Pivotable outlet port
11623059 · 2023-04-11
Assignee
Inventors
Cpc classification
A61M39/12
HUMAN NECESSITIES
F16L27/107
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16L53/38
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
A61M2205/0216
HUMAN NECESSITIES
International classification
A61M16/08
HUMAN NECESSITIES
A61M16/00
HUMAN NECESSITIES
A61M39/12
HUMAN NECESSITIES
Abstract
An apparatus for providing a pressurised flow of breathable gas to the airways of a patient includes a pivotable outlet port structured and arranged to connect to an air delivery tube configured to pass the pressurised flow of breathable gas to a patient interface. The pivotable outlet port is able to pivot about at least one axis.
Claims
1. An apparatus for providing a pressurised flow of breathable gas to airways of a patient, the apparatus comprising: a pivotable outlet port structured and arranged to connect to an air delivery tube configured to pass the pressurised flow of breathable gas to a patient interface, the pivotable outlet port being able to pivot about at least one axis, wherein the pivotable outlet port includes an outlet portion pivotally coupled to the apparatus, an inlet portion adapted to receive the pressurised flow of breathable gas, and a decoupling portion that provides a decoupling connection between the inlet portion and the outlet portion, wherein the outlet portion includes an outlet tube adapted to directly connect to the air delivery tube, wherein the outlet portion comprises a direct pivotal connection to the apparatus configured to provide the pivotal coupling of the outlet portion to the apparatus about the at least one axis, wherein the decoupling portion is structured and arranged to decouple pivotal movement of the outlet portion from the inlet portion, wherein the decoupling portion comprises a gusset or fold structured and arranged to expand and/or contract when the outlet portion is pivoted relative to the apparatus, and wherein the direct pivotal connection of the outlet portion is separate and distinct from the inlet portion and the decoupling portion.
2. The apparatus according to claim 1, wherein the decoupling portion is structured and arranged to allow the outlet portion to assume alternative positions or orientations relative to the apparatus for connection to the air delivery tube without impacting the inlet portion with respect to at least one plane associated with the apparatus.
3. The apparatus according to claim 1, wherein the outlet portion comprises a relatively rigid material and the inlet portion and the decoupling portion comprise a relatively soft and/or flexible material that is overmolded to the outlet portion.
4. The apparatus according to claim 3, wherein the outlet portion comprises a thermoplastic polymer.
5. The apparatus according to claim 3, wherein the inlet portion and the decoupling portion comprise a thermoplastic elastomer.
6. The apparatus according to claim 1, wherein the inlet portion includes an inlet seal.
7. The apparatus according to claim 1, wherein the outlet portion includes at least one pivot pin configured to provide the pivotal connection of the outlet portion.
8. The apparatus according to claim 1, wherein the outlet portion includes a pivotal range of movement, in at least one plane associated with the apparatus, which is within at least one of the following ranges; up to at least 30 degrees, up to at least 90 degrees, up to at least 180 degrees, and up to at least 270 degrees.
9. The apparatus according to claim 1, further comprising: a water reservoir including a cavity structured to hold a volume of water; and a water reservoir dock structured and arranged to receive the water reservoir in an operative position, wherein the pivotable outlet port is provided to a dock outlet of the water reservoir dock, the pivotable outlet port configured to pneumatically connect the water reservoir, or an outlet muffler, to the air delivery tube.
10. The apparatus according to claim 9, wherein the dock outlet includes a tapered side wall.
11. The apparatus according to claim 9, wherein the dock outlet is recessed with respect to an external wall of the apparatus.
12. The apparatus according to claim 11, wherein the dock outlet is located in a wall cavity so that no more than a portion of the outlet portion of the pivotal outlet port protrudes outside the wall cavity and beyond the external wall.
13. The apparatus according to claim 12, wherein no portion of the outlet portion of the pivotal outlet port protrudes outside the wall cavity.
14. The apparatus according to claim 1, wherein at least a portion of the outlet portion is configured to engage the decoupling portion to provide a stop to prevent further pivotal movement.
15. The apparatus according to claim 1, wherein the decoupling portion comprises an elastomeric material and is configured to resiliently return the outlet portion to an initial rest position when force applied to the air delivery tube is released.
