Abstract: A phyto material vaporization device is disclosed for being powered by an atomizer power supply having a central axis and a control button for being attached to an aromatherapy water pipe having an input port in fluid communication with an inhalation aperture. A water pipe engagement member is provided for being releasably coupled with the aromatherapy water pipe and a fastening mechanism for releasably fastening the water pipe engagement member to the aromatherapy water pipe. An atomizer power supply receptacle for releasably coupling with the atomizer power supply for receiving of electrical energy therefrom and a conduction heating element for receiving of the phyto material and for being disposed proximate the aromatherapy water pipe input port for restricting of ambient air flowing into the input port and having an electrical connection for electrically coupling with the atomizer power supply receptacle.

Abstract: Disclosed is an autoCPAP respirator which comprises a control unit, a respiration blower and a pressure sensor. The control unit comprises a controller for generating a first control signal, which induces the speed of the blower to generate a pressurized breathing gas flow, a controller for generating a periodically variable control signal, which activates the blower such that the speed of the blower varies in an oscillating manner at a frequency in the range of 1-20 Hz, and a sensor device, which ascertains one or more of instantaneous speed, instantaneous electrical current and instantaneous electrical power of the blower to determine the breathing gas flow and/or breathing gas volume generated by the blower while using characteristic data of the blower stored in a memory.

Abstract: A processor obtains input of a logistically attainable end tidal partial pressure of gas X (PetX[i]T) for one or more respective breaths [i] and input of a prospective computation of an amount of gas X required to be inspired by the subject in an inspired gas to target the PetX[i]T for a respective breath [i] using inputs required to utilize a mass balance relationship, wherein one or more values required to control the amount of gas X in a volume of gas delivered to the subject is output from an expression of the mass balance relationship. The mass balance relationship is expressed in a form which takes into account (prospectively), for a respective breath [i], the amount of gas X in the capillaries surrounding the alveoli and the amount of gas X in the alveoli, optionally based on a model of the lung which accounts for those sub-volumes of gas in the lung which substantially affect the alveolar gas X concentration affecting mass transfer.

Abstract: A medical device is provided with an alarm organization. A process for alarm organization of a medical device is also provided. Based on pressure measured values (99) and flow measured values (97) and with a comparison criterion it is determined whether an elevation of an airway pressure (105) of an anesthesia device or of a ventilator is caused by a coughing event. A visual and/or acoustic output (117, 121) of a warning or alarm (42) is adapted, indicating the elevated airway pressure PAW_High (105).

Abstract: Methods and apparatus for treating a respiratory disorder, in one aspect, include an apparatus that delivers backup breaths at a sustained timed backup rate that is a function of the patient's spontaneous respiratory rate. Other aspects include apparatus that delivers backup breaths at a rate that gradually increases from a spontaneous backup rate to a sustained timed backup rate or, alternatively, apparatus that oscillates a treatment pressure in antiphase with the patient's spontaneous respiratory efforts when a measure indicative of ventilation is greater than a threshold.

Abstract: Devices and systems with methods for detecting a sealing condition between a patient interface and a patient, and adjusting the patient interface to maintain the patient interface in sealing contact with the patient. The patient interface may include a sealing structure to form a seal on the patient, and a positioning structure to secure the sealing structure to the patient. The patient interface may include a sensor coupled to the sealing structure. A processor determines the sealing condition between the sealing structure and the patient based on a signal from the sensor, and adjusts at least one of the sealing structure and the positioning structure to maintain the sealing structure in sealing contact with the patient. A prediction system predicts a leak between the sealing structure and the patient based on the sensor signal. A learning system learns how to fit the sealing structure to the patient to form a seal.

Abstract: A patient interface for use in delivering a flow of breathable gas to an airway of a patient includes a first seal adapted to contact the patient's face and seal a first space between the patient interface and the patient's face at a first positive pressure; and a second seal adapted to contact the patient's face and seal a second space between the patient interface and the patient's face at a second positive pressure. The first seal also seals the first space from the second space. A leak reducing element may be provided on a seal to reduce and/or diffuse leakage of gas. A vacuum line configured to create a negative pressure may be provided in the second space to remove any gas leaking from the first space to the second space. A seal may be connected to a conduit for delivering the flow of gas that is incorporated into a frame of the patient interface.

