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, a tracheal tube may include signal sources for providing information at various locations on the tube or in an inflated cuff. The signals from the signal sources may be triangulated to determine the location of the tube in relation to a reference point on the body. The location information may provide an indication as to whether or not the tracheal tube is properly placed within the trachea.

Abstract: Provided herein are methods and apparatuses for certifying computers for use in conjunction with medical devices. These methods may be used in conjunction with a computer that includes software for operating the medical device. To certify a particular computer, one or more testing algorithms or routines for processing data, e.g., data representative of a typical output generated by use of the medical device on a patient, may be executed and the results may be compared to an expected result. In particular embodiments, the certification process may use data stored on the device itself to determine certification or may use data stored with or bundled with the software for operating the device.

Abstract: An apparatus and method for removing contaminant species from water by electrocoagulation are described. Alternating grounded, rotating, planar circular electrodes and stationary planar electrodes function as a Tesla fluid pump when placed in contact with the contaminated water, causing the water to flow between the rotating and stationary electrodes. An insoluble abrasive material introduced into the water removes scale from the electrodes while the water is pumped thereby. A direct electric current is caused to flow between each pair of rotating and stationary electrodes, thereby producing electrocoagulation of the contaminants in the water flowing therebetween. The electrocoagulated materials may be separated from the treated water by filtration or by permitting the treated water to stand for a chosen period.

Abstract: According to various embodiments, a tracheal tube may include signal sources for providing information at various locations on the tube or in an inflated cuff. The signals from the signal sources may be triangulated to determine the location of the tube in relation to a reference point on the body. The location information may provide an indication as to whether or not the tracheal tube is properly placed within the trachea.

Abstract: Systems and methods for measuring a physiological parameter of blood in a patient are provided herein. An example method includes establishing with a magnetic array, an first magnetic field along tissue of the patient inserted into the magnetic array and a second magnetic field perpendicular to the tissue, emitting optical signals into further tissue of the patient during at least a first alignment of the magnetic array around the tissue, detecting characteristics of the optical signals, and identifying a value of a physiological parameter based on at least the characteristics of the optical signals.

Abstract: According to various embodiments, an endotracheal tube ventilating device with a sealing cuff includes an anchoring device. The anchoring device may be secured to the tube above the sealing cuff and extend outwardly from the tubular body. In addition, the anchoring device may be configured to be positioned completely within the hypopharynx of a patient, in contact with the piriform fossa and a laryngeal surface of the epiglottis without creating an airtight seal of the hypopharynx or the esophagus.

Abstract: The present invention provides a method for measuring FeNO in a subject, wherein the FeNO data derived from a subject patient is normalized to compensate for variations of FeNO with flow rate.

Abstract: Various embodiments of an intubation system include a tracheal tube and an illumination assembly that is removably couplable to a tubular body of the tracheal tube. The tracheal tube may be a double lumen tracheal tube having a first cuff that is adapted to be inflated to seal against the walls of a patient's trachea and a second cuff that is adapted to be inflated to seal against the walls of the patient's bronchial stem. The illumination assembly may have one or more illumination devices that are adapted to produce light within the patient's trachea, the patient's bronchial stem, or both when the illumination assembly is coupled to the tubular body.

Abstract: The present disclosure describes systems and methods having a dual-lumen tube with an assembly end. The assembly end may be molded and coupled to an extruded portion of the tube to form a complete dual-lumen tube. The assembly end may form the distal portion of the dual-lumen tube, which may simplify the manufacturing process by eliminating cutting and shaping steps involved in forming the distal ends of the ventilation lumens. The assembly end may be molded or otherwise formed so that the distal portion is not cut to length. In addition, the assembly end may include addition functionality, such as a camera apparatus or one or more sensors.

Abstract: The present disclosure describes systems and methods that utilize a multi-lumen tube with an integral visualization apparatus, such as a camera. The multi-lumen tracheal tube system may include a camera apparatus that is positioned to facilitate left or right bronchial intubation. In addition, the camera apparatus may be a unitary assembly that functions to hold and position the camera relative to the tube and provides an acceptable profile for comfortable intubation. The camera apparatus may include additional components, such as integral light sources and flushing or cleaning devices to remove any buildup from the camera or optical components.

