NZ766039A

NZ766039A - Methods of detecting a quantity of water in a humidifier

Info

Publication number: NZ766039A
Application number: NZ766039A
Authority: NZ
Inventors: Ronald James Huby; Liam Holley; Andrew Roderick Bath; Matthew Rolf Harrington; Llewelyn Jones Richard; Ian Malcolm Smith
Original assignee: ResMed Pty Ltd
Priority date: 2013-10-21
Filing date: 2014-08-29
Publication date: 2022-03-25
Also published as: NZ733931A; NZ749883A

Abstract

Apparatus for humidifying a flow of air to be delivered to a patient, the apparatus including an inlet (5118) to receive the flow of air, an outlet (5122) to emit a humidified flow of air, a humidifier reservoir (5110) configured to contain a body of water for humidifying the flow of air, the humidifier reservoir being in fluid communication with the inlet and outlet, at least one sensor (e.g. vibration sensor 5234) configured to generate a signal indicative of a physical characteristic associated with the quantity of the body of water in the humidifier reservoir, and a controller. The controller is configured to: determine the quantity of the body of water in the humidifier reservoir, based on the signal; control a change to humidification output based on the determined reservoir water quantity so as to be able to deliver a humidified flow of air throughout a therapy session without running out of water; determine a rate of water usage based on the signal or determined reservoir water quantity; and control at least one of (i) a decrease in the humidification output if the determined rate of water usage is above a threshold value, and (ii) an increase in the humidification output if the determined rate of water usage is below the threshold value.

Description

DIV4/73 TITLE: S OF DETECTING A QUANTITY OF WATER IN A HUMIDIFIER 1 CROSS-REFERENCE TO RELATED APPLICATIONS The present application claims priority from Australian Provisional Patent Application Number AU 2013904049, the entire contents of which is orated herewithin by reference. 2 BACKGROUND OF THE TECHNOLOGY 2.1 FIELD OF THE TECHNOLOGY The present technology relates to one or more of the detection, diagnosis, treatment, prevention and amelioration of respiratory-related ers. The present technology also relates 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 patient.

The airways include a series of ing tubes, which become er, 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 air into the venous blood and carbon dioxide to move out. The trachea divides into right and left main bronchi, which further divide eventually into terminal bronchioles. The bronchi make up the conducting s, and do not take part in gas exchange. Further divisions of the s lead to the respiratory bronchioles, and eventually to the alveoli. The alveolated region of the lung is where the gas exchange takes place, and is referred to as the respiratory zone. See "Respiratory Physiology", by John B. West, Lippincott Williams & Wilkins, 9th edition published 2011.

A range of respiratory disorders exist. Certain disorders may be characterised by particular events, e.g. apneas, hypopneas, and hyperpneas. 505787DIV4/73 Obstructive Sleep Apnea (OSA), a form of Sleep Disordered Breathing (SDB), is characterized 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 ed t to stop breathing for periods typically of 30 to 120 s in duration, sometimes 200 to 300 times per night. It often causes ive 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 affected may have no awareness of the m. 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 a. 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).

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

Chronic Obstructive Pulmonary e (COPD) encompasses any of a group of lower airway diseases that have certain characteristics in common. These include increased resistance to air movement, 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 smoking (primary risk factor), occupational res, air pollution and genetic s. 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 505787DIV4/73 intrinsic muscle pathology, or indirectly via nerve pathology. Some NMD patients are characterised by ssive muscular impairment leading to loss of ambulation, being wheelchair-bound, swallowing ulties, respiratory muscle weakness and, eventually, death from respiratory failure. Neuromuscular disorders can be divided into y progressive and slowly progressive: (i) Rapidly progressive disorders: Characterised by muscle impairment that worsens over months and results in death within a few years (e.g.

Amyotrophic lateral sclerosis (ALS) and Duchenne muscular dystrophy (DMD) in teenagers); (ii) Variable or slowly progressive disorders: Characterised by muscle impairment that worsens over years and only mildly reduces life expectancy (e.g. Limb girdle, Facioscapulohumeral and Myotonic muscular dystrophy). Symptoms of respiratory failure in NMD include: increasing generalised weakness, dysphagia, dyspnea on on 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 cient coupling between the respiratory muscles and the thoracic cage. The disorders are usually characterised by a restrictive defect and share the potential of long term apnic respiratory failure. Scoliosis and/or kyphoscoliosis may cause severe respiratory failure. Symptoms of respiratory failure include: dyspnea on exertion, peripheral oedema, nea, repeated chest infections, morning headaches, fatigue, poor sleep quality and loss of appetite.

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

Furthermore, otherwise healthy individuals may take advantage of such therapies to prevent atory disorders from arising. r, these have a number of omings. 2.2.2 Therapy Continuous Positive Airway Pressure (CPAP) therapy has been used to treat Obstructive Sleep Apnea (OSA). The hypothesis is that continuous ve airway pressure acts as a pneumatic splint and may prevent upper airway ion 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, ult to use, ive and aesthetically unappealing. 505787DIV4/73 Non-invasive ventilation (NIV) provides ventilatory t to a patient through the upper airways to assist the patient in taking a full breath and/or maintain adequate oxygen levels in the body by doing some or all of the work of breathing. The ventilatory support is provided via a patient interface. NIV has been used to treat CSR, OHS, COPD, MD and Chest Wall disorders. In some forms, the comfort and effectiveness of these therapies may be improved.

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

A treatment system may comprise a Respiratory Pressure Therapy Device (RPT device), an air circuit, a humidifier, a patient interface, and data management. 2.2.3.1 Patient Interface A patient interface may be used to interface respiratory equipment to its wearer, for example by providing a flow of air to an ce to the s. The flow of air may be ed via a mask to the nose and/or mouth, a tube to the mouth or a ostomy 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 pressure at sufficient variance with ambient pressure to effect therapy, e.g., at a positive pressure of about 10 cmH2O relative to ambient pressure. For other forms of therapy, such as the delivery of oxygen, the patient interface may not include a seal sufficient to facilitate delivery to the airways of a supply of gas at a positive pressure of about 10 cmH2O.

The design of a t interface presents a number of challenges. The face has a complex three-dimensional shape. The size and shape of noses varies considerably between individuals. Since the head includes bone, age and soft tissue, different regions of the face respond differently to mechanical forces. The jaw or mandible may 505787DIV4/73 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 ive, aesthetically undesirable, , poorly fitting, ult to use, and uncomfortable especially when worn for long s of time or when a patient is unfamiliar with a system. For example, masks designed solely for aviators, masks designed as part of personal protection equipment (e.g. filter masks), SCUBA masks, or for the administration of hetics may be tolerable for their original application, but nevertheless such masks may be undesirably uncomfortable to be worn for extended periods of time, e.g., several hours. This discomfort may lead to a reduction in patient compliance with therapy. 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.

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 Respiratory Pressure Therapy (RPT) Device Air pressure generators are known in a range of applications, e.g. industrialscale ventilation s. However, air pressure generators for medical applications have particular requirements not fulfilled by more generalised air pressure generators, such as the reliability, size and weight requirements of l devices. In addition, even devices designed for l treatment may suffer from omings, ning to one or more of: comfort, noise, ease of use, efficacy, size, weight, manufacturability, cost, and reliability. 505787DIV4/73 An example of the special requirements of certain RPT devices is ic noise.

Table of noise output levels of prior RPT devices (one specimen only, measured using test method specified in ISO3744 in CPAP mode at 10 cmH2O).

