Abstract: A system, method and kit for treating obstructive sleep apnea. The system includes a first implant adapted for implantation in an inframandibular region and having at least one aperture therethrough, and a ribbon-like element having first and second ends and a substantially uniform, non-circular cross section along its length. The ribbon-like element is adapted for implantation in a tongue with the first and second ends extending through the at least one aperture in the first implant for coupling the ribbon-like element with the first implant.

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

Abstract: A system and method of providing bi-level CPAP therapy is provided that incorporates an infrared carbon-dioxide sensor to determine whether a patient is inhaling or exhaling. Patient exhalation causes the infrared light to be absorbed, while patient inhalation reduces the presence of carbon-dioxide causes little or no absorption of carbon-dioxide. The level of carbon-dioxide in an associated patient breathing interface is monitored for thresholds that trigger higher CPAP pressure upon inhalation and lower CPAP pressure upon exhalation.

Abstract: Methods and devices to determine rate of particle production and the size range for the particles produced for an individual are described herein. The device (10) contains a mouthpiece (12), a filter (14), a low resistance one-way valve (16), a particle counter (20) and a computer (30). Optionally, the device also contains a gas flow meter (22). The data obtained using the device can be used to determine if a formulation for reducing particle exhalation should be administered to an individual.

Abstract: A traction exercise apparatus comprises a rectangular shaped metal frame including a pair of metal vertical members, a metal horizontal member on a bottom side, and a pair of metal horizontal members on a top side. A first rotating metal shaft and a second rotating metal shaft are located across the pair of metal horizontal members. Further a pair of ankle braces is attached to a snap hook. A cable pulley on each side of the first rotating metal shaft supports a first metal cable attached to the snap hook. A first cable reel on each side of second rotating metal shaft supports the first metal cable. A second cable reel on each side of the second rotating metal shaft supports a second metal cable attached to a hand grab bar. Second rotating metal shaft rotates to transmit a tension to the first metal cable to perform different traction exercises.

Abstract: A patient interface device that includes a support member sized and configured to span at least a portion of a patient's face while remaining below the patient's eyes responsive to the patient interface device being donned by such a patient and a sealing assembly operatively coupled to the support member such that the support member is moveable relative to the support member. The support member defines a gas carrying conduit adapted to carry a flow of gas to the sealing assembly. The support member is a single-piece unitary member and includes a conduit coupling portion adapted to be coupled to a patient circuit.

Abstract: A breath responsive filter blower respirator system for a gas mask including a pressure and control device, such as an optoelectric device and/or a pressure sensor, to control the air flow produced by an air blower. The optoelectric device detects the position of the mask's outflow valve. The pressure sensor measures air pressure in the mask relative to ambient air or the absolute air pressure in the mask. During exhalation, the pressure detector detects an increase in air pressure in the mask and/or the optoelectric device detects the outflow valve in an open position, and then signals the central processing unit to signal the air blower to reduce speed. The reduction in speed reduces air flow in the mask and lowers air pressure in the mask.

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: Mask ports 180 for attaching supplemental oxygen tubes 510 or measurement devices to a respiratory mask are downwardly directed and recessed into the base 110 of the mask frame 100. The ports may comprise a pair of downwardly extending tubular spigots 185 each housed in a respective recess 190 in the base 110, with a shallow bridging recess 290 therebetween for receiving a bridging piece 300 of a closure cap 280.

Abstract: Medical devices and related methods are disclosed for delivering an implant into the body of a patient. The devices include a damping assembly having an internal chamber with a varying inner diameter, and a piston slideably disposed therein. The piston is operably connected with a catheter portion such that movement of the piston is associated with concurrent movement of the catheter for implant delivery. The varying inner diameter of the damping assembly results in a decrease in damping force during implant delivery, thus providing a substantially constant velocity of implant delivery.

Abstract: A system and method for endotracheal intubation of airways are disclosed. A malleable stylet having a distal end and a proximal end, a charged coupled device (CCD) at the distal end and a transmitter, at or near the proximal end or connected to the proximal end of the stylet with connectors, transmits video to a visualization device comprising a receiver means, a display means, and a display support adapted to be worn on an operator in a position so that the operator can view the display with one eye while simultaneously viewing the airway directly. The display support is typically worn on the head of a physician. A second display can be worn by a student or observer. In some instances, the transmitter means and receiver means are wireless.

Abstract: A method and apparatus for determining the presence or absence of a pulmonary embolism (PE) in a patient. The breathing gas CO2 partial pressure (PCO2) during the expiration of breathing gases by the patient, the end tidal (EtCO2), CO2 partial pressure, and the CO2 partial pressure (PaCO2) of the blood are measured. The volume (V) of breathing gases expired during the expiration of breathing gases by the patient is also measured and a relationship between changes in breathing gas CO2 partial pressure (PCO2) and changes in breathing gas volume (V) in an alveolar expiration phase of patient expiration is determined. The difference between the blood CO2 partial pressure (PaCO2) and the end expiration CO2 partial pressure is divided by the relationship between PCO2 and V produce a quantity which is compared to a threshold value. If the quantity is below the threshold value, the absence of a pulmonary embolism is indicated.