Abstract: A filled hollow structure includes an open hollow structure from a first material. The open hollow structure is at least partially closed by a closing structure. The hollow structure is filled with a filler medium. The filled hollow structure is overmoulded with a second material.

Abstract: A mask apparatus for a respiratory treatment can permit delivery of breathable gas to a user. In one example, the mask may employ a frame and cushion to form a seal for both mouth and nose. The frame may be adapted for coupling with a respiratory treatment apparatus so as to permit communication of a pressurized gas from the respiratory treatment apparatus. The cushion, which may be foam, and a frame component may be made in an overmoulding process that moulds the frame onto a pre- formed foam cushion. Such a moulding process may form a mechanical and/or chemical bonding of the foam and mask frame component. The mask frame component may be a shell of plenum chamber, such as for both nose and mouth. Various features of the cushion may further promote sealing and comfort for the under the nose design.

Abstract: A cushion support assembly for a respiratory interface device cushion is provided. The cushion support assembly includes a cushion support assembly ribbon-like body with an inner side, an outer side and a wide facial side. The cushion support assembly body facial side includes a support surface, the support surface is structured to support the respiratory interface device cushion engagement portion in a generally planar configuration. The cushion support assembly body facial side support surface is generally planar relative to the user's respiratory interface device contour radial aspect.

Abstract: An adjustable airflow diffuser for selectively diffusing a flow of treatment gas includes a first member adapted to be disposed in the flow and a second member movably coupled to the first member and also adapted to be disposed in the flow. The second member is selectively moveable from: (i) a first position with respect to the first member in which the first member and the second member form a first turbulating arrangement, and (ii) a second position with respect to the first member in which the first member and the second member form a second turbulating arrangement.

Abstract: Disclosed is a respiratory device comprising a connecting socket which is inserted at least partially into a rotary sleeve and is latched thereto. The connecting socket and the rotary sleeve are disposed between a respiration hose and a patient interface, the connecting socket having an external diameter which is smaller than the internal diameter of the rotary sleeve. The rotary sleeve comprises on its inner side latching elements which engage in latching elements on the external diameter of the socket.

Abstract: A portable oxygen concentrator designed for medical use where the sieve beds, adsorbers, are designed to be replaced by a patient. The concentrator is designed so that the beds are at least partially exposed to the outside of the system and can be easily released by a simple user-friendly mechanism. Replacement beds may be installed easily by patients, and all gas seals will function properly after installation.

Abstract: The present disclosure pertains to a system (10) configured to prevent damage from liquid spills in a humidified pressure support therapy device (50). The system is configured to decouple a humidification chamber (42) in a humidifier from a pressure generator (14) of the pressure support therapy device when a cover (48) of the humidifier is opened. This eliminates and/or reduces the possibility of liquid in an overfilled humidification chamber unintentionally and/or otherwise entering the pressure generator and damaging sensitive mechanical and/or electrical components. In some embodiments, the system includes one or more of the pressure generator, the humidifier, a subject interface (16), a sensor (18), a decoupler (100), a processor (20), electronic storage (22), a user interface (24), and/or other components.

Abstract: Medical gas delivery devices are provided. A garment or another object may include a hose assembly configured to couple the garment or the object to a medical gas source. The garment or the object can be configured to deliver a medical gas to a patient. Additionally, medical gas delivery devices configured to be removably coupled to a garment or another object are provided.

Abstract: Nebulizer systems, apparatus, and methods are disclosed. The apparatus includes a body, a breathing gas inlet and outlet, and a barrier. The body is sized to be positioned within an adaptor of the nebulizer system. The breathing gas inlet and the breathing gas outlet are at opposite ends of the body. The barrier is coupled to the body. A plurality of holes are formed in the barrier. The plurality of holes open in a direction orthogonal to the breathing gas inlet. The system employs the apparatus in conjunction with a nebulizer and an adaptor. The method includes generating an aerosolized medicament, providing the aerosolized medicament to the adaptor, passing the aerosolized medicament through the barrier of the apparatus, providing a breathing gas to the apparatus, and flowing the aerosolized medicament and the breathing gas through the breathing gas outlet of the apparatus.

