NZ796355A

NZ796355A - Patient interface

Info

Publication number: NZ796355A
Application number: NZ796355A
Authority: NZ
Inventors: Matthew Eves; Lachlan Goldspink; Ravikumar Baluchagi; Robin Yew
Original assignee: ResMed Pty Ltd
Priority date: 2018-03-28
Filing date: 2019-03-28
Publication date: 2024-08-30
Also published as: NZ796354A

Abstract

A patient interface comprising: a plenum chamber comprising: one or more plenum chamber inlet ports; and a seal-forming structure comprising a nasal portion having at least one nasal hole and an oral portion having an oral hole; and a positioning and stabilising structure configured to generate a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, wherein a first surface of the nasal portion configured to engage the patient’s face has a first surface finish and a second surface of the oral portion configured to engage the patient’s face has a second surface finish that is different from the first surface finish.

Description

A patient interface comprising: a plenum chamber comprising: one or more plenum chamber inlet ports; and a seal-forming structure comprising a nasal n having at least one nasal hole and an oral portion having an oral hole; and a positioning and ising structure configured to generate a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, n a first surface of the nasal portion configured to engage the patient’s face has a first surface finish and a second surface of the oral portion configured to engage the patient’s face has a second surface finish that is different from the first surface finish.

NZ 796355 P1419NZ4 PATIENT INTERFACE 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 facsimile reproduction by anyone of the patent document or the patent disclosure, as it appears in Patent Office patent files or records, but otherwise reserves all copyright rights whatsoever. 1 REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Application No. 62/649,376, filed March 28, 2018, and U.S. Provisional ation No. 62/731,456, filed September 14, 2018, each of which is orated herein by reference in its entirety. 2 BACKGROUND OF THE TECHNOLOGY 2.1 FIELD OF THE TECHNOLOGY The present technology relates to one or more of the screening, diagnosis, monitoring, treatment, prevention and amelioration of respiratory-related disorders.

The present technology also s to medical devices or apparatus, and their use. 2.2 DESCRIPTION OF THE RELATED ART 2.2.1 Human Respiratory System and its Disorders The respiratory system of the body facilitates gas exchange. The nose and mouth form the entrance to the airways of a t.

The airways include a series of branching tubes, which become narrower, r and more numerous as they penetrate deeper into the lung. The prime function of the lung is gas exchange, ng oxygen to move from the d air into the venous blood and carbon dioxide to move in the opposite direction. The trachea divides into right and left main bronchi, which r divide eventually into terminal bronchioles. The bronchi make up the ting airways, and do not take part in gas exchange. Further divisions of the airways lead to the respiratory bronchioles, and eventually to the alveoli. The alveolated region of the lung is where the gas exchange P1419NZ4 takes place, and is referred to as the respiratory zone. See "Respiratory Physiology", by John B. West, Lippincott Williams & Wilkins, 9th n published 2012.

A range of respiratory disorders exist. Certain disorders may be terised by particular , e.g. apneas, hypopneas, and hyperpneas.

Examples of respiratory disorders include ctive Sleep Apnea (OSA), Cheyne-Stokes Respiration (CSR), respiratory insufficiency, Obesity Hyperventilation me (OHS), Chronic Obstructive ary Disease , Neuromuscular Disease (NMD) and Chest wall disorders.

Obstructive Sleep Apnea (OSA), a form of Sleep Disordered Breathing (SDB), is characterised by events including occlusion or obstruction 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, soft palate and posterior oropharyngeal wall during sleep. The condition causes the affected t to stop breathing for periods typically of 30 to 120 seconds in duration, sometimes 200 to 300 times per night. It often causes excessive daytime somnolence, and it may cause cardiovascular disease and brain damage. The syndrome is a common er, particularly in middle aged overweight males, although a person ed may have no awareness of the problem. See US Patent No. 4,944,310 (Sullivan).

Cheyne-Stokes Respiration (CSR) is another form of sleep disordered breathing. CSR is a disorder of a patient's respiratory controller in which there are rhythmic alternating periods of waxing and waning ventilation known as CSR cycles.

CSR is characterised by 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 afterload. See US Patent No. 6,532,959 (Berthon-Jones).

Respiratory failure is an umbrella term for respiratory disorders in which the lungs are unable to inspire sufficient oxygen or exhale sufficient CO2 to meet the patient’s needs. Respiratory failure may encompass some or all of the ing disorders.

P1419NZ4 A t with respiratory insufficiency (a form of respiratory failure) may experience abnormal shortness of breath on exercise.

Obesity Hyperventilation Syndrome (OHS) is defined as the combination of severe obesity and awake chronic hypercapnia, in the e of other known causes for hypoventilation. Symptoms e dyspnea, morning he and excessive daytime sleepiness. c ctive Pulmonary Disease (COPD) encompasses any of a group of lower airway diseases that have certain characteristics in common. These include increased resistance to air nt, extended expiratory phase of respiration, and loss of the normal city of the lung. Examples of COPD are ema and chronic bronchitis. COPD is caused by chronic tobacco g (primary risk factor), occupational exposures, air pollution and genetic factors.

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

Neuromuscular Disease (NMD) is a broad term that encompasses many diseases and ailments that impair the functioning of the muscles either directly via intrinsic muscle pathology, or indirectly via nerve pathology. Some NMD patients are characterised by progressive muscular impairment leading to loss of ambulation, being wheelchair-bound, swallowing ulties, respiratory muscle weakness and, eventually, death from respiratory failure. uscular 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 ment that s over years and only mildly reduces life expectancy (e.g. Limb girdle, Facioscapulohumeral and Myotonic muscular dystrophy). Symptoms of respiratory failure in NMD include: increasing generalised weakness, dysphagia, dyspnea on exertion and at rest, fatigue, sleepiness, morning headache, and difficulties with concentration and mood changes.

Chest wall disorders are a group of thoracic deformities that result in inefficient coupling between the respiratory muscles and the thoracic cage. The P1419NZ4 disorders are usually characterised by a restrictive defect and share the potential of long term hypercapnic respiratory failure. Scoliosis and/or kyphoscoliosis may cause severe respiratory failure. Symptoms of respiratory failure include: dyspnea on exertion, peripheral oedema, orthopnea, repeated chest infections, morning headaches, fatigue, poor sleep quality and loss of appetite.

A range of therapies have been used to treat or rate such conditions.

Furthermore, otherwise healthy individuals may take advantage of such therapies to prevent respiratory disorders from g. However, these have a number of shortcomings. 2.2.2 Therapy Various therapies, such as Continuous ve Airway Pressure (CPAP) therapy, vasive ventilation (NIV) and Invasive ventilation (IV) have been used to treat one or more of the above respiratory ers.

Continuous Positive Airway Pressure (CPAP) y has been used to treat Obstructive Sleep Apnea (OSA). The mechanism of action is that continuous ve airway pressure acts as a pneumatic splint and may prevent upper airway occlusion, such as by pushing the soft palate and tongue forward and away from the posterior oropharyngeal wall. Treatment of OSA by CPAP therapy may be voluntary, and hence patients may elect not to comply with therapy if they find devices used to provide such therapy one or more of: uncomfortable, difficult to use, expensive and aesthetically aling.

Non-invasive ventilation (NIV) provides ventilatory support to a patient through the upper airways to assist the patient breathing and/or in adequate oxygen levels in the body by doing some or all of the work of breathing. The ventilatory support is provided via a vasive patient ace. NIV has been used to treat CSR and respiratory failure, in forms such as OHS, COPD, NMD and Chest Wall disorders. In some forms, the comfort and effectiveness of these therapies may be improved.

P1419NZ4 Invasive ventilation (IV) provides ventilatory support to patients that are no longer able to effectively breathe themselves and may be provided using a tracheostomy tube. In some forms, the comfort and effectiveness of these therapies may be improved. 2.2.3 Treatment Systems These therapies may be provided by a treatment system or device. Such systems and devices may also be used to screen, diagnose, or monitor a condition without treating it.

A treatment system may se a Respiratory Pressure Therapy Device (RPT device), an air circuit, a humidifier, a patient interface, and data ment. r form of treatment system is a ular repositioning device. 2.2.3.1 Patient Interface A patient interface may be used to interface respiratory equipment to its , for example by providing a flow of air to an entrance to the airways. The flow of air may be provided via a mask to the nose and/or mouth, a tube to the mouth or a tracheostomy tube to the trachea of a patient. Depending upon the therapy to be applied, the patient interface may form a seal, e.g., with a region of the patient's face, to facilitate the delivery of gas at a re at sufficient ce with ambient pressure to effect therapy, e.g., at a positive pressure of about 10 cmH2O ve to ambient pressure. For other forms of therapy, such as the delivery of oxygen, the patient interface may not include a seal sufficient to tate delivery to the airways of a supply of gas at a positive pressure of about 10 cmH2O.

Certain other mask systems may be functionally unsuitable for the present field. For example, purely ornamental masks may be unable to maintain a suitable re. Mask systems used for underwater swimming or diving may be configured to guard against ingress of water from an external higher pressure, but not to maintain air internally at a higher pressure than ambient.

Certain masks may be ally unfavourable for the present logy e.g. if they block airflow via the nose and only allow it via the mouth.

P1419NZ4 Certain masks may be uncomfortable or impractical for the present technology if they require a patient to insert a portion of a mask structure in their mouth to create and maintain a seal via their lips.

Certain masks may be impractical for use while ng, e.g. for ng while lying on one’s side in bed with a head on a pillow.

The design of a patient interface ts a number of challenges. The face has a complex three-dimensional shape. The size and shape of noses and heads varies considerably between individuals. Since the head includes bone, cartilage and soft tissue, different regions of the face respond differently to mechanical forces. The jaw or mandible may move relative to other bones of the skull. The whole head may move during the course of a period of respiratory therapy.

As a consequence of these challenges, some masks suffer from being one or more of obtrusive, aesthetically undesirable, costly, poorly fitting, difficult to use, and uncomfortable ally when worn for long s of time or when a patient is unfamiliar with a system. y sized masks can give rise to d compliance, reduced comfort and poorer patient outcomes. Masks designed solely for aviators, masks designed as part of personal protection equipment (e.g. filter masks), SCUBA masks, or for the administration of anaesthetics may be tolerable for their original application, but nevertheless such masks may be undesirably ortable to be worn for extended periods of time, e.g., several hours. This discomfort may lead to a reduction in patient compliance with y. This is even more so if the mask is to be worn during sleep.

CPAP therapy is highly effective to treat certain respiratory disorders, provided patients comply with therapy. If a mask is uncomfortable, or difficult to use a patient may not comply with therapy. Since it is often recommended that a patient regularly wash their mask, if a mask is difficult to clean (e.g., difficult to assemble or disassemble), patients may not clean their mask and this may impact on patient compliance.

P1419NZ4 While a mask for other applications (e.g. aviators) may not be suitable for use in treating sleep disordered breathing, a mask designed for use in treating sleep disordered breathing may be suitable for other applications.

For these reasons, patient interfaces for delivery of CPAP during sleep form a distinct field. 2.2.3.1.1 Seal-forming structure Patient interfaces may include a seal-forming structure. Since it is in direct contact with the patient’s face, the shape and configuration of the seal-forming structure can have a direct impact the effectiveness and comfort of the patient interface.

A t interface may be partly characterised according to the design intent of where the orming structure is to engage with the face in use. In one form of patient interface, a seal-forming structure may comprise a first sub-portion to form a seal around the left naris and a second sub-portion to form a seal around the right naris. In one form of patient interface, a seal-forming structure may comprise a single element that surrounds both nares in use. Such single element may be designed to for example overlay an upper lip region and a nasal bridge region of a face. In one form of patient ace a seal-forming structure may se an element that surrounds a mouth region in use, e.g. by forming a seal on a lower lip region of a face.

In one form of patient interface, a seal-forming structure may comprise a single element that surrounds both nares and a mouth region in use. These different types of patient interfaces may be known by a variety of names by their manufacturer including nasal masks, full-face masks, nasal pillows, nasal puffs and oro-nasal masks.

A seal-forming ure that may be ive in one region of a patient’s face may be inappropriate in another region, e.g. because of the ent shape, structure, ility and sensitivity regions of the patient’s face. For e, a seal on swimming goggles that overlays a patient’s ad may not be appropriate to use on a patient’s nose.

P1419NZ4 Certain seal-forming structures may be designed for mass manufacture such that one design fit and be comfortable and effective for a wide range of different face shapes and sizes. To the extent to which there is a mismatch between the shape of the patient’s face, and the seal-forming structure of the mass-manufactured t interface, one or both must adapt in order for a seal to form.

One type of orming ure extends around the periphery of the patient interface, and is intended to seal against the patient's face when force is d to the patient interface with the seal-forming structure in nting engagement with the patient's face. The orming structure may include an air or fluid filled cushion, or a moulded or formed e of a resilient seal element made of an elastomer such as a rubber. With this type of seal-forming structure, if the fit is not adequate, there will be gaps between the seal-forming structure and the face, and additional force will be required to force the patient interface against the face in order to achieve a seal.

Another type of seal-forming structure incorporates a flap seal of thin material positioned about the periphery of the mask so as to provide a self-sealing action against the face of the patient when positive pressure is applied within the mask. Like the previous style of seal forming portion, if the match between the face and the mask is not good, additional force may be required to achieve a seal, or the mask may leak. Furthermore, if the shape of the seal-forming ure does not match that of the t, it may crease or buckle in use, giving rise to leaks.

Another type of seal-forming structure may comprise a friction-fit t, e.g. for insertion into a naris, however some patients find these uncomfortable.

Another form of seal-forming structure may use adhesive to achieve a seal. Some patients may find it inconvenient to constantly apply and remove an adhesive to their face.

A range of patient interface seal-forming ure technologies are disclosed in the following patent applications, assigned to ResMed Limited: WO 1998/004,310; P1419NZ4 One form of nasal pillow is found in the Adam Circuit manufactured by Puritan t. Another nasal pillow, or nasal puff is the subject of US Patent 4,782,832 (Trimble et al.), ed to Puritan-Bennett Corporation.

ResMed Limited has ctured the following products that incorporate nasal pillows: SWIFTTM nasal pillows mask, SWIFTTM II nasal pillows mask, M LT nasal pillows mask, SWIFTTM FX nasal pillows mask and MIRAGE LIBERTYTM full-face mask. The following patent applications, assigned to ResMed Limited, describe examples of nasal pillows masks: International Patent Application WO2004/073,778 (describing amongst other things aspects of the ResMed Limited SWIFTTM nasal pillows), US Patent Application 2009/0044808 ibing amongst other things aspects of the ResMed Limited SWIFTTM LT nasal pillows); International Patent Applications (describing amongst other things aspects of the ResMed d MIRAGE LIBERTYTM full-face mask); International Patent ation (describing amongst other things s of the ResMed Limited SWIFTTM FX nasal pillows). 2.2.3.1.2 Positioning and ising A seal-forming structure of a patient 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 ure, 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 Application Publication No. US 2010/0000534. However, the use of adhesives may be uncomfortable for some.

Another technique is the use of one or more straps and/or ising harnesses. Many such harnesses suffer from being one or more of ill-fitting, bulky, uncomfortable and awkward to use. 2.2.3.2 Respiratory Pressure Therapy (RPT) Device A respiratory pressure therapy (RPT) device may be used individually or as part of a system to deliver one or more of a number of therapies described above, such as by operating the device to generate a flow of air for delivery to an interface to the airways. The flow of air may be pressurised. Examples of RPT s include a CPAP device and a ventilator. 2.2.3.3 Humidifier Delivery of a flow of air without humidification may cause drying of airways. The use of a humidifier with an RPT device and the patient interface es humidified gas that minimizes drying of the nasal mucosa and increases patient airway comfort. In on in cooler climates, warm air applied generally to the face area in and about the patient interface is more comfortable than cold air. 2.2.3.4 Data Management There may be clinical reasons to obtain data to determine whether the patient prescribed with atory therapy has been "compliant", e.g. that the patient has used their RPT device according to one or more "compliance rules". One example of a compliance rule for CPAP therapy is that a patient, in order to be deemed compliant, is required to use the RPT device for at least four hours a night for at least 21 of 30 utive days. In order to determine a patient's compliance, a provider of the RPT , such as a health care provider, may manually obtain data describing the patient's therapy using the RPT device, calculate the usage over a predetermined time period, and compare with the compliance rule. Once the health care provider has determined that the patient has used their RPT device according to the ance rule, the health care provider may notify a third party that the patient is ant.

There may be other aspects of a patient’s y that would benefit from communication of therapy data to a third party or external system.

Existing processes to communicate and manage such data can be one or more of costly, time-consuming, and error-prone.

P1419NZ4 2.2.3.5 Mandibular repositioning A mandibular repositioning device (MRD) or mandibular advancement device (MAD) is one of the treatment options for sleep apnea and snoring. It is an adjustable oral appliance available from a dentist or other supplier that holds the lower jaw (mandible) in a forward on during sleep. The MRD is a removable device that a patient inserts into their mouth prior to going to sleep and removes following sleep. Thus, the MRD is not designed to be worn all of the time. The MRD may be custom made or produced in a standard form and es a bite sion n designed to allow fitting to a patient’s teeth. This mechanical protrusion of the lower jaw expands the space behind the tongue, puts tension on the pharyngeal walls to reduce collapse of the airway and diminishes palate vibration.

In n examples a mandibular advancement device may comprise an upper splint that is intended to engage with or fit over teeth on the upper jaw or maxilla and a lower splint that is intended to engage with or fit over teeth on the upper jaw or mandible. The upper and lower splints are connected together laterally via a pair of connecting rods. The pair of ting rods are fixed symmetrically on the upper splint and on the lower .

In such a design the length of the connecting rods is selected such that when the MRD is placed in a patient’s mouth the mandible is held in an advanced position. The length of the connecting rods may be adjusted to change the level of protrusion of the le. A dentist may determine a level of protrusion for the mandible that will determine the length of the connecting rods.

Some MRDs are structured to push the mandible forward relative to the maxilla while other MADs, such as the ResMed Narval CC™ MRD are designed to retain the mandible in a forward position. This device also reduces or minimises dental and temporo-mandibular joint (TMJ) side effects. Thus, it is configured to minimises or prevent any movement of one or more of the teeth. 2.2.3.6 Vent technologies Some forms of treatment systems may e a vent to allow the washout of exhaled carbon dioxide. The vent may allow a flow of gas from an interior space of P1419NZ4 a patient interface, e.g., the plenum chamber, to an exterior of the t interface, e.g., to ambient.

The vent may comprise an orifice and gas may flow h the orifice in use of the mask. Many such vents are noisy. Others may become blocked in use and thus provide insufficient washout. Some vents may be disruptive of the sleep of a bed partner 1100 of the patient 1000, e.g. through noise or focussed airflow.

ResMed Limited has developed a number of ed mask vent technologies. See International Patent Application Publication No.

International Patent Application Publication No. 6,581,594; US Patent Application Publication No. US 2009/0050156; US Patent Application Publication No. 2009/0044808.

Table of noise of prior masks (ISO 17510-2:2007, 10 cmH2O pressure at Mask name Mask type A-weighted A-weighted Year (approx.) sound power sound pressure level dB(A) dB(A) (uncertainty) (uncertainty) Glue-on (*) nasal 50.9 42.9 1981 ResCare nasal 31.5 23.5 1993 standard (*) ResMed nasal 29.5 21.5 1998 MirageTM (*) ResMed nasal 36 (3) 28 (3) 2000 UltraMirageTM ResMed nasal 32 (3) 24 (3) 2002 Mirage ActivaTM ResMed nasal 30 (3) 22 (3) 2008 Mirage ResMed nasal 29 (3) 22 (3) 2008 MirageTM SoftGel P1419NZ4 ResMed nasal 26 (3) 18 (3) 2010 MirageTM FX ResMed nasal pillows 37 29 2004 Mirage SwiftTM ResMed nasal pillows 28 (3) 20 (3) 2005 Mirage SwiftTM ResMed nasal pillows 25 (3) 17 (3) 2008 Mirage SwiftTM ResMed AirFit nasal pillows 21 (3) 13 (3) 2014 (* one specimen only, measured using test method specified in ISO 3744 in CPAP mode at 10 cmH2O) Sound pressure values of a variety of objects are listed below Object A-weighted sound pressure dB(A) Notes Vacuum cleaner: Nilfisk 68 ISO 3744 at 1m Walter Broadly Litter Hog: B+ distance Grade sational speech 60 1m distance Average home 50 Quiet library 40 Quiet bedroom at night 30 Background in TV studio 20 2.2.4 ing, sis, and Monitoring Systems Polysomnography (PSG) is a tional system for sis and monitoring of cardio-pulmonary disorders, and typically involves expert clinical staff to apply the system. PSG typically involves the placement of 15 to 20 contact sensors on a patient in order to record various bodily signals such as electroencephalography (EEG), electrocardiography (ECG), electrooculograpy (EOG), electromyography (EMG), etc. PSG for sleep disordered breathing has involved two nights of P1419NZ4 observation of a patient in a clinic, one night of pure diagnosis and a second night of ion of treatment ters by a clinician. PSG is therefore expensive and inconvenient. In particular it is unsuitable for home screening / diagnosis / monitoring of sleep ered breathing.

Screening and diagnosis generally be the identification of a condition from its signs and symptoms. Screening typically gives a true / false result indicating whether or not a patient’s SDB is severe enough to warrant further igation, while sis may result in clinically actionable information.

Screening and diagnosis tend to be one-off processes, whereas monitoring the progress of a condition can continue indefinitely. Some screening / diagnosis systems are suitable only for screening / diagnosis, whereas some may also be used for monitoring.

Clinical experts may be able to screen, diagnose, or monitor patients adequately based on visual observation of PSG signals. However, there are circumstances where a al expert may not be available, or a clinical expert may not be able. Different clinical experts may disagree on a patient’s condition. In addition, a given clinical expert may apply a different standard at different times. 3 BRIEF SUMMARY OF THE TECHNOLOGY The present technology is directed s providing medical s used in the screening, diagnosis, monitoring, amelioration, treatment, or prevention of respiratory disorders having one or more of improved comfort, cost, efficacy, ease of use and manufacturability.

A first aspect of the present technology relates to apparatus used in the screening, diagnosis, monitoring, amelioration, ent or prevention of a respiratory disorder.

Another aspect of the present technology relates to methods used in the screening, diagnosis, monitoring, amelioration, ent or prevention of a respiratory disorder.

P1419NZ4 An aspect of certain forms of the present technology is to provide methods and/or apparatus that improve the compliance of patients with respiratory therapy.

An aspect of the t technology is directed to a t interface comprising: a plenum chamber comprising: a orming structure; and a shell; and a positioning and stabilising structure, wherein an at least partially anterior wall of a nasal portion of the seal-forming ure comprises two lateral support portions, each of the lateral support portions being spaced apart laterally, each of the lateral support portions having a higher resistance to deformation relative to an adjacent portion of the seal-forming structure.

An aspect of the present technology is directed to a patient interface comprising: a plenum chamber pressurisable to a therapeutic pressure of at least 6 cmH2O above ambient air pressure throughout a patient’s respiratory cycle in use, the plenum chamber having an oral portion and a nasal portion, the plenum r comprising: a seal-forming structure constructed and ed to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, said nasal portion of the seal-forming ure having at least one nasal hole configured to deliver a flow of air at said therapeutic re to an entrance to the patient’s nares in use, said oral portion of the seal-forming structure having an oral hole ured to deliver the flow of air at said therapeutic re to an entrance to the patient’s mouth in use, the seal-forming structure constructed and arranged to maintain said therapeutic re in the plenum r throughout the patient’s respiratory cycle in use; and a shell having one or more plenum chamber inlet ports sized and structured to receive the flow of air at the therapeutic pressure for breathing by a patient throughout the t’s respiratory cycle in use, and the shell supporting the seal-forming structure; and a positioning and stabilising structure configured to generate a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, wherein the shell is joined to the oral n of the plenum chamber, wherein the seal-forming structure forms substantially the entire nasal portion, wherein the nasal portion of the plenum chamber comprises posterior corners configured to engage the patient’s face proximate the nasolabial sulci, and wherein an at least lly anterior wall of the nasal portion of the seal-forming P1419NZ4 structure comprises two lateral support ns, each of the lateral support portions being spaced apart laterally, each of the lateral support portions having a higher resistance to deformation relative to an adjacent portion of the seal-forming structure.

In examples of the two ing s, (a) each of the lateral support portions may be thicker than the adjacent n of the seal-forming structure, (b) each of the lateral support portions may have a curved superior boundary, each of the l support portions may be substantially fin-shaped, (c) the nasal portion of the seal-forming structure may comprise a central portion configured to seal in use against an inferior periphery of the patent’s nose surrounding the patient’s nares and t the patient’s lip superior, the central portion being thinner than the lateral support portions, (d) the nasal portion of the seal-forming structure may comprise intermediate portions provided between the central portion and the lateral support portions, the intermediate portions being thicker than the central portion, (e) the intermediate portions may be thinner than the l support portions, (f) the shell may comprise iorly ding portions configured to reinforce the seal-forming structure at a base of the nasal portion in use, and/or (g) the seal-forming structure may be configured not to engage the patient’s face below the chin in use.

An aspect of the present technology is directed to a patient interface comprising: a plenum chamber comprising: a seal-forming structure; and a shell; and a positioning and stabilising structure, n the shell comprises two lateral t portions protruding in a superior ion into an at least partially anterior wall of a nasal portion of the seal-forming structure, each of the lateral support portions being spaced apart laterally.

An aspect of the present technology is directed to a patient interface comprising: a plenum r pressurisable to a therapeutic re of at least 6 cmH2O above ambient air pressure throughout a patient’s respiratory cycle in use, the plenum chamber having an oral portion and a nasal portion, the plenum chamber comprising: a seal-forming structure constructed and ed to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, said nasal n of the seal-forming structure having at least one nasal hole configured to deliver a flow of air at said therapeutic pressure to an entrance to the patient’s nares in P1419NZ4 use, said oral portion of the seal-forming ure having an oral hole ured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s mouth in use, the seal-forming ure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the patient’s respiratory cycle in use; and a shell configured to support the seal-forming structure, the shell having one or more plenum chamber inlet ports sized and structured to receive the flow of air at the eutic pressure for breathing by a patient throughout the patient’s respiratory cycle in use; and a positioning and stabilising structure configured to generate a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, wherein the shell comprises two lateral support portions protruding in a superior direction into an at least lly anterior wall of the nasal portion of the seal-forming structure, each of the lateral support portions being spaced apart laterally.

In examples of the two preceding aspects, (a) each of the lateral support portions may have a curved superior boundary, (b) a curvature of the curved superior boundary may ntially match or substantially follow a curvature of a superior periphery of the seal-forming structure, (c) the shell may comprise two plenum chamber inlet ports, and/or (d) a or boundary of each of the two plenum r inlet ports may be formed by a respective one of the lateral support portions.

