Abstract: The invention concerns a gas delivery system (1, 2) for providing gaseous Nitric Oxide (NO) to a patient comprising a medical ventilator (2) providing a respiratory gas, such as air, to a patient breathing circuit (3) having an inspiratory limb (31) with a flow sensor (100) and an NO injection module (110), and a NO-delivery device (1) for providing a NO-containing gas to the NO injection module (110) of the inspiratory limb (31), said NO delivery device (1) including a control unit (130) and a differential pressure sensor (104). The medical ventilator (2) can be a High Frequency Oscillatory (HFO) ventilator.

Abstract: A system and method is disclosed for performing diagnostics on patient devices (720). The patient devices (720) may include respiratory therapy devices that operate in accordance with instruction sets, such as software or firmware. A server (710) may maintain a database of diagnostic data (718) indicating faults in one or more of a plurality of patient devices (720). The server (710) may transmit this diagnostic data (718) to one or more computing devices (760), including identification of faults that have occurred. The server (710) may also transmit service data to the plurality of patient devices (720) in order to address the identified faults.

Abstract: A flowmeter has a disposable flow tube and a part of the shutter which are in direct contact with exhaled air and protect the rest of the device from potential contamination with harmful viruses.

Abstract: Techniques for determining a volume of exhaled CO2 as a function of time using side-stream capnography, including obtaining flow dynamics measurements of a subject from a flow sensor; obtaining CO2 concentration measurements of the subject from a side-stream CO2 monitor; determining a duration of time (?Ts1) for a sample of gas to flow from a reference point to the side-stream CO2 monitor; synchronizing in time the CO2 concentration measurement with the flow dynamics measurement, based on the determined ?Ts1; and determining a volume of CO2 exhaled as a function of time, based on the flow dynamics measurement and the synchronized CO2 concentration measurement.

Abstract: Systems, devices, and methods for determining a user's lung capacity may employ a sound-producing breathing device and a recording device such as a microphone included in a user electronic device (e.g., smart phone or tablet computer). A user may inhale or exhale through the sound-producing breathing device, thereby producing a sound that is received by the microphone and communicated to a processor. The processor may analyze the received sound recording to determine one or more sound intensity values over, for example, the duration of the received sound and/or points in time within the sound recording. The sound intensity values may then be used to determine the user's lung capacity.

Abstract: This description relates to insight into the asthma management habits of a patient or a plurality of patients. The provided information includes records of rescue medication usage events, records of controller medication events, and overall evaluations of a patients disease management. Users of the application may include both patients who may use the information to monitor their own habits or providers who may use the information to monitor patients or improve a patient's existing medication regimen.

Abstract: Recognizing mental states from physiological signal is a concern not only for medical diagnostics, but also for cognitive science, behavioral studies as well as brain machine interfaces. Embodiments of the present disclosure utilize respiration signals to decipher mental states wherein non-linear baseline drifts in signal is implemented to extract the respiratory features in most effective way. Presence of class imbalance, is effectively rectified using Synthetic Minority Oversampling Technique (SMOTE) to resolve class imbalance problem, which not only increased the classification accuracy, but also reduced classifier bias towards the majority class, which in turn exceedingly enhanced the classifier sensitivity.

Abstract: Telematics and external data relating to the real-time driving of a population of drivers vehicle may be collected and used to calculate a driving pattern map. The driving pattern map is used to determine a driving quotient for individual drivers wherein the driving quotient is a relative score. The driving quotient may be displayed to the driver.

Abstract: A system for calculating cardiac output (CO) of a patient undergoing veno-arterial extracorporeal oxygenation includes measuring first oxygenated blood flow rate by a pump in the extracorporeal blood oxygenation circuit as introduced into an arterial portion of the patient circulation system and a corresponding arterial oxygen saturation, then changing the pump flow rate, such as decreasing, to produce a corresponding change in arterial oxygen saturation (wherein such change is outside of normal operating variances, operating errors or drift), which change in the arterial oxygen saturation is measured. From the first flow rate and the second flow rate along with the corresponding measured arterial oxygen saturation, the CO of the patient can be calculated, without reliance upon a measure of venous oxygen saturation.

Abstract: Systems, apparatuses, and methods are disclosed for optimizing management of one or more implanted artificial heart pumps. An example method includes wirelessly retrieving, via one or more portable diagnostic devices, data regarding the one or more implanted artificial heart pumps. The example method further includes analyzing, by a server device, performance characteristics of the one or more implanted artificial heart pumps based on the retrieved data. The example method further includes causing rendering of the performance characteristics. Corresponding apparatuses and computer program products are contemplated.

