Abstract: The present invention provides methods for characterizing obstructive sleep apnea (OSA) patients in the treatment of OSA, and devices thereof. The methods comprise measuring polysomnography of said patients; analyzing polysomnography, and determining a characteristic of the polysomnography and selections of suitable treatments based on the patterns.

Abstract: An oral negative-pressure therapy system includes a container and absorbent insert for the container. The container includes a baffle inside an interior of the container. A fluid passageway extends along the baffle for delivering fluid (e.g., a mixture of air and saliva) into the container. The absorbent insert for absorbing liquid (e.g., saliva) in the container may is over the baffle. At least one of the baffle and the absorbent insert is configured to maintain a fluid flow path between the baffle and the absorbent insert to maintain fluid communication between a fluid inlet and a fluid outlet of the container. The absorbent insert and/or the container may be designed and constructed to burst air bubbles in the aspirated liquid. In one or more embodiments, the absorbent insert is replaceable so that a spent absorbent insert can be replaced with a new, fresh absorbent insert.

Abstract: The present invention provides a negative pressure generator comprising a vacuum pump having an intake end and an exhaust end, a soundproofing module having a compartment for accommodating the vacuum pump, the soundproofing module being configured to insulate noise and vibration generated when the vacuum pump is in operation, and a silencing tube module comprising a flexible intake tube having one open end communicating with the intake end of the vacuum pump and a flexible exhaust tube having one open end communicating with the exhaust end of the vacuum pump, the silencing tube module being configured to reduce noise generated at the intake end and/or the exhaust end of the vacuum pump when the vacuum pump is in operation. The negative pressure generator can provide a vacuum source to an oral interface device to favorably create a negative pressure environment in a user's oral cavity so that the patency of the user's upper airway is maintained.

Abstract: The present invention provides a negative pressure generator comprising a vacuum pump having an intake end and an exhaust end, a soundproofing module having a compartment for accommodating the vacuum pump, the soundproofing module being configured to insulate noise and vibration generated when the vacuum pump is in operation, and a silencing tube module comprising a flexible intake tube having one open end communicating with the intake end of the vacuum pump and a flexible exhaust tube having one open end communicating with the exhaust end of the vacuum pump, the silencing tube module being configured to reduce noise generated at the intake end and/or the exhaust end of the vacuum pump when the vacuum pump is in operation. The negative pressure generator can provide a vacuum source to an oral interface device to favorably create a negative pressure environment in a user's oral cavity so that the patency of the user's upper airway is maintained.

Abstract: An oral negative-pressure therapy system includes a container and absorbent insert for the container. The container includes a baffle inside an interior of the container. A fluid passageway extends along the baffle for delivering fluid (e.g., a mixture of air and saliva) into the container. The absorbent insert for absorbing liquid (e.g., saliva) in the container may is over the baffle. At least one of the baffle and the absorbent insert is configured to maintain a fluid flow path between the baffle and the absorbent insert to maintain fluid communication between a fluid inlet and a fluid outlet of the container. The absorbent insert and/or the container may be designed and constructed to burst air bubbles in the aspirated liquid. In one or more embodiments, the absorbent insert is replaceable so that a spent absorbent insert can be replaced with a new, fresh absorbent insert.

Abstract: The present invention provides methods for characterizing obstructive sleep apnea (OSA) patients in the treatment of OSA, and devices thereof. The methods comprise measuring polysomnography of said patients; analyzing polysomnography, and determining a characteristic of the polysomnography and selections of suitable treatments based on the patterns.

Abstract: A method for automatically controlling negative pressure supplied in oral cavity, for relieving sleep apnea and snoring is provided. The method includes: sensing a physiological signal from the user and outputting the sensed physiological signal; extracting a physiological status based on said sensed physiological signal; and automatically controlling said negative pressure provided to the user's oral cavity based on said physiological status.

Abstract: A method for automatically controlling negative pressure supplied in oral cavity, for relieving sleep apnea and snoring is provided. The method includes: sensing a physiological signal from the user and outputting the sensed physiological signal; extracting a physiological status based on said sensed physiological signal; and automatically controlling said negative pressure provided to the user's oral cavity based on said physiological status.

Abstract: An oral fixation device and an oral fixing method using the same are provided. The oral fixation device includes a U-shaped brace and an arch board. The arch board is connected to an inner wall of the U-shaped brace, wherein the central part of the arch board is thicker than the connecting part, and the maximum thickness of the arch board is larger than 2 mm.

Abstract: A method for automatically controlling negative pressure supplied in oral cavity, for relieving sleep apnea and snoring is provided. The method includes: sensing a physiological signal from the user and outputting the sensed physiological signal; extracting a physiological status based on said sensed physiological signal; and automatically controlling said negative pressure provided to the user's oral cavity based on said physiological status.