NZ756941A - Nasal mask system - Google Patents

Abstract

A mask system for use in delivering breathable gas to a patient in positive airway pressure therapy, including: a cushion assembly (250) configured to receive a flow of the breathable gas pressurised above atmospheric pressure, the cushion assembly including a flexible plenum chamber and a seal forming portion (270) adapted to form a seal with at least a portion of the patient’s nose, the cushion assembly configured to in use attach to a headgear assembly with a two-point connection; and a decoupling system configured to in use isolate the cushion assembly from air conduit drag forces such that sealing forces applied by the cushion assembly to the patient’s face are not affected by the drag forces. The decoupling system includes a first decoupling structure comprising an elbow assembly, the elbow assembly (125, 128) configured to connect to an air conduit in use and an attachment region of the cushion assembly and permit the flow of the breathable gas into the cushion assembly, the elbow assembly configured to rotate about a plurality of axes relative to the attachment region, and a second decoupling structure (decoupling gusset 158(1)) that is configured to in use allow movement of the attachment region about a plurality of axes relative to the seal forming portion.

Description

NASAL MASK SYSTEM 1 CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the bene?t of US. Provisional Application No. 61/648,807, filed May 18, 2012, which is orated herein by reference in its 2 BACKGROUND OF TECHNOLOGY 2.! (1) FIELD OF LOGY The present technology relates to treatment of respiratory ers, and to procedures to prevent respiratory disorders. In particular, the present technology relates to medical devices, and their use for treating respiratory disorders and for ting respiratory disorders. More particularly, the present technology relates to a nasal mask system used for treatment, e.g., of Sleep Disordered Breathing (SDB) with Continuous Positive Airway Pressure (CPAP) or Non-Invasive Positive Pressure Ventilation (NIPPV).

The t technology also relates to apparatus to deliver breathable gas to a patient including a positive airway pressure (PAP) device, an air delivery t or tube, and a patient interface. The patient interface contacts the patient’s face in use to deliver pressurized breathable gas to the patient from the PAP device. 2.2 (2) DESCRIPTION OF THE RELATED ART The respiratory system of the body facilitates gas exchange. The nose and mouth form the entrance to the airways of a t.

The airways t of a series of branching tubes, which become narrower, shorter and more numerous as they penetrate deeper into the lung. The prime function of the lung is gas exchange, allowing oxygen to move from the air into the venous blood and carbon dioxide to move out. The trachea divides into right and left main bronchi, which further divide eventually into terminal bronchioles. The bronchi make up the conducting airways, and do not take part in gas exchange. Further divisions of the airways lead to the atory bronchioles, and eventually to the alveoli. The RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 2013/000383 alveolated region of the lung is where the gas exchange takes place, and is referred to as the respiratory zone. See West, Respiratory Physiology- the essentials A range of respiratory disorders exist.

Obstructive Sleep Apnoea (OSA), a form of Sleep Disordered Breathing (SDB), is characterized by occlusion of the upper air passage during sleep. It results from a combination of an abnormally small upper airway and the normal loss of muscle tone in the region of the tongue, so? palate and ior oropharyngeal wall during sleep. The condition causes the affected patient to stop breathing for periods typically of 30 to 120 seconds duration, sometimes 200 to 300 times per night. It often causes excessive daytime ence, and it may cause cardiovascular e and brain damage. The syndrome is a common disorder, ularly in middle aged overweight males, although a person affected may have no awareness of the problem.

See US Patent 4,944,310 (Sullivan).

Cheyne-Stokes Respiration (CSR) is a disorder of a patient's respiratory ‘ controller in which there are rhythmic alternating periods of waxing and waning ventilation, g repetitive de-oxygenation and re-oxygenation of the arterial blood. It is possible that CSR is harmful because of the repetitive hypoxia. In some patients CSR is associated with repetitive arousal from sleep, which causes severe sleep disruption, increased sympathetic activity, and increased a?erload. See US Patent 6,532,959 (Berthon-Jones).

Obesity Hyperventilation Syndrome (OHS) is de?ned as the combination of severe obesity and awake chronic hypercapnia, in the e of other known causes for hypoventilation. Symptoms include dyspnea, morning headache and excessive daytime sleepiness.

Chronic Obstructive Pulmonary Disease (COPD) encompasses any of a group of lower airway diseases that have n characteristics in common. These include increased ance to air movement, ed expiratory phase of respiration, and loss of the normal city of the lung. Examples of COPD are emphysema and chronic bronchitis. COPD is caused by chronic tobacco smoking RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 (primary risk factor), occupational exposures, air pollution and genetic factors.

Symptoms include: dyspnoea on exertion, chronic cough and sputum production.

] Neuromuscular Disease (NMD) is a broad term that encompasses many diseases and ts that impair the functioning of the muscles either directly via intrinsic muscle pathology, or ctly via nerve pathology. Some NMD patients are characterised by progressive muscular impairment leading to loss of ambulation, being wheelchair-bound, swallowing difficulties, respiratory muscle weakness and, eventually, death from respiratory failure. Neuromuscular disorders can be divided into rapidly progressive and slowly progressive: (i) Rapidly progressive disorders: Characterised by muscle impairment that worsens over months and results in death within a few years (e.g. Amyotrophic lateral sclerosis (ALS) and Duchenne muscular dystrophy (DMD) in teenagers); (ii) Variable or slowly progressive disorders: Characterised by muscle impairment that worsens over years and only mildly reduces life ancy (e.g. Limb girdle, Facioscapulohumeral and Myotonic ar phy). Symptoms of respiratory failure in NMD include: increasing generalised weakness, dysphagia, dyspnoea on exertion and at rest, fatigue, sleepiness, morning headache, and difficulties with concentration and mood changes. [000121‘ Chest wall ers are a group of thoracic ities that .result in inef?cient coupling between the respiratory muscles and the ic cage. The disorders are usually characterised by a restrictive defect and share the potential of long term hypercapnic atory failure. Scoliosis and/or kyphoscoliosis may cause severe respiratory failure. Symptoms of atory failure include: dyspnoea on on, peripheral oedema, orthopnoea, repeated chest infections, morning headaches, fatigue, poor sleep quality and loss of appetite.

Otherwise y individuals may take advantage of systems and devices to prevent atory disorders from arising. 2.2.1 Systems One known t used for treating sleep disordered breathing is the S9 Sleep Therapy System, manufactured by ResMed.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2.2.2 Therapy Nasal Continuous Positive Airway Pressure (CPAP) therapy has been used to treat Obstructive Sleep Apnea (OSA). The hypothesis is that continuous positive airway re acts as a pneumatic splint and may prevent upper airway occlusion by pushing the 500 palate and tongue forward and away from the posterior oropharyngeal wall.

] Non-invasive ventilation (NIV) has been used to treat OHS, COPD, NMD and Chest Wall ers. 2.2.3 Patient Interface The application of a supply of air at ve pressure to the entrance of the airways of a patient, e.g., while a patient sleeps, is facilitated by the use of a patient interface, such as a nasal mask, full-face mask or nasal pillows.

Known patient interface s suffer from being one or more of obtrusive, aesthetically undesirable,'poorly ?tting, dif?cult to use and ortable, especially when worn for long periods of time or when a patient is unfamiliar with a system. 2.2.3.1 Seal-forming portion Patient interfaces typically include a seal-forming portion.

A range of patient interface seal-forming portion technologies are disclosed in the following patent ations, assigned to ResMed Limited: WO l998/004,310; ,513; ,785. 2.2.3.2 oning and stabilising A seal-fonning portion of a t interface used for positive air pressure therapy is subject to the corresponding force of the air pressure to disrupt a seal. Thus a variety of techniques have been used to position the seal-forming portion, and to maintain it in sealing relation with the appropriate portion of the face.

One technique is the use of adhesives. See for example US Patent ation US 2010/0000534.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Another technique is the use of one or more straps and stabilising ses. 2.2.3.3 Vent technologies Some forms of patient interface systems may include a vent to allow the t of exhaled carbon dioxide.

ResMed Limited has developed a number of mask vent logies.

See W0 l998/034,665; W0 2000/078,38l; US 6,581,594; US Patent Application; US 2009/0050] 56; US Patent Application 044808. 3 BRIEF SUMMARY OF LOGY An aspect of the present logy relates to an elbow and a connector assembly adapted to receive gases from a ?ow generator and deliver the gases to a t interface.

An aspect of the present technology relates to an elbow and a connector adapted to vent gases from a patient interface.

As aspect of the present technology is to have multiple functions in one part or component and/or manufactured together, e,g., quick release button(s)/member(s)/actuator(s), baf?e and swivel all formed together, so patient is not required to disassemble; this may increase potential for reduced overall part costs.

An aspect of the present technology relates to a multi-axis elbow assembly that allows movement of a connected tube in two te planes while substantially ing drag forces from the tube.

Another aspect of the present technology relates to a method for manufacturing an elbow for a patient interface assembly, sing providing a skeleton, e.g., of rigid or semi-rigid material and adapted to communicate air ?ow under pressure between an air delivery conduit and a mask; separately molding an anti-asphyxia valve (AAV) with a pull tab; and assembling the skeleton and the AAV by pulling the pull tab from inside the on and through an opening in the skeleton to position, retain and/or seal the AAV relative to the skeleton. The method may RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 include removing at least a n of the pull tab once pulled through such that an outer ?ange of the AAV sits ?ush with an exterior elbow surfaceThe method may r comprise providing a ?exible component to secure the AAV in position. The ?exible component may form one or more e s or actuators on the elbow.

] Another aspect of the t technology relates to an elbow for a patient interface assembly, comprisinga skeleton or frame, e.g., of rigid or semi-rigid . material, and adapted to communicate air ?ow under pressure between an air delivery conduit and a mask; an antiiasphyxia valve (AAV) with a pull tab, whereby to assembly the AAV to the skeleton, the pull tab is inserted or guided inside the skeleton and pulled through an opening in the skeleton to position, retain and/or seal the AAV relative to the skeleton. At least a portion of an outer ?ange of the AAV, once the pull tab is pulled through, sits ?ush with an or elbow e. The elbow may include a ?exible component to secure the AAV in position and/or to form one or more release buttons or actuators on the elbow, the release buttons adapted to remove the elbow from a frame.

Another aspect of the technology relates to a swivel elbow and connector assembly for a patient interface for ring pressurized able gas to a patient from a PAP device. According to one aspect, the swivel elbow and connector assembly is ted to a ?exible patient interface structure, e.g. a n, through an aperture in the patient interface structure. According to another aspect, the swivel elbow and connector assembly includes a connector, for e a ring, which is attachable to anddetachable from the patient interface structure at the aperture. The connector includes a plurality of slots for venting gases from the interior of the patient interface structure to the exterior of the patient interface structure.

Yet another aspect of the technology “relates to a swivel elbow connected to the connector and slots to permit g of gases between the ring and the swivel elbow. According to another aspect, the swivel elbow is connected to the connector and the slots permit venting of gases between the connector and the patient interface structure, e.g. cushion, and no venting occurs between the connector and the swivel elbow.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 A further aspect of the logy relates to a swivel elbow and anti- asphyxia valve assembly having a diffuse vent. A still further aspect of the logy relates to a swivel elbow and anti-asphyxia valve assembly having a diffuse vent that may be molded in one piece. An even further aspect of the technology relates to a swivel elbow and anti-asphyxia valve assembly having a diffuse vent that may have engagement portions that, when pressed, permit ment and disengagement of the swivel elbow and anti-asphyxia valve assembly from a patient interface, e.g. a mask.

According to an example of the technology, a swivel elbow and connector assembly for a patient interface system comprises a ring con?gured to be sealingly secured in an aperture of the patient interface system, the ring including a ?rst side in an interior of the patient interface system and a second side at an exterior of the patient interface system when the ring is secured in the aperture, the ring comprising a plurality of vents con?gured to permit ?ow of gases from the interior to the exterior of the patient interface system; and an elbow swivelably d in the ring. The ring comprises a ?rst ?ange on the ?rst side and a second ?ange on the second side, the ?rst and second ?anges de?ning a channel that sealingly engages the aperture of the patient ace system and the second ?ange comprises an angled surface that directs the ?ow of gases from the ity of vents at an angle to the longitudinal axis of the ring.

According to another example of the logy, a patient interface system for deliVering a ?ow of breathable gas to a user comprises a t interface structure con?gured to sealingly engage the face of the user, the patient interface ure comprising an aperture; and a swivel elbow and connector assembly as disclosed herein.

According to another example of the technology, an elbow for delivering gases to a patient interface ses a ?rst connecting portion, a second connecting portion and a venting portion. The ?rst connecting portion is adapted to receive a tube connection, the second ting portion is adapted to receive a patient interface assembly, and the venting portion ximal to the second ting portion. The venting portion may be diffused about the perimeter of the RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 second ting portion. The elbow may further comprise a baf?e to te the venting portion from an incoming air stream from the ?rst ting portion.

According to still another example of the technology, a swivel elbow and anti-asphyxia valve assembly for a patient interface assembly comprises a ?rst component including a ?rst connection portion con?gured to be sealingly secured in an aperture of the patient interface system, a second tion n con?gured to be connected to a swivel or a ry. conduit, one or more ?rst supports between the ?rst connection portion and the second tion portion, and a ?rst aperture and a second aperture are provided between the one or more ?rst supports; and a second ent including a valve member, engagement members, and a ?exible member, the valve member being between the one or more ?rst supports of the ?rst component and movable between a ?rst position in which the valve member occludes the ?rst aperture and a second position in which the valve member does not occlude the ?rst aperture, the engagement members being con?gured to engage the one or more ?rst supports when d by a user of the patient interface system, and the ?exible member being connected to the ment members and sealing the second aperture.

Another aspect of the present technology is directed towards providing medical devices used in the diagnosis, treatment or prevention of respiratory disorders having one or more of improved comfort, cost, ef?cacy, ease of use and manufacturability.

Another aspect of the present technology relates to tus used in diagnosis, ent or prevention of a respiratory disorder.

Another aspect of the present technology relates to methods used in diagnosis, treatment or prevention of a respiratory disorder.

'One aspect of the present technology is a patient interface that is one or more of comfortable, ive, simple to use, unobtrusive and with a wide ?t range.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 An aspect of one form of the present technology is a patient interface that avoids a jetting effect of nasal pillows or prongs, and/or a feeling of discomfort from locating‘a portion of a mask within a nasal cavity of’a patient.

An aspect of one form of the present technology is a nasal mask that is easy to put on, and may avoid a need for headgear straps to interfere with, or cross the ears in use, and may avoid interfering or crossing the ears while putting on or removing.

Anether aspect of one form of the present technology is a method of putting on or ng a mask.

In one form of the t technology, a small, unobtrusive nasal mask is provided.

In one form of the present technology, a nasal mask is provided that does not form a seal on a lower lip, or a chin of a patient.

In one form of the present technology, a t interface is provided that does not exert a rd force on the mandible, e.g. the patient interface does not push on the mandible from the anterior towards the posterior.

In one form of the present technology, a patient interface is provided that doesnot comprise a rigid shell or rigid frame.

In one form of the present logy, a patient interface is provided that comprises a plenum chamber constructed from a e or semi-rigid material, for example a ?exible rubber of a suitable thickness (e.g. silicone with a type A ss in the range of about 35 to about 45, and about 1.5mm to about 3mm thick).

In one form of the technology, a nasal mask is provided that does not require engagement or disengagement of a clip to don or remove the mask.

An aspect of one form of the present technology is a patient interface sing a seal-forming portion having a first sealing region that is constructed to have little nor no ance to compression, and a second sealing region that is constructed to substantially resist a compressive force (e.g. as a result of headgear RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 tension). In ple in use, the first sealing region is arranged to overlay a portion of the cartilaginous framework of the nose, and the second sealing region is arranged to overlay a portion of a bone region the face. In an example, the bone region of the face is a region adjacent the ala, and optionally adjacent to the alar crest point.

According to one form of the present technology, a patient interface is provided that comprises: (i) a orming portion that in use overlays at least part of a top lip region of a patient's face, and a portion of the cartilaginous ork of the nose; and (ii) a seal positioning and stabilising structure that may be donned and removed without interfering with the ears of the patient.

Another aspect of one form of the present technology is a patient interface having a seal—forming portion associated with a two point connection with a seal positioning and stabilising structure. In an e, the patient interface does not comprise a forehead support. In an onal or ative example, the seal positioning and stabilising structure comprises a non-rigid or ?exing connection element.

] Another aspect of one form of the present technology is a patient interface that is d or otherwise constructed with aclearly defined perimeter shape which is intended to match that of an intended wearer in use.

Another aspect of one form of the present technology is a patient ace that is constructed and arranged so that while forming a seal on at least part of the aginous framework of the nose, it avoids or reduces a tendency to restrict nasal air flow therethrough.

According to one form of the t technology, a patient interface is provided that comprises a first superior sealing portion that in use overlays a portion of the cartilaginous framework of the nose, and a second inferior sealing portion that in use overlays a portion of the upper lip and wherein in use, a relatively larger portion of a ar sealing force is ed towards the portion of the upper lip and the underlying maxilla, teeth or gum than is directed towards the cartilaginous framework of the nose.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Another aspect of one form of the present technology is a patient interface that is constructed and arranged to avoid or reduce a cy to put unnecessary pressure on the nasal .

According to one form of the present technology, a patient interface is provided that in use forms a seal on a portion of an upper lip of a patient, and which comprises a plenum chamber having a wall and wherein a ?rst portion of the wall that is constructed to be located adjacent the septum in use has a relatively less stiff spring constant that ns of the wall that are adjacent to said ?rst portion.

Another aspect of one form of the present technology is a patient interface that while forming a seal on a portion of the aginous framework of the nose, provides an effective or improved seal on the region of the nose near ajunction between the r alar cartilage and the lateral cartilage.

According to one form of the present technology, a patient interface is provided that comprises a g ?ange that de?nes a generally T-shaped, or three lobed ori?ce. In an example, thesealing ?ange includes a membrane and a sealing ?ap that protrudes from the edge of the membrane along its inner perimeter in each side of nose region. The edge of the membrane along its inner perimeter along with the edge of each sealing ?ap along its inner perimeter cooperate to de?ne an ori?ce into the plenum chamber. In an example, such ori?ce includes a general T-shape, or three lobed ori?ce, including an upper ori?ce portion (along vertical axis v as viewed in Fig. 3-20) and a lower ori?ce portion (along horizontal axis h as viewed in Fig. 3- ) that extends generally transverse to the upper ori?ce n.

] According to one form of the present technology, an inner edge of a sealing ?ange is spring biased towards the face of a wearer in use, e.g. with respect to a middle portion of the sealing ?ange.

Another aspect of one form of the present technology is a nasal mask that is ucted and e to pivot or rotate about a top lip region upon adjustment of a headgear n.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Another aspect of one form of the present technology is a method of manufacturing a patient interface. r aspect of one form of the present technology is a device for preventing, ng or ameliorating one or more of OSA, CSA, OHS, COPD, NMD and chest-wall disorders.

Another aspect of the present technology is a mask system that can accommodate a wide range of ent facial shapes including faces with high and low nose bridge regions, and narrow and wide noses. Another aspect of the present technology is a mask system with a wide ?t range.

Another aspect of one form of the present technology is a mask system that is small and unobtrusive, and yet is stable on the face while a patient is sleeping.

One aspect of the present technology is a mask that is ucted and arranged to seal at its upper extent on a region of the nose that is generally above or superior to the pronasale, or tip of the nose.

One aspect of one form of the present technology is a mask that is] ucted and arranged to seal at itsupper extent at locations that are generally below or inferior to the nasal bones.

In one form of the present technology, a mask is provided that is ucted and arranged to have a seal g portion that overlays a portion of the upper or or lip, and that overlays a portion of the cartilaginous framework of the nose, e.g., without overlaying the nasal bones.

In one form of the present technology a mask is provided that is constructed and arranged to have a ?rst seal forming portion that overlays a portion of the upper or superior lip, and a second seal-forming portion that overlays of the cartilaginous ork of the nose, e.g., without overlaying the nasal bones.

In one form of the present technology a mask is provided that is constructed and arranged to have a ?rst seal forming portion that is substantially in RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 compression, or subject to bending forces in use, and a second seal-fonning portion that is substantially in tension in use.

In one form of the present technology a mask is provided that is ucted and arranged to have a ?rst seal g portion that is relatively stiff before use, and a second seal-forming portion that is relatively ?oppy before use.

Another aspect of one form of the present technology is a mask system with an improved sealing cuff. In an example, the mask system includes a facial ?ap comprising a relatively thin member formed of a ?exible, e.g., and at least semi- resilient, material. In an example, the mask system further ses, in at least some regions, a back-up band. r aspect of the present technology is a mask that is formed, moulded or otherwise constructed with a clearly defined ter shape which is intended to match that of an intended wearer.

A further aspect of the present technology is a cushion for a mask that seals at its upper extent in a region of the nose that is generally superior to or above the pronasale or tip of the nose,‘and extends across the alar or ?ares of the patient’s nose.

A further aspect of the present technology is a cushion for a mask that seals at its upper extent in a region of the nose that is generally superior to or above the pronasale or tip of the nose, and extends across the alar or ?ares of the t’s nose, e.g., not extending over or across the nasal bones of the patient’s nose.

] One aspect of one form of the present technology is a cushion for a mask that seals at its upper extent in a region of the nose that is generally close to the junction between bone and cartilage on a range of people with larger noses, and which avoids impinging on the sight of people with smaller noses.

