equipamiento con el objetivo de aumentar la calidad, seguridad, cuidado, sin embargo, a pesar de tener uso universal y alta eficacia para la ventilación no está exenta de complicaciones. El objetivo de la presente Investigación fue identificar la frecuencia de complicaciones con el uso de mascara laríngea en los hospitales públicos Vicente Corral Moscoso y José Carrasco en la ciudad de Cuenca. Métodos: Es un estudio observacional, descriptivo, prospectivo, en 220 pacientes pediátricos, ASA I , II y III intervenidos en cirugías electivas y emergentes bajo anestesia general en un intervalo de tiempo de 30 a 240 minutos, de todas las especialidades médicas quirúrgicas del año 2018 ,se utilizaron los diferentes tipos de máscara. La muestra se obtuvo aplicando la fórmula para población desconocida (n = (Z2 x p x q)/ e2), nivel de confianza (Z): 95%. (1.96) Margen de error (e): 5% Probabilidad de ocurrencia del evento (p): 15% Probabilidad de no ocurrencia del evento (q): 85%. Resultados: 220 casos ingresados al estudio. El índice de complicaciones laríngeas es 5.9% , frecuentemente la tos y secreción sanguinolenta, asociándose factores como mascara clásica, edad (2-5 años), tiempo mayor de 60 minutos, mayor número de intentos, ASA> I, estado nutricional sobrepeso, e insertar en formación. Conclusión: La máscara laríngea es validada como dispositivo en anestesia pediátrica por aprendizaje rápido, baja tasa de fracaso, menores complicaciones y utilidad en vías aéreas difíciles, Es insuficiente la evidencia para respaldar el uso de un determinado dispositivo por encima de otro

Introduction: The laryngeal mask is the equipment with the aim of increasing quality, safety, care, however, despite having universal use and high efficacy for ventilation, it is not without complications. The objective of this research was to identify the frequency of complications with the use of a laryngeal mask in the Vicente Corral Moscoso and José Carrasco public hospitals in the city of Cuenca. Methods: It is an observational, descriptive, prospective study in 220 pediatric patients, ASA I, II and III who underwent elective and emergent surgeries under general anesthesia in a time interval of 30 to 240 minutes, of all surgical medical specialties of the year 2018, the different types of mask were used. The sample was obtained by applying the formula for unknown population (n = (Z2 x p x q) / e2), confidence level (Z): 95%. (1.96) Margin of error (e): 5% Probability of occurrence of the event (p): 15% Probability of non-occurrence of the event (q): 85%. Results: 220 cases entered the study. The rate of laryngeal complications is 5.9%, frequently cough and bloody discharge, associating factors such as classic mask, age (2-5 years), time greater than 60 minutes, greater number of attempts, ASA> I, nutritional status, overweight, and insert in formation. Conclusion: The laryngeal mask is validated as a device in pediatric anesthesia due to rapid learning, low failure rate, fewer complications and usefulness in difficult airways. The evidence is insufficient to support the use of a certain device over another.

Comparison of two supraglottic airway devices on postoperative sore throat in children: a prospective randomized controlled trial / Comparação entre dois dispositivos supraglóticos de vias aéreas na dor de garganta pós-operatória em crianças: estudo controlado prospectivo randomizado