Abstract: A non-invasive method and system is provided for determining an internal component of respiratory effort of a subject in a respiratory study. Both a thoracic signal (T) and an abdomen signal (A) are obtained, which are indicators of a thoracic component and an abdominal component of the respiratory effort, respectively. A first parameter of a respiratory model is determined from the obtained thoracic signal (T) and the abdomen signal (A). The first parameter is an estimated parameter of the respiratory model that is not directly measured during the study. The internal component of the respiratory effort is determined based at least on the determined first parameter of the respiratory model. The first model parameter is determined based on the thorax signal (T) and the obtained abdomen signal (A) without an invasive measurement.

Abstract: The present disclosure describes a system for metabolic monitoring comprising: collecting exhaled gas from nasal airways of a subject; a mixing chamber for receiving a portion of the exhaled gas; a plurality of sensors for outputting signals related to gas parameters related to inhaled gas and exhaled gas during one or more breaths; and processors configured to determine a flow rate of gas in the interface appliance; determine pressure changes near the mouth of the subject to detect mouth breathing of the subject; determine concentration measurements of O2 and CO2 of the portion of the exhaled gas in the mixing chamber, and discard concentration measurements corresponding to mouth breathing; determine a rate of oxygen consumption VO2 and a carbon dioxide production VCO2 of the subject based on the determined flow rate, the CO2 concentration, and the determined O2 concentration.

Abstract: Systems and methods are provided for an air flow sensor assembly for a medical gas flow device. In one embodiment, a system for an air flow sensor assembly for a medical gas flow device includes an air flow passage having a flexible reed positioned therein, the flexible reed fixedly coupled to the air flow passage via an attachment point and having an edge smaller than an inner passage wall of the air flow passage, a planar surface of the flexible reed extending into a flow path of air flow through the air flow passage, and a strain gauge coupled to the planar surface of the flexible reed.

Abstract: Determining sleep patterns of a user includes detecting a plurality of point clouds, each corresponding to a different position of the user at different times, forming a plurality of bounding boxes, each corresponding to coordinates of captured points of one of the point clouds, creating a wake/sleep classifier based on features of the point clouds, determining sleep positions of the user as a function of time based on the bounding boxes, and determining sleep patterns of the user based on the sleep positions of the user and on results of the sleep/wake classifier. Detecting a plurality of point clouds may include using a tracking device to capture movements of the user. The features of the point clouds may include intermediate data that is determined using scalar velocities of points in the point clouds, absolute velocities of points in the point clouds, and/or counts of points in the point clouds.

Abstract: A system (400) for monitoring an individual's sleep includes: (i) a patient monitor (410) configured to obtain a patient waveform, the patient waveform comprising information representative of a vital statistic of the patient; a processor (420) in communication with the patient monitor and configured to: (i) process the patient waveform to generate a segmented waveform; (ii) extract at least one feature from a segment of the waveform in a time domain and/or at least one feature from the segment of the waveform in the frequency domain; (iii) classify, using the at least one extracted feature, a sleep stage of the patient for the segment of the waveform; and (iv) generate, from classified sleep stages for a plurality of segments of the waveform, a sleep quality measurement; and a user interface (480) configured to report the generated sleep quality measurement.

Abstract: In vitro methods for diagnosing, prognosing and/or monitoring and treating neutrophilic or eosinophilic airway inflammation in a subject, including determining the amount of one or more volatile organic compounds (VOCs) in exhaled breath from said subject. The invention also provides devices for use in said methods.

Abstract: A breathing mask including a vent system for ventilating the mask, a detector for providing respiration data of a user and located for sensing at least one physical property of air inside the breathing mask when worn by a user and a controller configured to activate the vent system based on the respiration data. The controller may be configured to predict future respiration data based on historic respiration data of at least one earlier detected inhaling or exhaling cycle, determine whether a future inhaling or exhaling cycle will occur based on predicted future respiration data and activate the vent system before the determined future inhaling or exhaling cycle commences.