Abstract: An improved oscillating positive expiratory pressure (“OPEP”) device, for respiratory therapy having a self sterilizing flow valve capable of insertion into the curved OPEP body without tools or aids. The flow valve is also tear resistant and incorporates a flared reinforced proximal end. To maximize the benefit to patients, the adjustable therapy selector is constrained from withdrawal and is dimensioned to accept commercially available, standardized respiratory fittings adaptors, mouthpieces and “Tees” that are capable of connection to multiple respiratory therapy devices or medicated aerosol delivery units. The aesthetics have been altered by the addition of an arced handle.

Abstract: An apparatus for administering a respirable gas to an individual includes a body receivable against a facial area for enclosing a respiratory organ, a vacuum hose, and a scavenger valve. The body is cup shaped, and includes a first side and a second side. An inhalation member extends from the first side of the body. An exhalation member extends from the second side of the body. The vacuum hose is for coupling a vacuum source to the exhalation member. The scavenger valve is coupled to the vacuum hose. The inhalation member is for administering respirable gas into the body, the exhalation member is for exhausting exhaust gas from the body into the vacuum hose, and the scavenger valve is for exhausting exhaust gas therethrough from the vacuum hose to an atmosphere.

Abstract: The present technology relates generally to cough-assist devices with humidified cough assistance. In one example, a system includes a cough-assist device having a first phase configured to provide insufflating gas to a patient circuit and a second phase configured to draw exsufflating gas from the patient circuit. A humidifier is disposed between the cough-assist device and a distal end of the patient circuit, the humidifier including a chamber configured to contain heated water and fluidically coupled to the cough-assist device and the patient circuit. The system further includes a bypass configured to (a) direct insufflating gas from the cough-assist device through a first route to the patient circuit such that the insufflating gas is humidified in the chamber, and (b) route exsufflating gas from the patient circuit through a second route to the cough-assist device such that the exsufflating gas bypasses the chamber.

Abstract: This invention relates to a method for achieving the balance of the mind of an examinee, the method comprising a first step of showing a set of symbols to an examinee; a second step of applying the symbols to a feeling of the examinee and a state of the examinee's mind; a third step of making the examinee understand a recognition system represented by the set; and a fourth step of resolving a conflict in the examinee's mind to achieve the balance of the examinee's mind; the set including a first to seventh symbols 1 to 7.

Abstract: The present disclosure pertains to a system configured to a system configured to detect slow waves based on adjusted slow wave detection criteria and time delivery of the sensory stimulation to correspond to slow waves detected based on the adjusted criteria. The system is configured to adjust slow wave detection criteria to enhance detection of slow waves in a subject. Slow wave detection using adjustable slow wave detection criteria produces more stimulation relative to prior art systems because more individual stimuli are provided if more slow waves are detected. In some embodiments, the system includes one or more of a sensory stimulator, a sensor, a processor, electronic storage, a user interface, and/or other components.

Abstract: This disclosure is directed to a medical device including a surface that has been roughened to provide a roughened surface that inhibits the adhesion of microorganisms on the roughened surface.

Abstract: A combination flush catheter and selective catheter as one convertible catheter and methods of using the same. The selective catheter may be a reverse curve or guide catheter. The additional steps of removal of the flush catheter and re-insertion of the selective catheter may be eliminated, reducing the possibility of errors and making the procedure smoother and shorter.

Abstract: A multi-catheter infusion system and method for the localized delivery of medications while minimally affecting patient mobility for an extended period of time. The multi-catheter infusion system includes a cannula and a plurality of catheters. The cannula includes a first end for connecting to a drug delivery system and a second end for connecting to the plurality of catheters. The plurality of catheters are in fluid communication with the cannula for delivering a drug to a target area of a patient. Each catheter includes a multi-orifice distal end.

Abstract: Apparatuses of the type broadly applicable to numerous medical applications in which it is desirable to insert one or more steerable or non-steerable catheters or similar devices into a working channel of an associated device, such as an endoscope, catheter, etc., or passageway of a patient, are disclosed. The apparatuses may include catheters having a dedicated guide wire channel and one or more of the following: viewing capabilities, a working channel, and auxiliary channels, such as insufflation/irrigation channels. The catheters may include a guide wire channel that is configured to provide the catheter or other device with rapid exchange capabilities.