In one form of the present logy, a mask system is provided that does not require a rigid frame or skeleton, and which seals at its upper extent in a region of the nose that is generally above or superior to the pronasale, or tip of the nose.

RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 One aspect of the present technology is a cushion for a mask that includes a sealing membrane and a backup band or undercushion, in at least some regions.

Another aspect of the present technology is a n for a nasal mask that includes an undercushion or backup band in the region of the top lip.

Another aspect of one form of the present technology is a cushion for a nasal mask that includes an ushion or backup band in the region of the top lip, and no undercushion or backup band in the sides of the nose or ridge of the nose s to avoid relatively high sealing forces on the sides of the nose or ridge of the nose regions as these relatively high sealing forces may cause occlusion of the nasal airway.

Another aspect of the present technology includes a cushion for a nasal mask, the cushion having a sealing region, a side wall region and an attachment region, wherein the sealing region is adapted to form a seal with a patient, the side wall region connects the sealing region and attachment region, and the ment region is adapted to connect or otherwise attach to an air delivery system.

Another aspect of the present technology includes a cushion for a nasal mask, the cushion having a sealing region and an attachment region, wherein the attachment region comprises a decoupling element.

] Another aspect of the present technology includes a cushion for a nasal mask, the cushion having a sealing region and an attachment region, wherein the attachment region comprises a decoupling element, the decoupling element comprising a vely thinner wall section. For example, the relatively thinner wall section may be 50-85% r.

Another aspect of the t technology includes a cushion for a nasal mask, the cushion comprising headgear connectors integrally formed with a side wall, e.g., n the side wall is constructed of a ?exible mer or rubber.

Another aspect of the present technology includes a cushion for a nasal mask, the cushion comprising headgear connectors, the headgear connectors RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 constructed and arranged to position a portion of a sealing region superior to or above the pronasale or tip of the patient’s nose.

Another aspect of the present technology includes a cushion for a nasal mask, the cushion having a nose ridge region, the nose ridge region having a dip or curvature, e.g. a local saddle region, adapted to m to, or be complementary to the nose ridge of the patient.

A r aspect of the t technology includes a cushion for a nasal mask, the cushion having a nose ridge region, the nose ridge region having a relatively longer membrane length when compared to other regions of the cushion, the relatively longer membrane length adapted to engage a greater fit range of patient’s noseiridge heights.

Another aspect of the present technology includes a cushion for a nasal mask, the cushion having a sides of the nose , the sides of the nose region having a raised portion, the raised portion having a greater height when compared to the nose ridge'region, the raised portion adapted to engage with the sides of the patient’s nose and ensure engagement with tall nose ridges as well as ?at nose ridges.

Another aspect of the present technology includes a cushion for a nasal mask, the cushion having a comers of the nose region, generally ponding to the region of the face between and ing the subalare and the alar crest, the corners of the nose region having the greatest height when compared to all other s of the cushion, wherein the comers of the nose region anchors the cushion in position. The height of the comers of the nose region may be arranged to ensure seal in the comers of the nose, as this is a particularly dif?cult area of the face to seal on. \[00092] Another aspect of the present technology includes a cushion for a nasal mask, the cushion having a top lip region, the top lip region configured to conform to the ure of a patient’stop lip region. The top lip region may be lly d, extending from a trough or dip and continuing up to the sides of the nose region. The membrane at the top lip region may stretch across a patient’s top lip to ensure a seal with the patient’s top lip.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Another aspect of the present technology relates to a nasal mask system including a cushion assembly including a sealing region that provides a single ori?ce adapted to surround both nares of the patient’s nose and a headgear assembly including a pair of side straps and a rear strap. The side straps are adapted to extend along sides of the patient’s face n the t’s eyes and ears and engage respective headgear connectors provided to the cushion assembly to provide a two- point tion with the cushion assembly. The rear strap s between the side straps and is adapted to engage along the back or posterior of the patient’s head along, below or inferior to the occipital bone.

Another aspect of the present technology relates to a nasal mask system including a cushion assembly including a sealing region having a nose ridge region, sides of nose region, comers of nose region, and a top lip region adapted to seal around both nares of the patient’s nose. The nose ridge region is adapted to be positioned and “seal along a nasal cartilage region which is above or superior to the pronasale and below or inferior to a nasal bone region of the patient’s nasal bridge. In one form, the g region includes a membrane seal that s around an entire perimeter of the sealing region and an undercushion that is only provided in the top lip and comers of nose regions.

] Another aspect of the present technology relates to a nasal mask system including a cushion assembly including a sealing region adapted to seal around both nares of the patient’s nose, an attachment region adapted to receive an elbow assembly, and a side wall region extending between the sealing region and the attachment region. The sealing region has a nose ridge region, sides of nose region, comers of nose region, and a top lip region. The side wall region es an area adjacent the top lip region of the g region that includes a thickness that is less than ponding thicknesses adjacent the nose ridge, sides of nose, and comers of nose regions of the sealing region.

Another aspect of the t technology relates to a nasal mask system including a cushion assembly including a sealing region having a nose ridge region, sides of nose , comers of nose region, and a top lip region adapted to seal around both nares of the patient’s nose. The sides of nose region includes a RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 portion adapted to be positioned and seal along a region adjacent the on n the nasal greater alar cartilage and the lateral nasal cartilage of the patient’s nose.

Another aspect of the t technology relates to a patient interface for applying a supply of air at positive pressure to the entrance of a patient's airways.

The patient interface includes a nasal mask and a positioning and stabilising structure.

The nasal mask has a seal forming portion constructed and arranged to form a seal on a portion of an upper lip of a patient, and to form a seal on a portion of a cartilaginous framework of the patient's nose. The nasal mask further has a plenum chamber that receives in use a portion of the patient's nose including the pronasale. The positioning and stabilising structure includes a pair of side straps that provide a int connection to the nasal mask and being constructed and arranged to be donned or removed without the side straps passing inferior to the patient’s ears. ] r aspect of the present technology relates to a method for ?tting a patient interface to a patient. The method es positioning a sealing region of the patient interface with respect the t‘s nose such that the sealing region surrounds both nares and engaging ar straps of the patient ace with the patient’s head without passing straps inferior to the patient’s ears.

Another aspect of the present technology relates to a nasal mask for delivery of a supply of air to the entrance of a patient's airways. The nasal mask includes a superior sealing portion and an inferior sealing portion. The superior sealing portion is constructed and arranged to be located on a portion of the cartilaginous framework of the nose, and to form a seal therewith without ng a sealing force that would restrict a ?ow of air through the nasal cavity. The inferior sealing portion is constructed and arranged to be located in part on a n of an upper lip of a patient and to direct a sealing force to a portion of a maxilla bone of the patient. 0] Another aspect of the present technology relates to a nasal mask de?ning a breathing chamber for ry of a supply of gas at positive pressure to the airways of a patient. The nasal mask includes a vent ad a cushion. The vent is adapted to t breathable gas and is adapted to be suf?ciently rigid to avoid RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 collapse. The cushion includes a sealing cuff and headgear connectors. The sealing cuff comprises a membrane seal and an undercushion. The membrane seal extends about a perimeter of the cushion including a nose ridge region‘of the cushion and a side of the nose region of the cushion, and the undercushion is d in a top lip region of the cushion and does not extend to the nose ridge region of the cushion or the side of the nose region of the cushion. The headgear connectors are formed with a side wall of the cushion.

Another aspect of the present technology relates to a patient interface for applying a supply of air at positive re to the entrance of a patient's airways.

The patient interface includes a nasal mask and a oning and stabilising structure.

The nasal mask has a seal forming portion constructed and arranged to form a seal on a portion of an upper lip of a patient, and to form a seal on a portion of a cartilaginous framework of the patient's nose. The nasal mask further has a plenum chamber that receives in use a portion of the patient's nose including the pronasale. The positioning and stabilising structure provides a sealing vector oriented at an angle with respect to a Frankfort horizontal direction. The positioning and stabilising structure includes a two-point connection to the nasal mask.

Another aspect of the present logy s to a patient interface for applying a supply of air at positive pressure to the ce of a patient's airWays.

The patient interface includes a nasal mask and a positioning and stabilising structure.

The nasal mask has a seal forming portion constructed and arranged to form a seal on a portion of an upper lip of a patient, and to form a seal on a portion of a aginous framework of the patient's nose. The nasal mask further has a plenum chamber that es in use a portion of the patient's nose including the pronasale. The positioning and stabilising structure es a sealing vector oriented at an angle with respect to a ort horizontal direction. The nasal mask does not include a forehead support.

Another aspect of the present technology relates to a patient ace for applying a supply of air at positive pressure to the entrance of a patient's airways.

The patient interface includes a nasal mask and a positioning and ising structure.

The nasal mask has a seal forming n constructed and arranged to form a seal on a portion of an upper lip of a patient, and to form a seal on a portion of a cartilaginous RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 framework of the patient's 'nose. The nasal mask further has a plenum chamber that receives in use a portion of the patient's nose including the pronasalc. The positioning and stabilising structure provides a sealing vector oriented at an angle with respect to a Frankfort horizontal direction. The positioning and stabilising structure includes a pair of side straps d to extend towards and over a crown of the patient’s head.

Of course, portions of the aspects may form sub-aspects of the present technology. Also, various ones of the sub-aspects and/or aspects may be combined in various manners and also constitute additional s or sub-aspects of the present technology.

] Other features of the technology will be apparent from consideration of the information contained in the following detailed description, ct, drawings and claims. '4 BRIEF DESCRIPTION OF THE L VIEWS OF THE DRAWINGS The present technology is illustrated by way of example, and not by way of limitation, in the ?gures of the accompanying drawings, in which like reference numerals refer to similar elements including: 4.1 TREATMENT SYSTEMS Fig. la shows a system in ance with the present technology. A patient lOOO wearing a patient interface 3000, receives a supply of air at positive re from a PAP device 4000. Air from the PAP device is humidi?ed in a humidi?er 5000, and passes along an air circuit 4170 to the patient 1000. The PAP device 4000, humidi?er 5000 and air circuit 4170 may be connected to a patient interface 3000 in accordance with the present technology. 4.2 THERAPY 4.2.1 Respiratory system Fig. 2a shows an overview of a human atory system including the nasal and oral es, the larynx, vocal folds, oesophagus, a, bronchus, lung, alveolar sacs, heart and diaphragm.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 9] Fig. 2b shows a view of a human upper airway including the nasal , nasal bone, lateral nasal cartilage, greater alar cartilage, nostril, lip superior, lip inferior, larynx, hard palate, soft , oropharynx, tongue, epiglottis, vocal folds, oesophagus and trachea. 4.2.2 Facial anatomy Fig. 2c is a front view of a face with several features of e anatomy identi?ed including the lip superior, upper vermillion, lower vermillion, lip inferior, mouth width, endocanthion, a nasal ala, nasolabial sulcus and cheilion.

Fig. 2d is a side view of a head with several features of surface anatomy identi?ed including glabella, sellion, pronasale, subnasale, lip superior, lip inferior, supramenton, nasal ridge, otobasion or and otobasion inferior. Also indicated are the directions superior & inferior, and anterior & posterior.

Fig. 2e is a further side view of a head. The approximate locations of the Frankfort horizontal and nasolabial angle are indicated.

Fig. 2f shows a base view ofa nose. 4] Fig. 2g shows a side view of the super?cial features of a nose.

Fig. 2h shows subcutaneal structures of the nose, ing the cartilaginous framework comprising the lateral cartilage,septum age, greater alar cartilage, lesser alar cartilage and also shows the tty tissue.

Fig. 2i shows a medial dissection of a nose, approximately several millimeters from a sagittal plane, amongst other things g the septum cartilage and medial crus of greater alar cartilage.

Fig. 2j shows a front view of the bones of a skull including the frontal, temporal, nasal and zygomatic bones. Nasal concha are indicated, as are the maxilla, mandible and mental protuberance.

Fig. 2k shows a lateral view of a skull with the outline of the surface of a head, as well as several muscles. The following bones are shown: l, sphenoid, RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 nasal, zygomatic, maxilla, mandible, parietal, temporal and occipital. The mental protuberance is indicated. The following s are shown: digastricus, masseter stemocleidomastoid and trapezius. 4.3 PATIENT INTERFACE Fig. 3-l is a perspective view of a nasal mask system according to an e of the present technology.

Fig. 3-2 is a side view of a nasal mask system ing to an example of the present technology. The nasal mask system is shown overlaying a head to indicate the approximate relative location of the headgear in use.

Fig. 3-3 is a front view of a nasal mask system according to an example of the present technology.

Fig. 3-4 is a perspective from view of a cushion of a nasal mask system according to an example of the present technology. 3] Fig. 3-5 is a perspective rear view of a cushion of a nasal mask system according to an example of the present technology.

Fig. 3-6 is a bottom view of a cushion of a nasal mask system according to an example of the present technology.

Fig. 3-7. is a top view of a cushion of a nasal mask system according to an example of the present technology.

~ Fig. 3-8 is a front view of a n of a nasal mask system according to an e of the present technology.

Fig. 3-9 is a rear view of a cushion of a nasal mask system according to an example of the t logy.

Fig. 3—10 is a cross-sectional view of the cushion of the nasal mask system of Fig. 3-9.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Fig. 3-1 1 is a perspective view of an elbow assembly of a nasal mask system according to an example of the present technology.

Fig. 3-12 is a rear view of an elbow assembly of a nasal mask system ing to an example of the present technology.

Fig. 3-13 is a cross-sectional view of the elbow assembly of a nasal mask system of Fig. 3-12.

Fig. 3-14 is a perspective rear view of a cushion of a nasal mask system according to another example of the present technology.

Fig. 3-15 is a top view of the cushion of Fig. 3-14.

Fig. 3-16 is a bottom view ofthe cushion of Fig. 3-14.

] Fig. 3-17 is a front view of the cushion of Fig. 3-14.

Fig. 3-18 is a cross-section view of the cushion of Fig. 3-17.

Fig. 3-19 is an enlarged view ofa portion of Fig. 3-18.

Fig. 3-20 is a rear view ofthe cushion of Fig. 3-14. 9] Fig. 3-21 is a side view ofthe cushion of Fig. 3-14.

Fig. 3-22 is a rear view of the n of Fig. 3-14 showing cross- sectional lines. 1] Fig. 3-23 is a cross-section through line 3-23 - 3~23 of Fig. 3-22.

Fig. 3-24 is a cross-section through line 3-24 - 3-24 of Fig. 3-22.

Fig. 3-25 is a cross-section h line 3-25 - 3-25 of Fig. 3-22.

Fig. 3-26 is a cross-section through line 3-26 - 3-26 of Fig. 3-22.

Fig. 3-27 is a cross-section through line 3-27 - 3-27 of Fig. 3-22.

Fig. 3-28 is a cross-section through line 3-28 - 3-28 of Fig. 3-22.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2013/000383 Fig. 3-29 is a cross-section through line' 3~29 - 3-29 of Fig. 3-22.

Fig. 3-30 is a cross-section through line 3-30 - 3-30 of Fig”. 3-22.

Figs. 3-31 to 3-34 are sequential views showing exemplary steps for donning a nasal mask system according to an example of the present technology. 0] Fig. 3-35 is a cross-sectional view g a nasal mask system engaged with a patient’s face according to an example of the present technology.

Fig. 3-36 is a cross-sectional view showing a nasal mask system engaged with a patient’s face according to an example of the present technology.

Fig. 3-37 is another ctive view of the cushion of Fig. 3-14.

Fig. 3-38 shows a cushion assembly d with the patient’s face and under pressure or in?ated in use according to an example of the present technology.

Fig. 3-39 is a schematic rear view of a cushion assembly showing the sealing portions engaged with the patient’s face in use according to an example of the present technology.

Figs. 31 to 38 show various views of a cushion assembly according to another example of the present technology. 6] Figs. 3l to 310 show various views of a cushion assembly according to another example of the present technology.

Fig. 3-42 is an isometric cross sectional View of a swivel elbow and tor assembly ing to an example of the technology.

Fig. 3-43 is a cross sectional side view of the swivel elbow and connector assembly of Fig. 1.

Figs. 3-44 and 3-45 are exploded isometric views of the swivel elbow . and connector ly of Fig. 3-42; RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Figs. 3-46 and 3-47 are isometric views of a double swivel elbow and tor assembly according to r example of the logy in a ?rst on or con?guration. 1] Fig. 3-48 is a side view of the double swivel elbow and connector assembly of Figs. 3-46 and 3-47.

Fig. 3-49 is a side view of the double swivel elbow and connector assembly of Fig. 3-48 in a second position or con?guration.

Fig. 3-50 is a side view of the transition of the double swivel elbow and connector assembly from the ?rst position to the second position.

Fig. 3—51 is an isometric cross sectional view of the double swivel elbow and connector assembly in the ?rst position.

Fig. 3-52 is an isometric cross sectional view of the double swivel elbow and connector ly in the second position.

Fig. 3-53 is a cross sectional side view of the double swivel elbow and connector assembly in the ?rst position.

Fig. 3-54 is a cross sectional side view of the double swivel elbow and connector assembly in a third position or con?guration.

Fig. 3-55 is a cross sectional side view of the transition of the double swivel elbow and connector assembly from the ?rst position to the second position. 9] Fig. 3-56 is a cross sectional side view of the double swivel elbow and connector assembly in a fourth position or con?guration.

Fig. 3-57 is a cross sectional side view of the transition of the double swivel elbow and connector assembly from the third position to the fourth position.

Figs. 3-58 and 3-59 are isometric views of a triple swivel elbow and connector assembly including a second swivel cuff according to still another example of the technology in a ?rst position or con?guration.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Fig. 3-60 is an isometric view of the triple swivel elbow and connector assembly of Figs. 3-58 and 3-59 in a second position or con?guration.

Fig. 3-61 is a side view of the triple swivel elbow and connector assembly of Figs. 3-58 and 3-59.

Fig. 3-62 is a side view of the transition of the triple swivel elbow and connector assembly from the ?rst position to the second position.

Fig. 3-63 is side view of the triple swivel elbow and connector ly in the second position.

Fig. 3-64 is a cross sectional side view of the triple swivel elbow and connector assembly in the ?rst on.

Fig. 3-65 is a cross sectional side view of the triple swivel elbow and tor assembly in the second position.

Fig. 3-66 is side view of the transition of the triple swivel elbow and tor assembly from the ?rst position to the second position. 9] Fig. 3-67 is a cross sectional isometric view of the triple swivel elbow and connector assembly in the [?rst position.

Fig. 3-68 is a cross sectional isometric view of the triple swivel elbow and connector assembly in the second position.

Fig. 3-69 is a cross sectional side view of the triple swivel elbow and tor assembly in a third position or con?guration.

Fig. 3-70 is a cross sectional side view of the triple swivel elbow and connector assembly in a fourth position or con?guration.

Fig. 3-71 is a cross sectional side view of the transition of the swivel elbow and connector assembly from the third position to the fourth position.

Fig. 3-72 is a cross sectional view of a patient interface structure, or cushion, usable with examples of the technology.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2013/000383 Fig. 3-73 is an isometric view of a swivel elbow and connector assembly according to an example of the technology.

Fig. 3-74 is a partial side cross sectional view of the swivel elbow and connector assembly of Fig. 3-73.

Fig. 3-75 is a top cross nal view of the swivel elbow and connector assembly of Fig. 3-73.

Fig. 3-76 is an isometric view of a variation of the swivel elbow and connector assembly of Fig. 3-73. 9] Fig. 3-77 is a front view of the swivel elbow and connector assembly of Fig. 3-76.

Fig. 3-78 is a cross sectional view of the swivel elbow and connector assembly of Fig. 3-76.

' Fig. 3-79 is an isometric view of a ?rst component of a swivel elbow and anti-asphyxia valve assembly according to an example of the technology.

Fig. 3-80 is a side view of the ?rst component of Fig. 3-79.

Fig. 3-81 is a rear View ofthe ?rst component of Figs. 3-79 and 3-80.

Fig. 3-82 is a cross sectional side view of the ?rst component of Figs. 3479 to 3-81.

‘ Fig. 3-83 is an isometric view of the ?rst component and a second component of the swivel elbow and anti-asphyxia valve assembly.

Fig. 3-84 is a side view of the swivel elbow and anti-asphyxia valve ly of Fig. 3-83. 7] Fig. 3-85 is a rear view of the swivel elbow and anti-asphyxia valve assembly of Figs. 3-83 and 3-84.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Fig. 3-86 is a front view the swivel elbow and anti-asphyxia valve assembly of Figs. 2-83 to 3-85. 9] Fig. 3-87 is a cross sectional side view of the swivel elbow and antiasphyxia valve assembly of Figs. 3-83 to 3-86.

Fig. 3-88 is a top view of the swivel elbow and anti-asphyxia valve assembly of Figs. 3-83 to 3-87. 1] Fig. 3-89 is an isometric view of a patient interface including a swivel elbow and connector assembly according to another example of the technology.

Fig. 3-90 is an isometric view of a patient interface ing a swivel elbow and connector assembly according to another example of the technology.

Fig. 3-91 is an isometric view of the elbow of Fig. 3-90.

Fig. 3-92 is a cross sectional view of the patient interface of Fig. 3-90.

Fig. 3-93 is a cross sectional view of a patient interface ing a swivel elbow and connector assembly according to another example of the technology.

Fig. 3-94 is an isometric view of an elbow according to an example of the technology.