Abstract: A low-cost, magnetically-driven device that enables visualization and quantification of dynamic changes in cell behavior during mechanical stretch. Using this device, it was observed that nuclei of mouse embryonic skin fibroblasts underwent rapid but divergent responses to strain magnitude, showing nuclear area increase and chromatin decompaction during 5% (low) strain, but nuclear area decrease and chromatin condensation during 20% (high) strain. Only responses to low strain were dependent on calcium, while actin inhibition abrogated any nuclear response and increased stretch-induced DNA damage. Stretch-activation revealed a shift in actin filaments away from (low strain) or towards (high strain) the nuclear periphery. The findings suggest that different pathways control strain level-dependent cell behavior and that mechanical confinement of nuclei through actin may be a protective mechanism during high strain loads.

Abstract: Systems, devices, and methods for determining a user's lung capacity may employ a sound-producing breathing device and a recording device such as a microphone included in a user electronic device (e.g., smart phone or tablet computer). A user may inhale or exhale through the sound-producing breathing device, thereby producing a sound that is received by the microphone and communicated to a processor. The processor may analyze the received sound recording to determine one or more sound intensity values over, for example, the duration of the received sound and/or points in time within the sound recording. The sound intensity values may then be used to determine the user's lung capacity.

Abstract: A method of diagnosing an air leak in a lung compartment of a patient may include: advancing a diagnostic catheter into an airway leading to the lung compartment; inflating an occluding member on the catheter to form a seal with a wall of the airway and thus isolate the lung compartment; measuring air pressure within the lung compartment during multiple breaths, using the diagnostic catheter; displaying the measured air pressure as an air pressure value on a console coupled with the diagnostic catheter; and determining whether an air leak is present in the lung compartment based on the displayed air pressure value during the multiple breaths.

Abstract: A portable sampling device (1) for collecting particles in a stream of exhaled breath comprising a housing (10) with an inlet (11) and an outlet (12) arranged to guide the stream of exhaled breath therethrough, a collecting device holder (20) arranged at least partially inside the housing and comprising at least one flow path (21) in fluid connection with the inlet in which a collecting device (30) is arranged, the collecting device being adapted to collect the particles in the exhaled breath, wherein the collecting device has a diameter smaller than the flow path diameter and is movably arranged in the collecting device holder.

Abstract: In some implementations, a system may receive, from a differential pressure sensor, a differential pressure measurement associated with a differential pressure across an air filter within an airway of a manual ventilator. The system may determine, based on the differential pressure measurement, an air flow rate through the airway. The system may determine timing of a compression cycle of the manual ventilator. The system may determine, based on the timing, a flow threshold associated with a desired breathing cycle. The system may determine a difference between the flow threshold and the air flow rate. The system may provide, via a display associated with the manual ventilator, a representation associated with the difference to indicate whether a compression parameter of the compression cycle is to be adjusted.

Abstract: A system for determining a set of at least one cardio-respiratory descriptor of an individual during sleep comprises a memory device having a first accelerometer for a thoracic position, a second accelerometer synchronized with the first and for an abdominal position, and an optional sensor (e.g., a photoplethysmographic sensor). The system also includes memory for recording accelerometer and optional sensor data; memory with a reference model; and a device for filtering accelerometer data and configured to extract low-, medium-, and high- frequency ranges. A computer is configured for determining, within the extracted frequency ranges, at least one characteristic representative of a cardio-respiratory and physiological state and the time of the extraction thereof; comparing the determined characteristic(s) with similar characteristics from the reference model; and deducing therefrom a set of at least one probable corresponding event the individual experienced during a predetermined period of time.

Abstract: Approaches described herein can determine one or more breathing phase patterns over a period of time using audio data captured by at least one microphone. The audio data can include one or more snores. A breathing phase pattern included within the period of time can be determined based at least in part on sensor data captured by one or more sensors in the electronic device. A determination can be made that a first breathing phase pattern represented by the audio data and a second breathing phase pattern represented by the sensor data are correlated. A determination can be made that the first breathing phase pattern represented by the audio data and the second breathing phase pattern represented by the sensor data both correspond to a user wearing the electronic device.

Abstract: A method of cough detection in a headset, the method comprising: receiving a first signal from an external transducer of the headset; receiving a second signal from an in-ear transducer of the headset; and detecting a cough of a user of the headset based on the first and second signals.

Abstract: A breath parameter measuring device is described which takes into account breathing patterns which historically have been incompatible with accurate measurements. In particular, during fast breathing patterns, the sensor performing the measurement may not be able to respond quickly enough to provide the true reading. The disclosure may be useful for example in the case of neonatal breath carbon dioxide measurements.