Abstract Background and objective: Sore throat is well recognized complaint after receiving general anesthesia. This study is conducted to compare the severity and frequency of postoperative sore throat in children undergoing elective surgery, following the use of Ambu laryngeal mask airway or I-gel®, who are able to self-report postoperative sore throat. Method: Seventy children, 6 to 16 years-old, undergoing elective surgery randomly allocated to either Ambu laryngeal mask (Ambu Group) or I-gel® (I-gel Group). After the procedure, patients were interviewed in the recovery room immediately, after one hour, 6 and 24 hours postoperatively by an independent observer blinded to the device used intra-operatively. Results: On arrival in the recovery room 17.1% (n = 6) of children of the Ambu Group complained of postoperative sore throat, against 5.7% in I-gel Group (n = 2). After one hour, the results were similar. After 6 hours, postoperative sore throat was found in 8.6% (n = 3) of the children in Ambu group vs. 2.9% (n = 1) in I-gel Group. After 24 hours, 2.9% (n = 1) of the children in Ambu Group complained of postoperative sore throat compared to none in I-gel Group. There was no significant difference found in the incidence of postoperative sore throat in both devices on arrival (p = 0.28); after 1 hour (p = 0.28); after 6 hours (p = 0.30); and after 24 hours (p = 0.31). The duration of the insertion of Ambu laryngeal mask was shorter and it was easier to insert than I-gel® (p = 0.029). Oropharyngeal seal pressure of I-gel® was higher than that of Ambu laryngeal mask (p = 0.001). Conclusion: The severity and frequency of postoperative sore throat in children is not statistically significant in the I-gel Group compared to Ambu Group.

Resumo Justificativa e objetivo: Dor de garganta é uma queixa bem conhecida após anestesia geral. O presente estudo comparou a gravidade e a frequência da queixa de dor de garganta pós-operatória associada ao uso de máscara laríngea Ambu ou máscara laríngea I-gel® durante cirurgia eletiva, em crianças capazes de autoreferir a queixa no pós-operatória. Método: Setenta crianças, de 6 a 16 anos submetidas à cirurgia eletiva foram alocadas aleatoriamente para o emprego da máscara laríngea Ambu (Grupo Ambu) ou para o emprego da máscara laríngea I-gel® (Grupo I-gel). Após o procedimento, os pacientes foram entrevistados imediatamente após admissão na sala de recuperação pós-anestésica-SRPA, uma hora, 6 e 24 horas após a cirurgia por um observador independente e cego ao dispositivo de vias aéreas utilizado no intraoperatório. Resultados: Na admissão à SRPA, 17,1% das crianças no Grupo Ambu (n = 6) se queixaram de dor de garganta pós-operatória, contra 5,7% no Grupo I-gel (n = 2). Após uma hora, os resultados foram similares. Após 6 horas, houve dor de garganta pós-operatória em 8,6% (n = 3) das crianças no Grupo Ambu vs. 2,9% (n = 1) no Grupo I-gel. Após 24 horas, 2,9% (n = 1) das crianças no Grupo Ambu versus nenhuma criança no Grupo I-gel. Não houve diferença significante na incidência de dor de garganta pós-operatória nos dois dispositivos na admissão na SRPA (p = 0,28); após 1 hora (p = 0,28); após 6 horas (p = 0,30); e após 24 horas (p = 0,31). A duração da inserção foi menor no grupo da máscara laríngea Ambu, e a I-gel® foi mais fácil de inserir (p = 0,029). A pressão de selagem orofaríngea do I-gel® foi maior do que a da máscara laríngea Ambu (p = 0,001). Conclusão: A gravidade e a frequência da dor de garganta pós-operatória em crianças não foram estatisticamente significantes no grupo com máscara laríngea I-gel® em comparação ao grupo com máscara laríngea Ambu.

Comparison of channelled videolaryngoscope and intubating laryngeal mask airway for tracheal intubation in obese patients: a randomised clinical trial / Comparação de videolaringoscópio com canal e máscara laríngea na intubação traqueal de pacientes obesos: estudo clínico randomizado

Abstract Background: Obesity causes various difficulties in intubation and ventilation, which are confronted due to increased fat tissue in the upper airway and diminished compliance in the chest wall. Videolaryngoscopes and Intubating Laryngeal Mask Airway (ILMA) are good options as recommended by the American Society of Anesthesologists (ASA) difficult airway guidelines. We aimed to compare ILMA and Airtraq (a channeled videolaryngoscope) in obese patients. Methods: Eighty patients with ASA physical status 1-3, aged between 18 and 65 years and with a body mass index greater than 35 kg.m-2, who were undergoing elective surgery requiring orotracheal intubation, were included in the study. Patients were intubated with one of the devices cited. Results: There was no difference between the number of intubation attempts, insertion times and need for optimisation manoeuvres of Airtraq and ILMA. The intubation with Airtraq was accomplished in a shorter period of time than in that in the ILMA group (29.9 ± 22.1s vs. 50.7 ± 21.2s; p < 0.001). A significant difference was found when the times of total intubation were compared (29.9 ± 22.1s vs. 97.4 ± 42.7s; p < 0.001). The mean arterial pressure statistically increased after device insertion in the ILMA group (p < 0.05). Conclusions: Airtraq appears to be superior to ILMA in obese patients, with a total of time intubation of less than 60 seconds and with low mean arterial pressure changes. However, ILMA is still a useful tool that provides both ventilation and intubation throughout the whole intubation process.