An aspect of the present technology is directed to a patient interface comprising: a plenum chamber comprising: one or more walls; a seal-forming structure; and one or more plenum chamber inlet ports; a positioning and stabilising structure, wherein the seal-forming structure comprises a l portion configured to seal t an inferior periphery of the patient’s nose in use, and wherein the seal- forming structure comprises intermediate portions configured to contact the ala of the patient’s nose in use, the intermediate portions having a r stiffness than the central portion.

An aspect of the present technology is directed to a patient interface comprising: a plenum chamber for a patient interface, the plenum chamber being pressurisable to a therapeutic pressure of at least 6 cmH2O above ambient air pressure throughout a patient’s respiratory cycle in use, the plenum r comprising: one P1419NZ4 or more walls at least lly enclosing a volume of space; a seal-forming structure constructed and arranged to form a seal with a region of the t’s face surrounding an ce to the patient’s airways, the seal-forming structure comprising a nasal n having at least one nasal hole configured to deliver a flow of air at said therapeutic pressure to an entrance to the patient’s nares in use, the seal-forming structure comprising an oral portion having an oral hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s mouth in use, the seal- forming structure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the patient’s respiratory cycle in use; and one or more plenum chamber inlet ports sized and structured to receive the flow of air at the therapeutic re for breathing by the patient throughout the patient’s respiratory cycle in use, a positioning and stabilising structure configured to generate a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, wherein the orming structure comprises a central portion configured to seal against an inferior periphery of the t’s nose in use, and wherein the seal- g structure comprises intermediate portions configured to contact the ala of the patient’s nose in use, the intermediate portions having a greater stiffness than the central portion.

In examples of the two preceding aspects, (a) the intermediate portions may comprise a pair of exterior walls of the seal-forming structure facing in partially medial and partially superior directions, (b) the intermediate ns may be configured to resist creasing, (c) the intermediate portions may be configured to limit creases from forming leak paths past the inferior periphery of the patient’s nose to ambient, (d) the intermediate portions may be thicker than the central portion, and/or (e) the seal-forming structure may be configured not to engage the t’s face below the chin in use.

An aspect of the present technology is directed to a patient ace comprising: a plenum chamber comprising: one or more walls; a seal-forming structure; and one or more plenum r inlet ports sized and ured to receive a flow of air at the therapeutic pressure for breathing by the patient throughout the patient’s respiratory cycle in use; and a positioning and stabilising structure, wherein P1419NZ4 the seal-forming ure comprises l peripheral support portions provided at opposite lateral sides of an oral hole, the lateral peripheral support portions being adjacent to an oral hole eral portion, and the lateral peripheral support portions being r the oral hole peripheral portion.

An aspect of the present technology is directed to a patient interface comprising: a plenum chamber for a patient interface, the plenum chamber being risable to a therapeutic pressure of at least 6 cmH2O above t air pressure hout a patient’s respiratory cycle in use throughout a patient’s respiratory cycle in use, the plenum chamber comprising: one or more walls at least partially enclosing a volume of space; a seal-forming structure constructed and arranged to form a seal with a region of the t’s face surrounding an entrance to the t’s s, the seal-forming structure comprising a nasal portion having at least one nasal hole configured to deliver a flow of air at said therapeutic pressure to an entrance to the patient’s nares in use, the seal-forming structure comprising an oral portion having an oral hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s mouth in use, the seal-forming structure constructed and arranged to maintain said therapeutic pressure in the plenum r throughout the patient’s respiratory cycle in use; and one or more plenum chamber inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by the patient throughout the t’s respiratory cycle in use; and a positioning and stabilising structure configured to generate a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, wherein the seal-forming structure comprises an oral hole peripheral portion surrounding at least a ty of the oral hole configured to surround the patient’s mouth in use, and wherein the seal- forming structure comprises lateral peripheral support portions provided at opposite lateral sides of the oral hole, the lateral peripheral support portions being adjacent to the oral hole peripheral portion, and the lateral peripheral support portions being stiffer the oral hole peripheral portion.

In examples of the two preceding s, (a) the lateral peripheral support portions may be thicker than the oral hole peripheral portion, (b) the seal-forming structure may comprise posterior-facing l portions surrounding a majority of the P1419NZ4 oral hole peripheral portion, the ior-facing lateral portions being thicker than the oral hole peripheral portion, (c) the posterior-facing lateral portions may extend medially towards lateral-most edges of the oral hole to form the lateral peripheral support portions, and/or (d) the seal-forming structure may be configured not to engage the patient’s face below the chin in use.

An aspect of the present logy is directed to a plenum chamber for a patient interface comprising: one or more walls; one or more plenum chamber inlet ports; and a seal-forming ure; and a positioning and stabilising structure, wherein the seal-forming structure comprises a nasal portion configured to seal against an inferior periphery of the patient’s nose in use, the nasal n having a central portion configured to be located inferior to the t’s pronasale in use and intermediate portions configured to t the patient’s corresponding ala in use, the ediate portions being r than the central portion.

An aspect of the present technology is directed to a plenum chamber for a patient interface, the plenum chamber being pressurisable to a therapeutic pressure of at least 6 cmH2O above t air pressure throughout a t’s atory cycle in use, the plenum chamber sing: one or more walls at least partially enclosing a volume of space; one or more plenum chamber inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by the patient throughout the patient’s respiratory cycle in use; and a seal-forming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, the seal-forming structure comprising a nasal portion having at least one nasal hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s nares in use, the seal-forming structure comprising an oral portion having an oral hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s mouth in use, the seal-forming structure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the patient’s atory cycle in use; and a oning and stabilising structure configured to generate a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, wherein the seal-forming structure comprises a nasal portion configured to seal against an inferior periphery of the patient’s nose in use, the nasal portion having a central portion configured to be located inferior to the patient’s pronasale in use and intermediate portions configured to contact the patient’s corresponding ala in use, the intermediate portions being stiffer than the central portion.

In examples of the two preceding aspects, (a) the intermediate portions of the seal-forming structure may be r than the central portion, (b) the central portion of the seal-forming ure may comprise an anterior-facing central portion and a superior-facing l portion, (c) each of the intermediate portions may comprise a or-facing intermediate portion and an anterior-facing intermediate portion, and the anterior-facing central portion may be thinner than the anterior-facing intermediate portions, (d) sides of the nasal portion may be configured to be drawn inwards towards the patient’s nasal ala when a downwards force is exerted on the central portion by the patient’s nose, and/or (e) seal-forming structure may be configured not to engage the patient’s face below the chin in use.

An aspect of the present technology is directed to a patient interface comprising: a plenum chamber comprising: one or more walls; one or more plenum chamber inlet ports; and a seal-forming structure; and a positioning and stabilising structure, wherein the seal-forming structure comprises a nasal n ured to seal against an inferior periphery of the patient’s nose, the nasal portion of the seal- forming ure having a pair of nasal holes configured to deliver the flow of air to the patient’s ponding nares in use, the orming structure comprising a bridge portion between the pair of nasal holes, the bridge portion being provided n a central portion of the nasal portion that is configured to be positioned or to the patient’s pronasale in use and a lip superior portion of the nasal portion that is configured to seal against the patient’s lip superior in use, the bridge portion being slack to allow movement of the central portion away from the lip superior portion in use.

An aspect of the t technology is directed to a patient interface comprising: a plenum chamber for a patient interface, the plenum chamber being pressurisable to a eutic pressure of at least 6 cmH2O above ambient air pressure throughout a patient’s respiratory cycle in use, the plenum chamber comprising: one P1419NZ4 or more walls at least partially enclosing a volume of space; one or more plenum chamber inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by a patient throughout the patient’s respiratory cycle in use; and a seal-forming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, the seal-forming structure sing a nasal portion having at least one nasal hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s nares in use, the seal-forming structure comprising an oral portion having an oral hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s mouth in use, the seal-forming structure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the patient’s respiratory cycle in use; and a positioning and stabilising structure configured to generate a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, wherein the seal-forming structure comprises a nasal portion configured to seal against an or periphery of the patient’s nose, the nasal portion of the seal-forming structure having a pair of nasal holes configured to deliver the flow of air to the patient’s ponding nares in use, the seal-forming structure sing a bridge portion between the pair of nasal holes, the bridge portion being provided between a central portion of the nasal portion that is ured to be positioned or to the patient’s pronasale in use and a lip superior n of the nasal portion that is configured to seal against the patient’s lip superior in use, the bridge portion being slack to allow movement of the central portion away from the lip superior portion in use.

In examples of the two preceding aspects, (a) the bridge portion comprises a curved portion configured to hten when the central portion moves away from the lip superior portion, (b) in use, the curved n may be ured to extend away from the patient’s nose in an undeformed state and is ured to straighten when the central n is moved away from the lip superior portion, and/or (c) in use, the bridge portion may enable the central portion to move in an anterior direction relative to the patient to receive the pronasale of the patient to accommodate different nose lengths t disengaging the lip superior portion from the t’s lip superior when the patient dons the patient interface.

P1419NZ4 An aspect of the present logy is directed to a plenum chamber for a patient ace comprising: one or more plenum chamber inlet ports; and a sealforming structure, wherein a first surface of a nasal portion configured to engage the patient’s face has a first surface finish and a second surface of an oral portion has a second surface finish that is different from the first surface finish.

An aspect of the present technology is directed to a plenum chamber for a t interface, the plenum chamber pressurisable to a therapeutic pressure of at least 6 cmH2O above ambient air pressure throughout a patient’s respiratory cycle in use, the plenum r comprising: one or more plenum chamber inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by a patient; and a seal-forming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, the seal- forming structure sing a nasal portion having at least one nasal hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s nares in use, the seal-forming structure comprising an oral portion having an oral hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the t’s mouth in use, the seal-forming structure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the t’s respiratory cycle in use, wherein a first surface of the nasal portion configured to engage the patient’s face has a first surface finish and a second surface of the oral n has a second surface finish that is different from the first surface finish.

In examples of the two preceding aspects, (a) the first surface finish and the second surface finish may differ in such a way that a coefficient of friction between the seal-forming structure and the patient’s face is greater in the oral portion than in the nasal n, (b) the first surface finish may be configured to provide the nasal portion with a smooth feel on the patient’s face, (c) the second surface finish may be configured to provide the oral portion with added grip on the patient’s face, (d) the first surface finish may be a d e finish, (e) the second surface finish may be a polished surface finish, (f) a boundary between the first surface finish and the second surface finish may be located on a part of the seal-forming structure P1419NZ4 configured to contact the patient’s cheeks in use, and/or (e) the seal-forming structure is configured not to engage the patient’s face below the chin in use.

An aspect of the present technology is directed to a patient interface comprising: a plenum chamber according to any one of the preceding s or examples thereof; a positioning and stabilising structure configured to generate a force to hold the orming structure in a therapeutically effective position on the patient’s head, the positioning and stabilising structure comprising a tie, the tie being constructed and arranged so that at least a portion overlies a region of the patient’s head superior to an otobasion superior of the patient’s head in use; and a vent structure configured to allow a continuous flow of gases exhaled by the patient from an interior of the plenum chamber to ambient, said vent structure being sized and shaped to maintain the therapeutic pressure in the plenum chamber in use, wherein the patient interface is configured to allow the patient to breath from ambient through their mouth in the e of a flow of rised air through the one or more plenum chamber inlet ports.

According to an aspect of the present technology, there is ed a plenum chamber for a patient interface, the plenum r pressurisable to a eutic pressure of at least 6 cmH2O above ambient air pressure, the plenum chamber having an oral portion and a nasal portion, the plenum chamber comprising: a seal-forming ure constructed and arranged to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, said seal-forming structure having one or more holes therein such that the flow of air at said therapeutic pressure is red to an entrance to the patient’s nares and to the patient’s mouth via the one or more holes, the seal-forming structure constructed and arranged to maintain said therapeutic re in the plenum r throughout the patient’s atory cycle in use; a shell having one or more plenum chamber inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by a patient the shell supporting the seal-forming structure, wherein the shell is provided to the oral portion of the plenum chamber, and ntially the entire nasal portion is formed by the seal-forming structure; and wherein the seal-forming structure comprises lateral support portions located on laterally-spaced, at least partially P1419NZ4 anterior-facing sides of the nasal portion, the lateral support portions having a higher resistance to deformation in use in comparison to one or more adjacent portions of the seal-forming structure.

According to another aspect of the present technology, there is provided a plenum chamber for a patient interface, the plenum chamber risable to a therapeutic pressure of at least 6 cmH2O above ambient air pressure, the plenum chamber having an oral portion and a nasal portion, the plenum chamber comprising: a seal-forming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, said seal-forming structure having one or more holes therein such that the flow of air at said therapeutic pressure is delivered to an entrance to the t’s nares and to the patient’s mouth via the one or more holes, the seal-forming structure constructed and ed to maintain said therapeutic pressure in the plenum chamber throughout the patient’s respiratory cycle in use; n substantially the entire nasal portion is formed by the seal-forming structure; and wherein the seal-forming structure comprises lateral support portions located on laterally-spaced, at least partially or-facing sides of the nasal portion, the lateral support portions having a higher resistance to deformation in use in comparison to one or more adjacent portions of the seal-forming structure.

In examples: the l t portions are portions of the seal-forming ure having a relatively greater stiffness in ison to one or more adjacent portions of the seal-forming structure; the lateral support portions are portions of the seal-forming structure supported by a support structure; the t structure is a portion of a frame or a clip-on support; the lateral support portions comprise portions of the orming structure having relatively greater thickness in comparison to one or more adjacent portions of the seal-forming structure; the lateral t portions are provided substantially directly superior to portions the shell; the lateral support portions each have a substantially flat inferior boundary; the flat inferior boundary is provided adjacent a superior edge of the shell; the l t portions each have a curved or boundary. Curvature of the superior boundary substantially matches P1419NZ4 or follows curvature of a superior ery of the seal-forming structure; the lateral support ns are substantially fin-shaped.

In examples: the seal-forming structure comprises a central portion ured to form a seal to an inferior periphery of the patent’s nose surrounding the patient’s nares and to the patient’s lip superior in use, the central portion having a lesser thickness than the lateral support portions; the orming structure comprises intermediate portions provided between the central portion and the lateral support portions, the seal-forming structure having a r thickness in the intermediate portions than in the central portion; the seal-forming structure comprises a lesser thickness in the intermediate portions than in the lateral support portions; the sealforming structure comprises lateral-facing posterior portions provided between respective intermediate portions and lateral support portions on each side of the nasal portion, the seal-forming structure having a greater thickness in the posterior l facing portions than in the intermediate portions; at least part of each intermediate n is provided superior and anterior to a respective lateral support portion; at least part of each lateral-facing posterior portion is ed or and posterior to a respective lateral support portion.

In examples: the seal-forming structure comprises, on each lateral side of the nasal portion, a junction n a respective lateral support portion, intermediate portion and lateral-facing posterior portion, the junction being located proximate a superior-most point of the lateral support portion; the junction is located anterior to the or-most point of the lateral support portion.

In examples: the central n of the seal-forming ure comprises an anterior-facing central n and a superior-facing central portion; the superiorfacing central portion and anterior-facing central portion being connected to each other by a central saddle region of the nasal portion of the seal-forming structure; the superior facing central portion has a positive curvature in a lateral direction, sides of the superior-facing central portion facing in a partially medial direction.

In es: the intermediate portions each comprise a or-facing central portion and an or-facing l portion; the superior-facing central P1419NZ4 portion and anterior-facing central portion are connected to each other over a or periphery of the seal-forming structure; the nasal portion comprises a lip superior portion configured to seal against the lip superior of the patient in use; the lip superior portion has a stiffness similar to a stiffness of the central portion; the lip or portion has a wall thickness substantially equal to that of the central portion; the lip or portion comprises a wall thickness lesser than a wall thickness of the intermediate portions.

In examples: the nasal portion comprises posterior s configured to lie on the patients face proximate nasolabial sulci on the patient’s face; the posterior corners are configured to contact the patient’s face on respective lateral sides of the lip or; the posterior s are configured to contact the patient’s face proximate an area lateral and or to the nasal ala; the posterior corners are configured to fit n the t’s nasal ala and the patient’s nasolabial sulci.

In examples: the posterior corners have a stiffness r than a stiffness of the central portion of the nasal portion of the seal-forming structure; the posterior s have a wall thickness greater than that of the intermediate portions of the nasal portion; the posterior corners have a wall thickness lesser than the lateral-facing posterior portions of the nasal n; the posterior corners are substantially domeshaped ; the transition between the posterior corners and the lip superior portion is configured to be located inferior to the patient’s nasal ala in use.

In examples: the shell comprises posteriorly protruding portions reinforcing the seal-forming structure at a base of the nasal portion; the posteriorly protruding portions are provided at superior lateral corners of the shell; the posterior pointing portions are provided inferior to the lateral support portions; the posterior pointing portions have a flat superior edge; a flat or boundary of each l support portions is provided adjacent each posterior pointing portion.

In examples: the oral portion comprises a lip or portion configured to form a seal to the lip inferior of the patient, the lip or portion having a wall thickness substantially equal to that of the lip superior portion; the oral portion comprises an oral hole peripheral portion, the oral hole peripheral portion comprising P1419NZ4 a wall thickness substantially equal to lip superior portion; the oral hole peripheral portion is contiguous with either or both of the lip superior portion and the lip inferior portion; the oral portion comprises ior-facing lateral portions provided to either lateral side of the oral hole peripheral portion configured to seal against the patient’s cheeks in use; the posterior-facing lateral portions comprise a wall thickness greater than that of the oral hole peripheral portion; the posterior-facing lateral portions curve away from contact with the patient’s face; the lip inferior portion is approximately half the width of the oral opening; the transitions between the lip or portion and the posterior-facing lateral portions on either lateral side of the lip inferior portion are configured to lie at or proximate labiomandibular s of the patient’s face; the lip inferior portion is wider at the periphery of the oral hole than at the lower periphery of the seal-forming structure.

In examples: the oral portion comprises lateral portions at the lateral ery of the seal forming structure; the lateral ns comprise a wall thickness greater than that of the posterior-facing lateral portions; the oral portion comprises anterior-facing lateral portions on the anterior side of the seal-forming structure; the anterior-facing lateral ns comprise a greater wall ess than that of the lateral portions; the oral portion comprises or support portions on the anterior side of the seal-forming structure; the anterior support portions comprise a greater wall thickness than that of the or-facing lateral ns; the oral portion comprises two anterior support portions ate superior lateral corners of the shell; the oral n comprises two anterior support portions proximate inferior lateral corners of the shell.

In examples: the plenum chamber ses a single plenum r inlet port; the single plenum chamber inlet port is provided centrally in the shell; the plenum chamber inlet port is configured to connect to a frame; the plenum chamber inlet port is ntially circular.

According to r aspect of the present technology there is provided a plenum chamber for a patient interface, the plenum chamber pressurisable to a therapeutic pressure of at least 6 cmH2O above ambient air pressure, the plenum chamber having an oral portion and a nasal portion, the plenum chamber comprising: P1419NZ4 a seal-forming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, said seal-forming structure having one or more holes therein such that the flow of air at said therapeutic re is delivered to an entrance to the patient’s nares and to the patient’s mouth via the holes, the seal-forming structure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the t’s respiratory cycle in use; a shell configured to support the seal-forming structure, the shell having one or more plenum chamber inlet ports sized and structured to e a flow of air at the therapeutic pressure for breathing by a patient; wherein the shell comprises lateral support portions protruding in a superior direction into the nasal portion of the patient interface on laterally-spaced, at least partially anterior-facing sides of the nasal portion.

In examples: the lateral support portions each have a curved superior boundary; curvature of the superior ry substantially matches or follows curvature of a superior periphery of the seal-forming structure; the lateral t portions are substantially fin-shaped.

In examples: the plenum chamber comprises two plenum chamber inlet ports; the plenum chamber inlet ports are provided to lateral sides of the shell; the plenum r inlet ports are configured to connect to conduits; the plenum chamber inlet ports are approximately elliptical; the or periphery of each of the two plenum chamber inlet ports is formed by a tive one of the lateral support portions.

According to another aspect of the t technology there is provided a plenum chamber for a patient interface, the plenum chamber being pressurisable to a therapeutic re of at least 6 cmH2O above ambient air pressure, the plenum chamber comprising: one or more walls at least partially enclosing a volume of space; a seal-forming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an ce to the patient’s airways, said seal-forming structure having one or more holes therein such that the flow of air at said therapeutic pressure is delivered to an entrance to the patient’s nares and to the t’s mouth via the one or more holes, the seal-forming structure constructed and arranged to P1419NZ4 maintain said therapeutic pressure in the plenum chamber throughout the patient’s respiratory cycle in use, one or more plenum chamber inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by a patient; wherein the seal-forming structure comprises a central portion configured to seal to an or periphery of the patient’s nose surrounding the t’s nares and to the patient’s lip superior in use, and intermediate portions configured to be located against or proximate the ala of the patient’s nose in use, the intermediate portions having a greater stiffness than the central portion.

In examples: the one or more walls may comprise some or all of the sealforming structure; the one or more walls may be separate to the seal-forming structure; the intermediate portions comprise a pair of exterior walls of the sealforming structure facing in partially medial and partially or directions; the intermediate portions are configured to resist creasing; the intermediate portions are configured to limit creases from forming leak paths past the inferior periphery of the patient’s nose to ambient. ing to another aspect of the present technology there is ed a plenum chamber for a patient interface, the plenum r being pressurisable to a therapeutic pressure of at least 6 cmH2O above ambient air pressure, the plenum chamber comprising: one or more walls at least partially ing a volume of space; a seal-forming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, said orming structure having at least one hole therein such that the flow of air at said eutic pressure is delivered to an ce to the patient’s nares and to the patient’s mouth via the at least one hole, the seal-forming ure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the patient’s respiratory cycle in use; one or more plenum chamber inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by a patient; wherein the seal-forming structure comprises an oral hole eral n surrounding at least a majority of an oral hole configured to surround the patient’s mouth in use, and lateral eral support portions provided at opposite lateral sides of the oral hole, P1419NZ4 the lateral peripheral support portions having a stiffness r than a stiffness of the oral hole peripheral n.

In es: the l peripheral support portions comprise a wall thickness greater than a wall thickness of the oral hole peripheral portion; the sealforming structure comprises posterior-facing lateral portions surrounding a majority of the oral hole peripheral portion, the posterior-facing lateral ns having a thickness greater than the oral hole peripheral portion; the posterior-facing lateral portions form the lateral peripheral support portions. The posterior-facing lateral portions extend medially towards the lateral-most edges of the oral hole to form the lateral peripheral t ns; the lateral support portions provide resistance to buckling in the seal forming structure.

According to another aspect of the present logy there is provided a plenum chamber for a patient interface, the plenum chamber being risable to a therapeutic pressure of at least 6 cmH2O above ambient air pressure, the plenum chamber comprising: one or more walls at least partially enclosing a volume of space; one or more plenum chamber inlet ports sized and ured to receive a flow of air at the therapeutic pressure for breathing by a patient; a seal-forming structure constructed and ed to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, said seal-forming structure having one or more holes therein such that the flow of air at said therapeutic pressure is delivered to an entrance to the patient’s nares and to the patient’s mouth via the one or more holes, the seal-forming structure constructed and arranged to maintain said therapeutic pressure in the plenum chamber hout the patient’s respiratory cycle in use; n the seal-forming structure comprises a nasal portion configured to form a seal to an inferior periphery of the patient’s nose in use, the nasal portion having a central portion configured to be located inferior to the patient’s ale in use and intermediate ns configured to be located proximate to the patient’s ala in use, the seal-forming structure having a greater stiffness in the intermediate portions than in the l portion.

In examples: the intermediate portions of the seal-forming structure comprise a greater wall thickness than the central portion; the intermediate portions P1419NZ4 may each comprise a medially-facing wall configured to be lie at or proximate the nasal ala of the patient in use; the central n of the seal-forming structure comprises an or-facing central portion and a or-facing central portion; the or-facing central portion and anterior-facing central portion being ted to each other by a central saddle region of the nasal portion of the seal-forming structure; the superior facing central portion comprises a positive curvature in a lateral direction, sides of the or-facing central portion facing in a partially medial direction; the intermediate portions each comprise a superior-facing central portion an anteriorfacing central portion; the superior-facing central portion and anterior-facing central portion are connected to each other overall a superior periphery of the seal-forming structure; the central saddle portion comprises an equal wall thickness to the central portion; the anterior-facing central portion comprises a lesser wall thickness than the anterior-facing intermediate portions; when a downwards force is d on the central portion from the patient’s nose, the sides of the nasal portion are drawn inwards towards the patient’s nasal ala; the intermediate ns are drawn inwards to lie at or proximate the patient’s ala; the nasal portion comprises a lip superior portion configured to seal against the lip superior of the patient in use; the lip superior portion ses a stiffness similar to a stiffness of the central n; the lip superior portion comprises a wall thickness substantially the equal to a wall thickness of the central portion; the lip superior portion ses a wall thickness lesser than a wall thickness of the intermediate portions.

According to another aspect of the present technology there is provided a plenum chamber for a patient interface, the plenum chamber being pressurisable to a therapeutic pressure of at least 6 cmH2O above t air pressure, the plenum chamber having comprising: one or more walls at least partially enclosing a volume of space; one or more plenum chamber inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by a patient; a seal-forming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an entrance to the t’s airways, said seal-forming structure having a plurality of holes therein such that the flow of air at said therapeutic re is delivered to an entrance to the patient’s nares and to the patient’s mouth via the plurality of holes, the seal-forming structure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the patient’s respiratory cycle in use; wherein the plenum chamber comprises a nasal portion and the seal-forming structure in the nasal portion is configured to seal to an inferior periphery of the patient’s nose, the orming structure defining a pair of nasal holes configured in use to deliver the flow of air to the t’s nasal airways, the seal-forming structure comprising a bridge portion between the pair of nasal holes, the bridge portion being ed centrally n a central portion and a lip superior portion of the sealforming structure in the nasal portion, the bridge portion being slack to allow movement of the l portion away from the posterior region.

In examples: the bridge portion comprises a curved portion configured to straighten when the central portion moves away from the lip superior portion; the curved portion comprises a single curve; the curved portion ses two curves; the curved portion is approximately S-shaped when viewed from a lateral direction; the curved portion comprises a sawtooth shape; the curved portion comprises one or more folds; the bridge portion hangs or to the central portion and is able to straighten while the central portion moves away from the lip superior portion; the bridge portion enables the central portion to move to receive the patient’s nose when the patient dons the patient interface; the bridge portion enables the central portion to move in an anterior direction to e the pronasale of the patient when the patient dons the patient interface.

According to another aspect of the present technology there is provided a plenum chamber for a t ace, the plenum chamber pressurisable to a therapeutic pressure of at least 6 cmH2O above ambient air pressure, the plenum r comprising: one or more plenum r inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by a patient; a sealforming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an ce to the patient’s airways, said seal-forming structure having one or more holes therein such that the flow of air at said therapeutic pressure is delivered to an entrance to the patient’s nares and to the patient’s mouth via the one or more holes, the seal-forming structure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the patient’s P1419NZ4 respiratory cycle in use; wherein the seal-forming structure comprises a nasal portion configured to form a seal to the patient’s face at or ate the patient nose, and an oral portion configured to form a seal to the patient’s face around the patient’s mouth, the seal-forming structure having a first surface finish in the nasal portion and a second surface finish in the oral portion different from the first surface finish.