Abstract: A flow sensor for pulmonary function testing is provided, and the flow sensor is capable of preventing cross-infection and has a hollow tubular structure. The flow sensor includes a main breather tube and a pressure tapping hole arranged on a tube wall of the main breather tube. An outer wall of the main breather tube is provided with a pressure tapping stub in air communication with the pressure tapping hole. The volume of an inner cavity of the pressure tapping stub satisfies following condition: during the pulmonary function testing, air exhaled or inhaled by a tester enters the pressure tapping stub through the pressure tapping hole and is kept within the pressure tapping stub without contacting a connection pipeline outside of the flow sensor. The flow sensor can isolate contaminants, i.e., bacteria or viruses and prevent the contaminants from entering other connection pipelines or cavities of a pulmonary function instrument.

Abstract: A resuscitator has a patient airway interface device, a bag, a fluid passage coupled between the bag and patient airway interface device, and a sensor module. The patient airway interface device may be a mask or an endotracheal tube. The sensor module can have a display, at least one sensor coupled to the flow passage and configured to provide a measurement of at least one parameter, and a processor coupled to the display and the at least one sensor. The processor is configured to receive the measurement from the sensor and provide information on the display based on the received measurement. The information may include a current breath rate, a pressure-vs-time curve, and guidance to the user to assist in achieving a target breath rate.

Abstract: An apparatus for measuring fluid flow includes a housing, a first ultrasonic transducer, and a fluid flow path. The housing defines a smooth bore and a first cavity. The first cavity is separated from a fluid that flows through the smooth bore. The first ultrasonic transducer is disposed within the first cavity and transmits an ultrasonic pulse through the fluid. The fluid flow path extends from an upstream intake through the cavity.

Abstract: Methods, systems, and apparatus, including computer programs encoded on computer-storage media, for collecting monitoring data and predicting outcomes for communities. In some implementations, monitoring data is received, including location tracking data that indicates locations visited by individuals in a community. Community data for the community that describes characteristics of the community and a geographic region associated with the community is received. One or more predictive models are used to evaluate regions for potential for transmission of a disease based on behavior patterns of individuals in the community. The one or more predictive models can be models trained based on training data describing a plurality of different communities and behavior patterns and disease outcomes of individuals in the different communities over time.

Abstract: The present invention provides devices and methods for creating and/or maintaining patency of the upper airway passage. The device is configured to fit under the chin of a subject at an external location corresponding approximately with the subject's internal soft tissue associated with the neck's anterior triangle. The device includes structural elements designed to optimize comfort, compliance and seal achieved through minimizing the pressure variation along the contact surface of the therapy device.

Abstract: A device for monitoring breathing activity of, e.g., athletes while exercising includes a breathing activity sensor configured to be worn by a wearer and to provide a breathing activity signal indicative of the breathing activity of the wearer. A motion sensor is configured to be worn by the wearer and to provide a motion signal indicative of the motion activity of the wearer. A processing arrangement is coupled to the breathing activity sensor to process the breathing activity signal and produce a processed breathing activity signal. The processing arrangement includes filter circuitry having a first filtering bandwidth and a second filtering bandwidth. The first filtering bandwidth is larger than the second filtering bandwidth. The filter circuitry is coupled to the motion sensor and operates with one of the first filtering bandwidth and the second filtering bandwidth selected as a function of the motion signal from the motion sensor.

Abstract: A method of deriving one or more individual thoracic parameters of a subject. The method comprises instructing a subject to perform a thoracic volume manipulation, receiving a plurality of measurements of a plurality of EM signals from a thoracic intrabody area of lungs of the subject during the thoracic volume manipulation, deriving a plurality of thoracic volume values at a plurality of different intervals during the thoracic volume manipulation so that each the thoracic volume value correspond with another of a plurality of estimated thoracic volumes achieved during the thoracic volume manipulation, and calculating at least one individual thoracic parameter of the subject by combining between the plurality of measurements and the plurality of thoracic volume values.

Abstract: Devices, systems, and methods for visually depicting a vessel and evaluating treatment options are disclosed. The methods can include obtaining pressure measurements from first and second instruments positioned within a vessel of a patient while the second instrument is moved longitudinally through the vessel from a first position to a second position and the first instrument remains stationary within the vessel; and outputting a visual representation of the pressure measurements obtained by the first and second instruments on a display, the output visual representation including a graphical display of a pressure ratio of the obtained pressure measurements and at least a portion of a pressure waveform of the obtained pressure measurements identifying a diagnostic period utilized in calculating the pressure ratio.