16. An apparatus for providing a pressurised flow of breathable gas to airways of a patient, the apparatus comprising: a pivotable outlet port structured and arranged to connect to an air delivery tube configured to pass the pressurised flow of breathable gas to a patient interface, the pivotable outlet port being able to pivot about at least one axis, wherein the pivotable outlet port includes an outlet portion pivotally coupled to the apparatus, an inlet portion adapted to receive the pressurised flow of breathable gas, and a decoupling portion that provides a decoupling connection between the inlet portion and the outlet portion, wherein the outlet portion includes at least one pivot pin configured to provide the pivotal coupling of the outlet portion to the apparatus about the at least one axis, wherein the outlet portion includes an outlet tube adapted to directly connect to the air delivery tube, and wherein the decoupling portion is structured and arranged to decouple pivotal movement of the outlet portion from the inlet portion.
17. The apparatus according to claim 16, wherein the at least one pivot pin is configured to allow the outlet portion to pivot relative to the apparatus about only a single axis.
18. The apparatus according to claim 16, wherein the apparatus forms a bottom plane that is substantially horizontal when the apparatus is in a working orientation, and the outlet portion is pivotally coupled to the apparatus such that the at least one axis is oriented generally perpendicular to the bottom plane.
19. The apparatus according claim 16, wherein the decoupling portion comprises a gusset or fold structured and arranged to expand and/or contract when the outlet portion is pivoted relative to the apparatus.
20. The apparatus according to claim 16, further comprising: a water reservoir including a cavity structured to hold a volume of water; and a water reservoir dock structured and arranged to receive the water reservoir in an operative position, wherein the pivotable outlet port is provided to a dock outlet of the water reservoir dock, the pivotable outlet port configured to pneumatically connect the water reservoir, or an outlet muffler, to the air delivery tube.
Description
4 BRIEF DESCRIPTION OF THE DRAWINGS
(1) The present technology is illustrated by way of example, and not by way of limitation, in the figures of the accompanying drawings, in which like reference numerals refer to similar elements including:
4.1 Respiratory Therapy Systems
(2)
4.2 Patient Interface
(3)
4.3 RPT Device and Humidifier
(4)
(5)
(6)
(7)
(8)
(9)
(10)
(11)
(12)
(13)
(14)
(15)
(16)
(17)
(18)
(19)
(20)
(21)
(22)
5 DETAILED DESCRIPTION OF EXAMPLES OF THE TECHNOLOGY
(23) Before the present technology is described in further detail, it is to be understood that the technology is not limited to the particular examples described herein, which may vary. It is also to be understood that the terminology used in this disclosure is for the purpose of describing only the particular examples discussed herein, and is not intended to be limiting.
(24) The following description is provided in relation to various examples which may share one or more common characteristics and/or features. It is to be understood that one or more features of any one example may be combinable with one or more features of another example or other examples. In addition, any single feature or combination of features in any of the examples may constitute a further example.
5.1 Therapy
(25) In one form, the present technology comprises a method for treating a respiratory disorder comprising applying positive pressure to the entrance of the airways of a patient 1000.
(26) In certain examples of the present technology, a supply of air at positive pressure is provided to the nasal passages of the patient via one or both nares.
(27) In certain examples of the present technology, mouth breathing is limited, restricted or prevented.
5.2 Respiratory Therapy Systems
(28) In one form, the present technology comprises a respiratory therapy system for treating a respiratory disorder. The respiratory therapy system may comprise an RPT device 4000 for supplying a flow of air to the patient 1000 via an air circuit 4170 and a patient interface 3000, e.g., see
5.3 Patient Interface
(29)
(30) If a patient interface is unable to comfortably deliver a minimum level of positive pressure to the airways, the patient interface may be unsuitable for respiratory pressure therapy.
(31) The patient interface 3000 in accordance with one form of the present technology is constructed and arranged to be able to provide a supply of air at a positive pressure of at least 6 cmH.sub.2O with respect to ambient. The patient interface 3000 in accordance with one form of the present technology is constructed and arranged to be able to provide a supply of air at a positive pressure of at least 10 cmH.sub.2O with respect to ambient.