Abstract: Provided herein are methods and apparatuses for certifying computers for use in conjunction with medical devices. These methods may be used in conjunction with a computer that includes software for operating the medical device. To certify a particular computer, one or more testing algorithms or routines for processing data, e.g., data representative of a typical output generated by use of the medical device on a patient, may be executed and the results may be compared to an expected result. In particular embodiments, the certification process may use data stored on the device itself to determine certification or may use data stored with or bundled with the software for operating the device.

Abstract: Various embodiments of an intubation system include a tracheal tube, a heat source coupled to the tracheal tube, and a temperature sensor disposable in a patient's trachea to detect a temperature within the patient's trachea. The heat source is adapted to generate heat when the tracheal tube is disposed in the airway of the patient. A temperature control system coupled to the heat source is adapted to monitor the detected temperature and to control generation of heat from the heat source based on the detected temperature.

Abstract: Various embodiments of a tracheal tube having a suction lumen are provided. For example, the suction lumen may be associated with two spaced apart pressure transducers, whereby a pressure drop between the transducers indicates that the suction lumen is free of blockages and a characteristic lack of pressure drop and/or particular pressure curve is indicative of a blockage. In addition, embodiments may include a tracheal tube with sensors configured to sense a buildup of secretions. The sensors may be located proximate to an opening in the suction lumen. In other embodiments, a blockage-clearing system for a suction lumen may be provided that blows air into the suction lumen to clear blockages. In particular, in certain embodiments, the blockage-clearing system may operate to create its own pressurized air source by utilizing the pressure change created in the suction line by a blockage.

Abstract: Various embodiments of a tracheal tube having a multifunctional lumen disposed in a tracheal tube wall are provided. Provided tracheal tubes include a ventilation lumen, through which bidirectional airflow may be established to and from a patient during operation, as well as a multifunctional lumen adapted to receive a variety of interchangeable medical devices. Embodiments of the provided tracheal tubes may provide for insertion or removal of a medical device from the multifunctional lumen without extubation of the tracheal tube from a patient.

Abstract: According to various embodiments, methods and systems for determining pressure in the lungs may employ tracheal pressure measurements. The tracheal pressure measurements may be obtained through a pressure monitoring lumen associated with a tracheal tube. Such systems may include a purging or flushing mechanism to keep the pressure monitoring lumen free of any obstructions. The flushing mechanism may utilize fluids delivered through the pressure monitoring lumen at a predetermined point in the breathing cycle and/or at a predetermined pressure relative to the respiratory gases. The resulting pressure measurements may be used to determine a more accurate estimate of lung pressure, which in turn may be used to control a ventilator and provide breathing assistance to a patient.

Abstract: According to various embodiments, an endotracheal tube ventilating device with a sealing cuff includes an anchoring device. The anchoring device may be secured to the tube above the sealing cuff and extend outwardly from the tubular body. In addition, the anchoring device may be configured to be positioned completely within the hypopharynx of a patient, in contact with the piriform fossa and a laryngeal surface of the epiglottis without creating an airtight seal of the hypopharynx or the esophagus.

Abstract: According to various embodiments, a tracheal tube may include a cuff assembly that relies on mechanical pressure rather than inflation pressure to form a seal against a patient's trachea. Such cuff assemblies may include cone or umbrella-shaped structures that may form seals at substantially lower pressures than traditional inflation cuffs. One or more of such cuff assemblies may be used instead of or in addition to an inflation cuff to provide an improved seal.

Abstract: According to various embodiments, a tracheal tube may include a drug delivery system for nebulizing drug to droplets within a particular drop size range. The drug delivery system may include an integral nebulizer located towards a distal end of the tracheal tube. The nebulizer may comprise a micropump and may be in fluid communication with a drug delivery lumen, which in turn may be coupled to a system for monitoring the delivery of drug to the nebulizer. The nebulizer may be sized and shaped to be accommodated within a lumen that runs alongside a main respiratory lumen of the tracheal tube.

Abstract: An apparatus and method for removing contaminant species from water by electrocoagulation are described. Alternating grounded, rotating, planar circular electrodes and stationary planar electrodes function as a Tesla fluid pump when placed in contact with the contaminated water, causing the water to flow between the rotating and stationary electrodes. An insoluble abrasive material introduced into the water removes scale from the electrodes while the water is pumped thereby. A direct electric current is caused to flow between each pair of rotating and stationary electrodes, thereby producing electrocoagulation of the contaminants in the water flowing therebetween. The electrocoagulated materials may be separated from the treated water by filtration or by permitting the treated water to stand for a chosen period.