. Fig. 3~95 is a cross sectional view of the elbow of Fig. 3-94.

Fig. 396 is a cross sectional view of an elbow and tube tor assembly ing to the technology. 9] Fig. 3-97 is an enlarged view of a portion of Fig. 3-96.

Fig. 3-98 is an exploded assembly view of the elbow and tube connector assembly of Fig. 3-96.

Fig. 3-99 is an exploded assembly view of an elbow and tube connector assembly according to another e of the technology.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Fig. 3-100 is an assembly view of the elbow and tube connector assembly of Fig. 3-99.

Fig. 3-101 is a cross sectional View of the elbow and tube connector assembly of Fig. 3-100.

Fig. 3-102 is an exploded assembly view of an elbow and tube connector ly according to another example of the technology.

Fig. 3-103 is an assembly View of the elbow and tube tor assembly of Fig. 3-102‘. 6] Fig. 3-104 is a cross sectional view of the elbow and tube connector ly of Fig. 3-103.

Fig. 3-105 is an isometric view of the connector of the elbow and tube connector assembly of Fig. 3-104. 8] Fig. 3-106 is a cross sectional view of the connector of Fig. 3-105.

Fig. 3-107 is a cross sectional view of a tube connector assembly according to an example of the technology.

Fig. 3-108 is an isometric view of the tube connector assembly of Fig. 3-107.

Figs. 3-109A-D show a multi-step process for manufacturing an elbow with anti-asphyxia valve.

Fig. 3-110A shows a perspective View of a variant of the elbow.

Fig. 3-1 103 shows a cross section of the variant shown in Fig. .

Fig. 3-111 shows the AAV (a variant) in isolation.

Figs. 31 and 32 are a top view and related cross-sectional view showing a nasal mask system engaged with a patient’s face according to an example of the present technology, the nasal mask system in a static sealing position.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2013/000383 Figs. 31 and 32 are a side view and related cross-sectional view showing a nasal mask system engaged with a patient‘s face according to an e of the present technology, the nasal mask system in a static sealing on.

Figs. 31 and 32 are a top view and related sectional view showing a nasal mask system engaged with a patient’s face according to an example ofthe present technology, the nasal mask system in a dynamic sealing position with the nasal mask system being pulled sideways.

Figs. 31 and 32 are a side View and related cross-sectional View showing a nasal mask system engaged with a patient’s face according to an e of the present technology, the nasal mask system in a dynamic sealing position with the nasal mask system being pulled upwards.

Figs. 3-1 16-1 and 32 are an alternative side View and related cross-sectional view showing a nasal mask system in a dynamic g position with the nasal mask system being pulled upwards.

Figs. 3-1 17-1 and 3-1 17-2 are a side view and related cross-sectional view g a nasal mask system engaged with a patient’s face according to an example of the present technology, the nasal mask system in a dynamic sealing position with the nasal mask system being pulled downwards.

Figs. 1, 32, and 33 illustrate rotation ofan elbow assembly in the X-axis, Z-axis, and Y-axis according to an example of the present technology.

Fig. 3-1 19-1 is a perspective view of a nasal mask system with the short tube in a retracted position according to an example of the present logy.

Fig. 3-1 19-2 is a perspective view of a nasal mask system with the short tube in an extended position according to an example of the present technology.

Figs. 31 to 34 show various views of an elbow, short tube and swivel assembly ing to an e of the present technology.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Fig. 35 shows a cross-section through line 3-l20-5—3-l20-5 of Fig. 4.

Fig. 36 shows a cross-section through line 36—36 of Fig. 4. 4.4 PAP DEVICE Fig. 4a shows a PAP device in ance with one form of the present technology.

DETAILED DESCRIPTION ILLUSTRATED ES 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.

The following description is provided in relation to several examples which may share common teristics and features. It is to be understood that one or more es of any one e may be combinable with one or more features of the other examples. In addition, any single feature or combination of features in any of the examples may constitute additional examples.

In this specification, the word “comprising” is to be understood in its “open” sense, that is, in the sense of “including”, and thus not limited to its “closed” sense, that is the sense of sting only of". A corresponding meaning is to be attributed to the corresponding words ise", "comprised" and "comprises" where they appear.

The term "air" will be taken to include breathable gases, for example air with supplemental . Hence a supply of air may correspond to a supply of gas including air and supplemental oxygen. It is also acknowledged that the PAP devices or blowers described herein may be designed to pump ?uids other than air.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2] Examples of the technology are directed towards a nasal mask system that is easy and quick to ?t (e.g., with little or no adjustment), enable reduced strap tension, is manufacturable in high volumes, provides high consumer appeal, provides comfort and seal, provides reliable quality, unobtrusive, and/or fits a large majority of the population. 3] One or more examples may include exemplary metrics, e.g., dimensions, angles, percentages, etc. Although c metrics and ranges therefore may be provided, it is to be understood that these metrics and ranges are merely exemplary and other metrics and ranges are possible depending on application. For example, metrics/ranges that Vary from those provided +/- 10-20% may be suitable for particular applications. ' [000244] The present technology is adapted to e an arrangement or ly between a- patient interface and a tube that may be adapted to decouple tube drag forces, provide a freedom of movement for the tube to enable a patient to position the tube in a desired position without disrupting the seal, vent exhausted gases and provide a compact, unobtrusive design that is aesthetically acceptable to patients.

The venting arrangement may diffuse the exhausted air to prevent air jetting on ts or their bed partners, and to reduce noise.

The venting arrangement may cooperate with the elbow or connector assembly to further diffuse exhaled air, for e the elbow may be ed with a ridge to de?ect air in a diffused manner.

The elbow may be provided with one or more swivel connectors adapted to provide more degrees of movement and aid in ling tube drag .

The elbow may be referred to as an r, connector or may be described as any element attach an air delivery tube to a patient interface.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 .1.1 Nasal CPAP for OSA In one form, the present technology comprises a method of treating Obstructive Sleep Apnea in a patient by applying nasal continuous positive airway pressure to the patient. .2 PATIENT INTERFACE 3000 A patient interface 3000 in accordance with one aspect of the t technology ses the following functional aspects: a seal-forming structure 3100, a plenum chamber 3200, a oning and ising structure 3300 and a connection port 3600 for connection to an air circuit 4170 (e.g., see Fig. 3-2). In some forms a functional aspect may be provided by one or more physical components. In some forms, one physical component may provide one or more functional aspects. In use the seal-fonning structure 3100 is arranged to nd an entrance to the airways of the patient so as to facilitate the supply of air at positive pressure to the airways.

In an example, the plenum chamber 3200 and the seal forming structure 3100 are moulded in one piece. In another example they are formed as two 01' more separate components.

A patient interface 3000 in accordance with one form of the present technology is nasal mask system 100. As shown in Figs. 3-1 to 3—3, nasal mask system 100 in accordance with the t technology may comprise a headgear assembly 110, an elbow assembly 120, an air delivery assembly 130 and a cushion assembly or cushion 150. Figs. 3-4 to 3-10 show various views of the cushion assembly 150, and Figs. 3-11 to 3-12 show s views of the elbow assembly 120.

A plenum chamber 3200 in accordance with one form of the present technology is cushion assembly 150. Cushion assembly 150 may be adapted to sealingly engage with a patient’s airway, ing a patient’s nose. As shown in Figs 3-1 to 3-3, cushion assembly 150 may receive able gas from air ry assembly 130 and/or elbow assembly 120, and be supported in position by headgear assembly 110.

Cushion assembly 150 may se a sealing region or sealing cuff 151, two headgear tors 156, a side wall or side wall region 157 and an RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 ment region 158. In an example, n assembly 150 may be formed from a ?exible elastomer or rubber.

] Figs. 3-14 to 3-30, 3-35, and 31 to 32 show various views of a cushion assembly 250 according to another example of the present technology, which is similar to the cushion ly 150. Cushion assemblies 150, 250 are generally referred to as a compact nasal cushion in contrast to the embodiment depicted in Fig. 3-74 which is generally referred to as nasal pillows. As described below, the n assembly 250 includes a thinner wall section adjacent a top lip region of the sealing region of the cushion assembly 250 (e.g., toavoid excessive pressure on the patient’s columella and septum). Also, each side of the nose region of the sealing region includes a wing or sealing ?ap adapted to form a seal on the region adjacent the junction between the nasal greater alar cartilage and the lateral nasal age of the patient’s nose.

In the illustrated e of Figs. 3-l4 to 3-21, D. is about 85-105 mm (e.g., about 97 mm), D2 is about 35-55 mm (e.g., about 48 mm), D3 is about 35-55 mm (e.g., about 44 mm), D4 is about 30-50 mm (e.g., about 41 mm), D5 is about 25- 45 mm (e.g., about 35 mm), D, is about 20-30 mm (e.g., about 26 mm), D7 is about 40-60 mm (e.g., about 50 mm), and D8 is about 20-30 mm (e.g., about 23 mm).

Although speci?c dimensions are provided, it is to be understood that these dimensions are merely exemplary and other dimensions are possible depending on application. For e, the exemplary dimensions may vary by +/-lO-20% or more or less depending on application. .2.1 Seal-forming structure 3100 In one form of the present technology, a seal-forming structure 3100 provides a sealing-forming surface, and may additionally provide a ning function.

In an example, a seal-fonning structure 3100 in accordance with the present technology is constructed from a soft, ?exible, resilient material such as silicone.

RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 In one form, the seal-fonning structure 3100 comprises a sealing ?ange 3110 and a support ?ange 3120. In one form of the present technology, sealing ?ange 3110 includes membrane 160 of the sealing region 151 and support ?ange 3120 includes undercushion or backup band‘ 165 of the sealing region 151 (e.g., see Fig. 3-10). In an example, the sealing ?ange 3110 comprises a relatively thin member with a thickness of less than about lmm, for example about 0.25mm to about 0.45mm that extends around the perimeter 3210 of the plenum chamber 3200. In'ran example, the support ?ange 3120 is relatively thicker than the sealing ?ange 31 10. The support ?ange 3120 is disposed between the sealing ?ange 3110 and the al edge 3220 of the plenum chamber 3200, and extends at least part of the way around the perimeter 3210 of the plenum chamber 3200. The support ?ange 3120 is a spring-like element and functions to support the sealing ?ange 31 10 from buckling in use. In use the sealing ?ange 3110 can readily respond to system re in the plenum chamber 3200 acting on its underside to urge it into tight sealing engagement with the face.

In one form of the t technology, seal-forming structure 3100 comprises a superior sealing portion 3102 and an inferior sealing portion 3104 (e.g., see Figs. 3-10 and 3-21). The superior sealing portion 3102 and the inferior sealing portion 3104 are, e.g., d adjacent one another, and one region may blend into the other. .2.1.1 or sealing portion 3102 Superior sealing portion 3102 is constructed and arranged to form a seal on a portion of the cartilaginous framework of the nose. In an example, or sealing portion 3102 is constructed from a relatively thin material, e.g. a ?ap, ?ange or membrane of material e.g. a plastic elastomer, or a silicone rubber, and r, e.g., one that readily bends or folds in. response to light ?nger pressure when not in use. Depending on the shape of the nose with which it is being used, a relatively narrow width of superior sealing n 3102 may engage with nose ridge to form a seal. A relatively wider portion of superior sealing portion 3102 may engage with the skin adjacent lateral nasal cartilage to form a seal. See, e.g., Fig. 3-39. 2] The superior sealing portion 3102 is not designed to overlay the whole of the nose.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 In an example, the or sealing n 3102 is constructed and arranged, e.g. by being thin and ?exible, to be adaptable to different heights of nose ridge. In this way, the range of faces that will be able to get a good seal is increased.

Furthermore, for a given face and nose, the ?exibility of the superior g portion 3102 means that a seal may be maintained should the plenum chamber 3200 may be moved, e. g. in response to movement of the air circuit 4170.

While the or sealing portion is constructed so that it does not overlay the nasal bones in use, certain portions of the superior sealing portion may overlay some part of the nasal bones on some faces, depending on exactly how the patient interface is used and the size and shape of the ular face.

In an ative form, the superior sealing portion is constructed and arranged to form a seal on the nasal bones in use. .2.1.2 Inferior g portion 3104 Inferior sealing portion 3104 is constructed and arranged to form seal on a portion of the upper lip of a patient, and to direct at least part of a sealing force to the maxilla bone of the patient. In use, part of the inferior sealing portion 3104 is located close to the subalare and the alar crest point.

In one form, inferior g portion is con?gured to avoid excessive pressure on the upper teeth or gums. In an e, the inferior sealing portion does not extend along bone (e.g., l process of maxilla) superiorly to the alar crest point, however it should be appreciated that in other examples it might.

Inferior sealing portion 3104 may be constructed from a single, relatively thicker ?ap, rim or ?ange of material, e.g. a silicone , or themioplastic elastomer, e.g. with a thickness of about 1mm to 2mm. In one form, inferior sealing portion 3104 may be constructed from a dual ?ap, rim or ?ange, for example one being relatively thin and the other being relatively thick. Alternatively, inferior sealing portion 3104 may be constructed from a gel-filled bladder.

RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 .2.1.3 "W" shaped region Figs. 31 to 38 show various views of a cushion assembly 350 according to another example of the present technology. In this example, the cushion assembly includes a general “W” shape in the top lip region, i.e., general “W” shape along the outer (inferior) edge 360(0) of the membrane 360 in the top lip region as best shown in Fig. 34. 1] Figs. 3l to 38 show various views of a cushion assembly 450 according to another example of the present technology. This example shows a cushion assembly with a general “W” shape in the top lip region. In contrast to the example of Figs. 31 to 38, the cushion example of Figs. 31 to 38 includes general “W” shape along both the inner (superior) edge 460(i) of the membrane 460 and the outer (inferior) edge 460(0) of the membrane in the top lip region as best shown in Fig. 34.

In one form, the "W" portion of the top lip region is constructed and arranged so that a middle portion of the "W" may rest on the subnasale or columella in use, in the event of the seal forming portion ng upwards (superiorly) in use, leaving clearance (e.g.; indicated by c in Fig. 38 which is between an inner edge of the undercushion 465 and an inner surface of the plenum chamber) around the respective left and right subalare. 3] In an example, as best shown in Figs. , , and 310, a portion of the sealing portion may have a question-mark shaped, sickle shaped, or c- shaped cross-section. The question-mark , sickle shaped, or ed cross- section may provide the sealing portion with r range of movement or ?exibility towards the patient’s face in use. In the illustrated example, the question-mark shaped, sickle shaped, or c-shaped cross-section is provided to a lower portion of the undercushion 465 and/or the side wall region 457, which provides a space below the lower portion of the undercushion 465 and nt the side wall region 457. For example, the lower portion of the undercushion 465 is radially offset towards the outside of the side wall region 457. It should be appreciated that such cross-section may be provided around the entire perimeter of the cushion or may only be provided RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2013/000383 in selected regions of the cushion, e.g., only in the top lip region. Also, the size and/or con?guration of such cross-section may vary in selected regions. 4] In the illustrated example of Figs. 31 to 38 and 31‘to 3 8, D. is about 90-110 mm (e.g., about 105 mm), D2 is about 40-60 mm (e.g., about 51 mm), D3 is about 40-60 mm (e.g., about 51 mm), D4 is about 35-55 mm (e.g., about 44 mm), D5 is about 30-50 mm (e.g., about 38 mm), D6 is about 25-35 mm (e.g., about 32 mm), D7 is about 45-65 mm (e.g., about 58 mm), and D3 is about 20-30 mm (e.g., about 26 mm). Although speci?c dimensions are provided, it is to be understood that these dimensions are merely exemplary and other dimensions are possible depending on application. For example, the exemplary dimensions may vary by 20% or more or less depending on application. For example, the sealing portion and aperture may be wider, e.g., D. is about 100-120 mm (e.g., about 114 mm), D6 is about 40-50 mm (e.g., about 42 mm), D7 is about 55-75 mm (e.g., about 68 mm), and D3 is about 20-30 mm (e.g., about 24 mm). In another example, the sealing portion and re may be narrower, e.g., D. is about 90-110 mm (e.g., about 100 mm), D6 is about 25-35 mm (e.g., about 28 mm), D7 is about 45-65 mm (e.g., about 54 mm), and D8 is about 20-30 mm (e.g., about 24 mm). .2.1.4 Sealing Region In accordance with r form of the present technology seal forming structure 3100 comprises sealing region 15 1. Sealing region 151 may be adapted to interface with the patient and form a seal with the patient’s airways.

Sealing region 151 may include a nose ridge or nose ridge region 152, sides of the nose region 153, comers of the nose region 154 and top lip region 155. Sealing region 151 may comprise a membrane or flap type seal 160. In an example, as shown in Figs. 3-18 and 3-19, the inner edge of the membrane 260 may includes a bead 260-1, e.g., to prevent tearing, enhance sealing along the edge. Sealing region 151 may further comprise an ushion or backup band 165, extending around part of or the entire ter of the sealing region. A further aspect of the present technology is a n for a mask that seals at its upper extent in a region of the nose that is generally above the tip of the nose, and extends across the alar or ?ares of the patient’s nose.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 In an example, sealing regiOn 151 may be preformed or ise pre- shaped so as to conform to that patient’s facial topography.

Sealing Along Nasal Ridge 7] One aspect of the t technology relates to scaling of the sealing region in the nose ridge region. In an example, the sealing region in the nose ridge region is adapted to engage along the nasal ridge between the pronasale and sellion, and along the nasal cartilage region of the nasal ridge and below or inferior to the nasal bone. That is, the nasal mask system is constructed to have a seal-forming region that is substantially on at least part of the cartilaginous framework of the patient’s nose and not on the nasal bone, i.e., seal along nasal ridge without contacting nasal bridge/skin on the nasal bone.

For example, the sealing region 151 is adapted to be positioned and seal at its upper extent in a region of the nose that is generally above the tip of the nose (i.e., above the pronasale), and extends across the alar or ?ares of the patient’s nose, e.g., not extending over or across the bone of the patient‘s nose.

In an example, the sealing region 151 is positioned at its upper extent in a region of the nose that is generally close to the junction between bone and cartilage on a range of people with larger noses, and avoids impinging on the sight of people with smaller noses.

Nose ridge Region Nose ridge region 152 may be adapted to engage with a nose ridge of a patient. In an example, the nose ridge region may be shaped or preformed to accommodate a patient’s nose ridge, for example, as best shown on Fig. 3-7,-the nose ridge region may be lower (i.e., closer to the attachment region 158) than the sides of the nose region 153. Nose ridge region 152 may comprise a ne 160 for sealing without an ushion or backup band. In an example, such an arrangement ts excess pressure on the sensitive nose ridge region. In an example, the membrane at the nose ridge region 152 may be vely longer that the ne in other regions of the seal region, for example the top lip region 155. The membrane in RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 the nose ridge region 152 may be, for example, about 2-5mm in . In an example, the ne in the nose ridge region 152 may be about 2-4mm in length.

In an example, the membrane in the nose ridge region 152 may be about 3mm in length.

Sides of the Nose Region Sides of the nose region 153 may be adapted to engage with the sides of a patient’s nose. In an example, sides of the nose region 153 may be med to accommodate the sides of the patient’s nose and potentially their cheeks. As best shown on Fig. 3-5, sides of nose the region 153 extends from the apex of the cushion at nose ridge region 152 to the comers of the nose region 154. The sides of nose the region 153 slopes upwardly from the nose ridge region 152 to the comers of the nose region, see for example Fig. 3-6. Sides of the nose region 153 may se a membrane 160 for sealing without an undercushion or backup band. In an example, such arrangement prevents excess pressure on the sides of the patient's nose or alar or ?ares. Excess pressure on these s may cause the cartilage of the nose to collapse inwardly towards the septum, thereby occluding or partially occluding the patient’s airway.

Comers of the Nose Region Comers of the nose region 154 may be adapted to form a seal with the comers of the patient’s nose. Fig. 3-6 shows the comers of the nose region 154 having an apex or point generally indicated by H., being the maximum height of the sealing region 151. This height is to ensure that the most force is applied to the sealing region 151 in the comers of the nose region 154, as this is a honey region of the face and is therefore less ive to pressure. Furthermore, this region of the patient’s face is particularly difficult to seal on as the geometry of the face in this region is quite complex, so the greater the force applied to the seal in this region, the more likely a seal will form. In addition, since lower sealing forces are required on the nose ridge , region and the sides of the nose region (for t and to avoid occlusion), the sealing region must be anchored at the comers of the nose region. Comets of the nose region 154 may comprise a membrane or membrane seal 160 and an ushion or RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2013/000383 backup band 165. The use of both a membrane and an undercushion may ensure a higher g force in this region. In an example, the membrane may have a thickness about 0.1-O.5mm, for example about 0.3mm. In an e, the undercushion may have a thickness of about 0.3-2mm.