(32) The patient interface 3000 in accordance with one form of the present technology is constructed and arranged to be able to provide a supply of air at a positive pressure of at least 20 cmH.sub.2O with respect to ambient.
5.4 RPT Device
(33) An exploded view of an RPT device 4000 in accordance with one aspect of the present technology is shown in
(34) In one form, the RPT device 4000 is constructed and arranged to be capable of delivering a flow of air in a range of −20 L/min to +150 L/min while maintaining a positive pressure of at least 6 cmH.sub.2O, or at least 10 cmH.sub.2O, or at least 20 cmH.sub.2O.
(35) The RPT device 4000 may include an external housing having one or more panel(s) such as a main panel 4010, a front panel 4012 and a side panel 4014. The RPT device 4000 may also comprise an outlet muffler 4124 as shown in
(36) Electrical components may be mounted on a single Printed Circuit Board Assembly (PCBA) 4202. In an alternative form, the RPT device 4000 may include more than one PCBA 4202.
(37) Further examples and details of an exemplary RPT device are described in PCT Publication No. WO 2015/089582, which is incorporated herein by reference in its entirety.
(38) A power supply may be located internal or external of the external housing 4010 of the RPT device 4000.
(39) In one form of the present technology, power supply provides electrical power to the RPT device 4000 only. In another form of the present technology, power supply provides electrical power to both RPT device 4000 and humidifier 5000.
(40) In one form of the present technology, the RPT device includes a central controller including one or a plurality of processors suitable to control an RPT device 4000.
(41) Suitable processors may include an x86 INTEL processor, a processor based on ARM® Cortex®-M processor from ARM Holdings such as an STM32 series microcontroller from ST MICROELECTRONIC. In certain alternative forms of the present technology, a 32-bit RISC CPU, such as an STR9 series microcontroller from ST MICROELECTRONICS or a 16-bit RISC CPU such as a processor from the MSP430 family of microcontrollers, manufactured by TEXAS INSTRUMENTS may also be suitable.
(42) In one form of the present technology, the central controller is a dedicated electronic circuit.
(43) In one form, the central controller is an application-specific integrated circuit. In another form, the central controller comprises discrete electronic components.
(44) The central controller may be configured to receive input signal(s) from one or more transducers, one or more input devices, and the humidifier 5000.
(45) The central controller may be configured to provide output signal(s) to one or more of an output device, a therapy device controller, a data communication interface, and the humidifier 5000.
(46) In some forms of the present technology, the central controller is configured to implement the one or more methodologies described herein, such as the one or more algorithms expressed as computer programs stored in a non-transitory computer readable storage medium, such as memory. In some forms of the present technology, the central controller may be integrated with an RPT device 4000. However, in some forms of the present technology, some methodologies may be performed by a remotely located device. For example, the remotely located device may determine control settings for a ventilator or detect respiratory related events by analysis of stored data such as from any of the sensors described herein.
5.5 Air Circuit
(47) An air circuit 4170 in accordance with an aspect of the present technology is a conduit or a tube constructed and arranged to allow, in use, a flow of air to travel between two components such as RPT device 4000 and the patient interface 3000.
(48) In particular, the air circuit 4170 may be in fluid connection with the outlet of the pneumatic block 4020 and the patient interface. The air circuit may be referred to as an air delivery tube. In some cases there may be separate limbs of the circuit for inhalation and exhalation. In other cases a single limb is used.
(49) In some forms, the air circuit 4170 may comprise one or more heating elements configured to heat air in the air circuit, for example to maintain or raise the temperature of the air. The heating element may be in a form of a heated wire circuit, and may comprise one or more transducers, such as temperature sensors. In one form, the heated wire circuit may be helically wound around the axis of the air circuit 4170. The heating element may be in communication with a controller such as a central controller. One example of an air circuit 4170 comprising a heated wire circuit is described in U.S. Pat. No. 8,733,349, which is incorporated herewithin in its entirety by reference.
(50) 5.5.1 Supplementary Gas Delivery
(51) In one form of the present technology, supplementary gas, e.g. oxygen, is delivered to one or more points in the pneumatic path, such as upstream of the pneumatic block 4020, to the air circuit 4170, and/or to the patient interface 3000.