In examples: the first surface finish and the second surface finish differ in such a way that a coefficient of on between the seal-forming structure and the patient’s face is greater in the oral portion than in the nasal portion; the first surface finish is configured to provide the nasal portion with a smooth feel on the patient’s face (e.g. for t); the second surface finish is configured to provide the oral portion with grippy contact on the patient’s face (e.g. for a more robust seal); the first surface finish may be a frosted surface finish; the second surface finish may be a polished surface finish; a boundary between the first surface finish and the second surface finish may be d on a part of the seal-forming ure in contact with the patient’s cheeks in use; the nasal portion may comprise a lip superior portion having the first surface finish; non-patient contacting surfaces of the nasal portion may comprise a surface finish other than the first surface ; the non-patient contacting es of the nasal portion may comprise the second surface .

According to another aspect of the present technology, there is provided a patient interface comprising: a plenum chamber according to an aspect of the present technology bed above; a positioning and ising structure to provide a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, the positioning and ising structure comprising a tie, the tie being constructed and ed so that at least a portion overlies a region of the patient’s head superior to an otobasion superior of the patient’s head in use; and a vent structure to allow a continuous flow of gases exhaled by the patient from an interior of the plenum chamber to ambient, said vent ure being sized and shaped to maintain the therapeutic pressure in the plenum chamber in use; wherein the patient ace is configured to allow the patient to breath from ambient through their mouth in the absence of a flow of pressurised air through the plenum chamber inlet port.

P1419NZ4 Another aspect of one form of the present technology is a patient interface that is d or otherwise constructed with a perimeter shape which is complementary to that of an intended wearer.

An aspect of one form of the present logy is a method of manufacturing apparatus.

An aspect of certain forms of the present logy is a medical device that is easy to use, e.g. by a person who does not have medical training, by a person who has limited dexterity, vision or by a person with limited experience in using this type of l device.

An aspect of one form of the t technology is a portable RPT device that may be carried by a person, e.g., around the home of the .

An aspect of one form of the present technology is a patient interface that may be washed in a home of a patient, e.g., in soapy water, without requiring specialised cleaning equipment. An aspect of one form of the present technology is a humidifier tank that may be washed in a home of a patient, e.g., in soapy water, without requiring lised cleaning equipment.

The s, systems, devices and apparatus described may be implemented so as to improve the functionality of a processor, such as a processor of a specific purpose computer, respiratory monitor and/or a respiratory therapy apparatus. Moreover, the described methods, systems, devices and apparatus can provide improvements in the technological field of ted management, monitoring and/or treatment of respiratory conditions, including, for example, sleep disordered breathing.

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 aspects or sub-aspects of the t technology.

P1419NZ4 Other features of the logy will be apparent from consideration of the information contained in the following detailed description, abstract, drawings and claims. 4 BRIEF DESCRIPTION OF THE DRAWINGS The present technology is illustrated by way of example, and not by way of limitation, in the figures of the anying drawings, in which like reference numerals refer to similar elements including: 4.1 TREATMENT SYSTEMS Fig. 1A shows a system ing a t 1000 wearing a patient interface 3000, in the form of nasal pillows, receiving a supply of air at positive pressure from an RPT device 4000. Air from the RPT device 4000 is humidified in a humidifier 5000, and passes along an air circuit 4170 to the patient 1000. A bed partner 1100 is also shown. The patient is sleeping in a supine sleeping position.

Fig. 1B shows a system including a patient 1000 g a patient interface 3000, in the form of a nasal mask, receiving a supply of air at positive pressure from an RPT device 4000. Air from the RPT device is humidified in a humidifier 5000, and passes along an air circuit 4170 to the patient 1000.

Fig. 1C shows a system including a patient 1000 wearing a patient interface 3000, in the form of a ace mask, receiving a supply of air at positive pressure from an RPT device 4000. Air from the RPT device is humidified in a humidifier 5000, and passes along an air circuit 4170 to the patient 1000. The patient is ng in a side sleeping position. 4.2 ATORY SYSTEM AND FACIAL ANATOMY Fig. 2A shows an overview of a human respiratory system including the nasal and oral cavities, the larynx, vocal folds, oesophagus, trachea, bronchus, lung, alveolar sacs, heart and diaphragm.

Fig. 2B shows a view of a human upper airway including the nasal cavity, nasal bone, lateral nasal cartilage, greater alar cartilage, nostril, lip superior, lip P1419NZ4 or, larynx, hard palate, soft palate, oropharynx, tongue, epiglottis, vocal folds, agus and trachea.

Fig. 2C is a front view of a face with several es of e anatomy identified including the lip superior, upper vermilion, lower vermilion, lip inferior, mouth width, endocanthion, a nasal ala, nasolabial sulcus and cheilion. Also indicated are the directions superior, inferior, radially inward and ly outward.

Fig. 2D is a side view of a head with l features of e anatomy identified including glabella, sellion, pronasale, subnasale, lip or, lip inferior, supramenton, nasal ridge, alar crest point, otobasion superior 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. The coronal plane is also indicated.

Fig. 2F shows a base view of a nose with several es identified including naso-labial sulcus, lip inferior, upper Vermilion, naris, subnasale, lla, pronasale, the major axis of a naris and the midsagittal plane.

Fig. 2G shows a side view of the superficial features of a nose.

Fig. 2H shows subcutaneal structures of the nose, including lateral cartilage, septum cartilage, greater alar cartilage, lesser alar cartilage, sesamoid cartilage, nasal bone, epidermis, adipose tissue, frontal process of the maxilla and fibrofatty tissue.

Fig. 2I shows a medial dissection of a nose, approximately several millimeters from the midsagittal 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, nasal and zygomatic bones. Nasal concha are indicated, as are the maxilla, and mandible.

P1419NZ4 Fig. 2K shows a lateral view of a skull with the outline of the surface of a head, as well as several muscles. The ing bones are shown: frontal, sphenoid, nasal, zygomatic, maxilla, mandible, parietal, temporal and occipital. The mental protuberance is indicated. The following muscles are shown: digastricus, masseter, sternocleidomastoid and trapezius.

Fig. 2L shows an anterolateral view of a nose. 4.3 PATIENT INTERFACE Fig. 3A shows a t interface in the form of a nasal mask in accordance with one form of the present technology.

Fig. 3B shows a schematic of a cross-section h a structure at a point. An d normal at the point is indicated. The curvature at the point has a positive sign, and a relatively large magnitude when compared to the magnitude of the curvature shown in Fig. 3C.

Fig. 3C shows a schematic of a cross-section through a structure at a point. An d normal at the point is indicated. The curvature at the point has a positive sign, and a relatively small magnitude when compared to the magnitude of the curvature shown in Fig. 3B.

Fig. 3D shows a schematic of a cross-section through a structure at a point. An outward normal at the point is indicated. The curvature at the point has a value of zero.

Fig. 3E shows a schematic of a cross-section through a structure at a point. An d normal at the point is indicated. The curvature at the point has a negative sign, and a relatively small ude when compared to the ude of the curvature shown in Fig. 3F.

Fig. 3F shows a schematic of a cross-section through a structure at a point.

An outward normal at the point is indicated. The curvature at the point has a negative sign, and a relatively large magnitude when ed to the magnitude of the curvature shown in Fig. 3E.

P1419NZ4 Fig. 3G shows a cushion for a mask that includes two pillows. An exterior surface of the cushion is indicated. An edge of the surface is indicated. Dome and saddle regions are indicated.

Fig. 3H shows a cushion for a mask. An exterior e of the n is indicated. An edge of the surface is indicated. A path on the surface between points A and B is indicated. A straight line distance between A and B is indicated. Two saddle regions and a dome region are indicated.

Fig. 3I shows the surface of a structure, with a one dimensional hole in the surface. The rated plane curve forms the boundary of a one dimensional hole.

Fig. 3J shows a cross-section h the structure of Fig.3I. The illustrated surface bounds a two dimensional hole in the structure of Fig. 3I.

Fig. 3K shows a perspective view of the structure of Fig. 3I, including the two dimensional hole and the one dimensional hole. Also shown is the surface that bounds a two dimensional hole in the structure of Fig. 3I.

Fig. 3L shows a mask having an inflatable bladder as a cushion.

Fig. 3M shows a cross-section through the mask of Fig. 3L, and shows the interior surface of the bladder. The interior surface bounds the two dimensional hole in the mask.

Fig. 3N shows a further section through the mask of Fig. 3L. The interior surface is also indicated.

Fig. 3O illustrates a left-hand rule.

Fig. 3P illustrates a right-hand rule.

Fig. 3Q shows a left ear, including the left ear helix.

Fig. 3R shows a right ear, ing the right ear helix.

Fig. 3S shows a right-hand helix.

P1419NZ4 Fig. 3T shows a view of a mask, including the sign of the torsion of the space curve defined by the edge of the sealing membrane in different regions of the mask.

Fig. 3U shows a view of a plenum chamber 3200 showing a sagittal plane and a mid-contact plane.

Fig. 3V shows a view of a posterior of the plenum chamber of Fig. 3U.

The direction of the view is normal to the mid-contact plane. The sagittal plane in Fig. 3V bisects the plenum r into left-hand and right-hand sides.

Fig. 3W shows a cross-section through the plenum chamber of Fig. 3V, the cross-section being taken at the sagittal plane shown in Fig. 3V. A ‘mid-contact’ plane is shown. The mid-contact plane is perpendicular to the sagittal plane. The orientation of the mid-contact plane corresponds to the orientation of a chord 3209 which lies on the sagittal plane and just touches the cushion of the plenum chamber at two points on the sagittal plane: a superior point 3220 and an inferior point 3229.

Depending on the geometry of the cushion in this , the mid-contact plane may be a tangent at both the superior and inferior points.

Fig. 3X shows the plenum chamber 3200 of Fig. 3U in position for use on a face. The sagittal plane of the plenum chamber 3200 lly coincides with the midsagittal plane of the face when the plenum chamber is in position for use. The mid-contact plane corresponds generally to the ‘plane of the face’ when the plenum chamber is in position for use. In Fig. 3X the plenum chamber 3200 is that of a nasal mask, and the superior point 3220 sits approximately on the n, while the inferior point 3229 sits on the lip superior. 4.4 RPT DEVICE Fig. 4A shows an RPT device in accordance with one form of the t technology.

Fig. 4B is a schematic diagram of the pneumatic path of an RPT device in ance with one form of the present technology. The ions of upstream and downstream are indicated with reference to the blower and the patient interface. The P1419NZ4 blower is defined to be upstream of the patient ace and the t interface is defined to be downstream of the blower, regardless of the actual flow direction at any particular moment. Items which are located within the pneumatic path between the blower and the patient interface are downstream of the blower and upstream of the patient interface. 4.5 HUMIDIFIER Fig. 5A shows an isometric view of a humidifier in accordance with one form of the present logy.

Fig. 5B shows an isometric view of a humidifier in accordance with one form of the present technology, showing a humidifier reservoir 5110 removed from the humidifier reservoir dock 5130. 4.6 BREATHING WAVEFORMS Fig. 6A shows a model typical breath waveform of a person while sleeping. 4.7 PATIENT INTERFACE EXAMPLES OF THE PRESENT TECHNOLOGY Fig. 7 is a front view of a plenum chamber 3200 in accordance with one form of the present technology.

Fig 8 is a rear view of the plenum chamber 3200 of Fig. 7.

Fig 9 is a side view of the plenum r 3200 of Fig. 7.

Fig 10 is a top view of the plenum chamber 3200 of Fig. 7.

Fig 11 is a bottom view of the plenum chamber 3200 of Fig. 7.

Fig 12 is a perspective view of the plenum chamber 3200 of Fig. 7.

Fig 13 is another ctive view of the plenum chamber 3200 of Fig. 7.

Fig 14 is another ctive view of the plenum chamber 3200 of Fig. 7.

P1419NZ4 Fig. 15 is a front view of the plenum r 3200 of Fig. 7 with cross section lines 16-16 to 19-19 labelled.

Fig. 16 is a cross section view of the plenum chamber 3200 of Fig. 15 along the line 16-16.

Fig. 17 is a cross section view of the plenum chamber 3200 of Fig. 15 along the line 17-17.

Fig. 18 is a cross section view of the plenum chamber 3200 of Fig. 15 along the line 18-18.

Fig. 19 is a cross section view of the plenum chamber 3200 of Fig. 15 along the line 19-19.

Fig. 20 is a rear view of the plenum r 3200 of Fig. 7 with cross section lines 21-21 to 25-25 labelled.

Fig. 21 is a cross section view of the plenum chamber 3200 of Fig. 20 along the line 21-21.

Fig. 22 is a cross section view of the plenum chamber 3200 of Fig. 20 along the line 22-22.

Fig. 23 is a cross section view of the plenum chamber 3200 of Fig. 20 along the line 23-23.

Fig. 24 is a cross section view of the plenum chamber 3200 of Fig. 20 along the line 24-24.

Fig. 25 is a cross section view of the plenum chamber 3200 of Fig. 20 along the line 25-25.

Fig. 26 is a side view of the plenum chamber 3200 of Fig. 7 with cross section lines 27-27 to 33-33 labelled.

P1419NZ4 Fig. 27 is a cross section view of the plenum chamber 3200 of Fig. 26 along the line 27-27.

Fig. 28 is a cross section view of the plenum r 3200 of Fig. 26 along the line 28-28.

Fig. 29 is a cross section view of the plenum chamber 3200 of Fig. 26 along the line 29-29.

Fig. 30 is a cross section view of the plenum chamber 3200 of Fig. 26 along the line 30-30.

Fig. 31 is a cross section view of the plenum chamber 3200 of Fig. 26 along the line 31-31.

Fig. 32 is a cross section view of the plenum chamber 3200 of Fig. 26 along the line 32-32.

Fig. 33 is a cross section view of the plenum chamber 3200 of Fig. 26 along the line 33-33.

Fig. 34 is a rear view of another plenum chamber 3200 having various portions fied.

Fig. 35 is a front view of the plenum r 3200 of Fig. 34 having various portions identified.

Fig. 36 is a top view of the plenum chamber 3200 of Fig. 34 having various portions identified.

Fig. 37 is a bottom view of the plenum chamber 3200 of Fig. 34 having various portions identified.

Fig. 38 is a side view of the plenum chamber 3200 of Fig. 34 having various portions identified.

P1419NZ4 Fig. 39 is a view of another plenum chamber 3200 in accordance with one form of the present technology.

Fig. 40 is a cross section view of the plenum r 3200 of Fig. 39.

Fig. 41 is a front view of the shell 3210 of the plenum chamber 3200 of Fig. 7.

Fig. 42 is a rear view of the shell 3210 of the plenum r 3200 of Fig. 7.

Fig. 43 is a side view of the shell 3210 of the plenum chamber 3200 of Fig. 7.

Fig. 44 is a front perspective view of the shell 3210 of the plenum chamber 3200 of Fig. 7.

Fig. 45 is a rear perspective view of the shell 3210 of the plenum chamber 3200 of Fig. 7.

Fig. 46 is a top view of the shell 3210 of the plenum chamber 3200 of Fig.

Fig. 47 is a rear view of another plenum chamber 3200 in accordance with one form of the present technology.

Fig. 48 is a rear view of r plenum chamber 3200 in accordance with one form of the present technology having various portions identified.

Fig. 49 is a front view of a plenum chamber 3200 in accordance with one form of the present technology.

Fig 50 is a rear view of the plenum chamber 3200 of Fig. 49.

Fig 51 is a side view of the plenum chamber 3200 of Fig. 49.

Fig 52 is a top view of the plenum chamber 3200 of Fig. 49.

P1419NZ4 Fig 53 is a bottom view of the plenum chamber 3200 of Fig. 49.

Fig 54 is a perspective view of the plenum chamber 3200 of Fig. 49.

Fig 55 is r perspective view of the plenum chamber 3200 of Fig.

Fig 56 is another ctive view of the plenum chamber 3200 of Fig.

Fig. 57 is a front view of the plenum chamber 3200 of Fig. 49 with cross section lines 58-58 to 61-61 labelled.

Fig. 58 is a cross section view of the plenum chamber 3200 of Fig. 57 along the line 58-58.

Fig. 59 is a cross section view of the plenum chamber 3200 of Fig. 57 along the line 59-59.

Fig. 60 is a cross section view of the plenum chamber 3200 of Fig. 57 along the line 60-60.

Fig. 61 is a cross section view of the plenum chamber 3200 of Fig. 57 along the line 61-61.

Fig. 62 is a rear view of the plenum r 3200 of Fig. 49 with cross section lines 63-63 to 67-67 labelled.

Fig. 63 is a cross section view of the plenum chamber 3200 of Fig. 62 along the line 63-63.

Fig. 64 is a cross section view of the plenum chamber 3200 of Fig. 62 along the line 64-64.

Fig. 65 is a cross section view of the plenum chamber 3200 of Fig. 62 along the line 65-65.

P1419NZ4 Fig. 66 is a cross n view of the plenum chamber 3200 of Fig. 62 along the line 66-66.

Fig. 67 is a cross section view of the plenum chamber 3200 of Fig. 62 along the line 67-67.

Fig. 68 is a side view of the plenum chamber 3200 of Fig. 49 with cross n lines 69-69 to 75-75 labelled.

Fig. 69 is a cross n view of the plenum chamber 3200 of Fig. 68 along the line 69-69.

Fig. 70 is a cross section view of the plenum chamber 3200 of Fig. 68 along the line 70-70.

Fig. 71 is a cross section view of the plenum chamber 3200 of Fig. 68 along the line 71-71.

Fig. 72 is a cross section view of the plenum chamber 3200 of Fig. 68 along the line 72-72.

Fig. 73 is a cross section view of the plenum chamber 3200 of Fig. 68 along the line 73-73.

Fig. 74 is a cross section view of the plenum chamber 3200 of Fig. 68 along the line 74-74.

Fig. 75 is a cross section view of the plenum chamber 3200 of Fig. 68 along the line 75-75.

Fig. 76 is a rear view of another plenum chamber 3200 in accordance with one form of the present technology having various portions identified.

Fig. 77 is a front view of the plenum chamber 3200 of Fig. 76 having various portions identified.

P1419NZ4 Fig. 78 is a top view of the plenum chamber 3200 of Fig. 76 having various portions identified.

Fig. 79 is a bottom view of the plenum r 3200 of Fig. 76 having various portions identified.

Fig. 80 is a side view of the plenum chamber 3200 of Fig. 76 having various ns identified.

Fig. 81 is a front view of the shell 3210 of the plenum chamber 3200 of Fig. 49.

Fig. 82 is a rear view of the shell 3210 of the plenum chamber 3200 of Fig. 49.

Fig. 83 is a side view of the shell 3210 of the plenum chamber 3200 of Fig. 49.

Fig. 84 is a front perspective view of the shell 3210 of the plenum chamber 3200 of Fig. 49.

Fig. 85 is a rear perspective view of the shell 3210 of the plenum chamber 3200 of Fig. 49.

Fig. 86 is a top view of the shell 3210 of the plenum chamber 3200 of Fig.

Fig. 87 is a cross section view of a connection between a plenum chamber 3200 and a frame 3350 in accordance with one form of the present logy.

Fig. 88 is another cross-section view of the connection between the plenum chamber 3200 and the frame 3350.

Fig. 89 is a perspective view of a patient interface 3000 according to one example of the t technology.

Fig. 90 is a front view of the patient interface 3000 of Fig. 89.

P1419NZ4 Fig. 97A is a cross section view of the patient interface 3000 shown in Fig. 90 through the line 90A-90A.

Fig. 91 is a back view of the patient interface 3000 of Fig. 89.

Fig. 92 is a top view of the t interface 3000 of Fig. 89.

Fig. 93 is a bottom view of the patient interface 3000 of Fig. 89.

Fig. 94 is a side view of the patient interface 3000 of Fig. 89.

Fig. 95 is another back view of the patient interface 3000 of Fig. 89.

Fig. 96 is a perspective view of the t interface 3000 of Fig. 89 while worn by a patient.

Fig. 97 is a front view of the patient interface 3000 of Fig. 89 while worn by a patient.

Fig. 98 is a back view of the t interface 3000 of Fig. 89 while worn by a patient.

Fig. 99 is a top view of the patient interface 3000 of Fig. 89 while worn by a patient.

Fig. 100 is a bottom view of the patient interface 3000 of Fig. 89 while worn by a patient.

Fig. 101 is a side view of the patient ace 3000 of Fig. 89 while worn by a patient.

Fig. 102 is another back view of the patient interface 3000 of Fig. 89 while worn by a patient.

Fig. 103 is a perspective view of a frame 3350 according to one example of the present technology.

P1419NZ4 Fig. 104 is a front view of the frame 3350 of Fig. 103.

Fig. 105 is a back view of the frame 3350 of Fig. 103.

Fig. 106 is a top view of the frame 3350 of Fig. 103.

Fig. 107 is a bottom view of the frame 3350 of Fig. 103.

Fig. 108 is a side view of the frame 3350 of Fig. 103.

Fig. 109 is view of straps of the positioning and ising structure 3300 of the t interface 3000 of Fig. 89.

Fig. 110 is a cross section view of the plenum chamber 3200 of the patient interface 3000 of Fig. 89 in sealing position on a patient.

Fig. 111 is a cutaway view of the plenum chamber 3200 of the patient interface 3000 of Fig. 89 in sealing position on a patient.

Fig. 112 is a cross section view of a n of the plenum chamber 3200 of the patient interface 3000 of Fig. 89 before sealing to the nose of a t.

Fig. 113 is a cross section view of the portion of the plenum chamber 3200 of Fig. 112 in sealing position against the nose of a patient.

Fig. 114 is a cross section view of a n of the plenum chamber 3200 of the patient interface 3000 of Fig. 89 in sealing on against the nose of a patient without lateral loading.

Fig. 115 is a cross section view of the portion of the plenum chamber 3200 of Fig. 113 in sealing position against the nose of a patient while receiving lateral loading.

Fig. 116 is a rear view of a plenum chamber 3200 having various portions identified and having creases in a nasal portion 3230 of the plenum chamber 3200.

P1419NZ4 Fig. 117 is a side cross section view of the plenum chamber 3200 of the patient interface 3000 in isolation while in sealing position against the face of a patient having a short nose.

Fig. 118 is a side cross section view of the plenum chamber 3200 of Fig. 117 while in sealing position t the face of a t having a long nose.

Fig. 119 is a perspective view of a plenum chamber 3200 in accordance with another form of the present technology.

Fig. 120 is a front view of the plenum chamber 3200 shown in Fig. 119.

Fig. 121 is a rear view of the plenum r 3200 shown in Fig. 119.

Fig. 122 is a top view of the plenum chamber 3200 shown in Fig. 119.

Fig. 123 is a bottom view of the plenum chamber 3200 shown in Fig. 119.

Fig. 124 is a left side view of the plenum chamber 3200 shown in Fig.

Fig. 125 is a right side view of the plenum chamber 3200 shown in Fig.

Fig. 126 is a front perspective view of a plenum chamber 3200 according to another example of the present technology having a small size.

Fig. 127 is a rear perspective view of the plenum chamber 3200 shown in Fig. 126.

Fig. 128 is a front view of the plenum chamber 3200 shown in Fig. 126.

Fig. 129 is a rear view of the plenum chamber 3200 shown in Fig. 126.

Fig. 130 is a top view of the plenum r 3200 shown in Fig. 126.

Fig. 131 is a bottom view of the plenum chamber 3200 shown in Fig. 126.

Fig. 132 is a side view of the plenum chamber 3200 shown in Fig. 126.

P1419NZ4 Fig. 133 is a cross section view of the plenum chamber 3200 shown in Fig. 130 through the line 133-133.

Fig. 134 is a front perspective view of a plenum chamber 3200 according to r example of the present technology having a medium size.

Fig. 135 is a rear perspective view of the plenum chamber 3200 shown in Fig. 134.

Fig. 136 is a top view of the plenum chamber 3200 shown in Fig. 134.

Fig. 137 is a bottom view of the plenum chamber 3200 shown in Fig. 134.

Fig. 138 is a front view of the plenum chamber 3200 shown in Fig. 134.

Fig. 139 is a rear view of the plenum chamber 3200 shown in Fig. 134.

Fig. 140 is a side view of the plenum chamber 3200 shown in Fig. 134.

Fig. 141 is a cross section view of the plenum chamber 3200 shown in Fig. 136 though the line 141-141.

Fig. 142 is a front perspective view of a plenum chamber 3200 according to r example of the present technology having a small-wide size.

Fig. 143 is a rear perspective view of the plenum chamber 3200 shown in Fig. 142.

Fig. 144 is a top view of the plenum chamber 3200 shown in Fig. 142.

Fig. 145 is a bottom view of the plenum r 3200 shown in Fig. 142.

Fig. 146 is a front view of the plenum chamber 3200 shown in Fig. 142.

Fig. 147 is a rear view of the plenum chamber 3200 shown in Fig. 142.

Fig. 148 is a side view of the plenum chamber 3200 shown in Fig. 142.

P1419NZ4 Fig. 149 is a cross section view of the plenum chamber 3200 shown in Fig. 144 through the line 149-149.

Fig. 150 is a front perspective view of a plenum chamber 3200 according to another example of the present technology having a wide size.

Fig. 151 is a rear perspective view of the plenum chamber 3200 shown in Fig. 150.

Fig. 152 is a top view of the plenum chamber 3200 shown in Fig. 150.

Fig. 153 is a bottom view of the plenum chamber 3200 shown in Fig. 150.

Fig. 154 is a front view of the plenum r 3200 shown in Fig. 150.

Fig. 155 is a rear view of the plenum chamber 3200 shown in Fig. 150.

Fig 156 is a side view of the plenum chamber 3200 shown in Fig. 150.

Fig. 157 is a cross section view of the plenum chamber 3200 shown in Fig. 152 through the line 157-157.

Fig. 158 is a side view of the plenum chamber 3200 shown in Fig. 126 having various portions identified.

Fig. 159 is a bottom perspective view of the plenum chamber 3200 shown in Fig. 126 having various portions identified.

Fig. 160 is a top view of the plenum chamber 3200 shown in Fig. 126 having various ns identified.

Fig. 161 is a rear view of the plenum chamber 3200 shown in Fig. 126 having various portions identified.

Fig. 162 is a front view of the plenum r 3200 shown in Fig. 126 having various portions identified.

P1419NZ4 Fig. 163 is a front perspective view of the plenum chamber 3200 shown in Fig. 126 having various portions identified.

Fig. 164 is a rear perspective view of the plenum chamber 3200 shown in Fig. 126 having various portions identified.

Fig. 165 is a side view of the plenum chamber 3200 shown in Fig. 134 having various portions identified.

Fig. 166 is a bottom view of the plenum chamber 3200 shown in Fig. 134 having various portions identified.