Resumo Justificativa: A obesidade dificulta a ventilação manual e intubação traqueal devido ao acúmulo de tecido adiposo na via aérea superior e a complacência diminuída na caixa torácica. Os videolaringoscópios e as Máscaras Laríngeas para Intubação (MLI) são alternativas boas para o manuseio da via aérea difícil, de acordo com as diretrizes da Sociedade Americana de Anestesologia (ASA). O objetivo do estudo foi comparar o uso da MLI e do Airtraq, um videolaringoscópio com canal, em pacientes obesos. Método: Estudamos 80 pacientes com classificação ASA I-III, com idades entre 18 e 65 anos e índice de massa corporal acima de 35 kg.m-2, submetidos a cirurgia eletiva com indicação de intubação orotraqueal. Os pacientes foram intubados empregando-se um dos seguintes dispositivos: MLI ou Airtraq. Resultados: Não houve diferença entre o número de tentativas de intubação, tempo de inserção do dispositivo e necessidade de manobras de otimização para o Airtraq e MLI. A intubação com Airtraq foi realizada mais rapidamente do que no Grupo MLI (29,9 ± 22,1 s vs. 50,7 ± 21,2 s; p < 0,001). Houve diferença significante na comparação do tempo total para intubação (29,9 ± 22,1 s vs. 97,4 ± 42,7 s; p < 0,001). Houve aumento estatisticamente significante da pressão arterial média após a inserção do dispositivo no Grupo MLI (p < 0,05). Conclusões: Airtraq parece ser superior a MLI em pacientes obesos, apresentando tempo total de intubação abaixo de 60 segundos e com menor variação na pressão arterial média. Todavia, a MLI ainda é ferramenta útil que propicia tanto ventilação quanto intubação durante todo o processo de manejo da via aérea.

Feasibility of non-intubated anesthesia and regional block for thoracoscopic surgery under spontaneous respiration: a prospective cohort study

Data about the feasibility and safety of thoracoscopic surgery under non-intubated anesthesia and regional block are limited. In this prospective study, 57 consecutive patients scheduled for thoracoscopic surgery were enrolled. Patients were sedated with dexmedetomidine and anesthetized with propofol and remifentanil. Ropivacaine was used for intercostal nerve and paravertebral block. Lidocaine was used for vagal block. The primary outcomes were mean arterial pressure (MAP), heart rate (HR), oxygen saturation, and end-tidal carbon dioxide partial pressure (ETCO2) at T0 (pre-anesthesia), T1 (immediately after laryngeal mask/nasopharyngeal airway placement), T2 (immediately after skin incision), T3 (10 min after opening the chest), T4 (end of surgery), and T5 (immediately after laryngeal mask/nasopharyngeal airway removal). One patient required conversion to intubation, 15 developed intraoperative hypotension, and two had hypoxemia. MAP at T0 and T5 was higher than at T1-T4; MAP at T3 was lower (P<0.05 vs other time points). HR at T0 and T5 was higher (P<0.05 vs other time points). ETCO2 at T2 and T3 was higher (P<0.05 vs other time points). Arterial pH, PCO2, and lactic acid at T1 differed from values at T0 and T2 (P<0.05). The Quality of Recovery-15 (QoR-15) score at 24 h was lower (P<0.05). One patient experienced dysphoria during recovery. Thoracoscopic surgery with regional block under direct thoracoscopic vision is a feasible and safe alternative to conventional surgery under general anesthesia, intubation, and one-lung ventilation.