5.6 Humidifier
(52) 5.6.1 Humidifier Overview
(53) In one form of the present technology there is provided a humidifier 5000 (e.g. as shown in
(54)
(55) In the illustrated example, the RPT device 4000 is integrated with the humidifier 5000. In this arrangement, the water reservoir dock 5130 is structured to connect the water reservoir 5110 to the pneumatic path. As best shown in
(56) However, it should be appreciated that the reservoir dock 5130 may be provided separately to RPT device 4000 in an alternative arrangement. In such an arrangement, additional interfaces may be used to connect the reservoir dock 5130 to the RPT device 4000, e.g., directly coupled or coupled via an air circuit.
(57) In another arrangement, the water reservoir dock 5130 may comprise an opening in a substantially horizontal plane, so that the water reservoir 5110 may be inserted from above or below the water reservoir dock 5130.
(58) Further examples and details of such RPT device 4000 and integrated humidifier 5000 are described in PCT Publication No. WO 2014/138804, published Sep. 18, 2014, which is incorporated herein by reference in its entirety.
(59) 5.6.2 Humidifier Components
(60) 5.6.2.1 Water Reservoir
(61)
(62) According to one aspect, the water reservoir 5110 is configured to add humidity to a flow of air from the RPT device 4000 as the flow of air travels therethrough. In one form, the water reservoir 5110 may be configured to encourage the flow of air to travel in a tortuous path through the reservoir 5110 while in contact with the volume of water therein.
(63) According to one form, the reservoir 5110 may be removable from the humidifier 5000, for example in a lateral direction as shown in
(64) 5.6.2.2 Conductive Portion
(65) According to one arrangement, the reservoir 5110 comprises a conductive portion 5120 configured to allow efficient transfer of heat from the heating element to the volume of liquid in the reservoir 5110. In one form, the conductive portion 5120 may be arranged as a plate, although other shapes may also be suitable. All or a part of the conductive portion 5120 may be made of a thermally conductive material such as aluminium (e.g. approximately 2 mm thick, such as 1 mm, 1.5 mm, 2.5 mm or 3 mm), another heat conducting metal or some plastics. In some cases, suitable heat conductivity may be achieved with less conductive materials of suitable geometry.
(66) 5.6.2.3 Humidifier Reservoir Dock
(67) In one form, the humidifier 5000 may comprise a humidifier reservoir dock 5130 (as shown in
(68) Air Delivery Tube to Reservoir Dock Connection
(69)
(70) In the example, the pivotable outlet port 6500 is provided to the dock outlet 6090 of the reservoir dock 6050 to pneumatically connect a water reservoir or outlet muffler to the air delivery tube 4170. The pivotable outlet port 6500 is configured to deliver pressurized air that has been humidified in the water reservoir, or that has passed through the outlet muffler, to the air delivery tube 4170. In an example, the pivotable outlet port 6500 may also at least partially locate and secure the air delivery tube 4170 to the reservoir dock 6050. Whilst described in the context of an RPT device with an integrated humidifier, the pivotable nature of the described outlet port is not directly associated with the humidification of the provided air. The function of the outlet port is to conveniently pass on the pressurized air generated in the RPT device to the air circuit 4170 and the patient interface 3000. As such, the described pivotable outlet port 6500 may even be used with an RPT device without a humidifier. Thus, the pivotable outlet port 6500 may be located anywhere on the integrated RPT device and/or humidifier 6000.
(71) As best shown in
(72) As best shown in
(73) In addition, a single pin or a pair of opposed, protruding, and cylindrical pivot pins 6520 extend from the outlet tube 6512 (e.g., at superior and inferior sides of the outlet tube 6512) for forming a pivot or hinge connection with the reservoir dock 6050. As shown in
(74) As shown in
(75) In the illustrated example, the integrated RPT device and humidifier 6000 includes a bottom surface defining a bottom plane BP (e.g., see
(76)
(77) As best seen in
(78) In the illustrated example, e.g., see
(79) For example, as shown in
(80) In an alternative example, each of the outlet portion 6510 and the inlet portion 6530 may comprise a relatively rigid material (e.g., thermoplastic polymer (e.g., PC, ABS)), and the decoupling portion 6550 may comprise a relatively soft and/or flexible material (e.g., thermoplastic elastomer (TPE) or silicone) that is overmolded to the outlet portion 6510 and the inlet portion 6530 to flexibly connect the outlet portion 6510 and the inlet portion 6530.