Top Lip Region 3] Top lip region 155 may be adapted to engage the e between the patient’s top lip and base of the nose. In an e, top lip region may have a relatively shorter membrane length than the nose ridge region, for example a length of about 0.5-2.5mm, e.g., about 1.5-2.5mm. In an example, this shorter membrane length may be advantageous as some patient’s only have a small space between their top lip and the base of their nose. As best shown in Fig. 3-10, top lip region 155 may have a membrane seal 160 and an undercushion or backup band 165. The use of both a membrane and an undercushion may ensure a higher sealing force in this region. In an example, the membrane may have a thickness about 0.1-0.5mm, for example about 0.3mm. In an example, the undercushion may have a thickness of about 0.3-2mm, for example about 1.5mm. In an example, the thickness of the undercushion may vary along the length of the top lip region, for example from about 0.3mm at the comers of the nose region, to about 1.2mm at the centre of the top lip region. .2.1.5 Seal Use of the undercushion or back-up band s the membrane or facial ?ap to be made considerably thinner than if a single unsupported ?ap were used. This is highly advantageous in that a thinner ?ap is in turn more ?exible, so as to feel so?er and more comfortable and more readily conform to irregularities in the facial contour. It also permits the ?ap to more readily respond to system pressure in the breathing chamber acting on its'underside to urge it into tight sealing engagement with the face.

As noted above, the nasal mask system is ucted to have a seal- forming region that is substantially on the aginous framework on the nose (i.e., not on the nasal bone), and which does not block the nose. In an example, this may be achieved by providing a compression seal (e.g., using an undercushion structure) RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 along the patient’s top lip (e.g., or g portion) and not on the patient’s nose.

Seal on the patient’s nose (e.g., superior sealing portion) may be achieved by tension in the membrane and/or a pneumatic seal. 6] For example, as shown in the cushion example of Figs. 3-14 to 3-30 ’ and also described in the above example, the undercushion or backup band 265 is only provided in the top lip region 255 and the comers of the nose region 254 of the cushion, e.g., see Figs. 3-16, 3-18, 3-22, 3-23, 3-29, and 3-30. That is, the sealing region includes a single layer or membrane 260 only structure in the nose ridge region 252 and sides of the nose region 253 (e.g., see Figs. 3-18 and 3-22 to 3-28), and the sealing region includes a dual layer or membrane 260 and undercushion 265 structure in the top lip region 255 and comers of nose region 254. The dual layer structure provides a compression seal along the top lip region and comers of nose region. In contrast, the nose ridge region and sides of the nose region uses tension in the membrane (edge of the membrane stretched into sealing engagement due to n applied to membrane) and/or pressure in the breathing chamber acting on the membrane (pneumatic seal) to e a seal. The single layer is also provided in the nose ridge region and sides of the nose region to provide a softer and more e seal that avoids any potential for blocking the patient’s nose, , i.e., prevents excess pressure on the sides of the patient’s nose or alar or ?ares which may cause the cartilage to collapse inwardly and potentially at least partially occlude the patient’s airway.

Thus, the cushion assembly according to an example of the present technology provides different sealing mechanisms in different portions of the cushion.

For e, the cushion assembly may provide one mechanism of sealing in the superior portion of the cushion (e.g., sealing by tension in the membrane and/or a pneumatic seal) and a different mechanism of sealing in the inferior portion of the cushion (e.g., compression seal). In the illustrated example, the cushion ly provides a compression seal via a dual layer or membrane and undercushion structure. r, it should be appreciated that the compression seal may be ed by alternative structures, e.g., gel-?lled or foam-?lled pocket, thicker single wall (e.g., about 0.8 to 1.2mm thick silicone).

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Fig. 3-38 shows an example of the n assembly 250 engaged with the patient’s face and under pressure or in?ated in use, i.e., supply of air at positive pressure being d to the cushion ly 250. Fig. 3-39 shows a hatched area along the sealing portion of the cushion assembly 250 which illustrates a width or contact area 280 of the sealing portion engaged with the patient’s face in use. The width or contact area includes an inner edge 280(i) (e.g., along the edge of the ori?ce) and an outer edge 280(0). Fig. 3-36 also shows the outer edge 280(0) of the contact area in dashed lines. As illustrated, a relatively narrow width of superior sealing portion 3102 may engage with the nose ridge to form a seal, e.g., depending on the shape of the nose with which it is being used. A relatively wider portion of superior sealing portion 3102 may engage with the skin adjacent lateral nasal age to form a seal. In the inferior sealing portion 3104, substantially the entire width of the inferior g n may engage the skin along the comer of nose regibn and top lip region to form a seal. Thus, the width or contact area of the sealing portion engaged with the patient’s face in use may vary around the perimeter of the n assembly to form a seal. .2.1.6 Sealing Flap In an example, as shown in Figs, 3-14, 3-16, 3-20, 3-22, 3-26, 3-27, 3- , and 3-36, each side of nose region 253 of the sealing region includes a portion 270, e.g., a wing or sealing ?ap, that protrudes from the edge of the membrane 260 along its inner perimeter. As best shown in Figs. 3-35 and 3-36, each sealing ?ap 270 is adapted to form a seal on the region adjacent the junction n the nasal greater alar cartilage and the lateral nasal age of a patient’s nose (also referred to as the alar crease). The exact location of the sealing ?ap on a face in use may vary depending on the size and shape of the nose with which it is being used.

As illustrated, each sealing ?ap 270 is at least partially angled or pre- biased outwardly away from the breathing r of the n. When engaged with the patient’s nose, the sealing ?aps are de?ected towards the breathing chamber which provides a bias for sealing in the junction noted above. That is, the shape, ?exibility, and pre—bias of the sealing ?aps allows the ?aps to accommodate changes RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 in curvature or contour in this junction (e.g., which tend to continually vary when the nasal alar or “flare“ in use) so as to maintain seal and prevent leaks in use.

In an example, the sealing ?ange (including membrane 260 and sealing ?ap 270) de?nes a generally T-shaped ori?ce. The edge of the membrane 260 along its inner perimeter along with the edge of each sealing ?ap 270 along its inner perimeter cooperate to de?ne an ori?ce 275 into the plenum chamber. In an example, such ori?ce 275 includes a general T-shape including an upper ori?ce portion 275(1) (along vertical axis v as viewed in Fig. 3-20) and a lower ori?ce portion 275(2) (along horizontal axis has viewed in Fig. 3-20) that extends generally transverse to the upper ori?ce n 275(1).

As best shown in Fig. 3-14, the sealing ?ap 270 changes the curvature and/or angle of the edge de?ning the ori?ce 275, i.e., edge of the ori?ce 275 curves upwardly and outwardly away from the breathing chamber at least along the sealing flap 270.

The curvature of the cushion may vary along the t contacting surface of the membrane 260 in different regions of the cushion, e.g., to facilitate g in different regions of the t’s face. .. [000294] For example, as shown in Fig. 3-14, the nose ridge region 252 and the, top lip region 255 each e at least a portion that is locally saddle-shaped in curvature, e.g., curves up in one direction dl and curves down in a different direction d2. Fig. 3-37 is another view of the cushion 250 illustrating such saddle-shaped curvature in the nose ridge region 252 and the top lip region 255.

It should be iated that the above-noted shapes of curvature are approximate shapes and should not be limited to strict atical de?nitions of such .

In addition, it should be appreciated that regions may include similar ure shapes, but the magnitudes of such curvature may be different. For example, the nose ridge region 252 and the top lip region 255 may both include at least a n that is locally saddle-shaped, however the magnitude of curvature in RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2013/000383 one and/or both principle directions of such‘saddle-shape may be different in each region. .2.2 Aperture In an example, where a single mask should be used to ?t about 85% of the female population, the undercushion aperture width (e.g., indicated at uw in Fig. 341-9 for example) is about 36mm to about 42mm, or about 38mm to about 40mm.

In an example, where a single mask should be used to ?t about 85% of the male population, the undercushion aperture width is about 40mm to about 46mm, or about 42mm to about 44mm. In one form, to t for nose width variations of various ethnicities, to fit up to 95% of an average population, an undercushion aperture width is about 50mm to about 56mm, or about 52mm to about 54mm.

In an example, where a single mask should be used to fit about 85% of the female population, the membrane aperture width (e.g., indicated at mw in Fig. 3- 41-9 for example) is about 23mm to about 29mm, or about 25mm to about 27m. In an example, where a single mask should be used to ?t about 85% of the male population, the membrane aperture width is about 39mm to about 45mm, or about 41m to about 43mm. In one form, to account for nose‘width variations of various ethnicities, to ?t up to 95% of an average population, a membrane aperture width is about 49mm to about 55mm, or about 51mm to about 53mm. .2.3 Plenum chamber 3200 Plenum r 3200 is formed in part by a side wall. In one form, the side wall includes side wall region 157 of sealing region 151. The plenum chamber has a perimeter 3210 that is shaped to conform lly to the surface contour of the face of an average person (e.g., see Figs. 3-8 and 3-9). In use, a al edge 3220 of the plenum chamber 3200 is positioned in close proximity to an adjacent surface of the face (e.g., see Fig. 3-10). Actual contact with the face is provided by the seal- forming ure 3100. In an example, the seal-forming structure 3100 extends in use about the entire perimeter 3210 of the plenum chamber 3200. In an example, the plenum r is d to receive a portion of the patient's nose including the pronasale, e.g., the plenum chamber forms over and surrounds a portion of the cartilaginous framework of the nose ing the pronasale.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 In an example, the walls of the plenum chamber 3200 are ?exible, or igid. In an example, plenum chamber 3200 does not include a rigid frame or shell. In an example, the walls of the plenum chamber 3200 are not rigid, and, e.g., the walls of the plenum chamber 3200 are not floppy. In certain forms, ?exibility of the walls of the plenum chamber 3200 assists to decouple a tube drag force from disrupting a seal.

In one form, the walls of the plenum chamber 3200 are d from a silicone rubber. In an example, the walls of the plenum chamber 3200 are constructed from a silicone rubber with a Type A indentation ss of about 35 to about 40, and with a thickness in the range of about 2 mm to about 4mm. In certain forms of the present technology, the plenum chamber 3200 may have different thicknesses in different regions. .2.3.1 Side Wall Region Side wall region 157 may extend between sealing region 151 and attachment region 158. Side wall region 157 may be generally conical, that is, it may have a ?rst diameter at ate attachment region 158 and a second diameter proximate g region 151, with the ?rst diameter being less than the second diameter. Side wall region may have a thickness of about 1.5-5mm, e.g., about 1.5- 3mm, e.g., about 2mm. Such a thickness may provide some support to the sealing region 151, prevent the elbow assembly 120 contacting the patient’s nose, and ensure that the cushion does not collapse from headgear tension when in use.

Side wall region 157 may t or be formed with headgear connectors 156. Such an arrangement may replace the need for a rigid frame or skeleton, as the headgear tors are arrange proximal to the sealing region 151.

Headgear connectors 156 may be disposed on opposing sides of side wall 157. .2.3.2 r Wall Section In an example, as best shown in Figs. 3-16, 3-18, 3-23, and 3-30, the side wall region 257 between the g region 251 and the attachment region 258 includes an area 268 adjacent the top lip region 255 of the sealing region that includes a thickness that is less than corresponding thicknesses adjacent the nose ridge, sides of RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 2013/000383 nose, and comers of nose regions of the sealing region. That is, the area 268 includes a thinner walled cross-section adjacent the top lip region 255 of the g region.

Such area 268 of thinner cross-section lessens the force provided by the sealing region along this section of the top lip region 255. For example, such area 268 es less pressure along the top lip region 255 than the comers of nose region 254 (Le, stiffer along the corners of nose region than the top lip region thereby giving rise or effecting relatively greater pressure along the comers of nose region (along the comers of the lip adjacent the alars), in order to avoid excessive pressure on the columella or septum of the patient’s nose which is a more sensitive region of the patient’s nose.

Figs. 3-22 to 3-30 show exemplary cross-sectional views through various regions of the n assembly 250. For example, Fig. 3123 is a cross- sectional view through the nose ridge region 252 and the top lip region 255 g the single layer or membrane 260 only structure in the nose ridge region 252 and the dual layer or membrane 260 and undercushion 265 structure in the top lip region 255.

Fig. 3-23 also shows the thinner cross-section area 268 in the side wall region 257 adjacent the top lip region 255, e.g., to avoid excessive re on the columella or septum. In addition, Fig. 3-23 shows the attachment region 258 including r wall section 258(1), e.g., to permit decoupling of tube drag forces. 3-24 and 3-25 show the single layer or membrane 260 only structure in the sides of the nose region 253. Figs. 3-26 and 3-27 also show the single layer or membrane 260 only structure in the sides of the nose region 253 as well as at least part of the wing or sealing ?ap 270 that protrudes from the edge of the membrane 260. Fig. 3-27 and 3-28 show at least part of the headgear connector 256. 3-29 and 3-30 show the dual layer or ne 260 and undercushion 265 structure in the comers of nose region 254 and the top lip region 255. Fig. 3-30 shows the thinner cross-section area 268 in the side wall region 257 adjacent the top lip region 255. .2.4 Positioning and stabilising structure 3300 In an example, the seal-forming portion 3100 of the patient interface 3000 of the present technology is held in sealing position in use by the positioning and stabilising structure 3300.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 7] In one form, the seal-forming n 3100 of the patient ace 3000 of the present technology is held in sealing position via a two-point connection to a positioning and stabilising ure 3300.

In one form, the positioning and stabilising structure 3300 connects to plenum chamber 3200 via headgear tor 156.

In. an example, there are only two connectors 156 to the plenum chamber 3200. .2.4.] Headgear Connector — Headgear connector 156 may comprise a lug or interface 159 adapted to receive a cushion connector 116 on headgear 1 10. A similar arrangement is disclosed in PCT application number , ?led 22 October 2008, which is incorporated herein by reference in its entirety.

Headgear connectors 156 may be positioned at an angle relative to the vertical axis of the sealing region 151. As best shown in Figs. 3~6 and 3-7, headgear tors 156 may be positioned at angle a relative to the vertical axis of the sealing region 151. In an example, angle a may be approximately 90-135°. In an example, angle a may be approximately 90-120°. In an example, angle a may be approximately 90-100°. Angle a aligns the headgear connectors in such a way so as to ensure a g force between the cushion and the patient is suf?cient to effect a seal without causing discomfort or causing the cushion to collapse (for example, the closer angle a is to 180°, the more likely the cushion is to collapse inwardly towards the vertical axis when headgear tension is applied, thus pinching the patient’s nose), particularly in the sides of the nose region 153 of sealing regiOn 151.

In an alternative example, as best shown in Figs. 31, , 340- , 36, 31, 33, 35, 36, a hinge or thinner wall section 356(1), 456(1) may be provided to each headgear connector 356, 456 to enhance lity of the headgear connectors and allow suf?cient bending in use so headgear tensioning force is not transferred to collapse the cushion inwardly, e.g., to avoid pinching of the alar under ar tension. Also, as shown in Fig. , one or more wall sections 457(1) of the side wall region 457 between the lugs of the ar connectors may RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 be thickened, e.g., to prevent or reduce collapse of the side wall region under headgear tension. 3] ar connectors 156 may be positioned at an angle relative to the horizontal axis of the sealing region 151. As best shown in Fig. 3-9, headgear connectors 156 may be positioned at angle B relative to the horizontal axis of the sealing region 151. In an example, angle B may be approximately 90-135°. In an example, angle B may be approximately 90-120°. In an example, angle B may be approximately 90-IOO°. Angle B aligns the headgear connectors in such a way so as to ensure the sealing force provided by the headgear tors 156 is buted over the sealing region 151, with more force provided in the top lip region 155 and comers of the nose region 154, and less force provided in the nose ridge region 152. Such distribution may be more comfortable and stable.

As shown in Fig. 3-8, headgear connectors 156 may have a ?rst width w. at a region al to the side wall 157, and a second width W. at its extremity, with first width w. being greater than second width wz. In an example, ?rst width w. may be about lS-SOmm. In an example, first width w. may be about 15-30mm. In an example, ?rst width w. may be about 20-25mm. In an example, second width W2 may be about 15-30mm. In an e, second width W; may be about m. In an example, second width W; may be about 15-20mm. First width w. ensures that the force ed by the headgear is spread from the sides of the nose region 153 to the comers of the nose region 154, and also stabilizes the cushion in the horizontal plane.

Second width W; is arranged to reduce the visual bulk of the headgear tor 156 and permit connection with cushion connector 116.

Headgear c0nnectors 156 are advantageously disposed proximal to the sealing region 151. Headgear connectors 156 are positioned at a height H. from the sealing region 151, as shown on Fig. 3-6. In an example, height H. may be approximately 10-50mm. In an example, height H. may be approximately 10-30mm.

In an example, height H. may be approximately 10-20mm. In an example, height H. may be approximately 20-30mm. This arrangement ensures that headgear forces are ated directly to the sealing portion, and. the sealing region is able to wrap or conform to the patient’s nasal geometry.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 The position and size of the headgear tors s the sealing force to the sealing region in such a way so as to negate or eliminate the need for a forehead support or vertical headgear strap. For example, the width of the headgear connectors proximal to the side wall stabilizes the sealing region on the patient’s face.

The height of the headgear connectors 156 to the sealing region 151 ensures that headgear forces are translated directly to the sealing portion, thereby eliminating the need for additional stabilization from a forehead support.

In an alternative form of the present technology, headgear tors 156 are formed separately from the plenum r. .2.4.2 Headgear Assembly One form of positioning and stabilising structure 3300 in accordance with the present technology is headgear assembly 1 10. Headgear assembly 110 may be d to support, stabilize and/or position the cushion assembly 150 on the t’s face.

As shown in Figs. 3-1 to 3—3, headgear assembly 110 may comprise a pair of side straps l 15, ted to a rear strap 1 18. Side straps 115 de?ne a main headgear loop that may be positioned along the sides of the patient’s face, across the patient’s cheeks, extending between the eyes and the ears of the patient, e.g., overlaying at least a portion of the zygomatic bone, s the croWn of the patient‘s head where it e.g., overlays a portion of the parietal bone. Side straps 115 may have a cushion tor 116 adapted to receive a headgear connector 156 of cushion 150.

Side straps l 15 may have an adjustment portion 117, wherein side straps 115 interlock or ise connect to each other and are able to adjust in length relative to one another. Rear strap 118 extends between the side straps and may loop through a respective slot 114 provided to the side straps 115. Rear strap 1 18 de?nes a rear headgear loop that may be oned over the back of the patient’s head, e.g., engaging along or below the patient’s occiput. In an example, a portion of the headgear rear strap 1 18 or rear headgear loop overlays or engages a point on the head below‘ or inferior to the occipital bone, e.g. a portion of the strap lies on a portion of the trapezius muscle, adjacent the occipital bone in use. In an example, at least a n of the rear strap 1 18 engages below or inferior a lower edge of the occipital RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 bone, which lower edge helps to maintain the rear strap in position and prevent the rear strap from riding up the patient’s head, e.g., prevent sliding in a superior direction. Refer to Figs. 2i and 3-2 for location of the trapezius and an exemplary positioning of the rear strap 1 18 along a portion of the trapezius. In an example, the headgear straps are suf?ciently stretchy or ?exible, e.g., to e comfort and adjustability. For example, the headgear may not require length adjustment to don.

In one form, headgear assembly 1 10 comprises a silicone main n and a fabric rear portion. In another form, headgear assembly I 10 comprises a fabric main portion and a fabric rear portion. In another form, headgear assembly 110 comprises a silicone main portion and a silicone rear portion.

In one form, headgear assembly 1 10 is constructed and ed to be substantially ?oppy.

In one form, headgear assembly 1 10 comprises a main structural tie, and a rear structural tie.

An exemplary headgear assembly I 10 is disclosed in PCT application number , ?led 22 October 2008, which is incorporated herein by nce in its entirety. .2.5 Vent 3400 In one form, the patient ace 3000 es a vent 3400 constructed and arranged to allow for the washout of exhaled carbon dioxide.

One form of vent 3400 in ance with the t technology comprises a plurality of holes, for example, about 20 to about 80 holes, or about 40 to about 60 holes, or about 45 to about 55 holes. 6] In an example, the vent 3400 is located in a decoupling structure 3500, e.g. a swivel 3510. Alternatively, the vent 3400 is located in the plenum chamber 3200.

One form of vent 3400 in ance with the present technology is vent 126. Vent 126 may permit to expiration of exhaled gases from the nasal mask RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 system. Vent 126 may comprise a series of holes, a mesh or other arrangement d to permit the ?ow of gas. In an example, vent 126 may be suf?ciently rigid to avoid collapse of the air ls that exhaust the exhaled gas. Vent 126 may be positioned on the elbow 125 or other region such as the air delivery tube ly 130 or cushion ly 150 (including, for example, side wall 157).

In certain forms of the present technology, the vent 3400 may be constructed from a ?exible, or ?oppy material that is ted by a suf?ciently rigid frame to avoid collapse of the air channels that t the exhaled gas.

In an alternative form, the patient interface 3000 does not e a vent. .2.6 Decoupling structure(s) 3500 In one form the patient interface 3000 es at least one decoupling structure 3500, for example a swivel 3510 or a ball and socket 3520 (e.g., see Fig. 3- 13). In one form, decoupling structure 3500 may be formed at least in part by attachment region 158. .2.6.1 Attachment Region Attachment region 158 may be adapted to receive elbow assembly 120.