Abstract: Provided is a medical observation device which includes a detection unit configured to detect a pressing operation based on an operation signal according to the pressing operation which is output from an external operation device equipped with a switch pressed by a mouth, and a processing unit configured to perform a process corresponding to the detected pressing operation. The process corresponding to the pressing operation includes some or all of a process related to an imaging operation of an imaging device, a process related to a display of a medical captured image which is captured in the imaging device, and an identification process of identifying a user's input indicating the process related to the imaging operation or the process related to the display of the medical captured image.

Abstract: The sensor device includes a sensor unit that detects information of an object, an attachment portion detachably attached to one or more attachment positions on the object, and an acquisition unit that acquires information indicating the attachment position to which the attachment portion is attached.

Abstract: The invention relates to a respiratory flow sensor (11) comprising a flow tube (12) which has a flow channel (13) and tube connections for tubes at the free ends (15, 17) of the flow tube, a cover flap (32) which is arranged in the flow channel (13) and divides the flow channel (13) into a first flow channel section (18) and a second flow channel section (19), and comprising connections (22, 23) which open into the flow channel (13) on both sides of the cover flap (32) and which are used to decrease the pressure difference generated by the cover flap (32). A drainage device (41) which comprises drain grooves (42, 43) is provided in the flow channel (13), and the cover flap (32) has a hinge region which is formed by a first slot and a second H-shaped slot.

Abstract: A pulmonary health monitoring system aims at assessing pulmonary health of subjects. Conventional techniques used for pulmonary health monitoring are not convenient to the subjects and needs considerable cooperation from the subjects. But, there is a challenge in utilizing the conventional devices to the subjects not capable of providing considerable cooperation. The present disclosure includes a blow device applicable to all kind of subjects and doesn't need cooperation from the subjects. Further, in the present disclosure, the blow device generates a phase shifted signal corresponding to a breathe signal and the phase shifted signal is further processed to extract a set of physiological features. Further, pulmonary health of a subject is analyzed by processing the set of physiological features based on a ridge regression based machine learning technique.

Abstract: A method, apparatus, and system for measuring respiratory effort of a subject are provided. According to the method, a thoracic effort signal (T) is obtained, the thoracic effort signal (T) being an indicator of a thoracic component of the respiratory effort. An abdomen effort signal (A), the abdomen effort signal (A) being an indicator of an abdominal component of the respiratory effort. A respiratory flow (F) is obtained. The respiratory effort is determined by adjusting the components of a model of the respiratory system based on the thoracic effort signal (T), the abdomen effort signal (A), or the respiratory flow (F) or any combination of the thoracic effort signal (T), the abdomen effort signal (A), and the respiratory flow (F).

Abstract: A medical ventilator (10) performs a method including: receiving measurements of pressure of air inspired by or expired from a ventilated patient (12) operatively connected with the medical ventilator; receiving measurements of air flow into or out of the ventilated patient operatively connected with the medical ventilator; dividing a breath time interval into a plurality of fitting regions (60); and simultaneously estimating respiratory system's resistance and compliance or elastance, and respiratory muscle pressure in each fitting region by fitting to a time series of pressure and air flow samples in that fitting region. In one approach, the fitting includes parameterizing the respiratory muscle pressure by a continuous differentiable function, such as a polynomial function, over the fitting region.

Abstract: A medical measuring device (2), as well as to a ventilator (1), as well as to a method for operating a medical measuring device (2) or a ventilator are provided. The medical measuring device (1) includes a sensor system (14) and measuring, signal processing and calculating device (21), to detect an inspiratory measured variable, which represents an indicator for the transport of breathing gases into the lungs of a patient (80), and an expiratory measured variable, which represents an indicator for the transport of breathing gases out of the lungs of a patient (80), and to determine an indicator for a ventilation-related shifting of secretion from the expiratory measured variable and the inspiratory measured variable.

Abstract: A measurement module determines a fluid quantity which relates to a property of a fluid located in or flowing through a measurement tube. The measurement module contains a base body, a control device and first and second oscillation transducers fastened at a distance from one another on the base body. The first and/or the second oscillation transducer is controlled by the control device to excite an oscillation of a side wall of the measurement tube when a contact face of the measurement module is coupled to the side wall of the measurement tube directly or via a coupling layer. The oscillation of the side wall excites compression oscillations of the fluid, which are conducted through the fluid to the respective other oscillation transducer and recorded the control device to determine a measurement quantity. The fluid quantity can be determined by the control device in dependence on the measurement quantity.