RPT Device name A-weighted sound power Year (approx.) level dB(A) es TangoTM 31.9 2007 es TangoTM with Humidifier 33.1 2007 S8 EscapeTM II 30.5 2005 S8 EscapeTM II with H4iTM Humidifier 31.1 2005 S9 AutoSetTM 26.5 2010 S9 AutoSetTM with H5iTM Humidifier 28.6 2010 One known RPT device used for ng sleep disordered breathing is the S9 Sleep Therapy System, manufactured by ResMed Limited. Another e of an RPT device is a ventilator. Ventilators such as the ResMed Stellar™ Series of Adult and Paediatric Ventilators may provide support for invasive and non-invasive non-dependent ventilation for a range of patients for treating a number of conditions such as but not limited to NMD, OHS and COPD.

The ResMed Elisée™ 150 ventilator and ResMed VS III™ ventilator may provide support for invasive and vasive dependent ventilation suitable for adult or paediatric patients for ng a number of conditions. These ventilators e volumetric and barometric ventilation modes with a single or double limb circuit. RPT devices typically comprise a pressure generator, such as a motor-driven blower or a compressed gas reservoir, and are configured to supply a flow of air to the airway of a patient. In some cases, the flow of air may be supplied to the airway of the patient at positive re. The outlet of the RPT device is connected via an air circuit to a patient interface such as those described above. 2.2.4 Humidifier Delivery of a flow of air without humidification may cause drying of airways.

The use of a humidifier with a RPT device and the patient interface produces humidified 505787DIV4/73 gas that minimizes drying of the nasal mucosa and increases patient airway comfort. In addition, in cooler climates, warm air applied generally to the face area in and about the patient interface is more comfortable than cold air. A range of artificial fication devices and systems are known, however they may not fulfil the specialised ements of a medical humidifier.

Medical humidifiers are used to increase humidity and/or ature of the flow of air in on to ambient air when required, typically where the patient may be asleep or resting (e.g. at a hospital). A medical humidifier for bedside placement may be small. A medical humidifier may be configured to only humidify and/or heat the flow of air delivered to the patient without humidifying and/or heating the patient’s surroundings. ased systems (e.g. a sauna, an air conditioner, or an evaporative cooler), for example, may also humidify air that is breathed in by the t, however those systems would also humidify and/or heat the entire room, which may cause discomfort to the occupants. Furthermore medical humidifiers may have more stringent safety constraints than industrial fiers While a number of medical humidifiers are known, they can suffer from one or more shortcomings. Some medical humidifiers may provide inadequate humidification, some are difficult or inconvenient to use by patients.

Humidity refers to the quantity of water vapour present in the air. It is commonly measured in two ways: (2) Absolute Humidity (AH) is the actual content of water vapour in the air recorded in terms of weight per volume - usually in grams per cubic meter (g/m3) or rams per liter . (2) Relative Humidity (RH) is a percentage expression of the actual water vapour content of a gas compared to its capacity to carry water vapour at any given ature.

The capacity of air to hold water vapour increases as the temperature of the air increases. This means that for air with a stable AH, the RH will decline as the temperature of the air is increased. Conversely, for air saturated with water (100% RH), if the temperature is d then the excess water will condense out. Air breathed by humans 505787DIV4/73 is generally naturally heated and humidified by the patient’s airways to reach a temperature of 37°C and 100% humidity. At this ature the absolute humidity (AH) is 44 mg/L.

Medical fiers are ble in many forms and may be a lone device that is coupled to an RPT device via an air circuit, integrated with the RPT device or configured to be directly coupled to the relevant RPT device. While passive humidifiers can provide some relief, generally a heated humidifier is required to provide ient humidity and temperature to the air so that the patient will be comfortable.

Humidifiers typically comprise a humidifier reservoir (also referred to as water reservoir or tub) having a capacity of several hundred milliliters (ml), a heating element for heating the water in the reservoir, a control to enable the level of humidification to be , a gas inlet to receive gas from the flow generator or device, and a gas outlet adapted to be connected to an air circuit that delivers the humidified gas to the patient interface.

A heated passover humidifier is one common form of fier used with a RPT device. In such humidifiers the heating t may be incorporated in a heating plate which sits under, and is in thermal contact with, the humidifier reservoir. Thus, heat is transferred from the heating plate to the fier reservoir primarily by conduction.

The air flow from the RPT device or flow generator or ventilator passes over the heated water in the water tub resulting in water vapour being taken up by the air flow. The ResMed H4i™ and H5i™ Humidifiers are examples of such heated passover humidifiers that are used in combination with ResMed S8 and S9 CPAP systems respectively.

Other humidifiers may also be used such as a bubble or diffuser humidifier, a jet humidifier or a wicking humidifier.

An alternative form of humidification is provided by the ResMed re™ D900 humidifier that uses a CounterStream™ technology that directs the air flow over a large surface area in a first direction whilst supplying heated water to the large surface area in a second opposite direction. The ResMed HumiCare™ D900 humidifier may be used with a range of invasive and non-invasive ventilators. 505787DIV4/73 3 BRIEF SUMMARY OF THE TECHNOLOGY The present technology is directed towards providing medical devices used in the diagnosis, 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 diagnosis, amelioration, treatment or prevention of a respiratory disorder.

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

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

One form of the present technology relates to a method of determining a quantity of a body of liquid in a humidifier.

Some versions of the present technology may e a method of determining a quantity of water in a humidifier. The method may comprise providing a humidifier reservoir configured to retain the quantity of water and connected to an inlet of the humidifier. The method may further comprise delivering a flow of air to the humidifier reservoir through the inlet of the humidifier. The method may further comprise ining a first measure set of the flow of air. The method may r comprise determining the quantity of water based on the first measure set. [0043a] In some versions the first measure set may comprise one or more measures of one or more of: a pressure, a temperature, a flow rate and a noise. In some versions the first e set may be determined at a first location. In some ns the first location may be downstream of the humidifier reservoir. In some versions the first measure set may be determined by a first sensor. In some ns the quantity of water may be determined based on the first measure set and a reference set. In some ns the reference set may comprise a second e set. [0043b] In some versions the second measure set may comprise one or more measures of one or more of: a pressure, a temperature, a flow rate and a noise. In some versions the second measure set may be determined subsequent to determination of the first measure 505787DIV4/73 set. In some versions the second measure set may be determined at least a predetermined length of time subsequent to determination of the first e set. In some versions the reference set may se one or more estimates of one or more of: a pressure, a temperature, a flow rate and a noise. In some versions the one or more estimates may be based on one or more of: a motor current, a motor speed, a motor acceleration, an de, a therapy pressure and a flow rate. In some versions determining the ty of water may be based on a relationship between the reference set and the first measure set. [0043c] In some versions the onship may be a change in magnitude between the reference set and the first measure set. In some versions the relationship may be a change in phase between the reference set and the first measure set. In some versions the relationship may be a time lag between the reference set and the first measure set. In some versions the reference set may be ined for a second location. In some ns the second location may be upstream of the humidifier reservoir. In some versions the quantity of water may be determined using a look-up table. [0043d] In some versions the method may further comprise a step of performing a calibration cycle to populate the look-up table. In some versions the quantity of water may be ined using a function. In some versions the method may further comprise a step of ming a calibration cycle to determine the function. In some versions the calibration cycle may be performed while the humidifier reservoir is in use. In some versions the calibration cycle may be performed during a set-up process. In some versions the calibration cycle may be performed at predetermined intervals. [0043e] Some versions of the present technology may involve an apparatus for humidifying a flow of air to be delivered to a patient. The apparatus may comprise an inlet to receive the flow of air. The apparatus may further comprise a humidifier reservoir configured to retain a body of water for fying the flow of air. The apparatus may further comprise a first sensor ured to ine a first measure set of the flow of air. The apparatus may further comprise a ller, wherein the controller is configured to determine a quantity of the body of water based on the first measure set. [0043f] In some versions the first measure set may comprise one or more measures of one or more of: a pressure, a temperature, a flow rate and a noise. In some versions the first sensor may be configured to determine the first measure set downstream of the 505787DIV4/73 humidifier reservoir. In some versions the controller may be further configured to determine a quantity of the body of water based on the first measure set and a reference set. In some versions the reference set may comprise a second e set. In some versions the second measure set may se one or more measures of one or more of: a pressure, a temperature, a flow rate and a noise. In some versions the reference set may comprise one or more estimates of one or more of: a re, a temperature, a flow rate and a noise. [0043g] In some versions the one or more estimates may be based on one or more of: a motor current, a motor speed, a motor acceleration, an altitude, a therapy re and a flow rate. In some versions the controller may be further configured to determine the quantity of the body of water based on a relationship between the reference set and the first measure set. In some ns the relationship may include one or more of a change in magnitude, a change in phase or a time lag between the reference set and the first measure set. In some versions the controller may be further configured to ine the quantity of the body of water using a p table or a function. In some ns the controller may be further configured to perform a calibration cycle to determine the lookup table or the function.