Attachment region 158 may include a thinner wall section 158(1) than the side wall region 157, for example attachment region 158 may have a wall section of about 0.1- lmm, for example about 0.2-0.8mm, for example about 0.5mm. In an example, the thinner wall section 158(1) is con?gured to permit decoupling of the tube drag forces from the sealing forces. At the opening end or aperture of the attachment region 158 is a lip portion 158(2) having a thickness of about 2 mm to 3 mm. Also, the lip portion 158(2) reduces the diameter of the opening end from the side wall region 157 of about 26 mm to 27 mm to about 18 mm to 19 mm, which is approximately a 30% reduction in diameter. The thickness and reduced diameter of the lip portion 158(2) assist with ion of the connector ring 128 of the elbow 125 with the cushion assembly 250.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 .2.7 Connection port 3600 In one form, connection port 3600 to air circuit 4170 is made by elbow assembly 120 (e.g., see Figs. 3-1 and 3-2). .2.7.1 Elbow Assembly Elbow assembly 120 may be adapted to connect or serve as an interface between the cushion assembly 150 and the air delivery assembly 130. Elbow ly 120 may be formed with or integral with the air delivery assembly 130, or n assembly 150. Elbow assembly 120 may also be adapted to permit exhaust of exhaled gases.

As shown in Figs. 3-1 to 3-3 and 3-11 to 3-13, elbow assembly 120 may comprise an elbow 125, the elbow having a vent 126, the elbow connecting to or otherwise formed with tor ring 128. Elbow 125 may be formed with a ball joint and the connector ring 128, and may be constructed and arranged to permit rotation of the ball joint while ensuring a suf?cient seal with the elbow 125 to ensure Fair leakage does not compromise the patient’s treatment pressure. The ball joint provides a decoupling mechanism, e.g., decouple tube drag forces from sealing forces.

In one embodiment, the connector ring 128 is releasably or removably detachable from the elbow 125 by pulling the connector ring 128 off the elbow 125 to facilitate thorough cleaning of all surfaces of the connector ring 128 and elbow 125. The connector ring 128 has two raised edges 128(1), 128(2) that extend dly from the outer ferential surface at the distal ends of the tor ring 128, i.e., a ?rst raised edge or ?rst flange on a ?rst side of the ring adjacent an or of the cushion assembly in use and a second raised edge or second ?ange on a second side of the ring adjacent an exterior of the n assembly in use. A channel 128(3) is de?ned between the two raised edges 128(1), 128(2), as shown in Figs. 3-11 and 3-13, such channel 128(3) adapted to sealingly engage the lip portion 158(2) that de?nes the opening end or aperture of the attachment region 158. As shown in Fig. 3-13, the elbow 125 has a ?rst g 125(1) and a second opening 125(2) for directing the pressurised air through the elbow 125. The connector ring 128 is retained on the elbow 125 at the second opening 125(2) of the elbow 125, and is freely rotatable relative to the elbow 125. As shown in Fig. 3-13, the partially spherical or curved RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 inner ferential surface 128(4) of the connector ring 128 abuts the partially spherical, outer e 125(3) of the elbow 125 which allows relative tilting between the connector ring 128 and elbow 125. In an example, the lly spherical surfaces of the ring 128 and the elbow 125 have approximately equal radii of curvature. As depicted in 'Fig. 3-13, when the centers of the connector ring 128 and second opening 125(2) of the elbow 125 are aligned, the ?rst edge 128(1) of the connector ring 128 is co-planar to the edge 125(2)e of the second opening 125(2) of the elbow 125, i.e., annular surface provided by edge 125(2)e of the elbow 125 is ?ush with the r e provided by the first edge 128(1) of the ring 128 when the longitudinal axes of the elbow 125 and ring 128 are co-linear. gh Fig. 3-13 depicts the first edge 128(1) having substantially the same diameter as the second edge , it is possible that the ?rst edge 128(1) may have a larger diameter than the second edge 128(2) (e.g., see Fig. 35). This may minimise inadvertent detachment of the elbow 125 to the cushion assembly 250 when thelip portion 158(2) of the attachment region 158 is retained within the l 128(3) of the connector ring 128. When the lip portion 158(2) is engaged within the l 128(3), it is locked into a ?xed position and also unable to freely rotate relative to each other due to surface friction.

Elbow 125 may also be attached to or otherwise connected with swivel or swivel cuff 129, adapted to receive an air delivery tube assembly 130. Swivel 129 may be arranged such that it may form a seal or have a low leak with elbow 125, while still being able to freely rotate relative to elbow 125.

The swivel cuff 129 includes an annular engaging ring 129(1) that is received in an annular groove 125(4) of the elbow to rotatably connect the swivel cuff 129 to the elbow 125. The swivel cuff 129 also has a channel portion 129(2) de?ned on an outer circumferential surface to matingly receive a cuff or connector 135 provided to the air delivery tube assembly 130. The swivel cuff 129 and the cuff or connector of the air ry tube assembly 130 are removably detachable from each other. .2.8 Forehead support In an example, the patient ace 3000 does not include a forehead support, however in one alternative form, a forehead support may be included.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 .2.9 Anti-asphyxia in one form, the patient interface 3000 includes an anti-asphyxia valve. .2.10 Ports In one form of the present technology, a patient interface 3000 includes one or more ports that allow access to the volume within the plenum chamber 3200.

In one form this allows a clinician to supply supplemental oxygen. In one form this allows for the direct measurement of a property gases within the plenum chamber 3200, such as the pressure. .2.11 Air circuit 4170 An air circuit 4170 in ance with one form of the present technology is air delivery assembly 130. Air ry assembly 130 may be constructed to t a ?ow generator to mask system 100. As shown in Figs. 3-1 to 3-3, air delivery system 130 may comprise a tube 133 and a connector 135. Tube 133 may be relatively ?exible. Connector 135 may beadapted to receive swivel 129 of elbow assembly 120. .2.12 Donning and ng The nasal mask system provides a small, unobtrusive mask system that is easy to don, easy to remove, is stable, comfortable, effective, provides wide-?t range, unobtrusive, easy to use, and adjustable. In addition, the nasal mask system provides a non-prong or non-pillows arrangement (i.e., nasal mask system provides nasal-type cushion that provides single orifice adapted to surround both nares in use) that does not suffer from problems ofjetting effect, nor the ial discomfort ated with nasal prongs or pillows d to at least partiale extend up the patient’s nose. The nasal mask system is structured such that little or no ment may be needed to ?t the nasal mask system to the patient's head. In an example, no forehead support is provided to the mask system, though one can be provided if desired.

In the illustrated example, the nasal mask system 100 es a two- point connection with the cushion, i.e., two side straps l 15 of the headgear assembly engage tive headgear connector 156 alongside of the cushion 150 (e.g., see RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Figs. 3-1 to 3-3). The headgear assembly provides three adjustment points, e.g., adjustment portion 117 of the side straps 115 and tive adjustability of ends of the rear strap 118 with a respective slot 1 14 of the side straps 115. However, it should be appreciated that more or fewer adjustment points may be ed, e.g., side straps ‘ and rear strap may provide ?xed length with no adjustability.

In an example, the two-point connection does not does not require engagement or agement Of a clip in order to don or remove the mask system, i.e., no clips are provided to the mask system but they can be ed if desired.

Also, the main headgear loop de?ned by the side straps 115 s from an inferior anterior position to a superior posterior position, which avoids any headgear strap extending below the ears (i.e., straps do not pass inferior to the patient’s ear) as described below. 4] Figs. 3-3] to 3-34 provide a sequence of views to illustrate an exemplary method for ?tting the nasal mask system to a patient, e.g. prior to the application of air pressure to the plenum chamber. As shown in Fig. 3-31, the patient may grasp the nasal mask system such that one hand holds the cushion assembly 150 in a manner to orient the sealing region towards the patient’s face and the other hand holds the rear strap 1 18 in a manner to allow the main headgear loop de?ned by the side straps 1 15 to receive the patient’s head. Then, as shown in Fig. 3-32, the cushion assembly is engaged with the patient’s face, and the rear strap is held over the patient’s head as it passes through the main ar loop. The rear strap, along with the side straps ed thereto, may be pulled onto the patient’s head until the rear strap is positioned along the back of the patient’s head as shown in Fig. 3-33, i.e., straps rotated or pivoted about the cushion assembly onto the patient’s head until the straps engage and self-locate onto the patient’s head. Finally, as shown in Fig. 3-34, ends of the rear strap 1 18 and/or the adjustment portion 1 17 of the side straps may be adjusted as necessary to secure the nasal mask system on the patient's head.

This arrangement is simple to put on and take off as the straps do not have to be pulled down over the ears to don the mask system or pulled up over the ears to remove the mask system, i.e., headgear straps easily slid on/off over the RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 patient’s head like a cap. That is, the mask system includes ar that may be donned and removed like a cap without interfering with the ears of the patient.

In use, the side straps 115 are arranged to pull the nasal mask system in a superior posterior direction (e.g., as indicated by the arrow al in Fig. 3-34), which provides less compressive force along the nose ridge region of the cushion assembly 150 which is advantageous as. such region is along a more sensitive region of the patient’s nose, i.e., along the cartilage of the nose (not bone) as described above.

Masks with nasal-type cushions normally include headgear arrangements arranged to pull the mask along a direction that is ntially parallel to Frankfort horizontal (as indicated by the arrow a2 in Fig. 3-34) so as to provide a compressive sealing force substantially normal to the patient‘s face. To e such force, the headgear ement includes straps that extend under the patient’s ears so as to provide such force along the Frankfort horizontal direction. In the mask system according to an e of the present technology, the headgear assembly is arranged to pull the mask along the superior posterior direction, e.g., like an “under the nose” mask (e.g., pillows or cradle), which provides less compressive force along the nose ridge region while maintaining suf?cient seal as noted above. Thus, the nasal mask system es headgear that provides an effective sealing vector similar to “under the nose” masks (i.e., not parallel to Frankfort horizontal), but instead used for mask that covers part of the nose, i.e., the nasal mask system compromises sealing force ly along the Frankfort horizontal for an over the ear headgear arrangement to facilitate .2.13 ng adjustment of plenum chamber Fig. 3-9 shows a perpendicular ce h3 between a headgear connection point hp, i.e., line of headgear n as headgear connects to the cushion assembly 150, and a pivoting point or rotation axis pp of the cushion assembly 150 on the face, i.e., the top lip. This perpendicular distance h3 allows adjustment of the headgear tension to effect rotational or pivotal adjustment of the plenum chamber/cushion assembly about the pivoting point pp. As illustrated, the headgear connection point hp is superior to the pivoting point pp or point of contact of the cushion assembly with the top lip. This arrangement enables a user to /pivot the RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 cushion assembly via adjustment of headgear n and to use only a two point headgear connection to accommodate different nose ridge geometry. In an example, increasing the perpendicular distance h3 will se the moment.

Alternative Examples of Elbow Assemblies Figs. 3-42 to 3-11 1 show elbow assemblies according to ative examples of the technology. It should be appreciated that such elbow assemblies may be adapted for use with patient aces of the type described above. However, aspects of the technology may be adapted for use with other suitable ace types, e.g., nasal prongs, etc.

Swivel Elbow and Connector Assembly — Vented Connector or Ring Referring to Figs. 3-42 to 3-45, a swivel elbow and tor assembly 610 according to an example of the technology comprises a vented elbow connector, or ring, 620 and a swivel elbow 640. A sleeve 630 is provided between the vented elbow ring 620 and the swivel elbow 640. The sleeve 630 is provided between a ?rst end of the swivel elbow 640 and the vented elbow ring 620. A swivel cuff 650 is provided to asecond end of the swivel elbow 640 opposite the ?rst end. The swivel cuff 650 comprises a swivel cuff annular engaging ring 651 that is received in an annular groove 643 of the swivel elbow 640 so that the swivel cuff 650 is rotatable, or swivelable, with respect to the swivel elbow 640. In one embodiment, the swivel cuff annular engaging ring 651 and connector ring 620 are made from nylon, and the elbow 640 is made from polypropylene.

The tor ring 620 and swivel cuff annular engaging ring 651 are inserted in an elbow mold. Next, the elbow 640 is molded while previously the molded tor ring 620 and molded swivel cuff annular engaging ring 651 is in the elbow mold. Since the connector ring 620 and swivel cuff annular engaging ring 651 are made from nylon their melt temperature is higher than the polypropylene molding temperature, and therefore they do not undergo plastic deformation when the elbow 640 that is made from polypropylene is molded. This process enables an accurate and snug ?t n these three components 620, 651, 640 which addresses the problem of uncontrolled leak at the connection locations which has been a RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 problem in the past. Also, it eliminates at least one post-molding ly step usually required when attaching le plastic parts er, i.e., ring 620 and ring 651 are insert molded in the elbow mold at substantially the same time. The second end portion of the swivel elbow 640 also es a tapered ?ange 644 that is received in an annular groove 652 of the swivel cuff 650 to secure the swivel elbow 640 to the swivel elbow 640. The swivel elbow 640 also includes an end portion 653 that is con?gured to be connected to an air delivery hose or conduit that is con?gured to deliver a ?ow of breathable gas generated by a ?ow generator, or blower.

Referring to Fig. 3-43, the vented elbow ring 620 comprises an inner ?ange 622 and an outer ?ange 623. A patient interface structure, e.g. n, 65 of a patient interface system may be ?tted into a channel 624 of the vented elbow ring 620 de?ned by the ?anges 622, 623. The cushion 605 may be a nasal cushion, a full face cushion, or a nasal s or prongs cushion. The patient interface system may also e, for example, a support structure, or frame, that supports the cushion 605; a tube, conduit, or hose con?gured to deliver a ?ow of breathable gas to the cushion; and/or a patient interface positioning and izing system (e.g. headgear). It should also be appreciated that the .vented elbow ring 620 may be provided in, for example, the t structure or frame.

Referring to Fig. 3-72, a cushion 605 usable with the swivel elbow and connector assembly 610 may include a sealing portion 6950 having an upper lip engagement portion 6962 that is supported by a supporting portion 6953. The g portion 6950 is separated from the supporting portion 6953 by a front gap in an area of a nose tip engagement portion 6952. The nose tip engagement portion 6952 is ?exible and can extend downward when contacted by a t’s nose, but will be limited in how far it can extend if it reaches the supporting portion 6953. The nose tip engagement n 6952 is extended in length from the aperture 6955 to ?t nose tips of different size, so that the nose tip of different patients may engage the nose tip engagement portion at different locations. A stem 6954 supports the supporting portion 6953 and the g portion 6950. The cushion 605 may be as disclosed in, for example, International Application ( Al), the entire contents of which are incorporated herein by reference. However, it should be appreciated that the swivel elbow and connector assemblies disclosed herein may RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 be used with other patient interface structures or systems, e.g. cushions, such as those sed in, for example, US. Application ,623 or US. 2009/0044808 Al, the entire contents of each being incorporated herein by reference.

The stem 6954 may receive the vented elbow ring 620. The vented elbow ring 620 may be inserted into the aperture of the cushion 605 such that the stem 6954 is gly located in the channel 624 between the ?anges 622, 623. The sealing portion 6950, the stem 6954, and the supporting portion 6953 may be a ?exible material such as liquid silicone rubber material or another elastomeric material, e.g., TPE, gel or foam. The stem 6954 and the supporting portion 6953 may be formed together such as in a mold, and the g portion 6950 may be formed separately and then joined together, e. g. such as by gluing. Alternatively, the stem 6954 and the supporting n 6953 may be formed together such as in a mold, and then the sealing portion 6950 may be bonded to the supporting portion 6953 and the stem 6954 in the mold.

The cushion 605 may comprise a ?exible gusset 6965, which may include the supporting portion 6953 and the stem 6954. The ting portion 6953 and the stem 6954 may be formed as a single unitary element. The ?exible gusset 6965 may be ucted of a ne with a hardness of about 20 to 90 Shore A, preferably about 40 Shore A. The ?exible gusset 6965 could also be made from polycarbonate, polypropylene, nylon, thermoplastic elastomer (TPE), HytrelTM, etc.

Referring again to Figs. 3-42 to 3-44, the vented elbow ring 620 comprises a plurality of vent slots 625 that extend through the inner ?ange 622 across the channel 624 and through the outer ?ange 623. As shown in Fig. 3-43, the sleeve 630 includes a sleeve ?ange 63] provided between a ?ange 64] of the swivel elbow 640 and the ?ange 623 of the vented elbow ring 620. As shown in Fig. 3-42, the connection of the sleeve 630 between the swivel elbow 640 and the vented elbow ring 620 provides a plurality of vents 621 for the g of exhalation gases from the interior of the cushion 605 to the exterior of the cushion 605 through the vent slots 625.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 The shape of the vent hole in one example of the present technology may be such that the cross n (e.g., round) is larger on or towards the inside (entry of air) compared to the r outside cross sections (e.g., diameter) where the air exits to atmosphere. Also, the exit point or region may be angled to diffuse air away from bed r/bed clothes, e.g., not dicular.

A smooth transition may be provided at the vent passage to help reduce/ensure low noise providing vents along the swivel effectively increase overall length of vents, which may allow for laminar ?ow development, and result in less noise.

The ?rst end portion of the swivel elbow 640 includes a tapered ?ange 642 that engages an annular surface 632 of the sleeve 630. A rical portion 633 of the sleeve 630 s between the sleeve ?ange 631 and the tapered ?ange 642 of the swivel elbow 640. The sleeve 630.in the swivel elbow 640 may be permanently assembled by the tapered ?ange 642 as shown in Fig. 3-43, although it should be appreciated that the sleeve 630 may be under , co molded or otherwise formed with the swivel elbow 640 to reduce assembly costs.

Refening to Fig. 3-42, the swivel elbow and connector assembly 610 may be provided with a plurality of vents 621, for example, 20-60 vents, for example -50 vents, for example 38 vents, 40 vents or 42 vents. The cross sectional area of the vents may vary from, for example, 0.5 mm x 0.5 mm, for example, 1.0 mm x 1.0 mm, or 0.7 mm x 0.7 mm. 0] The sleeve ?ange 631 and the ?ange 64] of the swivel elbow 640 may be provided at an angle that provides for venting of the exhalation gases from the interior of the cushion 605, 360° around the swivel elbow 640 and in direction away from the face of the patient. The sleeve 630 provides good diffusivity, and the vent path is contained and easily adjustable. The formation of the vents 62] by the sleeve 630 also reduces the noise of the venting from the interior of the cushion 605.

Although the vented elbow ring 620 is shown in Figs. 3-42 to 3-45 as circular, it should be appreciated that the vented elbow ring may be, for example, elliptical in cross section, as show in Figs. 3-76 and 3-77, RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Swivel Elbow and Connector Assembly — Vented Elbow 2] Referring to Figs. 3-73 to 3-78, a swivel elbow and connector ly 6120 according to another e comprises a swivel elbow 6140 and a connector, or ring, 6150. A cushion 6130 comprises a ?exible base 6133 comprising an aperture for sealingly receiving the ring 6150. The ?exible base may comprise a ?ange, or stem, 6138 that is con?gured to be received in a channel 6154 of the ring 6150 that is de?ned between an inner ?ange 6152 and an outer ?ange 6153. The cushion 6130 may comprise nasal pillows 6131 for sealingly engaging the nares of a patient or user and connectors 6132 for connecting the cushion 6130 to a patient interface structure positioning and stabilizing system (e.g. headgear). The cushion 6130 may be as sed in, for example, International Application ‘ ( Al), the entire contents of which are incorporated herein by reference. It should be iated that other cushions or patient interface structures may also be used with the assembly 6120, including rigid or semi-rigid t interface support structures (cg. frames).

The elbow 6140 includes a ?rst end 6143 con?gured for connection to, for example, a delivery hose or conduit. The elbow includes a tapered ?ange 6142 at a second end for securing the elbow 6140 to the ring 6150. ediate the ?rst and second ends, the elbow 6140 includes an angled ?ange 6141 having a plurality of vents 6145 spaced around the ?ange 6141. The ?ange 6141 is angled with respect to the longitudinal axis of the elbow 6140. The number and size of the vents may be as described above. It should also be appreciated that the vents 6145 may be distributed around the angled ?ange 6141 evenly or randomly. It should further be iated that the vents 6145 may not extend around the entire circumference of the angled ?ange 6141 of the elbow 6140, for example as shown in Fig. 3-76.

A radial ?ange 6146 may nd the angled ?ange 6141 that engages the outer ?ange 6153 of the ring 6150. The ring 6150 is secured between the d ?ange 6142 and the radial ?ange 6146; The elbow 6140 may further comprise a baf?e 6144 to separate the venting portion 6147 from an incoming ?ow of breathable gas from the ?rst end 6143, although it may be circular or have other shapes as well.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Referring to Figs. 3-76 to 3-78, the ring 6150 may have an elliptical con?guration (e.g. elliptical cross section). A circular radial ?ange 6155 may be provided on the ring 6150 to form a sealing interface with the radial ?ange 6146 of theelbow 6140. As also shown in Fig. 3-76, the vents 6145 may not be provided around the entire circumference of the elbow, for example the lower portion 6159 of the angled ?ange 6141 may not include vents 6145, and/or the angled ?ange 6141 may have a reinforced n 6157 n vents 6145. As shown in Fig. 3-78, the baf?e 6144 of the elbow 6140 also has an elliptical ration that provides venting portions 6147 and non-venting portion 6149 to the elbow 6140.