Abstract: Described herein are devices and methods for guide catheters having one or more regions of increased flexibility. A flexibility region comprises one tubular segment of the guide catheter with a non-linear seam between two non-concentric layers of material having different durometers. A non-linear seam, such as a zig-zag or sinusoidal configuration, permits controlled compression of lower durometer material between portions of higher durometer material.

Abstract: The invention addresses the problem of limited functionality of the distal end of a steerable medical device due to the presence of the pull wire ring in the distal end portion. It relates to a steerable medical device (1) comprising a pull wire ring (100a-e) for imparting a bending movement on the steerable medical device. By providing the pull wire ring (100a-e) with an eccentric recess (105a-f) which defines a passage between a first end face (101) and a second end face (105) of the ring, it becomes possible to guide ancillary elements such as electrical lines, data cables and fiber optics past the pull wire ring (100a-e) further towards the distal end of the steerable medical device. By this measure, functionality of the distal end of the medical device is enhanced without obstructing a main lumen of the device.

Abstract: A medical device or catheter management system comprises several layers where a top layer has one or more channels to receive one or more elongated medical devices or members and a bottom layer comprises adhesive to secure the catheter management system to a patient or other secure site in the operating field. A firm upper surface causes the elongated medical devices or members to stay in the channels, whereas a firm inner layer facilitates maintaining the shape of the catheter management system and providing resistance for an operator to easily release an elongated medical device or member.

Abstract: Dislodging an anchor sleeve from an implanted device may be accomplished with a tool that includes a support portion and a sleeve dislodging element, wherein a collar of the support portion engages a distal end of the anchor sleeve while the dislodging element, positioned at a proximal end of the sleeve, is moved toward the collar to dislodge the anchor sleeve. The tool preferably includes a handle member held in sliding engagement with a base member, for example, by a snap-fit, wherein the support portion is part of the handle member, and a distal segment of the base member is terminated by the dislodging element. A tool kit may include a plurality of base members, each one including a different type of dislodging element, from which an operator may select for snap-fitting to a handle member of the kit.

Abstract: A transcranial fastening device (1) for a drainage catheter (3), comprising an external body (5) being equipped with a passage (P), the passage (P) being equipped with blocking means (9) of the drainage catheter (3) adapted to allow a sliding of the drainage catheter (3) through the passage (P) along a first movement direction (M1) and to prevent a sliding of the drainage catheter (3) through the passage (P) along a second movement direction (M2).

Abstract: Disclosed herein is an IV catheter system., comprising a catheter hub (100), a needle hub (200) and a needle shield (300), wherein the needle of the needle hub is provided with a high friction surface part (207). Furthermore, an open and closed IV catheter system is described. Also disclosed is a needle hub (200) and a shielded needle system (600).

Abstract: A catheter insertion device includes a housing, a needle, a catheter, and a guide wire. The needle has a proximal end positioned in the housing and a distal end extending beyond a distal end of the housing. The catheter is positioned coaxially over the needle, and includes a flexible tube and a catheter hub on a proximal end of the flexible tube. A proximal portion of the flexible tube and the catheter hub are positioned in the housing. The guide wire has a proximal end positioned in the housing and a distal end positioned in a lumen of the needle. The catheter insertion device also includes a handle coupled to the catheter, wherein movement of the handle relative to the housing moves the catheter hub from a position in the housing to a position outside of the housing.

Abstract: An interventional catheter is adapted for treating a blood vessel. In an embodiment, the catheter includes an elongate shaft sized for insertion in a blood vessel and a stent positioned on a distal region of the elongate shaft. An expandable dilation member is coupled to a distal region of the elongate shaft. The expandable dilation member is adapted to expand outward. A stent containment member is positioned over the elongate shaft and the stent to contain the stent in a collapsed state.

Abstract: A system and method providing a catheter assembly for engaging a stenosis. The assembly includes a catheter defining a first lumen and a second lumen spaced apart and disposed about a longitudinal axis. The catheter includes an opening in communication with the first lumen to define a flow path having an angle incident to the longitudinal axis. A first marker; and a second marker disposed on the catheter are spaced equidistantly from the opening. The assembly includes a balloon having a first end and a second end each sealed about the catheter and equidistantly from the opening to define a holding volume therebetween. The opening is disposed within the holding volume thereby placing the first lumen in sealed fluid communication with the holding volume. In a preferred embodiment, the catheter assembly includes a stem disposed about the balloon, and the balloon is configured to engage the stent with a stenosis.