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 present technology.

Other features of the technology 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 accompanying gs, in which like reference numerals refer to r elements including: 4.1 TREATMENT SYSTEMS Fig. 1a shows a system including a patient 1000 wearing a patient interface 3000, in the form of a nasal s, receiving a supply of air at ve pressure from a 505787DIV4/73 RPT device 4000. Air from the RPT device is humidified in a humidifier 5000, and passes along an air circuit 4170 to the t 1000. A bed partner 1100 is also shown.

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

Fig. 1c shows a system including a patient 1000 g a patient ace 3000, in the form of a full-face mask, receiving a supply of air at positive pressure from a 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 4.2 RESPIRATORY 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, r alar cartilage, nostril, lip or, lip inferior, larynx, hard palate, soft , oropharynx, tongue, epiglottis, vocal folds, oesophagus and trachea.

Fig. 2c is a front view of a face with several features of surface anatomy identified including the lip superior, upper vermilion, lower vermilion, lip inferior, mouth width, nthion, a nasal ala, nasolabial sulcus and cheilion. Also indicated are the directions superior, inferior, radially inward and radially outward. 4.3 PATIENT INTERFACE Fig. 3a shows a patient interface in the form of a nasal mask in accordance with one form of the present technology. 4.4 RPT DEVICE Fig. 4a shows a RPT device in accordance with one form of the present technology. 505787DIV4/73 Fig. 4b is a schematic diagram of the pneumatic path of a RPT device in accordance with one form of the present technology. The directions of upstream and downstream are indicated.

Fig. 4c is a tic diagram of the electrical components of a RPT device in accordance with one form of the present logy. 4.5 HUMIDIFIER Fig. 5a shows an isometric view of a humidifier in accordance with one form of the present technology.

Fig. 5b shows a schematic of a humidifier in accordance with one form of the present technology.

Fig. 5c shows an isometric view of a humidifier in accordance with one form of the present technology.

Fig. 5d 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.

Fig. 6 shows an ary schematic of a respiratory treatment system sing a humidifier according to one aspect of the present technology, wherein the humidifier comprises a first sensor located upstream of the oir and a second sensor located downstream of the reservoir.

Fig. 6a shows an exemplary schematic of a atory ent system sing a humidifier ing to one aspect of the present technology, wherein the humidifier comprises a first pressure sensor located upstream of the reservoir and a second pressure sensor located downstream of the reservoir.

Fig. 6b shows an exemplary schematic of a respiratory treatment system comprising a humidifier according to one aspect of the present technology, wherein the humidifier comprises a first microphone located upstream of the reservoir and a second microphone located downstream of the reservoir. 505787DIV4/73 Fig. 6c shows an exemplary schematic of a respiratory treatment system comprising a humidifier according to one aspect of the present technology, wherein the fier comprises a first sensor located in the reservoir and a second sensor located downstream of the reservoir, proximal to a t interface.

Fig. 7 shows an exemplary one-dimensional look-up table according to one aspect of the present technology.

Fig. 8 shows an exemplary two-dimensional look-up table according to one aspect of the t technology.

Fig. 9 shows an exemplary tic of a respiratory treatment system comprising a humidifier ing to one aspect of the present technology, wherein the humidifier ses a sensor located downstream of the reservoir.

Fig. 9a shows an exemplary schematic of a atory treatment system sing a humidifier according to one aspect of the present technology, wherein the humidifier comprises a re sensor located downstream of the oir.

Fig. 9b shows an exemplary schematic of a respiratory treatment system comprising a fier according to one aspect of the present technology, wherein the humidifier comprises a flow rate sensor located downstream of the reservoir.

Fig. 9c shows an exemplary schematic of a respiratory treatment system comprising a humidifier according to one aspect of the present technology, wherein the humidifier comprises a microphone located downstream of the reservoir.

Fig. 10 shows an exemplary schematic of a respiratory treatment system comprising a humidifier according to one aspect of the t technology, wherein the respiratory treatment system comprises a vibration source and a vibration sensor.

Fig. 11a shows an exemplary schematic of a respiratory treatment system comprising a humidifier according to one aspect of the present technology, wherein the respiratory treatment system comprises a movable portion and an optical sensor. 505787DIV4/73 Fig. 11b shows an exemplary schematic of a atory treatment system comprising a fier according to one aspect of the present logy, n the respiratory treatment system comprises a movable portion and an angular sensor.

Fig. 11c shows an exemplary schematic of a respiratory treatment system comprising a humidifier according to one aspect of the present technology, wherein the respiratory treatment system comprises a movable portion and a proximity sensor.

Fig. 12a shows an exemplary schematic of a respiratory treatment system comprising a humidifier according to one aspect of the present logy, wherein the fier ses a rotatable paddle.

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 bed herein, which may vary. It is also to be understood that the terminology used in this disclosure is for the purpose of describing only the particular es discussed herein, and is not intended to be limiting.

The following description is provided in relation to various examples which may share one or more common characteristics and/or features. It is to be understood that one or more features of any one example may be able with one or more es of another example or other examples. In addition, any single feature or combination of features in any of the examples may tute a further example. .1 THERAPY In one form, the present technology comprises a method for treating a respiratory disorder comprising the step of applying positive pressure to the entrance of the airways of a patient 1000.

In n 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. 505787DIV4/73 .2 TREATMENT SYSTEMS In one form, the present technology comprises an apparatus or device for treating a atory disorder. The apparatus or device may comprise a RPT device 4000 for supplying pressurised air to the patient 1000 via an air circuit 4170 to a t interface 3000. .3 PATIENT INTERFACE A non-invasive patient interface 3000 in accordance with one aspect of the present technology comprises the ing functional aspects (see Fig. 3a): a sealforming structure 3100, a plenum r 3200, a positioning and stabilising structure 3300 and one form of connection port 3600 for connection to air circuit 4170. In one form, the patient interface 3000 includes a ad support 3700. In one form, the patient interface 3000 includes a vent 3400 constructed and arranged to allow for the washout of exhaled carbon dioxide. In one form, the patient interface 3000 includes at least one decoupling ure 3500, for example, a swivel or a ball and socket. In some forms a functional aspect may be provided by one or more physical ents. In some forms, one al ent may provide one or more functional aspects. In use the sealforming structure 3100 is ed to surround an entrance to the airways of the patient so as to facilitate the supply of air at positive pressure to the airways. .4 RPT DEVICE An RPT device 4000 in accordance with one aspect of the present technology (see Fig. 4a) comprises mechanical and pneumatic ents 4100, electrical components 4200 and is configured to execute one or more 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 include 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 sensors 4270, such as re sensors 4272 and flow rate sensors 4274. 505787DIV4/73 One or more of the air path items may be d within a removable y ure which will be referred to as a pneumatic block 4020. The pneumatic block 4020 may be located within the external housing 4010. In one form a pneumatic block 4020 is supported by, or formed as part of the chassis 4016.