Different anesthesia management in preterm infants undergoing surgeries for retinopathy of prematurity: A retrospective study / 北京大学学报(医学版)

OBJECTIVE@#To evaluate the effect of different anesthesia management on clinical outcomes in former prematurely born infants undergoing surgeries for retinopathy of prematurity (ROP).@*METHODS@#In this retrospective study, electronic medical record database was searched for all former prematurely born infants (gestational age < 37 weeks and post conceptual age < 60 weeks) who received ROP surgery under inhalational general anesthesia between November 2016 and October 2018. The patients were divided into two groups based on anesthesia management: laryngeal mask airway (LMA) insertion without intravenous muscle relaxant injection and with pressure support ventilation (LMA group) or airway secured with endotracheal tube (ETT) with intravenous muscle relaxant injection and pressure controlled ventilation (ETT group). Primary outcomes included perioperative adverse events and complications. Extubation time and length of stay after surgery were also recorded.@*RESULTS@#Sixty eight preterm infants in the LMA group and 100 preterm infants in the ETT group were included. The incidence of adverse events during surgery (including airway management change and desaturation) was similar in LMA group and ETT group (4.4% vs. 1.0%, P =0.364). During the early recovery period after surgery, the incidence of difficult extubation (extubation time >30 min) was significantly lower in LMA group compared with ETT group (4.4% vs.15.0%, RR=0.262, 95%CI:0.073－0.942, P=0.029). The incidence of respiratory events was similar between the two groups (20.6% vs. 27.0%, P =0.342). However, the incidence of apnea was significantly lower in the LMA group than in the ETT group (5.9% vs.19.0%, RR=0.266, 95%CI: 0.086－0.822, P =0.015). No significant difference was observed between the LMA group and ETT group in incidences of cardiovascular events (0% vs. 1.0%, P =1.000) and unplanned admission to neonatal intensive care unit (5.9% vs. 7.0%, P=0.774). No airway spasm, re-intubation, aspiration or regurgitation was observed during early recovery. During late recovery after returning to ward, the incidence of adverse events was also similar between the two groups (0% vs. 2.0%, P =0.241). The median (IQR) extubation time was 6 (5, 10) min in LMA group and 10 (6, 19) min in ETT group (P < 0.001). The median length of stay after surgery was significantly shortened in LMA group compared with ETT group [20 (17, 22) hours vs. 22 (17, 68) hours, P =0.002].@*CONCLUSION@#Compared with endotracheal intubation with intravenous muscle relaxant injection, laryngeal mask airway insertion without muscle relaxant could achieve an early extubation, and reduce the incidence of apnea during early recovery period in former prematurely born infants undergoing ROP surgery.

Systematic review and meta-analysis comparing ventilatory support in chemical, biological and radiological emergencies / Revisão sistemática e metanálise comparando técnicas de suporte ventilatório em emergências químicas, biológicas e radiológicas / Comparación de técnicas de soporte ventilatorio en situaciones de emergencia química, biológica y radiológica: revisión sistemática y meta-análisis

Objective: to compare the mean development time of the techniques of direct laryngoscopy and insertion of supraglottic devices; and to evaluate the success rate in the first attempt of these techniques, considering health professionals wearing specific personal protective equipment (waterproof overalls; gloves; boots; eye protection; mask). Method: meta-analysis with studies from LILACS, MEDLINE, CINAHL, Cochrane, Scopus and Web of Science. The keywords were the following: personal protective equipment; airway management; intubation; laryngeal masks. Results: in the "reduction of the time of the procedures" outcome, the general analysis of the supraglottic devices in comparison with the orotracheal tube initially presented high heterogeneity of the data (I2= 97%). Subgroup analysis had an impact on reducing heterogeneity among the data. The "laryngeal mask as a guide for orotracheal intubation" subgroup showed moderate heterogeneity (I2= 74%). The "2ndgeneration supraglottic devices" subgroup showed homogeneity (I2= 0%). All the meta-analyses favored supraglottic devices. In the "success in the first attempt" outcome, moderate homogeneity was found (I2= 52%), showing a higher proportion of correct answers for supraglottic devices. Conclusion: in the context of chemical, biological or radiological disaster, the insertion of the supraglottic device proved to be faster and more likely to be successful by health professionals. PROSPERO record (CRD42019136139).

