Abstract:
Disclosed is a device for determination of the content of higher oxides of nitrogen in exhaled breath condensate which comprises a conduit (7) having an exhaling condensing portion with an inlet and an outlet (the inlet can be configured to fit with a mechanical respirator, or for direct use by a patient, an inlet assembly providing one-way ingress (2) of ambient atmosphere so the device can be associated with the inlet of the conduit exhaling condensing portion); a coolant jacket (6) coaxially surrounding said exhaling condensing portion; a gas release port; and, in an enclosed fluid communication with said conduit exhaling condensing portion outlet, a sample assay assembly (9) comprising the following: (a) a translucent analysis chamber attached to the outlet to receive condensate fluid and having a reagent port; (b) a reagent chamber in enclosed fluid communication with the reagent entry port; and (c) a pliable element connecting the oulet and the analysis chamber and forming a portion of the reagent chamber such that flexion of the pliable element closes communication between the oulet and the analysis chamber and contracts the reagent chamber so as to deliver to the analysis chamber controlled amounts of condensate and reagent. The device is disposable and inexpensive, and is used to collect human exhaling for colorimetric assay of liquid and gas phase nitrogen oxides to assist in evaluation of airway inflammation.
Abstract:
A non-invasive system and procedure for deriving the blood gas content for a patient. The system measures the carbon dioxide concentration of the expiratory breath relative to volume. This data is then processed to derive arterial blood gas levels of carbon dioxide. If data sampling is in the time domain, the processing shifts the data from the time domain to the volume domain. The processing also iteratively assesses the significance of numerous variables. The resulting relationship provides a fast and accurate measure of blood gas content for both healthy and diseased lung patients.
Abstract:
This invention is a spirometric device (100) for analyzing the strength of the exhalation of a patient. The device (100) is designed to sense and measure exhaled airflow rate, exhaled breath temperature, determine airflow volume, and record and display the respiratory movement of the patient for helping make medication recommendations. The device (100) includes an electronic package (336) mounted inside a housing (110) for computing and recording the strength, the temperature, and the volume of the exhalation along with the time and date. The device (100) includes a replaceable airflow chamber (130) mounted on the housing (110). A disposable mouthpiece (140) is releasably attached to the airflow chamber. A hot wire (430) is disposed inside the airflow chamber (130) and provides for measuring both airflow rate and temperature. An output of the hot wire (430) is connected to electronic circuitry (305) inside the housing for determining the proper volumes along with recording the time and date of the event.
Abstract:
Single hand supportable and operable apparatus (30) for providing an output signal characteristic of the morphology of a respiratory tract includes an acoustic pipe (30) for exchanging acoustical energy with the tract. The pipe has an open first end (34) in communication with an opening in the respiratory tract. A transducer (38), such as a loudspeaker, is coupled to the pipe, producing an incident wave towards to opening in the tract and a reflected wave to form a transient wave filed in the pipe representative of the morphology of the tract. Preferably, first (40) and second pressure wave sensing transducers (42), such as microphones, mounted along the length of the pipe in spaced relationship provide first and second transduced signals representative of the transient wave field. A processor (66) processes the first and second transduced signals to provide an output signal characteristic of the morphology of the tract, such as the cross-sectional area as a function of the distance from the opening of the tract.
Abstract:
A calorimeter for generating signals representative of the oxygen consumption and carbon dioxide production of a subject over a test period (12) includes two flow sensors (48, 64) and a carbon dioxide scrubber (66) connected to a patient mouthpiece (60). Interconnections (44, 46, 52, 54, 56, 58, 62) are such that the air inhaled by the subject passes through one flow meter and the exhaled breath passes first through the other flow meter, the carbon dioxide scrubber and then through the first flow meter. The electrical output signals from the flow meters are provided to a microprocessor based computer (50) which integrates the volume differences between the inhaled gas, and the exhaled gas after the carbon dioxide has been removed from it, over the period of the test.
Abstract:
A volume change sensor (11, 12) having an elongated tubular enclosure (15) with a thin deformable wall having a conduit (13) for connection to a pressure monitor (14), there being an elongated insert material (24) within the tubular enclosure that is wider than it is thick at some locations formed from resiliently deformable open cell foam. An elastic belt (16) against which the tubular enclosure is positioned is used to wrap it about a respirating subject (10) undergoing corresponding changes to measure same.
Abstract:
An apparatus and method are disclosed for monitoring physiological parameters associated with the ventilation of infants during assisted ventilation. The infant is placed in a plethysmograph and various sensor means are used to measure flow of gas into and out of the plethysmograph and infant respiration. The outputs of the sensor means are supplied to a microcomputer system for processing. A unique calibration system is provided which constantly corrects for changing system parameters such as plethysmographic chamber air leaks, compliance and the like. Additionally, a heating system which exhibits radiant as well as convective heating properties is provided to maintain the infant in a constant temperature environment with a minimal amount of temperature fluctuation. From this data, ventilator breaths are discriminated from infant breaths.
Abstract:
A quick occlusion controlled device particularly intended to evaluate the sensitivity of respiratory centres comprises a body (1) connected to the respiratory apparatus of the patient through a buccal connector (2), provided with a pressure tap (3). According to the invention, the device is characterized in that the body (1) comprises an inspiration connector (4) which opens into the inner volume of the body (1) through a valve (5), as well as a respiration connector (6) which opens into the inner volume of the body (1) through a second valve (7), said device being further provided with an occlusion means of both/either of the valves (5) and (7).
Abstract:
An arrangement for measuring bidirectional respiration flow, including a hose (1) which is connected to the breathing passages of a patient in which, via a Y-piece (2) is also connected to a tube (3) for inspiration gas and to a tube (4) for expiration gas. The tubes (3, 4) are connected to a breathing apparatus. Each tube has a venturi means arranged therein. According to the invention a pressure differential meter (8) having two inlets is connected with one inlet to each venturi means. A magnet valve (7) is arranged to periodically connect both inlets together, and there is provided an electronic means (9) for calculating the valve measured and for controlling the zero-setting, to which end the control means is connected electrically to the pressure differential meter (8) and to the magnet valve (7).
Abstract:
Apparatus for providing a measure of extravascular lung water of a subject using a single thermal indicator, including means (16) for providing an injection of the thermal indicator into the bloodstream of the subject at a position proximal to or in the right heart (10) means (26) for detecting a first time-temperature concentration curve of the bloodstream at a position in the pulmonary artery, means (104) responsive to the first time-temperature concentration curve detected in the pulmonary artery for calculating a characteristic time for the first time-temperature concentration curve, means (28) for detecting a second time temperature concentration curve of the bloodstream at a position in a systemic artery, means (104) responsive to the second time-temperature concentration curve detected in the systemic artery for calculating a characteristic time for the second time-temperature concentration curve, means (104) for calculating the flow of blood through the heart and lungs, and means (104) for calculating a measure of extra-vascular lung water in accordance with the difference between the products of the blood flow times the first characteristic time and the blood flow times the second characteristic time.