The RPT device 4000 may have an electrical power supply 4210, one or more input devices 4220, a central controller 4230, a therapy device controller 4240, a pressure generator 4140, one or more protection circuits 4250, memory 4260, sensors 4270, data communication interface 4280 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 e more than one PCBA 4202. .4.1 RPT device mechanical & pneumatic components An RPT device may comprise one or more of the following components in an integral unit. In an alternative form, one or more of the ing components may be d as respective separate units. .4.1.1 Air filter(s) A RPT device in accordance with one form of the t logy may include an air filter 4110, or a plurality of air filters 4110.

In one form, an inlet air filter 4112 is located at the beginning of the pneumatic path upstream of a pressure generator 4140. See Fig. 4b.

In one form, an outlet air filter 4114, for example an antibacterial filter, is located between an outlet of the pneumatic block 4020 and a patient interface 3000. See Fig. 4b. .4.1.2 Muffler(s) In one form of the present technology, an inlet muffler 4122 is located in the pneumatic path upstream of a pressure generator 4140. See Fig. 4b.

In one form of the present technology, an outlet muffler 4124 is located in the pneumatic path between the pressure generator 4140 and a patient interface 3000. See Fig. 505787DIV4/73 .4.1.3 Pressure generator 4140 In one form of the present technology, a pressure generator 4140 for producing a flow, or a supply, of air at positive pressure is a controllable blower 4142. For example the blower 4142 may include a brushless DC motor 4144 with one or more ers housed in a volute. The blower may be capable of delivering a supply of air, for example at a rate of up to about 120 litres/minute, at a positive pressure in a range from about 4 cmH2O to about 20 cmH2O, or in other forms up to about 30 cmH2O. The blower may be as described in any one of the following patents or patent applications the contents of which are incorporated herein by reference in their entirety: U.S. Patent No. 7,866,944; U.S. Patent No. 8,638,014; U.S. Patent No. 8,636,479; and PCT Patent Application Publication No.

The pressure generator 4140 may be under the control of the therapy device controller 4240.

In other forms, a pressure generator 4140 may be a -driven pump, a pressure regulator connected to a high pressure source (e.g. compressed air reservoir), or a bellows. .4.1.4 Sensor(s) s may be internal of the RPT device, or external of the RPT device.

External sensors may be located for example on or form part of the air circuit, e.g., the patient interface. External sensors may be in the form of non-contact s such as a Doppler radar movement sensor that transmit or er data to the RPT .

In one form of the present logy, one or more sensors 4270 are located upstream and/or downstream of the re generator 4140. The one or more sensors 4270 may be constructed and arranged to measure properties such as a flow rate, a pressure or a temperature at that point in the pneumatic path.

In one form of the t technology, one or more s 4270 may be located proximate to the patient interface 3000.

In one form, a signal from a sensor 4270 may be filtered, such as by low-pass, high-pass or band-pass filtering. 505787DIV4/73 .4.1.4.1 Flow rate sensor A flow rate sensor 4274 in accordance with the present technology may be based on a differential pressure transducer, for example, an SDP600 Series differential pressure transducer from SENSIRION.

In one form, a signal from the flow rate sensor 4274 is received by the central controller 4230. .4.1.4.1.1 Pressure sensor 4272 A pressure sensor 4272 in accordance with the present technology is located in fluid communication with the pneumatic path. An example of a suitable re transducer is a sensor from the HONEYWELL ASDX series. An ative suitable pressure transducer is a sensor from the NPA Series from L ELECTRIC.

In one form, a signal from the pressure sensor 4272 is received by the central controller 4230. .4.1.4.1.2 Motor speed sensor In one form of the present technology a motor speed sensor 4276 is used to ine a rotational velocity of the motor 4144 and/or the blower 4142. A motor speed signal from the motor speed sensor 4276 may be provided to the therapy device controller 4240. The motor speed sensor 4276 may, for example, be a speed sensor, such as a Hall effect sensor. .4.1.5 Anti-spill back valve In one form of the present technology, an anti-spill back valve 4160 is located between the humidifier 5000 and the pneumatic block 4020. The anti-spill back valve 4160 is ucted and arranged to reduce the risk that water will flow upstream from the humidifier 5000, for example to the motor 4144. .4.1.6 Air t An air circuit 4170 in accordance with an aspect of the present technology is a t or a tube constructed and ed in use to allow a flow of air to travel between two components such as the pneumatic block 4020 and the patient interface 3000. 505787DIV4/73 In particular, the air circuit 4170 may be in fluid connection with the outlet of the pneumatic block and the patient ace. The air circuit may be ed to as an air delivery tube. In some cases there may be separate limbs of the circuit for inhalation and exhalation. In other cases a single limb is used.

In some forms, the air circuit 4170 may comprise one or more heating ts 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 sensors, such as temperature sensors. In one form, the heated wire circuit may be lly wound around the axis of the air circuit 4170. The heating element may be in communication with a ller such as a central controller 4230 or a humidifier controller 5250. One example of an air circuit 4170 comprising a heated wire circuit is described in United States Patent Application No. US/2011/0023874, which is orated herewithin in its entirety by reference. .4.1.7 Supplemental oxygen In one form of the present technology, supplemental oxygen 4180 is delivered to one or more points in the pneumatic path, such as upstream of the pneumatic block 4020, to the air circuit 4170 and/or to the patient interface 3000. .4.2 RPT device electrical components .4.2.1 Power supply A power supply 4210 may be located internal or external of the external g 4010 of the RPT device 4000.

In one form of the present technology power supply 4210 provides electrical power to the RPT device 4000 only. In another form of the present technology, power supply 4210 provides electrical power to both RPT device 4000 and humidifier 5000. .4.2.2 Input devices In one form of the present technology, a RPT device 4000 includes one or more input devices 4220 in the form of buttons, switches or dials to allow a person to interact with the device. The buttons, switches or dials may be physical devices, or software devices accessible via a touch screen. The buttons, es or dials may, in one form, be physically connected to the al housing 4010, or may, in another form, be in 505787DIV4/73 wireless communication with a receiver that is in electrical connection to the central controller 4230.

In one form, the input device 4220 may be constructed and ed to allow a person to select a value and/or a menu option. .4.2.3 l ller In one form of the present logy, the central controller 4230 is one or a plurality of processors suitable to control a RPT device 4000. le processors may include an x86 INTEL processor, a sor based on ARM® Cortex®-M processor from ARM Holdings such as an STM32 series ontroller from ST MICROELECTRONIC. In certain alternative forms of the present technology, a 32-bit RISC CPU, such as an STR9 series microcontroller from ST MICROELECTRONICS or a 16-bit RISC CPU such as a processor from the MSP430 family of microcontrollers, manufactured by TEXAS INSTRUMENTS may also be suitable.

In one form of the present technology, the central controller 4230 is a dedicated electronic circuit.

In one form, the central controller 4230 is an application-specific integrated circuit. In another form, the central controller 4230 comprises discrete electronic components.

The central controller 4230 may be configured to receive input signal(s) from one or more sensors 4270, and one or more input devices 4220.