Objetivo: comparar o tempo médio do desenvolvimento das técnicas de laringoscopia direta e de inserção de dispositivos supraglóticos e avaliar a taxa de sucesso na primeira tentativa dessas técnicas, considerando a utilização de equipamentos de proteção individual específicos (macacão impermeável; luvas; botas; proteção ocular; máscara) pelos profissionais de saúde. Método: metanálise com estudos das bases LILACS, MEDLINE, CINAHL, Cochrane, Scopus e Web of Science. As palavras-chave foram: personal protective equipment; airway management; intubation; laryngeal masks. Resultados: no desfecho redução "do tempo dos procedimentos" a análise geral dos dispositivos supraglóticos em comparação com o tubo orotraqueal apresentou inicialmente alta heterogeneidade dos dados (I2 = 97%). A análise por subgrupos impactou na redução da heterogeneidade entre os dados. O subgrupo "máscara laríngea como guia para intubação orotraqueal" demonstrou heterogeneidade moderada (I2 = 74%). O subgrupo "dispositivos supraglóticos de 2ª geração" evidenciou homogeneidade (I2 = 0%). Todas as metanálises foram favoráveis aos dispositivos supraglóticos. No desfecho "êxito na primeira tentativa" foi encontrada homogeneidade moderada (I2 = 52%), demonstrando maior proporção de acerto para dispositivos supraglóticos. Conclusão: no contexto do desastre químico, biológico ou radiológico, a inserção do dispositivo supraglótico revelou ser mais rápida e apresentar maior chance de acerto por profissionais de saúde. Registro PROSPERO (CRD42019136139).

Objetivo: comparar el tiempo medio de desarrollo de las técnicas de laringoscopia directa y de inserción de dispositivos supraglóticos y evaluar la tasa de éxito obtenida en el primer intento de dichas técnicas con profesionales sanitarios provistos de equipos de protección individual específicos (mono impermeable, guantes, botas, protección ocular, mascarilla). Método: meta-análisis con estudio de las bases de datos LILACS, MEDLINE, CINAHL, Cochrane, Scopus y Web of Science. Las palabras clave fueron las siguientes: personal protective equipment; airway management; intubation; laryngeal masks. Resultados: en el resultado "reducción del tiempo de los procedimientos", el análisis general de los dispositivos supraglóticos en comparación con el tubo orotraqueal presentó, inicialmente, una alta heterogeneidad de los datos (I2= 97%). El análisis por subgrupos dio como resultado una reducción de la heterogeneidad entre los datos. El subgrupo "mascarilla laríngea como guía para la intubación orotraqueal" mostró una heterogeneidad moderada (I2= 74%). El subgrupo "dispositivos supraglóticos de 2ª generación" mostró homogeneidad (I2= 0%). Todos los meta-análisis fueron favorables a los dispositivos supraglóticos. En el resultado "éxito en el primer intento" se halló una homogeneidad moderada (I2= 52%), obteniendo una mayor proporción de aciertos con el uso de dispositivos supraglóticos. Conclusión: en el contexto de un desastre químico, biológico o radiológico, se ha demostrado que la inserción del dispositivo supraglótico es más rápida y que los profesionales sanitarios obtienen una mayor probabilidad de acierto. Registro PROSPERO (CRD42019136139).