Abstract: An implantable, body-driven shunt pump includes a pump body defining a fluid inlet, a fluid outlet and a fluid chamber therebetween; an inlet valve arranged in the fluid inlet, the inlet valve being a one-way valve arranged such that it is operable to allow fluid flow into the fluid chamber and to prevent fluid flow out of the fluid chamber; and an outlet valve arranged in the fluid outlet, the outlet valve being a one-way valve arranged such that it is operable to allow fluid flow out of the fluid chamber and to prevent fluid flow into the fluid chamber. The pump body includes an expandable and contractible component in a portion of the pump body that defines the fluid chamber such that the fluid chamber changes volume in response to a change in pressure of fluid in the fluid chamber.

Abstract: A blood coagulating device can include an absorbent body; and a hemostatic lysine composition associated with the body. The body can have a cylindrical or conical member having a first end having the hemostatic composition, the first end being configured for insertion into a nasal passageway. A method for coagulating blood can include providing a powdered hemostatic lysine composition; and applying the powdered hemostatic lysine composition to blood so as to cause the blood to coagulate and form a clot. The coagulation can occur in a nasal passageway away from a blood vessel. The method can include providing at least one absorbent member having the powdered hemostatic lysine composition; and applying the at least one absorbent member to the blood so that the powdered hemostatic lysine composition causes the blood to coagulate and clot.

Abstract: Methods to collect use data of a user during customized skin care by using a specimen dispensing device are presented. Methods to utilize the embedded memory and electrical interface of the dispensing device and dispensers to collect use data of said user are also presented. The invention may also be applied to health care and personal care needs.

Abstract: A medical fluid suspension generating apparatus for performing medical procedures includes a Venturi-agitating tip assembly composed of a multi-channel arrangement at a proximal first end thereof and a tip at a distal second end thereof. The apparatus also includes a compressed medical fluid unit fluidly connected to the multi-channel arrangement at a proximal first end of the Venturi-agitating tip assembly and a medical solution fluidly connected to the multi-channel arrangement at a proximal first end of the Venturi-agitating tip assembly. Pressurized gas, from the compressed medical fluid unit, and the medical solution are combined within the Venturi-agitating tip assembly in a manner generating an enriched medical suspension that is ultimately dispensed from the suspension delivery apparatus.

Abstract: A system and method includes delivery of a redox gas solution to treat onychomycosis, wherein the redox gas solution comprises a reactive species dissolved in a perfluorocarbon liquid, and wherein the perfluorocarbon liquid comprises of an anti-inflammatory in a perfluorocarbon liquid and wherein the reactive species may include, alone or in combination, one or more of reactive oxygen, reactive nitrogen, reactive chlorine, or reactive bromine species, and the perfluorocarbon liquid may include perfluorodecalin.

Abstract: An applicator for a microprojection array is described. In one embodiment, the applicator comprises an energy-storing element. Application of force causes the compressed energy-storing element to extend or transition from first and second configurations, releasing stored energy to deploy a holding member in the application which is configured to hold an array of microprojections. In another embodiment, the applicator comprises an energy storing element with two stable configurations, a first stable configuration and second stable configuration. Application of force causes the energy-storing element to transition from the higher energy first stable configuration to the lower energy second stable configuration, releasing the difference in energies of the two states to deploy a holding member in the application which is configured to hold an array of microprojections.

Abstract: Provided are a transdermal absorption sheet capable of achieving control of the dissolution rate and suppression of diffusion of a drug, and a method of producing the same. A transdermal absorption sheet includes a sheet portion, and a plurality of needle-like protruding portions formed by a plurality of frustum portions arranged on the sheet portion and needle portions arranged on the frustum portions, in which at least one of the needle-like protruding portions has a cavity portion extending from the sheet portion to the frustum portion.

Abstract: Provided is a transdermal absorption sheet capable of improving strength against impact at the time of puncture. A transdermal absorption sheet includes a sheet portion and a plurality of needle-like protruding portions arranged on a first principal surface of the sheet portion, in which the sheet portion has a center portion which is a region in which the plurality of needle-like protruding portions are formed, and an outer edge portion which is a region from the center portion to an end portion, and a maximum thickness of a thickness portion of the outer edge portion is larger than an average thickness of the center portion.