The central ller 4230 may be configured to provide output signal(s) to one or more of an output device 4290, a therapy device controller 4240, a data communication interface 4280 and humidifier controller 5250.

In some forms of the present technology, the central controller 4230 is configured to implement the one or more methodologies described , such as the one or more algorithms expressed as computer programs stored in a non-transitory er readable storage medium, such as memory 4260. In some forms of the present technology, the central controller 4230 may be integrated with a RPT device 4000. 505787DIV4/73 However, in some forms of the present technology, some methodologies may be performed by a remotely located device. For example, the remotely located device may determine control settings for a ventilator or detect respiratory related events by analysis of stored data such as from any of the sensors described herein. .4.2.4 Clock The RPT device 4000 may include a clock 4232 that is connected to the central controller 4230.

Therapy device ller In one form of the t technology, therapy device controller 4240 is a control module that forms part of the algorithms executed by the central controller 4230.

In one form of the present technology, therapy device controller 4240 is a dedicated motor control integrated circuit. For example, in one form a MC33035 brushless DC motor controller, manufactured by ONSEMI is used. 6 tion circuits The one or more protection circuits 4250 in accordance with the t technology may comprise an ical protection circuit, a temperature and/or pressure safety circuit. .4.2.7 Memory In accordance with one form of the present technology the RPT device 4000 includes memory 4260, e.g., non-volatile memory. In some forms, memory 4260 may include battery powered static RAM. In some forms, memory 4260 may include volatile Memory 4260 may be located on the PCBA 4202. Memory 4260 may be in the form of EEPROM, or NAND flash.

Additionally or alternatively, RPT device 4000 includes a removable form of memory 4260, for example a memory card made in accordance with the Secure Digital (SD) standard. 505787DIV4/73 In one form of the t technology, the memory 4260 acts as a nontransitory computer readable storage medium on which is stored computer program instructions expressing the one or more methodologies described , such as the one or more algorithms. .4.2.8 Data communication systems In one form of the present technology, a data communication interface 4280 is provided, and is connected to the central controller 4230. Data communication interface 4280 may be connectable to a remote external communication network 4282 and/or a local external communication network 4284. The remote external communication network 4282 may be connectable to a remote external device 4286. The local external communication network 4284 may be connectable to a local external device 4288.

In one form, data communication interface 4280 is part of the central controller 4230. In another form, data ication interface 4280 is separate from the central ller 4230, and may comprise an integrated circuit or a processor.

In one form, remote al ication network 4282 is the Internet.

The data communication interface 4280 may use wired communication (e.g. via Ethernet, or l fibre) or a wireless protocol (e.g. CDMA, GSM, LTE) to connect to the Internet.

In one form, local external communication network 4284 utilises one or more communication standards, such as Bluetooth, or a consumer infrared ol.

In one form, remote external device 4286 is one or more computers, for example a cluster of networked computers. In one form, remote external device 4286 may be virtual ers, rather than physical computers. In either case, such remote external device 4286 may be accessible to an appropriately authorised person such as a clinician.

The local external device 4288 may be a personal er, mobile phone, tablet or remote control. 505787DIV4/73 .4.2.9 Output devices ing optional display, alarms An output device 4290 in accordance with the present technology may take the form of one or more of a visual, audio and haptic unit. A visual display may be a Liquid Crystal Display (LCD) or Light Emitting Diode (LED) display. .4.2.9.1 Display driver A display driver 4292 receives as an input the characters, symbols, or images intended for display on the display 4294, and ts them to commands that cause the display 4294 to y those characters, symbols, or images. .4.2.9.2 Display A display 4294 is configured to visually display characters, s, or images in response to ds received from the display driver 4292. For e, the display 4294 may be an segment display, in which case the display driver 4292 converts each character or symbol, such as the figure "0", to eight logical signals indicating whether the eight respective segments are to be activated to display a particular character or . .5 HUMIDIFIER .5.1 Humidifier overview In one form of the present technology there is provided a humidifier 5000 (e.g. as shown in Figs. 5a, 5c and 5d) to change the absolute humidity of air or gas for delivery to a patient relative to ambient air. Typically, the humidifier 5000 is used to increase the absolute ty and increase the temperature of the flow of air (relative 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 humidifier outlet 5004 to deliver a humidified flow of air. In some forms, as shown in Fig. 5c and Fig. 5d, an inlet 5118 and an outlet 5122 of the humidifier reservoir 5110 may coincide with the humidifier inlet 5002 and the humidifier outlet 5004 tively. 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. 505787DIV4/73 .5.2 fier mechanical components 1 Humidifier reservoir According to one arrangement, the humidifier 5000 may comprise a humidifier 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 humidifier reservoir 5110 is typically configured to hold a predetermined maximum volume of water in order to provide adequate humidification for at least the on of a respiratory y session, such as one evening of sleep. Typically, the reservoir 5110 is configured to hold several d 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 external water source such as a building’s water supply system.

In one arrangement as shown in Fig. 6, the humidifier reservoir 5110 comprises an inlet 5118 configured to receive a flow of air to the interior of the humidifier reservoir 5110. The humidifier reservoir 5110 may be configured so that the flow of air would be further humidified as it passes through the interior of the humidifier reservoir 5110. The fier reservoir 5110 also comprises an outlet 5122 configured to deliver the humidified flow of air. The outlet 5122 may be connected to an air circuit 4170 through which the humidified flow of air may be delivered to the patient 1000 via the patient interface 3000. In one form, the fier reservoir 5110 may be configured to age the flow of air to travel in a tortuous path through the reservoir 5110 while in t with the volume of water therein.

According to one form, the reservoir 5110 may be removable from the humidifier 5000, for example in a horizontal direction as shown in Fig. 5c and 5d.

The reservoir 5110 may also be configured to discourage 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 sub-components.

As the flow of air to be fied by the humidifier 5000 is typically pressurised, the reservoir 5110 may also be configured to prevent losses in pneumatic pressure h leak and/or flow impedance. 505787DIV4/73 .5.2.2 Conductive portion According to one arrangement, the reservoir 5110 comprises a conductive portion 5152 configured to allow ent transfer of heat from the heating element 5240 to the volume of liquid in the reservoir 5110. In one form, the conductive n 5152 may be arranged as a plate, although other shapes may also be suitable. All or a part of the conductive portion 5152 may be made of a thermally conductive material such as aluminium (e.g. approximately 2 mm thick, such as 1 mm, 1.5 mm, 2.5 mm or 3 mm), r heat conducting metal or some cs. In some cases, suitable heat conductivity may be achieved with less conductive materials of suitable geometry.