High-flow nasal cannula oxygen therapy in acute respiratory failure due to acute exacerbation of fibrotic interstitial lung disease

High flow nasal cannula oxygen therapy (HFNC) has become frequent in the treatment of patients with acute hypoxemic respiratory failure. Methods. Eleven patients with acute exacerbation of fibrotic interstitial lung disease (ILD) were treated with HFNC after failure of conventional therapy (SatO2 < 90% offering 100% FiO2 by non-rebreathing mask or noninvasive ventilation). Ten patients had success with HFNC (not requiring orotracheal intubation) during emergency department admission. HFNC significantly improves clinical variables after 2h: respiratory rate decreased from 33 ± 6 breaths/ min to 23 ± 3 breaths/min; PaO2 increased from 48.7 (38-59) mmHg to 81.1 (76-90) mmHg; PaO2/FiO2 ratio increased from 102.4 ± 32.2 to 136.6 ± 29.4; SatO2 increased from 85 (66-92)% to 96 ± (95-97)%. HFNC could be an effective alternative in the treatment of acute respiratory failure from acute exacerbations of fibrotic ILD.(AU)

Intérêt du masque laryngé en anesthésie pédiatrique: expérience d'une mission humanitaire

Introduction: L'optimisation du réveil anesthésique repose en grande partie sur la gestion des voies aériennes. Notre travail avait pour objectif d'évaluer l'impact du masque laryngé lors d'une mission ponctuelle de chirurgie pédiatrique.Patients et méthodes : Il s'agit d'une étude prospective, descriptive, observationnelle et comparative portant sur les patients de 0-16 ans ayant bénéficié d'une chirurgie sous anesthésie générale. Deux groupes ont été constitués, un groupe masque laryngé (ML) et un groupe intubation trachéale (IT). Les paramètres étudiés étaient : âge, risque anesthésique (ASA), type de chirurgie, protocole anesthésique, temps opératoire et délai de réveil anesthésique.Résultats: Trente-cinq patients ont été inclus, 12 ML et 23 IT. Les enfants de 1 à 8 ans étaient majoritaires dans les deux groupes. La classe ASA 1 constituait 83% de ML et 95,7% d'IT. Les chirurgies viscérales, urologiques et orthopédiques étaient les plus réalisées. Le recours à la curarisation a été noté uniquement chez 56,5% d'IT. La majorité des patients des deux groupes a présenté un temps opératoire de 1 et 2 heures, soit 83,3% (ML) et 60,9% (IT).Presque la moitié des patients ML (41,7%) a eu un réveil rapide en moins de 10 minutes après la fin de la chirurgie, aucun dans le groupe IT mais par contre 26,1% de patients avec un réveil plus retardé. Conclusion : Notre étude montre que le masque laryngé a contribué à atteindre l'objectif de cette mission de chirurgie pédiatrique dans laréalisation d'un grand nombre d'actes dans les temps requis

Airway management strategies under the situation of prevention and control of nosocomial infections for coronavirus disease 2019 / 中南大学学报(医学版)

Since the outbreak of COVID-19, the prevention and control of nosocomial infections has been highly valued. Airway management, including endotracheal intubation, extubation, and suction, has been considered as the high-risk virus-spreading procedures, which can put the health providers at a high risk of nosocomial infections. As hospitals at all levels will gradually resume their routine medical work, effective managements for the airway of the silent asymptomatic carriers and patients with delayed symptoms, treatment for severe patients, and prevention of cross infection in hospital have become the focus for the current prevention and control of nosocomial infections. Under the guidance of partitioned and graded prevention and differential control strategies at this stage, we comprehensively analyzed four main intubation methods used in the current clinical work including rapid sequence intubation, laryngeal mask insertion, intubation guided by video flexible intubating scope and awake tracheal intubation. Furthermore, we discussed and summarized intubation and protection strategies for 3 categories of patients during the COVID-19 pandemic, providing evidence for protecting medical stuff in operating room and ICU against severe acute respiratory syndrome coronavirus 2 infection.

