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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Форма поиска

Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 6604. Отображено 100.
26-01-2012 дата публикации

Modified Liquid Trap Cup and a Liquid Trap Assembly

Номер: US20120017907A1
Автор: Fei-Fang Hsiao
Принадлежит: CHINA MEDICAL UNIVERSITY

A liquid trap cup is provided. The liquid trap cup comprises a hollow cup tube with a upper portion and a lower portion, a piston element with a top portion and a tail portion and a liquid discharge structure, in which the piston element is arranged airtight in the lower portion and is movable between a start point and an end point of the lower portion so as to control the opening and the closing of the liquid discharge structure. A liquid trap assembly using the liquid trap cup is provided. The liquid trap assembly comprises said liquid trap cup and a multi-necked adapter tube with an expanded-plate structure, in which expanded-plate structure can be tightly sealed with the liquid trap. When applying the liquid trap assembly to a breathing system, it can simply drain the liquid collected in the liquid trap cup without disassembling the liquid trap assembly so as to prevent the infection problems of patients and reduce the burden of the medical staff.

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24-05-2012 дата публикации

Respiratory system

Номер: US20120125333A1
Принадлежит: PLASTIFLEX BELGIUM

The present invention relates a modular respiratory system to which different parts can be added in a convenient way enabling such upgraded respiratory system to deliver the most comfortable respiratory conditions at an acceptable cost of ownership.

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31-05-2012 дата публикации

Arrangement in a Patient Breathing Tube and a Patient Breathing Tube

Номер: US20120136272A1
Принадлежит: General Electric Co

Arrangement in a patient breathing tube and a patient breathing tube. The breathing tube is provided with a patient end and a ventilator end. The arrangement comprises a sampling conduit having a sampling tip provided at a pre-determined point of the patient end to define a sampling point. The arrangement further comprises a support structure locating the sampling tip of the sampling conduit apart from the inner surface of the patient breathing tube.

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14-06-2012 дата публикации

Sound dampening in positive airway pressure devices

Номер: US20120145155A1
Принадлежит: ResMed Pty Ltd

A CPAP system includes a PAP device ( 5 ) structured to generate a supply of pressurized air, a patient interface ( 15 ) adapted to engage with the patient's face to provide a seal, an air delivery conduit ( 102,104 ) provided between the PAP device and the patient interface to deliver the supply of pressurized air along a gas delivery path from the PAP device to the patient interface, and a muffler ( 100 ) provided along the gas delivery path downstream of the PAP device.

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21-06-2012 дата публикации

Connector part and fluid connection structure

Номер: US20120153613A1
Автор: Heikki Haveri, Jani Kauppi
Принадлежит: General Electric Co

Connector part comprising a body part for connecting to a counterpart for creating a fluid tight seal when fitted together. The connector part also comprises a seal element made of resilient material and a space which is capable to receive the seal element made of resilient material when the fluid tight seal is made. The connector part can be used for forming a fluid tight connection structure.

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25-10-2012 дата публикации

Double-ended blower and volutes therefor

Номер: US20120266887A1
Принадлежит: ResMed Pty Ltd

A variable speed blower for Continuous Positive Airway Pressure (CPAP) ventilation of patients includes two impellers in the gas flow path that cooperatively pressurize gas to desired pressure and flow characteristics. Thus, the blower can provide faster pressure response and desired flow characteristics over a narrower range of motor speeds, resulting in greater reliability and less acoustic noise.

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01-11-2012 дата публикации

Two-phase surgical procedure for creating a pneumostoma to treat chronic obstructive pulmonary disease

Номер: US20120277584A1
Принадлежит: Portaero Inc

A two-phase surgical procedure is disclosed for creating a pneumostoma to treat chronic obstructive pulmonary disease The first phase is a procedure to induce creation of a localized pleurodesis and is preferably performed as an outpatient procedure. The second phase is a procedure to introduce a surgical instrument into the lung via the pleurodesis to create the pneumostoma. An interval of about one of more days between the first and second phases allows the formation of a stable pleurodesis to prevent pneumothorax during the procedure.

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15-11-2012 дата публикации

Mechanical Insufflation/Exsufflation Airway Clearance Apparatus

Номер: US20120285460A1
Принадлежит: LUNG ASSIST Inc

An MIE apparatus has a blower, a direction valve, an oscillator, and a mask hose connector. The blower is connected to the direction valve, which is connected to the oscillator, which is connected to the hose connector. During insufflation, a direction valve connects exhaust of a blower to an oscillator, causing positive pressure at the hose connector. During exsufflation, the direction valve connects the blower intake to the oscillator, causing negative pressure at the hose connector. The oscillator is a butterfly valve with a 360° rotating disc. During insufflation, the disc is fixed to steadily modulate the airflow. During exsufflation, the oscillator is inactive or in flutter mode. When inactive, the disc is fixed to allow maximum air flow. In flutter mode, the disc continuously rotates so that the air flow rapidly alternates between maximum and minimum.

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06-12-2012 дата публикации

Interface

Номер: US20120305001A1
Автор: Stanislav Tatkov
Принадлежит: Fisher and Paykel Healthcare Ltd

A user interface comprising a non-sealing nasal cannula and a mask arranged about the nasal cannula, the mask including a seal configured with a user's face to allow the interface to be pressurised, the cannula configured to deliver breathing gases to the nares of a user at a flow rate exceeding the intended user's peak inspiratory flow requirements so that the mask and the user's pharynx are flushed continuously with fresh breathing gases to reduce dead space.

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27-12-2012 дата публикации

System, Method and Apparatus for Removal of Volatile Anesthetics for Malignant Hyperthermia

Номер: US20120325213A1
Принадлежит: Individual

Systems, methods, and apparatus for removing volatile anesthetics from an anesthesia or ventilation system to minimize the effects of malignant hyperthermia in susceptible patients. According to one aspect of the present invention, a system for removing volatile anesthetics is provided. A first filter component placed in fluid communication with an inspiratory limb of an anesthesia or ventilation system such that volatile anesthetics will pass through the first filter component during operation of the anesthesia or ventilation system. A second filter component is operably coupled to the expiration port of the anesthesia or ventilation system such that gases passing through the expiratory limb of the anesthesia or ventilation system pass through the second filter component. The first filter component and second filter component are adapted to effectively remove volatile anesthetics passing through the respective filters.

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10-01-2013 дата публикации

Elbow assembly

Номер: US20130008439A1
Принадлежит: ResMed Pty Ltd

An elbow assembly for a mask system includes an elbow including a slot and a port, an anti-asphyxia valve adapted to be received within the slot and including a flap portion adapted to selectively close the port depending on the presence of pressurized gas, and a clip member to secure the anti-asphyxia valve to the elbow. The clip member includes a slot that is adapted to interlock with a protrusion provided to the anti-asphyxia valve.

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10-01-2013 дата публикации

Adapters for use with an anesthetic vaporizer

Номер: US20130008441A1

Adapters are provided for establishing fluid communication between an anesthetic agent container and an anesthetic vaporizer having a fluid port. The adapter may be mountable on the vaporizer to cooperate with the spout of an anesthetic agent container or may be mountable on an anesthetic agent container to cooperate with the fluid port of an anesthetic vaporizer to provide a sealing and/or retaining relationship therebetween.

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09-05-2013 дата публикации

Disposable protective device for suction tube

Номер: US20130112196A1
Автор: Tien-Hsiung Ku
Принадлежит: CHANGHUA CHRISTIAN HOSPITAL

The disposable protective device for suction tube includes an encapsulating bag unit and a connective tubular unit. The encapsulating bag unit has a protruding circular portion. The encapsulating bag unit has an interior space which may house a suction tube. The encapsulating bag unit has a first opening and a second opening at its two ends, with the diameter of the second opening larger than or equal to that of the first opening. The connective tubular unit has a first connector, a second connector and a third connector. The first connector may connect with the second opening. A cover may cover the first connector. The second connector may connect with a ventilator. The third connector is provided at the bottom part of the connective tubular unit and may connect with a tracheostomy tube or a tube inside the trachea.

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16-05-2013 дата публикации

Anesthetic Inhalation Aid Device and Attachment Used for the Same

Номер: US20130118484A1
Автор: Naoyuki ISHIKITA
Принадлежит: Individual

An inhalation mask, an artificial nose unit, an anesthetic gas concentration detector, an extension tube, an anesthesia attachment, and an elastic bag are in communicative connection in sequence. The elastic bag has a mixing chamber formed therein and has an anesthetic inlet, an air inlet, and an outlet port each formed at the boundary to the exterior. The anesthesia attachment includes a hollow structure and an evaporation injector syringe. The outlet port of the elastic bag is in communicative connection with the hollow structure through its opening, and the evaporation injector syringe tightly mates with the interior of another opening. The anesthetic introduced into the mixing chamber is vaporized and then mixed with air introduced from the air inlet into mixed gas. The mixed gas is supplied from the outlet port to the inhalation mask by compressing the elastic bag or other procedures.

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30-05-2013 дата публикации

Oscillating Positive Expiratory Pressure Device

Номер: US20130133649A1
Принадлежит: Individual

An oscillating positive expiratory pressure apparatus having a housing defining a chamber, a chamber inlet, a chamber outlet, a deformable restrictor member positioned in an exhalation flow path between the chamber inlet and the chamber outlet, and an oscillation member disposed within the chamber. The deformable restrictor member and the oscillation member are moveable between an engaged position, where the oscillation member is in contact with the deformable restrictor member and an disengaged position, where the oscillation member is not in contact with the deformable restrictor member. The deformable restrictor member and the oscillation member move from the engaged position to the disengaged position in response to a first exhalation pressure at the chamber inlet, and move from the disengaged position to an engaged position in response to a second exhalation pressure at the chamber inlet.

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30-05-2013 дата публикации

METHOD AND APPARATUS FOR ADJUSTING RESPIRATORY MASK SEALING FORCE

Номер: US20130133657A1
Автор: Berthon-Jones Michael
Принадлежит: RESMED LIMITED

A mask assembly includes a mask with an inflatable bladder. The internal pressure of the inflatable bladder can be set to be higher than the delivered therapeutic pressure. The pressure offset may be constant, or it may vary over the range of therapeutic pressures. Thus, the force necessary to maintain a contact seal between the mask and the patient can be reduced, thereby providing a system that is more comfortable to the patient, which increases patient compliance. 1. A patient interface comprising:a frame;a cushion provided to the frame and defining a chamber structured to be in communication with a first source that is adapted to provide a first pressure to the chamber; anda bladder associated with the cushion and configured to engage a face of a patient, the bladder having a side wall, and the side wall being thinner in a face contacting region of the bladder than in a face non-contacting region, the side wall thickness being progressively thicker from the face contacting region to the face non-contacting region,wherein a rate of change in the thickness of the side wall varies around the face contacting region of the bladder, andwherein the bladder is configured to be in communication with a second source that provides a second pressure to the bladder that is higher than the first pressure by a positive offset amount.2. The patient interface of claim 1 , wherein the bladder is configured to receive gas from the chamber.3. The patient interface of claim 2 , wherein the chamber is configured to be in fluid communication with both the first and second sources.4. The patient interface of claim 3 , wherein the chamber comprises an inlet port configured to be in fluid communication with the first source and comprises an outlet port configured to be in fluid communication with the second source.5. The patient interface of claim 4 , wherein the bladder includes an inlet port configured to be in fluid communication with the second source.6. The patient interface of ...

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30-05-2013 дата публикации

MASK SYSTEM

Номер: US20130133658A1
Принадлежит: RESMED LIMITED

A full face mask system for treatment of respiratory disorder with Continuous Positive Airway Pressure equipment suitable to generate a supply of gas at positive pressure to be delivered to a patient's airways, the mask system comprising a frame module; a cushion module provided to the frame module and adapted to form a seal with the patient's face; an elbow module provided to the frame module and adapted to be connected to an air delivery tube to deliver breathable gas to the patient; and headgear removably attachable to the frame module. 1. A full face mask system for treatment of respiratory disorder with Continuous Positive Airway Pressure equipment suitable to generate a supply of gas at positive pressure to be delivered to a patient's airways , the mask system comprising:a frame module;a cushion module provided to the frame module and adapted to form a seal with the patient's face;an elbow module provided to the frame module and adapted to be connected to an air delivery tube to deliver breathable gas to the patient; andheadgear removably attachable to the frame module, wherein:the frame module is structured to assist in maintaining the cushion module and the elbow module in an operative position with respect to the patient's face,the frame module includes an open construction, said frame module being structured to retain the elbow module,the frame module includes two headgear connectors to connect with the headgear, the two headgear connectors each includes a slot at a free end of the connector adapted to receive a respective headgear strap of the headgear,each said headgear connector is removably coupled to the frame module, each said headgear connector including a clip structure adapted to removably engage with a corresponding portion of the frame module,the cushion module is structured to interface with the frame module and form a seal with the patient's nose and mouth,the cushion module includes a main body of relatively harder material and a cushion of ...

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06-06-2013 дата публикации

MASK SYSTEM

Номер: US20130139822A1
Принадлежит:

A mask system including a headgear and cushion module and a seal and frame module provided to the headgear and cushion module. The seal and frame module includes a sealing portion adapted to form a seal with the patient's face and a frame portion adapted to form a breathing chamber. The headgear and cushion module includes a cushion region adapted to support and shape the sealing portion and a headgear region adapted to support and stabilize the mask system on the patient's face. 1. A mask system comprising:a headgear and cushion module; anda seal and frame module provided to the headgear and cushion module,the seal and frame module including a sealing portion adapted to form a seal with the patient's face and a frame portion adapted to form a breathing chamber, and the headgear and cushion module including a cushion region adapted to support and shape the sealing portion and a headgear region adapted to support and stabilize the mask system on the patient's face.2. A mask system according to claim 1 , wherein the headgear and cushion module includes a single piece construction.3. A mask system according to claim 1 , wherein the headgear and cushion module is cut by ultrasonic die cutting to provide the headgear and cushion module with substantially rounded edges.4. A mask system according to claim 1 , wherein the cushion region includes at least one layer of foam.5. A mask system according to claim 4 , wherein the cushion region includes a first softer layer of foam and a second harder layer of foam.6. A mask system according to claim 1 , wherein the seal and frame module include a single piece construction.7. A mask system according to claim 1 , wherein the seal and frame module is constructed of silicone.8. A mask system according to claim 1 , wherein the frame portion is structured to receive an elbow.9. A mask system according to claim 1 , wherein the headgear and cushion module includes outer fabric layers.10. A mask system according to claim 1 , wherein the ...

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13-06-2013 дата публикации

ERGONOMIC AND ADJUSTABLE RESPIRATORY MASK ASSEMBLY WITH FRAME

Номер: US20130146059A1
Принадлежит: RESMED LIMITED

A respiratory mask assembly for delivering breathable gas to a patient includes a frame having a front surface and a rear surface, opposite the front surface, and adapted in use to face the patient. The frame defines an inner wall and an outer wall extending from the rear surface, the inner and outer walls being spaced to define a channel therebetween. A cushion is removably attachable to the frame such that the cushion and frame are repeatably engagable with and disengagable from one another. The cushion includes a side wall to be inserted into the channel of the frame, the side wall having a first interlocking surface that engages a second interlocking surface provided in the channel when the cushion and frame are engaged with one another. The first and second interlocking surfaces interlock with one another to removably attach the cushion to the frame. 156-. (canceled)57. A frame for a respiratory mask assembly that delivers breathable gas to a patient , the frame comprising:a main body having a front surface and a rear surface adapted in use to face the patient, the main body having an aperture extending through the front surface for the introduction of breathable gas into a nasal breathing cavity defined by the frame; andan inner wall and an outer wall each extending rearwardly from the rear surface, the inner and outer walls being spaced to define a channel therebetween that is structured to receive a side wall of a cushion such that the cushion may be repeatedly attached to and detached from the frame, wherein the main body and the inner and outer walls are formed in one piece and the inner and outer walls are spaced in parallel, wherein a length of the inner wall is different than a length of the outer wall such that the inner wall protrudes away from the rear surface a distance that is different than a distance the outer wall protrudes away from the rear surface,wherein at least a portion of the channel is shaped and dimensioned to generally follow a ...