Fig. 167 is a top view of the plenum chamber 3200 shown in Fig. 134 having s portions identified.

Fig. 168 is a rear view of the plenum r 3200 shown in Fig. 134 having various portions identified.

Fig. 169 is a front perspective view of the plenum r 3200 shown in Fig. 134 having various portions identified.

Fig. 170 is a rear ctive view of the plenum chamber 3200 shown in Fig. 134 having various portions identified.

Fig. 171 is a front view of the plenum chamber 3200 shown in Fig. 134 having various portions identified.

Fig. 172 is a side view of the plenum chamber 3200 shown in Fig. 142 having various portions identified.

Fig. 173 is a bottom ctive view of the plenum chamber 3200 shown in Fig. 142 having various portions identified.

Fig. 174 is a top view of the plenum chamber 3200 shown in Fig. 142 having various portions identified.

P1419NZ4 Fig. 175 is a rear view of the plenum chamber 3200 shown in Fig. 142 having various portions identified.

Fig. 176 is a front view of the plenum chamber 3200 shown in Fig. 142 having various portions identified.

Fig. 177 is a side view of the plenum chamber 3200 shown in Fig. 150 having s portions identified.

Fig. 178 is a bottom view of the plenum chamber 3200 shown in Fig. 150 having various portions identified.

Fig. 179 is a top view of the plenum r 3200 shown in Fig. 150 having s portions fied.

Fig. 180 is a rear view of the plenum chamber 3200 shown in Fig. 150 having s portions identified.

Fig. 181 is a front view of the plenum chamber 3200 shown in Fig. 150 having various portions identified.

Fig. 182 is a front perspective view of the plenum chamber 3200 shown in Fig. 150 having s portions identified.

Fig. 183 is a rear perspective view of the plenum chamber 3200 shown in Fig. 150 having various portions identified.

Fig. 184 is a perspective view of a patient interface 3000 according to another example of the present technology.

Fig. 185 is a perspective view of a patient interface 3000 according to another e of the present technology.

DETAILED DESCRIPTION OF EXAMPLES OF THE TECHNOLOGY 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 P1419NZ4 herein, which may vary. It is also to be understood that the ology used in this sure is for the purpose of describing only the particular examples discussed herein, and is not intended to be limiting.

The ing description is provided in relation to various examples which may share one or more common characteristics and/or features. It is to be understood that one or more features of any one example may be combinable with one or more features of another example or other examples. In addition, any single feature or combination of features in any of the examples may constitute a further example.

Where anatomical directional terms are used in describing aspects and examples of the present technology, such as "anterior", "posterior", "superior", "inferior", al", "medial" and the like, the directions are to be d in the context of the present technology during use by a patient. For example, an anterior side of a patient ace refers to the side of the t interface which is anterior with respect to the patient when the patient has donned the patient interface in the intended manner.

Where surfaces or portions are described as facing a direction, e.g. "superior-facing", "anterior-facing" and the like, unless the context clearly es ise the surfaces or portions are to be understood as at least partially facing in the particular direction. A portion may be "superior-facing" if the portion generally faces a superior direction, even if it partially also faces another direction. .1 THERAPY In one form, the present technology comprises a method for ng a respiratory disorder comprising the step of ng positive pressure to the entrance of the airways of a patient 1000.

In certain examples of the present technology, a supply of air at positive pressure is provided to the nasal passages of the patient via one or both nares.

In certain examples of the present technology, mouth breathing is limited, restricted or prevented.

P1419NZ4 .2 TREATMENT SYSTEMS In one form, the present technology comprises an apparatus or device for treating a respiratory disorder. The apparatus or device may comprise an RPT device 4000 for supplying pressurised air to the t 1000 via an air circuit 4170 to a patient interface 3000. .3 PATIENT INTERFACE A non-invasive t interface 3000 in accordance with one aspect of the present technology comprises the following functional aspects: a plenum chamber 3200 comprising a seal-forming structure 3100, a positioning and stabilising structure 3300, a vent 3400, one form of connection port 3600 for tion to air t 4170, and a forehead support 3700. 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-forming structure 3100 is arranged to surround an entrance to the airways of the patient so as to facilitate the supply of air at positive pressure to the airways.

In some examples of the present technology, the plenum chamber 3200 is at least partially formed by a shell 3210 and the seal-forming structure 3100. The plenum chamber 3200 may comprise a cushion module or cushion assembly, for e. The shell 3210 may on as a chassis for the seal-forming structure 3100.

The t interface 3000 in some examples of the technology is an oronasal patient interface. That is, the patient interface 3000 is configured to seal around both the patient’s nasal airways and oral airway. In some examples the t interface 3000 comprises separate seals around each of the nasal airways and oral airway. The patient interface 3000 may comprise a plenum chamber 3200 having a nasal portion 3230 and an oral portion 3260, as shown in Figs. 7 to 14, 49 to 56, 119 to 125 and 126 to 157, for e. The seal g structure may be ured to nd the nasal airways at the nasal portion 3230 and to seal around the patient’s mouth at the oral portion 3260. As such, the seal-forming structure 3100 may also be considered to have a nasal portion and an oral portion, the nasal portions and oral P1419NZ4 portions of the seal-forming structure sing those parts that seal around the t’s nasal s and mouth tively.

In the examples shown in Figs. 7 to 14, 49 to 56, 119 to 125 and 126 to 157, the seal-forming structure 3100 at the nasal portion 3230 does not lie over a nose bridge region or nose ridge region of the patient’s face and instead seals against inferior surfaces of the patient’s nose. The nasal portion 3230 may seal against the lip or, the ala and the anterior surface of the pronasale and/or the inferior surface of the pronasale. The actual sealing locations may differ between patients. The nasal portion 3230 may also be configured to contact and/or seal to a region of the patient’s face between the ala and the nasolabial sulcus and at the lateral portions of the lip superior proximate the nasolabial sulcus.

The seal-forming structure 3100 of the oral portion 3260 may be configured to form a seal to a ery of the patient’s mouth in use. The oral portion 3260 may be configured to form a seal to the patient’s face at the lip superior, nasolabial sulcus, cheeks, lip inferior, supramenton, for example.

The seal-forming structure 3100 may have one or more holes n such that the flow of air at a therapeutic pressure is delivered to the patient’s nares and to the patient’s mouth via the one or more holes. The seal-forming structure may define an oral hole and one or more nasal holes to deliver the flow of air to the patient. In the es shown in Figs. 7 to 14, 49 to 56, 119 to 125 and 126 to 157, the plenum chamber 3200 comprises a seal-forming structure 3100 comprising an oral hole 3271 and two nasal holes 3272. Each of the nasal holes 3272 may be positioned on the plenum chamber 3200 to be substantially aligned with a nare of the t in order to deliver a flow of air thereto in use.

If a patient interface is unable to comfortably deliver a minimum level of positive pressure to the airways, the patient interface may be unsuitable for respiratory pressure y.

The patient interface 3000 in accordance with one form of the present technology is constructed and arranged to be able to provide a supply of air at a positive re of at least 6 cmH2O with respect to ambient.

P1419NZ4 The patient ace 3000 in accordance with one form of the present logy is constructed and arranged to be able to provide a supply of air at a positive pressure of at least 10 cmH2O with respect to ambient.

The patient ace 3000 in accordance with one form of the t technology is constructed and arranged to be able to provide a supply of air at a positive pressure of at least 20 cmH2O with t to ambient. .3.1 Plenum chamber The plenum chamber 3200 has a perimeter that is shaped to be complementary to the surface contour of the face of an average person in the region where a seal will form in use. In the examples shown in Figs. 7 to 14, 49 to 56, 119 to 125 and 126 to 157 the plenum chamber comprises a shell 3210 and a seal-forming structure 3100. In these examples a marginal edge of the plenum chamber 3200 is positioned in close ity to an adjacent surface of the face. Actual contact with the face is provided by the orming structure 3100. The seal-forming structure 3100 may extend in use about the entire perimeter of the plenum chamber 3200. In some forms, the plenum r 3200 and the seal-forming structure 3100 are formed from a single homogeneous piece of material.

In certain forms of the present technology, the plenum chamber 3200 does not cover the eyes of the patient in use. In other words, the eyes are outside the pressurised volume defined by the plenum chamber. Such forms tend to be less obtrusive and/or more table for the wearer, which can improve compliance with therapy.

In certain forms of the present technology, a portion of the plenum chamber 3200 is constructed from a transparent material, e.g., a transparent polycarbonate. In the examples shown in Figs. 7 to 14, 49 to 56, 119 to 125 and 126 to 157, the shell 3210 is constructed from transparent polycarbonate. The use of a transparent material can reduce the obtrusiveness of the patient interface, and help improve compliance with therapy. The use of a transparent al can aid a clinician to observe how the patient interface is located and functioning. In some examples, the shell 3210 may be formed from silicone.

P1419NZ4 In certain forms of the present technology, the plenum chamber 3200 is constructed from a translucent al. The use of a translucent material can reduce the obtrusiveness of the patient interface, and help improve compliance with therapy.

Figs. 7 to 47, 49 to 75, and 119 to 183 show plenum chambers 3200 according to examples of the present technology which are formed partially by a shell 3210. Additionally, the plenum r 3200 is formed partially by the seal-forming structure 3100. In some examples the seal-forming structure 3100 is overmoulded to the shell 3210. The seal-forming structure 3100 may alternatively be formed separately from the shell 3210 and be configured to permanently or removably connect to the shell 3210. The seal-forming structure 3100 and shell 3210 may be integrally formed.

In the examples shown in Figs. 7 to 47, 49 to 75 and 119 to 183, the shell 3210 is formed from polycarbonate and the seal-forming structure 3100 is formed from silicone. The silicone may have a Shore A hardness of 30 or 40 Durometer. A silicone or similar material with this hardness is advantageous for t and flexibility to conform and seal to the patient’s face. The use of polycarbonate (or other stiffer material), with its higher ss and stiffness than silicone is advantageous in providing portions of higher resistance to deformation with less material than would be required to e the same resistance with silicone. Using less material can be advantageous in keeping overall bulk and weight down, which may reduce obtrusiveness to the user. In alternative examples the shell 3210 may be formed from nylon or polypropylene. The orming structure 3100 may alternatively be formed from silicone, a suitable foam or any suitable thermoplastic elastomer.

As shown in Figs. 40-46, the shell 3210 may have posteriorly protruding portions 3215 at superior lateral corners of the shell 3210. The posteriorly ding portions 3215 may rce a base of the nasal portion and may help e stability to the seal-forming structure 3100. The posteriorly ding portions 3215 also help reinforce the locations of the seal-forming structure proximate ior corners 3131 (shown in Figs. 10 and 52, among others) which also support the nasal portion of the plenum chamber on the patient’s face, and also advantageously fit into the patient’s nasolabial sulci. The ior protruding portions 3215 may protrude from the shell P1419NZ4 3210 towards the location of the patient’s nasolabial sulcus or the patient’s cheeks alongside the nasolabial sulcus. The ior protruding portions 3215 may be provided inferior to lateral support portions 3151 ibed below). .3.1.1 Lateral Support Portions In some examples of the present technology, the plenum chamber 3200 comprises lateral support portions 3151 on the anterior side of the nasal portion 3230 of the plenum chamber 3200, as shown in Figs. 18, 19, 32, 35, and 38, among others.

The lateral support portions 3151 may have a higher ance to deformation than one or more adjacent ns of the seal-forming structure 3100. The lateral support portions 3151 may be stiffer than regions of the plenum r 3200 superior to lateral t portions 3151. Additionally, or alternatively, the lateral support portions 3151 may be stiffer than a central region of the plenum chamber 3200. The regions of relatively greater stiffness may be in the form of fins configured to provide areas of relatively high rigidity in comparison to nding areas of the plenum chamber. The seal-forming structure 3100 shown in Figs. 34 to 38 ses lateral t portions 3151 n. Additionally, the plenum chamber 3200 shown in Figs. 49 to 56 comprises lateral support portions 3151 in the shell 3210. The shell 3210 of the plenum chamber 3200 of Figs. 49 to 56 is shown in isolation in Figs. 81-86. As shown, the lateral support portions 3151 are formed by superior lateral portions of the shell 3210 itself.

The lateral support portions 3151 may assist in providing lateral stability to the nasal portion 3230 of the plenum chamber 3200. In the examples of Figs. 7 to 38 the lateral support portions 3151 are provided to laterally-spaced, at least partially anterior-facing sides of the of the plenum chamber 3200. In particular, the lateral support portions 3151 are provided to the non-patient facing side (e.g., anterior side or at least partially anterior-facing sides) of the nasal portion 3230. In these examples one lateral support portion 3151 is provided on each l side of the plenum chamber 3200 to an at least partially anterior-facing wall. The plenum chamber 3200 is configured so that the lateral support ns 3151 are positioned in the sealforming structure 3100 approximately opposite the patient’s ala in use.

P1419NZ4 The lateral support portions 3151 may comprise regions of the plenum chamber 3200 having an increased material thickness relative to surrounding or adjacent areas. Alternatively, or additionally, the lateral support portions 3151 may be formed by a material stiffer than the material in surrounding or adjacent areas.

The lateral support portions 3151 may be substantially fin shaped (e.g. having a curved or boundary and a flatter inferior boundary). As shown in Figs. 34 to 38, the lateral support portions 3151 of the seal-forming structure 3100 comprise curved superior boundaries 3153 and r inferior boundaries 3152. Similarly, the lateral support portions 3151 of the shell 3210 as shown in Figs 49 to 56 have curved superior boundaries 3153 ugh in this example there are no distinct or boundaries of the lateral support portions 3151). A fin shape, in particular the provision of a curved superior boundary or edge, is ageous as the superior edge or boundary of the lateral support portion 3151 follows the curvature of the superior periphery 3232 of the nasal portion 3230. This provides a consistent height of the nasal portion 3230 above the shell 3210, which may be useful for providing consistent or controlled stiffness to the structure of the nasal portion 3230 (as discussed below).

Additionally, the curved superior boundaries 3153, rather than a flat boundary around the entire or side of the nasal n 3230, mean that the l anterior-facing portion of the nasal portion remains flexible to avoid excessive force on the patient’s pronasale.

The lateral support portions 3151 may control collapsibility of the anterior side of the plenum r 3200. The height (e.g., amount of or extension) of the lateral support portions 3151 may be ed to balance collapsibility with structural rigidity. A certain amount of flexibility in the structure of the seal-forming structure 3100 is desirable as it enables the seal-forming structure 3100 to odate a wide range of nose shapes and sizes. However, if the lateral support portions 3151 extend too far in the superior direction, the seal-forming structure 3100 may not be accommodating enough or may not be sufficiently comfortable. atively, if the lateral support ns 3151 do not extend far enough in the superior direction, then the seal-forming structure 3100 may be so prone to collapse P1419NZ4 that it may not be able to prevent blowout of the g engagement with the patient’s face.

Additionally, some flexibility in the overall structure of the seal-forming ure 3100 can be advantageous for accommodating long and/or narrow noses.

When the orming structure 3100 is moved upwards into t with the underside of a narrow nose, an amount of flexibility in the l structure of the nasal portion 3230 is desirable as it enables the lateral sides of the orming structure 3100 to be drawn inwards as a result of downwards force applied to the centre of the seal-forming structure 3100 by the patient’s nose. Figs. 112 and 113 show the seal-forming structure 1000 before and after being brought into sealing position with the nose of the patient 1000. As shown in Fig. 113, when the sealforming structure 3100 in the nasal portion 3230 is brought into contact with the patient’s nose, the outwardly-facing lateral sides of the seal-forming structure 3100 are pulled ly to assist the inwardly-facing lateral sides of the seal-forming structure 3100 to conform to the lower periphery of the patient’s nose. If there is insufficient flexibility in the lateral sides of the seal-forming structure 3100, the rming structure 3100 may be less accommodating to narrow noses and/or may be uncomfortable if the patient is required to tighten the headgear to compensate. Excess flexibility may result in the seal-forming structure 3100 being incapable of holding its shape and maintaining an effective seal.

The height of the lateral support portions 3151, should be appropriate to e sufficient structural rigidity to the nasal portion 3230 while remaining flexible enough to enable the seal-forming structure 3100 to seal comfortably to a wide range of noses. The lateral support portions 3151 may extend superiorly approximately 35- 65% of the height of the nasal portion 3230, such as 40-60% or 50%, in examples, of the distance between a base of the nasal portion 3230 on an anterior side of the plenum chamber 3200 and the most superior point of the plenum chamber 3200.

In other examples, the lateral support portions 3151 could be substituted by other stiffening/rigidising structures or features. In some examples, ribs are provided to the or or the exterior of the nasal n 3230 of the seal-forming structure 3100 generally in the locations of the l support portions 3151, to P1419NZ4 provide structural rigidity to the nasal portion 3230. In other examples, the lateral t portions 3151 may be rigidised. The seal-forming structure 3100 may comprise supportive inserts (e.g., rigidiser elements) provided to the lateral t portions 3151. In one example, the seal-forming structure 3100 may be overmoulded to one or more rigidiser ts to provide rigidity to the lateral t portions 3151.

In other examples, the plenum chamber 3200 may comprise an undercushion that provides the necessary support to the ure of the nasal portion 3230. The undercushion may be thicker than the face-contacting portions of the sealforming structure 3100, ng the patient-contacting walls to be thin for comfort and able to conform to the patient’s nose and face. r still, in some examples a separate component is provided to support the structure of the nasal portion 3230 of the seal-forming structure 3100. For example, a frame to which the plenum chamber 3200 connects may have portions that reinforce the seal-forming structure 3100 in the areas of the lateral support portions 3151. .3.1.1.1 Lateral support portions formed by seal-forming structure The plenum chamber 3200 shown in Figs. 7 to 40 comprises lateral support portions 3151 provided by the seal-forming structure 3100. The lateral support portions 3151 are provided to the anterior side of the plenum chamber 3200 and on each lateral side of the nasal portion 3230. In this example, the lateral support portions 3151 are provided at inferior regions of each lateral side of the nasal portion 3230.

At least a majority of the nasal portion 3230 is formed by the seal-forming structure 3100 in this example. The majority of the nasal n 3230 of the plenum chamber 3200 is formed from a soft, flexible resilient material. The majority of the nasal portion 3230 is formed from ne in this example. In the es of Figs. 7 to 33, substantially the entire nasal portion is formed by the orming structure 3100. In the examples of Figs. 49 to 75, portions of the nasal portion are formed by the shell 3210.

P1419NZ4 In these examples, the lateral support portions 3151 are regions of the seal-forming ure 3100 having relatively greater stiffness in comparison to one or more adjacent regions of the seal-forming structure 3100. In particular, the lateral support portions 3151 have a greater material thickness than regions of the sealforming ure 3100 superior to the lateral support portions 3151. This greater al thickness provides an amount of stiffness or structural ty to the ure of the seal-forming structure 3100 and in particular the nasal portion 3230. Much of the posterior side of the nasal portion 3230 has a low wall thickness for comfort and ability to seal against the patient’s face, which may not provide icant structural rigidity to the shape of the nasal portion 3230. The lateral support portions 3151 compensate for the lack of structural rigidity provided by the patient-contacting walls and increase the overall structural rigidity to the nasal portion 3230.

As shown in Figs. 35 and 38, the lateral support portions 3151 each se a substantially flat or boundary 3152. While the substantially flat inferior boundaries 3152 are approximately flat, they may still have a small amount of ure, for example due to some curvature being required for the base of the nasal portion to transition into the oral n 3260 of the plenum chamber 3200. Each flat or boundary 3152 may be adjacent a respective posteriorly protruding portion 3215 of the shell 3210. The lateral support portions 3151 each comprise a curved superior boundary 3153 in this example. Additionally, the curved superior boundaries 3153 may have a curvature which substantially matches or follows curvature of a superior periphery 3232 of the orming structure 3100 at the nasal portion 3230. .3.1.1.2 Lateral support portions formed by shell The plenum chambers 3200 shown in Figs. 49 to 75 and 126 to 157 each comprises lateral support portions 3151 provided by the shell 3210 of the plenum chamber 3200. Figs. 81-86 show the shell 3210 of the plenum chamber 3200 shown in Figs. 49 to 75 in isolation. The lateral t portions 3151 in these examples comprise superior portions of the shell 3210. The l support portions 3151 extend in a superior direction into the nasal portion 3230 of the plenum chamber 3200. The lateral support portions 3151 comprise portions of the shell 3210 provided to the nasal portion 3230 in these examples. While the shell 3210 has a generally flat top edge in P1419NZ4 the example shown in Figs. 7 to 33, the shell 3210 in the example shown in Figs. 49 to 75 and 81 to 86 comprises a curved top edge 3211 which comprises lateral support portions 3151 that extend in a superior direction to a greater extent than a central portion of the top edge 3211, g the two lateral support ns 3151. Each of the lateral support portions 3151 in these examples comprises a curved superior edge or boundary. The ure of each superior edge substantially matches or follows a curvature of a superior periphery 3232 of the seal-forming structure. The lateral support portions 3151 of the shell 3210 occupy s of the or and lateral facing sides of the nasal portion 3230 approximately opposite from the patient’s nasal ala in use.

The lateral support portions 3151 in the examples shown in Figs. 49 to 75 and 81 to 86 provide similar functions to the lateral support portions 3151 shown in the examples of Figs. 7 to 33. The l support portions 3151 provide structural ty to the nasal portion 3230 of the seal-forming structure 3100. Since the patientcontacting (posterior) side of the orming structure 3100 comprises relatively low thickness, flexible walls, the lateral support portions 3151 provide a level of structural rigidity to the nasal portion 3230. .3.1.2 Plenum chamber inlet port The shell 3210 may comprise one or more plenum chamber inlet ports 3240. The one or more plenum chamber inlet ports 3240 may allow for a connection to other components, such as a frame, decoupling structure, vent arrangement, heat and moisture exchanger (HMX), constant-flow vent (CFV), anti-asphyxia valve (AAV) and/or connection port to a conduit in various examples.

In the example shown in Figs. 7 to 14, the plenum chamber 3200 comprises a single inlet port 3240. The inlet port 3240 is ed ntially centrally in the shell 3210. The inlet port 3240 in this example may be configured to connect to a frame to which headgear or other positioning and stabilising structure components can be connected. The inlet port 3240 is substantially circular in this exemplary form of the technology.

P1419NZ4 In the examples shown in Figs. 49 to 56 and 126 to 183, the plenum chamber 3200 comprises two inlet ports 3240. The inlet ports 3240 are provided to lateral sides of the shell 3210. The inlet ports 3240 in these examples are configured to connect to conduits which connect to a decoupling component located above the patient’s head where the conduits are connected to the air circuit. The ts may form part of the positioning and stabilising ure 3300, i.e., they may be ear conduits". In some examples the inlet ports 3240 may receive combined headgear and conduit connection assemblies, in order to provide multiple functions such as g, supply of the flow of air and headgear attachment points. The combined headgear and conduit connection assemblies may also comprise an AAV. The inlet ports 3240 in these examples are approximately elliptically shaped, e.g., oval.

In some examples, the plenum chamber 3200 shown in Figs. 7-14 may be provided with one or two inlet ports 3240 on the lateral sides of the shell 3210 to connect with conduit headgear. It would be understood that any of the features described herein of seal-forming structures 3100 (including that of the plenum chamber 3200 shown in Fig. 7-48) may be incorporated in a patient interface including conduit headgear.

The superior ery of each inlet port 3240 in the examples shown in Figs. 49 to 56 is formed by a lateral support portion 3151 of the nasal portion 3230. In examples where the inlet ports 3240 connect to headgear conduits, this ageously enables the connections of the plenum r 3200 to the headgear conduits to be made in superior positions of the plenum chamber 3200. This may enable r conduits, more favourable force vectors and/or a smaller t int over the patient’s face, in comparison to inlet ports 3240 provided at inferior positions of the plenum chamber 3200.

In one example, the plenum chamber 3200 connects to a frame and is supported in front of the patient’s face via a positioning and stabilising structure 3300 (e.g. headgear). The connection to the frame may be a snap fit connection.

Alternatively, the connection may be a press fit, bayonet connection or other suitable connection.

P1419NZ4 In one example the frame 3350 comprises snap fit hooks 3351 that fit over a rim of the shell 3210. In some examples two snap fit hooks 3351 provided to the frame snap over a rim 3218 provided to the air inlet port 3240 of the plenum chamber 3200. Figure 87 is a cross section view of the tion between the frame 3350 and the plenum chamber 3200 in a ntal plane, showing horizontal snap fit hooks 3351 snapped over the rim 3218 of the air inlet port 3240. In this example, the two snap fit hooks 3351 are horizontally opposed across the air inlet port 3240. In other examples the arms are vertically opposed. Providing horizontally opposed snap fit arms (e.g., at 9 k and 3 o’clock positions around the air inlet 3240) may advantageously provide ance to disengagement when lateral forces are exerted on the plenum chamber 3200 or frame 3350. Figure 88 is a cross section view of the connection between the frame 3350 and the plenum chamber 3200 in a vertical plane, showing a lack of snap fit connections at the vertically opposed sides of the connection. Since the patient may sleep with their head on its side, the plenum r 3200 may be more likely to receive lateral forces in use than al forces.

Providing horizontally opposed snap fit connections means that the patient can rotate the plenum r 3200 upwards or downwards with respect to the frame 3350 to disassemble it, but that lateral forces on the plenum chamber 3200 during use may be unlikely to disengage plenum chamber 3200 from the frame. .3.1.3 Seal-forming structure In one form of the present technology, a seal-forming structure 3100 provides a target orming region, and may additionally provide a cushioning function. The target seal-forming region is a region on the orming structure 3100 where sealing may occur. The region where sealing actually occurs - the actual sealing surface - may change within a given treatment session, from day to day, and from patient to patient, depending on a range of factors including for example, where the t interface was placed on the face, tension in the positioning and stabilising structure and the shape of a patient’s face.

In one form the target seal-forming region is located on an outside surface of the seal-forming structure 3100.

P1419NZ4 In certain forms of the present technology, the seal-forming structure 3100 is constructed from a biocompatible material, e.g., liquid silicone rubber (LSR).

A seal-forming structure 3100 in ance with the present technology may be constructed from a soft, flexible, resilient al such as liquid silicone rubber (LSR).

In certain forms of the present technology, a system is provided comprising more than one seal-forming structure 3100, each being configured to correspond to a ent size and/or shape range. For e the system may comprise one form of a seal-forming structure 3100 le for a large sized head, but not a small sized head and another suitable for a small sized head, but not a large sized head. .3.1.3.1 Sealing isms In one form, the seal-forming structure 3100 includes a sealing flange utilizing a pressure assisted sealing mechanism. In use, the sealing flange can readily respond to a system positive pressure in the interior of the plenum chamber 3200 acting on its underside to urge it into tight sealing engagement with the face. The pressure assisted mechanism may act in ction with elastic tension in the positioning and stabilising structure.