(81) In an example, the pivotable outlet port 6500 may comprise a port, e.g., pressure port for measuring air pressure at the dock outlet 6090.
(82) When the pivotable outlet port 6500 is connected to the dock outlet 6090 of the reservoir dock 6050, the outlet portion 6510 and outlet tube 6512 thereof protrudes out of the cavity of the reservoir dock 6050 to allow engagement with the air delivery tube 4170, e.g., see
(83)
(84) When the dock connector 4600 is engaged with the pivotable outlet port 6500, the pivotable outlet port 6500 is structured and arranged to allow pivoting of the outlet portion 6510 and hence the attached air delivery tube 4170 within a horizontal plane that extends generally parallel to the bottom surface and bottom plane BP thereof of the integrated RPT device and humidifier 6000. That is, the outlet portion 6510 may be pivoted within the horizontal plane about its pivot axis PA to a maximum left position (as viewed in
(85) In the illustrated example, the axis OA of the outlet tube 6512 in the maximum left position (as viewed in
(86) However, it should be appreciated that the outlet portion 6510 may include alternative ranges of movement, e.g., range of movement 0 to 180°, e.g., 20° to 140°, e.g., 40° to °120. In an example, the outlet portion 6510 may include a pivotal range of movement, in at least one plane associated with the apparatus, between the maximum left and right positions, within at least one of the following ranges: at least 30°, at least 90°, at least 180°, and at least 270°. If the outlet portion 6510 is arranged on a flat surface of a device, e.g., along a side of a device as illustrated in
(87) In an example, the end wall 6516 of the outlet portion 6510 may engage the gusset or fold 6556 of the decoupling portion 6550 which provides a stop to prevent further rotation when the outlet portion 6510 reaches the maximum left position and the maximum right position (as viewed in
(88) As shown in
(89) In an example, the outlet portion 6510 may freely rotate to any position between the maximum left and right positions, e.g., depending on force applied to the air delivery tube 4170. In an alternative example, the pivotable outlet port 6500 may include a ratcheting or locking arrangement structured and arranged to provide one or more discrete and predetermined angular positions of the outlet portion 6510.
(90) In a further alternative arrangement, not shown in the drawings, a ball joint type connection between the dock connector 4600 and the outlet port 6500 may also be used. Such an arrangement will allow decoupling of the outlet portion 6510 relative to the inlet portion 6530, and therefore decoupling of the air delivery tube 4170 from the RPT device in a plurality of planes, and not only in a single horizontal plane illustrated in
(91) 5.6.2.4 Water Level Indicator
(92) The humidifier reservoir 5110 may comprise a water level indicator. In some forms, the water level indicator may provide one or more indications to a user such as the patient 1000 or a care giver regarding a quantity of the volume of water in the humidifier reservoir 5110. The one or more indications provided by the water level indicator may include an indication of a maximum, predetermined volume of water, any portions thereof, such as 25%, 50% or 75% or volumes such as 200 ml, 300 ml or 400 ml.
(93) 5.6.2.5 Humidifier Transducer(s)
(94) As shown in
(95) 5.6.2.5.1 Pressure Transducer
(96) One or more pressure transducers 5212 may be provided to the humidifier 5000 in addition to, or instead of, a pressure sensor 4272 provided in the RPT device 4000.
(97) 5.6.2.5.2 Flow Rate Transducer
(98) One or more flow rate transducers 5214 may be provided to the humidifier 5000 in addition to, or instead of, a flow rate sensor provided in the RPT device 4000.
(99) 5.6.2.5.3 Temperature Transducer
(100) The humidifier 5000 may comprise one or more temperature transducers 5216. The one or more temperature transducers 5216 may be configured to measure one or more temperatures such as of the heating element 5240 and/or of the flow of air downstream of the humidifier outlet. In some forms, the humidifier 5000 may further comprise a temperature sensor 5216 to detect the temperature of the ambient air.