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13-06-2013 дата публикации

CUSHION FOR A PATIENT INTERFACE DEVICE

Номер: US20130146060A1
Принадлежит: KONINKLIJKE PHILIPS ELECTRONICS N.V.

A cushion () for a patient interface device includes a patient contacting portion () and wall portions ( ). The wall portions include a plurality of voids () and/or orifices therein. The patient contacting portion and the wall portions may be made of a material having a hardness of between 5 and 60 on the Shore 00 scale. Also, the parts of the wall not having the plurality of voids/orifices provided therein may have a cross-sectional thickness of 4 mm or greater. The voids may include a first void provided in an inner side of a first one of the wall portions and a second void provided in an outer side of the first one of the wall portions. The first void and the second void are positioned across from and overlapping one another. 1103056846. A cushion ( , ) for a patient interface device ( , ) , comprising:{'b': 12', '32', '60, 'a patient contacting portion (, ); and'}{'b': 18', '20', '22', '24', '34', '66', '68', '70', '72', '26', '74, 'one or more wall portions (, , , , , , , , ) adjacent the patient contacting portion, wherein the one or more wall portions include a plurality of voids (, ) therein, wherein the patient contacting portion and the one or more wall portions are made of a material having a hardness of between 5 and 60 on the Shore 00 scale.'}2. The cushion according to claim 1 , wherein the patient contacting portion and the one or more wall portions are made of a unitary piece of the material.3. The cushion according to claim 2 , wherein the material is an RTV-2 silicone.4. The cushion according to claim 1 , wherein the plurality of voids comprise at least one first void provided in an inner side of the one or more wall portions and at least one second void provided in an outer side of the one or more wall portions.5. The cushion according to claim 1 , wherein the parts of the one or more wall portions not having the plurality of voids provided therein have a cross-sectional thickness of 4 mm or greater.6. The cushion according to claim 5 , wherein ...

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20-06-2013 дата публикации

Tracheal tube adaptor and flaring jig

Номер: US20130152355A1
Принадлежит: COVIDIEN LP

The present disclosure describes systems and methods that utilize a tracheal tube adaptor system. The tracheal tube adaptor system includes a tracheal tube adaptor and/or a flaring jig. A proximal end of a tracheal tube may be flared and the tracheal tube adaptor may be coupled to the proximal end of the tracheal tube. The tracheal tube adaptor may be configured to easily attach and detach an end connector. The end connector may be used to couple a variety of medical devices such as a ventilator, a manual respirator, a nebulizer, a vaporizer, suctioning equipment, and so forth, to the tracheal tube. The use of the tracheal tube adaptor system and methods enables the rapid detachment and attachment of various end connectors, thus allowing the coupling of the tracheal tube to a variety of medical devices.

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20-06-2013 дата публикации

Patient interface device with a frame assembly having a double-y supporting structure

Номер: US20130152937A1
Принадлежит: KONINKLIJKE PHILIPS ELECTRONICS NV

A patient interface device ( 2,102 ) is includes a cushion ( 6,106 ) and a frame assembly ( 60,160 ) coupled to the cushion, the frame assembly including a main frame member ( 4,104 ) and a stiffening structure ( 62,162 ) coupled to the main frame member, the stiffening structure having a main arm ( 64,164 ), a first Y-portion coupled to a first end of the main arm having first and second front branches extending at upward and downward angles, respectively, from the first end of the main arm, and a second Y-portion coupled to a second end of the main arm having first and second rear branches extending at upward and downward angles, respectively, from the second end of the main arm.

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20-06-2013 дата публикации

PATIENT INTERFACE DEVICE WITH AUTO-ADJUSTING CUSHION

Номер: US20130152938A1
Принадлежит: KONINKLIJKE PHILIPS ELECTRONICS N.V.

A patient interface device () includes a frame member () and a cushion () having a main body, a sealing portion, and first and second posts extending from the main body. The frame member defines a first orifice and a second orifice. The first post of the cushion is rotateably received within the first orifice and the second post is rotateably received within the second orifice in a manner that permits the cushion to rotate relative to the frame member. 1. A patient interface device , comprising:a frame member defining a first orifice and a second orifice, the frame member including a generally annular central member defining a central orifice, a first main arm that extends from a first side of the central member and a second main arm extends from a second side of the central member; anda cushion having a main body, a sealing portion provided at a first end of cushion, and a first post extending from a first side of the main body and a second post extending from a second side of the main body, wherein a second end of the cushion opposite the sealing portion defines a fluid coupling orifice structured to be coupled to a fluid connector, wherein the second end including the fluid coupling orifice is inserted through the central orifice of the central member of the frame member, and wherein the first post is rotateably received within the first orifice and the second post is rotateably received within the second orifice in a manner that permits the cushion to rotate relative to the frame member.2. The patient interface device according to claim 1 , wherein the first orifice and the second orifice are circular and the first post and the second post are cylindrical.3. The patient interface device according to claim 2 , wherein the first post and the second post each include an inner cylindrical portion claim 2 , an outer cylindrical portion claim 2 , and an enlarged portion provided between the inner cylindrical portion and the outer cylindrical portion.4. The patient ...

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27-06-2013 дата публикации

MASK VENT

Номер: US20130160769A1
Принадлежит: RESMED LIMITED

A mask system includes a mask component including one or more openings for gas washout and a vent component provided to the mask component. The vent component includes one or more tracks or grooves along its outer surface adapted to guide gas washout. The vent component is adapted to cover the one or more openings in the mask component so that gas washout escapes along the one or more tracks or grooves between an outer surface of the mask component and the vent component. 199-. (canceled)100. A mask system comprising:a mask component including one or more openings for gas washout; anda vent component provided to the mask component, the vent component including one or more tracks or grooves along its outer surface adapted to guide gas washout,the vent component being adapted to cover the one or more openings in the mask component so that gas washout escapes along the one or more tracks or grooves between an outer surface of the mask component and the vent component.101. A mask system according to claim 100 , wherein the mask component is an elbow.102. A mask system according to claim 100 , wherein the mask component is a mask frame.103. A mask system according to claim 100 , wherein one of the openings in the mask component provides an entry/exit window to receive the vent component.104. A mask system according to claim 100 , wherein the one or more tracks or grooves are provided on one or both sides of the vent component.105. A mask system according to claim 104 , wherein the track or groove is radially arched in a first direction on a first side of the vent component claim 104 , and the track or groove is radially arched in a second direction on a second side of the vent component claim 104 , further wherein the first direction is opposite the second direction.106. A mask system according to claim 100 , wherein the vent component is deformable to assemble or disassemble to the mask component.107. A mask system according to claim 106 , wherein the vent component ...

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11-07-2013 дата публикации

ERGONOMIC AND ADJUSTABLE RESPIRATORY MASK ASSEMBLY WITH ELBOW ASSEMBLY

Номер: US20130174839A1
Принадлежит: RESMED LIMITED

A respiratory mask assembly for delivering breathable gas to a patient includes a frame having a front surface and a rear surface adapted in use to face the patient. The frame includes a main body providing an aperture therethrough for the introduction of breathable gas into a nasal breathing cavity. An elbow assembly is swivelably coupled to the front surface of the frame. The elbow assembly includes a swivel elbow that defines an intake port and an exhaust port separated from the intake port using a baffle. The elbow assembly includes an end portion that interfaces with the aperture of the frame. 120-. (canceled)21. A respiratory mask assembly for delivering breathable gas to a patient comprising:a mask frame comprising a left first connector portion and a right first connector portion;a mask cushion attached to the mask frame; anda headgear assembly comprising a left second connector portion and a right second connector portion adapted for interconnection with the left and right first connector portions of the mask frame, respectively, whereinthe left first connector portion is only connectable to the left second connector portion, and the right first connector portion is only connectable to the right second connector portion.22. A respiratory mask assembly according to claim 21 , wherein each of the first and second connector portions includes a magnet.23. A respiratory mask assembly according to claim 22 , wherein the magnets of the left first connector portion and the right second connector portion are oriented to repulse each other claim 22 , and the magnets of the right first connector portion the and the left second connector portion are oriented to repulse each other.24. A respiratory mask assembly according to claim 23 , wherein the left second connector portion comprises a first bore configured to receive the magnet of the left first portion claim 23 , and the right second connector portion comprises a second bore configured to receive the magnet of the ...

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11-07-2013 дата публикации

SUPPORT FOR TRACHEOSTOMY OR ENDOTRACHEAL TUBES

Номер: US20130174844A1
Принадлежит:

A device for securing a tracheostomy or endotracheal tube to a patient. 1. A device for securing a medical tube comprising a tracheostomy or endotracheal tube and a slotted flange having a first and a second slot , said device constructed to retain the medical tube to a ventilator tube connector , the device comprising:a neckband having a first and a second end, the neckband comprising an interior foam material, an inner textile surface suitable for placement against human skin, and an outer textile fastening material;a neckband fastening strip having a first end and a second end, the first end of the neckband fastening strip being connected to the first end of the neckband, the neckband and neckband fastening strip having a length sufficient to encircle a human neck, a majority of a length of the neckband fastening strip comprising a non-hook, textile material, the second end of the neckband fastening strip having a hook face surface constructed to releasably fasten to the outer textile fastening material, the second end of the neckband fastening strip being tapered and the neckband fastening strip being sized for insertion into the first and second slots when the flange is pediatric sized; anda ventilator fastener comprising a textile strip having a first end and second end, the textile strip comprising an inner surface that is suitable for placement against skin, the first end of the ventilator fastener being connected to the first end of the neckband, the second end of the ventilator fastener constructed to releasably fasten to the outer textile fastening material, and the ventilator fastener having a length sufficient to encircle a connector and have the second of the ventilator fastener fasten to the outer textile fastening material.2. A device according to claim 1 , wherein a majority of a length of the ventilator fastener being free of a hook surface and the second end of the ventilator fastener comprises a hook surface.3. A method of securing a medical tube ...

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18-07-2013 дата публикации

DEVICE AND METHOD FOR DILATING AN AIRWAY STENOSIS

Номер: US20130184568A1
Принадлежит:

A medical device and a system and for dilating a stenotic airway of a patient are described. The medical device comprises a proximal end, a distal end, and a shaft system having an inflation lumen and a ventilation lumen the proximal end. The shaft system has a proximal shaft section and a distal shaft section. An inflatable balloon is attached to the distal shaft section in a position that is proximal to the distal end. The ventilating tip is distal to the balloon on the distal shaft section and has one or more radially facing openings. A method for treating a stenotic airway includes inserting the medical device into a patient's airway, and dilating and ventilating the airway. 1. A medical device for dilating an airway stenosis , said device comprising:a proximal end;a distal end;a shaft system having an inflation lumen and a ventilating lumen between said proximal end and said distal end, said shaft system having a proximal shaft section and a distal shaft section;an inflatable balloon on said distal shaft section, proximal to the distal end of the medical device; anda ventilating tip on the distal shaft section, distal to the inflatable balloon, said ventilating tip comprising a tip opening and one or more radially facing openings.2. The medical device of wherein the one or more radially facing openings comprise 4 openings.3. The medical device of wherein the radially facing openings have a diameter of between 1 mm and 2 mm.4. The medical device of wherein the radially facing opening are spaced 90 degrees apart.5. The medical device of wherein the inflation lumen and the ventilating lumen are adjacent lumens.6. The medical device of further comprising an atraumatic tip portion.7. The medical device of further comprising one or more direct visualization markers.8. The medical device of wherein the markers are located on the shaft system.9. The medical device of wherein the markers are located on the balloon.10. The medical device of further comprising one or more ...

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25-07-2013 дата публикации

SYSTEMS AND METHODS FOR PROVIDING RESPIRATORY THERAPY

Номер: US20130186395A1
Принадлежит: Vapotherm, Inc.

Systems and methods for respiratory therapy are disclosed. The system may include a nebulizer, an adaptor, and a nasal cannula. The nebulizer is operable to generate an aerosolized medicament and pass the aerosolized medicament through a nebulizer outlet port. The adaptor has a nebulizer coupling port configured to be coupled to the nebulizer outlet port. The nasal cannula is configured to provide a flow of breathing gas from a breathing gas source to the patient. The nasal cannula comprises at least one nasal prong and an attachment device positioned adjacent the at least one nasal prong. The attachment device is configured to secure the adaptor outlet port adjacent an outlet of the nasal prong. The method includes securing a nasal cannula to the patient, attaching an adaptor to the nasal cannula, generating an aerosolized medicament, transferring the aerosolized medicament into the adaptor, and providing a flow of breathing gas to the patient. 1. A system for providing respiratory therapy to a patient comprising:a nebulizer having a nebulizer outlet port, the nebulizer operable to generate an aerosolized medicament and pass the aerosolized medicament through the nebulizer outlet port;an adaptor having an adaptor body, a nebulizer coupling port, and an adaptor outlet port, the nebulizer coupling port of the adaptor configured to be coupled to the nebulizer outlet port of the nebulizer; anda nasal cannula configured to provide a flow of breathing gas from a breathing gas source to the patient, the nasal cannula comprising at least one nasal prong and an attachment device positioned adjacent the at least one nasal prong, the attachment device configured to secure the adaptor outlet port adjacent an outlet of the at least one nasal prong.2. The system of claim 1 , wherein the adaptor outlet port has a cross-sectional area less than the nebulizer coupling port.3. The system of claim 2 , wherein the adaptor body comprises an approximately cone-shaped body extending ...

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25-07-2013 дата публикации

Ventilation Mask with Integrated Piloted Exhalation Valve

Номер: US20130190643A1
Автор: Brambilla Enrico
Принадлежит: Breathe Technologies, Inc.

In accordance with the present invention, there is provided various tubing arrangements and an associated Y-connector which may be used to facilitate the operative interface of the mask to a ventilator within a ventilation system. The tubing arrangement may comprise a pair of bi-lumen tubes. One end of each of the bi-lumen tubes is fluidly connected to the mask, with the opposite end being fluidly connected to the Y-connector. The Y-connector is in turn fluidly connected to one end of either a tri-lumen tube or a quad-lumen tube also included in the tubing arrangement, the opposite end of such tri-lumen tube or quad-lumen tube being fluidly connected to the ventilator. The Y-connector is uniquely configured to fluidly connect certain lumens of the tri-lumen tube or the quad-lumen tube to dedicated, corresponding ones of the lumens included in respective ones of the bi-lumen tubes, and to further allow for the selective detachment of the tri-lumen tube or the quad-lumen tube from the bi-lumen tubes. 1. A respiratory assistance system , comprising:a flow generator;a ventilation mask; and a multi-lumen tube which is fluidly coupled to the flow generator;', 'a first bi-lumen tube which has a generally teardrop-shaped cross-sectional configuration, and is fluidly coupled to and extends between the multi-lumen tube and the ventilation mask; and', 'a second bi-lumen tube which has a generally teardrop-shaped cross-sectional configuration, and is fluidly coupled to and extends between the multi-lumen tube and the ventilation mask., 'a fluid conduit fluidly coupling the flow generator to the ventilation mask, and comprising2. The respiratory assistance system of wherein:the multi-lumen tube defines at least a gas delivery lumen, a valve pilot lumen and a pressure sensing lumen which are each fluidly coupled to the flow generator;the first bi-lumen tube defines a gas delivery lumen which is fluidly coupled to and extends between the gas delivery lumen of the multi-lumen tube ...

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01-08-2013 дата публикации

BREATHING SYSTEM WITH FLOW ESTIMATION

Номер: US20130192600A1
Принадлежит:

A breathing system for ventilating a patient has a gas channel enclosing a gas channel volume (V), and a compliance (C). The system has a flow calculation unit operative to determine a gas flow estimate (Fe) at a flow estimate location in the gas channel. The gas flow estimate (Fe) is based on a relationship between a monitored gas flow (Fm) in the gas channel and a compressible gas flow (Fc) which depends on the compliance (C) in the gas channel. The monitored gas flow (Fm) is a gas flow at a monitoring location in the gas channel and the compressible gas flow (Fc) is a flow of gas in the gas channel between the flow estimate location and the monitoring location, and the flow estimate location is remote from the monitoring location. 1. A breathing system for ventilating a patient , said system having a gas channel having a gas channel volume (V) and a compliance (C) , said system comprising:a flow calculation unit operative to determine a gas flow estimate (Fe) at a flow estimate location in said gas channel, wherein said gas flow estimate is based on a relationship between a monitored gas flow (Fm) in said gas channel and a compressible gas flow (Fc) dependent on said compliance (C) in said gas channel, wherein said monitored gas flow is a gas flow at a monitoring location in said gas channel and said compressible gas flow (Fc) is a flow of gas in said gas channel between said flow estimate location and said monitoring location, and wherein said flow estimate location is remote from said monitoring location.2. System according to claim 1 , wherein said system comprises at least one pressure sensor in communication with said system for measuring at least one pressure at a pressure measurement location in said system respectively claim 1 ,a pressure estimator unit connected to said at least one pressure sensor and operative to determine an estimated pressure (Pe) in said system based on said at least one measured pressure, and{'b': '125', 'wherein said flow ...

