Reducing Patient Harm From Manual Ventilation

Improve your manual ventilation today
98%

Of responders delivered at least one breath that was inadequate or excessive per 90-second period.(1)

The Problem

The manual resuscitator, also known as the bag valve mask (BVM), is the standard means of providing emergency ventilatory support. Despite the widespread use of these devices, poor manual ventilation technique is a well-documented problem that occurs irrespective of a provider’s qualifications, training, experience, and confidence. Currently, there are no limitations or restrictions on the way a provider can ventilate with a BVM. This results in high provider variability in breath delivery and can lead to serious complications. (1)

High Provider Variability

71%

Of the time, air enters the stomach when ventilating the lungs with a manual resuscitator (2)

Sotair Image

The Solution

Sotair employs a flow blocking and pressure control valve mechanism to minimize complications associated with overventilation. The Sotair minimizes excessive pressure in the airway system without venting air by capping peak flow rates at 55 L/min.

Pressure Delivered During Manual Ventilation

Sotair blocks the flow of air at 55 L/min. For an average adult, this corresponds to a maximum pressure generated of approximately 20 cmH2O. Air enters the stomach beyond this corresponding pressure threshold.

Sotair Image

Improve Your Manual Ventilation Today

UMLRI

Awarded a small business grant for the development and commercialization of SafeBVM’s technology

Opportunity Health

Selected for the 2021 program focused on healthcare companies that are looking to improve care,reduce cost sand create new efficient approaches to problems with in the medical industry

BMJ Journals

Publication showing the enefits of Sotair as a potential solution to reduce barotrauma, overventilation, and under ventilation in periods of extended manual ventilation

NIH, one Phase II SBIR/STTR grant

Awarded 2 grants by the NIH, one Phase II SBIR/STTR grant, and one grant in collaboration with Umass Memorial Medical Center

AFWERX/AF Ventures initiative of the US Air Force.

Awarded a Phase ISBIR contract by the AFWERX/AFV entures initiative of the US AirForce

NASDAQ’s

SafeBVM was selected in the highly competitive NASDAQ’s Milestone Makers Program

MassChallenge Boston

SafeBVM was a part of the 100 companies that were selected for the 2020 Mass Challenge Boston cohort

Out of 130 companies, SafeBVM was one of the two companies that were awarded grants by the AHA

Out of 130 companies, SafeBVM was one of the two companies that were awarded grants by the AHA

2019 European Product Design Awards.

won the Gold Prize in the Life Science Design category in the 2019 European Product Design Awards

SafeBVM was awarded Phase I & Phase II SBIR/STTR grants by the National Science Foundation

These projects will advance the science of emergency airway management. The technology will fit into the existing treatment workflow and supply chain while addressing the need for safer ventilation during COVID-19

SafeBVM was selected as International Top 20 out of 1800 applicants.

The James Dyson Award is an international design award that celebrates, encourages and inspires the next generation of design engineers

SafeBVM wins 1st place at the University of Minnesota’s Design of Medical Devices Conference. 

1st place at the University of Minnesota’s 2019 Design of Medical Devices Conference

2022 EMS WORLD EXPO Innovation Awards

SafeBVM selected as finalist at the 2022 EMS WORLD EXPO Innovation Awards & winner at the 2019 EMS WORLD EXPO Innovation Awards

Testimonials

safeBVM’s device does limit pressure delivered and can be utilized with monitoring devices if needed. This inexpensive accessory to manual ventilation is a must at reducing harmful pressure during emergency care in and out of the hospital. Once approved, this device will be a tool that Respiratory Therapists (RTs) around the world will utilize to provide a safe means for resuscitation. I look forward to a successful collaboration that can assist in making manual ventilation safer in the future

Joe Holley,

MD FACEP FAEMS

Medical Director of the State of Tennessee EMS,
Associate Professor in Emergency Medicine at University of Tennessee Health Science Center

 

safeBVM’s device does limit pressure delivered and can be utilized with monitoring devices if needed. This inexpensive accessory to manual ventilation is a must at reducing harmful pressure during emergency care in and out of the hospital. Once approved, this device will be a tool that Respiratory Therapists (RTs) around the world will utilize to provide a safe means for resuscitation

Douglas S. Gardenhire,

EdD, RRT-NPS, FAARC

Chairman, Department of Respiratory Therapy,
Georgia State University

 

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