Abstract: A method for communicating with medical devices includes receiving, at a medical device communication interface, patient parameters from a first and second medical device in a respective first and second format. The method further includes identifying, at the medical device communication interface, a first and second protocol associated with the patient parameters by comparing the patient parameters and the first and second format to a predefined schema. The method further includes modifying, at the medical device communication interface, a respective configuration parameter for each of the first and second medical devices. The method further includes translating the patient parameters based on the first and second identified protocols and the respective configuration parameter for each of the first and second medical devices.

Abstract: This disclosure describes systems and methods for monitoring and evaluating ventilatory parameters, analyzing those parameters and providing useful notifications and recommendations to clinicians. That is, modern ventilators monitor, evaluate, and graphically represent multiple ventilatory parameters. However, many clinicians may not easily recognize data patterns and correlations indicative of certain patient conditions, changes in patient condition, and/or effectiveness of ventilatory treatment. Further, clinicians may not readily determine appropriate ventilatory adjustments that may address certain patient conditions and/or the effectiveness of ventilatory treatment. Specifically, clinicians may not readily detect or recognize the presence of asynchrony during ventilation.

Abstract: A tracheal tube assembly includes an outer cannula configured to be positioned in a patient airway and an inner cannula configured to be disposed inside the outer cannula. The tracheal tube assembly further includes a flange member secured about the outer cannula, and an outer cannula connector coupled to a proximal end of the outer cannula. The inner cannula includes a compressible proximal end region that is compressed while secured inside the outer cannula connector.

Abstract: A method for patient monitoring includes receiving first patient parameters from at least one machine. The method further includes transforming the first patient parameters into display parameters comprising at least one of a patient identifier, a patient status, and an alarm condition. Transforming is performed such that a first set of the display parameters is operable to be displayed on a screen, a second set of the display parameters is operable to be displayed on the screen in response to a rotation of the screen in a first direction, and a third set of the display parameters is operable to be displayed on the screen in response to a rotation of the screen in a second direction. The second set of the display parameters is not identical to the third set of the display parameters. The method further includes updating the display parameters in response to receiving second patient parameters.

Abstract: A tracheal tube assembly includes an outer cannula having a distal end and a proximal end, the distal end being adapted to be inserted into an airway of a patient. The assembly also includes an inner cannula adapted to be inserted into the outer cannula, a flange member disposed about the proximal end of the outer cannula, and a connector coupled to the proximal end of the outer cannula. The inner cannula and the connector form a contiguous passageway for exchanging fluid with the airway of the patient in operation. The assembly further includes an inner cannula status indication system that receives information regarding whether or not the inner cannula is an operable position with respect to the outer cannula, and, via the status indicator, provides a visual indication of whether or not the inner cannula is an operable position with respect to the outer cannula.

Abstract: This disclosure describes improved systems and methods for displaying respiratory data to a clinician in a ventilatory system. Respiratory data may be displayed by any number of suitable means, for example, via appropriate graphs, diagrams, charts, waveforms, and other graphic displays. The disclosure describes novel systems and methods for determining and displaying ineffective patient inspiratory or expiratory efforts or missed breaths in a manner easily deciphered by a clinician.

Abstract: This disclosure describes systems and methods for a ventilator-derived CPAP system that mimics the flow and/or pressure oscillations or fluctuations of the B-CPAP system creating a breath type referred to herein as a mimicked-bubble-CPAP (M-CPAP) mode. Further, the disclosure describes systems and methods for delivery of other breath types with flow and/or pressure oscillations or fluctuations that mimic the oscillation observed during ventilation with the B-CPAP system, referred to herein as adjusted breath types.

Abstract: A method for automating complex alerts includes receiving, at a complex alert interface, first parameters from at least one medical device and a first comparison operator. The first parameters and the first comparison operator are indicative of a first condition. The method further includes receiving, at the complex alert interface, second parameters from the at least one medical device and a second comparison operator. The second parameters and the second comparison operator are indicative of a second condition. The method further includes generating, at the complex alert interface, a complex alert expression based on a mathematical aggregate of the first condition and the second condition. The method further includes evaluating the complex alert expression to initiate display of at least one alert.

Abstract: Systems and methods for measuring a physiological parameter of tissue in a patient are provided herein. In a first example, a method of measuring a physiological parameter of blood in a patient is provided. The method includes emitting at least two optical signals for propagation through tissue of the patient, detecting the optical signals after propagation, identifying propagation pathlengths of the optical signals, and identifying detected intensities of the optical signals. The method also includes processing at least the propagation pathlengths to scale the detected intensities for determination of a value of the physiological parameter.