In one form, the seal-forming structure 3100 comprises a sealing flange and a support flange. The sealing flange comprises a relatively thin member with a thickness of less than about 1mm, for example about 0.25mm to about 0.45mm, which extends around the perimeter of the plenum chamber 3200. Support flange may be vely thicker than the sealing flange. The support flange is disposed between the sealing flange and the marginal edge of the plenum chamber 3200, and s at least part of the way around the perimeter. The support flange is or includes a springlike element and functions to t the sealing flange from buckling in use.

In one form, the seal-forming structure may comprise a compression sealing portion or a gasket sealing portion. In use the ssion sealing portion, or P1419NZ4 the gasket sealing portion is constructed and arranged to be in compression, e.g. as a result of c tension in the positioning and stabilising structure.

In one form, the seal-forming structure comprises a tension portion. In use, the tension portion is held in tension, e.g., by adjacent regions of the sealing flange.

In one form, the seal-forming structure ses a region having a tacky or adhesive surface.

In certain forms of the present technology, a seal-forming structure may comprise one or more of a pressure-assisted sealing flange, a ssion sealing portion, a gasket g portion, a tension portion, and a portion having a tacky or adhesive surface. .3.1.3.2 Nasal region In certain forms of the present technology, the seal-forming structure 3100 comprises a central portion ured to form a seal to inferior surfaces of the patient’s nose. The central portion may seal to an inferior periphery of the patient’s nose (e.g., surrounding the t’s nares and to the patient’s lip or). In examples, the seal-forming structure 3100 may be configured to contact the patient’s face below the bridge of the nose or below the pronasale.

As shown in Figs. 34 to 80 and 158 to 183, the seal-forming structure 3100 comprises a central portion configured to seal to an inferior periphery of the patient’s nose in use and intermediate portions ured to be located against or proximate the ala of the patient’s nose in use. More particularly, the central portion includes a superior-facing central portion 3111 and an anterior-facing central portion 3115. Most or all of the t of the l portion with the patient’s nose is made by the superior-facing central portion 3111. Additionally, the intermediate portions comprise a superior-facing intermediate portion 3121 and an or facing intermediate portion 3125. Most or all of the contact of the intermediate portions with the patient’s nose is made by the superior-facing intermediate portion 3121.

P1419NZ4 It will be appreciated that the actual amount of contact made by the sealforming structure 3100 to the patient’s face will depend on the particular implementation of the present logy and the anatomy of a particular patient. The seal-forming structures 3100 of the plenum chambers 3200 shown in Figs. 4 (a small size plenum chamber 3200) and Figs. 165-171 (a medium size plenum chamber 3200) are configured for use by patients having nose shapes that are long and narrow.

In contrast, the seal forming structures 3100 of the plenum chambers 3200 shown in Figs. 172-176 (a wide size plenum r 3200) and Figs. 177-183 (a wide size plenum chamber 3200) are configured for use by patients having relatively short and wide noses. In the small and medium-sized plenum chambers 3200 shown in Figs. 158-171, a greater amount of contact may be made to lateral inferior surfaces of the patient’s nose by the superior-facing intermediate portions 3121 than in the small- wide and wide size plenum chambers 3200 shown in Figs. 172-183, since patients that use the small and -sized plenum chambers 3200 may generally have narrower noses and since the small and medium size plenum chambers 3200 may have a greater concavity in the nasal portion 3230 of the seal forming structure 3100. In each of these particular examples of the present logy, the superior facing central portion 3111 makes the majority of contact with the inferior surfaces of the patient’s nose.

The lip superior portion 3116 may also make significant contact with or surfaces of the patient’s nose along with the patient’s lip superior. In some examples a majority of the seal formed by the seal-forming surface 3100 to the inferior periphery of the patient’s nose may be made by the superior-facing central portion 3111 and lip superior portion 3116. The or-facing l portion 3111 and lip or portion 3116 may each comprise a lower stiffness than other ns of the seal forming structure 3100, which in some examples of the present technology is provided by a lower wall thickness than other portions of the seal forming structure 3100. The inferior surfaces of the patient’s nose and lip superior can have complex geometry and can also be very sensitive to pressure. Accordingly, it is advantageous for the areas of the plenum chamber 3200 that will contact or seal against these locations to be flexible and compliant, to avoid exerting excessive pressure on the face at these s. The low stiffness, which in these es is provided by a thin P1419NZ4 wall thickness in the central portion of the nasal portion 3230 of the seal-forming structure 3100 proximate the nasal holes 3272, enable the cushion to readily deform to seal against the surfaces on the underside of the patient’s nose, e.g., against the pronasale s the anterior direction, the nasal ala on either lateral side and the lip superior. Fig. 110 shows a cross section view of the plenum chamber 3200 in sealing contact with the lower periphery of the nose of a patient 1000. While the overall shape and ure of the outwardly-facing regions of the nasal portion 3230, such as the posterior corners 3131, anterior-facing intermediate portions 3125 and the anteriorfacing central portion 3115 is generally ined in use, the more flexible superiorfacing central portion 3111 is able to conform to the lower periphery of the patient’s nose.

The low wall thickness of the superior-facing central portion 3111 and lip superior portion 3116 also enables the seal-forming structure to e in these portions to conform to the ry of inferior surfaces and periphery of the patient’s nose. As shown in Fig. 110, the thin wall of the seal-forming structure 3100 in the superior-facing central portion 3111 and lip superior portion 3116 is ageous in creating a good seal to the complex geometry under and around the nose. The thin wall can deform and inflate under pressure, conforming to the surfaces of the patient’s face to create an effective and yet comfortable seal.

The superior-facing central region 3111 superior and anterior to the nasal holes 3272 of the orming structure is intended to seal against the inferior and partially anterior surfaces of the patient’s ale. This area of the seal-forming structure 3100 may be ed with a low wall thickness because the ale can be a relatively sensitive area to many ts. The central portion may extend from a superior-facing central portion 3111 on the posterior (i.e., patient facing) side of the cushion over a l saddle portion 3112 and peripheral edge and into an anteriorfacing l portion 3115 on the anterior (i.e., non-patient facing) side of the sealforming structure. A thin wall thickness in this region avoids exerting excessive pressure on the sensitive pronasale area.

A lip superior portion 3116 of the seal-forming structure 3100 is intended to seal against the lip or. The lip superior portion 3116 is provided centrally and inferior and ior to the nasal holes 3272. The lip superior portion 3116 may comprise a low wall stiffness. In some es the low wall ess is provided by a low wall thickness. Similarly to the area of the seal-forming structure 3100 intended to seal against the pronasale, a low wall thickness extends over the central inferior/posterior region of the nasal portion 3230 of the orming ure 3100 because the lip superior can be a sensitive area. The low wall thickness may exert lower forces on the lip superior than would be exerted by a relatively thick wall thickness.

While there is an advantage for comfort in g the wall thickness low in the regions configured to contact the ive pronasale and lip superior regions, in examples of the present technology the wall thickness in these regions is not reduced to the extent that the seal-forming structure 3100 is no longer able to in a stable seal to the patient’s face. If the wall thickness is too low in these regions, the seal- forming structure could be prone to creasing, which can break the seal and create a leak path through which air can flow to the surroundings between the patient’s face and the cushion.

The superior-facing intermediate portions 3121 may be located around some or all of the inferior periphery of the patient’s nose in use. For example, the superior-facing intermediate portions 3121 may be configured to lie just outside of a patient’s nose at the base of the nose, e.g., proximate or in contact with the ala. The superior-facing intermediate portions 3121 of the seal-forming structure 3100 may comprise a pair of exterior walls facing towards partially medial and partially superior ions (e.g., having external or exterior surfaces facing in medial and superior directions) and in some examples also partially posteriorly. As shown in Fig. 113, the superior-facing intermediate ns 3121 of the nasal portion 3230 lie proximate the lower periphery of the nose of a patient 1000. The seal-forming ure 3100 comprises a greater stiffness in the superior-facing intermediate portions 3121 in comparison to the central portions 3111, 3115. In these examples, the seal-forming structure 3100 comprises a greater wall thickness in the intermediate portions 3121 and 3125 than in the central portions 3111, 3115 and lip superior portion 3116.

In general, a greater stiffness in regions of the seal-forming structure 3100 compared to other regions of the seal-forming structure 3100 may be ed by a r wall thickness, a stiffer material (e.g., higher durometer silicone or other material), a reinforcing structure such as a tie or a rib, an undercushion, portion or a chassis, or the like, across various examples of the present technology.

In the examples of Figs. 34 to 38 and 76 to 80, the nasal portion has a l saddle portion 3112 which may seal to anterior or inferior areas of the patient’s pronasale in addition to the superior-facing central portion 3111. The intermediate portions are, in these examples, provided to l sides of the nasal portion 3230 of the seal-forming structure 3100 on either side of the superior-facing l portion 3111, but not to the l saddle portion 3112, which in these examples of the present technology comprises the same low stiffness as the superior facing central portion 3111 and anterior-facing central portion 3115.

The seal-forming structure 3100 may have a wall thickness of between .4mm in the superior-facing central portion 3111, anterior-facing central n 3115, and/or lip superior portion 3116, for example, n 0.2mm and 0.3mm, such as 0.25mm. The wall thickness in the superior-facing intermediate ns 3121 and anterior facing intermediate portions 3125 may be in the range of 1mm, such as between 0.6mm-0. 9mm, for example 0.75mm.

In some examples, the superior-facing intermediate portions 3121 of the seal-forming structure 3100 reinforces the superior-facing central portion 3111 of the seal-forming ure 3100. In further examples, the superior-facing intermediate portions 3121 provides a barrier to creases and prevents leak paths from forming in the seal-forming structure 3100. Additionally, the superior-facing intermediate portions 3121 may provide flexibility and support against sideward loading on the plenum chamber 3200 to help prevent breaking the seal under lateral forces.

As the or-facing central portion 3111 has a thin wall thickness and is therefore very flexible, it may be prone to creasing in some conditions. The superior-facing intermediate portions 3121 are stiffer than the superior-facing central n 3111 due to greater wall thickness and are therefore less prone to creasing. In P1419NZ4 some examples, the nasal portion 3230 of the seal-forming structure 3100 may be particularly prone to creasing proximate the lateral sides of the patient’s nose. If a crease begins in the seal-forming surface and continues outside of the seal forming surface, the crease may create a leak path through which gas can leak through the crease from the or of the plenum chamber 3200 to t, past the patient’s face.

In some es, the superior-facing intermediate portion 3121 due to its increased wall stiffness, resists creasing of the seal-forming structure 3100. If a crease occurs in the superior-facing central portion 3111 of the seal-forming structure 3100, the superior-facing intermediate portions 3121 and/or the r posterior corner regions 3131 can limit the size of the crease to prevent it from continuing up the patient-facing sides of the nasal portion 3230 and past the seal forming surface (e.g., part of the periphery of the patient’s nose). Accordingly, the or-facing intermediate portions 3121 act as a barrier to creases that closely follow the shape of the t’s nose, by being ured to lie at or proximate the edges of the patient’s ala around the base of the nose. Fig. 116 shows a plenum chamber 3200 with various portions of the seal-forming structure 3100 identified. As illustrated, creases 3110 have formed in the superior-facing central portion 3111, yet the superior-facing intermediate ns 3121 and the posterior corners 3131 effectively e a barrier ting the creases 3110 from propagating outwardly and forming leak paths past the seal formed with the t’s face. The posterior corners 3131 may provide a barrier to the creases 3110 inferior to and laterally of the superior-facing central portion 3111. The superior-facing intermediate portions 3121 may provide a barrier to the creases 3110 superior to and laterally of the superior-facing central portion 3111.

Furthermore, the intermediate portions 3121 or 3125 may assist in resisting or ting creases forming in the thinner central portions 3111 or 3115.

When the patient dons the patient interface 3000, the intermediate portions may stretch the thinner central portion onto the base of the nose (e.g., to the inferior periphery). The increased resistance to deformation that is provided by the intermediate portions proximate the patient’s ala may resist or t creases from P1419NZ4 forming in the l portion by stretching the central portion onto the base of the nose.

The seal-forming structure 3100 may also comprise a lateral-facing posterior portion 3141 on lateral tient facing regions of the nasal portion 3230 of the seal-forming structure 3100. The l-facing posterior portions 3141 of the nasal portion 3230 may comprise a greater stiffness than the or-facing intermediate portions 3121 and anterior-facing intermediate portions 3125. The lateral-facing posterior portions 3141 may se a greater wall thickness than the intermediate portions, central portions and or lip superior n 3116.

The superior-facing intermediate portions 3121 are positioned to contact the sides of the patient’s nose when the patient dons the patient interface 3000, yet are flexible enough that they can be deformed laterally by the patient’s nose. In use, the seal-forming structure 3100 is biased at the superior-facing intermediate portions 3121 into contact with the patient’s nasal ala. The patient’s nose exerts forces outwardly on the sides of the seal-forming structure 3100 when the patient dons the patient ace 3000. In turn, the sides of the seal-forming ure 3100 in the nasal portion 3230 conform to the periphery of the patient’s nose to form a stable and robust seal. Figs. 112 and 113 show the nasal portion 3230 before and after the patient 1000 dons the patient interface 3000. As illustrated, the seal-forming structure 3100 is shaped in the nasal portion 3230 to conform to the lower periphery of the patient’s nose when the t 1000 dons the patient interface 3000. Fig. 113 shows that the seal-forming structure 3100, in the or-facing central portion 3111 proximate the superior facing ediate portions 3121 conforms to the periphery of the nose of the patient 1000 to form a good seal. The stiffness of the orming structure 3100 in the superior-facing intermediate portions 3121 is advantageously large enough that the nasal portion 3230 can fit to and create a robust seal with a narrow nose but is not so stiff that it would be uncomfortable for a wider nose.

Additionally, the preload on the sides of the nose provided by the superior-facing intermediate portions 3121 provides decoupling between the patient’s nose and the rest of the plenum chamber 3200 and patient ace 3000, tolerating some lateral movement of some portions of the plenum chamber 3200, e.g. the shell P1419NZ4 3210, without ting the seal in use. Fig. 114 illustrates a seal-forming structure 3100 in sealing contact with the nose of a patient 1000 and in the e of lateral displacement of the plenum chamber 3200. Fig. 115 shows the same view as Fig. 114 but after the orming structure 3100 has been displaced laterally (for example by tube drag). As shown in Fig. 115, the bias of the seal forming structure 3100 into contact with the nose of the patient 1000 enables the seal-forming structure 3100 to remain in sealing contact with both sides of the nose even under relatively large displacement of the plenum chamber 3200.

As shown in Figs. 7-8, 49-50, 9, 138-139, 146-147, 154-155, the nasal portion 3230 of the seal-forming ures 3100 in these examples comprises two lateral portions 3231. Each lateral portion 3231 of a nasal portion 3230 may comprise a patient-facing side and a tient-facing side. The t-facing side may face in a medial and posterior direction while the non-patient-facing side may face in a lateral and anterior direction. Both the patient-facing side and the nonpatient-facing side may face partially in a superior direction. The patient-facing side of a lateral portion 3231 of the nasal portion 3230 may comprise a portion of the superior-facing central surface 3111 and an adjacent superior-facing intermediate portion 3121. The non-patient-facing side of a lateral portion 3231 of the nasal portion 3230 may comprise an anterior-facing intermediate portion 3125 and a lateral-facing posterior portion 3134.

The lateral portions 3231 of the nasal portion 3230 of the seal-forming ure 3100 in some examples of the present technology may be taller than in other examples of the present technology. That is, the lateral portions 3231 may project from the oral n 3260 by a greater distance in the or direction in use. The plenum chambers 3200 shown in Figs. 7-8 and 49-50 comprise tall lateral portions 3231 in the nasal portion 3230. These plenum chambers 3200 may fit well to ts comprising relatively long, narrow noses, and/or noses comprising ala that are higher than the columella. The plenum chambers 3200 shown in Figs. 128-129 and 138-139 comprise lateral portions 3231 in the nasal n 3230 which are not as tall as the examples shown in Figs. 7-8 and 49-50 but which comprise a moderate height. These lateral portions 3231 may also fit well to patients having long and narrow noses. The P1419NZ4 lateral portions 3231 shown in Figs. 146-147 and 154-155 have shorter lateral portions 3231 in the nasal portion 3230. These plenum chambers 3200 may fit well to patient’s having wider, shorter and/or flatter noses.

The anterior areas of the nasal portion 3230 are ured to be table while able to form a stable seal to the patient’s nose.

The or-facing central portion 3115 has in some examples a thickness of approximately 0.15-0.4mm, for example 0.2-0.3mm, and in the illustrated example comprises a wall thickness of approximately 0.25mm. The anterior-facing intermediate portions 3125 may comprise a wall thickness that is r than a wall thickness in the anterior-facing central portion 3115, and may be between 0.5mm and 1mm, such as between 0.65mm and 0.85mm or, in the illustrated examples, approximately . In some examples the thickness of the seal-forming structure 3100 tapers between regions having different thicknesses. In other examples the thickness s relatively abruptly, e.g., in steps. The anterior areas of the nasal portion 3230 is configured to be at compliant and is therefore not as thick and stiff as other s of the nasal portion 3230, such as the posterior s 3131 of the nasal portion 3230 (which may be in the range of 1-1.5mm in thickness). The anterior areas of the nasal portion 3230 may generally be sufficiently thick that it is stiff enough to hold its general shape when donned by a patient.

Providing flexibility in the anterior portion of the nasal portion 3230 allows the seal-forming structure 3100 to deform somewhat when receiving a patient’s nose, especially a longer nose. Fig. 117 shows a plenum chamber 3200 according to one example in sealing contact with the face of a patient 1000 with a short nose, while Fig. 118 shows the plenum chamber 3200 in sealing contact with the face of a patient 1000 with a longer nose. The seal-forming structure 3100 in this example is able to deform to a r extent to receive the longer nose. This may be achieved without adversely affecting patient comfort. The patient’s ale can be a particularly sensitive area and the flexibility of the anterior portion of the nasal portion 3230 may help reduce forces applied to the patient’s nose from the sealforming structure 3100. This flexibility is particularly advantageous at the on of the pronasale, and therefore the central portions are less stiff than the anterior-facing P1419NZ4 intermediate portions 3125. The superior-facing central portions 3111 and anteriorfacing central portions 3115 may be around 0.25mm in thickness while the anteriorfacing intermediate portions 3125 may have a wall thickness of about 0.75mm. The reduced thickness of the l portions reduces pressure on the pronasale while the thicker intermediate portions 3125 provide some support to the overall structure of the nasal portion 3230.

A further age of a flexible central region of the nasal portion 3230 is that it enables the sides of the nasal portion 3230 to be pulled inwardly (e.g., in a medial direction) when the patient dons the patient interface 3000 and the patient’s nose exerts a downward force on the superior-facing central portion 3111 of the sealforming structure. The inwards pull on the sides of the nasal portion 3230 towards the sides of the patient’s nose may improve the seal since the seal-forming structure 3100 is pulled into and around the or ery of the patient’s nose. Fig. 113 illustrates a orming structure 3100 conforming to the periphery of the patient’s nose. gh the lateral sides of the nasal portion 3230 are pulled s, the anterior portion, and in particular the anterior-facing intermediate ns 3125 on either side of the more flexible anterior-facing central portion 3115, retains enough structural rigidity to maintain the overall shape of the seal-forming structure 3100 and prevent creases from creating leak paths. In alternative examples, the anterior-facing central portion 3115 may be closer in thickness to the anterior-facing intermediate portions 3125 to e further crease resistance at the central saddle portion 3112 of the nasal portion 3230.

It is advantageous that the nasal portion 3230 of the seal-forming structure 3100, and in particular the region between the nasal holes 3272 and the central saddle region 3112 of the nasal portion 3230, is vely long in the anterior-posterior directions. This part of the nasal portion 3230 of the seal-forming structure 3100 is relatively unsupported in comparison to other regions. A long area in this part of the seal-forming ure 3100 allows ample room for the nasal n 3230 of the sealforming structure 3100 to deform, which is ageous as it receives the nose. If the seal-forming structure 3100 has a stiffer structure in this region, excessive force could P1419NZ4 be exerted on the patient’s pronasale, especially in longer noses. It is advantageous to avoid this excessive force for t, given the pronasale can be a particularly sensitive region. However, some patients have shorter noses, which may also be relatively wide. The plenum rs 3200 shown in Figs. 142-149 and 150-157 are suited to patients with shorter noses. These plenum chambers 3200 and comprise nasal portions 3230 which are shorter in length between the lip or portion 3116 and the central saddle region 3112. These plenum chambers 3200 still have a e in the superior-facing central portion 3111 between the apertures 3272 and the central saddle region 3112 which can e the pronasale in a manner which is comfortable for the patient, but are not as long between the lip superior portion 3116 and the central saddle region 3112 as the plenum chambers 3200 shown in Figs. 126-133 or 134-141, which are better suited to patients having longer noses. The plenum chambers 3200 shown in Figs. 126-133 and 134-141 also comprise central saddle regions 3112 that are d more anteriorly with respect to the chassis 3210 than the central saddle regions 3112 of the plenum chambers 3112 shown in Figs. 9 and 150-157.

The superior-facing central portion 3111 of the nasal portion 3230 of the seal-forming structure 3100 has a bridge portion 3113, connecting the anterior region of the superior-facing central portion 3111 with the lip superior portion 3116 of the nasal portion. The bridge portion 3113 therefore lies inferior to the patient’s columella in use and partly defines the two nasal holes 3272 (one on either lateral side) through which air can be supplied to the patient.

The bridge n 3113 is flexible and curved to be slack when the patient ace 3000 is not donned by the patient. The slack provided to the bridge portion 3113 allows the anterior part of the central portion 3111 (anterior of the bridge, which contacts the patient’s pronasale in use) to move away from the lip superior portion 3116 when the patient dons the patient ace 3000.

Advantageously, this allows a nose with a longer length to still be comfortably accommodated by the seal-forming structure 3100. A longer and/or narrower nose could comfortably push the anterior part of the superior-facing central portion 3111 in an anterior ion. By allowing deformation of the nasal portion 3230 in this way, the forces exerted by the seal-forming structure 3100 back onto the patient’s pronasale (which is generally quite sensitive) can be kept to a tolerable level.

Figs. 117 and 118 show a plenum chamber 3200 and orming structure 3100 having a bridge portion 3113 that is formed to have slack, worn by a patient 1000 having a short nose and long nose, respectively. As shown in Fig. 117, the bridge portion 3113 is generally curved and slack since the nose of the patient 1000 has not pushed the anterior part of the superior-facing l portion 3111 anteriorly to a significant extent. However, as illustrated in Fig. 118, the longer nose has pushed the anterior part of the superior-facing central portion 3111 anteriorly to such an extent that the bridge portion 3113 has stretched into a straighter configuration. The bridge portion 3113 is therefore advantageous in enabling the seal-forming structure to accommodate a range of nose sizes while still be comfortable and able to achieve a good seal.

The bridge portion 3113 may be S-shaped so that it can hten out to tolerate movement of the superior-facing central n 3111 of the seal-forming structure 3100 away from the lip superior portion 3116. The bridge portion 3113 may be bowed, curved or . The bridge portion 3113 may have concertina or bellows.

The bridge portion 3113 may comprise only one curve so that the bridge is C-shaped, or may comprise two bows so that it is S-shaped, to e even more slack. The bridge portion 3113 may be in the form of a sling (e.g., a portion that hangs between its end). The bridge portion 3113 is longer and is comprised of more material than is necessary to bridge the gap between the anterior and posterior portions of the superior-facing central portion 3111 of the nasal portion 3230. The extra material allows for extension while the bridge portion 3113 straightens out, before becoming taut. The more extra al is provided, the more extension can be ed by the bridge portion 3113 before it becomes taut upon a force applied to the anterior part of the superior-facing central portion 3111. Since the bridge portion 3113 does not need to seal to the patient’s lla in order to create a full seal to the patient’s nose, a good seal can be made to a small nose even if the bridge portion 3113 remains somewhat slack.

P1419NZ4 The bridge portion 3113 may have a thickness of about 0.2mm-045mm, or 0.3-0.4 mm for example 0.35mm. The bridge portion 3113 may have a greater material thickness than the surrounding superior-facing central portion 3111 of the seal-forming structure 3100 which helps resist or prevent the bridge portion 3113 from tearing. The bridge n 3113 could alternatively be wider and thinner. In one example, a thicker and narrower bridge portion 3113 is provided so that the nasal holes 3272 are relatively large.

The bridge portion 3113 may serve other purposes as well. For example, it may in the integrity of the l portion 3111 in the thin zone. If there were no bridge n 3113 and d a single nasal hole, due to the relatively thin wall thickness of the l portion, whilst under pressure if the seal-forming structure is refitted (e.g. via pulling of the face and reseating) or if it receives aggressive dynamic loading, there is a chance that blowout may occur at the superior-facing l portion 3111. The bridge portion 3113 ties the superior-facing central portion 3111 to the lip superior n 3116 to reduce the chance of blowout at the superior-facing central portion 3111.

Additionally, the bridge portion 3113 may help prevent the patient from setting up the patient interface 3000 incorrectly. If the bridge portion 3113 was not provided and there was instead a single nasal hole, a patient may inadvertently insert their nose into the nasal hole. Since in some examples the seal-forming structure 3100 is configured to seal to an inferior periphery of the patient’s nose, the orming structure may not achieve a suitable seal if the patient inserts their nose into the nasal hole.

Notwithstanding the advantages of the bridge portion 3113 in some forms of the technology, in some alternative examples there is no bridge n 3113 provided and there is only a single hole in the nasal portion 3230 of the seal-forming structure 3100. This allows the superior-facing central portion 3111 of the nasal portion 3230 to move ve to the inferior portion, and also makes the seal-forming structure 3100 easier to clean. However, there may be an increased risk of blowout for some patients if the superior-facing central portion 3111 of the seal-forming structure 3100 is not tied to the lip superior portion 3116. Additionally, the patient could P1419NZ4 attempt to insert their nose into the single hole. Provided steps are taken to mitigate these risks (e.g., by providing the seal-forming structure with a r, smaller or tighter membrane around the hole), then a single hole (i.e., no bridge) may be provided in some examples of the technology. Seal-forming structures 3100 of patient interfaces 3000 according to examples of the present logy may comprise either one or two apertures to provide a flow of air to the t’s nasal es.

While, in the areas of the seal-forming ure 3100 discussed above, it is advantageous for the seal-forming structure 3100 to have a low wall thickness to allow it to comfortably conform to complex geometry, in some regions of the sealforming structure 3100 a relatively thicker wall thickness is advantageous in other forms of the technology.

For example, the nasal portion 3230 of the seal-forming ure 3100 comprises posterior s 3131 configured to seal to the patient’s face proximate the nasaolabial sulcus. These ior corners 3131 have a greater wall thickness in comparison to the l portion of the nasal portion 3230 of the seal-forming structure 3100. The greater wall thickness provides significant structural rigidity to the seal-forming structure 3100 in these regions, which may provide a number of advantages.

