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Vol. 43. Issue 8.
Pages 474-479 (November 2019)
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Vol. 43. Issue 8.
Pages 474-479 (November 2019)
DOI: 10.1016/j.medine.2018.06.008
Safety of aerosol therapy in children during noninvasive ventilation with helmet and total face mask
Seguridad de la aerosolterapia durante la ventilación mecánica no invasiva con helmet y mascarilla facial total en población pediátrica
L. Rodriguez Garciaa,
Corresponding author

Corresponding author.
, A. Medinab,c, V. Modesto i Alapontd, M.L. Palacios Loroe, J. Mayordomo-Colungab,c, A. Vivanco-Allendeb, C. Reyf,g
a Paediatric Intensive Care Unit, Department of Paediatrics, Complejo Asistencial Universitario de León, León, Spain
b Paediatric Intensive Care Unit, Department of Paediatrics, Hospital Universitario Central de Asturias, Oviedo, Spain
d Department of Anesthesiology and Critical Care, Hospital Universitari i Politècnic La Fe de Valencia, Valencia, Spain
e Department of Paediatrics, Hospital Universitario Central de Asturias, Oviedo, Spain
f Paediatric Intensive Care Unit, Hospital Universitario Central de Asturias, Oviedo, Spain
g Universidad de Oviedo, Oviedo, Spain
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Tables (4)
Table 1. Characteristics of patients and interface used.
Table 2. Characteristics of patients according to the use of nebulized drugs.
Table 3. Comparison between patients with or without nebulized drugs according to the type of interface.
Table 4. Logistic regression and Cox regression studies according to the type of interface.
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To evaluate the consequences of using nebulized drugs in patients subjected to noninvasive ventilation (NIV) with total face mask (TFM) and helmet.


A descriptive analytical study of a prospective patient cohort was carried out.


Pediatric intensive care unit (PICU) of a tertiary hospital.


Consecutive sampling was used to include all patients admitted to the PICU and requiring NIV with helmet or TFM over a period of 29 months. No patients were excluded.


Nebulized treatment was added according to medical criteria.

Variables of interest

Independent variables were age, sex, diagnosis, disease severity, ventilation parameters and nebulized drugs (if administered). Secondary outcomes were duration and failure of NIV, and length of PICU stay.


The most frequent diagnoses were bronchiolitis (60.5%) and asthma (23%). Patients received NIV for a median of 43h. Nebulized drugs were administered in 40% of the cases during NIV, and no adverse effects were registered. Using Bayesian statistics, the calculated probability of suffering an adverse effect was 1.3% with helmet and 0.5% with TFM (high density 95% probability intervals). Patients with helmet and nebulized therapy were in more serious condition than those who did not receive nebulization; nevertheless, no differences were observed regarding the need to change to bilevel modality. With TFM, PICU stay was shorter for the same degree of severity (p=0.033), and the NIV failure rate was higher in patients who did not receive inhaled drugs (p=0.024).


The probability of suffering an adverse effect related to nebulization is extremely low when using a helmet or TFM. Inhaled therapy with TFM may shorten PICU stay in some patients.

Noninvasive ventilation (NIV)
Drug side effect
Bronchial spasm
Nebulizers and vaporizers
Total face mask

Evaluar las consecuencias de la medicación nebulizada en pacientes con ventilación no invasiva (VNI) con mascarilla facial total (MFT) y casco.


Estudio analítico descriptivo sobre una cohorte prospectiva de pacientes.


UCIP de hospital de tercer nivel.


Todos los pacientes ingresados en UCIP (muestreo consecutivo) con VNI con casco o MFT durante 29 meses. No se excluyeron pacientes.


Se añadió tratamiento nebulizado según criterio médico.

Variables de interés

Independientes: edad, sexo, diagnóstico, gravedad, parámetros ventilatorios y medicación nebulizada (si se utilizaba). Secundarias: duración, fallo de VNI y estancia en UCIP.


Los diagnósticos más frecuentes fueron bronquiolitis (60,5%) y asma (23%). La mediana de conexión a VNI fue de 43 horas. Se administraron nebulizaciones durante la VNI en un 40% sin registrarse efectos adversos. La probabilidad calculada de tener un efecto adverso fue 1,3% con casco y 0,5% con MFT (estadística bayesiana, intervalo de probabilidad 95%). Los pacientes con casco y aerosolterapia tenían mayor gravedad que los que no recibieron nebulizaciones, sin encontrarse diferencias en la necesidad de cambiar a modalidad con doble nivel de presión. En los pacientes con MFT la estancia en UCIP fue menor (p=0,033) a pesar de no existir diferencias en el nivel de gravedad; la tasa de fallo de VNI fue mayor en los que no recibieron nebulizaciones (p=0,024).


La probabilidad de tener un efecto adverso relacionado con la nebulización es baja utilizando casco o MFT. La terapia inhalada con MFT puede disminuir la estancia en UCIP en algunos pacientes.

Palabras clave:
Ventilación no invasiva (VNI)
Efectos secundarios
Mascarilla facial total


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