Abstract: A monitoring system (10) includes at least one video camera (14), a motion unit (40), and a segmentation unit (42). The at least one video camera (14) is configured to continuously receive video of a subject in normal and darkened room conditions. The motion unit (40) identifies clusters of motion of the subject based on respiratory and body part motion in the received video of the subject. The segmentation unit (42) segments body parts of the subject based on the identified clusters of subject motion.

Abstract: A system for a medical system includes a position sensing unit to sense a displacement of a medical device from a medically operational point on a subject, and a signal processing circuit to output, based on the sensed displacement, a signal to disable an alert system when the medical device is for sensing a physiological parameter of a subject during a medical procedure and the displacement is greater than a first threshold value, or to output a signal to enable the alert system when the medical device is for delivering treatment to the subject and the displacement is greater than a second threshold value.

Abstract: According to an aspect, a testing instrument that is used for testing an airway protection function includes: a pipe portion continuous from an inlet port to an outlet port, the pipe portion having a plurality of holes penetrating the pipe portion from an outer surface of the pipe portion to an inner surface of the pipe portion, the holes being provided for guiding a reagent gas mixture to the inside of the pipe portion; and a guide portion covering all of the holes to form a closed space and guiding the reagent gas mixture to the closed space from an inflow port.

Abstract: A CPAP apparatus is provided that determines the presence of a snore by the simplified method of using filtered expiratory noise as the measure of intrinsic device noise and comparing that to filtered inspiratory noise. The filtering time constants for inspiratory and expiratory noise are adjusted such that treatment pressure does not cause false snore detection.

Abstract: A method, apparatus, and system for measuring respiratory effort of a subject are provided. A thorax effort signal and an abdomen effort signal are obtained. The thorax effort signal and the abdomen effort signal are each divided into a volume-contributing component of the respiratory effort and a paradox component. The paradox component represents a non-volume-contributing component of the respiratory effort. The abdomen paradox component is negatively proportional to the thoracic paradox component. The thorax effort signal or the abdomen effort signal or both are weighted by a weight factor to obtain a volume-proportional signal. The volume-proportional signal is proportional to the actual respiratory volume of the respiratory effort. A calibration factor for calibrating the thorax effort signal and the abdomen effort signal is obtained by optimizing the weight factor by minimizing thoracic paradox component and the abdomen paradox component.

Abstract: Assessing the sleep quality of a user in association with an electronic device with one or more physiological sensors includes detecting an attempt by the user to fall asleep, and collecting physiological information associated with the user. The disclosed method of assessing sleep quality may include determining respective values for one or more sleep quality metrics, including a first set of sleep quality metrics associated with sleep quality of a plurality of users, and a second set of sleep quality metrics associated with historical sleep quality of the user, based at least in part on the collected physiological information and at least one wakeful resting heart rate of the user, and determining a unified score for sleep quality of the user, based at least in part on the respective values of the one or more sleep quality metrics.

Abstract: Methods and systems to measure a volumetric fluid flow rate through a fluid flow passage, such as an air handler of a HVAC system, are described. The system includes an air intake conduit. The air intake conduit includes a partition, an airflow measuring passage through the partition, and an airflow flow-through passage. The partition and the airflow flow-through passage are arranged in a side-by-side fashion. The airflow measuring passage is equipped with an airflow measuring device to measure the air pressure drop in the airflow measuring passage and has a minimal air pressure drop requirement. The air intake conduit has a minimal volumetric air intake requirement. When the air intake conduit has the minimal volumetric air intake, the air pressure drop measured at the airflow measuring passage is at the minimal air pressure drop requirement.

Abstract: A respiratory therapy instrument providing a telehealth platform for pulmonary care includes a housing with opposed extension arms, an airway tube removably clamped between the opposed extension arms, a pair of pressure sensors, and a circuit board retained within the housing. The pressure sensors are in communication with an interior of the airway tube and are configured to detect pulmonary flow data within the airway tube. The circuit board is configured to collect the pulmonary flow data detected by the pair of pressure sensors and includes a transmitter to send data, including the collected pulmonary flow data, wirelessly to a computing device. The collected pulmonary flow data is utilized in game play for an incentivization game operated on the computing device.