The ior corners 3131 may assist in supporting the seal-forming structure on the patient’s face and therefore need to have sufficient structural rigidity so that they do not collapse and mise the seal achieved by the central portion of the seal-forming structure 3100 (e.g., the superior-facing central portion 3111 and/or lip or portion 3116). In alternative examples, the posterior corners 3131 are provided with an undercushion for reinforcement. In the illustrated examples in which a single wall seal-forming structure 3100 is provided, ural rigidity is provided by a iently high wall thickness, which may be around 0.8-1.6mm thick, for example 1.1mm to 1.45mm, or 1.25mm in one example. The posterior corners 3131 are configured to lie on the patient’s face in a region inferior to the ala of the patient’s nose as well as inferior and laterally outwards of the patient’s nose, for example between the nasolabial sulcus and the regions of the lip superior located inferior to the ala.

P1419NZ4 As shown in Figs. 27, 34, 69, and 76, there is an abrupt transition (e.g., an abrupt taper or step) between the higher wall thickness in the posterior corners 3131 and the low wall thickness in the lip or portion 3116 of the seal-forming structure 3100 (i.e., the region that seals against the lip superior). The thick posterior corners 3131 may provide support to the seal-forming structure where t is required/advantageous while the lip superior portion 3116 lies t and seal to against the patient’s lip superior and may be much more flexible to conform to the contours of the t’s face while keeping forces to a minimum. While facial ry can vary widely between patients, the abrupt transitions may be located almost directly inferior to the nasal ala on the lip superior.

In some examples of the present technology, the seal-forming ure 3100 comprises lateral corner regions 3114 forming part of the l portion, which are configured to contact and seal against the ala. As shown in Figs. 34, 76, 160, 161, 164, 168 and 170 , superior to the location of the junction between the thicker of the posterior corners 3131 and the thinner wall thickness at the lip superior portion 3116 of the nasal n 3230 of the seal-forming structure 3100 are lateral corner regions 3114 of the superior-facing central portion 3111 that extend in a lateral, posterior and superior direction on either side of the target seal g region (e.g., they extend up the medially-facing sides of the seal-forming structure 3100). The ala can be significantly , and many patients may have very concave pockets or cavities where the ala meets the face. The pockets can result from ala that curve back towards a medial ion (e.g., towards the sagittal plane) between the widest part of the nose and the junction of the ala and the face. Providing a low stiffness (which in these examples is achieved by a low wall thickness) at these lateral corner regions 3114 enables the seal-forming structure 3100 to deform to match the curvature of the ala.

This flexibility and ability to conform may assist the seal-forming structure 3100 in filling the concavities which may exist at the inferior s of the patient’s nose.

The seal-forming structure 3100 may be configured so that each transition between the thick posterior corner 3131 and the thin lip superior portion 3116 may be located on the t’s face laterally of the ala but close to the ala. The regions of the seal-forming structure 3100 contacting the patient’s face on either inferior lateral side P1419NZ4 of the nose may be part of the thick posterior corners 3131 to provide good t and stability to the seal-forming structure 3100. Fig. 111 shows a cutaway view of the plenum chamber 3200 according to one example of the present technology in sealing position on the patient’s face. The or-facing l portion 3111 seals to the lower periphery of the nose of the patient 1000 while the lip super portion 3116 seals against the patient’s upper lip. The superior-facing intermediate n 3121 lie proximate the sides of the patient’s nose (e.g. proximate the ala).Additionally, the lateral corner regions 3114 of the superior-facing l portion 3111 may deform to receive the patient’s ala. For example, the lateral corner regions 3114 may cup the patient’s ala. They may deform to create shelves in the cushion on which the proximal portions of the patient’s ala may be supported in use, enabling the seal-forming structure 3100 to conform well to the inferior periphery of the patient’s nose in use, especially proximate the lip superior.

As illustrated in Fig. 111, the boundary between the thick walls forming the posterior corners 3131 and the medially adjacent portions of the seal-forming structure 3100 may track upwardly, outwardly and then inwardly to follow the curvature of the patient’s nose in a superior direction ng from under patient’s ala.

The medial boundaries of the walls forming the thick posterior s 3131 may follow a path up the patient’s face on either side of the nose following the curvature along either side of the nose. This may provide good support where needed (e.g., against the patient’s face just below and on either side of the patient’s nose) while enabling the thinner portions, such as the superior-facing central portion 3111 and the lip superior portion 3116 to m and seal to the ala and underside of the patient’s nose.

As shown in the side views such as Figs. 18, 19, 30, 31, 32, 38, 58, and 80, the seal-forming structure 3100 is even thicker s its anterior side closer to the shell 3210 (shell 3210 not shown in Figs, 38 or 80 but shown in Figs 9 and 51). As discussed above, the orming structure 3100 comprises l support portions 3151 in the form of thickened regions on the partially-anterior facing lateral sides of the nasal portion 3230 of the seal-forming structure 3100. The thicker regions of the P1419NZ4 seal-forming structure 3100 proximate the shell 3210 provide good t and structural rigidity to the seal-forming structure 3100.

While thick areas proximate the shell 3210 are advantageous in ing structural rigidity, the nasal n 3230 of the seal-forming structure 3100 still retains a degree of flexibility to enable the sides of the seal-forming structure 3100 to be pushed outwardly or pulled inwardly to accommodate noses of different widths.

For example, the non-patient facing sides or regions (e.g., anterior sides, at least partially anterior-facing sides) of the nasal portion 3230 of the seal-forming structure 3100 (particularly the non-patient contacting regions on either side of nasal portion 3230 of the seal-forming structure 3100) are thick enough to provide sufficient ural rigidity to the seal-forming structure 3100, but are thin enough so that when the seal-forming structure 3100 is donned by a patient with a long narrow nose, the downward forces d by the patient’s nose on the superior-facing central region 3111 are able to pull the sides of the nasal portion 3230 inwardly somewhat to bring the patient-contacting surfaces of the seal-forming structure 3100 on either side of the patient’s nose into good t with the patient’s nose. Similarly, the structure of the nasal portion 3230 of the seal-forming structure 3100 is sufficiently flexible that, if a t with a wider nose dons the seal-forming structure 3100, there are not ive s forces on the sides of the patient’s nose (which may occur if the seal-forming structure is too stiff to tolerate a wider nose). A number of different sizes for the seal-forming structure 3100 are also able to be provided to accommodate ent ranges of nose widths.

As shown in Figs. 7, 8 and 49, 55, 126, 129, 138-139, 146, 147, 154, 155, for example, there is an oronasal transition 3275 at the periphery of the plenum chamber 3200 where the nasal portion 3230 and oral portion 3260 t. The periphery of the seal-forming structure 3100 varies at this location between examples of the technology. As shown in Fig. 7 the oronasal transition 3275 is relatively sharp and there is relatively large positive curvature at the periphery of the seal-forming structure 3100 between the nasal portion 3230 and oral portion 3260. In st, as shown in Fig. 49, the oronasal transition 3275 is relatively gradual and there is relatively small positive curvature at the periphery of the seal-forming structure 3100 P1419NZ4 between the nasal portion 3230 and oral portion 3260. In both cases, the oronasal transition 3275 comprises a saddle region. The plenum chambers 3200 shown in Figs. 128, 138, 146 and 154 comprise ct but gradual oronasal transitions 3275.

While the periphery of the orming structure 3100 should preferably be sufficiently stiff that it can support the overall shape of the seal-forming structure 3100 and t large creases and buckling, the shape of the periphery may be varied more than the regions that are in contact with the patient’s face and the nearby regions (i.e. the thin zones and the thicker zones which t s from creating leak paths past the patient’s face). In any case, the oronasal tion 3275 between the nasal portion and oral portions of the seal-forming structure 3100 is relatively stiff (e.g., by being relatively thick) in comparison to low stiffness portions of the rming structure 3100 such as the superior-facing central portion 3111 in order to prevent creases or buckling from ing and creating leaks between theses portions. Alternatively, the oronasal transition 3275 may be rced by any suitable means such as an undercushion, ribs, a portion of the shell or a frame or the like.

In some examples, the oral portion 3260 of the seal-forming structure 3100 comprises features to prevent creasing. The lateral periphery of the oral hole 3271 may be more susceptible to ng or buckling than the top and bottom portions of the oral hole 3271, due to the downward forces on the nasal portion of the cushion and the wide oval shape of the oral opening.

In the examples shown in Figs. 34 to 80, the seal-forming structure 3100 comprises an oral hole eral portion 3117 at the periphery of the oral hole 3271, which is thinner than other portions of the seal-forming structure 3100. Additionally, the seal-forming structure in those examples comprises posterior-facing lateral portions 3135 which are thicker than the oral hole peripheral portion 3117 and which resist creasing and buckling in the cushion which could lead to leak paths forming.

The seal-forming ures 3100 shown in Figs. 126-157 may also be provided with an oral hole peripheral portion comprising a lower stiffness than posterior-facing lateral portions of the oral portion 3260 in some examples of the present technology.

In some examples, such as the plenum chamber 3200 shown in Fig. 48, the seal-forming structure comprises lateral peripheral support portions 3136 at opposite lateral sides of the oral hole 3271. In this example, the posterior-facing lateral portions 3135 form the l peripheral support portions 3136. The iorfacing lateral portion 3135 extends medially towards the most lateral edges of the oral hole 3271 to provide the lateral peripheral support portions 3136. The lateral eral support portions 3136 provide extra resistance to buckling. The sealforming structures 3100 shown in Figs. 126-157 may also be provided with lateral peripheral support portions 3136 in some examples of the t technology. .3.1.3.3 Oral-region In one form, the non-invasive t interface 3000 comprises a sealforming structure 3100 that forms a seal in use on an upper lip region (that is, the lip superior) of the patient's face. The seal forming ure 3100 may comprise a lip superior portion 3116 configured to form a seal to the lip superior of the patient.

In one form, the seal-forming structure 3100 es a saddle-shaped region constructed to form a seal in use on an upper lip region of the patient's face.

In one form the non-invasive patient ace 3000 comprises a sealforming structure 3100 that forms a seal in use around the patient’s mouth at an oral portion 3260. The seal-forming structure 3100 may form a seal on a chin-region of the patient's face.

In one form, the seal-forming structure 3100 includes a saddle-shaped region constructed to form a seal in use on a chin-region of the patient's face.

The seal-forming structure 3100 as shown in Figs. 34 to 80 and 126-183 comprises a lip or portion 3118 which forms a seal against the chin region of the patient. In an example, the seal-forming structure 3100, including the lip inferior portion 3118, does not extend below the patient’s chin (i.e., below the mental protuberance) in use or engage the patient’s face below the chin (i.e., below the mental protuberance) in use. The lip inferior n 3118 of the seal-forming structure may seal against the lip inferior and supramenton of the patient.

P1419NZ4 Additionally, in these examples, the seal-forming structure 3100 comprises an oral hole peripheral portion 3117. The lip inferior portion 3118 may be connected to (e.g., contiguous with) the lip or n 3116 via the oral hole peripheral portion 3117. The seal-forming structure 3100 comprises a relatively low wall thickness at the oral hole peripheral n 3117 and at the lip inferior portion 3118 of the sealforming structure 3100 which lies against the chin region (in comparison to other s). The low wall ess in these locations assists in achieving an effective, comfortable seal. The seal-forming structure 3100 in these regions is able to readily conform to any x geometry (e.g. the labiomandibular creases).

In these examples, the oral portion 3260 comprises posterior-facing l portions 3135 on the patient-contacting side of the orming structure 3100. As discussed above, immediately around the oral hole 3271 at the oral hole peripheral portion 3117 the wall thickness is low in comparison to other regions of the sealforming structure 3100, however in these examples there are posterior-facing lateral portions 3135 on either lateral side of the oral hole peripheral portion 3117 which are thicker than the oral hole peripheral portion 3117. These regions may have a wall thickness of around 1mm to 1.5mm, such as 1.15 mm to 1.35mm, for example around 1.25mm thick. The areas that these regions contact in use, i.e., the t’s cheeks, may generally not be as sensitive as other areas of the face and therefore patients may lly tolerate the orming structure 3100 having a greater wall thickness/stiffness in these areas. Additionally, the posterior-facing lateral portions 3135 of the oral portion 3260 curve away from contact with the patient’s face which reduces the area of contact on the patient’s face at these regions. In ative examples the posterior-facing lateral portions 3135 of the oral portion 3260 may not be thicker and may instead be stiffened by another means, such as by reinforcing structures (e.g., ribs), a stiffer al, an undercushion or the like.

The posterior-facing lateral portions 3135 may provide resistance to creases that may form proximate the oral hole 3271, thereby preventing leak paths from being d. The posterior-facing lateral portions 3135 may provide a barrier to creases that form at the thinner oral hole peripheral portion 3117, limiting the extent of creases away from the oral hole 3271. This function of the posterior-facing P1419NZ4 lateral portions 3135 may be similar to the crease ance function provided by the or-facing intermediate portions 3121 of the nasal n 3230 described above.

The lip or portion 3118 of the oral portion 3260 is approximately half the width of the oral portion 3260 and centered inferior to the oral hole 3271. As bed above, the lip inferior portion 3118 may be relatively thin. The transitions between the thinner lip inferior portion 3118 and the thicker posterior-facing lateral portions 3135 on either lateral side may be configured to lie at or proximate a patient’s labiomandibular creases. The lip inferior portion 3118 is wider at the periphery of the oral hole 3271 than at the lower periphery of the seal-forming structure 3100. The width of the lip inferior portion 3118 therefore tapers down from the oral hole 3271. In the example shown in Figs. 49-80, the lip inferior portion 3118 extends from a ior-facing side of the seal-forming structure 3100 to an inferiorfacing periphery. The actual amount of the lip inferior portion 3118 that makes contact with the patient’s face may depend on the shape of the t’s chin. Patient’s having a more anteriorly protruding chin may make more contact with the lip inferior portion 3118. In the plenum chambers 3200 shown in Figs. 158-183, the inferior periphery of the shell 3210 is not as inferior as the inferior periphery of the shell 3210 of the plenum r 3200 shown in Figs. 49-80, and seal forming structure 3100 and lip inferior portion 3118 around the inferior periphery of the seal-forming structure 3100 to form a partially anterior-facing portion of the lip inferior portion 3118. r from contact with the patient (e.g., closer to the shell 3210) than the posterior-facing lateral portions 3135 at the lateral periphery of the oral portion 3260 are lateral portions 3145 of the oral portion 3260. In these examples, the lateral ns 3145 are thicker than the posterior-facing lateral ns 3135 of the oral portions. In some examples, the lateral portions 3145 of the oral portion have a ess in the range of 1.5-2.2mm, such as 1.7-2mm. Most, or all, of the lateral portions 3145 are unlikely to be in contact with the patient’s face in use and ingly, patient comfort is a less important design consideration for these regions and the wall thickness can be higher in these regions than in the patient-contacting regions. The higher wall thickness may provide structural rigidity to the overall shape P1419NZ4 of the oral portion 3260 of the seal-forming structure 3100. In some examples, the further away from the patient’s face a particular region of the seal-forming ure 3100 is, the thicker that region is, unless there is a reason for providing flexibility to that region (e.g., to enable the sides of the nasal portion of the seal-forming structure 3100 to deform). The lateral portions 3145 define a lateral periphery of the sealforming structure 3100 in the oral portion 3260.

On the anterior side of the seal-forming structure 3100, the wall thickness is generally higher in these examples, with the exceptions of the anterior sides of the nasal portion and the central inferior region of the oral portion of the seal-forming structure 3100). In these examples the seal-forming structure 3100 comprises anteriorfacing lateral portions 3155. The l or facing portions 3155 in these es have a wall thickness r than the lateral portions 3145 (and posteriorfacing lateral portions 3135). The anterior-facing lateral portions may have a wall thickness in the range of 1.7-2.7mm, for e in the range of 2.0-2.5mm. These thicker areas provide substantial support and structural rigidity to the overall shape of the seal-forming structure 3100. The lateral anterior-facing portions 3155, in ation with other portions of the seal-forming structure that are provided with high wall thickness, such as the l portions 3145, hold the general shape of the seal-forming ure 3100 and may resist creases and/or buckling etc., while the thinner areas provided to the patient-facing side of the seal-forming structure 3100 deform against the patient’s face under the forces exerted on the plenum chamber 3200 by the positioning and stabilising structure 3300.

Also on the anterior side of the seal-forming ure 3100 are anterior support portions 3161 of the oral portion 3260. The anterior support portions 3161 are even thicker zones of the seal-forming structure 3100 at the base of the nasal portion on the anterior side, where the nasal portion joins the oral n, proximate the frame, and at the inferior lateral corners of the oral portion 3260. The wall thickness in these s may be in the range of 2-3mm, for example 2.5-3mm. These regions may provide even further structural stiffness to the seal-forming structure. The anterior support ns 3165 may have a greater wall thickness in comparison to the anterior-facing lateral portions 3155. Generally, the cushion has a greater wall P1419NZ4 thickness further away from the seal forming region gh immediately proximate the shell 3210, the thickness may be similar to the thickness of the anterior-facing lateral portions 3155, even though the anterior support portions 3165 are r. The silicone immediately adjacent the shell 3210 in some examples may require a lesser wall thickness since it may be reinforced by the peripheral edge of the shell 3210. .3.1.3.4 ad region In one form, the seal-forming structure forms a seal in use on a forehead region of the patient's face. In such a form, the plenum chamber may cover the eyes in use. .3.1.3.5 Nasal pillows In one form the seal-forming structure of the vasive patient interface 3000 comprises a pair of nasal puffs, or nasal pillows, each nasal puff or nasal pillow being constructed and arranged to form a seal with a respective naris of the nose of a patient.

Nasal pillows in accordance with an aspect of the present technology include: a frusto-cone, at least a portion of which forms a seal on an underside of the patient's nose, a stalk, a flexible region on the underside of the frusto-cone and connecting the frusto-cone to the stalk. In addition, the structure to which the nasal pillow of the t technology is connected includes a flexible region nt the base of the stalk. The flexible regions can act in concert to facilitate a universal joint structure that is accommodating of relative movement both displacement and angular of the frusto-cone and the structure to which the nasal pillow is connected. For example, the frusto-cone may be axially displaced towards the structure to which the stalk is connected. 3.6 e finish In some examples, different regions of the seal-forming structure 3100 comprise different surface finishes.

Referring to Fig. 47, the plenum r 3200 ses a seal-forming structure 3100 comprising a nasal portion 3230 and an oral portion 3260. The The P1419NZ4 seal-forming structure comprises a first surface finish in the nasal portion and a second surface finish in the oral portion different from the first surface finish. In the illustrated example the region 3101 has a first surface finish and the region 3103 has a second surface finish. The ry between the first surface finish and the second surface finish is identified by the lines 3102, which may contact the t’s cheeks in use.

A coefficient of friction between the seal-forming structure 3100 and the t’s face is greater in the oral portion 3260 than in the nasal portion 3230. The first surface finish in region 3101 may be configured to provide the nasal portion with a smooth feel on the t’s face, which may be more comfortable. The second surface finish in region 3103 may be configured to provide the oral n with grippy contact on the patient’s face, which may enable a more robust seal. In some examples, the first surface finish at region 3101 may be a frosted surface . In some embodiments the second surface finish at region 3103 may be a polished surface finish. The nasal portion 3230 in this example comprises a lip superior portion 3116 having the first surface finish.

The polished surface finish may have a grippy, sticky feel to it so that there is higher friction acting against movement of the seal-forming ure 3100 against the t’s face. This is generally desired as it helps prevent movement of the plenum chamber 3200 when donned by a patient, thereby assisting in maintaining a seal. However, patients may consider the feeling of a polished surface finish to be less comfortable on their face than a smoother feeling low-friction surface finish.

Patients may tolerate the feeling of the polished finish on their cheeks and below their mouth, but may not tolerate the feeling of the polished e on and around their nose, given the nose is lly a more ive area. Therefore, a polished finish is provided around the oral portion 3260, while a frosted finish is provided to the nasal portion 3230 of the seal-forming structure 3100, in this example. The frosted finish at the nasal portion 3230 may also assist the seal-forming structure 3100 to move against the nose as it conforms to the surfaces around the nose, which may also help in forming a seal.

P1419NZ4 Additionally, the added grip ed by the higher friction in the region of the second e finish at region 3103 assists the oral portion 3260 to maintain a seal during movement of the patient’s lower jaw. The jaw may have a tendency to move relative to the head (and drop, in particular). The added grip helps the seal maintain its position around the patient’s mouth during movement of the jaw.

The boundary 3102 between the polished finish at 3103 and the frosted finish at 3101 is close to the boundary between the nasal portion 3230 and the oral portion 3260 of the seal-forming structure 3100, slightly closer to the oral portion 3260 than the nasal portion 3230. The ry 3102 lies across the seal-forming structure 3100 roughly perpendicular to a path on the oral portion 3260 circumscribing the oral hole 3271. At the periphery of the oral hole 3271 the boundary 3102 may lie on the lip superior. At the periphery of the oral portion 3260 of the orming structure 3100 the boundary may lie ate the patient’s zygomatic bone. .3.2 Positioning and stabilising structure The seal-forming structure 3100 of the patient ace 3000 of the t technology may be held in sealing position in use by the positioning and stabilising structure 3300.

In one form the positioning and stabilising structure 3300 provides a retention force at least sufficient to overcome the effect of the positive pressure in the plenum chamber 3200 to lift off the face.

In one form the positioning and stabilising structure 3300 provides a retention force to overcome the effect of the gravitational force on the patient interface 3000.

In one form the positioning and stabilising structure 3300 es a retention force as a safety margin to overcome the potential effect of disrupting forces on the patient interface 3000, such as from tube drag, or accidental interference with the t interface.

In one form of the present technology, a positioning and stabilising structure 3300 is provided that is configured in a manner consistent with being worn by a patient while sleeping. In one example the positioning and ising structure 3300 has a low profile, or cross-sectional thickness, to reduce the perceived or actual bulk of the apparatus. In one example, the positioning and stabilising ure 3300 comprises at least one strap having a rectangular cross-section. In one example the positioning and stabilising structure 3300 comprises at least one flat strap.

In one form of the present technology, a positioning and stabilising ure 3300 is provided that is configured so as not to be too large and bulky to t the patient from lying in a supine sleeping position with a back region of the patient’s head on a pillow.

In one form of the present technology, a positioning and stabilising structure 3300 is provided that is configured so as not to be too large and bulky to t the patient from lying in a side sleeping position with a side region of the t’s head on a pillow.

In one form of the present technology, a positioning and stabilising structure 3300 is provided with a decoupling portion located between an anterior portion of the positioning and stabilising structure 3300, and a posterior n of the positioning and stabilising structure 3300. The decoupling portion does not resist ssion and may be, e.g. a flexible or floppy strap. The decoupling portion is constructed and arranged so that when the patient lies with their head on a pillow, the presence of the decoupling portion ts a force on the posterior portion from being transmitted along the positioning and stabilising ure 3300 and disrupting the seal.

In one form of the present technology, a positioning and stabilising structure 3300 comprises a strap constructed from a laminate of a fabric patientcontacting layer, a foam inner layer and a fabric outer layer. In one form, the foam is porous to allow moisture, (e.g., sweat), to pass through the strap. In one form, the fabric outer layer comprises loop material to engage with a hook material portion.

P1419NZ4 In certain forms of the present technology, a positioning and stabilising structure 3300 comprises a strap that is extensible, e.g. resiliently extensible. For example the strap may be configured in use to be in n, and to direct a force to draw a seal-forming structure into sealing contact with a portion of a patient’s face. In an example the strap may be configured as a tie.

In one form of the present technology, the positioning and stabilising structure ses a first tie, the first tie being constructed and arranged so that in use at least a portion of an inferior edge thereof passes superior to an otobasion superior of the patient’s head and overlays a n of a parietal bone without overlaying the tal bone.

In one form of the present technology suitable for a nasal-only mask or for a full-face mask, the positioning and stabilising structure includes a second tie, the second tie being constructed and arranged so that in use at least a portion of a superior edge thereof passes inferior to an otobasion inferior of the t’s head and overlays or lies inferior to the occipital bone of the patient’s head.

In one form of the present logy suitable for a nasal-only mask or for a full-face mask, the positioning and ising structure es a third tie that is constructed and arranged to interconnect the first tie and the second tie to reduce a tendency of the first tie and the second tie to move apart from one another.

In certain forms of the present technology, a positioning and stabilising structure 3300 comprises a strap that is bendable and e.g. non-rigid. An advantage of this aspect is that the strap is more comfortable for a patient to lie upon while the patient is sleeping.

In certain forms of the present technology, a positioning and stabilising ure 3300 comprises a strap constructed to be breathable to allow moisture vapour to be transmitted h the strap.

Figs. 89-95 show a patient interface 3000 according to one example of the t technology having a positioning and stabilising structure 3300 and a plenum chamber 3200 having a seal forming structure 3100. The positioning and stabilising P1419NZ4 ure 3300 in this example comprises a frame 3350 and a plurality of headgear straps connected to the frame 3350.

The plenum chamber 3200 of the patient interface 3000 is ted to the frame 3350. The plenum chamber 3200 of the exemplary t interface 3000 shown in Figs. 89-95 is the plenum chamber 3200 shown in Figures 7-14, although the positioning and stabilising structure 3300 may also be used with other plenum chambers 3200 in alternative examples of the present technology. The plenum chamber 3200 may connect to the frame 3350 via a snap fit tion. In one example, the plenum chamber 3200 may connect to the frame 3350 in the manner described with reference to Figs. 87-88. In other examples, the plenum chamber 3200 may form a different type of removable connection to the frame 3350, snap fit, removable press fit or otherwise, or may be permanently ted to the frame 3350.

The positioning and stabilising ure 3300 may comprise a ity of straps or strap portions connecting to the frame 3350 and passing around the patient’s head in order to support the plenum chamber 3200 in sealing position against the patient’s face. It will be understood that a single "strap" may be formed by multiple lengths of material(s) that have been cut or formed separately and then joined together at their ends to create a longer length or single "strap" may be a single length of material(s).

In the example illustrated in Figs. 89-95 the positioning and stabilising structure 3300 comprises a pair of upper straps 3310. Each upper strap 3310 is configured to pass between a respective eye and ear of the patient. Additionally, the positioning and stabilising structure 3300 ses a pair of lower straps 3320 configured to lie over the patient’s cheeks below the patient’s cheekbones. In this example, the plenum chamber 3200 is held in position via a oint connection to headgear straps via the frame 3350.

The frame 3350 is shown in isolation in Figs. 103-108. The frame 3350 comprises a frame inlet tion port 3354. The frame inlet connection port 3354 may be configured to connect to a source of pressurised breathable gas, such as air. In one example, such as the patient interface shown in Figs. 89-95, the frame inlet P1419NZ4 connection port 3354 may be configured to enable connection to a swivel elbow assembly 3610 which provides a connection port 3600 for connection with an air circuit 4170. The frame inlet connection port 3354 in this example comprises a connection rim 3355. The connection rim 3355 may comprise a radially outwardly extending flange. The swivel elbow assembly 3610 may form a releaseable snap-fit with the tion rim 3355, creating a fluid connection between the swivel elbow assembly and the frame 3350. The opposite side of the frame inlet connection port 3354 is configured to fluidly connect to the plenum chamber, as shown in Figs. 87-88 and Fig 90A. The frame 3350 therefore enables a fluid connection between the swivel elbow ly 3610 and the interior of the plenum chamber 3200.

