Abstract: A method and devices for facilitating fixating and joining of bone fractures utilizing expandable devices that are positioned within the bone and across the fracture site. The stress from the expanded may enhance and expedite bone healing.

Abstract: Methods and devices are disclosed for manipulating the airway, such as to treat obstructive sleep apnea. An implant is positioned within the body with respect to the airway. The spatial orientation of the airway is manipulated, directly or indirectly, to affect the configuration of the airway. In general, the implant is manipulated to displace the trachea in an inferior direction, resist superior displacement of the trachea and/or to alter the tracheal wall tension. The implant restrains the trachea in the manipulated configuration.

Abstract: A veterinary anesthesia monitor system useful in establishing, maintaining, and reporting upon the anesthesia gas mixture delivered to or exhaled by a patient.

Abstract: In order to prevent tainting of a cougher's hand with germs, the product from a cough is carried in contact with a germicide inside a hollow article, and is vented out of the hollow article, in directions away from the user's face and hand holding the article. More specifically, the cough catcher has a hollow region for accepting the product from a cough therein. This hollow region has a filter element containing a germicide mounted therein, and a series of channels formed between the filter element and a bottom surface of the hollow region. The channels communicate with vent ports around a rim portion of the cough catcher. The vent ports are oriented away from both the mouth opening and the outside surface of the cough catcher for conveying the product from a cough away from both the face and the hand of a user.

Abstract: An apparatus and methods for treating sleep apnea and/or snoring are provided. The apparatus includes an appliance sized and structured to be placed in the pharyngeal region of a human or animal. The appliance, when so placed is effective in treating sleep apnea and/or snoring, for example in maintaining openness of an oropharyngeal region of a human or animal during natural sleep. Preferably, the appliance is non-circumferential in form and includes rounded, spaced apart end portions.

Abstract: A liquid evaporator includes a liquid reservoir (3) with a liquid to be evaporated, a heater (9) and an evaporator tube (12). The evaporator tube (12) has a first porous element (1) having a first porosity and with an area in contact with the liquid in the liquid reservoir (3) and a second porous element (2) with a second porosity and with an area present on an evaporator side (50) used to dispense the evaporated liquid, and an area outside the liquid reservoir heated by the heater (9) which is not directly in connection with the liquid. The first porous element and the second porous element are in contact in contact areas with the first porous element forming a wick delivering liquid from the reservoir to the contact area.

Abstract: A method and a CPAP apparatus for characterizing different mask systems, e.g., masks and hoses, are provided. The apparatus can be calibrated for different mask systems and hoses by including sensors for measuring flow and pressure at a flow generator of the apparatus. When the flow generator is fitted to a new system, or changes are made to an existing system, mask or patient interface, and/or hose, a method of calibrating the flow generator is provided. The method includes determining air flow characteristics of the hose using flow measurements made during a first test period when flow through the system is open, measuring or estimating pressure in the system during a second test period when flow through the system is blocked, and determining air flow characteristics of the diffuser using the air first test period flow characteristics of the air delivery hose and the second test period pressure measurements.

Abstract: An infant nasal interface prong device for use with an nCPAP system. The device includes first and second nasal prongs and a base. Each prong includes a bellows segment, a tip, and a lumen. The tip extends from the bellows segment to a tip end and is adapted for insertion with an infant's naris. The lumen extends through the tip and the bellows segment. In an undeflected state, a central axis of the lumen along the bellows segment is transversely offset from the lumen axis at the tip end. The base is connected to each of the nasal prongs and is adapted for coupling to a CPAP generator. The bellows segment renders the corresponding prong highly flexible relative to the base. The offset positioning of the tip end promotes desired positioning of the base/CPAP generator, relative to the patient and more closely conforms to the expected nasal anatomy.

Abstract: The present invention discloses a pivotal disc is pivotally coupled to a first brace and a second brace. The pivotal disc has a motion-limit member and a positioning member limiting the angle by which the second brace rotates with respect to the first brace with the pivotal disc being the axis and fixing the angle between the first and second braces. The present invention is characterized in that the motion-limit member uses a range-adjust member to push a slide block and determine the range that a block portion of the second brace is blocked by the slide block, and that the positioning member uses a switch knob actuates on end of a positioning rod to engage with or depart from a positioning notch on the pivotal disc, and that the pivotal disc has two limit elements to define the maximum movement range of the first brace and the second brace.