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08-08-2013 дата публикации

HUMIDIFIER BYPASS VALVE

Номер: US20130199524A1
Принадлежит: KONINKLIJKE PHILIPS ELECTRONICS N.V.

A valve () for controlling a flow of fluid, the valve having a conduit, first valve portion having an inlet, a first humidifier interface, and a first conduit opening to the conduit. The first valve portion defines a switchable flow path between the inlet and either the first humidifier interface or the first conduit opening. A second valve portion has an outlet, a second humidifier interface, and a second conduit opening to the conduit. The second valve portion defines a switchable flow path between the outlet and either the second humidifier interface or the second conduit opening. Responsive to the first and/or second humidifier interfaces being connected to a humidifier chamber, the fluid flows from the inlet to the outlet through the humidifier chamber, and responsive to the first and second humidifier interfaces being disconnected from the humidifier chamber, the fluid flows from the inlet to the outlet through the conduit. 1. A valve configured to control a flow of fluid through the valve , the valve comprising:a conduit;a first valve portion disposed at a first end of the conduit, the first valve portion having an inlet configured to interface with a respiration circuit, a first humidifier interface configured to be removably connected to a humidifier chamber, and a first conduit opening in fluid communication with an interior of the conduit, the first valve portion being configured to define a switchable flow path between the inlet and either the first humidifier interface or the first conduit opening;a second valve portion disposed at a second end of the conduit, the second valve portion having an outlet configured to interface with a respiration circuit, a second humidifier interface configured to be removably connected to the humidifier chamber, and a second conduit opening in fluid communication with the interior of the conduit, the second valve portion being configured to define a switchable flow path between the outlet and either the second humidifier ...

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08-08-2013 дата публикации

Aerosol therapy device

Номер: US20130199526A1
Автор: Davide Fraccaroli
Принадлежит: MED 2000 Srl

The present invention relates to an aerosol-therapy device, comprising a casing, a compressor group mounted in the casing and air intake and delivery means respectively to and from said compressor group. The compressor group comprises a motor and a compressor device which can be driven by the motor to draw in and deliver air respectively through the air delivery and intake means. In addition, the compressor device comprises a piston attached and supported solely by the casing and a cylinder sliding on the piston and eccentrically connected to the drive shaft of the motor.

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08-08-2013 дата публикации

Apparatus for control of oxygen and/or air flow to nasal prongs

Номер: US20130199531A1
Принадлежит: Neotech Products Inc

An air or oxygen flow supply system between a supply source and nasal prongs applicable to a patient, comprising a succession of flow ducts having different flow areas, there being junctions between successive of the ducts, the flow areas defined by A 1 , A 2 - - - A n where n>2, the flow areas decreasing at the junctions, in the direction of the flow.

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08-08-2013 дата публикации

GAS DELIVERY VENTURI

Номер: US20130199535A1
Принадлежит: Aeon Research and Technology, LLC

A venturi connector includes a housing having a mixing chamber defined therein and at least one window that is in fluid communication with the mixing chamber and is open to atmosphere to allow air to be entrained into the mixing chamber. The connector includes a nozzle actuator member includes a body having a plurality of discrete nozzles formed therein. The nozzles are defined by different sized venturi orifices through which gas flows, thereby allowing the concentration of the gas delivered to the patient to be varied. The nozzle actuator member is disposed within one window formed in the housing between the gas port and the mixing chamber such that the position of the nozzle actuator member within the housing can be adjusted so as to position one of the discrete nozzles into the gas flow path, thereby controlling the flow rate of the gas into the mixing chamber and ultimately the concentration of gas delivered to the patient. 1. A venturi connector comprising:a housing having a mixing chamber defined therein and at least one window that is in fluid communication with the mixing chamber and is open to atmosphere to allow air to be entrained into the mixing chamber to form a venturi effect;a gas port extending outwardly from the housing for connecting to a supplemental gas source, the gas port defining a gas flow path for delivering the supplemental gas to the mixing chamber; anda nozzle actuator member comprising a body having a plurality of discrete nozzles formed therein, the nozzles being defined by different sized venturi orifices through which gas flows; the nozzle actuator member being disposed within one window formed in the housing between the gas port and the mixing chamber such that the position of the nozzle actuator member within the housing can be adjusted so as to position one of the discrete nozzles into the gas flow path, thereby controlling the flow rate of the supplemental gas into the mixing chamber and a concentration of the supplemental gas ...

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08-08-2013 дата публикации

Breathing mask for feeding a breathing gas to a mask user and discharge device for discharging breathing gas

Номер: US20130199536A1
Автор: Achim Biener, Bernd Lang
Принадлежит: ResMed R&D Germany GmbH

A breathing mask arrangement for delivering breathable gas to a patient includes a reinforcement element, a mask engaged with the reinforcement element and having a mask base body defining a mask interior and a sealing lip structured to engage a patient's face, a forehead rest including forehead padding that is structured to engage a patient's forehead, and a fixing mechanism to fix the forehead rest relative to the reinforcement element. The mask base body and the sealing lip are two pieces that are fixedly attached to one another. The forehead rest is moveably coupled to the reinforcement element to allow movement of the forehead rest relative to the reinforcement element. The forehead rest includes a pair of coupling structures structured to be coupled to an upper head band arrangement and the reinforcement element includes a pair of coupling structures structured to be coupled to a lower head band arrangement.

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08-08-2013 дата публикации

MASK SYSTEM

Номер: US20130199537A1
Принадлежит: RESMED LIMITED

A mask system for delivery of respiratory therapy to a patient includes a nares portion and a mouth portion and an inlet conduit connected to at least one of the nares portion and the mouth portion to deliver the pressurized, breathable gas. The mask system is adapted to selectively utilize the nares portion and/or the mouth portion in a first mode utilizing both the nares portion and the mouth portion, and in a second mode utilizing the nares portion and not utilizing the mouth portion. 1. A mask system for delivery of respiratory therapy to a patient , comprising:a nares portion adapted to form a seal with the patient's nares;a mouth portion including a mouth chamber and a mouth sealing portion adapted to form a seal with the patient's mouth, the mouth chamber including an opening adapted to selectively receive pressurized, breathable gas; andan inlet conduit connected to at least one of the nares portion and the mouth portion to deliver the pressurized, breathable gas,wherein the mask system is adapted to selectively utilize the nares portion and/or the mouth portion in a first mode utilizing both the nares portion and the mouth portion, and in a second mode utilizing the nares portion and not utilizing the mouth portion.2. The mask system according to claim 1 , further comprising a plug adapted to plug the opening in the mouth chamber in the first mode so that the mouth chamber is utilized as a mouth seal that does not deliver any of the pressurized claim 1 , breathable gas to the patient's mouth.3. The mask system according to any one of or claim 1 , wherein the inlet conduit is connectable to the nares portion to deliver the pressurized claim 1 , breathable gas to the nares of the patient.4. The mask system according to claim 1 , wherein when in use in the first mode claim 1 , the opening in the mouth chamber is connectable to the inlet conduit to deliver the pressurized claim 1 , breathable gas to the patient's mouth.5. The mask system according to claim 4 , ...

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08-08-2013 дата публикации

FLUID COUPLING CONDUIT WITH EXHAUST GAS NOISE REDUCTION

Номер: US20130199538A1
Принадлежит: KONINKLIJKE PHILIPS ELECTRONICS N.V.

A fluid coupling conduit () includes an inlet end () structured to receive a flow of breathing gas, an outlet end () fluidly coupled to the inlet end and defining an outlet opening, a central chamber portion () positioned between the inlet end and the outlet end, the central chamber portion having an outer wall () positioned opposite the outlet opening. The outer wall has a plurality of exhaust gas orifices () extending therethrough. A number of sound attenuating structures are disposed in the central chamber portion between the outlet opening and the outer wall. The sound attenuating structures including a plurality of surfaces structured to reflect sound waves associated with exhaust gas flow through the fluid coupling conduit. 1. A patient interface device , comprising:(a) a cushion;(b) a frame, the cushion being coupled to the frame, the frame having an orifice in fluid communication with the cushion; and an inlet end,', 'an outlet end fluidly coupled to the inlet end, wherein the inlet end is structured to receive a flow of breathing gas, wherein the outlet end is structured to be fluidly coupled to the orifice of the frame,', 'a central chamber portion positioned between the inlet end and the outlet end, the central chamber portion having an outer wall structured to be positioned opposite the orifice of the frame when the outlet end is fluidly coupled to the orifice,', 'a plurality of exhaust gas orifices disposed on the outer wall and extending therethrough, and', 'a number of sound attenuating structures disposed in the central chamber portion between the outlet end and the outer wall, the sound attenuating structures including a plurality of surfaces structured to reflect sound waves associated with exhaust gas flow through the orifice of the frame., '(c) a fluid coupling conduit comprising2. The patient interface device according to claim 1 , wherein the exhaust gas orifices are oval-shaped.3. The patient interface device according to claim 2 , wherein a ...

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22-08-2013 дата публикации

PATIENT INTERFACE SYSTEMS

Номер: US20130213400A1
Принадлежит: RESMED LIMITED

A patient interface structure for delivery of respiratory therapy to a patient includes a front plate configured to conform to the shape of the patient's face; a mouth cushion defining a breathing chamber and provided to the front plate and configured to seal around the patient's mouth; and a nasal cushion configured to seal the patient's nasal airways. The nasal cushion is supported by the mouth cushion, does not contact a bridge of the patient's nose in use, and extends at least partially into the breathing chamber. A patient interface system includes a patient interface structure and a patient interface structure positioning system configured to position, stabilize and secure the patient interface structure in sealing engagement with the patient's face. 1. A patient interface structure for delivery of respiratory therapy to a patient , comprising:a front plate configured to conform to the shape of the patient's face;a mouth cushion defining a breathing chamber and provided to the front plate and configured to seal around the patient's mouth; anda nasal cushion configured to seal the patient's nasal airways, wherein the nasal cushion is supported by the mouth cushion, has a dual wall construction including a sealing wall and a supporting wall, does not contact a bridge of the patient's nose in use, and extend at least partially into the breathing chamber.2. A patient interface structure according to claim 1 , wherein the front plate is flexible.3. A patient interface structure according to claim 1 , wherein the front plate is formed of clear material claim 1 , such as nylon or polycarbonate.4. A patient interface structure according to claim 1 , wherein the front plate is formed of nearly clear material claim 1 , such as polypropylene.5. A patient interface structure according to claim 1 , wherein the front plate is shaded.6. A patient interface structure according to claim 5 , wherein the front plate is selectively shaded claim 5 , such as a graded shading claim ...

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22-08-2013 дата публикации

EXHAUST GAS ASSEMBLY FOR A PATIENT INTERFACE DEVICE

Номер: US20130213401A1
Принадлежит: KONINKLIJKE PHILIPS ELECTRONICS N.V.

A patient interface device () includes a cushion (), a frame () having a faceplate portion. The cushion is coupled to the frame. The faceplate portion has a main orifice and holes adjacent the main orifice. The device further includes a coupling conduit () having an inlet end, an outlet end coupled to the inlet end, and a hood member having openings provided on an outer periphery thereof. The inlet end is structured to receive a flow of breathing gas. The outlet end is coupled to the main orifice to deliver the flow of breathing gas to the main conduit. The hood member surrounds the outlet end and is disposed over the holes such that exhalation gasses will through the holes and be captured by the hood member and directed through the openings. 1. A patient interface device , comprising:a cushion;a frame having a faceplate portion, the cushion being coupled to the frame, wherein the faceplate portion has a main orifice and one or more holes adjacent the main orifice, and wherein the main orifice and the one or more holes extend through the frame; anda fluid coupling conduit having an inlet end, an outlet end fluidly coupled to the inlet end, and a hood member having one or more openings provided on an outer periphery thereof, wherein the inlet end is structured to receive a flow of breathing gas, wherein the outlet end is fluidly coupled to the main orifice to deliver the flow of breathing gas to the main orifice, and wherein the hood member surrounds the outlet end, is disposed over the one or more holes, and engages the faceplate portion in a manner such that exhalation gasses will flow through the one or more holes and be captured by the hood member and directed through the one or more openings.2. (canceled)3. The patient interface device according to claim 1 , wherein the one or more holes comprises a plurality of holes spaced around the main orifice.4. The patient interface device according to claim 3 , wherein the hood member includes a plurality of contacting ...

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29-08-2013 дата публикации

BREATH INDICATOR

Номер: US20130220326A1
Принадлежит: FISHER & PAYKEL HEALTHCARE LIMITED

This invention relates to a breath indicator that is receivable by a part of a breathing assistance apparatus that supplies gas to a patient. The indicator comprises an elongate body having a gas sampling end and an attachment end. The attachment end is adapted to attach to a part of a breathing assistance apparatus and for locating the gas sampling end. The gas sampling end is to be located in a region where gas from the patient is to be exhaled. The gas sampling end being in communication with a sensor comprising a detector material changeable between a first visual indicator state relating to an inhalation phase of the patient, and a second visual indicator state relating to an exhalation phase of the patient. The detector material is capable of changing between the visual indicator states at a sufficient rate to substantially correspond with the inhalation and exhalation phases of the patient. 1. A breath indicator receivable by a part of a breathing assistance apparatus that supplies gas to a patient , the indicator comprising:an elongate body having a gas sampling end and an attachment end,the attachment end adapted to attach to a part of a breathing assistance apparatus and adapted to locate the gas sampling end in a region where gas from the patient is to be exhaled,the gas sampling end being in communication with a sensor, the sensor comprising a detector material changeable between a first visual indicator state relating to an inhalation phase of the patient and a second visual indicator state relating to an exhalation phase of the patient, andwherein the detector material is capable of changing between the first and second visual indicator states at a sufficient rate to substantially correspond with the inhalation and exhalation phases of the patient.2. The breath indicator as claimed in claim 1 , wherein the detecting material is COdetecting material.3. The breath indicator as claimed in claim 1 , wherein the detecting material changes from the first ...

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05-09-2013 дата публикации

Respiratory therapy device having standard and oscillatory pep with nebulizer

Номер: US20130228174A1
Принадлежит: Hill Rom Services Pte Ltd

A respiratory therapy device has both a standard positive expiratory pressure (PEP) device and an oscillatory PEP device packaged together. A manually operable member is movable to select which of the standard and oscillatory PEP device is placed in communication with a patient's airway. A nebulizer connector may also be provided for connection of a nebulizer.

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12-09-2013 дата публикации

LEAK-COMPENSATED PROPORTIONAL ASSIST VENTILATION

Номер: US20130233314A1
Принадлежит: COVIDIEN LP

This disclosure describes systems and methods for compensating for leakage when during delivery of gas from a medical ventilator in a proportional assist mode to a patient. The technology described herein includes systems and methods to compensate the delivery of PA ventilation for leakage in the patient circuit by using leak-compensated lung flows as well as leak-compensated respiratory mechanics parameters (lung compliance and lung resistance) estimated in a manner that compensates for elastic and inelastic leaks from the ventilation system. 120.-. (canceled)21. A method of compensating for leakage in a ventilation tubing system during delivery of proportional assist ventilation to a patient comprising:receiving a support setting identifying an amount of proportional assistance to provide to the patient;receiving at least one of a pressure measurement and a flow measurement in the ventilation tubing system;modeling leakage from the ventilation tubing system as a first leakage component through a first orifice of a fixed size and a second leakage component through a second orifice of a varying size;estimating a lung compliance of the patient and a lung resistance of the patient based on the first leakage, the second leakage, and the at least one of the pressure measurement and the flow measurement;estimating patient effort based on the first leakage, the second leakage, the lung compliance, the lung resistance, and the at least one of the pressure measurement and the flow measurement; anddelivering ventilation to the patient based on the estimated patient effort and the support setting.22. The method of claim 21 , wherein one or more of modeling leakage claim 21 , estimating lung compliance and lung resistance claim 21 , and estimating patient effort occurs every computational cycle.23. The method of claim 21 , wherein estimating the lung compliance further comprises:generating a plurality of leak-compensated lung flows associated with a period of time based on the ...