The conductive portion 5152 may be coupled with a heating element 5240 to introduce heat to the interior of the humidifier oir 5110. Humidifier reservoir dock In one form, the humidifier 5000 may comprise a fier reservoir dock 5130 (as shown in Fig. 5d) configured to receive the humidifier reservoir 5110. In some arrangements, the humidifier reservoir dock 5130 may comprise a locking e such as a locking lever 5135 configured to retain the reservoir 5110 in the oir dock 5130. .5.2.3 Water level reference The humidifier reservoir 5110 may comprise a water level reference 5150 as shown in Fig. 5c-5d. In some forms, the water level reference 5150 may provide one or more references to a user such as the patient 1000 or a care giver regarding a quantity of the volume of water in the humidifier oir 5110. The one or more references provided by the water level reference 5150 may include an indication of a maximum, predetermined volume of water, any portions thereof, such as 25%, 50% or 75% or s such as 200 ml, 300 ml or 400ml. .5.2.4 Heating plate 5120 According to another aspect of the present technology, the fier 5000 may comprise a heating plate 5120 which is used to transfer heat to the humidifier reservoir 5110 as shown in Fig. 6. The heating plate 5120 may comprise a heating element 5240 located on or near the base of the humidifier 5000. In one form, the heating plate 5120 may simply cover a heating element 5240. The heating plate 5120 may be formed, for example, of a nickel chrome alloy, stainless steel or anodised aluminium. 505787DIV4/73 .5.3 Humidifier electrical & thermal components The humidifier 5000 may comprise a number of ical and/or thermal components such as those listed below. .5.3.1 Humidifier sensor(s) The humidifier 5000 may comprise one or more humidifier sensors (transducer) 5202 instead of, or in addition to, sensors 4270 described above. Humidifier sensors 5202 may include one or more of a re sensor 5205, a flow rate sensor 5210, a temperature sensor 5220, or a humidity sensor 5218 as shown in Fig. 5c. A fier sensor 5202 may produce one or more output signals which may be communicated to a controller such as the central controller 4230 and/or the humidifier controller 5250. In some forms, a humidifier sensor may be located externally to the humidifier 5000 (such as in the air circuit 4170) while communicating the output signal to the ller. The term ‘sensor’ will be taken to include transducers in the present document unless otherwise explicitly stated. .5.3.1.1 Pressure sensor One or more pressure sensors 5205 may be provided to the humidifier 5000 in addition to, or instead of, a pressure sensor 4272 provided to the RPT device 4000. .5.3.1.2 Flow rate sensor One or more flow rate sensors 5210 may be provided to the humidifier 5000 in addition to, or instead of, a flow rate sensor 4274 provided to the RPT device 4000. .5.3.1.3 ature sensor The humidifier 5000 may comprise one or more temperature sensors 5220.

The one or more temperature sensors 5220 may be configured to measure one or more temperatures such as of the heating t 5240 and/or of the flow of air (e.g. downstream of the humidifier outlet 5004). In some forms, the fier 5000 may further comprise a temperature sensor 5220 configured to detect the temperature of the ambient air. 505787DIV4/73 .5.3.1.4 Humidity sensor In one form, the fier 5000 may comprise one or more humidity sensors 5218 to detect a humidity of a gas, such as the t air. The humidity sensor 5218 may be placed towards the humidifier outlet 5004 in some forms to e a humidity of the gas delivered from the fier 5000. The ty sensor may be an absolute humidity sensor or a relative humidity . .5.3.2 Heating element A heating element 5240 may be provided to the humidifier 5000 in to provide a heat input. For example, the heating element 5240 may provide a heat input to one or more of the volume of water in the humidifier reservoir 5110 and to the flow of air. The heating t 5240 may comprise a heat generating component such as an electrically resistive heating track. One suitable example of a heating element 5240 is a d g element such as one described in the PCT Patent ation Publication No. WO 2012/171072, which is incorporated herewith by reference in its entirety.

In some forms, the heating element 5240 may be provided in the humidifier base 5006 where heat may be provided to the humidifier reservoir 5110 primarily by conduction as shown in Fig. 5d. According to one arrangement, the heating element 5240 may be moulded into a resin forming a tub, as disclosed in the PCT patent application .5.3.3 Humidifier controller According to one arrangement of the present technology, a humidifier 5000 may comprise a fier controller 5250. In one form, the humidifier controller 5250 may be a part of the l controller 4230. In another form, the humidifier controller 5250 may be a separate controller, which may be in communication with the central controller 4230 as shown in Fig. 4c.

In one form, the humidifier controller 5250 may receive as inputs measures of properties (such as temperature, humidity, pressure and/or flow rate), for example of the flow of air, the water in the reservoir 5110 and/or the humidifier 5000. The humidifier controller 5250 may also be configured to execute or implement humidifier algorithms and/or deliver one or more output signals. 505787DIV4/73 As shown in Fig. 5b, the humidifier controller 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 4170 and/or a g element ller 5252 configured to control the temperature of a heating element 5240.

In some cases, humidifier algorithms may also utilise outputs from one or more sensors. 4 Water quantity (level/volume) determination As discussed in further detail above, the humidifier reservoir 5110 may contain a body of , such as water, which is evaporated to add humidity to the flow of air travelling through the humidifier 5000. In some cases, it may be desirable to determine the quantity of liquid that is present in a humidifier oir 5110. It is noted that where references are made to determination of ‘water quantity’, it is to be understood that such techniques are not to be limited to applications in determining a quantity of water, but would be applicable to other s also.

In some forms, it may be desirable to determine the quantity of water in the reservoir 5110 by indirect measurements. For example, ct measurements of the quantity of water may allow determination of the water quantity without use of sensors that form a part of a disposable component. Furthermore, indirect measurements of the quantity of water may be carried out using sensors which may have other ons, such as control of y pressure, or control of temperature of the air flow delivered to the patient, which may lead to improved efficiency. ct measurements of water quantity are described in further detail below.

The quantity of water may be determined and/or processed in terms of any number of units, relative or absolute. For example, the quantity of water may be ed in a unit of volume, such as litres, millilitres or cc, in a unit of mass such as in grams, kilograms or ounces, in relative measures such as a percentage or a fraction, in any arbitrary units such as a number out of five or a number out of 10, and in some cases by a measure of the size of the void or the quantity of air in the reservoir 5110. In some forms, the water quantity may be expressed as a ‘level’ to indicate a height, however it will be understood that a reference to any ular form of measure (e.g. water level, water volume or water mass) is not intended to be limiting to the express form. 505787DIV4/73 .5.3.4.1 Use of determined water quantity One age associated with being able to determine the quantity of water present in the reservoir 5110 may be in being able to inform, or alert a user, such as a caregiver or a patient 1000, of the determined water quantity. Additionally, or alternatively, the user may be informed or alerted based on other information which may be inferred from the determined water quantity. According to one aspect of the present logy, the patient 1000 may be alerted of a low water quantity prior to commencement of a therapy session. For example, the patient may be alerted if the determined water quantity is below a predetermined old level.

According to another aspect, a controller may ine whether the determined water ty may be sufficient for humidification of air flow throughout a remainder of a therapy session. In one form, the user may be prompted to re-fill the reservoir 5110 before cing y. In one form, the user may be alerted upon completion of therapy to re-fill the reservoir 5110 if the determined water quantity may not be sufficient for humidification of air throughout another therapy session.

According to another , an alarm may be activated when the oir 5110 is out of water or the water level is determined to be low (e.g. below a threshold).

An alarm may be raised at any time, such as prior to commencement of a therapy session, at the completion of a therapy session, or during a therapy session. In one form, a controller such as a central controller 4230 or the fier controller 5250 may activate an alarm. In some cases where the patient 1000 requires humidified air and may not be able to re-fill the reservoir 5110 themselves, the alarm may alert a caregiver (e.g. a nurse) that ling is required.

In another form, determination of water quantity in the reservoir 5110 may allow for a humidification output to suit the available water quantity and/or the rate of water usage as will be described below in further detail.

In some arrangements, the reservoir 5110 may be disposable and may require replacement (e.g. periodically, based on usage or for individual patients) throughout a life of the humidifier 5000. In such arrangements the introduction of any additional components, such as a sensor, may not be ble as this may se the cost of the disposable reservoir 5110, particularly if the additional components are relatively 505787DIV4/73 expensive. Yet further, in order to introduce a sensor into the reservoir 5110, one or more electrical tions may be required between the humidifier oir 5110 and other components such as the humidifier controller 5250 and/or a power source (e.g. power supply 4210). The presence of such electrical connections may also be not preferable as they may increase system complexities, increase the cost of the disposable reservoir 5110 and introduce potential failure points in a disposable component.