Abstract: A cartridge for propellant-free administration of a liquid pharmaceutical composition by inhalation includes: an elongate displacing device including an upper end and a lower end, the lower end for at least partial insertion into a container; a cartridge chamber disposed at the lower end of the displacing device and operable store a pharmaceutical formulation, the cartridge chamber including at least one pierceably sealed opening; and a cannula guide extending from the upper end of the displacing device to the cartridge chamber, wherein insertion of a cannula through the guide pierces the sealed opening and releases the pharmaceutical formulation into a liquid solvent in the container to form the liquid pharmaceutical composition.

Abstract: The present invention relates to a nasal delivery device for and a method of delivering a substance, in particular one of a liquid, as a suspension or solution, or a powder containing a medicament, especially systemic or topical pharmaceuticals, or a vaccine to the nasal airway of a subject.

Abstract: A method of conveying humid breathing gases from a patient through a breathable breathing tube. The breathing tube includes a heater associated, at least in part, with a portion of hydrophilic material. The purpose of the heater is to evaporate any condensed liquid collecting in the conduit, which is first sucked up by the hydrophilic material. The heated wick reduces the risk of collected water being passed to the patient and causing choking fits or discomfit. It is preferred that the heated wick lies freely in the conduit to settle at low points in the conduit where condensation may collect.

Abstract: Concentrated oxygen product gas is produced and delivered to a patient. Product gas is produced by (a) introducing ambient air into a first end of a column containing an adsorbent material that preferentially adsorbs nitrogen and removes oxygen-rich product gas out a second end of the column; (b) evacuating the column through the first end to remove adsorbed gas from the column; (c) repressurizing the column by introducing ambient air into the first end of the column until the column is near 1.0 atmosphere; and (d) repeating steps (a)-(c). Product gas is delivered as needed to the patient.

Abstract: A waterproof structure of a respiratory tube is provided. The waterproof structure comprises a hollow body and a lid. The hollow body has a first opening end and a second opening end opposing to the first opening end. The lid pivots onto the hollow body at the first opening end. Before the lid is immersed into liquid, the gravity of the lid can keep the lid at a certain position so that the respiratory tube is well-ventilated. After a part of the lid is immersed into the liquid, the buoyancy provided by the liquid forces the closing surface thereof to substantially seal the first opening end and prevent liquid from going into the tube.

Abstract: An electrosurgical apparatus for coagulating tissue used in combination with an endoscope which includes an elongated flexible tube having a plurality of side-ports located therethrough. The tube extends through a working channel of the endoscope and an ionizable gas is supplied to the tube at or near the proximal end of the tube. A diffusing member directs the ionizable gas from the proximal end of the tube through each of the side-ports towards the tissue. An electrode is used for ionizing the gas prior to the gas exiting the side-ports.

Abstract: A blister pack for use with inhalation therapy inhalers comprises an elongate bottom element having an overlying top element defining a plurality of spaced top crowned areas containing powder or liquid medications or drugs.

Abstract: An underwater exhaust system and method which includes an exhaust valve having a sealing edge, an exhaust outlet for exiting an exhaust gas, and a projection for directing water flow away from the exhaust valve. The exhaust valve includes a valve head and a valve stem, the valve stem being coupled with the valve head. The system and method prevent a siphoning effect, whereby leakage of water into the exhaust valve is minimized or prevented.

Abstract: A cardiopulmonary resuscitation device that combines ventilation of a patient's lungs with chest compressions on the patient's sternum area. The device includes a self-inflating bag having an outlet port through which the content of the bag is forced when bag is compressed; target indicia on the bag to indicate the proper position of the bag on the patient's sternum area and to indicate the proper location on the bag for applying force to the top side thereof; a face mask for placement over the patient's mouth and nose; and a tube extending from the bag to the face mask. The device may include indicia for indicating the amount of pressure applied to the self-inflating bag, and a backboard including belt/motor structure for providing repeated and rapid chest compression and forced ventilation of the patient's lungs.

Abstract: A device and method for facilitating the delivery of medication/humidity to a patient without breaking a ventilator circuit that contains a two-position flow control valve in the circuit, so as to permit manual switching from a first position in which humidified air/oxygen will be supplied to a patient and a second position in which atomized medication will be supplied to the patient.

Abstract: An improved ventilator which delivers ventilatory support that is synchronized with the phase of the patients respiratory efforts and guarantees a targeted minimum ventilation. Improved synchronization is achieved through an instantaneous respiratory phase determination process based upon measured respiratory airflow as well as measured respiratory effort using an effort sensor accessory, preferably a suprasternal notch sensor. The ventilator processes a respiratory airflow signal, a respiratory effort signal and their respective rates of change to determine a phase using standard fuzzy logic methods. A calculated pressure amplitude is adjusted based upon the calculated phase and a smooth pressure waveform template to deliver synchronized ventilation.