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12-09-2013 дата публикации

INTERCHANGEABLE MASK ASSEMBLY

Номер: US20130233316A1
Принадлежит: RESMED LIMITED

A mask assembly adapted for use with a positive airway pressure device includes a mask frame, a cushion provided to the frame, a forehead support assembly, and a neck to connect the frame to the forehead support assembly. The neck includes at least one wall including a first edge and a second edge, wherein lower ends of the first edge and the second edge converge towards one another in an upward direction and upper ends of the first edge and second edge diverge from one another in an upward direction. The mask assembly is configured so that a relatively narrow portion of the neck overlies the bridge of the nose or is between the eyes of a user. The relatively narrow portion is a portion of the neck where a distance between the first edge and second edge is smallest. 142-. (canceled)43. A mask assembly adapted for use with a positive airway pressure device , comprising:a mask frame;a cushion provided to the frame;a forehead support assembly; anda neck to connect the frame to the forehead support assembly, the neck comprising at least one wall comprising a first edge and a second edge, whereinlower ends of the first edge and the second edge converge towards one another in an upward direction and upper ends of the first edge and second edge diverge from one another in an upward direction, andthe mask assembly is configured so that a relatively narrow portion of the neck overlies the bridge of the nose or is between the eyes of a user, the relatively narrow portion being a portion of the neck where a distance between the first edge and second edge is smallest.44. The mask assembly according to claim 43 , wherein at least a portion of the neck is integrally molded with the frame.45. The mask assembly according to claim 43 , wherein a width of the neck as seen in front view is substantially larger than a thickness of the at least one wall.46. The mask assembly according to claim 43 , wherein the first edge and second edge of the at least one wall has a compound shape ...

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12-09-2013 дата публикации

Connector for a respiratory mask and a respiratory mask

Номер: US20130233317A1
Принадлежит: ResMed Pty Ltd

A respiratory mask assembly for delivering breathable gas to a patient includes a frame and an elbow assembly. The frame has a front surface and a rear surface adapted in use to face the patient. The frame includes a main body providing an aperture therethrough for the introduction of breathable gas into a nasal breathing cavity. The elbow assembly is swivelably coupled to the front surface of the frame. The elbow assembly includes a swivel elbow that defines an intake port and an exhaust port separated from the intake port using a baffle. The elbow assembly includes an end portion that interfaces with the aperture of the frame.

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19-09-2013 дата публикации

Modularized respiratory treatment apparatus

Номер: US20130239960A1
Принадлежит: ResMed Pty Ltd

A modularized respiratory treatment apparatus provides various respiratory pressure treatments. The apparatus may be formed by discrete connectable modules such as a flow generator module, alarm module and/or humidifier module. Each module may include its own external casing or housing to independently retain or enclose the respective components that serve the function of the module. Different modules may be adapted with different components and functionalities and may be readily coupled using standardized gas and electrical connection configurations that have flow and communication paths that extend through the modules. When coupled, operation of the respiratory treatment apparatus may be controlled by detection of different modules, such as the alarm module that generates visual and/or audible alarms based on detected conditions, so as to selectively enable or disable different respiratory treatments. The discrete modules of the medical treatment apparatus may include tamper resistant locking mechanisms to impede unauthorized separation of some modules.

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19-09-2013 дата публикации

FLOW RATE COMPENSATION FOR TRANSIENT THERMAL RESPONSE OF HOT-WIRE ANEMOMETERS

Номер: US20130239967A1
Принадлежит: COVIDIEN LP

Systems and methods are described for application of a transitory corrective modification to a hot-wire anemometer flow voltage and/or calculated flow rate to compensate for transient thermal response of the anemometer during a change in mixture of a mixed gas being measured. According to one embodiment a method of applying the transitory corrective modification is provided. An output signal of an exhalation flow sensor of a medical ventilator is received. The flow sensor includes a hot-wire anemometer. The output signal is indicative of a rate of flow of expired gas by a patient. Transient thermal response of the hot-wire anemometer is compensated for by applying a corrective modification to the output signal or a value based thereon. The corrective modification is based at least in part on a fraction of inspired oxygen (FiO2) being supplied by the medical ventilator to the patient. 118.-. (canceled)19. A method comprising:one or more flow sensor processing modules of a medical ventilator receiving an output signal of an exhalation flow sensor including a hot-wire anemometer, the output signal indicative of a rate of flow of expired gas by a patient;the one or more flow sensor processing modules compensating for transient thermal response of the hot-wire anemometer resulting from a change in concentration of gas types included within the expired gas by applying a corrective modification to the output signal or a value based thereon that is based at least in part on a mixed gas being supplied to the patient by the medical ventilator; andwherein the one or more flow sensor processing modules are implemented in one or more microprocessors and one or more computer-readable media, the one or more computer-readable media having instructions tangibly embodied therein that are executable by the one or more microprocessors.20. The method of claim 19 , wherein the corrective modification involves a constant and an exponentially decaying factor.21. The method of claim 20 , ...

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26-09-2013 дата публикации

NEBULIZER FOR USE IN MECHANICAL RESPIRATORY VENTILATION THERAPY

Номер: US20130247909A1
Автор: Dotan Mordechai
Принадлежит:

A nebulizer for use in mechanical respiratory therapy that allows for the introduction of medicaments in the form of aerosols into the system without causing interruption to the therapy being provided to the patient. 1. A nebulizer for use in conjunction with apparatus providing mechanical respiratory ventilation therapy to a patient , the nebulizer comprising:a container having a volume sufficient to hold a therapeutically effective amount of a liquid medicament and to enable aerosolizing therein of the medicament upon the inflow thereto of a respiratory gas, the container comprising:a first port adapted for attachment to a source of a respiratory gas,a second port adapted for attachment to the apparatus providing respiratory ventilation to the patient,a third port adapted for inserting the medicament into the container without causing interruption to the respiratory ventilation therapy being provided to the patient; anda fourth port adapted for draining residual liquid from said nebulizer without causing interruption to the respiratory ventilation therapy being provided to the patient.2. The nebulizer according to wherein the container is of a unitary structure.3. The nebulizer according to wherein the third port is a one-way valve allowing introduction of the medicament without allowing outflow of any respiratory gas or aerosol.4. The nebulizer according to wherein the third port comprises a sealed insertion point for insertion of a needle of a syringe.5. The nebulizer according to wherein the insertion point is sealed with an elastomeric material.6. The nebulizer according to wherein the container comprises an internal configuration that is adapted to facilitate the aerosolizing of the medicament therein.7. The nebulizer according to wherein the configuration comprises a bottom portion that is tapered downward.8. The nebulizer according to wherein the configuration comprises a narrow tube extending from the first port and directing the inflow of respiratory gas ...

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26-09-2013 дата публикации

PATIENT INTERFACE DEVICE WITH MULTI-AXIS ELBOW CONDUIT

Номер: US20130247915A1
Принадлежит: KONINKLIJKE PHILIPS ELECTRONICS N.V.

A patient interface device () includes a frame (), a cushion () coupled to the frame, and a fluid coupling conduit () having a first conduit member () and a second conduit member (), the first conduit member being fluidly coupled to at least one of the frame and the cushion and being rotatable with respect to the frame and about a longitudinal axis of the first conduit member, the second conduit member being fluidly coupled to first conduit member and being rotatable with respect to the first conduit member and about an axis that is transverse to the longitudinal axis of the first conduit member. 1. A patient interface device , comprising:a frame;a cushion coupled to the frame; anda fluid coupling conduit having a first conduit member and a second conduit member, the first conduit member being fluidly coupled to at least one of the frame and the cushion and being rotatable with respect to the frame and about a longitudinal axis of the first conduit member, the second conduit member being fluidly coupled to first conduit member and being rotatable with respect to the first conduit member and about an axis that is transverse to the longitudinal axis of the first conduit member,wherein the first conduit member comprises a first connector portion defining a first fluid chamber, and a first mating portion coupled to the first connector portion, the first mating portion defining a second fluid chamber,wherein the second conduit member comprises a second connector portion defining a third fluid chamber, and a second mating portion coupled to the second connector portion, the second mating portion defining a fourth fluid chamber,wherein the first mating portion is fluidly coupled to the second mating portion,wherein the first mating portion includes a first back surface connected to a first angled surface, the first angled surface being disposed at a first angle with respect to a plane defining a flat top of the first connector portion,wherein the second mating portion ...

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03-10-2013 дата публикации

DIRECTION SWITCHING VALVE UNIT AND COUGH ASSISTING DEVICE USING THE SAME

Номер: US20130255689A1
Принадлежит: Seoil Pacific Corp.

Provided is a direction switching valve unit and a cough assisting device using the same for inhaling to and exhaling from a patient's respiratory organ to induce a cough, the cough assisting device has a case body () having an inhaling space () formed on and passing through a lower surface thereof; an air pressure generating unit () provided in the case body (), the air pressure generating unit generating an air pressure through a rotation force for suctioning air into an air inlet () and discharging suctioned air via an air outlet (); a direction switching valve unit () provided in the inhaling space () formed through the case body (), the direction switching valve unit converting a flow direction of the air for forcedly suctioning air toward a patient's respiratory organ or forcedly discharging air from a patient's respiratory organ by means of air pressure generated in the air pressure generating unit (), whereby the device can be operated with low electric power. 1. A direction switching valve unit , comprising:{'b': 310', '311', '312', '311', '313', '311', '314', '311', '315', '311', '316', '312, 'claim-text': [{'b': 330', '311', '310', '331', '311, 'a receiving body () fixed in the receiving space () of the housing () and having communication ports () formed at and penetrating locations corresponding to four (4) opened portions of the receiving space ();'}, {'b': 340', '330', '341', '342', '343', '344', '341', '342', '345', '346', '347, 'a rotating body () placed on the receiving body (), the rotating body having an upper plate (), a lower plate () and first and second partitions () and () connecting the upper plate () and the lower plate () to form a first direct passage (), a second direct passage () and a third direct passage (), both sides of each of the direct passages being opened; and'}, {'b': 350', '310', '340, 'a two-directional motor () provided at an upper side of the housing () and connected to a shaft of the rotating body ().'}], 'a housing () ...

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10-10-2013 дата публикации

VENTILATOR APPARATUS AND METHOD

Номер: US20130263854A1
Принадлежит:

A respiratory treatment apparatus configured to provide a flow of breathable gas to a patient, including a breathable air outlet, an outside air inlet, and an pneumatic block module, wherein the pneumatic block module includes: a volute assembly including an inlet air passage, a mount for a blower and an outlet air passage; the blower being mounted in the mount such that an impeller of the blower is in a flow passage connecting the inlet air passage and the outlet air passage; a casing enclosing the volute assembly, wherein air passages within the casing connect air ports on the volute assembly, wherein the inlet air passage of the volute assembly is in fluid communication with the outside air inlet and the outlet air passage of the volute assembly is in fluid communication with the air outlet. 1. A respiratory treatment apparatus configured to provide a flow of breathable gas to a patient , including a breathable air outlet , an outside air inlet , and an pneumatic block module , wherein the pneumatic block module comprises:a volute assembly including an inlet air passage, a mount for a blower and an outlet air passage;the blower being mounted in the mount such that an impeller of the blower is in a flow passage connecting the inlet air passage and the outlet air passage; anda casing enclosing the volute assembly, wherein air passages within the casing connect air ports on the volute assembly,wherein the inlet air passage of the volute assembly is in fluid communication with the outside air inlet and the outlet air passage of the volute assembly is in fluid communication with the air outlet.2. The respiratory treatment apparatus of wherein the apparatus is a ventilator.3. The respiratory treatment apparatus of wherein the volute assembly is a molded rigid plastic device.4. The respiratory treatment apparatus of wherein the casing is metallic having a lower portion and top cover.5. The respiratory treatment apparatus of wherein the casing includes an air passage ...

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17-10-2013 дата публикации

Apparatus for humidifying a respiratory gas

Номер: US20130269696A1
Принадлежит: ResMed R&D Germany GmbH

The invention concerns an apparatus for supplying a respiratory gas, a humidifying apparatus, a respiratory gas tube and a connecting apparatus therefor. The apparatus of the invention includes a blowing device for delivering the respiratory gas, a housing device which has a bottom region, a top surface region and a side region extending upwardly between the top surface region and the cover region, as well as a connecting device for connecting a humidifying apparatus for humidifying the respiratory gas, wherein the connecting device is arranged in the side region of the apparatus in such a way that the humidifying apparatus can be laterally coupled thereto. The humidifying apparatus according to the invention is distinguished by a partial amount discharge device for passing a partial amount of the liquid pre-stored in a liquid storage space into a humidifying region. The respiration tube according to the invention includes a connecting plug structure which has both a respiratory gas connecting portion and also a pressure measuring tube connecting portion.

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24-10-2013 дата публикации

MULTIPURPOSE THERAPEUTIC FACE MASK

Номер: US20130276784A1
Автор: Flynn, SR. Stephen Donald
Принадлежит:

A therapeutic face mask comprises a face-engaging portion and a single connector having a mask-engaging end and a single treatment-receiving end which has a single attachment mounting for detachably sealingly receiving a treatment attachment, such as an oxygen reservoir bag or a nebulizer. A one-way inhalation valve in the connector permits fluid flow from the treatment-receiving end to the mask-engaging end during inhalation and inhibits fluid flow in the other direction. The mask also includes a valve-governed exhalation port and an anti-asphyxia valve assembly configured to permit fluid flow from ambient to the face-engaging portion during inhalation only when inspiratory effort during inhalation exceeds fluid flow to the treatment-receiving end of the connector. Also provided is an oxygen reservoir bag having a neck shaped for removable coupling to a mating connector of a therapeutic face mask. An oxygen reservoir bag may have a metered-dose inhaler port defined in its neck. 1. A therapeutic face mask , comprising:a face-engaging portion having a fluid aperture; the mask-engaging end of the connector is coupled to the face-engaging portion in fluid communication with the fluid aperture;', 'the connector has only a single attachment mounting for detachably sealingly receiving a treatment attachment in fluid communication therewith, the attachment mounting being defined at the treatment-receiving end of the connector; and', 'the connector has at least one inhalation valve interposed in the fluid passageway between the mask-engaging end and the treatment-receiving end thereof, each inhalation valve being a one-way valve and being oriented to permit fluid flow from the treatment-receiving end to the mask-engaging end during inhalation and to inhibit fluid flow from the mask-engaging end to the treatment-receiving end;, 'only a single connector, the connector having a mask-engaging end and a only a single treatment-receiving end, the connector defining a fluid ...

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24-10-2013 дата публикации

VENTILATOR WITH INTEGRATED BLOWER TO PROVIDE NEGATIVE OR POSITIVE PRESSURE IN A VENTILATOR SYSTEM

Номер: US20130276789A1
Принадлежит: KONINKLIJKE PHILIPS ELECTRONICS N.V.

A ventilator system () includes an integrated blower (). In one case, the ventilator system includes: an inspiration port () for connection to an inspiratory limb () of a dual-limb patient circuit (), and an expiration port () for connection to an expiratory limb () of the dual-limb patient circuit; a gas delivery device () connected to the inspiration port to supply a pressurized flow of gas to the inspiration port to generate a positive pressure; and a blower having an inlet () that is operatively connected to the expiration port and configured to be controlled to selectively supply a negative pressure level between 4 and 120 cmHO to the expiration port, and an outlet () to exhaust gas received from the expiration port. In another case, the ventilator system includes a blower to generate positive pressure/flow to augment flow for noninvasive ventilation. 1100200300. A ventilator system ( , , ) , comprising:{'b': 122', '222', '322', '112', '212', '312', '110', '210', '310', '142', '242', '342', '114', '214', '314, 'an inspiration port (, , ) configured to be connected to an inspiratory limb (, , ) of a dual-limb patient circuit (, , ), and an expiration port (, , ) configured to be connected to an expiratory limb (, , ) of the dual-limb patient circuit;'}{'b': 120', '220', '320, 'a gas delivery device (, , ) operatively connected to the inspiration port and configured to supply a pressurized flow of gas to the inspiration port to generate positive pressure; and'}{'b': 130', '230', '330', '132', '232', '332', '134', '234', '334, 'sub': '2', 'a blower (, , ) having an inlet (, , ) that is operatively connected to the expiration port and configured to be controlled to selectively supply a negative pressure level between 4 and 120 cmHO to the expiratory limb, and further having an outlet (, , ) configured to exhaust gas received via the expiration port.'}2100200300140240340. The ventilator system ( claim 1 , claim 1 , ) of claim 1 , further comprising an exhalation ...