DOuble Swivel Elbow and Connector Assembly — Vented Connector or Ring 6] Referring to Figs. 3-46 to 3-57, a double swivel elbow and connector assembly 660 according to a example comprises a ball and socket connection i.e. a ball joint vented elbow ring 670, a ball joint swivel elbow 680 swivelably connected to the ball joint vented elbow ring 670, and a swivel cuff 690 swivelably connected to the ball joint swivel elbow 680. The ball joint vented elbow ring 670 includes a plurality of vent slots 671 extending around the periphery of the elbow ring 670. As shown in Fig. 3-48, the slots 67] extend through an inner ?ange 673 of the elbow ring 670 and through an outer ?ange 674 of the elbow ring 670. A cushion 605 having an aperture may be received in a channel 675 between the inner ?ange 673 and the outer ?ange 674. When the elbow ring 670 is positioned in the aperture of the cushion 605, vent holes are created between the vent slots 671 in the elbow ring 670 and the cushion 605. The cushion 605 is secured to the double swivel elbow and connector assembly 660 when the stem 6454 of the cushion is received in the channel 675 of the vented elbow ring 670. As used herein, the term “sealingly secured” means that the ?ow of breathable gas delivered to the patient interface system, e.g. cushion, through the swivel elbow will not pass from the interior to the exterior of the patient interface system through the vents in the absence of exhalation by the patient or wearer of the patient interface system. 7] ing to Fig. 3-47, the vented elbow ring 670 includes an annular e 672 that may be ?ush or in line with an annular e 681 of the ball joint swivel elbow 680 when the double swivel elbow and connector assembly 660 is in the RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 position or con?guration shown in Figs. 3-46 to 3-48, i.e., with the elbow pointing lly downward. As shown in Fig. 3-51, the ball joint swivel elbow 680 includes an e r, or lly spherical, outer surface 682 that is swivelably contained by an arcuate annular, or partially spherical, inner surface 676 of the vented elbow ring 670. The vented elbow ring 670 and the ball joint swivel elbow 680 thus act as a ball joint connection between the vented elbow ring 670 and the swivel elbow 680. The inner surface 676 and the outer surface 682 have radii of curvature that are approximately equal. The substantially equal radii of curvature may be achieved by molding the vented elbow ring 670 and the swivel elbow 680 together, without the vented elbow ring 670 and the swivel elbow 680 chemically bonding or mechanically . bonding in the mold, e.g., by shrinkage. The inner surface 676 and the outer surface 682 are engaged essentially over the area of contact between the surfaces so that no or little gas ?ows between the ring 670 and the elbow 680.

The swivel elbow 680 may swivel from the position shown in Fig. 3- 53, in which the annular surface 68] is flush with the annular surface 672 of the vented elbow ring 670 and the longitudinal axes of the ring 670 and the elbow 680 are co-linear, to the position shown in Figs. 3-54, 3-56 and 3-57, in which the annular surfaces 672, 681 are not ?ush and the longitudinal axes are at an angle to each other.

An annularjunction 685 between the arcuate annular outer surface 682 of the swivel elbow 680 and the end portion of the swivel elbow 680 limits the ing of the elbow 680 within the vented elbow ring 670, as shown in Figs. 3-54, 3-56 and 3-57. ing to Figs. 3-51 to 3-57, the end portion of the swivel elbow 680 includes an annular groove 683 that receives a tapered r engaging ring 691 of the swivel cuff 690. A tapered ?ange 684 of the swivel elbow 680 engages the tapered annular engaging ring 691 of the swivel cuff 690 to retain the swivel cuff 690 to the swivel elbow 680. As shown in Figs. 3-53 and 3-54, the swivel cuff 690 includes an angled groove 692 that allows the swivel cuff 690 to rotate from the position shown in Fig. 3-53 to the position shown in Fig. 3-54.

Referring to Figs. 3-50 and 3-55, the pivoting of the swivel cuff 690 allows a longitudinal axis of the double swivel elbow and tor assembly 660 to rotate through an angle a of, for example, 40-60°, for example 50°.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 The double swivel elbow and connector assembly 660 allows for swiveling of the connection of an air delivery tube or conduit to the swivel cuff end portion 693 in two directions. For example, as shown in Figs. 3-48 and 3-49, the swivel cuff 690 may swivel from the position shown in Fig. 348 to the position shown in Fig. 3-49 while the swivel elbow 680 remains in a position such that the annular surface 681 of the swivel elbow is flush with the annular surface 672 of the vented elbow ring 670. The transition from the ent shown in Fig. 3-48 to the alignment shown in Fig. 3-49 is shown in Fig. 3-50 as a central axis of the swivel cuff 690 rotates h the angle 0. of, for example, 50°. The swiveling of the cuff 690 from the position shown in Fig. 3-48 to the on shown in Fig. 3-49 allows a short air delivery tube or conduit to straighten out y reducing torque forces applied to the vented elbow ring 670 and n 605. In other masksvwithout this swivel, if the tube is pulled in a direction that is perpendicular to the central axis of the elbow, because the elbow has an L shaped ration and no swivel, it cannot rotate to be in line with the tube; therefore this pulling force is directly applied to the mask and can disrupt the seal. The ball joint (or ball and socket connection) design allows the elbow and the swivel to re-align depending on the forces being exerted by the tube.

The double swivel elbow and connector assembly 660 also s the swivel elbow 680 to swivel with respect to the vented elbow ring 670, for e, from the position shown in Fig. 3-54 to the position shown in Fig. 3-56.

The pivoting or swiveling of the swivel elbow 680 is limited by the annularjunction ' 685 between the arcuate annular outer surface 682 of the swivel elbow 680 and the end portion of the swivel elbow 680. The swivel elbow 680 may also swivel from the position shown in Fig. 3-54 to the position shown in Fig. 3-57 while the swivel cuff 690 may also pivot or swivel with respect to the swivel elbow 680.

Triple Swivel Elbow and Connector Assembly — Vented Connector or Ring Referring to Figs. 3-58 to 3-71, a triple swivel elbow and connector assembly 660 according to another example comprises a second swivel cuff 6100 swivelably connected to the end portion of the swivel cuff 690. The second swivel cuff 61 00 comprises a tapered annular engaging ring 610] that is received in an annular groove 695 in the end portion of the swivel cuff 690. A tapered ?ange 694 is RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 provided at the end of the swivel cuff 690 to engage and retain the annular ng ring 6101 of the second swivel cuff 6100. The second swivel cuff 6100 includes an annular groove 6102 that receives the tapered ?ange 694 of the swivel cuff 690. The second swivel cuff 6100 includes an end portion 6103 that is con?gured to receive an air ry tube or conduit for receiving a ?ow of breathable gas provided by a flow generator, or blower, for delivery into a t interface including the cushion 605.

The swivel cuff 690 and the swivel elbow 680 of the examples shown in Figs. 3-58 to 3-71 are swivelable in the same manner as described with respect to the e sed in Figs. 3-46 to 3-57. As shown in Figs. 3-62 and 3-66, the pivoting of the swivel cuff 690 allows a longitudinal axis of the triple swivel elbow and connector ly 660 to rotate through an angle [3 of, for example, 40-60°, for example 50°. Although the second swivel cuff 6100 is shown as including an annular groove 6102 that receives the tapered ?ange 694 of the swivel cuff 690, it should be appreciated that the second swivel cuff 6100 may be provided with an angled groove similar to the angled groove 692 of the first swivel cuff 690 to permit the second swivel cuff 6100 to swivel through an angle similar to the manner in which the swivel cuff 690 swivels with respect to the swivel elbow 680.

Swivel Elbow and sphyxia Valve Assembly Referring to Figs. 3-79 to 3-88, a swivel elbow and anti-asphyxia valve assembly 6300 according to an example of the technology may be provided having a diffuse vent. The assembly may also include engagement portions, e.g. buttons or actuators, for engaging and disengaging the assembly 6300 to a patient interface, e.g. a mask. The assembly 6300 may be molded in one piece. This arrangement is advantageous as the patient is not required to dismantle the component (thereby preventing potential loss of components or misalignment when reassembling), the cost of the component may be lower, and the anti-asphyxia valve may be positioned such that it carmot be tampered with or accidentally removed.

The assembly 6300 may comprise a ?rst elbow component, base moulding, collar or on portion 6200, as shown in Figs. 3-79 to 3-82. The skeleton portion 6200 may provide the underlying structure of the assembly 6300 to RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 support the assembly in an open or patent on. As shown in Fig. 3-79, the skeleton portion 6200 may include vent holes 6230 adapted to permit the exit of ted gases from a patient interface as per previously described examples. As shown in Fig. 3-82, the skeleton portion 6200 may further se a baf?e 6260 d to separate the incoming gases from the outgoing gases in the assembly 6300 as per previously described examples.

The skeleton portion 6200 may also include a ?rst connection region 6245 comprising engagement tabs 6240 for interfacing or connecting with a patient interface, for example. The ?rst connection region 6245 may be ntially arcuate or de?nea first arcuate region when viewed from the front. The skeleton portion 6200 may also include a second connection region 6250 for interfacing or connecting with a tube or swivel, for example. The on portion 6200 may further include a stop 6255 to position the assembly 6300 with respect to a mask, for example, and t the assembly 6300 from travelling through the connection with the mask or insertion of the assembly 6300 into the mask.

The skeleton portion 6200 may be formed of a relatively rigid, or stiff, material so that the structure may remain open to permit the ?ow of gases. Stiffer materials may ze the noise of the air exiting the vent holes. The skeleton portion 6200 may be formed of, for example, polycarbonate, polypropylene, or nylon.

A rigid material may also assist in maintaining the assembly 6300 in an open position under certain loads, e.g. the patient lying on the assembly. A rigid material may also be easier for the user to connect and disconnect from the mask, tube and/or swivel.

As shown in Fig. 3-80, the skeleton portion 6200 may further comprise supports, arms or interconnecting regions 6290 adapted to connect the ?rst connection region 6245 with the second connection region 6250. The supports 6290 may also form the boundaries of a ?rst aperture 6210 and a second aperture 6220.

The supports 6290 may be e and resilient, i.e. the supports 6290 may return to their original shape after deformation. The first aperture 6210 may be structured and ed to receive an anti asphyxia valve or other valve. The second aperture 6220 may be structured and arranged to receive a ?exible member or web. The second RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 aperture 6220 may extend to an g, gap or relief 6280 at the ?rst connection region 6245, as shown in Fig. 3-81. 0] Referring to Fig. 3-80, the vent holes 6230 may be positioned on a e 6235 that is generally circular or d to better diffuse exiting air streams.

The surface 6235 may be tapered to prevent moisture build up on the elbow - this can cause vent whistle i.e. air exiting the vent holes to create a high d whistle-like noise. The vent holes 6230 may be scattered around the surface 6235 to diffuse the air ?ow. It should be appreciated that the vent holes 6230 may be uniformly spaced around the surface 6235, or provided as ise described herein.

The skeleton portion 6200 may further include second supports or stops 6270 adapted to receive a button or other engagement mechanism. The second supports 6270 may be adapted to transmit a force from an engagement feature or mechanism, such as a button, to the skeleton portion 6200. The second supports 6270 may also reinforce or provide a foundation for an engagement feature or mechanism, such as a button, such that when the button is pressed it does not collapse, rather it transmits a force to the skeleton portion 6200. The second supports 6270 may be an alignment feature to align the skeleton portion 6200 in a tool or mold. The second supports 6270 may form a surface for a second component, for example an over- mould, to abut or be formed against.

The skeleton portion 6200 may be over-moulded or otherwise formed with a second component (also referred to as a ?exible portion or deformable region) 6335, e.g. an assembly over-mould. For example, the skeleton portion 6200 may be moulded in a first tool and then erred to a second tool for over-moulding with the second component 6335, or could be done all in one tool. That is, second —/ component 6335 may be chemically, mechanically or otherwise formed to the on portion 6200. The second component 6335 may be formed of a relatively e material, such as thermoplastic elastomer (TPE), ne, gel or other The second component 6335 may include engagement portions 6320, a ?exible member or web 6330, a lip 6315 and a valve member 6310, The RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 engagement portions 6320 may be, for example, buttons, grips, tabs or other arrangements adapted to receive a pressing force or other motion from a patient or clinician. The engagement portions 6320 may be supported and/or reinforced by the second supports 6270. The engagement portions 6320 may, when pressed, squeeze towards one another thereby displacingthe ?rst supports 6290 inwards. The ?rst supports 6290 may then deform the ?rst tion region 6245 from a ?rst, resting position (e.g. a circular shape) to a second, pressed position (e.g. an oval or elliptical shape). The gap or relief 6280 may be adapted to permit the ?rst connection region 6245 to ?ex. This change in shape may move the engagement tabs 6240 from a ?rst, engaged position, to a second, disengaged position. The gap or relief 6280 may form a second arcuate region, such that when combined with the ?rst arcuate region of the ?rst connection region 6245, the two components form a circle and hence a cylinder.

The ?exible member or web 6330 may be connected to the engagement ns 6320 and also seal the second aperture 6220. The ?exible member 6330 may be in the form of a membrane or other readily deformable shape, as when engagement portions 6320 are pressed, the ?exible member 6330 may buckle or bend.

The lip 6315 may be formed about and positioned around the perimeter of the ?rst aperture 6210. The lip 6315 may be adapted to t objects from entering the ?rst re 6210. The lip 6315 may also serve as a blank off for molding elbow ly 6300.

The valve member 6310, as shown in Fig. 3-87, may be positioned within the body of the elbow assembly 6300, i.e. n the ?rst supports 6290. The valve member 6310 may act as an anti-asphyxia valve, i.e. when air is delivered from the second connection region 6250 to the ?rst tion region 6245, the valve member 6310 may move into a ?rst position (not shown) to occlude the ?rst aperture 6210; and when there is no air being red from the second connection region 6250 to the ?rst connection region 6245, the valve member 6310 may move to a second position (Fig. 3-87) that does not occlude the ?rst aperture 6210, y permitting the patient to receive air from atmosphere through the ?rst aperture 6210.

The valve member 6310 may be a ?ap. The valve member 6310 may be integrally RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 formed with the second component 6335, e.g. through a living hinge attached to the lip. It should be appreciated that the valve member 6310 may be formed separately from the second component 6335 and attached to the second component 6335. The valve member 6310 may be larger than the ?rst aperture 6210, so as to occlude the first aperture 6210 when air is delivered from the second connection region 6250 to the ?rst tion region 6245.

The valve member 6310, the lip 6315, the ment portions 6320, and the ?exible member 6330 may be formed from the same material in a single piece. Alternatively, one or more of these components may be formed separately and/or from an alternative material. 8] In a further example of the present logy, e.g., shown in Figs. 3- 109A to 3-1 11 an elbow 680 may be formed or constructed in a multi-step process, e.g., three step process, to achieve a single component with multiple functions. The elbow 6800 may comprise a skeleton or frame 6805, e.g., constructed of rigid or semi- rigid material, and adapted to communicate air ?ow from an air delivery tube to a mask. The skeleton 6805 may be ?rst formed or molded in a tool. Skeleton 6805 may be constructed of a polymer such as polypropylene, polycarbonate, and nylon.

The elbow 6800 may further comprise an AAV (anti-asphyxia valve) 6810 having a ?ap 6812 adapted to provide the patient with access to atmospheric gas should a ?ow generator fail to deliver air to the mask. The AAV 6810 may be formed or molded within the skeleton 6805 or formed or molded and then subsequently assembled to the on 6805. For example, as shown in Figs. 3-lO9A to 3-109D, the AAV 6810 may be molded and then pulled through an opening 6815 in the skeleton. A pull tab 6820 of the AAV may enable the AAV 6810 to be pulled through the opening 6815 so as to on. retain and/or seal the AAV relative to the skeleton.

The pull tab 6820 may be a sacri?cial component that once utilized (e.g., pulled through the opening) it may be cut off (such that an outer surface 6810.2 of an outer ?ange 6810.1 is substantially ?ush with the elbow surface) as shown in Fig. 3-110A or ise removed (e.g., once an inner ?ange 6825 is pulled and ed against the inner surface of the skeleton, r applied force will tear the pull tab away from the AAV, possibly assisted by a perforation(s) between pull tab and outer ?ange RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 6810.1). Al‘tematively the AAV 6810 may be molded in the opening 6815 and extending through the skeleton 6805 t the need for pull tab 6820. The AAV 6810 may include an inner ?ange 6825 to seal the AAV 6810 against the inner wall 6830 ofthe skeleton 6805.

The elbow 6800 may comprise a ?exible component 6832 (Fig. 3- 110A) d to secure the AAV 6810 in position and/or form one or more release buttons 6835 of the elbow 6800. For example, the ?exible component 6832 may be a silicone or TPE which is molded over the on 6805 to form the outer portions of the release buttons 6835, thereby allowing the release buttons 6835 to ?ex; and may be molded over the AAV 6810 at the opening 6830 to seal and hold the AAV 6810 in position relative to the skeleton 6805.

] The arrangement may have one or more of the following advantages: 1. The AAV is sealed in position and cannot be removed from the elbow thereby preventing the patient from accidentally disassembling the AAV and thus rendering the device unsafe. 2. The ?exible component can be molded in a single shot - if there was no ?exible component over the AAV then the ?exible component may be molded on either side of the elbow at each button. Since it is molded in a single shot, it may be more efficient and less ive to tool 3. The elbow may be more ly appealing.

Swivel Elbow and Connector Assembly Including Cushion Referring to Fig. 3-89, a patient interface system 6400 for ring a?ow of breathable gas to a patient may include a swivel elbow 6410, a swivel or ring or connector 6420, and a cushion 6430 for sealingly engaging the t‘s airways. Although the cushion 6430 as shown includes nasal pillows or prongs or puffs, it should be appreciated that other cushions may be provided, for example a nasal cushion or a full face cushion. The swivel 6420 may be removably attachable to the n 6430 by a bayonet type connection 6440 that includes detents 6421 on the swivel 6420 to engage with tabs 6431 on the cushion 6430. Vents 641 l are provided RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 between the elbow 6410 and the swivel 6420. The vents 641 1 may include slots provided on the elbow surface to create venting gaps between the elbow 6410 and the swivel 6420. It should be appreciated that the slots may be provided in the swivel instead of the elbow, or that slots may be proyided in both the elbow and the swivel.

Referring to Figs. 3-90 to 3-92, according to another example a patient interface system 6450 may include a swivel elbow 6460, a swivel or ring or connector 6470, and a cushion 6490. The swivel 6470 may be connected to a ring 6480 that is attached to the cushion 6490 at 6481. The ring 6480 may be permanently or removably attached to the cushion 6490. For example, the cushion 6490 may be ulded to the ring 6480 or the cushion 6490 and the ring 6480 may be attached by adhesive. As r example, the cushion 6490 and the ring 6480 may be press ?t er.

The elbow 6460 may be bly attached to the swivel 6470 or the elbow may be permanently attached to the swivel 6470. The elbow 6460 may have ?exible buttons 6462 provided between s 6463 formed in the elbow 6460. The buttons 6462 may be pressed or ?exed to connect and disconnect the elbow 6460 from the swivel 6470.

Vents 6461 are provided between the elbow 6460 and the swivel 6470. The vents 6461 may include slots provided on the elbow surface to create g gaps between the elbow 6460 and the swivel 6470. It should be appreciated that the slots may be provided in the swivel instead of the elbow, or that slots may be provided in both the elbow and the swivel. ' Referring to Fig. 3-93, a patient interface system 6500 ing to another example may include a swivel elbow 6510, a swivel or ring or connector 6520, and a cushion 6530. The cushion 6530 may be permanently or bly ted to the swivel 6520 at 6521. The elbow 6510 may be press fit to the swivel 6520 and be releasable by pressing buttons 6512 provided between grooves 6513 as per grooves 6463. Grooves 6463 are made air tight by either being thinned regions of material or an over-molded second material (e.g., TPE, silicone). The elbow 6510 RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 2013/000383 may further include slots 6511 to vent exhaled gases and a baf?e 6514 to reduce noise and increase exhaust gas washout.

Referring to Figs. 3-94 and 3-95, an elbow 5550 according to an example of the technology may e slots 6551 to vent exhaled gases and a baf?e 6554 to reduce noise and increase exhaust gas washout. An aperture 6552 may be provided in the elbow 6550 to permit the patient to breathe in the event that the ?ow of breathable gas is interrupted or stopped. An AAV ?ap 6555 is provided to close the aperture 6552 when a ?ow of breathable gas is in the elbow 6550 (i.e. the ?ow of breathable gas biases the ?ap 6555 into a closed position to cover the aperture 6552).

As shown in Figs. 3-94 and 3-95, the AAV ?ap 6555 is in the open position. The elbow 6550 may be moulded from, for example, a rigid material to improve vent ?ow noise and to prevent the slots 6551 from occluding. The AAV ?ap 6555 may be formed of, for example, a ?exible material to enable movement of the AAV ?ap 6555 from the open to the closed position under the in?uence of the ?ow of breathable gas.

Elbow and Tube Connector Assembly ing to Figs. 3-96 to 3-98, an elbow and tube connector assembly 6560 may e an 6570 and a tube connector 6580 that clips into the inner surface of the elbow 6570. Clipping the tube tor 6580 into the elbow 6570 reduces the overall visual bulk of the assembly 6560 and may also create a tube- speci?c ?tting such that only tubes 6590 provided by a certain manufacturer or provided can be used with the elbow 6570.

The elbow 6570 may include a lip or e element 6571 adapted to engage with an outer surface, e.g. a groove, 6581 of the tube connector 6580 to ensure a more robust seal. The tube connector 6580 may also include a series of ridges 6582 adapted to engage with the inner surface of the elbow 6570, thereby causing a seal, while avoiding sed friction between the tube connector 6580 and the elbow 6570 to permit rotation of the components relative to one another.