The frame 3350 also comprises a pair of d upper strap connection points 3315 to which the upper straps 3310 connect. In this example, each upper strap connection point 3315 ses an aperture formed in the frame 3350. Each upper strap 3310 is able to t to a respective upper strap connection point 3315 by passing through the aperture, looping back onto itself and securing to itself. Each upper strap 3310 may secured to itself via hook and loop materials configured to releasably bind to each other upon contact. In ative examples, each upper strap 3310 may pass h a respective aperture, loop back onto itself and be d onto itself with a band, clip or the like. In r alternative examples, the upper straps 3310 may connect to the frame via side release buckle connections.

The frame 3350 also comprises a pair of opposed lower strap connection points 3325 to which the lower straps 3320 connect. In this example, each lower strap connection point 3325 comprises a magnet. Each lower strap 3320 comprises a lower strap clip 3326 comprising a magnet or al that is attracted to the magnet at the lower strap connection point 3325. In this example, each lower strap clip 3326 comprises an aperture through which the end of a respective lower strap 3320 and is able to pass and then loop back and be secured onto itself, for example with hook and loop material, a band, a clip or the like. In alternative examples, the lower straps 3320 may connect to the frame 3350 via side release buckle connections, onto hooks or via any other suitable connection.

P1419NZ4 In an example, the frame 3350 and upper strap connection points 3315 are structured and arranged to direct a force/tension provided by the upper straps 3310 into a partially superior and partially posterior force vector applied to the plenum chamber 3200. The partially superior and partially posterior force vector urges, in ular, the nasal portion 3230 of the seal forming structure 3100 into sealing contact with the lower periphery of the t’s nose and the patient’s upper lip.

The upper straps 3310 may each by selectively adjustable. For example, the effective length of each of the upper straps 3310 may be varied by changing how much of the upper strap 3310 is passed through the aperture at the respective upper strap connection point 3315 and looped back on itself. Passing more of the upper strap 3310 through the aperture effectively reduces the length of the upper strap 3310, allowing the force vectors to be modified and the fit of the patient interface 3000 to be adjusted.

In an example, the frame 3350 and the lower strap connection points 3325 are structured and arranged to direct a force/tension ed by the lower straps 3320 into a lly posterior and partially inferior force vector applied to the plenum chamber 3200. The partially posterior and partially inferior force vector urges, in particular, the oral portion 3260 into sealing contact with the t’s face around the periphery of the patient’s mouth. The partially inferior force applied to the frame 3350 by the lower straps 3320 may balances the partially superior force applied by the upper straps 3310 along with any inferiorly directed force that the patient’s nose may apply onto the seal forming structure 3100.

The lower straps 3320 may each by selectively adjustable. For example, the effective length of each of the lower straps 3320 may be varied by changing how much of each lower strap 3310 is passed through the re in the tive lower strap clip 3326 and looped back on itself. Passing more of each lower strap 3320 through the aperture ively reduces the length of the lower strap 3320, allowing the force vectors to be modified and the fit of the patient ace 3000 to be adjusted.

P1419NZ4 The oning and stabilising structure 3300 may also comprise one or more of a top crown strap 3330, a pair of lateral crown straps 3332 and a neck strap 3334. In the example illustrated in Figs. 89-95, the upper straps 3310 and lower straps 3320 are connected to ends of a top crown strap 3330. The top crown strap 3330 is configured to pass around the patient’s head and lie against superiorly and iorly facing surfaces. The top crown strap 3330 may be configured to overlie the parietal bone of the patient’s skull. Each end of the top crown strap 3330 connects to a respective one of the upper straps 3310 and also to a respective one of a pair of lateral crown straps 3332. Each one of the lateral crown straps 3332 connects between the upper strap 3310 and the lower strap 3320 on a respective side of the patient’s head.

The inferior ends of the lateral crown straps 3332 are connected to each other by a neck strap 3334. The neck strap 3334 may be ured to pass across the sagittal plane and lie against inferior and/or posterior facing surfaces of the patient’s head or lie against the back of the patient’s neck. The neck strap 3334 may overlie, or lie inferior to, the tal bone of the patient’s skull.

The length of the top crown strap 3330 may be selectively able. In the example illustrated in Figs. 89-95 the top crown strap 3330 is formed by two strap portions which are connected by a link having a pair of apertures. Each of the two strap portions forming the top crown strap 3330 is able to pass through a respective one of the apertures then loop back and secure to itself, for example via hook and loop material, a further clip, a band or the like. The amount of each top strap portion that passes through the link can be varied to adjust the length of the top crown strap 3330 and in turn adjust the fit of the positioning and stabilising structure 3300.

Once all the headgear straps have been ed and the desired fit of the patient interface 3000 has been achieved, the magnetic clip connection provided by the lower strap clips 3326 enables the lower straps 3320 to be quickly disengaged from the lower strap connection points 3325 on the frame 3350, allowing the patient ace 3000 to be removed from the patient without adjustment of straps. Similarly, when the patient dons the patient interface again, the lower strap clips 3326 can be y engaged at the lower strap connection points 3325 to fit the patient interface 3000 t the need to adjust straps. Further advantages and features of a P1419NZ4 positioning and stabilising structure comprising magnetic clips are described in WO 2014/110622, the entire contents of which are incorporated herein by reference.

In certain forms of the present technology, a system is provided comprising more than one positioning and stabilizing structure 3300, each being configured to provide a retaining force to correspond to a different size and/or shape range. For example the system may comprise one form of positioning and stabilizing structure 3300 suitable for a large sized head, but not a small sized head, and another. suitable for a small sized head, but not a large sized head.

Figs. 184 and 185 show a patient interface 3000 comprising the plenum chamber 3200 shown in Figs. 134 to 141. The patient interface 3000 in this example also comprises a oning and stabilising structure 3300 to hold the plenum chamber 3200 in sealing position on the patient’s face in use. The oning and stabilising structure 3300 in this e comprises a pair of headgear tubes 3340.

The pair of headgear tubes 3340 are connected to each other at their or ends and are each configured to lie t or and lateral surfaces of the t’s head in use. Each of the headgear tubes 3340 may be configured to lie between and eye and an ear of the t in use. The inferior end of each headgear tube 3340 is configured to fluidly connect to the plenum chamber 3300. In this example, the or end of each headgear tube 3340 connects to a headgear tube connector 3344 configured to connect to the shell 3210 of the plenum chamber 3200. The positioning and stabilising structure 3300 comprises a conduit headgear inlet 3390 at the junction of the two headgear tubes 3340. The conduit headgear inlet 3390 is configured to receive a pressurised flow of gas, for example via an elbow comprising a connection port 3600, and allow the flow of gas into hollow interiors of the headgear tubes 3340. The headgear tubes 3340 supply the pressurised flow of gas to the plenum chamber 3200.

The positioning and stabilising structure 3300 may comprise one or more straps in on to the headgear tubes 3340. In this example the positioning and stabilising ure 3300 comprises a pair of upper straps 3310 and a pair of lower straps 3320. The posterior ends of the upper straps 3310 and lower straps 3320 are joined together. The junction between the upper straps 3310 and lower strap 3320 is configured to lie t a posterior surface of the patient’s head in use, providing an P1419NZ4 anchor for the upper strap 3310 and lower straps 3320. Anterior ends of the upper straps 3310 connect to the headgear tubes 3340. In this example each headgear tube 3340 comprises a tab 3342 having an opening through which a respective upper strap 3310 can be passed through and then looped back and secured onto itself to secure the upper headgear strap 3310 to the headgear tube 3340. The positioning and ising structure 3300 also comprises a lower strap clip 3326 ed to the anterior end of each of the lower straps 3320. Each of the lower strap clip 3326 is configured to connect to a lower connection point 3325 on the plenum chamber 3200. In this example, the lower strap clips 3326 are secured magnetically to the lower connection points 3325. In some examples, there is also a mechanical engagement between the lower strap clips 3326 and the lower connection points 3325.

The headgear tube connectors 3344 may be configured to allow the patient to breathe ambient air in the absence of pressure within the plenum chamber 3200. Each headgear tube connector 3344 may comprise an anti-asphyxia valve (AAV). The AAV in each headgear tube connector 3344 may be configured to open in the absence of pressure within the plenum chamber 3200 in order to allow a flow of air between the interior of the plenum chamber 3200 and ambient. Each AAV may be biased into a configurations which blocks the flow of air from the interior of the plenum chamber 3200 into a respective headgear tube 3340 but allows for the ge of air between the plenum chamber 3200 and ambient. When the ar tubes 3340 are pressurised the AAV in each ar tube tor 3344 may prevent the exchange of air between the interior of the plenum chamber 3200 and ambient but allow for a flow of air from the respective headgear tube 3340 into the plenum chamber 3204 breathing by the patient. .3.3 Vent In one form, the patient interface 3000 includes a vent 3400 ucted and ed to allow for the washout of exhaled gases, e.g. carbon dioxide.

In certain forms the vent 3400 is configured to allow a continuous vent flow from an interior of the plenum chamber 3200 to ambient whilst the pressure within the plenum chamber is positive with respect to ambient. The vent 3400 is P1419NZ4 ured such that the vent flow rate has a magnitude sufficient to reduce rebreathing of exhaled CO2 by the patient while maintaining the therapeutic pressure in the plenum chamber in use.

One form of vent 3400 in accordance with the present 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.

The vent 3400 may be located in the plenum chamber 3200. atively, the vent 3400 is located in a decoupling structure, e.g., a swivel.

In the example illustrated in Figs. 89-95, the patient interface 3000 comprises a vent 3400. The vent 3400 in this example comprises passages within the frame 3350 and swivel elbow ly 3610 through which air can flow from the interior of the plenum chamber 3200 to atmosphere. As shown in Figs. 91, 95 and 103-105, the frame 3350 comprises four holes g part of the vent 3400 around the periphery of the frame inlet connection port 3354. In other examples any number of vent holes, including a single vent hole, may be provided to the frame 3350. As shown in Fig. 90, air can flow into the swivel elbow assembly 3610 and then out to atmosphere through exterior holes of the swivel elbow assembly 3610 g part of the vent 3400. The swivel elbow assembly 3610 may be substantially as described in International ation No. incorporated herein by reference.

The plenum chambers 3200 shown in Figs. 126-157 comprise a vent 3400. In this example, the vent 3400 comprises a plurality of holes. In these examples the vent 3400 is provided to the shell 3210. The holes of the vent 3400 are formed in the shell 3210 in this example. In other examples of the present technology the patient interface 3000 may comprises a vent module, either permanently or detachably connected to the plenum chamber 3200. In some examples of the present technology the t interface 3000 comprises a diffuser configured to diffuse air flowing though the vent 3400. In the plenum chambers 3400 shown in Fig. 126-157, the vent 3400 is provided lly. A vent 3400 provided centrally with respect to the plenum chamber 3200 advantageously is less prone to being blocked during side sleeping.

P1419NZ4 Additionally, the vent 3400 in these examples is provided at an inferior location on the shell 3210. The inferior location on the shell 3210 means that the vent 3400 is aligned approximately with the patient’s mouth. A large tion of the exhaled gas from the patient may come from the t’s mouth, so a vent 3400 located opposite the patient’s mouth may provide for good gas washout. Furthermore, since the inlet ports 3240 of the plenum chamber 3200 are provided at a superior location on the plenum chamber 3200, a bias flow of air received at the inlet ports 3240 may flow through a large volume (e.g. from a superior location to an inferior on), which may provide for efficient gas washout and may reduce the likelihood of stagnant air pockets bypassed by the bias flow. .3.4 Decoupling structure(s) In one form the patient ace 3000 includes at least one decoupling structure, for e, a swivel or a ball and socket. .3.5 Connection port Connection port 3600 allows for connection to the air t 4170. .3.6 Forehead support In one form, the patient interface 3000 includes a forehead support 3700 such as that shown in Fig. 3A. In other es, e.g., as shown in Figs. 7-125, the patient interface 3000 may e a forehead support. Furthermore, the patient interface 3000 may be configured not to contact the patient’s forehead at all. .3.7 Anti-asphyxia valve In one form, the patient interface 3000 includes an anti-asphyxia valve.

As described above, the patient interface 3000 may comprise one or more headgear tubes 3340 connected to a plenum chamber 3200 via a headgear tube connector 3344 comprising an anti-asphyxia valve. Alternatively, or additionally, the patient interface 3000 may comprise a swivel elbow configured to connect to a supply conduit, the swivel elbow comprising an anti-asphyxia valve. In other examples, an anti-asphyxia valves may be built into a plenum chamber 3200, for example by being ed to a shell 3210 of the plenum chamber 3200.

P1419NZ4 .3.8 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 ian to supply supplemental oxygen. In one form, this allows for the direct measurement of a property of gases within the plenum chamber 3200, such as the re. .4 RPT DEVICE An RPT device 4000 in accordance with one aspect of the present technology comprises mechanical, pneumatic, and/or electrical components and is configured to execute one or more algorithms, such as any of the methods, in whole or in part, described herein. The RPT device 4000 may be configured to generate a flow of air for delivery to a patient’s airways, such as to treat one or more of the respiratory ions described elsewhere in the present document.

In one form, the RPT device 4000 is constructed and ed to be capable of ring a flow of air in a range of -20 L/min to +150 L/min while maintaining a positive pressure of at least 6 cmH2O, or at least 10cmH2O, or at least cmH2O.RPT device algorithms The RPT device may have an external housing 4010, formed in two parts, an upper portion 4012 and a lower portion 4014. Furthermore, the external housing 4010 may include one or more panel(s) 4015. The RPT device 4000 comprises a chassis 4016 that supports one or more internal components of the RPT device 4000.

The RPT device 4000 may e a handle 4018.

The pneumatic path of the RPT device 4000 may comprise one or more air path items, e.g., an inlet air filter 4112, an inlet muffler 4122, a pressure generator 4140 capable of supplying air at positive pressure (e.g., a blower 4142), an outlet muffler 4124 and one or more transducers 4270, such as pressure sensors and flow rate s.

As mentioned above, in some forms of the t technology, the central controller may be configured to implement one or more algorithms expressed as P1419NZ4 computer programs stored in a non-transitory computer readable storage medium, such as memory. The algorithms are generally grouped into groups ed to as modules.

The RPT device 4000 may have an ical power supply 4210, one or more input devices 4220, a central controller, a y device controller, a pressure generator 4140, one or more protection circuits, memory, transducers 4270, data communication interface and one or more output devices 4290. Electrical components 4200 may be mounted on a single Printed Circuit Board Assembly (PCBA) 4202. In an alternative form, the RPT device 4000 may include more than one PCBA 4202.

An RPT device in accordance with one form of the present technology may include an air filter 4110, or a plurality of air filters 4110.

In one form, an outlet air filter 4114, for e an antibacterial filter, is located between an outlet of the pneumatic block 4020 and a patient interface 3000.

An RPT device in accordance with one form of the present technology may include a muffler 4120, or a ity of mufflers 4120.

In one form of the present technology, an anti-spill back valve 4160 is d between the humidifier 5000 and the pneumatic block 4020. The anti-spill back valve is constructed and ed to reduce the risk that water will flow upstream from the humidifier 5000, for example to the motor 4144. .5 AIR CIRCUIT An air circuit 4170 in accordance with an aspect of the present technology is a conduit or a tube constructed and arranged to allow, in use, a flow of air to travel between two components such as RPT device 4000 and the patient interface 3000.

In particular, the air circuit 4170 may be in fluid connection with the outlet of the pneumatic block 4020 and the patient interface. The air circuit may be referred to as an air ry tube. In some cases there may be separate limbs of the circuit for tion and exhalation. In other cases a single limb is used.

P1419NZ4 In some forms, the air circuit 4170 may se one or more heating elements configured to heat air in the air circuit, for example to maintain or raise the temperature of the air. The heating element may be in a form of a heated wire circuit, and may comprise one or more transducers, such as temperature sensors. In one form, the heated wire circuit may be helically wound around the axis of the air circuit 4170.

The heating element may be in communication with a ller such as a central controller. One example of an air circuit 4170 comprising a heated wire circuit is bed in United States Patent 8,733,349, which is incorporated herewithin in its entirety by reference. .5.1 Oxygen delivery In one form of the present technology, supplemental oxygen 4180 is delivered to one or more points in the tic path, such as upstream of the pneumatic block 4020, to the air circuit 4170 and/or to the patient interface 3000. .6 HUMIDIFIER .6.1 Humidifier overview In one form of the present logy there is provided a humidifier 5000 (e.g. as shown in Fig. 5A) to change the absolute humidity of air or gas for ry to a patient relative to ambient air. Typically, the humidifier 5000 is used to increase the absolute humidity and increase the temperature of the flow of air ive to ambient air) before delivery to the patient’s airways.

The humidifier 5000 may comprise a humidifier reservoir 5110, a humidifier inlet 5002 to receive a flow of air, and a fier outlet 5004 to deliver a humidified flow of air. In some forms, as shown in Fig. 5A and Fig. 5B, an inlet and an outlet of the humidifier reservoir 5110 may be the humidifier inlet 5002 and the humidifier outlet 5004 respectively. The humidifier 5000 may further comprise a humidifier base 5006, which may be adapted to receive the humidifier reservoir 5110 and comprise a heating element 5240.

As shown in Fig. 5C, the humidifier controller 5250 may comprise one or more controllers, such as a central humidifier controller 5251, a heated air circuit controller 5254 configured to control the temperature of a heated air circuit 4171 and/or a heating element controller 5252 configured to control the temperature of a heating element 5240. .6.2 Humidifier components .6.2.1 Water reservoir According to one arrangement, the humidifier 5000 may comprise a water reservoir 5110 configured to hold, or retain, a volume of liquid (e.g. water) to be evaporated for humidification of the flow of air. The water reservoir 5110 may be configured to hold a predetermined maximum volume of water in order to provide adequate humidification for at least the duration of a respiratory therapy session, such as one evening of sleep. Typically, the reservoir 5110 is configured to hold several hundred millilitres of water, e.g. 300 millilitres (ml), 325 ml, 350 ml or 400 ml. In other forms, the humidifier 5000 may be configured to receive a supply of water from an al water source such as a building’s water supply system.

According to one aspect, the water reservoir 5110 is configured to add humidity to a flow of air from the RPT device 4000 as the flow of air travels hrough. In one form, the water oir 5110 may be configured to encourage the flow of air to travel in a tortuous path through the reservoir 5110 while in contact with the volume of water n. ing to one form, the oir 5110 may be removable from the humidifier 5000, for example in a lateral direction as shown in Fig. 5A and Fig. 5B.

The reservoir 5110 may also be configured to rage egress of liquid therefrom, such as when the reservoir 5110 is displaced and/or rotated from its normal, working orientation, such as through any apertures and/or in between its subcomponents.

As the flow of air to be humidified by the humidifier 5000 is typically pressurised, the reservoir 5110 may also be configured to prevent losses in pneumatic re through leak and/or flow impedance.

P1419NZ4 .6.2.2 Conductive portion According to one arrangement, the reservoir 5110 ses a conductive portion 5120 ured to allow efficient transfer of heat from the heating element 5240 to the volume of liquid in the reservoir 5110. In one form, the conductive n 5120 may be arranged as a plate, although other shapes may also be suitable.

All or a part of the conductive portion 5120 may be made of a lly conductive material such as aluminium (e.g. approximately 2 mm thick, such as 1 mm, 1.5 mm, 2.5 mm or 3 mm), another heat conducting metal or some plastics. In some cases, suitable heat conductivity may be achieved with less conductive als of suitable geometry. .6.2.3 Humidifier reservoir dock In one form, the humidifier 5000 may comprise a humidifier oir dock 5130 (as shown in Fig. 5B) configured to receive the humidifier reservoir 5110.

In some arrangements, the humidifier reservoir dock 5130 may comprise a locking feature such as a locking lever 5135 ured to retain the reservoir 5110 in the humidifier reservoir dock 5130. .6.2.4 Water level indicator The humidifier reservoir 5110 may comprise a water level indicator 5150 as shown in Fig. 5A-5B. In some forms, the water level indicator 5150 may provide one or more indications to a user such as the patient 1000 or a care giver regarding a quantity of the volume of water in the humidifier reservoir 5110. The one or more indications provided by the water level indicator 5150 may include an indication of a maximum, predetermined volume of water, any portions f, such as 25%, 50% or 75% or volumes such as 200 ml, 300 ml or 400ml. .6.2.5 Humidifier ucer(s) The humidifier 5000 may comprise one or more humidifier transducers (sensors) 5210 instead of, or in addition to, transducers 4270 described above.

Humidifier transducers 5210 may include one or more of an air pressure sensor 5212, an air flow rate ucer 5214, a temperature sensor 5216, or a humidity sensor 5218 as shown in Fig. 5C. A humidifier transducer 5210 may produce one or more P1419NZ4 output signals which may be communicated to a controller such as the central controller and/or the humidifier controller 5250. In some forms, a humidifier transducer may be located externally to the fier 5000 (such as in the air circuit 4170) while communicating the output signal to the controller. .7 BREATHING WAVEFORMS Fig. 6A shows a model typical breath waveform of a person while sleeping. The horizontal axis is time, and the vertical axis is respiratory flow rate.

While the parameter values may vary, a typical breath may have the following approximate values: tidal volume Vt 0.5L, inhalation time Ti 1.6s, peak inspiratory flow rate Qpeak 0.4 L/s, exhalation time Te 2.4s, peak expiratory flow rate Qpeak -0.5 L/s. The total duration of the , Ttot, is about 4s. The person typically breathes at a rate of about 15 breaths per minute (BPM), with Ventilation Vent about 7.5 L/min.

A typical duty cycle, the ratio of Ti to Ttot, is about 40%. .8 RESPIRATORY PRESSURE THERAPY MODES Various respiratory pressure therapy modes may be implemented by the RPT device 4000 depending on the values of the parameters A and P0 in the ent pressure equation (Error! Reference source not found.) used by the therapy parameter ination thm in one form of the present technology. .9 GLOSSARY For the purposes of the present technology sure, in certain forms of the present technology, one or more of the following definitions may apply. In other forms of the present logy, alternative definitions may apply. .9.1 General Air: In certain forms of the present technology, air may be taken to mean atmospheric air, and in other forms of the present technology air may be taken to mean some other combination of breathable gases, e.g. atmospheric air enriched with oxygen.

P1419NZ4 t: In certain forms of the present technology, the term ambient will be taken to mean (i) external of the treatment system or patient, and (ii) immediately surrounding the treatment system or patient.

For example, ambient humidity with respect to a humidifier may be the humidity of air immediately nding the humidifier, e.g. the humidity in the room where a patient is ng. Such ambient humidity may be different to the humidity outside the room where a patient is sleeping.

In another example, ambient pressure may be the pressure immediately surrounding or external to the body.

In certain forms, ambient (e.g., acoustic) noise may be considered to be the background noise level in the room where a patient is located, other than for example, noise generated by an RPT device or emanating from a mask or t interface. Ambient noise may be generated by sources outside the room.

Automatic Positive Airway re (APAP) therapy: CPAP therapy in which the treatment pressure is automatically adjustable, e.g. from breath to breath, between minimum and maximum limits, depending on the ce or absence of indications of SDB events. uous ve Airway Pressure (CPAP) therapy: Respiratory pressure therapy in which the treatment pressure is approximately nt through a respiratory cycle of a patient. In some forms, the pressure at the entrance to the airways will be slightly higher during exhalation, and slightly lower during tion.

In some forms, the pressure will vary between different respiratory cycles of the patient, for e, being increased in response to detection of indications of partial upper airway obstruction, and decreased in the absence of indications of partial upper airway obstruction.

Flow rate: The volume (or mass) of air delivered per unit time. Flow rate may refer to an instantaneous quantity. In some cases, a reference to flow rate will be a nce to a scalar quantity, namely a quantity having magnitude only. In other cases, a reference to flow rate will be a reference to a vector quantity, namely a P1419NZ4 quantity having both magnitude and direction. Flow rate may be given the symbol Q.

‘Flow rate’ is sometimes shortened to simply ‘flow’ or ‘airflow’.

Humidifier: The word humidifier will be taken to mean a humidifying tus constructed and arranged, or configured with a physical structure to be capable of providing a therapeutically cial amount of water (H2O) vapour to a flow of air to ameliorate a medical respiratory condition of a patient.

Leak: The word leak will be taken to be an unintended flow of air. In one example, leak may occur as the result of an incomplete seal between a mask and a patient's face. In another example leak may occur in a swivel elbow to the ambient.

Noise, conducted tic): Conducted noise in the present document refers to noise which is carried to the patient by the pneumatic path, such as the air circuit and the t interface as well as the air therein. In one form, conducted noise may be quantified by measuring sound pressure levels at the end of an air circuit.

Noise, radiated (acoustic): Radiated noise in the present document refers to noise which is carried to the t by the ambient air. In one form, radiated noise may be fied by measuring sound power/pressure levels of the object in question according to ISO 3744.

Noise, vent (acoustic): Vent noise in the present document refers to noise which is generated by the flow of air through any vents such as vent holes of the patient interface. t: A person, whether or not they are suffering from a respiratory condition.

Pressure: Force per unit area. Pressure may be expressed in a range of units, including cmH2O, g-f/cm2 and hectopascal. 1 cmH2O is equal to 1 g-f/cm2 and is approximately 0.98 hectopascal. In this specification, unless otherwise , pressure is given in units of cmH2O.

The pressure in the patient interface is given the symbol Pm, while the treatment pressure, which represents a target value to be achieved by the mask pressure Pm at the current instant of time, is given the symbol Pt.

Respiratory Pressure Therapy (RPT): The application of a supply of air to an entrance to the airways at a treatment pressure that is typically positive with respect to atmosphere.

Ventilator: A mechanical device that provides pressure support to a patient to perform some or all of the work of breathing. .9.1.1 Materials Silicone or Silicone Elastomer: A synthetic rubber. In this specification, a reference to ne is a reference to liquid ne rubber (LSR) or a compression d silicone rubber (CMSR). One form of commercially available LSR is IC ded in the range of products sold under this trademark), ctured by Dow Corning. Another manufacturer of LSR is Wacker. Unless otherwise specified to the contrary, an exemplary form of LSR has a Shore A (or Type A) indentation hardness in the range of about 35 to about 45 as measured using ASTM D2240.

Polycarbonate: a thermoplastic r of Bisphenol-A Carbonate. .9.1.2 Mechanical properties Resilience: Ability of a material to absorb energy when deformed elastically and to release the energy upon unloading.

Resilient: Will e substantially all of the energy when unloaded.

Includes e.g. certain silicones, and thermoplastic elastomers.

Hardness: The ability of a material per se to resist deformation (e.g. described by a Young’s Modulus, or an ation hardness scale measured on a standardised sample size).