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24-10-2013 дата публикации

Articulating headgear connector for respiratory masks

Номер: US20130276790A1
Принадлежит: SleepNet Corp

Applicants have disclosed an “Articulating Headgear Connector for Respiratory Masks” which allows three-dimensional movement of the headgear connector to alleviate the mechanical forces incurred from a wearer's head movement, and thus maintain an effective seal. In the preferred embodiment, the invention comprises: a CPAP mask having a plastic shell; the mask has a stub tube extending outwardly from the shell; a headgear connector mounted loosely onto the stub tube; a T-shaped nib on the elbow guides the headgear's movement; whereby the headgear connector can slide forward on the stub tube (i.e., move along the Z axis), guided by the nib; and, whereby the headgear connector can rock (i.e., about the X-Y axes) and its sides seesaw on the stub tube (i.e., along the Z-axis), with the amount of rotation and seesawing limited by the nib.

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21-11-2013 дата публикации

ELBOW ASSEMBLY

Номер: US20130306066A1
Принадлежит: RESMED LIMITED

An elbow assembly for a mask system includes an elbow including a slot and a port, an anti-asphyxia valve adapted to be received within the slot and including a flap portion adapted to selectively close the port depending on the presence of pressurized gas, and a support member to secure the anti-asphyxia valve to the elbow. The support member includes a slot that is adapted to interlock with a protrusion provided to the anti-asphyxia valve. 1. An elbow assembly adapted to connect an air delivery tube to a mask assembly , the elbow assembly comprising:an elbow body with a first end, a second end and a bend between the first and second ends;a slot;an anti-asphyxia valve (AAV) assembly with a flap portion adapted to be received within the slot;a port adjacent the slot, the port being selectively closed by the flap portion; anda support member having an inside surface to which the flap portion is attached, the support member and the flap portion as a unit being attached to the elbow body,wherein the support member comprises an alignment member configured to cooperate with the elbow body to prevent assembly when the flap portion is misaligned with respect to the elbow body,wherein the support member is adapted to be flush with the port when secured to the elbow body, andwherein the support member is securable to the elbow body in only one orientation.2. An elbow assembly according to claim 1 , wherein the elbow body comprises a flange proximate the second end claim 1 , and the support member is adapted to abut the flange when secured to the elbow body.3. An elbow assembly according to claim 2 , wherein only one side of the support member is adapted to be flush with a surface of the elbow body when the support member is secured to the elbow body.4. An elbow assembly according to claim 3 , wherein the support member comprises grip members that protrude outward from the elbow body when the support member is clipped to the elbow body.5. An elbow assembly according to claim ...

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28-11-2013 дата публикации

MASK SYSTEM

Номер: US20130312758A1
Принадлежит: RESMED LIMITED

A mask system for treating sleep disordered breathing, comprising headgear, a shell/cushion including a channel adjacent a front aperture, a frame, an elbow including at least one undercut on a proximal end, a retaining ring including a rear flange adapted to be retainably insertable in the channel of the shell/cushion, and a front flange adapted to retainably engage with the at least one undercut of the elbow. 1. A mask system for treating sleep disordered breathing comprising headgear , a frame , and a shell/cushion including at least a pair of spaced frame-receiving channels formed between opposed flange portions , wherein the frame is adapted to be removably insertable in the frame-receiving channels of the shell/cushion.2. The mask system as claimed in claim 1 , wherein the shell/cushion has a generally triangular shape.3. The mask system as claimed in claim 2 , wherein said pair of channels includes four channels.4. The mask system as claimed in claim 2 , wherein one of the channels is positioned at the apex of the generally triangular shape.5. The mask system as claimed in claim 2 , wherein one of said channels is provided on each side of the generally triangular shape.6. The mask system as claimed in claim 4 , wherein the shell/cushion includes a strap aperture through which an end of a headgear strap may be threaded claim 4 , said aperture being aligned with each channel positioned on each side of the generally triangular shape.7. The mask system as claimed in claim 2 , wherein at least one of the channels is positioned along a base portion of the generally triangular shape.8. The mask system as claimed in claim 7 , wherein the opposed flange portions comprise a front flange and a rear flange associated with the at least one channel positioned along the base portion claim 7 , further comprising one or more vent holes for COgas washout from the shell/cushion.9. The mask system as claimed in claim 8 , wherein the front and/or rear flanges project away from an ...

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05-12-2013 дата публикации

Headgear

Номер: US20130319418A1
Автор: Amal S. Amarasinghe
Принадлежит: ResMed Pty Ltd

A mask assembly suitable for the treatment of sleep disordered breathing, comprising: a mask to provide pressurized air to a patient; upper and lower slot features located on each side of the mask; a headgear assembly, comprising: a back portion; a pair of upper straps provided to the back portion, each upper strap having a loop portion and a hook portion at a free end thereof for releasably attaching to the loop portion; a pair of lower straps extending away from the back portion, each lower strap having a loop portion and a hook portion at a free end thereof for releasably attaching to the loop portion; and a connection region of each loop portion of each strap, the connection region being adapted to receive a respective hook portion, the connection region being wider than each respective hook portion along each respective hook portion's entire length.

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12-12-2013 дата публикации

System and device for neonatal resuscitation and initial respiratory support

Номер: US20130327332A1
Принадлежит: VENTINVENT AB

The present invention relates to a device and a system for positive pressure ventilation and continuous positive airway pressure (CPAP) treatment for neonatal resuscitation and initial respiratory support. The device and system are designed and tested for preterm and term neonatal use. The device is easy to use and allows rapid switch between PPV and CPAP without change of equipment and significantly reduces the imposed work of breathing for a breathing child treated with CPAP.

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12-12-2013 дата публикации

Mask system

Номер: US20130327333A1
Принадлежит: ResMed Pty Ltd

A full-face mask system for delivery of a supply of gas at positive pressure to a patient for medical treatment includes a shroud, a cushion module adapted to form a seal with the patient's nose and mouth, an elbow, and headgear. The cushion module includes a frame and a cushion. The frame includes an opening that releasably receives a distal end of the elbow with a snap-fit, wherein an inner edge of the opening and the distal end of the elbow together form a retention structure to retain the elbow to the frame.

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12-12-2013 дата публикации

Mask vent

Номер: US20130327336A1
Принадлежит: ResMed Pty Ltd

A vent arrangement is provided to a mask to discharge exhaled gas from the mask to atmosphere. The vent arrangement is structured to diffuse the exhaust vent flow to produce less air jetting, thereby increasing the comfort of the patient and their bed partner. The vent may include a first wall, a second wall defining an outer perimeter, and a plurality of gas washout vent holes positioned between the first wall and the second wall, the vent holes having an inner edge positioned within the outer perimeter of the second wall.

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26-12-2013 дата публикации

HIGH FLOW THERAPY DEVICE UTILIZING A NON-SEALING RESPIRATORY INTERFACE AND RELATED METHODS

Номер: US20130340752A1
Принадлежит:

A gas delivery conduit adapted for fluidly connecting to a respiratory gases delivery system in a high flow therapy system, the gas delivery conduit includes a first connector adapted for connecting to the respiratory gases delivery system, a second connector adapted for connecting to a fitting of a patient interface, tubing fluidly connecting the first connector to the second connector where the first connector has a gas inlet adapted to receive the supplied respiratory gas, one of electrical contacts and temperature contacts integrated into the first connector. The gas delivery conduit further can include a sensing conduit integrated into the gas delivery conduit, where the first connector of the gas delivery conduit is adapted to allow the user to couple the first connector with the respiratory gases delivery system in a single motion. 1. A gas delivery conduit adapted for fluidly connecting to a respiratory gases delivery system , the gas delivery conduit comprising:a first connector adapted for connecting to the respiratory gases delivery system;a second connector adapted for connecting to a fitting of a patient interface; andtubing fluidly connecting the first connector to the second connector;wherein the first connector has a gas inlet adapted to receive the supplied respiratory gas.2. The gas delivery conduit of claim 1 , further comprising one of electrical contacts and temperature contacts integrated into the first connector.3. The gas delivery conduit of claim 1 , further comprising a sensing conduit integrated into the gas delivery conduit.4. The gas delivery conduit of claim 3 , wherein the sensing conduit is adapted to facilitate monitoring one of pressure claim 3 , pulse oximetry claim 3 , carbon dioxide and oxygen.5. The gas delivery conduit of claim 1 , wherein the first connector is adapted to allow the user to couple the first connector with the respiratory gases delivery system in a single motion.6. The gas delivery conduit of claim 1 , wherein ...

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26-12-2013 дата публикации

COMPLIANT COUPLER OR ADAPTOR

Номер: US20130340757A1
Принадлежит: RESMED LIMITED

A CPAP device includes a flow generator including an outlet, a humidifier including an inlet, and an adaptor connector between the outlet of the flow generator and the inlet of the humidifier. The connector includes a flexible and conformable sealing portion that is movable to accommodate misalignment. 1. A connector for a CPAP system , the CPAP system including a flow generator configured to generate a flow of breathable gas to be delivered to a patient and a tub configured to contain a supply of liquid , the connector comprising:a main body having a first end and a second end;a channel extending axially through the main body from the first end to the second end and configured to deliver the flow of breathable gas to the tub;an attaching portion provided at the first end of the main body; anda flexible sealing portion provided at the second end of the main body, the flexible sealing portion comprising at least one bellows convolution, said bellows convolution shaped and arranged such that, in use, said bellows convolution will fill with breathable gas and expand due to the breathable gas to establish a face seal wherein a flat facing surface of said at least one bellows convolution is pressurized against a surface surrounding an inlet opening provided in the tub.2. A connector according to claim 1 , wherein the connector is formed as one piece.3. A connector according to claim 2 , wherein the connector has a round shape.4. A connector according to claim 1 , wherein the connector is formed of a flexible material.5. A connector according to claim 4 , wherein the flexible material is silicone.6. A connector according to claim 4 , wherein the face seal is axially claim 4 , laterally claim 4 , angularly claim 4 , pivotally claim 4 , and/or rotationally flexible.7. A connector according to claim 6 , wherein the face seal is axially flexible within a range of about 1 mm to 5 mm.8. A connector according to claim 7 , wherein the face seal is axially flexible within a range ...

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02-01-2014 дата публикации

System, apparatus and method for supplying gases

Номер: US20140000610A1
Принадлежит: Fisher and Paykel Healthcare Ltd

A system, apparatus and methods are provided for supplying gases to a user. The supply includes a sub-therapeutic mode and a pressure support mode for delivering therapy to a user. A flow diversion device or valve switches from a first mode corresponding with the sub-therapeutic mode of the system to a second mode corresponding with the pressure support mode of the system. In the first mode, the valve opens a larger flow path between the interior of the user interface and ambient air than in the second mode.

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02-01-2014 дата публикации

Systems and Methods for Therapeutic Intrathoracic Pressure Regulation

Номер: US20140005566A1
Принадлежит: ResQSystems, Inc.

Embodiments of the present invention provide systems and methods for delivering respiratory treatment to a patient. For example, a treatment system may include a mechanism for delivering a positive pressure breath to a patient, and one or more limb flow control assemblies which modulate gas flow to and from the patient. Exemplary treatment techniques are embodied in anesthesia machines, mechanical ventilators, and manual ventilators. 1109-. (canceled)110. A system for providing intrathoracic pressure regulation (IPR) to an individual , the system comprising:a patient connection mechanism for coupling with an airway of the individual;a flow control assembly comprising a housing having a vent, an impeller disposed within the housing, and a motor in operative association with the motor; andan external pressure source selected from the group consisting of a manual bag valve mask mechanism, a mechanical ventilator machine, and an anesthesia machine,wherein the external pressure source is in fluid communication with the housing vent of the flow control assembly,wherein the impeller of the flow control assembly is disposed between the patient connection mechanism and the external pressure source, along a fluid passage that extends between the patient connection mechanism and the external pressure source, andwherein the flow control assembly is configured to allow retrograde airflow from the external pressure source to the patient connection mechanism while simultaneously compelling airflow from the patient connection mechanism to the housing vent.111. The system according to claim 110 , wherein the impeller of the flow control assembly is configured to produce a continuous pressure differential within a range from about 3 cm HO to about 16 cm HO.112. The system according to claim 110 , wherein the external pressure source is configured to provide a respiratory cycle duration of about 5 seconds.113. The system according to claim 110 , wherein operation of the flow control ...

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16-01-2014 дата публикации

Methods, Devices and Formulations for Targeted Endobronchial Therapy

Номер: US20140014103A1

The present invention provides a method and novel devices for treating tracheobronchitis and pneumonia in the intubated patient, preferably with aerosolized anti gram-positive and anti-gram negative antibiotics administered in combination or in seriatim in reliably sufficient amounts for therapeutic effect. In one embodiment the result is achieved mechanically. In another embodiment, the result is achieved by aerosol formulation. In a preferred embodiment, the invention assures the result when aerosol is delivered directly to the airways distal of the ventilator circuit. The devices eliminate the dosage variability that ventilator systems engender when aerosols are introduced via the ventilator circuit. The treatment also concentrates the therapeutic agent specifically at affected sites in the lung such that therapeutic levels of administrated drug are achieved without significant systemic exposure of the patient to the drug. The invention further provides a dose control device to govern this specialized regimen.

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27-02-2014 дата публикации

Optimized Breathing Assistance Device

Номер: US20140053841A1
Автор: Jeffrey B. Ratner
Принадлежит: Mercury Enterprises Inc

A breathing assistance device with improved pressure characteristics is disclosed. The device is capable of providing a high level of CPAP per unit of supplementary respirable gas consumed while maintaining low CPAP fluctuations throughout the breath cycle. The invention further optionally comprises a manometer for monitoring pressure and a safety pressure relief valve as additional safety measures against overpressure delivered to a patient. The device may be made to be completely disposable for one-time or single patient use.

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06-03-2014 дата публикации

PATIENT INTERFACE DEVICE

Номер: US20140060544A1
Принадлежит: Ric Investments LLC

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. 1. A patient interface device , comprising: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, the support member being a single-piece unitary member and having a coupling portion configured to continuously span from a first side of a patient's face on a first side of the patient's nose to a second, opposite side of the patient's face on a second, opposite side of the patient's nose responsive to the patient interface device being donned by such a patient;an elbow coupling adapted to be coupled to a patient circuit, the elbow coupling being coupled to an end of the support member through a joint, the joint allowing the support member to rotate relative to the elbow coupling; anda sealing assembly operatively coupled to the support member at the coupling portion in a manner wherein the sealing assembly is, independent of rotation of the support member relative to the elbow coupling, rotatable relative to the support member about a longitudinal axis of the coupling portion or slideable relative to the support member along the longitudinal axis of the coupling portion while remaining in fluid communication with an interior of the support member, wherein the support member defines a gas carrying conduit adapted to ...

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13-03-2014 дата публикации

Low profile mask attachment element

Номер: US20140069433A1
Принадлежит: Koninklijke Philips NV

A patient interface device that includes a mask with a shell having a recess defined therein, thereon, or by a material coupled thereto and a headgear component for attaching the patient interface device to the head of a patient. The headgear component includes a strap and an attachment element provided between the mask and the strap, wherein the attachment element has a strap attachment portion coupled to the strap and a mask attachment portion disposed in the recess in a manner that selectively couples the headgear component to the mask.