Thus, it may be preferable to determine a quantity of water in a humidifier reservoir 5110 using one or more s which do not form a part of the reservoir 5110.

Furthermore, it may be preferable to determine the water ty using the sensors which may be also otherwise used in a humidifier 5000 and/or a RPT device 4000, for example to measure one or more properties of the air flow. .5.3.4.2 Determination of effects of varying water quantity According to some arrangements of the fier reservoir 5110 according to the present technology, a variation in the quantity of water present in the humidifier reservoir 5110 may affect one or more measurable characteristics or properties, such as those of: the water, the flow of air, the reservoir 5110 and/or the humidifier 5000. The characteristic(s) or property(s) affected by a variation in the quantity of water (and thus may be used to infer the ty of water) may include, but not be limited to, pressure, flow rate, noise, temperature or vibration. They will be referred hereafter as indicative characteristics. A person skilled in the art would understand that there may be other, r, characteristics to those ‘indicative characteristics’ disclosed in the present document, which may also be used to determine a water quantity in the reservoir 5110 in a manner ntially equivalent to those disclosed herewithin.

Thus one or more es of one or more indicative characteristics may be used to determine the ty of water in the reservoir 5110. A quantity of water may be determined for a particular time, or a change in the ty of water in the reservoir 5110 between a first time and a second time may be determined. For example a measure of the indicative characteristic may be used as a variable in a look-up table or a function to determine an estimate of the quantity of water in the reservoir 5110 or the change in the quantity of water in the reservoir 5110. 505787DIV4/73 As will be described in further detail below, a measure of an indicative characteristic may be of an aspect of the indicative teristic, such as a magnitude or a direction of a vector quantity. For example, where a noise is an indicative characteristic, a measure of an indicative characteristic may be a measure of amplitude of the noise, a measure of phase of the noise or a combination of both aspects.

In some forms, each ‘measure’ herein may in fact refer to a set of measures (e.g. a plurality of measures), such that for e a first set of measures and a second set of measures may be used to determine the quantity of water.

In one form, a plurality of measures such as a first measure and a second measure of the indicative characteristic(s) may be used to determine the quantity of water.

The ity of measures may be of one indicative characteristic or a plurality of indicative characteristics. For e, a measure of pressure of the flow of air from a pressure sensor and a measure of flow rate of the flow of air from a flow rate sensor may be used to determine the quantity of water.

The plurality of measures may be obtained from a single sensor, or a plurality of sensors. As an example, a first microphone, may measure a first measure of noise and a second measure of noise. Or, a first microphone and a second microphone may respective measure a first measure of noise and a second measure of noise. The first measure of noise and the second measure of noise may then be used to determine the quantity of water in the reservoir. In another form, one measure of an indicative characteristic may be used to determine the water quantity in the reservoir 5110. For example, a single measure of noise from a microphone may be used to determine the ty of water.

The system may generate a nce signal such as a waveform (e.g. with a ermined shape, frequency and/or amplitude), or an impulse, for use in determination of water quantity. To this end, the system may comprise a reference tor configured to generate the reference signal, such as a loudspeaker, or the blower 4142. In some forms, the reference signal may be measured by one or more s to determine a reference set, to which a measure set may be compared to determine a ty of water. A measure set may be determined (e.g. first measure set measured) after at least a predetermined length of time has passed uent to the reference set (e.g. second measure set). 505787DIV4/73 In some forms, the reference set may be determined from estimation, whereby water ty may be determined from a resulting measure set (e.g. from a single sensor 5202-3 as shown in Fig. 9) and the estimated reference set. For example, a reference set may include an estimated pressure based on a measure of motor speed. In one form, a time taken for a reference signal to travel from the reference generator, through the reservoir 5110, and to the sensor may be measured to ine a time lag. Yet further, any transformation, such as a phase change, or a change in amplitude, that the reference signal undergoes prior to arriving at the sensor may then be measured and used to infer the volume of water in the reservoir 5110.

Further s of determination of the quantity of water in the reservoir 5110 by use of indicative characteristics will be discussed below. .5.3.4.3 Measures of the air flow According to one aspect of the present technology, a quantity of water in the oir 5110 may be ined from a measure set (one or more es) of the air flow, for example as measured in the reservoir 5110 or downstream of the reservoir 5110.

A property of the reservoir 5110 and the water contained n, such as its ic transmission loss, flow impedance, thermal mass or thermal conductivity, may vary according to the quantity of water present in the reservoir 5110. In turn, one or more characteristics of the flow of air that travels through the reservoir 5110 may be affected, such as pressure, flow rate, temperature, noise, or vibration. Thus, the affected characteristic(s) of the air flow may indicate the quantity of water in the reservoir 5110 when measured in the reservoir 5110 or downstream of the reservoir 5110, and in some cases, when ed upstream of the reservoir 5110. For e, a decrease in the quantity of water in the reservoir 5110 may decrease the overall thermal mass of the reservoir 5110.

Fig. 6 shows an arrangement of a system according to the present technology that comprises a first sensor 5202-1 and a second sensor 5202-2. Three exemplary, possible quantities of water in the reservoir 5110 are indicated by three water levels WL- 1, WL-2 and WL-3 in Fig. 6. An ary travel path for the flow of air through the reservoir 5110 is indicated by the arrows AF. 505787DIV4/73 The flow of air may undergo a pressure drop (e.g. a decrease in static or total pressure) as it travels through the reservoir 5110, for example as measured n the reservoir inlet 5118 and the reservoir outlet 5122. A magnitude of the drop in pressure of the flow of air may vary ing to a flow impedance of the reservoir 5110. As the ty of water in the reservoir 5110 is varied, the flow impedance of the reservoir 5110 may be altered due to a change in a path for the air flow through the reservoir 5110 as the effective boundaries of the reservoir 5110 change (e.g. from WL-1 to WL-2 in Fig. 6). As a result, a difference between the air pressure at the reservoir inlet 5118 and at the reservoir outlet 5122 may be affected by the change in the quantity of water in the reservoir 5110. Thus a pressure of the flow of air may be a suitable indicative characteristic of the quantity of water present in the reservoir 5110.

Similarly, any number of properties of the flow of air may be suitable indicative characteristics of the quantity of water present in the reservoir 5110. Suitable indicative characteristics of the flow of air may include pressure, flow rate, temperature, density, noise or vibration or other characteristics of the flow of air. Thus one or more of the indicative characteristics may be measured from the air flow to determine the ty of water in the oir 5110.

According to the arrangement shown in Fig. 6, the first sensor 5202-1 may determine a first measure set M1 of an indicative characteristic of the flow of air, and the second sensor 5202-2 may determine a second measure set M2 of an indicative characteristic the flow of air. The first measure set M1 and the second measure set M2, and/or their relationship, such as a difference in amplitude, or a ence in phase, may then be ated to a quantity of water in the reservoir 5110 using a function or a lookup table as will be discussed in more detail below.

Locations of the sensor(s) need not be limited to the particular ary locations discussed herein in order to take advantage of the present technology as disclosed. es of suitable locations for the (s) may include the inlet or the outlet of the RPT device 4000, the inlet or the outlet of the humidifier 5000, interior of the reservoir 5110, interior of the air circuit 4170, interior of the patient interface 3000 or other locations in fluid ication with the flow of air. In some cases, the sensor(s) may be located between or near any of the above listed components. In one arrangement, DIV4/73 at least a part of the reservoir 5110 is located between at least two sensors when a plurality of sensors is employed. ing to Fig. 6, the first sensor 5202-1 is shown at a first location, upstream of the reservoir 5110, and the second sensor 5202-2 is shown at a second location, downstream of the reservoir 5110. atively, the sensors 5202-1 and/or 5202-2 may be arranged as shown in Fig. 6c, where the first sensor 5202-1 is located within the reservoir 5110 and the second sensor 5202-2 is located proximal to the patient interface 3000. A sensor may be integrally formed with another ent such as the RPT device 4000, an air t 4170 or the humidifier 5000 (or a sub-component thereof). In other arrangements, a sensor may be removably connected to another component.