Abstract: A physiological monitoring system may use photonic signals to determine physiological parameters. The system may vary parameters of a light drive signal used to generate the photonic signal from a light source such that power consumption is reduced or optimized. Parameters may include light intensity, firing rate, duty cycle, other suitable parameters, or any combination thereof. In some embodiments, the system may use information from a first light source to generate a light drive signal for a second light source. In some embodiments, the system may vary parameters in a way substantially synchronous with physiological pulses, for example, cardiac pulses. In some embodiments, the system may vary parameters in response to an external trigger.

Abstract: A physiological monitoring system may use photonic signals to determine physiological parameters. The system may vary parameters of a light drive signal used to generate the photonic signal from a light source such that power consumption is reduced or optimized. Parameters may include light intensity, firing rate, duty cycle, other suitable parameters, or any combination thereof. In some embodiments, the system may use information from a first light source to generate a light drive signal for a second light source. In some embodiments, the system may vary parameters in a way substantially synchronous with physiological pulses, for example, cardiac pulses. In some embodiments, the system may vary parameters in response to an external trigger.

Abstract: Processing circuitry may process a physiological signal such as a light signal attenuated by a subject. The physiological signal may include a desired component and an undesired component. A first filtering operation may be performed to remove at least a portion of the undesired component and a second filtering operation may be performed to reduce an undesired distortion introduced by the first filter. The transfer function of the second filter may be substantially the inverse of the transfer function of the first filter. One or more physiological parameters may be determined based on the filtered physiological signal.

Abstract: A physiological monitoring system may use photonic signals to determine physiological parameters. The system may vary parameters of a light drive signal used to generate the photonic signal from a light source such that power consumption is reduced or optimized. Parameters may include light intensity, firing rate, duty cycle, other suitable parameters, or any combination thereof. In some embodiments, the system may use information from a first light source to generate a light drive signal for a second light source. In some embodiments, the system may vary parameters in a way substantially synchronous with physiological pulses, for example, cardiac pulses. In some embodiments, the system may vary parameters in response to an external trigger.

Abstract: A system to optically measure a physiological parameter of tissue of a patient is provided. The system includes a tissue interface assembly configured to emit an optical signal into the tissue, receive a first measurement signal based on the optical signal propagating along a first path, receive a second measurement signal based on the optical signal propagating along a second path, and transfer the first measurement signal and the second measurement signal for delivery to a processing system. The processing system is coupled to the tissue interface assembly and configured to receive the first measurement signal and the second measurement signal, determine a phase delay between the first measurement signal and the second measurement signal based on a cross correlation analysis, and identify a value of the physiological parameter of the patient based on at least the phase delay between the first measurement signal and the second measurement signal.

Abstract: According to various embodiments, methods and systems for determining pressure in an inflatable cuff of a tracheal tube may employ pressure transducers associated with a cuff inflation line or a pilot balloon assembly. The pressure transducers may be implemented to provide continuous or intermittent cuff pressure. Also provided are tracheal tubes with adapters or other devices that incorporate pressure transducers. The tracheal tubes may facilitate wireless cuff pressure monitoring.

Abstract: Embodiments described herein may include systems and method for monitoring physiological parameters of a patient. Specifically, embodiments disclose wireless, reusable, rechargeable medical sensors that include an inductive coil coupled to a rechargeable battery. Additionally, embodiments disclose systems and methods for recharging and disinfecting the disclosed medical sensors.

Abstract: Embodiments described herein may include systems and method for monitoring physiological parameters of a patient. Specifically, embodiments disclose wireless, reusable, rechargeable medical sensors that include an inductive coil coupled to a rechargeable battery. Additionally, embodiments disclose systems and methods for recharging and disinfecting the disclosed medical sensors.

Abstract: Embodiments described herein may include systems and method for monitoring physiological parameters of a patient. Specifically, embodiments disclose wireless, reusable, rechargeable medical sensors that include an inductive coil coupled to a rechargeable battery. Additionally, embodiments disclose systems and methods for recharging and disinfecting the disclosed medical sensors.

Abstract: This disclosure describes systems and methods for providing an optimized proportional assist breath type during ventilation of a patient. The disclosure describes a novel breath type that delivers a target airway pressure calculated based on a desired patient effort range to a triggering patient.

Abstract: This disclosure describes systems and methods for controlling an exhalation valve based on pressure and/or flow measurements during exhalation. The disclosure describes novel exhalation valve controls for ventilating a patient.