An apparatus such as a fluid mixer, suitable for use with a respirator, including a venturi nozzle for flow of a pressure-controlled fluid; an ambient fluid aperture in fluid communication with the venturi nozzle; a fluid port; a pressure force multiplier in fluid communication with the fluid port; and a valve moveable relative to the venturi nozzle between a start flow position and a stop flow position; where the pressure force multiplier is configured such that fluid forced into the fluid port actuates the valve relative to the venturi nozzle; and where the pressure force multiplier is configured such that fluid withdrawn from the fluid port actuates the valve relative to the venturi nozzle.

The present ventilator system, for detecting and treating concurrent chronic obstructive pulmonary disease (COPD) and obstructive sleep apnea (OSA event(s)) overlap syndrome, comprises a pressure generator for generating a pressurized flow of breathable gas for delivery to an airway of a subject; sensor(s) for generating output signals conveying information related to breathable gas parameters; and processor(s) operatively connected to the sensor(s) and the pressure generator, configured to: detect presence of OSA event(s) and/or expiratory flow limitation (EFL) in the subject based on the output signals. Responsive to detecting concurrent presence of OSA event(s) and EFL, the processors are configured to determine OSA EVENT(S) therapy parameters for treating the detected OSA event(s) in the subject; determine EFL therapy parameters for treating the detected EFL in the subject; determine a priority treatment based on a comparison between the OSA event(s) therapy parameters and the EFL therapy parameters; and control the pressure generator to deliver the determined priority treatment.

The present technology relates to the field of medical monitoring, and, in particular, to non-contact detecting and monitoring of patient breathing. Systems, methods, and computer readable media are described for calculating a change in depth of a region of interest (ROI) on a patient. In some embodiments, the systems, methods, and/or computer readable media can identify steep changes in depths. For example, the systems, methods, and/or computer readable media can identify large, inaccurate changes in depths that can occur at edge regions of a patient. In these and other embodiments, the systems, methods, and/or computer readable media can adjust the identified steep changes in depth before determining one or more patient respiratory parameters.

A device for respiratory therapy of a patient comprises a respiratory gas source for specifying different respiratory gas parameters, comprising at least one control unit, and comprising a signal unit for outputting at least one signal. The at least one signal is used for signaling changing respiratory gas parameters and is sensorially perceptible by the patient.

The present disclosure pertains to a portable handheld pressure support system configured to deliver a pressurized flow of breathable gas to the airway of a subject. The pressure support system is configured to treat COPD and/or other patients suffering from dyspnea and/or other conditions. The pressure support system is configured to be small and lightweight so that a subject may carry the system and use the system as needed without requiring a device to be worn on the face. The present disclosure contemplates that the portable handheld pressure support system may be used to treat symptoms and/or conditions related to dyspnea, and/or for other uses. In one embodiment, the system comprises one or more of a pressure generator, a subject interface, one or more sensors, one or more processors, a user interface, electronic storage, a portable power source, a housing, a handle, and/or other components.

Liquid ventilator and methods integrating the concept of total liquid ventilation (TLV) using liquid volumes below functional residual capacity (FRC) of mammal's lungs are disclosed. Beyond the automatization of the whole process, the technology has been up-scaled to confirm that TLV at residual volumes below FRC can provide a safe procedure while enabling the full potential of TLV in a mammal such as humans or adult-sized animals. Such tidal liquid ventilation strongly differs from the previously known TLV approach, opening promising perspectives for a safer clinical translation. Also disclosed are apparatus and method for safe and fast induction of hypothermia during liquid ventilation of a mammal.

A ventilator that utilizes a cam lever to raise a piston within a cylinder is provided. The weight of the piston can push breathable air out of the cylinder to a patient. A motor assembly provides the only electronic component necessary to operate the ventilator. Adjustments to volume, speed, and pressure can be made by adjusting mechanical components of the ventilator.

An exemplary example of a medical device can include a retention structure for at least partially encircling a patient's body, the retention structure including a central member and a support portion configured to be placed underneath a patient, a piston extending from the central member, a driver coupled to the piston configured to retract and extend the piston, a patient contact member attached to the piston, the patient contact member configured to adhere to the patient's body, and a controller. The controller can be configured to cause the driver during a session to perform at least two cycles of negative pressure ventilation, each of the at least two cycles of negative pressure ventilation including positioning the piston at a reference position, retracting the piston from the reference position to an expansion position to expand a chest of a patient to generate negative pressure ventilation, and returning the piston from the expansion position to the reference position.

Devices and methods for delivering air to a patient are provided. A device includes a first portion having a first airflow inlet and a sensor configured to sense airflow, the first portion defining a first airflow path, and a second portion comprising a second airflow inlet, an impeller, and an outlet for communicating airflow to a patient, the second portion defining a second airflow path. The device includes means for coupling the first portion and the second portion, such that the sensor sensing airflow in the first portion causes corresponding movement of the impeller, wherein the impeller is configured to impel air through the second airflow inlet and out of the outlet to the patient, upon movement of the impeller.

Embodiments of the present invention provide systems and methods for delivering respiratory treatment to a patient. For example, a treatment system may include a mechanism for delivering a positive pressure breath to a patient, and one or more limb flow control assemblies which modulate gas flow to and from the patient. Exemplary treatment techniques are embodied in anesthesia machines, mechanical ventilators, and manual ventilators.