Straight Swivel for Elbow and Tube Connection RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Referring to Figs. 3-99 to 3-101, a tube and elbow connector assembly 6600 may include a swivel elbow 6610, a tube tor 6630 and a swivel or connector or ring 6620. The assembly 6600 may be used to connect the elbow 6610, such as the elbow disclosed in, for example, US. 2010/0307502 A1 , the entire contents of which are incorporated herein by reference, to a short retractable tube, having a length of, for example 150 m, such as disclosed in, for example, U.S. 2009/0078259 Al, the entire contents of which are incorporated herein by reference.

The assembly 6600 may reduce onal / torque forces between the tube and the elbow. For example, as disclosed in US. 2010/0000534 A1 , a patient interface system may include a “pillow cushion” that is adhesively applied to the patient’s face.

As the patient interface system has no headgear, it therefore has little to no resistance to rotational forces being d to the pillow cushion. The patient interface system may include a ling gusset, a ring elbow and a short, retractable tube attached to the elbow. A longer tube, e.g. a 2 m tube, may be connected to the short, retractable tube by a swivel. As the short, retractable tube is stretched, it may rotate almost a full revolution. This in turn rotates the elbow and distorts the pillow cushion and may pull the prongs or pillows out of the nose. In the patient ace of US. 2010/0000534 A1, thevshort, table tube assembly is designed to be ‘semi-permanent’ and have minimal leak through the tube-elbow interface. As such, there is no ability to rotate at the short, retractable tube and elbow interaction site and the elbow acts as a solid ?xture and increases the torque onto the cushion.

By altering the location of the swivel in the patient interface system, for example by placing the swivel between the short, retractable tube and the elbow, all the rotational forces of both the longer tube and the short, retractable tube would be onally decoupled from the cushion.

By g the geometry of the external surface of the elbow, and the internal surface of the short tube cuff and offsetting each by, for example, 0.2 mm, preferably 0.1 mm, there would be clearance between both parts. As the tube is stretched and starts to rotate, the e with the least resistance will swivel. The swivel may either ‘fuse’ (i.e. not ) on one side, and rotate 100% on the other, or take up 50% of the on on either side so that the cushion would only experience a tensile force.

RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 2013/000383 Referring to Figs. 3-102 to 3-106, a tube and elbow connector assembly 6650 ing to r example includes an elbow 6660 table to a tube or tube cuff 6690 by a swivel component 6670, 6680 made by, for example, overmoulding a ?rst swivel component 6680 over a second swivel component 6670 in a mould assembly to form a freely rotating swivel in a r footprint, i.e. minimising the extension of the elbow length. The internal geometry of the cuff 6690 and the external geometry of the elbow 6660 were replicated to ensure a tight ?t with no leak, yet the age of the in-mould assembly would allow a smooth rotation.

The swivel components 6670, 6680 form a two part swivel d as one.

Referring to Figs. 3-107 and 3-108, a tube cuff-to-tube cuff connector 6700 assembly may also provide a swivel configured to join cuffs 6710, 6730 of short tubes with no multiplication of the torque forces. A cuff connector 6720 may be provided between two short tubes of, for example, 150 mm in length, rather than one 300 mm tube with 100% clockwise torque force. The cuff connector 6720 connects the two short tubes, and each the two short tubes may be wound in different directions, (i.e. 50% clockwise, 50% anti-clockwise) to cancel each other’s torque out.

Static and Dynamic Sealing Positions ] , Figs. 31 to 32 and 31 and 32 are exemplary views showing the cushion assembly 250 with the membrane 260 engaged with the patient’s face in a static sealing position. Fig. 32 also shows the sealing ?aps 270 engaged with the junction between the nasal major alar age and the lateral nasal cartilage of the patient’s nose as noted above.

Figs. 3-1 14-1 to 32 show the cushion assembly 250 in various dynamic sealing positions as the n assembly 250 adjusts to accommodate external forCes applied to the cushion assembly, e. g., tube drag forces and tube torque applied to the cushion assembly 250. As illustrated, the thinner wall section provided to the attachment region 158 of the cushion assembly, the ball joint mechanism and the swivel provided to the elbow assembly 120, and the ?exibility provided by the 260 and sealing ?aps 270 permit sideways, upwards, and/or downwards . membrane RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 forces to be applied by the elbow assembly while ensuring a suf?cient seal of the cushion assembly with the patient’s face.

In the illustrated example, the patient interface is provided with a decoupling system having multiple decoupling structures to permit decoupling of tube torque and/or tube drag forces from the sealing forces applied by the cushion ly 250 to the patient’s face. That is, the decoupling structures function together to absorb and/or displace forces d by the air delivery tube so such tube forces do not adversely affect the sealing force ed by the cushion assembly 250 and forces provided by the headgear tension.

Decoupling Gusset The thinner wall n 158(1) (e.g., also referred to as a decoupling gusset or a decoupling wall) provided to the attachment region 158 of the cushion assembly provides suf?cient ?exibility and durability to allow the attachment region 158 to tilt, pivot or move relative to the side wall region 157. The thickness of the wall of the decoupling gusset 158(1) is thinner than its adjacent walls of the cushion assembly 250. Suf?cient nce is provided between the decoupling gusset 158(1) and the connector ring 128 supported by the attachment region 158, e.g., to prevent tor ring 128 and/or elbow 125 from piercing through the decoupling gusset 158(1) when tilting of the elbow 125 s a predetermined angle. In one embodiment, the attachment region 158 has a width of about 6 mm to 7 mm, and the decoupling gusset 158(1) has a width of about 3 mm to 4 mm. The decoupling gusset 158( 1) functions in a similar manner as a spheroidal joint because it enables ve motion around an ite number of axes between two ents which have one common center.

Ball and socketjoint/Spheroidal joint The ball and socketjoint provided by the elbow 125 and ring 128 allows for extra degrees of freedom of movement (i.e., in two planes) to permit rotation of the elbow 125 and provide a decoupling structure. For example, the ball and socket joint not only allows for full 360° rotation in the X-axis (see Fig. 3-1 18-1) but also adds an extra 30-405, e.g., 35°, of rotational nt/tilt in the Z-axis (see RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2013/000383 Fig. 2). As a result, the elbow 125 can pivot, swivel, and/or rotate with respect to the ring 128 so that pulling forces (e.g., sideways, upwards, and downwards as shown in Figs. 31 to 3-1 17-2) and/or torque forces applied to the elbow 125 are not directly applied to the cushion assembly 250 and do not disrupt the seal with the patient.

The pivoting or swiveling of the elbow 125 relative to the ring 128 is limited by annularjunction 127 between the partially spherical, outer surface 125(3) of the elbow 125 and the end portion ofthe elbow I25 (e.g., see Fig. 3-13). When the elbow 125 s this pivot or swivel point (e.g., rjunction 127 s the edge 128(2) (see Fig. 3-13) of the ring 128), pulling forces are transferred to the decoupling gusset 158(1) which deforms or pivots as described above to allow further pivoting to permit decoupling of tube drag. The type of deformation for the decoupling gusset 158(1) is typically compressive on one circumferential side and hing on the opposing circumferential side.

In an e, as shown in Fig. 31, a maximum angle a1 accommodated by the decoupling gusset 158(1) when the elbow 125 is tilted upwards relative to the cushion assembly 250 is about 9-10°, e.g., before deformation of the side wall region 157 of the cushion assembly 250 starts to occur.

In an example, as shown in Fig. 31, a maximum angle a2 accommodated by the decoupling gusset 158(1) during downwards tilting is about 13-15°, e.g., before deformation of the side wall region 157 of the cushion assembly 250 starts to occur.

Swivel The swivel or cuff swivel 129 is provided to the lower end or base of the elbow 125 and ts to the air delivery tube assembly 130 e.g., short tube. As illustrated, the air delivery tube assembly 130 includes a tube 133 and a connector 135 adapted to e swivel 129. As shown in Fig. 3-13, the swivel cuff 129 comprises a swivel cuff annular engaging ring 129(1) that is received in an annular groove 125(4) of the swivel elbow 125 so that the swivel cuff 129 is rotatable, or swivelable, with respect to the swivel elbow 125. The swivel cuff 129 allows for full 360° RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 rotation in the Y-axis (see Fig. 33), which provides a decoupling structure to decouple the connection with the air delivery tube assembly 130.

Short Tube 4] In an example, as shown in Figs. 3-1 19-1 and 32, the air delivery tube assembly 130 may be in the form of a short tube arranged to interconnect the patient interface with tubing communicated with the PAP device.

] As shown in Figs. 1 to 36, the short tube includes tube 133, end cuff or tor 135 provided to one end of the tube 133 and adapted to receive swivel 129, and end cuff or connector 137 provided to the opposite end of the tube 133 and adapted to receive swivel 136. The swivel 136 is adapted to engage the tubing communicated with the PAP device 4000.

The tube 133 is in the form of a helical tube which generates torque when the short tube is moved from its neutral state or original, retracted position (Fig. 31) to an extended position (Fig. 3-1 19-2). The tube 133 has a helical coil comprised of a plurality of adjacent coils each separated by a width and has an outer surface de?ning a coil diameter. The tube 133 also has a web of material coaxial to the helical coil that is attached, e.gi, integrally bonded, to the helical coil. The helical coil and web of material may be made from a plastic material such as TPE or TPU.

The end cuffs 135, 137 are overmolded to respective ends of the tube 133. The end cuffs 135, 137 are permanently connected to the tube 133. On the inner circumferential e of the end cuffs 135, 137 are ar ridges to matingly receive and form a rotational relationship with components such as the elbow 125 and cuff tor 6720. in the example shown in Fig. 3-120—5, the swivel cuff 129 is in the form of a swivel cuff r engaging ring that is received in an annular groove or channel 125(4) provided to the end of elbow 125 to provide a rotatable connection with the elbow 125. The swivel cuff annular engaging ring 129 es an annular groove or channel 129(2) along an outer circumferential surface to matingly receive RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 the circular ridge 135(1) of the end cuff 135, e.g., snap-?t connection. Theend cuff 135 is removably able from the swivel cuff annular engaging ring 129.

As shown in Fig. 36, the swivel 136 is provided to a tube connector 138 structured to connect the swivel 136 to the end cuff 137 of the tube 133. As illustrated, one end of the tube connector 138 es an annular groove or channel 138(1) along an outer circumferential e to matingly receive the circular ridge 137(1) of the end cuff 137, e.g., snap-fit connection. The end cuff 137 is removably detachable from the tube connector 138. The opposite end of the tube connector 138 rotatably supports the swivel 136 to allow the swivel to rotate 360° with respect to the tube connector 138. The opposite end may include an outwardly tapered edge 138(2) to retain the swivel 136 to the tube connector 138.

As shown in Figs. 31 to 34, the exterior e of the tube tor 138 may include finger grips 139 to facilitate manual attachment and detachment of the tube connector 138 and swivel 136 f to and from the tube 133 as well as tubing communicated with the PAP device 4000. As illustrated, such finger grip 139 may be a generally ed protrusion provided on opposing sides of the tube connector 138. In example, raised branding and/or raised es may be provided within each U-shaped protrusion to assist in providing grip to the tube connector 138.

The swivel 129 provided to the elbow 125, as well as the swivel 136 provided to the end of the tube 133, are able to rotate up to 180° or more in order to absorb or redirect such torque such that it has little to no effect on the cushion assembly 250. In an e, the swivel 129 may rotate about 30° with minimal extension of the short tube 133, about 120° with intermediate extension of the short tube 133, and about 180° or more with full extension of the short tube. Both ends of the tube 133 are able to rotate 360° by virtue of the proximal swivel 129 and distal swivel 136. Elongation of the tube 133 causes the helical coil of the tube 133 to twist.

This tendency to twist is fully absorbed by both swivels 129, 136 and the tube 133 is easily and freely rotatable relative to the swivels 129, 136 without noticeable frictional resistance when the tube 133 is elongated from its neutral state (see direction arrow on Fig. 3-1 19-1). Therefore, elongation of the tube 133 does not RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 transmit tube torque forces to components connected downstream from the tube 133 such as the elbow 125, seal-forming structure 3100 or a plenum chamber 3200. cally, elongating the tube 133 in a direction parallel to the udinal axis of the tube 133 does not result in immediate rotation (and preferably, little to no rotation) of the elbow 125, which would typically be in the clockwise or anti-clockwise direction corresponding to the ity (left or right handedness) of the helical coil of the tube 133.

In a typical scenario, a patient may don the patient interface 3000 and be sitting up prior to sleeping. The PAP device 4000 may be positioned on a bed side table next to the bed that the t is seated on. Due to gravity, the tube 133 tends to elongate and the elbow 125 rotates to a downward position such that the ?rst opening 125(1) of the elbow 125 faces the ground. The swivels 129, 136 decouple the rotation of the tube 133 when elongation occurs. When the patient falls asleep on their back or on their side facing away from the PAP device 4000, the ball and socket joint of the elbow 125 and swivels 129, 136 decouple tube drag forces. The angle of the elbow 125 is particularly suited in positions where the longitudinal axis of the tube 133 is perpendicular to the ort horizontal ion. In a small proportion of the time, if the patient is sleeping on their side and faces the PAP device 4000, the elbow 125 is tilted up due to the tube 133 aligning and positioning itself to be co-linear with the opening end of the attachment region 158. When the elbow 125 has exceeded its maximum tilting range, the decoupling gusset 158(1) deforms to absorb the tube drag forces before the side wall region 157 of the cushion assembly 150 starts to deform and destabilise from the tube drag forces. A patient interface 3000 having a non- elbowed component (straight component) with a ball and socket joint is unlikely to experience tube drag forces when the patient is sleeping on their side facing the PAP device 4000, however would experience tube drag forces in every other position.

Therefore, an elbow 125 with a ball and socketjoint is preferable for the majority of the time and majority of positions that the t is in when they are ing therapy instead of a non-elbowed component with ball and socket joint.

The decoupling system generally includes the ball and socket elbow 125, decoupling gusset 158(1) and tube 133 with dual swivel connections. In the ment where there is headgear ly 1 10 with two-point connection to the RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 2013/000383 n assembly 250 ing only two sealing vectors, the ling system is capable of minimising the impact of tube drag forces affecting stability without over- tightening of the headgear tension. In other words, any loss of stability caused by the type of headgear used is’at least partially compensated by the decoupling system. This widens the range of headgear that could be used with the patient interface 3000 including unobtrusive headgear (with very little surface contact with the patient’s face) without requiring a high and possibly uncomfortable level of headgear tension to maintain a seal.

PAP DEVICE 4000' A PAP device 4000 in accordance with one aspect of the present technology comprises mechanical and pneumatic components, electrical components and is programmed to execute one or more thms. In an example, PAP device has an external housing, e.g., formed in two parts, an upper portion 4012 of the external housing, and a lower n 4014 of the external housing. In ative forms, the external housing may include one or more panel(s) 4015. In an example, the PAP device 4000 comprises a chassis 4016 that supports one or more internal ents of the PAP device 4000. In one form a pneumatic block is supported by, or formed as part of the chassis 4016. The PAP device 4000 may include a handle 4018.

In an example, pneumatic path of the PAP device 4000 comprises an inlet air filter 4112, an inlet muf?er, a controllable source of air at positive pressure (e.g., a blower 4142), and an outlet muf?er. One or more pressure sensors and ?ow sensors are included in the pneumatic path. 6) In an example, pneumatic block comprises a portion of the pneumatic path that is located within the external housing.- In an example, the PAP device 4000 has an electrical power supply 4210, one or more input devices 4220, a processor, a pressure device ller, one or more protection ts, memory, transducers, data communication interface and one or more output devices. ical components may be mounted on a single Printed Circuit Board Assembly (PCBA) 4202. In an-altemative form, the PAP device 4000 may include more than one PCBA 4202.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 The processor of the PAP device 4000 is programmed to execute a series of algorithm modules in use, e.g., including pre-processing transducer signals module, a therapy engine module, a pressure control module, and further e.g., a fault condition module. .3 RY In certain forms of the present technology, one or more of the following de?nitions may apply. In other forms of the present technology, alternative de?nitions may apply. .3.1 General Air: Air will be taken to include breathable gases, for example air with supplemental oxygen.

Positive Airway Pressure (PAP): PAP ent will be taken to mean the application of a supply of air or breathable gas to the entrance to the airways at a pressure that is positive with t to atmosphere. In one form, the pressure will be continuously positive (CPAP) and e.g., approximately constant through a respiratory cycle of a patient. In some forms, the pressure at the entrance to the airways will vary by a few centimeters of water within a single respiratory cycle, for example being higher during inhalation and lower during exhalation. In some forms, the pressure'at the entrance to the airways will be slightly higher during exhalation, and slightly lower during tion. In some forms the pressure will be a number of centimeters, e.g. about 5-15 cm of water pressure higher during inhalation than exhalation, and provide ventilatory support. In some forms, the pressure will vary between different respiratory cycles of the t, for example being increased in response to detection of tions of l upper airway obstruction, and decreased in the absence of indications of partial upper airway obstruction. .3.2 Anatomy of the face 2] Ala: the external outer wall or "wing" of each nostril (plural: alar) 3] Alare: The most l point on the nasal ala.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Alar curvature (or alar crest) point: The most ior point in the curved base line of each ala, found in the crease formed by the union of the ala with the cheek.

Auricula or Pinna: The whole external visible part of the ear. (nose) Bonyframework: The bony framework of the nose comprises e.g. the nasal bones, the frontal s of the maxillae and the nasal part of the frontal bone. 7] (nose) Cartilaginousframework: The cartilaginous framework of the nose comprises, e.g., the septal, lateral, major and minor cartilages.

Columella: the strip of skin that separates the nares and which runs from the pronasale to the upper lip.

Columella angle: The angle between the line drawn through the midpoint of the nostril aperture and a line drawn perpendicular to the Frankfurt horizontal while intersecting subnasale.

Fran/Jar! horizontal plane: A line ing from the most inferior point of the orbital margin to the left tragion.

Glabella: Located on the soft , the most prominent point in the midsagittal plane of the ad. ' Lateral nasal cartilage: A generally triangular plate of cartilage. Its superior margin is attached to the nasal bone and frontal process of the a, and its inferior margin is connected to the greater alar cartilage.

Greater alar cartilage: A plate of cartilage lying below the lateral nasal cartilage. It is curved around the anterior part of the naris. lts posterior end is connected to the frontal process of the maxilla by a tough ?brous membrane containing three or four minor cartilages of the aIa.

RECTIFIED'SHEET (RULE 91) ISA/AU W0 2013/170290 Nares (Nostrils): Approximately ellipsoidal res forming the entrance to the nasal cavity. The singular form of nares is naris (nostril). The nares are separated by the nasal septum. abial sulcus or Naso-Iabialfold: The skin fold or groove that runs from each side of the nose to the comers of the mouth, separating the cheeks from the upper lip.

Nam-labial angle: The angle between the columella and the upper lip, while ecting subnasale. [000447.] 0t0basi0n inferior: The lowest point of attachment of the auricle to the skin of the face.

Otobasion superior: The highest point of attachment of the auricle to the skin of the face.

Pronasale: the most protruded point or tip of the nose, which can be identi?ed in lateral view of the rest of the portion of the head.

. Philtrum: the midline groove that runs from lower border of the nasal septum to the top of the lip in the upper lip region.

Pogom'on: Located on the soft tissue, the most anterior midpoint of the chin.

Ridge ): The nasal ridge is the midline prominence of the nose, extending from the Sellion to the Pronasale.

Sagittal plane: A vertical plane that passes from or (front) to posterior (rear) dividing the body into right and left halves. 4] Sellion: Located on the soft tissue, the most e point overlying the area of the nasal suture.

Septal cartilage (nasal): The nasal septal cartilage forms part of the septum and divides the front part of the nasal cavity.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Subalare: The point at the lower margin of the alar base, where the alar base joins with the skin of the superior (upper) lip.

Subnasal point: Located on the soft tissue, the point at which the columella merges with the upper lip in the midsagittal plane.

Supramentale: The point of st concavity in the midline of the lower lip between labrale inferius and so? tissue pogonion .3.3 Anatomy of the skull l bone: The frontal bone includes a large vertical portion, the squamafrontalis, corresponding to the region known as the forehead.

Mandible: The mandible forms the lower jaw. The mental protuberance is the bony protuberance of the jaw that forms the chin.

Maxilla: The maxilla forms the upper jaw and is located above the mandible and below the orbits. ntal process ofthe maxilla projects upwards by the side of the nose, and forms pan of its lateral boundary; Nasal bones: The nasal bones are two small oblong bones, g in size and form in different individuals; they are placed side by side‘at the middle and upper part of the face, and form, by theirjunction, the "bridge" of the nose.

: The intersection of the frontal bone and the two nasal bones, a depressed area directly between the eyes and or to the bridge of the nose.

Occipital bone: The occipital bone is situated at the back and lower part of the cranium. It includes an oval aperture, theforamen magnum, through which the cranial cavity communicates with the vertebral canal. The curved plate behind the foramen magnum is the squama occipitalis.

Orbit: The bony cavity in the skull to contain the eyeball. al bones: The parietal bones are the bones that, when joined er, form the roof and sides of the cranium.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Temporal bones: The temporal bones are situated on the bases and sides of the skull, and support that part of the face known as the temple.

Zygomatic bones: ‘The face es two zygomatic bones, d in the upper and lateral parts of the face and forming the ence of the cheek. .3.4 Anatomy of the respiratory system Diaphragm: A sheet of muscle that s across the bottom of the rib cage. The diaphragm tes the thoracic cavity, containing the heart, lungs and ribs, from the nal cavity. As the diaphragm contracts the volume of the thoracic cavity increases and air is drawn into the lungs.