Abstract: An airway positioning device facilitates the maintenance of a patent airway by correctly positioning a patient's head during anesthesia. A flat base supports a supine patient's head. A pair of rails slope downward from a first end of the base to a second end of the base. A track mounts with at least one of the rails. At least one adjustable support arm movably mounts with the track via a locking coupling device at an end of the arm distal to the patient's head. A patient engaging member mounted with an end of the arm proximal to the patient's head supports the patient's head in a desired position during an operation or procedure.

Abstract: A drape having a pair of elongated sheets connected at distal ends to define a skirt, with opposing side walls in a first portion of the elongated sheets having a first width and in a second portion having a different width so the drape has a stair-step structure, with a paper and plastic laminated first and second tier panels attached to the elongated sheets in spaced-relation and a central panel attached therebetween, for covering a tiered surgical operating table.

Abstract: A respiratory mask assembly for delivering breathable gas to a patient includes a frame and a headgear assembly removably attachable to the frame. The headgear assembly includes a pair of side portions and a rear portion that interconnects the pair of side portions. The pair of side portions includes at least one strap. The rear portion has at least one strap constructed of at least two layers of material. One of the layers of material has a more rigid construction than the other of the layers of material to resist compression of the at least one strap of the rear portion in a first direction which resists movement of the at least one strap of the pair of side straps in the first direction.

Abstract: A dental appliance for maintaining a separation between the occlusal plane surfaces of the posterior teeth in order to avoid or minimize the adverse effects of bruxism, especially while sleeping. The appliance comprises bitepad assemblies, side assemblies for adjustably receiving the bitepad assemblies, and a strap assembly for connecting the side assemblies. Bitepad cores are provided with solid projections and mechanical locks that enhance bonding with associated overmolds for improved durability. Side assembly flanges are divided to achieve independent flexibility and improved conformity for enhanced stability and comfort. A mesial area of the connecting strap assembly is thickened and rigidified to create a flare in the areas of the cuspid roots to minimize irritation and discomfort to the gum tissue.

Abstract: A method for treating a user's back, a user's neck, or combinations thereof. The method can include the steps of: inserting a traction device into a pouch of a fabric garment; disposing the fabric garment over a user; engaging the traction device with a surface; and applying a pressure to the traction device using the user's back. The traction device can provide a therapeutic pressure to the user's back, to the user's neck, or to combinations thereof. The method can use a customizable traction device having a shearable fraction head and body. The shearable traction head and body can each be cut to a custom size to fit a user. The method can use a removable fabric chair cover disposed over a chair. A user can sit on the chair and apply a pressure to the traction device using the user's back.

Abstract: The adjustable mouth shield device provides an adjustably fitted mouth shield with adjustable headband for secure fit. The adjustable headband is fastened to the padded earpiece. The straight first extension from the earpiece is angled downwardly and forwardly to terminate in a swivel joint providing almost 360 degrees of swivel. The second extension is arced both downwardly and forwardly. The u-shaped mouthpiece is fitted to the adjustable spring mount for horizontal pivot of the mouthpiece. The mouthpiece may, by virtue of the swivel joint and the spring mount, be moved completely away from a user's mouth and, in turn, pivoted and swiveled to be directly in front of the user's mouth. The inward curves at the distal end of the mouthpiece aid in sliding on the disposable pads that shield a user from objects, foods and other materials.

Abstract: A method of intubating a subject is disclosed. The method comprises inserting an endotracheal tube into the tracheal airway of the subject; inflating a cuff associated with the endotracheal tube within the airway below the vocal cords; measuring a level of at least one measure being indicative of leakage of secretion past the cuff to the lungs; comparing the level of the measure with an optimal level of the measure; and adjusting inflation of the cuff based on the comparison so as to generally minimize leakage of secretion from above the cuff to the lungs, while minimizing pressure associated damages to the airway. The measure(s) can be carbon dioxide concentration, a proxy measure from which such concentration can be inferred, or the level of one or more additives delivered to a subject during intubation.

Abstract: A method and apparatus for providing an average signal characteristic profile derived from signals obtained from different cycles of a cyclically recurring physiological phenomenon. A signal produced from first and second cycles of the physiological phenomenon is sampled at a series of data points to obtain second physiological property values at the data points. The change in the second physiological property values for the first cycle signal between a pair of successive data points and the change in the second physiological property values for the second cycle signal between the same pair of successive data points are determined and averaged. The average change amount is applied to a value of the average signal characteristic profile at one of the pair of successive data points to produce a new second physiological property value for the average signal characteristic profile at the other of the data points of the pair.