P1419NZ4 • ‘Soft’ materials may include silicone or thermo-plastic elastomer (TPE), and may, e.g. readily deform under finger pressure.

• ‘Hard’ materials may include polycarbonate, polypropylene, steel or aluminium, and may not e.g. readily deform under finger pressure.

Stiffness (or rigidity) of a structure or component: The ability of the ure or component to resist deformation in response to an applied load. The load may be a force or a , e.g. compression, n, bending or torsion. The structure or component may offer different resistances in different directions.

Floppy structure or ent: A structure or component that will change shape, e.g. bend, when caused to support its own weight, within a relatively short period of time such as 1 second.

Rigid structure or component: A structure or component that will not substantially change shape when subject to the loads lly encountered in use. An example of such a use may be setting up and maintaining a patient interface in sealing relationship with an entrance to a patient's airways, e.g. at a load of approximately 20 to 30 cmH2O pressure.

As an example, an I-beam may comprise a different bending stiffness (resistance to a bending load) in a first direction in comparison to a second, orthogonal direction. In another example, a structure or component may be floppy in a first ion and rigid in a second direction. .9.2 Respiratory cycle Apnea: According to some definitions, an apnea is said to have occurred when flow falls below a predetermined threshold for a duration, e.g. 10 s. An obstructive apnea will be said to have occurred when, despite patient , some obstruction of the airway does not allow air to flow. A central apnea will be said to have occurred when an apnea is detected that is due to a reduction in breathing effort, or the absence of breathing , despite the airway being . A mixed apnea occurs when a reduction or absence of breathing effort coincides with an obstructed airway.

Breathing rate: The rate of spontaneous respiration of a patient, usually measured in breaths per .

Duty cycle: The ratio of inhalation time, Ti to total breath time, Ttot.

Effort (breathing): The work done by a spontaneously ing person attempting to breathe.

Expiratory portion of a breathing cycle: The period from the start of expiratory flow to the start of inspiratory flow.

Flow limitation: Flow limitation will be taken to be the state of affairs in a patient's respiration where an increase in effort by the patient does not give rise to a corresponding increase in flow. Where flow limitation occurs during an inspiratory portion of the breathing cycle it may be bed as inspiratory flow limitation.

Where flow limitation occurs during an expiratory portion of the breathing cycle it may be described as expiratory flow limitation. ea: ing to some definitions, a hypopnea is taken to be a reduction in flow, but not a cessation of flow. In one form, a hypopnea may be said to have occurred when there is a reduction in flow below a threshold rate for a duration.

A l hypopnea will be said to have occurred when a hypopnea is ed that is due to a reduction in ing effort. In one form in adults, either of the following may be regarded as being hypopneas: (i) a 30% reduction in patient breathing for at least 10 seconds plus an associated 4% desaturation; or (ii) a reduction in patient breathing (but less than 50%) for at least 10 seconds, with an associated desaturation of at least 3% or an arousal.

Hyperpnea: An increase in flow to a level higher than normal.

Inspiratory portion of a breathing cycle: The period from the start of inspiratory flow to the start of expiratory flow will be taken to be the inspiratory portion of a breathing cycle.

P1419NZ4 Patency (airway): The degree of the airway being open, or the extent to which the airway is open. A patent airway is open. Airway y may be quantified, for example with a value of one (1) being patent, and a value of zero (0), being closed (obstructed).

Positive End-Expiratory Pressure (PEEP): The pressure above atmosphere in the lungs that exists at the end of expiration.

Peak flow rate ): The maximum value of flow rate during the inspiratory portion of the atory flow waveform.

Respiratory flow rate, patient airflow rate, respiratory airflow rate (Qr): These terms may be understood to refer to the RPT ’s estimate of atory flow rate, as opposed to "true respiratory flow rate" or "true respiratory flow rate", which is the actual respiratory flow rate experienced by the patient, usually expressed in litres per minute.

Tidal volume (Vt): The volume of air inhaled or exhaled during normal breathing, when extra effort is not applied. In principle the inspiratory volume Vi (the volume of air inhaled) is equal to the expiratory volume Ve (the volume of air exhaled), and therefore a single tidal volume Vt may be defined as equal to either quantity. In practice the tidal volume Vt is estimated as some combination, e.g. the mean, of the inspiratory volume Vi and the expiratory volume Ve. (inhalation) Time (Ti): The duration of the inspiratory portion of the respiratory flow rate waveform. (exhalation) Time (Te): The on of the expiratory portion of the respiratory flow rate waveform. (total) Time (Ttot): The total on between the start of one inspiratory portion of a respiratory flow rate waveform and the start of the following inspiratory portion of the respiratory flow rate waveform.

P1419NZ4 Typical recent ventilation: The value of ventilation around which recent values of ventilation Vent over some predetermined timescale tend to r, that is, a measure of the central tendency of the recent values of ation.

Upper airway obstruction (UAO): includes both partial and total upper airway obstruction. This may be ated with a state of flow limitation, in which the flow rate increases only slightly or may even decrease as the pressure difference across the upper airway increases (Starling resistor behaviour).

Ventilation (Vent): A measure of a rate of gas being exchanged by the patient’s respiratory system. Measures of ventilation may include one or both of atory and tory flow, per unit time. When sed as a volume per minute, this quantity is often referred to as "minute ventilation". Minute ventilation is sometimes given simply as a volume, understood to be the volume per minute. .9.3 Anatomy .9.3.1 Anatomy of the face Ala: the external outer wall or "wing" of each l (plural: alar) Alare: The most lateral point on the nasal ala.

Alar curvature (or alar crest) point: The most posterior point in the curved base line of each ala, found in the crease formed by the union of the ala with the cheek.

Auricle: The whole external visible part of the ear. (nose) Bony framework: The bony framework of the nose comprises the nasal bones, the frontal s of the maxillae and the nasal part of the frontal bone. (nose) Cartilaginous framework: The cartilaginous framework of the nose comprises 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.

P1419NZ4 Columella angle: The angle between the line drawn through the midpoint of the nostril aperture and a line drawn perpendicular to the Frankfort horizontal while ecting subnasale.

Frankfort horizontal plane: A line extending from the most inferior point of the orbital margin to the left tragion. The tragion is the deepest point in the notch or to the tragus of the auricle.

Glabella: Located on the soft tissue, the most prominent point in the midsagittal plane of the forehead.

Lateral nasal cartilage: A generally triangular plate of cartilage. Its superior margin is attached to the nasal bone and frontal s of the maxilla, and its inferior margin is connected to the greater alar cartilage.

Lip, lower le us): Lip, upper (labrale superius): Greater alar cartilage: A plate of cartilage lying below the l nasal cartilage. It is curved around the anterior part of the naris. Its posterior end is connected to the l process of the maxilla by a tough fibrous membrane containing three or four minor cartilages of the ala.

Nares (Nostrils): Approximately ellipsoidal apertures 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-labial fold: The skin fold or groove that runs from each side of the nose to the corners of the mouth, separating the cheeks from the upper lip.

Naso-labial angle: The angle between the columella and the upper lip, while intersecting subnasale.

Otobasion inferior: The lowest point of attachment of the auricle to the skin of the face.

P1419NZ4 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 identified 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.

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

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

Sagittal plane: A vertical plane that passes from anterior (front) to posterior (rear). The midsagittal plane is a sagittal plane that s the body into right and left halves.

Sellion: d on the soft tissue, the most concave point overlying the area of the frontonasal suture.

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

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. enton: The point of greatest concavity in the midline of the lower lip between labrale inferius and soft tissue pogonion .9.3.2 Anatomy of the skull Frontal bone: The frontal bone includes a large vertical portion, the squama frontalis, corresponding to the region known as the forehead.

P1419NZ4 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 d above the mandible and below the orbits. The l process of the maxilla projects upwards by the side of the nose, and forms part of its lateral boundary.

Nasal bones: The nasal bones are two small oblong bones, varying 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 their junction, the "bridge" of the nose.

Nasion: 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, the foramen magnum, h which the cranial cavity communicates with the vertebral canal. The curved plate behind the n magnum is the squama occipitalis.

Orbit: The bony cavity in the skull to contain the eyeball.

Parietal bones: The parietal bones are the bones that, when joined together, form the roof and sides of the cranium.

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 includes two zygomatic bones, located in the upper and l parts of the face and forming the prominence of the cheek. .9.3.3 Anatomy of the respiratory system Diaphragm: A sheet of muscle that extends across the bottom of the rib cage. The diaphragm separates the thoracic cavity, containing the heart, lungs and ribs, from the abdominal cavity. As the diaphragm contracts the volume of the thoracic cavity increases and air is drawn into the lungs.

P1419NZ4 Larynx: The , or voice box houses the vocal folds and connects the inferior part of the pharynx (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 ar 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 fin 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 or to (below) the nasal cavity, and superior to the oesophagus and . The pharynx is conventionally divided into three sections: the nasopharynx (epipharynx) (the nasal part of the pharynx), the rynx (mesopharynx) (the oral part of the pharynx), and the laryngopharynx (hypopharynx). .9.4 Patient interface Anti-asphyxia valve (AAV): The component or sub-assembly of a mask system that, by opening to atmosphere in a failsafe manner, reduces the risk of excessive CO2 rebreathing by a patient.

Elbow: An elbow is an example of a structure that s an axis of flow of air travelling therethrough to change direction through an angle. In one form, the angle may be approximately 90 s. In another form, the angle may be more, or less than 90 degrees. The elbow may have an approximately circular cross-section. In another form the elbow may have an oval or a rectangular cross-section. In certain forms an elbow may be rotatable with respect to a mating component, e.g. about 360 degrees. In certain forms an elbow may be ble from a mating component, e.g.

P1419NZ4 via a snap connection. In certain forms, an elbow may be assembled to a mating component via a one-time snap during manufacture, but not ble by a patient.

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 ght.

Headgear: Headgear will be taken to mean a form of positioning and stabilizing structure designed for use on a head. For example the headgear may comprise a collection of one or more , ties and stiffeners configured 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, flexible, elastic material such as a laminated composite of foam and fabric.

Membrane: Membrane will be taken to mean a typically thin element that has, preferably, ntially no resistance to bending, but has resistance to being stretched.

Plenum chamber: a mask plenum r will be taken to mean a portion of a t interface having walls at least lly enclosing a volume of space, the volume having air therein pressurised above heric pressure in use. A shell may form part of the walls of a mask plenum chamber.

Seal: May be a noun form ("a seal") which refers to a structure, or a verb form ("to seal") which refers to the . Two elements may be constructed and/or arranged to ‘seal’ or to effect ‘sealing’ therebetween without requiring a separate ‘seal’ element per se.

Shell: A shell will be taken to mean a curved, relatively thin structure having bending, tensile and compressive stiffness. For example, a curved structural wall of a mask may be a shell. In some forms, a shell may be faceted. In some forms a shell may be airtight. In some forms a shell may not be airtight.

P1419NZ4 Stiffener: A stiffener will be taken to mean a ural component designed to increase the bending resistance of another ent in at least one direction.

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

Swivel (noun): A subassembly of components configured to rotate about a common axis, preferably independently, preferably 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 preferably comprises a matched pair of cylindrical ts. There may be little or no leak flow of air from the swivel in use.

Tie (noun): A structure designed to resist tension.

Vent: (noun): A structure that allows a flow of air from an interior of the mask, or conduit, to ambient air for clinically effective washout of exhaled gases. For example, a clinically effective t may involve a flow rate of about 10 litres per minute to about 100 litres per minute, depending on the mask design and treatment pressure. .9.5 Shape of structures Products in accordance with the present technology may comprise one or more three-dimensional ical structures, for example a mask cushion or an impeller. The three-dimensional structures may be bounded by two-dimensional surfaces. These surfaces may be distinguished using a label to describe an associated surface orientation, location, function, or some other characteristic. For example a structure may comprise one or more of an anterior surface, a posterior surface, an interior surface and an exterior surface. In r example, a seal-forming structure may comprise a face-contacting (e.g. outer) e, and a separate non-facecontacting (e.g. underside or inner) surface. In r example, a ure may comprise a first surface and a second surface.

P1419NZ4 To tate describing the shape of the three-dimensional structures and the surfaces, we first consider a cross-section through a surface of the structure at a point, p. See Fig. 3B to Fig. 3F, which illustrate examples of cross-sections at point p on a surface, and the resulting plane curves. Figs. 3B to 3F also rate an outward normal vector at p. The outward normal vector at p points away from the surface. In some examples we describe the surface from the point of view of an imaginary small person ng upright on the e. .9.5.1 Curvature in one dimension The curvature of a plane curve at p may be bed as having a sign (e.g. positive, negative) and a magnitude (e.g. 1/radius of a circle that just touches the curve at p).

Positive curvature: If the curve at p turns towards the outward normal, the curvature at that point will be taken to be positive (if the ary small person leaves the point p they must walk uphill). See Fig. 3B (relatively large positive curvature compared to Fig. 3C) and Fig. 3C (relatively small ve curvature compared to Fig. 3B). Such curves are often referred to as concave.

Zero curvature: If the curve at p is a straight line, the ure will be taken to be zero (if the imaginary small person leaves the point p, they can walk on a level, r up nor down). See Fig. 3D.

Negative curvature: If the curve at p turns away from the outward normal, the curvature in that direction at that point will be taken to be negative (if the imaginary small person leaves the point p they must walk ll). See Fig. 3E (relatively small negative curvature compared to Fig. 3F) and Fig. 3F (relatively large negative curvature compared to Fig. 3E). Such curves are often referred to as convex. .9.5.2 Curvature of two dimensional surfaces A description of the shape at a given point on a two-dimensional surface in accordance with the present technology may include multiple normal crosssections.

The multiple cross-sections may cut the surface in a plane that includes the outward normal (a "normal plane"), and each cross-section may be taken in a different P1419NZ4 direction. Each cross-section results in a plane curve with a corresponding ure.

The different curvatures at that point may have the same sign, or a different sign.

Each of the curvatures at that point has a magnitude, e.g. relatively small. The plane curves in Figs. 3B to 3F could be examples of such multiple sections at a particular point.

Principal curvatures and directions: The directions of the normal planes where the curvature of the curve takes its maximum and minimum values are called the principal directions. In the examples of Fig. 3B to Fig. 3F, the maximum curvature occurs in Fig. 3B, and the minimum occurs in Fig. 3F, hence Fig. 3B and Fig. 3F are cross sections in the principal directions. The principal curvatures at p are the curvatures in the principal directions.

Region of a surface: A connected set of points on a surface. The set of points in a region may have similar characteristics, e.g. curvatures or signs.

Saddle region: A region where at each point, the pal curvatures have opposite signs, that is, one is positive, and the other is negative (depending on the direction to which the imaginary person turns, they may walk uphill or downhill).

Dome region: A region where at each point the principal curvatures have the same sign, e.g. both positive (a "concave dome") or both negative (a "convex dome"). rical region: A region where one pal curvature is zero (or, for example, zero within manufacturing tolerances) and the other principal curvature is non-zero.

Planar region: A region of a surface where both of the principal ures are zero (or, for e, zero within manufacturing tolerances).

Edge of a surface: A ry or limit of a surface or region.

Path: In certain forms of the present technology, ‘path’ will be taken to mean a path in the mathematical – topological sense, e.g. a continuous space curve from f(0) to f(1) on a surface. In certain forms of the present technology, a ‘path’ may P1419NZ4 be described as a route or course, including e.g. a set of points on a surface. (The path for the imaginary person is where they walk on the surface, and is analogous to a garden path).

Path length: In certain forms of the present technology, ‘path length’ will be taken to mean the distance along the surface from f(0) to f(1), that is, the ce along the path on the surface. There may be more than one path n two points on a surface and such paths may have different path lengths. (The path length for the imaginary person would be the ce they have to walk on the surface along the path).

Straight-line distance: The straight-line ce is the distance between two points on a surface, but without regard to the surface. On planar regions, there would be a path on the surface having the same path length as the straight-line distance between two points on the surface. On non-planar surfaces, there may be no paths having the same path length as the straight-line distance between two points.

(For the imaginary person, the straight-line distance would correspond to the distance ‘as the crow .) .9.5.3 Space curves Space curves: Unlike a plane curve, a space curve does not necessarily lie in any particular plane. A space curve may be closed, that is, having no endpoints. A space curve may be considered to be a one-dimensional piece of three-dimensional space. An imaginary person walking on a strand of the DNA helix walks along a space curve. A typical human left ear comprises a helix, which is a and helix, see Fig. 3Q. A typical human right ear comprises a helix, which is a right-hand helix, see Fig. 3R. Fig. 3S shows a right-hand helix. The edge of a ure, e.g. the edge of a membrane or impeller, may follow a space curve. In general, a space curve may be described by a curvature and a torsion at each point on the space curve. Torsion is a measure of how the curve turns out of a plane. Torsion has a sign and a magnitude.

The torsion at a point on a space curve may be characterised with nce to the tangent, normal and binormal vectors at that point.

P1419NZ4 Tangent unit vector (or unit tangent ): For each point on a curve, a vector at the point specifies a direction from that point, as well as a ude. A tangent unit vector is a unit vector pointing in the same direction as the curve at that point. If an imaginary person were flying along the curve and fell off her vehicle at a particular point, the ion of the tangent vector is the direction she would be travelling.

Unit normal vector: As the imaginary person moves along the curve, this tangent vector itself changes. The unit vector pointing in the same direction that the tangent vector is changing is called the unit principal normal vector. It is dicular to the tangent vector.

Binormal unit vector: The binormal unit vector is perpendicular to both the tangent vector and the principal normal vector. Its direction may be determined by a right-hand rule (see e.g. Fig. 3P), or alternatively by a left-hand rule (Fig. 3O). ting plane: The plane containing the unit tangent vector and the unit pal normal vector. See Figures 3O and 3P.

Torsion of a space curve: The torsion at a point of a space curve is the magnitude of the rate of change of the binormal unit vector at that point. It measures how much the curve deviates from the osculating plane. A space curve which lies in a plane has zero torsion. A space curve which deviates a relatively small amount from the osculating plane will have a relatively small magnitude of n (e.g. a gently sloping helical path). A space curve which deviates a relatively large amount from the osculating plane will have a relatively large ude of torsion (e.g. a steeply sloping helical path). With reference to Fig. 3S, since T2>T1, the magnitude of the torsion near the top coils of the helix of Fig. 3S is greater than the magnitude of the torsion of the bottom coils of the helix of Fig. 3S With reference to the right-hand rule of Fig. 3P, a space curve turning towards the ion of the right-hand binormal may be considered as having a righthand positive torsion (e.g. a right-hand helix as shown in Fig. 3S). A space curve g away from the direction of the right-hand binormal may be considered as having a right-hand negative torsion (e.g. a left-hand helix).

P1419NZ4 Equivalently, and with reference to a left-hand rule (see Fig. 3O), a space curve turning towards the direction of the left-hand binormal may be considered as having a left-hand positive torsion (e.g. a left-hand helix). Hence left-hand positive is equivalent to right-hand negative. See Fig. 3T. .9.5.4 Holes A surface may have a one-dimensional hole, e.g. a hole bounded by a plane curve or by a space curve. Thin structures (e.g. a membrane) with a hole, may be described as having a one-dimensional hole. See for example the one dimensional hole in the surface of structure shown in Fig. 3I, bounded by a plane curve.

A structure may have a two-dimensional hole, e.g. a hole bounded by a e. For example, an inflatable tyre has a two dimensional hole bounded by the interior surface of the tyre. In another example, a bladder with a cavity for air or gel could have a two-dimensional hole. See for e the n of Fig. 3L and the example cross-sections therethrough in Fig. 3M and Fig. 3N, with the interior surface bounding a two ional hole indicated. In a yet another example, a conduit may se a one-dimension hole (e.g. at its entrance or at its exit), and a two-dimension hole bounded by the inside surface of the conduit. See also the two dimensional hole through the structure shown in Fig. 3K, bounded by a surface as shown. .10 OTHER REMARKS Unless the context clearly es otherwise and where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit, between the upper and lower limit of that range, and any other stated or intervening value in that stated range is encompassed within the technology. The upper and lower limits of these intervening ranges, which may be independently ed in the intervening ranges, are also assed within the technology, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the technology.

Furthermore, where a value or values are stated herein as being ented as part of the technology, it is understood that such values may be P1419NZ4 imated, unless ise stated, and such values may be utilized to any suitable significant digit to the extent that a practical technical entation may permit or require it.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this technology belongs. Although any methods and als r or equivalent to those described herein can also be used in the ce or testing of the present technology, a limited number of the exemplary methods and materials are described herein.

When a particular material is identified as being used to construct a component, obvious alternative materials with similar properties may be used as a substitute. Furthermore, unless specified to the contrary, any and all components herein described are understood to be capable of being manufactured and, as such, may be manufactured together or separately.

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.

All publications mentioned herein are incorporated herein by reference in their ty to disclose and describe the methods and/or materials which are the subject of those publications. The publications sed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the present technology is not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided may be different from the actual publication dates, which may need to be independently confirmed.

The terms "comprises" and "comprising" should be interpreted as referring to elements, components, or steps in a clusive manner, indicating that the referenced elements, components, or steps may be present, or utilized, or combined with other ts, components, or steps that are not expressly referenced.

P1419NZ4 The t 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.

Although the technology herein has been described with nce to particular examples, it is to be understood that these examples are merely rative of the principles and applications of the technology. In some ces, the terminology and symbols may imply specific details that are not required to practice the technology. For example, although the terms "first" and "second" may be used, unless otherwise specified, they are not intended to indicate any order but may be utilised to distinguish between distinct elements. Furthermore, although process steps in the methodologies may be bed or illustrated in an order, such an ordering is not required. Those skilled in the art will recognize that such ordering may be modified and/or aspects thereof may be conducted concurrently or even synchronously.

It is therefore to be understood that numerous modifications may be made to the illustrative es and that other arrangements may be devised t departing from the spirit and scope of the technology. .11 REFERENCE SIGNS LIST patient 1000 bed partner 1100 t interface 3000 seal - forming structure 3100 region 3101 boundary 3102 region 3103 P1419NZ4 superior - facing central portion 3111 central saddle n 3112 bridge portion 3113 lateral corner regions 3114 or - facing central portion 3115 lip superior portion 3116 oral hole peripheral portion 3117 lip inferior portion 3118 superior - facing intermediate portion 3121 anterior facing intermediate portion 3125 posterior corners 3131 posterior - facing lateral portion 3135 lateral peripheral support portions 3136 l - facing posterior portion 3141 lateral ns 3145 lateral support portion 3151 flat inferior boundary 3152 curved or boundary 3153 anterior - facing lateral portions 3155 anterior support portions 3161 P1419NZ4 anterior t portions 3165 plenum chamber 3200 chord 3209 shell 3210 top edge 3211 protruding portions 3215 rim 3218 superior point 3220 inferior point 3229 nasal portion 3230 lateral portions 3231 superior periphery 3232 inlet port 3240 oral portion 3260 oral hole 3271 nasal holes 3272 oronasal transition 3275 oning and stabilising structure 3300 upper strap 3310 upper strap connection point 3315 P1419NZ4 lower strap 3320 lower connection point 3325 lower strap clip 3326 top crown strap 3330 lateral crown strap 3332 neck strap 3334 headgear tube 3340 tab 3342 headgear tube connector 3344 frame 3350 snap fit hooks 3351 frame inlet connection port 3354 connection rim 3355 conduit headgear inlet 3390 vent 3400 tion port 3600 swivel elbow assembly 3610 forehead support 3700 RPT device 4000 external housing 4010 P1419NZ4 upper portion 4012 lower n 4014 panel 4015 chassis 4016 handle 4018 pneumatic block 4020 air filter 4110 inlet air filter 4112 outlet air filter 4114 muffler 4120 inlet muffler 4122 outlet muffler 4124 pressure generator 4140 blower 4142 motor 4144 anti - spill back valve 4160 air circuit 4170 heated air circuit 4171 supplemental oxygen 4180 electrical components 4200 P1419NZ4 Printed Circuit Board Assembly (PCBA) 4202 electrical power supply 4210 input devices 4220 transducers 4270 output devices 4290 humidifier 5000 humidifier inlet 5002 humidifier outlet 5004 humidifier base 5006 reservoir 5110 conductive portion 5120 humidifier reservoir dock 5130 locking lever 5135 water level indicator 5150 humidifier ucer 5210 air pressure sensor 5212 air flow rate transducer 5214 ature sensor 5216 heating element 5240 humidifier controller 5250 central humidifier controller 5251 heating element controller 5252 air circuit controller 5254 P1419NZ4 6

Claims

1. A patient interface comprising: a plenum chamber for a patient interface, the plenum chamber pressurisable to a therapeutic pressure of at least 6 cmH2O above ambient air pressure hout a t’s respiratory cycle in use, the plenum chamber comprising: one or more plenum r inlet ports sized and structured to receive a flow of air at the therapeutic pressure for breathing by a patient; and a seal-forming structure constructed and arranged to form a seal with a region of the patient’s face surrounding an entrance to the patient’s airways, the seal-forming structure comprising a nasal portion having at least one nasal hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s nares in use, the seal-forming structure comprising an oral portion having an oral hole configured to deliver the flow of air at said therapeutic pressure to an entrance to the patient’s mouth in use, the seal-forming structure constructed and arranged to maintain said therapeutic pressure in the plenum chamber throughout the patient’s respiratory cycle in use; and a oning and stabilising structure configured to generate a force to hold the seal-forming structure in a therapeutically effective position on the patient’s head, wherein a first surface of the nasal portion configured to engage the patient’s face has a first surface finish and a second e of the oral portion configured to engage the patient’s face has a second surface finish that is ent from the first e finish.

2. The patient interface of claim 1, wherein the first surface finish and the second e finish differ in such a way that a coefficient of friction between the P1419NZ4 seal-forming structure and the patient’s face is greater in the oral portion than in the nasal portion.

3. The patient interface of claim 1 or 2, wherein the first surface finish is configured to provide a smoother feel on the patient’s face than the second e finish, and wherein the second surface finish is configured to provide the oral portion with added grip on the patient’s face.

4. The patient ace of any one of claims 1 to 3, wherein the first surface finish is a frosted surface .

5. The patient interface of any one of claims 1 to 4, n the second surface finish is a ed surface finish.

6. The patient interface of any one of claims 1 to 5, wherein a boundary between the first surface finish and the second surface finish is located on a part of the seal-forming structure configured to contact the patient’s cheeks in use.

7. The patient interface of any one of claims 1 to 6, wherein the seal-forming structure is configured not to engage the patient’s face below the chin in use.

8. The patient interface of any one of claims 1 to 7, n the seal-forming structure comprises a central portion configured to seal against an or periphery of the patient’s nose in use.

9. The t interface of any one of claims 1 to 8, wherein the plenum chamber ses a shell, the seal-forming structure being connected to the shell.

10. The patient interface of any one of claims 1 to 9, wherein the plenum chamber comprises a single inlet port.

11. The patient interface of any one of claims 1 to 10, wherein the plenum chamber comprises a pair of inlet ports to connect with conduit headgear of the patient interface.