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20-03-2014 дата публикации

Trachea pressure determination method and device

Номер: US20140081164A1
Принадлежит: COVIDIEN LP

According to various embodiments, methods and systems for determining pressure in the lungs may employ intracuff pressure measurements. The intracuff pressure measurements may calibrated or adjusted based on a set of calibration coefficients or a set of calibration curves, which may reflect patient parameters and cuff/tube geometry factors. The resulting calibration may be used to determine a more accurate estimate of lung pressure, which in turn may be used to control a ventilator and provide breathing assistance to a patient. Also provided are tracheal tubes with couplers or other memory devices for storing calibration information. Such tubes may allow calibration at the level of an individual tracheal tube to account for changes in tube geometry and individual patient factors.

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27-03-2014 дата публикации

COMBINATION ANESTHESIA AND SCAVENGER SURGICAL MASK

Номер: US20140083425A1
Автор: JR. John E., Moenning
Принадлежит:

A surgical mask for administering and/or scavenging medical gases includes a nasal mask and an oral mask that envelops the nasal mask. The nasal mask is secured to the oral mask and may be removable from it. 1. A surgical mask assembly for administering and scavenging medical gases , comprising:an outer shell having a gas port, the outer shell defining a chamber with a rear-facing opening defined by a rim, the rim having an inner edge and an outer edge, andan inner shell having a gas port, the inner shell defining a chamber with a rear-facing opening defined by a rim, the rim having an inner edge and an outer edge,wherein a superior-most point of the inner edge of the rim of the inner shell is positioned inferiorly and anteriorly relative to a superior-most point of the inner edge of the rim of the outer shell.2. The surgical mask assembly of claim 1 , wherein the entire inner shell is located in the chamber of the outer shell.3. The surgical mask assembly of claim 1 , further comprising a flexible seal secured to the rim of the inner shell claim 1 , wherein the flexible seal is located in the chamber of the outer shell.4. The surgical mask assembly of claim 1 , wherein:the outer shell envelops a patient's nose and mouth when the surgical mask assembly is positioned on the face of the patient, andthe inner shell envelops the patient's nose when the surgical mask assembly is positioned on the face of the patient.5. The surgical mask assembly of claim 1 , further comprising:a flexible seal secured to the rim of the inner shell, anda flexible seal secured to the rim of the outer shell.6. The surgical mask of claim 1 , wherein:the gas port of the inner shell comprises a first tube,the gas port of the outer shell comprises a second tube, andthe first tube is positioned within the second tube.7. A surgical mask assembly for administering and scavenging medical gases claim 1 , comprising:an oral mask configured to envelop a patient's nose and mouth when the surgical mask ...

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27-03-2014 дата публикации

RESPIRATORY MASK AND METHOD FOR MANUFACTURING A RESPIRATORY MASK

Номер: US20140083431A1
Принадлежит: ResMed R&D Germany GmbH

A respiratory mask, a mould for a respiratory mask, as well as to a method for producing a respiratory mask are disclosed, in which manufacturability and usability of respiratory masks are improved. A respiratory mask is disclosed for administering a breathable gas to a patient, the respiratory mask comprising a first component formed from a flexible material and a second component formed from a material that is more rigid than the flexible material, wherein the first component is formed onto the second component by an overmoulding process. 1. A respiratory mask comprising:a substrate made of a relatively rigid material, wherein the substrate includes at least one treated portion inclined to accept a reactive substance; andan elastomer that is made of a relatively more flexible material compared to the relatively rigid material of the substrate, said elastomer being applied to the substrate and secured to the substrate via an induced adhesive bond formed between said treated portion and a surface of the elastomer abutting the treated portion,wherein the mask includes a frame and an element configured to provide fluid communication between a conduit and the frame, wherein the element or frame includes at least one selected portion including said substrate and said elastomer is provided to the selected portion, andwherein the elastomer is in the form of a seal.2. The respiratory mask according to claim 1 , wherein the element is an elbow.3. The respiratory mask according to claim 2 , wherein the elbow includes a plurality of components and the selected portion includes the interface between any two elbow components.4. The respiratory mask according to claim 1 , wherein the frame includes a socket defining said substrate.5. The respiratory mask according to claim 1 , wherein the element is configured to be rotatable in relation to the frame.6. The respiratory mask according to claim 2 , wherein the seal includes a relatively long elastomer lip flexibly positionable and ...

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03-04-2014 дата публикации

PORTS CAP FOR MASK ASSEMBLY

Номер: US20140090643A1
Принадлежит: RESMED LIMITED

A ports cap for a mask assembly includes two closure portions adapted to seal respective ports of the mask assembly, a bridge piece that joins the two closure portions, and two gripping tabs extending outwardly from respective closure portions. Each gripping tab includes one or more ribs on at least one side thereof. 1. A mask assembly comprising:a frame including two ports each comprising a tubular spigot that forms a male connector; and two closure portions adapted to seal respective ports of the mask assembly, each closure portion being adapted to receive and seal a respective spigot on the respective port;', 'a bridge piece that joins the two closure portions; and', 'two gripping tabs extending outwardly from respective closure portions, each gripping tab including one or more ribs on an outer surface of at least one side thereof,', 'wherein, in a side view in which the closure portions extend at an angle to the bridge piece, the bridge piece and gripping tabs extend along an arc, and', 'wherein the bridge piece and the two gripping tabs extend from similar ends of the closure portions., 'a ports cap comprising2. The mask assembly according to claim 1 , wherein the ports cap is formed of a relatively soft elastomeric material.3. The mask assembly according to claim 1 , wherein each closure portion includes an opening adapted to receive a respective port.4. The mask assembly according to claim 3 , wherein surfaces defining the opening are adapted to engage the port to provide a seal and retain the closure portion on the port.5. The mask assembly according to claim 1 , wherein each closure portion includes an asymmetrical shape.6. The mask assembly according to claim 1 , wherein the one or more ribs are provided along a free end of the gripping tab to enhance gripping of the gripping tab at least for disassembly of the closure portion from the respective port.7. The mask assembly according to claim 1 , wherein the gripping tab includes a rib along both sides ...

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03-04-2014 дата публикации

Respiratory Mask with Disposable Cloth Body

Номер: US20140090649A1
Принадлежит: Circadiance LLC

The invention is a frameless, disposable cloth body for use with a respiratory mask, such as for continuous positive airway pressure therapy for those having sleep apnea. The cloth body is inflatable and moisture-vapor breathable and has an inner side having a nasal interface portion disposed on it and an outer side, and also has a circular aperture formed in a central location on the body, sized to sealingly receive an air delivery arrangement. The cloth body also has a pair of wings on opposite sides with slits arranged at optimal angles for receiving headgear straps.

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10-04-2014 дата публикации

RESPIRATORY MASK

Номер: US20140096768A1
Автор: Lee Gary C.J.
Принадлежит:

A respiratory mask includes a mask body and an air inlet connector. The mask body is formed with an air inlet. The air inlet connector is integrally formed at the air inlet. The respiratory mask can be direct connected to an oxygen tube, an air storage bag, a mist spray tank, a medicine feed tank or a standard air tube of 22 mm, without the need for a separate connector. The respiratory mask decreases the number of the parts and is easy to operate for medical workers to change different pipes, without changing the respiratory mask. 1. A respiratory mask , comprising a mask body and an air inlet connector , the mask body being formed with an air inlet , the air inlet connector being integrally formed at the air inlet.2. The respiratory mask as claimed in claim 1 , wherein the air inlet connector is adapted to mate with a standard connector of an oxygen tube claim 1 , a standard air tube of 22 mm claim 1 , an air storage bag claim 1 , a medicine feed tank or a mist spray tank.3. The respiratory mask as claimed in claim 1 , wherein an inner side of the air inlet is provided with a one-way inlet valve plate.4. The respiratory mask as claimed in claim 3 , wherein two sides of the mask body are respectively formed with an air outlet. 1. Field of the InventionThe present invention relates to a mask, and more particularly to a respiratory mask.2. Description of the Prior ArtFor a serious patient, the patient needs to wear a respiratory mask to cover the mouth and the nose of the patient to assist the patient in breathing or in pouring medial gas along with breath so that the patient can maintain normal physiological functions. A conventional respiratory mask has a mask body. The mask body is formed with an air inlet for connecting an oxygen tube, an air storage bag, a mist spray tank, a medicine feed tank or a standard air tube of 22 mm. Because all the mask body, the oxygen tube, the air storage bag, the mist spray tank, the medicine feed tank and the standard air tube of ...

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10-04-2014 дата публикации

INTERFACE COMPRISING A ROLLING NASAL BRIDGE PORTION

Номер: US20140096774A1
Принадлежит: FISHER & PAYKEL HEALTHCARE LIMITED

An interface for positive pressure therapy includes a mask assembly, a headgear assembly and a connection port assembly. The mask assembly comprises a seal member that has an upper portion movably connected to an integrated lower portion, wherein the upper portion rolls during hinging movement of the upper portion relative to the lower portion. The headgear assembly allows connection to the mask assembly in a direction substantially normal to a direction of strap tension. The connection port assembly includes a swivel elbow with a valve member that controls flow through a port that opens toward the user. 1. A mask assembly comprising a mask seal , the mask seal comprising an upper portion and a lower portion , the upper portion being pivotable relative to the lower portion , the upper portion comprising a region of reduced stiffness that is positioned between a first boundary and a second boundary , the first boundary being defined by a stiffness greater than that in the region of reduced stiffness , the second boundary being defined by a stiffness greater than that in the region of reduced stiffness , wherein when the first boundary is moved toward the second boundary , the region of reduced stiffness buckles in a single direction to define a roll of material that changes in size as the first boundary continues to move toward the second boundary.2. The mask assembly of claim 1 , wherein the region of reduced stiffness facilitates movement of the upper portion of the seal member relative to the lower portion of the seal member.3. The mask assembly of claim 2 , wherein the upper portion comprises a nasal bridge portion of the mask and movement of the first boundary toward the second boundary facilitates movement of the nasal bridge portion of the mask relative to the lower portion of the mask.4. The mask assembly of claim 1 , wherein the second boundary is positioned between the upper portion and the lower portion.5. The mask assembly of claim 4 , wherein the mask ...

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06-01-2022 дата публикации

FILTERING FACEPIECE RESPIRATOR

Номер: US20220000575A1
Автор: Ugbeye Tosan A.
Принадлежит:

Provided is a filtering facepiece respirator. The respirator includes a mask body having an anterior side portion, a posterior side portion, a middle portion, a first side portion, a second side portion, a top side portion, a bottom side portion and outer edge portions. The respirator further includes a primary port positioned at the anterior middle portion of the mask body and a detachable primary port adapter which is positioned over and engages the primary port. The respirator may further include an oxygen port and oxygen port adapter and a luer port and luer port adapter. 1. A filtering facepiece respirator comprising:a mask body having an anterior portion, a posterior portion, a middle portion, a first side portion, a second side portion, a top side portion, a bottom side portion and outer edge portions;a primary port positioned at the anterior middle portion of the mask body;a detachable primary port adapter which is positioned over and engages the primary port; and,fasteners for attaching and securing adjustable bands to the first side portion and at the second side portion of the mask body.2. The filtering facepiece respirator of claim 1 , wherein the mask body comprises a nose bridge positioned at the top anterior portion of the mask body claim 1 , wherein the mask body is comprised of silicone or a medical grade plastic material and wherein the mask body is transparent.3. (canceled)4. The filtering facepiece respirator of claim 1 , wherein the detachable primary port adapter comprises a cap assembly claim 1 , wherein the cap assembly is in the shape of a circular conduit.5. (canceled)6. The filtering facepiece respirator of claim 4 , wherein the cap assembly comprises a first end and a second end claim 4 , wherein the first end of the cap assembly comprises a snap coupling or screw threads for engaging the cap assembly to the primary port and wherein the second end of the cap assembly comprises a snap coupling or screw threads for engaging the cap assembly ...

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01-01-2015 дата публикации

CATHETER SYSTEMS AND METHODS OF USE

Номер: US20150000650A1
Принадлежит:

A method of using a catheter system which includes inserting a first distal end portion of an outer catheter into a first body lumen, coupling a first key joint component on an inner catheter with a second key joint component on a proximal end portion of the outer catheter to fix a rotational orientation of the inner catheter relative to a rotational orientation of the outer catheter about a longitudinal axis of the first body lumen, wherein the second key joint component runs along a partial length of the outer catheter, and wherein a distal end portion of the inner catheter includes a pre-formed bend that extends at a non-zero angle relative to the longitudinal axis of the first body lumen, and advancing the distal end portion of the inner catheter through a lumen of the outer catheter, away from the distal end portion of the outer catheter, and into a second body lumen, the second body lumen branching from the first body lumen. 1. A method of using a catheter system , comprising:inserting a first distal end portion of an outer catheter into a first body lumen;coupling a first key joint component on an inner catheter with a second key joint component on a proximal end portion of the outer catheter to fix a rotational orientation of the inner catheter relative to a rotational orientation of the outer catheter about a longitudinal axis of the first body lumen, wherein the second key joint component runs along a partial length of the outer catheter, and wherein a distal end portion of the inner catheter includes a pre-formed bend that extends at a non-zero angle relative to the longitudinal axis of the first body lumen; andadvancing the distal end portion of the inner catheter through a lumen of the outer catheter, away from the distal end portion of the outer catheter, and into a second body lumen, the second body lumen branching from the first body lumen.2. The method of claim 1 ,wherein the proximal end portion of the outer catheter comprises a detachable fitting ...

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01-01-2015 дата публикации

Fluid inlet adapter

Номер: US20150000653A1
Автор: Jeffrey Harold MILLER
Принадлежит: CareFusion 303 Inc

An adapter for selectively providing fluid to a device from one of multiple fluid sources has a body with a first inlet for connecting a first one of the multiple fluid sources to the device and a second inlet for connecting a second one of the multiple fluid sources to the device. The adapter also includes a handle that is movably coupled to the body and includes an access control element. The handle is configured to secure the body to a device when the adapter is in either of a first position or a second position that is rotated relative to the first configuration. The access control element obstructs access to the second inlet when the adapter is secured to the device in the first position and the access control element obstructs access to the first inlet when the adapter is secured to the device in the second position.

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01-01-2015 дата публикации

FLUID INLET ADAPTER

Номер: US20150000669A1
Автор: Miller Jeffrey Harold
Принадлежит:

An adapter is described for providing fluid to a device from a fluid source. The adapter has a housing with an inlet extending through the housing for connecting the fluid source to the device. The adapter also includes a latching component to secure the adapter to the device. The adapter further includes a tab having embedded magnets in a specific magnet configuration. The device has a sensor capable of detecting the specific magnet configuration. The device can be connected to other adapters, and identifies the fluid source based on the magnet configurations of the adapters. 1. An adapter for providing fluid from a fluid source to a device , the adapter comprising:a housing;an inlet extending through the housing for connecting the fluid source to the device, the inlet comprising a first end for connecting to the fluid source and a second end for connecting to the device;a latching component configured to secure the adapter to the device; anda machine-readable indicator for identifying the fluid source, the machine-readable indicator extending away from the first end of the inlet and beyond the second end of the inlet.2. The adapter of claim 1 , wherein the machine-readable indicator comprises a tab comprising a magnet claim 1 , and wherein a position of the magnet on the tab indicates the fluid source.3. The adapter of claim 2 , wherein the tab extends parallel to the inlet.4. The adapter of claim 2 , wherein the magnet is embedded in the tab.5. The adapter of claim 1 , wherein the latching component comprises a threaded nut.6. The adapter of claim 5 , wherein the housing comprises at least one pin for holding the threaded nut.7. The adapter of claim 5 , wherein the threaded nut comprises a groove claim 5 , and wherein the at least one pin is configured to interface with the groove.8. The adapter of claim 1 , wherein the housing comprises a first protrusion having a first width and a second protrusion having a second width claim 1 , the first width is different ...