(101) 5.6.2.5.4 Humidity Transducer
(102) In one form, the humidifier 5000 may comprise one or more humidity sensors 5218 to detect a humidity of a gas, such as the ambient air. The humidity sensor 5218 may be placed towards the humidifier outlet in some forms to measure a humidity of the gas delivered from the humidifier 5000. The humidity sensor may be an absolute humidity sensor or a relative humidity sensor.
(103) 5.6.2.6 Heating Element
(104) A heating element 5240 may be provided to the humidifier 5000 in some cases to provide a heat input to one or more of the volume of water in the humidifier reservoir 5110 and/or to the flow of air. The heating element 5240 may comprise a heat generating component such as an electrically resistive heating track. One suitable example of a heating element 5240 is a layered heating element such as one described in the PCT Patent Application Publication No. WO 2012/171072, which is incorporated herewith by reference in its entirety.
(105) In some forms, the heating element 5240 may be provided in the humidifier base where heat may be provided to the humidifier reservoir 5110 primarily by conduction.
5.7 Glossary
(106) For the purposes of the present technology disclosure, in certain forms of the present technology, one or more of the following definitions may apply. In other forms of the present technology, alternative definitions may apply.
(107) 5.7.1 General
(108) Air: In certain forms of the present technology, air may be taken to mean atmospheric air, and in other forms of the present technology air may be taken to mean some other combination of breathable gases, e.g. atmospheric air enriched with oxygen.
(109) Ambient: In certain forms of the present technology, the term ambient will be taken to mean (i) external of the treatment system or patient, and (ii) immediately surrounding the treatment system or patient.
(110) For example, ambient humidity with respect to a humidifier may be the humidity of air immediately surrounding the humidifier, e.g. the humidity in the room where a patient is sleeping. Such ambient humidity may be different to the humidity outside the room where a patient is sleeping.
(111) In another example, ambient pressure may be the pressure immediately surrounding or external to the body.
(112) In certain forms, ambient (e.g., acoustic) noise may be considered to be the background noise level in the room where a patient is located, other than for example, noise generated by an RPT device or emanating from a mask or patient interface. Ambient noise may be generated by sources outside the room.
(113) Automatic Positive Airway Pressure (APAP) therapy: CPAP therapy in which the treatment pressure is automatically adjustable, e.g. from breath to breath, between minimum and maximum limits, depending on the presence or absence of indications of SDB events.
(114) Continuous Positive Airway Pressure (CPAP) therapy: Respiratory pressure therapy in which the treatment pressure is approximately constant through a respiratory cycle of a patient. In some forms, the pressure at the entrance to the airways will be slightly higher during exhalation, and slightly lower during inhalation. In some forms, the pressure will vary between different respiratory cycles of the patient, for example, being increased in response to detection of indications of partial upper airway obstruction, and decreased in the absence of indications of partial upper airway obstruction.
(115) Flow rate: The volume (or mass) of air delivered per unit time. Flow rate may refer to an instantaneous quantity. In some cases, a reference to flow rate will be a reference to a scalar quantity, namely a quantity having magnitude only. In other cases, a reference to flow rate will be a reference to a vector quantity, namely a quantity having both magnitude and direction. Flow rate may be given the symbol Q. ‘Flow rate’ is sometimes shortened to simply ‘flow’ or ‘airflow’.
(116) In the example of patient respiration, a flow rate may be nominally positive for the inspiratory portion of a breathing cycle of a patient, and hence negative for the expiratory portion of the breathing cycle of a patient. Device flow rate, Qd, is the flow rate of air leaving the RPT device. Total flow rate, Qt, is the flow rate of air and any supplementary gas reaching the patient interface via the air circuit. Vent flow rate, Qv, is the flow rate of air leaving a vent to allow washout of exhaled gases. Leak flow rate, Ql, is the flow rate of leak from a patient interface system or elsewhere. Respiratory flow rate, Qr, is the flow rate of air that is received into the patient's respiratory system.
