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The Airway Pressures During Bag-Valve-Mask Ventilation

13 de mayo de 2026 actualizado por: Erkan Göksu, Akdeniz University Hospital

The Airway Pressures During Bag-Valve-Mask Ventilation: A Randomized Crossover Trial

Background and Objective Bag-valve-mask (BVM) ventilation is commonly used in emergency airway management, but the positive pressure generated may increase aspiration risk. This prospective, randomized, simulation-based manikin study aimed to assess how airway pressures change during BVM ventilation using different techniques and neck mobility scenarios.

Methods The study was conducted in a tertiary university hospital between July 15 and August 15, 2024. Emergency medicine residents (PGY-1 to PGY-4) performed ten ventilations using one-hand, two-hand CE, and modified two-hand TE techniques on a manikin under normal and restricted neck mobility. Airway pressures were measured with a real-time pressure sensor. The primary outcome was peak airway pressure; the secondary was the number of ventilations exceeding 20 cmH₂O. All data were automatically recorded, and analyses were performed using SPSS 16.0 with p < 0.05 considered significant.

Descripción general del estudio

Descripción detallada

Introduction:

Emergency department (ED) patients are considered to have an elevated risk of gastric distention and aspiration of gastric contents, making rapid sequence induction (RSI) the preferred intubation procedure. Pre-oxygenation is likely the most critical step in RSI, as it extends the duration of safe apnea time, providing the operator with more time for the intubation process. Although a facemask with a high FiO2 oxygen reservoir is recommended for pre-oxygenation, bag-valve-mask (BVM) ventilation is frequently used in emergency airway management.

Since its development during the polio epidemic in 1953, the BVM has been used for oxygenation and ventilation of critically ill patients. However, the positive pressure generated by the BVM can increase the risk of regurgitation and aspiration of gastric contents into the lungs. Excessive volumes and flow generated with the BVM can not only lead to gastric distention but also increase intrathoracic pressures, potentially causing negative cardiovascular effects.

The aim of this randomized crossover manikin study is to investigate how airway pressures change during ventilation with a BVM using different scenarios and techniques.

Methods:

This is a randomized crossover trial performed in the simulation lab of a tertiary care facility between 15.07.2024 to 15.08.2024. The ethical committee of XXX approved the study and informed consent was obtained from the participants. The participants were emergency medicine residents ranging from postgraduate year 1 (PGY) to PGY4.

In this study, airway pressures during BVM ventilation were continuously recorded using a calibrated pressure sensor placed between the facemask and the bag. All participants were requested to ventilate the Resusci Anne QCPR airway mannequin (Laerdal Medical, Stavanger, Norway) in a randomized manner using one-hand, two-hand (CE method), and modified two-hand (TE method) techniques, while the airway pressures were measured. Two different scenarios were applied to simulate normal and difficult airways while ventilating the airway mannequin. For the difficult airway scenario, a cervical collar was applied to the airway mannequin. To reduce potential bias, the purpose of the study was not explained to the participants Each participant was asked to provide a sufficient amount of air with the BVM to raise the mannequin's chest and to repeat these 10 times in a randomized order. All the pressure values measured during ventilation were recorded as cmH2O. The highest-pressure value measured during ventilations, as well as the number of ventilations during which the pressure exceeded 20 cmH2O, were recorded.

The differences in the pressure values measured using different hand techniques in normal and difficult airway scenarios were evaluated. Additionally, it was assessed which scenario and technique resulted in pressures exceeding 20 cmH2O, based on the theoretical assumption that pressures above this value would open the lower esophageal sphincter and inflate the stomach with air. This assumption was based on previous studies indicating that lower esophageal sphincter pressure is typically exceeded, and gastric inflation begins, when airway pressure surpasses 20 cmH₂O.

Statistical analysis:

The study data were analyzed using the SPSS software version 16.0 for Windows (SPSS Inc., Chicago, IL, USA). Demographic and baseline characteristics were summarized as a mean ± standard deviation for continuous variables and as a percentage of the group for categorical variables. Non-normally distributed data are presented as medians (interquartile range). For each scenario and technique, the participant was considered the unit of analysis. For every participant, the highest pressure value among the 10 ventilations and whether ≥5 of 10 ventilations exceeded 20 cmH2O were used in the analyses The chi-square test was used to compare the ventilations exceeding the 20 cmH2O pressure value with PGY levels. P < 0.05 was accepted as statistically significant.

Tipo de estudio

Intervencionista

Inscripción (Actual)

46

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Descripción

Inclusion Criteria:

  • 18 years or older.
  • Medical residents (Post-graduate years 1-4) or practicing emergency medicine physicians.
  • Ability and willingness to provide informed consent to participate in the simulation.
  • Experience with basic airway management and BVM ventilation in a clinical setting.

Exclusion Criteria:

  • Lack of Experience:
  • Any musculoskeletal or neurological condition that would prevent the participant from performing manual BVM maneuvers effectively.
  • Refusal to Participate: Inability to provide informed consent.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Investigación de servicios de salud
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Otro: PGY juniors (under 2 yrs)
Residents who have been working as assistants for less than two years
Describes the CE hand-holding position during the balloon mask ventilation.
Describes the TE hand-holding position during the balloon mask ventilation.
Describes the One hand-holding position during the balloon mask ventilation.
Otro: PGY Senior ( above 2 years)
Residents who have been working as assistants for more than two years.
Describes the CE hand-holding position during the balloon mask ventilation.
Describes the TE hand-holding position during the balloon mask ventilation.
Describes the One hand-holding position during the balloon mask ventilation.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Incidence of airway pressure exceeding 20 cmH2O
Periodo de tiempo: During the ventilation procedure (a continuous 10-breath sequence per technique/scenario
The frequency of breaths delivered with a peak airway pressure greater than 20 cmH2O (the threshold for gastric inflation risk) during Bag-Valve-Mask (BVM) ventilation.
During the ventilation procedure (a continuous 10-breath sequence per technique/scenario

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

  • 1- Weingart SD, Levitan RM. Preoxygenation and prevention of desaturation during emergency airway management. Ann Emerg Med. 2012 Mar;59(3):165-75.e1. doi: 10.1016/j.annemergmed.2011.10.002. 2- Lee CP, Yip YY. Understanding your bag-valve-mask resuscitator. BJA Educ. 2023 Jun;23(6):208-211. doi: 10.1016/j.bjae.2023.03.003. 3- Lawes EG, Campbell I, Mercer D. Inflation pressure, gastric insufflation, and rapid sequence induction. Br J Anaesth. 1987 Mar;59(3):315-8. doi: 10.1093/bja/59.3.315. 4- Bowman FP, Menegazzi JJ, Check BD, Duckett TM. Lower esophageal sphincter pressure during prolonged cardiac arrest and resuscitation. Ann Emerg Med. 1995 Aug;26(2):216-9. doi: 10.1016/s0196-0644(95)70154-0. 5- von Goedecke A, Wagner-Berger HG, Stadlbauer KH, Krismer AC, Jakubaszko J, Bratschke C, Wenzel V, Keller C. Effects of decreasing peak flow rate on stomach inflation during bag-valve-mask ventilation. Resuscitation. 2004 Nov;63(2):131-6. doi: 10.1016/j.resuscitation.2004.04.012.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

15 de julio de 2024

Finalización primaria (Actual)

15 de agosto de 2024

Finalización del estudio (Actual)

15 de agosto de 2024

Fechas de registro del estudio

Enviado por primera vez

30 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

13 de mayo de 2026

Publicado por primera vez (Actual)

18 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

18 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

13 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • AkdenizUH

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Anonymized data can be shared if deemed appropriate when requested.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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