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05-01-2017 дата публикации

AIRWAY ASSIST DEVICE AND METHOD

Номер: US20170000641A1
Принадлежит:

Airway assist device (AAD) is provided. The device includes an upper AAD component and a lower AAD component. The upper AAD component includes and upper tooth guide connected to an upper plate. The upper AAD component further includes an upper force receiving plate. The AAD also includes a lower AAD component. The lower AAD component includes a lower tooth guide connected to a lower plate. The lower AAD component further includes a lower force receiving plate. The upper and lower AAD components are connected in a way that allows relative movement between the two components between a neutral position and a plurality of extended positions to protrude and distract a patient's mandible. A ratchet mechanism inhibits movement of the lower plate from any extended position. The ratchet mechanism may be manually disengaged to allow the lower AAD component to return to the neutral position. The lower AAD component includes a chin guide. The chin guide includes a chin support member that is engageable with a patient's chin. 1. An airway assist device comprising:a first airway assist device component including an upper plate and an upper tooth guide connected to the upper plate, the upper plate including a first portion and a descending portion connected to the first portion and extending at an angle relative to the first portion;a second airway assist device component including a lower plate and a lower tooth guide connected to the lower plate, the lower plate including a first portion and a descending portion connected to the first portion and extending at an angle relative to the first portion;the first airway assist device component connected with the second first airway assist device component to allow relative movement between the first and second first airway assist device components between a neutral position and at least one extended position; anda ratchet mechanism acting between the first and second first airway assist device components, the ratchet mechanism acting ...

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07-01-2021 дата публикации

SYSTEMS, METHODS, AND DEVICES FOR OZONE SANITIZATION OF CONTINUOUS POSITIVE AIRWAY PRESSURE DEVICES

Номер: US20210000992A1
Автор: Leyva Timothy
Принадлежит:

The present invention is generally related to a device and method for sanitizing a medical instrument with ozone, in particular the invention relates to a system, method and a device for sanitizing a continuous positive airway pressure (CPAP) device. The device has an ozone compartment, an ozone operating system and one or more ozone distribution lines that distribute ozone to a continuous positive airway pressure device. The device may further include a heater adapter unit to connect heating systems in CPAP devices while distributing ozone to sanitize the CPAP device in accordance with the present invention. 1. A system for sanitizing continuous positive airway pressure (CPAP) equipment , comprising:an ozone device comprising a housing, the housing comprising a compartment and an ozone operating system separate from the compartment, wherein:the compartment is configured to house at least a portion of a CPAP mask;the ozone operating system is configured to generate ozone gas and to convey at least a portion of the ozone gas outside of said ozone device; andthe compartment is configured to receive at least a portion of the ozone gas from outside said ozone device.2. The system of claim 1 , further comprising an air pump that is configured to cause ozone gas generated by said ozone operating system to flow outside said ozone device.3. The system of claim 2 , wherein said air pump is within said housing.4. The system of claim 1 , further comprising a CPAP part claim 1 , wherein the ozone device is configured such that at least a portion of the ozone gas generated by the ozone operating system can flow into the CPAP part.5. The system of claim 4 , further comprising an ozone distribution line claim 4 , wherein:the ozone distribution line is configured to fluidly couple to the ozone operating system and to the CPAP part; andthe ozone device is configured such that at least a portion of the ozone gas generated by the ozone operating system can flow into the CPAP part at ...

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07-01-2021 дата публикации

ERGONOMIC AND ADJUSTABLE RESPIRATORY MASK ASSEMBLY WITH FRAME

Номер: US20210001073A1
Принадлежит:

A respiratory mask assembly for delivering breathable gas to a patient includes a frame having a front surface and a rear surface, opposite the front surface, and adapted in use to face the patient. The frame defines an inner wall and an outer wall extending from the rear surface, the inner and outer walls being spaced to define a channel therebetween. A cushion is removably attachable to the frame such that the cushion and frame are repeatably engagable with and disengagable from one another. The cushion includes a side wall to be inserted into the channel of the frame, the side wall having a first interlocking surface that engages a second interlocking surface provided in the channel when the cushion and frame are engaged with one another. The first and second interlocking surfaces interlock with one another to removably attach the cushion to the frame. 1. (canceled)2. A patient interface assembly for therapy of a patient having a breathing disorder , comprising:a frame with a central aperture by which a flow of pressurized breathable gas is introduced in use; anda cushion supported by the frame, the cushion being made of a material that is relatively softer than the frame;a hose to deliver the flow of pressurized breathable gas to the central aperture of the frame;an intermediate piece between the hose and the frame, the intermediate piece being releasably connected to the central aperture via a snap-action connection; and wherein each of the rear strap portions includes a rear strap end, and', 'wherein the front fabric material of the front strap portions includes stiffening support structure having a pair connector elements each having a slot to receive a respective one of the rear strap ends in a length adjustable manner, the stiffening support structure being formed of a relatively rigid material compared to the front fabric material, the stiffening support structure having a degree of flexibility in one direction such that variations in patient physiology ...

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07-01-2016 дата публикации

APPARATUS AND METHOD FOR PROVIDING GASES TO A USER

Номер: US20160001031A1
Принадлежит:

A connector and tubing combination includes a tubing segment with an end piece, such as a tubing flange. The tubing flange can be secured within the connector by an outer sleeve and an inner sleeve of the connector. Both of the inner sleeve and the outer sleeve are located outside of the tubing flange and the tubing segment. In addition, the inner sleeve, outer sleeve and the tubing flange are mechanically connected. 1. A tubing and connector combination comprising:a tubing segment and a tubing flange that are connected together;an inner sleeve;an outer sleeve; andthe inner sleeve and the outer sleeve being mechanically secured together and being positioned outside of a flow path through the tubing segment and the tubing flange.2. The tubing and connector combination of claim 1 , wherein the outer sleeve comprises an inner passage that tapers in the proximal direction and the inner sleeve comprises a proximal portion with distally-extending slots that allow compression of the proximal portion of the inner sleeve.3. The tubing and connector combination of claim 1 , wherein the tubing flange comprises an outer peripheral surface and an inner surface of the inner sleeve forms a seal around the outer peripheral surface of the tubing flange.4. The tubing and connector combination of claim 1 , wherein the inner sleeve comprises a distal portion having a structure configured to mate with a complementary structure.5. The tubing and connector combination of claim 4 , wherein the distal portion is formed along an internal surface.6. The tubing and connector combination of claim 5 , wherein the inner sleeve comprises an inner shoulder claim 5 , the inner shoulder and a portion of the tubing segment and tubing flange abutting following connection and the structure configured to mate with the complementary structure is positioned entirely distal of the shoulder.7. The tubing and connector combination of claim 6 , wherein at least a portion of the structure configured to mate ...

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04-01-2018 дата публикации

PATIENT INTERFACE SYSTEMS

Номер: US20180001046A1
Принадлежит:

A patient interface system for delivery of a supply of air at positive pressure to the entrance of a patient's airways for treatment of sleep disordered breathing includes an air delivery tube connected to a flexible portion of a plenum; a vent structure having sufficient rigidity to support its own weight under gravity and/or not to block or fold under tube movement or tube drag; and a patient interface structure. The patient interface structure includes a seal forming structure arranged on a top portion of the plenum; and a seal positioning and stabilizing structure connected to a flexible portion of the plenum. The seal-forming structure is substantially decoupled from a tube drag force. 110-. (canceled)11. A patient interface system for delivery of a supply of air at positive pressure to an entrance of a patient's airways for treatment of sleep disordered breathing , the patient interface system comprising:a patient interface structure comprising a flexible one-piece silicone structure at least partially forming a plenum having a seal provided thereto, the seal being adapted to, in use, engage and form a seal with the underside of the patient's nose; and ["a pair of main portions comprising a silicone material, each main portion being configured to, in use, engage a corresponding side of the patient's face between the patient's eye and ear, each main portion having a patient interface structure connector provided at a bottom portion thereof, each patient interface structure connector being removably connected to a corresponding side of the patient interface structure; and", "a rear strap connected at respective end portions thereof to the main portions of the seal positioning and stabilizing structure and being configured to, in use, extend around the back of the patient's head at a position above the patient's ears."], "a flexible seal positioning and stabilizing structure to position and stabilize the patient interface structure in sealing engagement with the ...

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04-01-2018 дата публикации

BREATHING ASSISTANCE APPARATUS

Номер: US20180001047A1
Принадлежит:

A CPAP system for supplying humidified gases to a user is disclosed in which various interfaces are described for gas delivery. A mask cushion including a deformable cushion and thin sheath is described. 1. (canceled)2. An elbow connector adapted to connect a patient interface with a supply of gases , the elbow connector comprising:a hollow body having an inlet and an outlet, the hollow body defining an air flow channel, the inlet configured to be in fluid communication with the supply of gases in use and the outlet configured to be in fluid communication with the patient interface in use;a wall of the hollow body defining the air flow channel, the wall being cylindrical, the cylindrical wall having a proximal portion closest to a user and a distal portion furthest from the user, the cylindrical wall also having a curved portion that bends in a first direction such that a length of the distal portion is longer than a length of the proximal portion, the distal portion comprising a flexible thin portion along the curved portion of the cylindrical wall such that the flexible thin portion is curved in two dimensions; andthe thin portion comprising a plurality of apertures configured to externally vent gases exhaled by the user.3. The elbow connector of claim 2 , wherein the elbow connector has at least a portion formed from polycarbonate.4. The elbow connector of claim 2 , wherein the elbow connector has at least a portion formed from Hytrel plastic.5. The elbow connector of claim 2 , wherein the apertures have rounded peripheries.6. The elbow connector of claim 2 , wherein the plurality of apertures are configured to reduce noise caused by venting of the gases exhaled by the user.7. The elbow connector of claim 2 , wherein the plurality of apertures are arranged in a circle.8. The elbow connector of claim 7 , wherein the flexible thin portion is circular.9. An elbow connector adapted to connect a patient interface with a supply of gases claim 7 , the elbow connector ...

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05-01-2017 дата публикации

CUSTOMIZABLE FACIAL SEALING SEGMENT FOR RESPIRATORY DEVICE AND METHOD OF CUSTOMIZING

Номер: US20170000964A1
Автор: SHAFER SANDY JANE
Принадлежит:

A facial sealing segment for a respiratory device includes a sealing flap adapted to sealingly engage the face of a user. The sealing flap is disposed about, and defines, a cutout adapted to receive one or both of the mouth or nares of the user. The facial sealing segment further includes a number of selectively removable portions formed in the sealing flap about the cutout. Each removable portion is defined in the sealing flap by a tear portion. 1. A facial sealing segment for a respiratory device , the sealing segment comprising:a sealing flap adapted to sealingly engage the face of a user, the sealing flap disposed about, and defining a cutout adapted to receive one or both of the mouth or nares of the user; anda number of selectively removable portions formed in the sealing flap about the cutout, each removable portion being defined in the sealing flap by a tear portion.2. The facial sealing segment of claim 1 , wherein the sealing flap comprises a first thickness (t)and wherein the tear portion comprises a localized thickness (t) less than the first thickness.3. The facial sealing segment of claim 1 , wherein the tear portion comprises a groove formed in the sealing flap.4. The facial sealing segment of claim 1 , wherein the groove is formed in a surface of the sealing flap opposite from a surface which sealingly engages the face of the user.5. The facial sealing segment of claim 1 , wherein the tear portion comprises a plurality of perforations formed in the sealing flap.6. The facial sealing segment of claim 1 , wherein the number of removable portions comprise a first portion adapted to be disposed adjacent a first side of the mouth of the user and a second portion adapted to be disposed adjacent a second side of the mouth of the user.7. The facial sealing segment of claim 1 , wherein at least one removable portion of the number of removable portions comprises a pull tab extending from a surface of the sealing flap opposite from a surface which sealingly ...

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02-01-2020 дата публикации

TRACHEOSTOMY TUBE MONITOR AND ALERTING APPARATUS

Номер: US20200001028A1
Автор: Mehta Deepak Kumar
Принадлежит:

A tracheostomy tube monitor and alerting apparatus includes: (i) a passive humidification device; and (ii) an integrated monitoring assembly fitted in an opening of a rear sidewall of the passive humidification device. The passive humidification device is configured to be connected to a connector of a tracheostomy tube of a patient. Once connected, the monitoring assembly of the apparatus can begin measuring one or more physiological parameters, such as, air flow, oxygen level, carbon dioxide level, pressure, and moisture. The measurements are compared against threshold values that denote blockage or decannulation. When these threshold values are surpassed, an alarm is actuated to alert a caregiver that the patient may be experiencing obstruction or decannulation of the tracheostomy tube. 1. A tracheostomy tube monitor and alerting apparatus , comprising:(i) a passive humidification device, the passive humidification device is configured to be connected to a connector of a tracheostomy tube; and(ii) an integrated monitoring assembly, the monitoring assembly configured to be fitted within an opening of a rear sidewall of the passive humidification device.2. The apparatus according to claim 1 , wherein the passive humidification device comprises a central housing and a tubular element.3. The apparatus according to claim 2 , wherein the central housing defines an enclosure having:a substantially C-shaped primary sidewall;a substantially D-shaped left sidewall and a substantially D-shaped right sidewall, the left and right sidewalls flanking a left side and a right side of the primary sidewall; andthe rear sidewall.4. The apparatus according to claim 3 , wherein the tubular element is configured to protrude from an external surface of the primary sidewall.5. The apparatus according to claim 4 , wherein a first end of the tubular element includes a port claim 4 , and wherein the port is configured to be connected to the connector of the tracheostomy tube.6. The apparatus ...

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02-01-2020 дата публикации

PATIENT INTERFACE HAVING ADAPTIVE SYSTEM, RESPIRATORY MASK AND CUSHION MODULE ADAPTED WITH ADAPTIVE SYSTEM

Номер: US20200001034A1
Принадлежит:

The present invention discloses a patient interface having an adaptive system, a respiratory mask and a cushion module adapted with the adaptive system. The adaptive system includes a forehead pressure diffusing portion, a cheek buffering portion and a connecting portion. The forehead pressure diffusing portion is disposed in a frame module. The cheek buffering portion is disposed in a cushion module. The connecting portion is positioned between the forehead pressure diffusing portion and the cheek buffering portion. The connecting portion is configured to transmit pressure between the forehead pressure diffusing portion and the cheek buffering portion. Thus, when a user wears a mask or other devices with the adaptive system, a force received by the face of the user could be automatically and appropriately distributed, further improving comfort of the wearer. 1. A patient interface , comprising:a cushion module;an elbow module;a frame module positioned between the cushion module and the elbow module;a headgear removably attached to the frame module; and a forehead pressure diffusing portion disposed in the frame module;', 'a cheek buffering portion disposed in the cushion module; and', 'a connecting portion positioned between the forehead pressure diffusing portion and the cheek buffering portion, wherein the connecting portion is configured to transmit pressure between the forehead pressure diffusing portion and the cheek buffering portion., "an adaptive system, adapted to fit the contours of patient's face when the cushion module, the elbow module, and the headgear are assembled, the adaptive system comprising:"}2. The patient interface according to claim 1 , wherein the forehead pressure diffusing portion comprises a headgear connecting portion claim 1 , and two side wings deformable by a pressure applied on the headgear.3. The patient interface according to claim 1 , wherein a forehead pad is absent between the forehead pressure diffusing portion and the patient ...

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02-01-2020 дата публикации

Systems and methods for evaluation of electrophysiology systems

Номер: US20200001036A1
Принадлежит: Biosig Technologies Inc

A signal processing evaluator and methods that compare a digital waveform of a cardiac signal to a first processed signal generated by a test system such as an EP recorder or an EP mapping system and generates a first finding evaluating how well the test system filters non-cardiac signals or simulated body impedance. A simulator and methods that send cardiac signals including non-cardiac signals or simulated body impedance to a test system and to a signal processing evaluator for evaluation of the test system.

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03-01-2019 дата публикации

WIRE HEATED TUBE WITH TEMPERATURE CONTROL SYSTEM, TUBE TYPE DETECTION, AND ACTIVE OVER TEMPERATURE PROTECTION FOR HUMIDIFIER FOR RESPIRATORY APPARATUS

Номер: US20190001091A1
Принадлежит:

A PAP system for delivering breathable gas to a patient includes a flow generator to generate a supply of breathable gas to be delivered to the patient; a humidifier including a heating plate to vaporize water and deliver water vapor to humidify the supply of breathable gas; a heated tube configured to heat and deliver the humidified supply of breathable gas to the patient; a power supply configured to supply power to the heating plate and the heated tube; and a controller configured to control the power supply to prevent overheating of the heating plate and the heated tube. 1. A control system for a heated conduit for use in a respiratory apparatus , the control system comprising:a power supply to provide power to the heated conduit;an over-temperature control circuit to prevent the overheating of the heated conduit;a heating control circuit configured to control heating to obtain a predetermined temperature;a sensing circuit including a sensing resistor configured to indicate the temperature of a sensor positioned in the heated conduit; anda bias generator circuit configured to provide a first source voltage to the sensing circuit so that the temperature of the heated conduit is continuously monitored.2. A control system according to claim 1 , wherein the over-temperature control circuit comprises a first transistor switch that is turned on when the temperature is below the predetermined temperature and is turned off when the temperature is at or above the predetermined temperature.3. A control system according to claim 2 , wherein the predetermined temperature is between the range of about 30° C. and about 45° C.4. A control system according to claim 2 , wherein the over-temperature control circuit further comprises a first comparator that controls the switching of the first transistor switch by comparing a reference voltage representing the predetermined temperature to a voltage determined from a first amplifier of the sensing circuit.5. A control system ...