(117) Flow therapy: Respiratory therapy comprising the delivery of a flow of air to an entrance to the airways at a controlled flow rate referred to as the treatment flow rate that is typically positive throughout the patient's breathing cycle.
(118) Humidifier: The word humidifier will be taken to mean a humidifying apparatus constructed and arranged, or configured with a physical structure to be capable of providing a therapeutically beneficial amount of water (H.sub.2O) vapour to a flow of air to ameliorate a medical respiratory condition of a patient.
(119) Leak: The word leak will be taken to be an unintended flow of air. In one example, leak may occur as the result of an incomplete seal between a mask and a patient's face. In another example leak may occur in a swivel elbow to the ambient.
(120) Noise, conducted (acoustic): Conducted noise in the present document refers to noise which is carried to the patient by the pneumatic path, such as the air circuit and the patient interface as well as the air therein. In one form, conducted noise may be quantified by measuring sound pressure levels at the end of an air circuit.
(121) Noise, radiated (acoustic): Radiated noise in the present document refers to noise which is carried to the patient by the ambient air. In one form, radiated noise may be quantified by measuring sound power/pressure levels of the object in question according to ISO 3744.
(122) Noise, vent (acoustic): Vent noise in the present document refers to noise which is generated by the flow of air through any vents such as vent holes of the patient interface.
(123) Patient: A person, whether or not they are suffering from a respiratory condition.
(124) Pressure: Force per unit area. Pressure may be expressed in a range of units, including cmH.sub.2O, g-f/cm.sup.2 and hectopascal. 1 cmH.sub.2O is equal to 1 g-f/cm.sup.2 and is approximately 0.98 hectopascal (1 hectopascal=100 Pa=100 N/m.sup.2=1 millibar 0.001 atm). In this specification, unless otherwise stated, pressure is given in units of cmH.sub.2O.
(125) The pressure in the patient interface is given the symbol Pm, while the treatment pressure, which represents a target value to be achieved by the interface pressure Pm at the current instant of time, is given the symbol Pt.
(126) Respiratory Pressure Therapy (RPT): The application of a supply of air to an entrance to the airways at a treatment pressure that is typically positive with respect to atmosphere.
(127) Ventilator: A mechanical device that provides pressure support to a patient to perform some or all of the work of breathing.
(128) 5.7.1.1 Materials
(129) Silicone or Silicone Elastomer: A synthetic rubber. In this specification, a reference to silicone is a reference to liquid silicone rubber (LSR) or a compression moulded silicone rubber (CMSR). One form of commercially available LSR is SILASTIC (included in the range of products sold under this trademark), manufactured by Dow Corning. Another manufacturer of LSR is Wacker. Unless otherwise specified to the contrary, an exemplary form of LSR has a Shore A (or Type A) indentation hardness in the range of about 35 to about 45 as measured using ASTM D2240.
(130) Polycarbonate: a thermoplastic polymer of Bisphenol-A Carbonate.
(131) 5.7.1.2 Mechanical Properties
(132) Resilience: Ability of a material to absorb energy when deformed elastically and to release the energy upon unloading.
(133) Resilient: Will release substantially all of the energy when unloaded. Includes e.g. certain silicones, and thermoplastic elastomers.
(134) Hardness: The ability of a material per se to resist deformation (e.g. described by a Young's Modulus, or an indentation hardness scale measured on a standardised sample size). ‘Soft’ materials may include silicone or thermo-plastic elastomer (TPE), and may, e.g. readily deform under finger pressure. ‘Hard’ materials may include polycarbonate, polypropylene, steel or aluminium, and may not e.g. readily deform under finger pressure.
(135) Stiffness (or rigidity) of a structure or component: The ability of the structure or component to resist deformation in response to an applied load. The load may be a force or a moment, e.g. compression, tension, bending or torsion. The structure or component may offer different resistances in different directions. The inverse of stiffness is flexibility.
(136) Floppy structure or component: A structure or component that will change shape, e.g. bend, when caused to support its own weight, within a relatively short period of time such as 1 second.
