Techniques described herein can identify usage information for sensors. In one example, an anesthesia device can include a processor to obtain usage information from a first flow sensor coupled to the anesthesia device. The processor can also determine the usage information exceeds a predetermined limit and generate an alert indicating the first flow sensor is to be replaced.

Systems and methods for lung-protective ventilation are disclosed. In examples, volume-targeted, pressure-controlled ventilation may deliver mandatory breaths to a patient without a rise time setting. Inputs into the ventilation may include a peak inspiratory flow value (Q.sub.peak) and a target tidal volume (V.sub.T,set). Respiratory parameters of the patient may be determined based on test breaths. The inputs and the respiratory parameters may be used to calculate a target inspiratory pressure (P.sub.i) and target rise time constant (τ). Breaths may then be delivered based on the calculated target inspiratory pressure and target rise time constant. Mechanical power delivered to the patient may also be monitored as an additional measure for patient lung protection.

A method of, or system for, ventilating lungs in breathing and non-breathing patients—including applications for anesthesia—may comprise maintaining an inspiratory flow rate at an inspiratory setpoint at a low flow setting. Lung pressure in a patient may be regulated between a high pressure setpoint and a low pressure setpoint with periodic expiratory flows and continuous inspiratory flow. An expiratory control valve may be adjusted to an open position when a lung pressure is at or above a high pressure setpoint. An expiratory control valve may be adjusted to a closed position when a lung pressure is at or below a low pressure setpoint. Concurrent venting outflow and CO.sub.2 offloading through flow within the lungs may be facilitated by providing an intermittent expiratory flow to the patient while providing the continuous inspiratory flow.

A respiratory treatment apparatus configured to provide a flow of breathable gas to a patient, including a breathable air outlet, an outside air inlet, and an pneumatic block module, wherein the pneumatic block module includes: a volute assembly including an inlet air passage, a mount for a blower and an outlet air passage; the blower being mounted in the mount such that an impeller of the blower is in a flow passage connecting the inlet air passage and the outlet air passage; a casing enclosing the volute assembly, wherein air passages within the casing connect air ports on the volute assembly, wherein the inlet air passage of the volute assembly is in fluid communication with the outside air inlet and the outlet air passage of the volute assembly is in fluid communication with the air outlet.

A pathogen detection system includes a pathogen sensing adaptor that detect pathogens present in the breathing circuit associated with a ventilated patient. A pathogen sensing adaptor may include a conduit, removable cartridges with testing strips, an optical sensor, and communication circuitry. Upon detecting a colorimetric change on the testing strip, the optical sensor generates a signal indicative of the presence and/or level of pathogens.

A breathing apparatus (1) is disclosed comprising an inspiratory channel (3), an expiratory channel (4), a patient interface (5), an oxygen valve (13) and a blower (7) comprising blower driving means (9). The blower (7) is arranged to produce a flow of air to the inspiratory channel (3). The oxygen valve (13) is configured to selectively deliver a flow of oxygen to the inspiratory channel (3). The breathing apparatus further comprises a control unit (19) configured to control the blower driving means (9) so that the blower (7) produces substantially no flow of air to the inspiratory channel (3) during a time period (tp). The present disclosure further relates to a method (100) of controlling operation of a breathing apparatus (1), a computer program and a computer program product (300) for performing a method (100) of controlling operation of a breathing apparatus (1).

A respiratory ventilation apparatus configured to deliver a respiratory gas to a patient interface is provided. The apparatus may include a gas pressurization unit configured to generate a pressurized respiratory gas, a gas inlet port configured to introduce the respiratory gas into the respiratory ventilation apparatus, a gas outlet port configured to discharge the pressurized respiratory gas to a respiration tube, a detection module configured to detect the pressure of the pressurized respiratory gas, at least one non-volatile memory configured to store a plurality of parameters and a plurality of programs, and one or more controllers. The one or more controllers may be configured to initiate the respiratory ventilation apparatus upon a boot operation, and/or initiate a program that constantly reads information from the detection module, and controls the pressure of the pressurized respiratory gas using the information read from the detection module and at least one parameter.

A computer-implemented method for detecting onset of a spontaneous breath by a patient coupled to a ventilation system includes receiving, at a processor, an electromyography (EMG) signal from an EMG sensor disposed on the patient. The method also includes pre-conditioning, via the processor, the EMG signal to separate the EMG signal into a plurality of components having EMG information utilizing a set of bandpass filters. The method further includes individually analyzing, via the processor, each component of the plurality of components to detect an onset of the spontaneous breath by the patient. The method still further includes determining, via the processor, the onset of the spontaneous breath by the patient is occurring when at least two components of the plurality of components indicate the onset of the spontaneous breath by the patient.

Systems and methods are provided for delivering anesthetic agent to a patient. In one embodiment, an anesthetic vaporizer includes a housing defining a sump, the sump configured to hold a self-contained supply of liquid anesthetic agent, a heating element electrically coupled to an electrical mating component, a gas inlet passage and a gas outlet passage, a manifold fluidically coupled to the gas inlet passage and the gas outlet passage, the manifold coupled to the housing and forming a gas-tight seal with the sump, and a quick disconnect pneumatic system coupled to the gas inlet passage and the gas outlet passage, sealing the gas inlet passage and the gas outlet passage from atmosphere.

A ventilator system, comprising: an inhalation pathway comprising an ambient air inlet, a bi-directional emergency valve, and a dynamic blower; and an exhalation pathway comprising a bi-directional exhalation valve and an exhalation port; wherein when a blockage occurs in the inhalation pathway, ambient air can be drawn from the exhalation port and through the bi-directional exhalation valve, and during exhalation exhalant exits the ventilator through the bi-directional exhalation valve and the exhalation port; wherein when a blockage occurs in the exhalation pathway, inhalant is delivered by the dynamic blower, and during exhalation the dynamic blower lowers its speed or stops and the exhalant exits the ventilator through the bi-directional emergency valve, the dynamic blower, and the ambient air inlet.