A shroud for a mask system includes a retaining portion structured to retain a frame, a pair of upper headgear connectors each including an elongated arm and a slot at the free end of the arm adapted to receive a headgear strap, and a pair of lower headgear connectors each adapted to attach to a headgear strap. The retaining portion, the upper headgear connectors, and the lower headgear connectors are integrally formed as a one piece structure.

An inspiratory resistor valve system (IRV) to regulate intrathoracic pressure during positive pressure breathing, spontaneous inspirations, and CPR may include an inspiratory port. The IRV system may include patient port. The IRV system may include a separate expiratory port. The IRV may include a plurality of atmospheric pressure sensitive valves. The plurality of atmospheric pressure sensitive valves may isolate the expiratory port and the inspiratory port from one another.

The present disclosure describes a ventilator. The ventilator includes tubing configured to receive an input gas and a flow outlet airline in fluid communication with the tubing. The flow outlet airline includes an airline outlet, and the flow outlet airline is configured to supply an output gas to a user via the airline outlet. The ventilator includes an aerosol generator in fluid communication with the flow outlet airline. The aerosol generator is configured to receive an input liquid through an inlet tube and transform the liquid input into an aerosol. The ventilator further includes a breath detection airline including an airline inlet, wherein the airline inlet is separated from the airline outlet of the flow outlet airline, and configured to receive breathing gas from the user during exhalation by the user via the airline inlet. A method of supplying respiratory gas containing an aerosol is disclosed.

A passive valve for use as a fixed leak valve. The valve includes a body having an internal chamber, first and second body ports in fluid communication with the chamber with the first port configured for fluid communication with a patient connection and the second body port configured for fluid communication with a ventilator, a body passageway in fluid communication with the chamber and with ambient air exterior of the body, and a check valve seal positioned to seal the body passageway to permit the flow of gas within the chamber through the body passageway to the exterior of the body and to prevent the flow of ambient air exterior of the body through the body passageway into the chamber. In alternative embodiments, the valve is incorporated into the patient connection or constructed as a separate part connectable to the patient connection.

A blower includes a housing including an inlet and an outlet, a motor to drive a rotatable shaft, first and second impellers provided to the shaft, the first and second impellers each including a plurality of impeller blades, a first stationary component provided to the housing and including stator vanes downstream of the first impeller, and a second stationary component provided to the housing and including stator vanes downstream of the second impeller. A first set of stator vanes of the first stationary component is provided around the motor and are configured and arranged to direct airflow along the motor, to de-swirl the airflow and to decelerate air to increase pressure. A blower including a third impeller and third stationary component positioned above the first impeller is also described.

A respiratory valve, such as a positive end expiratory pressure valve, permits pressure control for respiratory apparatus such as a ventilator or positive airway pressure device. The valve may include a flexible gas passage cover. The cover may be configured with a first side surface to operatively block and open an aperture of the gas passage at a valve seat to respectively prevent and permit gas flow through the aperture defined by the valve seat. The cover may include a second side surface opposite the first surface. The second surface may include at least one drop section forming a reduction in thickness of the cover between the first surface and the second surface. The first surface may include a coating to reduce friction of a membrane material of the first surface. The rim of the valve seat may comprise a variation in height relative the flexible cover.

A connection device, for mechanical ventilation and monitoring of spontaneous breathing of a patient (P), includes a fluid-guiding unit (9, 11, 15) and establishes a fluid connection between a medical arrangement (100) and a patient-side coupling unit (19). A volume flow sensor (90) measures an indicator of volume flow of fluid through the fluid-guiding unit. A volume flow sensor component (2) engages with an interior of the fluid-guiding unit. A homogenization unit (10) is nonrotatably inserted into the interior between the patient-side coupling unit and the component and includes two sieves and a connection element, which connects the sieves together. The homogenization unit homogenizes the flow of fluid through the fluid-guiding unit. An inner profile of the fluid-guiding unit and an outer profile of the homogenization unit together form a mechanical coding, which determines a defined rotation position of the homogenization unit in relation to the fluid-guiding unit.

The present technology is directed to ventilator systems that can provide both ventilation therapy and oxygen therapy. The systems described herein may include a ventilation assembly that can provide inspiratory gas to a patient circuit and an oxygen assembly that can provide pulses of oxygen to an oxygen delivery circuit. In some embodiments, the oxygen delivery circuit is distinct from the patient circuit. For example, the patient circuit can include a corrugated conduit coupled a ventilation mask, and the oxygen delivery circuit can include a nasal cannula. The ventilation mask can be positioned over the nasal cannula so that the patient can receive both the inspiratory gases and the pulses of oxygen.

Embodiments generally relate to a device for monitoring air pressure in the body of a patient. The device comprises a tube comprising a feeding lumen; a sensor lumen positioned parallel to the feeding lumen; at least one sensor positioned in the sensor lumen; and at least one perforation positioned to expose the at least one sensor to an air pressure within the body of a patient when the device is positioned at least partially in the airway of the patient. The at least one sensor is configured to generate data related to the pressure to which the sensor has been exposed.

A wye connector has a patient coupling end. The patient coupling end has a first connector surface and a second connector surface. The first connector surface has a first diameter at an axial location along the patient coupling end. The second connector surface has a second diameter at the same axial location along the patient coupling end. The first diameter is larger than the second diameter. The second connector surface projects axially outward beyond the first connector surface.