Abstract: A method of producing a transdermal absorption sheet includes: filling needle-like recessed portions of a mold with a drug solution that is a polymer solution containing a drug; drying the drug solution filling the needle-like recessed portions to form a drug layer containing the drug; supplying a polymer layer forming solution to the mold, the mold provided with a step portion that has a height different from a height of a region in which the needle-like recessed portion is formed in a periphery of the region in which the needle-like recessed portion is formed in a range of equal to or greater than the step portion as seen from above, and then fixing a contact position of the polymer layer forming solution and the mold to the step portion while reducing the polymer layer forming solution; and drying the polymer layer forming solution to form a polymer layer.

Abstract: Aspects herein relate to a medical device for providing a leak-resistant seal for use in a vascular access device. In various embodiments, a device for vascular access hemostasis is included. The device can include an enclosure configured to at least partially receive a medical device, the enclosure defining a cavity. The enclosure can have a first seal portion and a second seal portion, the cavity disposed between the first seal portion and the second seal portion. The enclosure can include the second seal portion comprising a split, septum seal. The enclosure can include a barrel in structural communication with the second seal portion. The device can include a constriction ring disposed around the barrel, the constriction ring interfacing with the second seal portion to limit movement of the split, septum seal.

Abstract: The subject invention is directed to a new and useful coupling system for connecting a tube set to a trocar. More particularly, the system includes a trocar connector having no more than two coaxial flow passages formed therein including an inner flow passage and an outer flow passage. The inner flow passage is defined by an inner annular wall and the outer flow passage is defined between the inner annular wall and an outer annular wall. A dual lumen tube set is included with a first tube having a first diameter and a second tube having a second diameter that is greater than the diameter of the first tube. The system further includes a coupling including a generally cylindrical body having a first end portion configured to mate with the two coaxial flow passages of the trocar connector and a second end portion configured for attachment to the two tubes of the dual lumen tube set.

Abstract: Cap and cleaning devices antiseptically maintain patient fluid line access valves to minimize the risk of infection via catheters. The devices have a cap that may contain a dry pad impregnated with an antimicrobial agent. The cap covers the access portion of the access valve when not in use. The devices have a hood that contains a wet pad impregnated with a cleaning solution and, optionally, an antimicrobial agent. The wet pad cleans the access portion of the access valve prior to and optionally, after the access valve is utilized to access the patient fluid line.

Abstract: A flow control clamp having a first member and a second member movable from a first open position to a second irreversibly closed position wherein flow through a tube associated with the clamp is irreversibly prevented and cannot be restored. Systems and methods using such clamps are also disclosed.

Abstract: A method of preparing an electrode for use with an implantable medical device, the electrode including a titanium surface, the method including: maintaining a nitrogen gas environment proximate to the titanium surface, delivering energy to a portion of the titanium surface, modifying the portion of the titanium surface with the energy delivered to the titanium surface, and forming titanium nitride by reacting titanium at the portion of the titanium surface with nitrogen from the nitrogen gas environment. Modifying includes increasing a surface area of the portion of the titanium surface, and removing titanium from the portion of the titanium surface. The titanium nitride is formed at the portion of the titanium surface where titanium has been removed.

Abstract: A method of forming an electrode array is disclosed, the method comprising: forming an elongate comb structure comprising a plurality of longitudinally-spaced electrode contacts extending from and supported by a spine; electrically connecting each of a plurality of electrically conductive pathways to a respective one of the plurality of electrode contacts; placing the conductive pathways adjacent the contacts; placing silicone over the conductive pathways and contacts; curing the silicone so as to substantially retain the longitudinal spacing between neighboring contacts; and severing the spine from the plurality of electrode contacts.

Abstract: The present disclosure generally relates to a system for treating headaches and other pain associated with the occipital nerves. More particularly, the disclosure relates to a system of treating pain by selectively activating specific nerve fibers with a single, fault-resistant contact situated proximate to, but not in direct contact with, portions of one or more the occipital nerves. Additional measures ensure the lead does not migrate or fracture, resulting in long-lasting pain relief.