Lingual tonsillar hypertrophy, an unknown enemy: a case report / Hipertrofia de amígdala lingual, un enemigo desconocido. A propósito de un caso

Abstract We report an unexpected difficult airway in a patient with unrecognized lingual tonsillar hypertrophy. A 54-year-old hypertensive woman presented for resection of a mediastinal mass under general anesthesia (GA). After induction, mask ventilation was impossible. Laryngeal mask airway (LMA) was used, achieving suboptimal ventilation. Fiberoptic intubation through LMA was attempted but tube advancement was hindered by a protrudingmass. Finally, intubation was achieved using the Frova introducer. After completion of the surgery, the patient was transferred, intubated, to the postanesthesia care unit. Ear, nose, and throat assessment concluded that the mass was a hyper-trophied lingual tonsil. Unexpected lingual tonsillar hypertrophy can complicate GA, making mask ventilation, and even intubation impossible. It is considered a frequent cause of unexpected difficult airway. Diagnosis cannot be made by standard airway physical examination. Once recognized, fiberoptic intubation is mandatory in subsequent surgeries.

Resumen Presentamos el caso de una vía aérea difícil imprevista debido a hipertrofia de la amígdala lingual no conocida. Mujer de 54 años, hipertensa, que ingresa para resección de masa mediastínica bajo anestesia general. Tras la inducción, la ventilación mediante mascarilla facial resultó imposible. Se coloca mascarilla laríngea (ML) y se consigue ventilación de forma subóptima. Se intenta intubación guiada por fibroscopia a su través, pero se objetiva masa protruyente que impide la progresión del tubo. Finalmente se intuba mediante introductor Frova. Tras finalizar la cirugía, la paciente se traslada intubada a la Unidad de Reanimación Postanestésica (URPA). Se realiza evaluación por otorrinolaringología (ORL), que concluye que la masa corresponde a una amígdala lingual hipertrófica. La hipertrofia de la amígdala lingual puede complicar la anestesia, dificultando la ventilación e intubación. Se considera una causa frecuente de vía aérea difícil imprevista. El diagnóstico no puede realizarse mediante exploración anestésica estándar. Una vez conocida, las intubaciones siguientes deben ser guiadas por fibroscopia.

Efectividad de la máscara laríngea Ambu® Aura40TM para anestesia general en cirugía ortopédica pediátrica / Effectiveness of Ambu® Aura40TM laryngeal mask for general anesthetic in pediatric orthopedic surgery

RESUMEN Introducción: las máscaras laríngeas son dispositivos supraglóticos utilizadas ampliamente en anestesia para el abordaje y mantenimiento de la vía respiratoria. Una de ellas, la Ambu® Aura 40TM, tiene un diseño que le permite ajustarse al entorno de la hipofaringe con su lumen dirigido a la apertura laríngea. Ha demostrado ser adecuada para procedimientos quirúrgicos donde no es necesaria la intubación endotraqueal. Objetivo: determinar la efectividad dicha máscara laríngea para anestesia general en cirugía ortopédica pediátrica. Materiales y métodos: se realizó un estudio descriptivo, prospectivo, transversal, en 135 pacientes intervenidos quirúrgicamente de forma electiva en el Hospital Pediátrico Eliseo Noel Caamaño, de Matanzas, en el periodo enero de 2015- junio 2017. Se tuvo en cuenta el número de intentos y el tiempo para insertar la máscara laríngea, la necesidad de reemplazarla por un tubo endotraqueal y las complicaciones relacionadas con su uso. Resultados: la ML Ambu® Aura 40TM fue efectiva en la mayoría de los pacientes ya que permitió realizar la cirugía sin necesidad de sustituirla por el tubo endotraqueal y la aparición de complicaciones relacionada con su uso fue baja. Conclusiones: la ML Ambu® Aura 40TM fue efectiva ya que en la mayoría de los pacientes fue insertada correctamente en el primer intento y un tiempo inferior a los 20 segundos. Solo una minoría necesitó que fuera reemplazada por el tubo endotraqueal, y la aparición de complicaciones relacionada con su uso fue baja (AU).