(137) Rigid structure or component: A structure or component that will not substantially change shape when subject to the loads typically encountered in use. An example of such a use may be setting up and maintaining a patient interface in sealing relationship with an entrance to a patient's airways, e.g. at a load of approximately 20 to 30 cmH.sub.2O pressure.
(138) As an example, an I-beam may comprise a different bending stiffness (resistance to a bending load) in a first direction in comparison to a second, orthogonal direction. In another example, a structure or component may be floppy in a first direction and rigid in a second direction.
5.8 Other Remarks
(139) Unless the context clearly dictates otherwise and where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit, between the upper and lower limit of that range, and any other stated or intervening value in that stated range is encompassed within the technology. The upper and lower limits of these intervening ranges, which may be independently included in the intervening ranges, are also encompassed within the technology, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the technology.
(140) Furthermore, where a value or values are stated herein as being implemented as part of the technology, it is understood that such values may be approximated, unless otherwise stated, and such values may be utilized to any suitable significant digit to the extent that a practical technical implementation may permit or require it.
(141) Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this technology belongs. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present technology, a limited number of the exemplary methods and materials are described herein.
(142) When a particular material is identified as being used to construct a component, obvious alternative materials with similar properties may be used as a substitute. Furthermore, unless specified to the contrary, any and all components herein described are understood to be capable of being manufactured and, as such, may be manufactured together or separately.
(143) It must be noted that as used herein and in the appended claims, the singular forms “a”, “an”, and “the” include their plural equivalents, unless the context clearly dictates otherwise.
(144) All publications mentioned herein are incorporated herein by reference in their entirety to disclose and describe the methods and/or materials which are the subject of those publications. The publications discussed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the present technology is not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided may be different from the actual publication dates, which may need to be independently confirmed.
(145) The terms “comprises” and “comprising” should be interpreted as referring to elements, components, or steps in a non-exclusive manner, indicating that the referenced elements, components, or steps may be present, or utilized, or combined with other elements, components, or steps that are not expressly referenced.
(146) The subject headings used in the detailed description are included only for the ease of reference of the reader and should not be used to limit the subject matter found throughout the disclosure or the claims. The subject headings should not be used in construing the scope of the claims or the claim limitations.
(147) Although the technology herein has been described with reference to particular examples, it is to be understood that these examples are merely illustrative of the principles and applications of the technology. In some instances, the terminology and symbols may imply specific details that are not required to practice the technology. For example, although the terms “first” and “second” may be used, unless otherwise specified, they are not intended to indicate any order but may be utilised to distinguish between distinct elements. Furthermore, although process steps in the methodologies may be described or illustrated in an order, such an ordering is not required. Those skilled in the art will recognize that such ordering may be modified and/or aspects thereof may be conducted concurrently or even synchronously.
(148) It is therefore to be understood that numerous modifications may be made to the illustrative examples and that other arrangements may be devised without departing from the spirit and scope of the technology.
5.9
(149) TABLE-US-00002 REFERENCE SIGNS LIST Feature Item Number patient 1000 bed partner 1100 patient interface 3000 patient interface 3000 seal - forming structure 3100 plenum chamber 3200 positioning and stabilising structure 3300 vent 3400 connection port 3600 forehead support 3700 RPT device 4000 main panel 4010 front panel 4012 side panel 4014 chassis 4016 pneumatic block 4020 outlet muffler 4124 air circuit 4170 PCBA 4202 dock connector 4600 humidifier 5000 water reservoir 5110 heater plate 5120 water reservoir dock 5130 cavity 5160 dock air outlet 5168 dock air inlet 5170 humidifier outlet 5172 humidifier transducer 5210 air pressure sensor 5212 air flow rate transducer 5214 temperature sensor 5216 humidity sensor 5218 heating element 5240 humidifier controller 5250 central humidifier controller 5251 heating element controller 5252 air circuit controller 5254 integrated RPT device and humidifier 6000 reservoir dock 6050 dock outlet 6090 side wall 6092 opening 6095 pivotable outlet port 6500 outlet portion 6510 outlet tube 6512 flange 6514 end wall 6516 pivot pins 6520 inlet portion 6530 inlet tube 6532 flange 6534 inlet seal 6536 decoupling portion 6550 outlet end 6552 inlet end 6554 fold 6556