Larynx: The larynx, or voice box houses the vocal folds and connects the inferior part of the x (hypopharynx) with the trachea.

Lungs: The organs of respiration in humans. The conducting zone of the lungs contains the trachea, the bronchi, the bronchioles, and the terminal bronchioles. The respiratory zone contains the respiratory bronchioles, the alveolar ducts, and the alveoli.

Nasal cavity: The nasal cavity (or nasal fossa) is a large air filled space above and behind the nose in the middle of the face. The nasal cavity is divided in two by a vertical ?n called the nasal septum. On the sides of the nasal cavity are three horizontal outgrowths called nasal conchae (singular "concha") or turbinates. To the front of the nasal cavity is the nose, while the back blends, via the choanae, into the nasopharynx.

Pharynx: The part of the throat situated ately inferior to (below) the nasal cavity, and superior to the oesophagus and larynx. The pharynx is conventionally divided into three sections: the nasopharynx (epipharynx) (the nasal part of the pharynx), the oropharynx (mesopharynx) (the oral part of the pharynx), and the laryngopharynx (hypopharynx).

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 .3.5 Materials Silicone or Silicone Elastomer: A tic rubber. In this speci?cation, a reference to silicone is a reference to liquid ne rubber (LSR) or a ssion 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 speci?ed to the contrary, an exemplary form of LSR has a Shore A (or Type A) indentation ss in the range of about 35 to about 45 as measured using ASTM D2240. .3.6 Aspects of a patient interface sphyxia valve (AA V): The component or sembly of a mask system that, by g to atmosphere in a failsafe manner, s the risk of excessive C02 rebreathing by a patient.

Elbow: A conduit that directs an axis of ?ow or air to change direction through an angle. In one form, the angle‘may be approximately 90 degrees. in another form, the angle may be less than 90 degrees. The conduit may have an approximately circular cross-section. In another form the conduit may have an oval or rectangular cross-section.

Frame: Frame will be taken to mean a mask structure that bears the load of tension between two or more points of connection with a headgear. A mask frame may be a non-airtight load bearing structure in the mask. However, some forms of mask frame may also be air-tight.

Headgear: Headgear will be taken to mean a form of positioning and stabilizing structure designed for use on a head. in an example, the headgear comprises a collection of one or more , ties and stiffeners con?gured to locate and retain a patient interface in position on a patient’s face for delivery of respiratory therapy. Some ties are formed of a soft, ?exible, elastic material such as a laminated composite of foam and fabric.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 Membrane: Membrane, e.g., in the context of a g portion and/or face-contacting portion, will be taken to meana typically thin element that has, e.g., substantially no resistance to bending, but has resistance to being stretched.

Plenum chamber: a mask plenum chamber will be taken to a mean n of a t interface having walls enclosing a volume of space, the volume having air therein pressurised above atmospheric pressure in use. A shell may form part of the walls of a mask plenum chamber. In one form, a region of the patient's face forms one of the walls of the plenum chamber.

Seal: The noun form ("a seal") will be taken to mean a structure or barrier that intentionally resists the ?ow of air through the interface of two surfaces.

The verb form ("to seal") will be taken to mean to resist a flow of air.

Shell: In an example, a shell will be taken to mean a curved structure having bending, e and compressive stiffness, for example, a portion of a mask that forms a curved ural wall of the mask. In an example, compared to its l dimensions it is relatively thin. In some forms, a shell may be faceted. In an example, such walls are airtight, although in some forms they may not be ht. 3] Stiffener: A stiffener will be taken to mean a structural component designed to increase the bending resistance of another component in at least one direction.

Strut: A strut will be taken to be a structural component designed to increase the compression ance of another component in at least one direction.

Swivel : (noun) A subassembly of ents con?gured to rotate about a common axis, e.g., independently, e.g., under low torque. In one form, the swivel may be constructed to rotate through an angle of at least 360 degrees. In another form, the swivel may be constructed to rotate through an angle less than 360 degrees. When used in the context of an air delivery conduit, the sub-assembly of components, e.g.,\comprises a matched pair of cylindrical conduits. Preferably there is little or no leak ?ow of air from the swivel in use.

RECTIFIED SHEET (RULE 91) ISA/AU W0 70290 Tie: A tie will be taken to be a structural component designed to resist tension. 7] Vent: (noun) the structure that allows a deliberate controlled rate leak of air from an interior of the mask, or t to ambient air, to allow washout of exhaled carbon e (C02) and supply of oxygen (02). .3.7 Terms used in relation to patient interface Floppy: A quality of a material, structure or composite that is the combination of features of: o Readily conforming to ?nger pressure. 0 Unable to retain its shape when caused to support its own weight. 0 Not rigid.

The quality of being ?oppy may have an associated direction, hence a particular material, ure or composite may be ?oppy in a ?rst direction, but stiff or rigid in a second direction, for example a second direction that is orthogonal to the ?rst direction.

Resilient: Able to deform substantially cally, and to release ntially all of the energy upon ing, within a relatively short period of time such as 1 second.

Rigid: Not readily deforming to ?nger pressure, and/or the ns or loads typically encountered when setting up and maintaining a patient interface in sealing relationship with an entrance to a patient's airways.

Semi-rigid: means being suf?ciently rigid to not substantially distort under the effects of mechanical forces typically applied during positive airway pressure therapy. .4 OTHER REMARKS A portion of the disclosure of this patent document contains material which is subject to copyright protection. The copyright owner has no objection to the RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 facsimile uction by anyone of the patent document or the patent disclosure, as it appears in the Patent and Trademark Of?ce patent ?le or records, but otherwise es all copyright rights whatsoever.

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 ening value in that stated range is encompassed within the technology.

The upper and lower limits of these intervening ranges, which may be independently ed in the intervening ranges, are also encompassed within the technology, subject to any cally ed 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.

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 signi?cant digit to the extent that a practical technical implementation may permit or require it. 6] Unless de?ned otherwise, all cal and scienti?c terms used herein have the same meaning as commonly understood by one of ordinary skill in the an 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.

When a particular material is identi?ed as being preferably used or as being an example to construct a component, obvious alternative materials with similar ties may be used as a substitute. 8] 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.

RECTIFIED SHEET (RULE 91] ISA/AU W0 2013/170290 All publications mentioned herein are incorporated by reference to disclose and be the methods and/or materials which are the subject of those publications. The publications discussed herein are ed solely for their disclosure prior to the ?ling date of the t 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 con?rmed.

Moreover, in interpreting the disclosure, all terms should be interpreted in the broadest reasonable manner consistent with the context. In particular, the terms "comprises" and "comprising" should be interpreted as referring to elements, ents, or steps in a non-exclusive manner, indicating that the referenced elements, components, or steps may be present, or ed, or combined with other ts, components, or steps that are not expressly referenced.

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. 2] Although the technology herein has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and ations of the technology. In some instances, the terminology and symbols may imply speci?c details that are not required to ce the technology. For example, although the terms "?rst" and "second" may be used, unless otherwise speci?ed, they are not intended. to te 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 suchordering may be modi?ed and/or aspects thereof may be ted concurrently or even synchronously.

RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 3] It is therefore to be understood that numerous modi?cations may be made to the illustrative embodiments and that other arrangements may be devised without departing from the spirit and scope of the technology. 6 Reference signs list 100 mask system 1 10 headgear assembly 1 14 respective slot 115 side straps 1 16 cushion connector 1 17 ‘ adjustment portion 1 18 rear strap 120 elbow assembly 125 elbow 125(1) ?rst opening 125(2) second opening 125(2)(e) edge 125(3) partially spherical, outer e 125(4) annular groove 127 r junction 128 connector ring 128(1) ?rst raised edge 128(2) second raised edge 128(3) channel 128(4) curved inner circumferential e 129 swivel cuff 129(1) annular engaging ring 129(2) channel portion 130 air delivery tube assembly 133 tube 135 connector 136 distal swivel 150 cushion assembly 151 sealing region 152 nose ridge region 153 sides of the nose region 154 comers of the nose region 155 top lip region RECTIFIED SHEET (RULE 91) ISA/AU 2013/000383 156 headgear connectors 157 side wall region 158 attachment region 158(1) ling gusset 158(2) lip portion 159 lug or interface 160 membrane 165 undercushion or backup band 250 cushion assembly ._ 251 sealing region 252 nose ridge region 253 sides of the nose region 254 comers of nose region 255 top lip region 256 headgear connector 257 side wall region 258 attachment region 260 membrane 260-1 bead 265 undercushion 268 thinner cross-section area 270 sealing ?ap 275 ori?ce 275(1) upper ori?ce portion 275(2) lower ori?ce portion 280 width or contact area 280(i) inner edge 280(6) outer edge 350 cushion assembly . 356 headgear connector 356(1) thinner wall section 360 ne 450 cushion assembly 456 headgear connector 456(1) thinner wall section 457 side wall region 457(1) wall ns 460 membrane 465 undercushion 605 cushion RECTIFIED SHEET (RULE 91) ISA/AU 610 swivel elbow and connector assembly 620 connector ring 621 vents 622 inner ?ange 623 outer ?ange 624 channel 625 vent slots 630 sleeve 631 sleeve ?ange 632 annular surface 633 cylindrical portion 640 swivel elbow 641 ?ange 642 tapered ?ange 643 annular groove 644 tapered ?ange 650 swivel cuff 651 swivel cuff annular engaging ring 652 annular groove 653 end portion 660 swivel elbow and connector assembly 670 elbow ring 671 vent slots 672 annular surface 673 inner ?ange 674 outer ?ange 675 channel 676 inner e 680 ball joint swivel elbow 681 annular surface 682 arcuate annular outer surface 683 annular groove 684 tapered ?ange 685 annular junction 690 swivel cuff 691 tapered r engaging ring 692 angled groove 693 swivel cuff end portion 694 tapered ?ange 695 annular groove RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 1000 patient 3000 patient interface 3100 seal g structure 3102 superior sealing portion 3104 inferior sealing portion 3110 sealing ?ange 3120 support ?ange 3200 plenum chamber 3210 perimeter 3220 marginal edge 3300 positioning and stabilising structure 3400 vent 3500 decoupling structure 3510 swivel 3520 ball and socket 3600 connection port 4000 , pap device 4012 upper portion 4014 lower portion 4016 chassis 4018 handle 41 12 inlet air ?lter 4142 blower ‘ 4170 air circuit 4202 pcba 4210 ical power supply 4220 input devices 5000 humidi?er 5550 elbow 6100 second swivel cuff 6101 d r engaging ring 6102 annular groove 6103 end portion 6120 swivel elbow and connector assembly 6130 cushion 6 l 32 connectors 6133 ?exible base 6140 swivel elbow 6141 angled ?ange 6142 tapered ?ange REC'l'IFIED SHEET (RULE 91) ISA/AU 6143 ?rst end 6144 baf?e 6145 vents 6146 radial ?ange 6147 venting portions 6150 ?ng 6152 inner?ange 6153 outer ?ange 6154 channel 6155 circular radial ?ange 6157 reinforced portion 6159 lower portion 6200 skeleton portion 6210 ?rst re 6220 second aperture 6230 venthoks 6235 sudace 6240 engagement tabs 6245 ?rst connection region 6250 second tion region 6255 stop 6260 baf?e 6270 secondsuppons 6280 gap or relief 6290 ?rst supports 6300 elbow assembly 6310 valve member 6315 Hp 6320 engagement portions 6330 ?exible member 6335 second component 6400 patient interface system 6410 swivel elbow 6411 vents 6420 sudvel 6421 detents 6430 cushkm 6431 tabs 6431 tabs 6440 t type connection RECTIFIED SHEET (RULE 91) ISA/AU W0 2013/170290 6450 patient interface system 6454 stem 6460 swivel elbow 6461 vents 6462 ?exible buttons 6463 grooves 6470 swivel 6480 ring 6490 cushion 6500 patient interface system 6510 swivel elbow 651 1 slots 6512 buttons 6513 grooves 6514 baf?e 6520 swivel 6530 cushion 6550 elbow 1’ 6551 slots 6552 aperture 6554 baf?e 6555 aav ?ap 6560 elbow and tube tor assembly 6570 elbow 6571 lip or ?exible element 6580 tube connector 6580 tube connector 6582 ridges 6590 tubes 6600 tube and elbow connector assembly 6610 swivel elbow 6620 swivel 6630 tube connector 6650 tube and elbow connector assembly 6660 elbow 6670 second swivel component 6680 ?rst swivel ent 6690 cuff 6710 cuff 6720 cuff connector RECTIFIED SHEET (RULE 91) ISA/AU 6730 cuff 6800 elbow 6805 on 6810 aav 68101 outer ?ange 68102 outer surface ‘6812 ?ap 6812 ?ap 6815 opening 6815 opening 6820 pull tab 6825 inner ?ange 6830 inner wall 6832 e component 6835 release buttons 6950 sealing portion 6952 nose tip engagement portion 6953 supporting portion 6954 stem 6955 Japerture 6962 upper lip engagement portion 6965 ?exible gusset RECTIFIED SHEET (RULE 91) ISA/AU JAWS Ref: 505857DIV2

Claims (48)

WHAT WE CLAIM IS:

1. A mask system for use in delivering breathable gas to a patient in positive airway pressure therapy, comprising: a cushion assembly configured to receive a flow of the breathable gas pressurised above atmospheric pressure, wherein the cushion assembly includes a flexible plenum chamber and a seal forming n adapted to form a seal with at least a portion of the patient’s nose, wherein the cushion assembly is configured to in use attach to a headgear assembly with a twopoint connection; a decoupling system configured to in use isolate the cushion assembly from air conduit drag forces such that sealing forces applied by the cushion assembly to the patient’s face are not affected by the drag , wherein the decoupling system comprises: a first decoupling ure comprising an elbow assembly, wherein the elbow assembly is configured to connect to an air conduit in use and an attachment region of the cushion ly and permit the flow of the breathable gas into the n assembly, wherein the elbow assembly is configured to rotate about a plurality of axes relative to the attachment region, and a second decoupling ure that is configured to in use allow movement of the attachment region about a plurality of axes relative to the seal g portion.

2. The mask system as claimed in claim 1, wherein the cushion assembly is formed from a flexible elastomer.

3. The mask system as claimed in either claim 1 or 2, wherein the plenum chamber is configured to receive in use a portion of the t's nose which includes the pronasale.

4. The mask system as claimed in any one of claims 1 to 3, n the plenum chamber comprises flexible walls which assist in decoupling the air t drag forces from disrupting the seal formed by the seal forming portion and at least the patient’s nose.

5. The mask system as claimed in any one of claims 1 to 4, wherein the plenum chamber is integrally formed with the seal forming portion.

6. The mask system as d in any one of claims 1 to 5, wherein the plenum chamber releasably attaches to the seal forming portion. JAWS Ref: 505857DIV2

7. The mask system as claimed in any one of claims 1 to 6, wherein the cushion assembly is configured to connect to a pair of side straps of the headgear assembly with the two-point connection.

8. The mask system as claimed in any one of claims 1 to 7, n the cushion assembly comprises a pair of headgear connectors.

9. The mask system as claimed in claim 8, wherein the pair of headgear connectors are configured on the plenum chamber.

10. The mask system as claimed in either claim 8 or 9, wherein each of the pair of the headgear connectors attaches to a tive one of the pair of side .

11. The mask system as claimed in either claim 8 or 9, wherein each of the pair of the headgear connectors attaches to a connector configured on a tive one of the pair of side straps.

12. The mask system as claimed in claim 11, wherein each of the pair of headgear connectors comprise a structure adapted to receive the connector.

13. The mask system as claimed in claim 12, wherein the ure comprises a lug adapted to interface with the tor.

14. The mask system as claimed in any one of claims 1 to 13, wherein the cushion assembly includes a side wall region extending between the seal g portion and the attachment region.

15. The mask system as claimed in claim 14 when dependent on any one of claims 8 to 13, wherein each of the pair of headgear connectors releasably attach to the side wall region.

16. The mask system as claimed in claim 14 when dependent on any one of claims 8 to 13, wherein each of the pair of headgear connectors are integrally formed with the side wall region.

17. The mask system as claimed in any one of claims 8 to 16, wherein each of the pair of headgear connectors comprise a thinner wall section relative to the thickness of the adjacent walls of each of the pair of headgear connectors, wherein the thinner wall section is configured to move in use JAWS Ref: 505857DIV2 such that a headgear tensioning force is not transferred to the cushion assembly during ar tensioning.

18. The mask system as claimed in any one of claims 8 to 17, wherein each of the pair of headgear connectors is configured at an angle of substantially between 90 to 135 degrees relative to an xaxis defined by a longitudinal plane of the cushion assembly.

19. The mask system as claimed in any one of claims 8 to 18, wherein each of the pair of headgear connectors is configured at an angle of substantially n 90 to 135 degrees relative to a yaxis defined by a longitudinal plane of the cushion assembly.

20. The mask system as claimed in any one of claims 1 to 19, wherein a lower portion of the seal forming portion is configured to form a seal with part of an upper lip of the patient.

21. The mask system as claimed in claim 20, wherein the two-point connection is above a ng point or point of contact of the seal g portion with the upper lip.

22. The mask system as claimed in any one of claims 1 to 21, wherein the elbow assembly comprises an elbow configured with a first end g and second end opening and further ured to permit the passage of the breathable gas through the elbow.

23. The mask system as claimed in claim 22, wherein the elbow assembly comprises a connector for connecting the elbow to the attachment region.

24. The mask system as claimed in claim 23, wherein the connector is a ring ured to be sealingly secured in an opening configured in the ment .

25. The mask system as claimed in claim 24, wherein the ring comprises a channel defined between two raised edges, wherein the channel is configured to sealingly engage a lip portion of the attachment region that defines the opening.

26. The mask system as claimed in either claim 24 or 25, wherein the ring is detachable from the elbow. JAWS Ref: 505857DIV2

27. The mask system as claimed in any one of claims 24 to 26, wherein the ring is ed to an upper end region of the elbow.

28. The mask system as claimed in any one of claims 23 to 27, wherein the elbow is rotatable relative to the connector.

29. The mask system as claimed in any one of claims 22 to 28, wherein the elbow is a swivel elbow.

30. The mask system as claimed in any one of claims 23 to 29, wherein the elbow comprises a ball joint and with the connector forms a ball and socket joint which permits rotation of the elbow assembly about a plurality of axes relative to the attachment region such that the air conduit drag forces are decoupled from the sealing forces.

31. The mask system as claimed in any one of claims 22 to 30, wherein a first swivel is provided to a lower end region of the elbow.

32. The mask system as claimed in claim 31, wherein the first swivel comprises a first swivel cuff.

33. The mask system as claimed in claim 32, wherein the elbow ses an annular groove configured to receive an annular engaging ring configured on the first swivel cuff such that the elbow and first swivel cuff rotatably connect.

34. The mask system as d in any one of claims 31 to 33, wherein the first swivel ts in use to an end portion of the air t and is configured to permit rotation of the air conduit relative to the elbow assembly.

35. The mask system as claimed in any one of claims 31 to 33, wherein a second swivel is provided to the first swivel, and wherein the second swivel is rotatable relative to the first swivel.

36. The mask system as claimed in claim 35, wherein the second swivel ts in use to an end portion of the air conduit and is configured to permit rotation of the air conduit relative to the elbow assembly.

37. The mask system as d in either claim 35 or 36, wherein the second swivel comprises a second swivel cuff. JAWS Ref: 505857DIV2

38. The mask system as claimed in any one of claims 1 to 37, wherein the second decoupling structure is configured to deform to allow further movement of the elbow assembly such that the air conduit drag forces are led from the sealing forces.

39. The mask system as claimed in any one of claims 1 to 38, n the second decoupling structure is formed at least in part by the attachment region.

40. The mask system as claimed in any one of claims 1 to 39, wherein the second decoupling structure is formed by a thinner wall section of the cushion ly, thinner relative to the ess of adjacent wall sections of the cushion assembly.

41. The mask system as d in 40, wherein the attachment region comprises the thinner wall section.

42. The mask system as claimed in claim 42, wherein the thinner wall section is between 50 to 85 % thinner relative to the thickness of wall sections adjacent to the thinner wall section.

43. The mask system as d in either claim 41 or 42, wherein the thinner wall section is configured to allow the ment region to move relative to the seal forming portion such that the air conduit drag forces are decoupled from the sealing forces.

44. The mask system as claimed in any one of claims 40 to 43, wherein the thinner wall section comprises a decoupling gusset.

45. The mask system as claimed in claim 44, wherein the decoupling gusset deforms to absorb the air t drag forces before adjacent portions of the cushion assembly deform and destabilise.

46. The mask system as claimed in claim 45, wherein regions of the decoupling gusset are configured to compress or extend when the air conduit drag forces are applied to the attachment region.

47. The mask system as claimed in any one of claims 23 to 46, wherein the elbow is configured to limit the movement of the elbow relative to the connector to a point at which the air conduit drag forces are transferred to the second ling structure. JAWS Ref: 505857DIV2

48. The mask system as claimed in claim 47, wherein the elbow comprises an annular junction between a partially spherical outer surface of the elbow, and an adjacent outer surface of the elbow, n the movement of the elbow relative to the connector is limited to a point at which the annular junction s an edge of the ring such that the air conduit drag forces are transferred to the second decoupling structure. W0 70290