ABSTRACT Introduction: laryngeal mask are supra glottal devices widely used in anesthetics for approaching and maintaining the airway. One of them, the Ambu® Aura 40TM, has a design allowing to adjust to the surroundings of hypo-pharynx with its lumen directed to the pharyngeal opening. It has demonstrated to be adequate for surgical procedures when there is no need of endotracheal intubation. Objective: to determine the effectiveness of that laryngeal mask for general anesthetic in pediatric orthopedic surgery. Materials and methods: a cross-sectional, prospective, descriptive study was carried out in 135 patients who underwent elective surgical intervention in the Pediatric Hospital ?Eliseo Noel Caamaño?, of Matanzas, in the period January 2015- June 2017. The number of attempts and the time needed to insert laryngeal mask, the necessity of changing it for an endotracheal tube, and complications related to its usage were taking into account. Results: Ambu® Aura 40TM laryngeal mask was effective in most patients, due to it allowed to perform the surgery without need of changing it for an endotracheal tube, and the low appearance of complications related to its use. Conclusions: Ambu® Aura 40TM laryngeal mask was effective because it was inserted correctly at the first attempt, in a time less than 20 seconds. Only a minority needed to replace it by endotracheal tube, and the appearance of complications related to its use were low (AU).

Máscara laríngea vs tubo orotraqueal no atendimento pré-hospitalar - desfechos hospitalares / Laringeal mask vs orotraqueal tube in pre-hospital care - hospital outcomes

INTRODUÇÃO: Em situações emergenciais, se torna crucial o manejo adequado das vias aéreas, pois falhas neste processo contribuem consideravelmente para piores desfechos clínicos. OBJETIVO: comparar a utilização do tubo endotraqueal e da máscara laríngea no atendimento pré- -hospitalar em relação aos desfechos hospitalares tais como tempo de ventilação mecânica, tempo de permanência na UTI e taxa de óbito. MATERIAIS E MÉTODOS: estudo observacional retrospectivo, desenvolvido no Hospital Santa Cruz, Rio Grande do Sul. Foram incluídos pacientes maiores de 18 anos, de ambos os sexos, que foram atendidos pelo SAMU durante o atendimento pré-hospitalar, e após o encaminhados para o Pronto Atendimento ou Ambulatório do Hospital Santa Cruz. As variáveis analisadas foram extraídas dos prontuários médicos dos indivíduos selecionados. RESULTADOS: foram analisados 27 indivíduos, maioria do sexo masculino, com média de idade de 46,5±22 anos, sendo a causa predominante do atendimento pré-hospitalar o politraumatismo. Ao compararmos os pacientes que utilizaram tubo endotraqueal com os que utilizaram máscara laríngea, não foram observadas diferenças significativas em relação ao tempo de atendimento pré-hospitalar. Na fase intra-hospitalar, observamos diferença significativa em relação ao tempo de ventilação mecânica e tempode internação na UTI, não sendo o mesmo observado em relação a taxa de óbito. CONCLUSÃO: Os pacientes submetidos a utilização da máscara laríngea no atendimento pré-hospitalar apresentaram menor tempo de ventilação mecânica e menor tempo de internação na UTI, em relação aos pacientes intubados com tubo endotraqueal.

INTRODUCTION: In emergency situations, proper management of the airways becomes crucial, because flaws in this process contribute considerably to worse clinical outcomes. OBJECTIVE: To compare the use of the endotracheal tube and laryngeal mask in prehospital care in relation to hospital outcomes such as mechanical ventilation time, length of stay in the ICU and death rate. MATERIALS AND METHODS: a retrospective observational study, developed in a Hospital Santa Cruz, Rio Grande do Sul. Patient records were used from the Emergency Mobile Service (SAMU) of Santa Cruz do Sul, sent to the Emergency Department or Ambulatory of Santa Cruz Hospital. RESULTS: 27 individuals, mostly males, with an average age of 46.5 ± 22 years, were analyzed, being the predominant cause of pre-hospital care the polytrauma. When comparing the patients who used the endotracheal tube with those who used laryngeal mask, no significant differences were observed in relation to the time of prehospital care. In the in-hospital phase, we observed a significant difference in relation to the time of mechanical ventilation and length of stay in the ICU, and the same was not observed in relation to the death rate. CONCLUSION: The patients submitted to the use of the laryngeal mask in the pre-hospital care presented a shorter time of mechanical ventilation and a shorter time of hospitalization in the ICU than the patients intubated with an endotracheal tube.