A fluid dynamic valve passively allows fluid flow out of a moving stream in one flow direction and not in the reverse. This allows the collection of fluid from a single direction of an AC fluid flow. The siphoned portion of the flow has a flow rate proportional to the mainstream flow. This device can collect exhaled breath or selective entrenchment during inhale. In one orientation, it can meter aerosolized particles into an inhale breath stream for pulmonary delivery, without complicated breath timing or possible large scale drug loss due to drug adsorption to the back of the throat. Alternatively, a user can breathe through the device and a proportional amount, relative to the volumetric flow rate, of each exhale can flow into an auxiliary chamber for analysis. In this arrangement, the fluid dynamic valve replaces the mechanical pump in a metabolic measurement apparatus. It collects a proportional volume of the exhale and none of the inhale for mixing-chamber breath analysis. In addition, the device also has to have a low respiratory burden and be comfortable to use.

A conventional flow tube for a metabolic cart is usually a straight length of pipe whose inner diameter is fixed by the respiratory burden imposed by the flow tube on the user, with a smaller diameter imposing a higher respiratory burden. The ratio of the straight flow tube's length to diameter is fixed by fluid dynamics, so increasing the flow tube's diameter causes the flow tube's length to increase. As the flow tube gets longer, it exerts more torque on the user's neck and jaw, creating discomfort. Reducing the flow tube's length causes an undesired increase in the respiratory burden but increasing the flow tube's diameter to reduce the respiratory burden makes the flow tube less comfortable, making the flow tube unconformable, hard to breathe through, or both. Bending the flow tube, e.g., in an L shape, makes it possible to increase the flow tube's propagation length without increasing the flow tube's lever arm length.

A portable inhalator device includes a housing with a mouthpiece for a user; a gas conduit coupled to the mouthpiece and configured to guide inhaling and exhaling gas flow within the device; a pressure sensor configured to monitor the gas flow in the gas conduit and to provide pressure differential signal for indicating direction of the gas flow through the gas conduit; a detection sensor configured to monitor the gas flow in the gas conduit and to provide characteristics signal for indicating composition of the gas flow through the gas conduit; and a dispenser configured to dispense a drug to the gas conduit.

A respiratory function testing system includes an air transforming device, a sound reception device and an operation device. The air transforming device is configured to collect exhaled and/or inhaled air for a predetermined period and generate a wide frequency range sound signal according to the collected respired air. The wide frequency range sound signal at least contains an ultrasonic signal. The sound reception device is configured to receive and record the wide frequency range sound signal as an audio file. The operation device is in communication with the sound reception device and is configured to receive and compute the audio file to generate a respiratory function parameter. Besides, the recorded wide frequency range sound signal may be converted into a spectrogram for further applications, and the computation of the audio file can be replaced by analyzing the spectrogram. A respiratory function testing method corresponding to the respiratory function testing system is also provided.

In particular embodiments, a method includes accessing, by a computing device, sensor data from a sensor of a client device corresponding to a user. The method further includes determining one or more segments of sensor data and selecting at least one segment of sensor data. The method further concludes determining, based at least on the selected segments of sensor data, one or more features corresponding to the user's pulmonary condition. The method further includes determining, based at least on the determined features, an assessment of the user's pulmonary condition.

A system for assessing extubation includes a respiratory assistance device, an artificial intelligence platform, and a hospital information system. The respiratory assistance device is adapted to communicate with a trachea of a patient. The artificial intelligence platform includes a prediction module. A method for assessing extubation includes the following steps. Measured values of respiratory parameters of the patient are recorded by the respiratory assistance device. The recorded times and the measured values of the respiratory parameters corresponding to each of the recording times are transmitted to the artificial intelligence platform. The prediction module analyzes the measured values of respiratory parameters within a predetermined time period according to a prediction model to generate a prediction result. The prediction result is transmitted to the hospital information system and is recorded into a medical record of the patient. With such design, a reference for extubation assessment that is more accurate is provided.

A method includes receiving, by an electronic device, sensor data during a spirometry test of a user, the sensor data comprising audio data of the user and distance data of a distance from a face of the user to the electronic device. The method also includes obtaining, by the electronic device, an amount of air volume exchange and at least one pulmonary health parameter that are determined based on the audio data and the distance data. The method also includes presenting an indicator on a display of the electronic device for use by the user or a medical provider, the indicator representing the amount of air volume exchange.

Devices and methods for allowing for improved assisted ventilation of a patient. The methods and devices provide a number of benefits over conventional approaches for assisted ventilation. For example, the methods and devices described herein permit blind insertion of a device that can allow ventilation regardless of whether the device is positioned within a trachea or an esophagus.

A system for monitoring the state of health of a patient suffering from respiratory disease including a portable medical device, the device including: a) a flow measurement device performing a spirometry measurement, and b) a reflecting photometric sensor performing an oxygen measurement or a measurement of blood oxygen saturation and heart rate. The system includes storage and comparison units in which a personalised plan of action for the patient is stored against which the spirometry and/or oxygen measurement data found are compared, displaying the result of such comparison on the display of a device connected to the internet so as to define the patient's state of health and identify exacerbation of the disease on the basis of data obtained from both such spirometry and oxygen measurements. A method for monitoring the health of a patient suffering from respiratory disease implemented through the system indicated above is also claimed.

Devices and methods for allowing for improved assisted ventilation of a patient. The methods and devices provide a number of benefits over conventional approaches for assisted ventilation. For example, the methods and devices described herein permit blind insertion of a device that can allow ventilation regardless of whether the device is positioned within a trachea or an esophagus. In addition, the methods and device allow for timed delivery of ventilations based on a condition of a thoracic cavity to increase the amount and efficiency of blood flow during a resuscitation procedure.