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03-01-2019 дата публикации

POSITIVE EXPIRATORY PRESSURE DEVICE

Номер: US20190001187A1
Принадлежит: TRUDELL MEDICAL INTERNATIONAL

A positive exhalation pressure device increases the pressure gradient in the airways, thereby increasing oxygen saturation levels and decreasing the severity of hypoxia. Various embodiments of the device may be inserted into the nasal and/or oral cavities, or configured as mask devices covering the nasal and/or oral cavities. In some embodiments, the resistance of the device may be varied. 143-. (canceled)44. A positive expiratory pressure device comprising:a mask comprising a body shaped to cover the user's mouth and nose, wherein the mask is configured with a first port configured with an inhalation valve, and a second exhalation port sized to produce an exhalation pressure between 1-15 cmH2O; anda neck tube coupled to the mask and extending downwardly therefrom.45. The positive expiratory pressure device of wherein the neck tube is releasably coupled to the mask.46. The positive expiratory pressure device of wherein the neck tube is releasably coupled to the mask with a magnet.47. The positive expiratory pressure device of wherein the neck tube does not cover the first or second ports.48. The positive expiratory pressure device of wherein the mask comprises fabric catches for aligning one or more openings in the neck tube with the first and second ports on the mask.49. The positive expiratory pressure device of wherein the neck tube comprises an elastic member configured to engage the user.50. The positive expiratory pressure device of further comprising a drawstring mechanism for adjusting the elastic member.51. The positive expiratory pressure device of wherein the neck tube is the only feature for securing the mask to the user.52. The positive expiratory pressure device of wherein the body defines a dead space external to the user.53. The positive expiratory pressure device of wherein the expiratory port comprise a single orifice having an area of between 3.142 mmand 78.540 mm.54. A method of using a positive expiratory pressure device comprising:positioning a ...

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03-01-2019 дата публикации

Connector for multiple sized connections

Номер: US20190003625A1
Принадлежит: Fisher and Paykel Healthcare Ltd

A connector is used to connect a gases supply to a user. The user can be fitted with an interface, such as a cannula, while the gases supply can include a conduit. The connector interfaces between the conduit and the interface. The connector has a female assembly and a male assembly that connect together, such as by push fit. The male assembly includes an inner portion sized and configured to mate with a first female connector and an outer portion sized and configured to alternatively mate with a second female connector.

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20-01-2022 дата публикации

CPAP DEVICE

Номер: US20220016377A1
Принадлежит:

The CPAP device includes a main unit and a second unit to be attached to or detached from the main unit. The main unit includes a first housing having a first lead-out part, an air blower for leading out air from the first lead-out part, and a first electrical connection part provided on the first housing. The second unit includes a second housing having a second lead-in part and a second lead-out part, a humidifier which humidifies air led therein from the second lead-in part, and a second electrical connection part to be connected to the first electrical connection part. The first lead-out part and the second lead-in part are configured to guide, with a connection between them, the first electrical connection part and the second electrical connection part to a position where they are connectable to each other. 1. A CPAP device for feeding air led inside the device to an airway of a user , the CPAP device comprising:a first unit; anda second unit attachable to or detachable from the first unit, whereinthe first unit includes a first housing having a first lead-in part and a first lead-out part, an air blower for leading out air led in from the first lead-in part from the first lead-out part, a first electrical connection part provided on the first housing, and a first guide part,the second unit includes a second housing having a second lead-in part and a second lead-out part, a humidifier which humidifies air led therein from the second lead-in part, a second electrical connection part electrically connectable to the first electrical connection part, and a second guide part, andthe first guide part and the second guide part are configured to guide, with a connection between the first lead-out part and the second lead-in part, the first electrical connection part and the second electrical connection part to a position where the first electrical connection part and the second electrical connection part are electrically connectable to each other.2. The CPAP device ...

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20-01-2022 дата публикации

HUMIDIFIER AND/OR FLOW GENERATOR FOR CPAP DEVICE

Номер: US20220016382A1
Принадлежит:

A CPAP device is configured to deliver a pressurized flow of respiratory gas to a patient's airways and includes a flow generator with a blower configured to pressurize the flow of respiratory gas. A flexible face seal is positioned at an outlet end of a blower discharge path. The flexible face seal includes an aperture and a lip curling inwardly from a perimeter of the flexible face seal. A tub configured to hold a body of water and humidify the pressurized flow of respiratory gas includes a heat conducting base plate and a side wall. The side wall has a substantially flat portion that surrounds an air inlet opening. A base supports both the flow generator and the tub and includes a floor with a heater plate. A laterally positioned guide prevents the tub from being removed from the base in a vertical direction and includes a pair of C-shaped channel portions with open sides that face each other. 120-. (canceled)21. A CPAP device configured to deliver a pressurized flow of respiratory gas to a patient's airways , the CPAP device comprising:a flow generator comprising a blower configured to pressurize the flow of respiratory gas and a blower wall with a blower discharge path configured to convey the pressurized flow of respiratory gas from the blower;a flexible face seal connected to the blower wall and positioned at an outlet end of the blower discharge path, the flexible face seal comprising an aperture and a lip curling inwardly from a perimeter of the flexible face seal toward the aperture;a tub configured to hold a body of water and humidify the pressurized flow of respiratory gas, the tub comprising a heat conducting base plate and a tub side wall, the tub side wall having a substantially flat portion that surrounds an air inlet opening;a base that supports both the flow generator and the tub and comprises a floor with a heater plate, the tub being horizontally removable from the base by sliding the tub away from the blower wall and being horizontally ...

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08-01-2015 дата публикации

VENTILATOR SYSTEM

Номер: US20150007815A1
Принадлежит:

Described herein is a modular ventilator. The ventilator has modular flow control devices, which are connected to fluid inlet adapters. The modular flow control devices have sensors for controlling fluid flow through the modular flow control devices. The fluid inlet adapters are removable, and can include magnetic indicators, and the ventilator can identify the fluid from the magnetic indicator. The ventilator can also contain or be connected to a device having a low-noise blower. 1. A ventilator comprising: a housing defining an impeller cavity;', 'an impeller plate disposed within the impeller cavity and comprising an outside edge; and', 'one or more vanes disposed on the impeller plate and comprising a leading surface and a trailing surface connecting at a tip; and, 'a blower comprising a fixed magnetic field;', 'a drive coil configured to move within the fixed magnetic field in response to a low frequency signal and configured to receive a high frequency signal;', 'a detection coil adjacent the drive coil and configured to detect the high frequency signal in the drive coil, the detected high frequency signal corresponding to a position of the drive coil; and', 'a processor coupled to the high frequency source and the low frequency source and configured (i) to receive the detected high frequency signal form the detection coil and (ii) to adjust the low frequency signal to move the drive coil,, 'a flow control device comprisingwherein the blower is in fluid communication with the flow control device.2. The ventilator of claim 1 , wherein the blower is before the flow control device in a fluid path of the ventilator.3. The ventilator of claim 1 , wherein the blower is after the flow control device in a fluid path of the ventilator.4. The ventilator of claim 1 , further comprising a sensor configured to provide sensor information of the blower and the flow control device claim 1 , and a ventilation control system configured to send the sensor information to the flow ...

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08-01-2015 дата публикации

CUSHION TO FRAME ASSEMBLY MECHANISM

Номер: US20150007816A1
Принадлежит:

A patient interface for delivery of a supply of pressurised air or breathable gas to an entrance of a patient's airways including: a cushion member that includes a face contacting portion, a retaining structure and a resiliently flexible lip; and a frame member, wherein the retaining structure and the frame member are repeatedly engageable with and disengageable from one another, wherein a gas chamber is formed at least in part by engagement of the cushion member and the frame member, and wherein the resiliently flexible lip is configured to provide a sealing force between the cushion member and the frame member. 1. A patient interface for delivery of a supply of pressurised air or breathable gas to an entrance of a patient's airways comprising:a cushion member that includes a face contacting portion, a retaining structure and a resiliently flexible lip; anda frame member,wherein the retaining structure and the frame member are repeatedly engageable with and disengageable from one another,wherein a gas chamber is formed at least in part by engagement of the cushion member and the frame member, andwherein the resiliently flexible lip is configured to provide a sealing force between the cushion member and the frame member and the resiliently flexible lip projects laterally from a wall that forms part of a groove in a tongue and groove arrangement.2. The patient interface of claim 1 , wherein the resiliently flexible lip comprises a sealing lip that seals against the frame member when the retaining structure and frame member are attached to one another claim 1 , and when air pressure increases within the cushion member claim 1 , the sealing force is increased.3. The patient interface of claim 2 , wherein the sealing lip is a continuous inner peripheral edge integral to the resiliently flexible lip.4. The patient interface of claim 3 , wherein the sealing lip has an overall non-planar shape.5. The patient interface of claim 1 , wherein the retaining structure and the ...

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12-01-2017 дата публикации

Systems and Methods for Treating An Airway

Номер: US20170007792A1
Автор: Nye Hoyt
Принадлежит:

Some embodiments described herein may include a system or a method in which an air delivery lumen of an endotracheal tube, a laryngeal mask, or other airway device is configured to optionally provide a suction effect. 1. A method of removing blood or bodily secretions located in a throat region , the method comprising:disconnecting a proximal connector port of an airway device from a gas supply source, a distal tube portion of the airway device being inserted through a patient's mouth and positioned in a patient's trachea or posterior pharynx;releasably connecting a first end of an adapter device to the proximal connector port of the airway device by inserting the proximal connector port into a tapered lumen of the first end of the adapter device; andreleasably connecting a second end of the adapter device to a vacuum source so that at least the adapter device and the distal tube portion of the airway device define a suction path to remove blood or bodily secretions located in the throat region.2. The method of claim 1 , wherein the airway device is one of an endotracheal tube or a laryngeal mask claim 1 , the method further comprising delivering from the gas supply source a gas having a higher concentration of oxygen as compared to air claim 1 , the gas being delivered through the distal tube portion of the airway device before said disconnecting the proximal connector port of the airway device from the gas supply source.3. The method of claim 1 , wherein releasably coupling a first end of an adapter device to the proximal connector port comprises inserting and compressing the proximal connector port into a female fitting of the adapter device.4. The method of claim 1 , wherein the inserting and compressing the proximal connector port into a female fitting of the adapter device creates an interference fit.5. The method of claim 1 , wherein said releasably coupling the second end of the adapter device to the vacuum source comprises sealingly mating the second end of ...

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12-01-2017 дата публикации

Non-Rebreather Face Mask

Номер: US20170007793A1
Автор: Salvino Chris, White Scott
Принадлежит:

The invention is an improved non-rebreather face mask (NRB). The mask enables users to obtain high purity oxygen, over 80%, while minimizing the amount of pure oxygen needed to run the system by reducing dead space within the mask. The mask also features safety mechanisms to ensure users will never suffocate. 1. A non-rebreather face mask for oxygen supplementation comprising:A face mask with a balloon disposed along the circumference of the inner surface of the mask, that may be inflated to a volume of between 10-100 milliliters, further disposed with a standard valve at the center bottom of the mask for inflation by a tube connected to an external gas source, further disposed with two one way check valves for releasing gas from within the mask, further disposed with a luer lock for attachment to a semi-compliant elastic reservoir bag, which may be 0.1-5 liters, which is further disposed with a luer lock for attachment to a hose connected to a source of pure oxygen.2. A non-rebreather face mask for oxygen supplementation comprising:An elastic reservoir bag, a face mask with an inflatable inner lining, one way CO2 check valves, an O2 line.3. A non-rebreather face mask for oxygen supplementation comprising:a face mask with a reservoir bag attached to a bottom portion of the face mask, an oxygen line inlet on the reservoir bag for receiving oxygen, an exhaust valve for a user's exhaled breath, and a balloon attached to an inner surface of the face mask and wherein the balloon is inflated to occupy a dead space in the face mask but does not obstruct a user's nostril or mouth airways.4. Wherein the balloon is incorporated into the circumference of the face mask in a generally circular configuration.5. Wherein the balloon is configured in the shape of two saddle bags that rest over the user's nose and onto the user's cheeks.6. Wherein the balloon is inflatable with a luer lock configured port on the face mask.7. Wherein the balloon has a volume of between 10-25 ...

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14-01-2016 дата публикации

RECOGNITION SYSTEM FOR AN APPARATUS THAT DELIVERS BREATHABLE GAS TO A PATIENT

Номер: US20160008560A1
Автор: Kwok Philip Rodney
Принадлежит:

An adapter for use with a flow generator includes a conduit attachable to the outlet of the flow generator and an identifying element supported by the conduit and providing an identifying feature unique to a specific peripheral component attachable to the flow generator. The identifying feature is communicatable to the flow generator so that appropriate operating parameters of the flow generator may be automatically selected by the flow generator to coordinate with the specific peripheral component. 115-. (canceled)16. A continuous positive airway pressure (CPAP) system comprising:a flow generator configured to generate a supply of pressurized breathable gas that is delivered, via an airflow path that includes at least an outlet formed in the flow generator, a delivery conduit, and a patient interface, to a patient for treatment, the flow generator including a first connector structure;a peripheral CPAP component that is operable to be a component of the CPAP system and assist in application of treatment for the patient;a connector removably attachable to the first connector structure and separate from the peripheral CPAP component and, when attached, is configured to communicate the pressurized breathable gas delivered from the outlet to other components included in the airflow path, the connector including an identifying element disposed on or in the connector with the identifying element including an identifying feature related to the peripheral CPAP component; automatically recognize, via the first connector structure, the peripheral CPAP component connected to the first connector structure based on the identifying feature; and', 'automatically adjust at least one operating parameter of the flow generator based on recognition of the peripheral CPAP component, where adjustment of the operating parameter changes how the supply of pressurized breathable gas is delivered to the patient., 'an electronic controller electronically coupled to the first connector ...

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11-01-2018 дата публикации

SCENT DELIVERY ADAPTOR FOR CPAP

Номер: US20180008796A1
Автор: Le Son Q.
Принадлежит:

Embodiments of an adaptor for delivering diffused aromatic agents to a user of a CPAP machine is disclosed in this document. The adaptor may include a connector body, a diffuser pad disposed within the connector body, and at least one coupling mechanism on the connector body coupling the connector body within the air supply and positioning the diffuser pad within the airflow of a CPAP machine. The adaptor may be configured to couple directly to a CPAP mask. Similarly, the adaptor may be configured to be placed in the airflow between the CPAP air generator and the mask. The adaptor may be configured such that no modification of the existing CPAP hose, machine, or mask is required. 1. An adaptor , the adaptor comprising:a connector body;a diffuser pad disposed within the connector body; andat least one coupling mechanism on the connector body for coupling the connector body to a portion of a CPAP machine such that an airflow of the CPAP machine flows through the connector body and in contact with the diffuser pad.2. The adaptor of claim 1 , wherein the adaptor is configured to couple directly to a CPAP mask.3. The adaptor of claim 1 , wherein the adaptor is configured to be placed in the airflow between an air generator and a mask of the CPAP machine.4. The adaptor of claim 1 , wherein the adaptor is configured such that when used with a CPAP machine claim 1 , no modification of the existing CPAP hose claim 1 , machine claim 1 , or mask is required.5. The adaptor of claim 1 , further comprising essential oils permeated into the pad.6. The adaptor of claim 1 , wherein the pad is formed of polyester felt.7. The adaptor of claim 1 , wherein the connector body includes a hose attachment and a mask attachment.8. The adaptor of claim 1 , wherein the at least one coupling mechanism includes a tube formed of a pliable material.9. A method of diffusing aromatic agents into the air supply of a CPAP machine claim 1 , the method comprising:providing a CPAP machine having an air ...

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