In an arrangement of the present technology as shown in Fig. 6a, a first pressure sensor 5205-1 and a second re sensor 5205-2 may each determine measures of pressure of the flow of air. The first pressure sensor 5205-1 may determine a first measure of pressure Pm1 of the flow of air at a first location, and the second pressure sensor 5205-2 may determine a second measure of pressure Pm2 of the flow of air at a second location. A measure of pressure drop ∆Pm between the first location and the second location may be determined using the formula ∆Pm=Pm1-Pm2. The measure of pressure drop ∆Pm may then be used to determine the quantity of water in the reservoir (e.g. as shown in Fig. 7) as described in further detail below.

In an illustrative example, a maximum allowable quantity (in volume) of water in the reservoir 5110 may be imately 350 ml. In Fig. 6, the ponding water level may be WL-1. When the water volume is 350 ml, at a therapy re (i.e. a pressure at the patient interface 3000) of 10cm H2O, a first measure of pressure Pm1 at the first pressure sensor 5205-1 may be called Pm1350 and a second measure of pressure Pm2 at the second pressure sensor 5205-2 may be called Pm2350. Based on the first measure of pressure Pm1350 and the second measure of pressure Pm2350, a measure of pressure drop at 350 ml of water ∆Pm350 may be calculated using the ing formula ∆Pm350=Pm1350- Pm2350. However if the water volume was to decrease to 240 ml for instance, it may lower the water level to WL-2, increasing the effective internal volume of the reservoir 5110. In this case, the measure of pressure drop may change to ∆Pm240, and similarly at 130 ml of water volume at water level WL-3, the measure of pressure drop may then change further 505787DIV4/73 to ∆Pm130. Thus the quantity of water may be determined based on the measure of pressure drop.

In some forms, the quantity of water in the oir may be determined based on the e of pressure drop ∆Pm using one or more functions and/or look-up tables.

An example of a look-up table is shown in Fig. 7, where a series of pressure drop values (measured in pressure) are correlated to water quantity values (measured in volume). ing to one arrangement, a memory 4260, in communication with the controller, may store the look-up tables (and/or functions). The controller may receive the measure of pressure drop ∆Pm as an input and determine the water quantity based on the look-up table (and/or ons).

In some forms, the controller may be configured to determine the water ty from the closest value of pressure drop available ∆P in the look-up table to the measure of re drop ∆Pm. For instance, in the look-up table shown in Fig. 7, the t pressure drop value ∆P to the measured pressure drop at 350 ml of water ∆Pm350 may be ΔP_350, and the determined water volume may be 350 ml. Or, the closest pressure drop value ∆P to the measured re drop at 240 ml of water ∆Pm240 may be ΔP_250, and the determined water volume may be 250 ml Alternatively, the controller may be configured to olate between listed values in the look-up table by any suitable interpolation methods such as linear, polynomial, piecewise constant interpolation or a combination thereof. Using interpolation, two closest values of re drop ∆P to the measured pressure drop at 240 ml of water ∆Pm240 may be ΔP_250 and ΔP_225, and the controller may determine the quantity of water by interpolating between the two values.

In one form, a look-up table may be multi-dimensional as shown in Fig. 8.

This may allow effects of additional les (such as therapy pressure (Ptherapy), pressure at pressure generator, pressure generator motor speed, pressure generator motor current, flow rate, length of air circuit 4170, type of humidifier reservoir 5110 or other indicative characteristics) to be taken into consideration in determining the water quantity.

In one form, the look-up table may be populated by a manufacturer by characterisation of the oir 5110 and stored in a memory (e.g. in the RPT device 4000 or humidifier 5000). Additionally, or alternatively, the humidifier controller 5250 505787DIV4/73 may also comprise the ability to calibrate and populate the look-up table by using a learn mode during therapy, and/or by executing or performing a calibration cycle, both of which will be described in r detail below.

In one form, the quantity of water may be determined from measures of indicative teristic(s) based on one or more functions. The one or more ons may be predetermined and made available to a controller such as the humidifier controller 5250, for example stored in a memory (e.g. in the RPT device 4000 or humidifier 5000).

In some forms, the on correlating the indicative characteristic(s) to the quantity of water may be selected from a plurality of functions, for example according to a variable (e.g. therapy pressure). Alternatively, or additionally, the function may be calibrated by a learn mode during therapy or by performing a calibration cycle. Thus, in one example, the function may determine the quantity of water, in volume Vw based on a measure of the pressure drop ∆Pm, using a linear equation Vw = A×∆Pm + B, where A and B are values that may be predetermined and/or adjusted by calibration/learn mode. The function may also take one or more of any number of le forms, such as a linear, polynomial, logarithmic or a combination thereof.

Fig. 9 shows an arrangement of a system that comprises a sensor 5202-3. In this arrangement, a measure M3 determined by the sensor 5202-3 may be used as an input to a look-up table or a function to determine the quantity of water in the reservoir 5110. In another example, a reference value Mref may be used to e to the output or the measure M3 produced by the sensor 5202-3 to determine the quantity of water. The reference value Mref may be a fixed and/or a predetermined value. The reference value Mref may additionally or alternatively be determined from another characteristic such as a motor speed, motor current, t temperature, ambient pressure or ambient density among . Yet r, the reference value Mref may be based at least partly on a previous measure determined by the sensor .

In the exemplary arrangement shown in Fig. 9a, a pressure sensor 5205-3 is located downstream of the humidifier reservoir 5110, and the pressure sensor 5205-3 may determine a measure of pressure Pm3. The measure of re Pm3 may be used as an input to a look-up table or a function to ine the quantity of water. Alternatively, or additionally, the measure of pressure Pm3 may be compared to a reference pressure Pref, for example to produce an estimated pressure drop ∆Pe=Pref-Pm3 (where Pref is upstream 505787DIV4/73 of Pm3). A look-up table or a function may be used to determine the quantity of water based on the estimated pressure drop rly to the method described above. The reference pressure may be predetermined, or variable, for example the reference pressure may be estimated from parameters such as motor current, motor speed, motor acceleration and/or altitude as disclosed in PCT Application Number for example, the entire contents of which is ed herewithin by reference. In a yet another alternative, the measure of pressure Pm3 may be used as an input to a look-up table or a on, wherein the look-up table or the on may vary according to the reference pressure Pref.

In some forms, the quantity of water in the reservoir 5110 may be determined from a plurality of measures of tive characteristics over time. For example, measures of indicative characteristics over time may include effects of one or more breath waveforms, such as inspiratory or expiratory waveforms. teristics of the flow of air such as its pressure, flow rate or temperature may be affected due to breathing of the patient 1000. For example, when the patient 1000 breathes out, the air pressure may increase, including at or near the humidifier reservoir 5110. When the patient 1000 breathes in, the air pressure may decrease, including at or near the humidifier reservoir 5110. A magnitude of a ion of the indicative characteristics (such as pressure) may depend on a quantity of water in the reservoir 5110. The effect that the patient’s breathing has to the characteristics of the flow of air may thus be measured to determine the quantity of water in the reservoir 5110.

In another example, one or more of a t’s breath waveforms (or a part f), such as inspiratory or tory waveforms may be determined using an arrangement as shown in Fig. 9b. For instance, a difference in flow rates n expiration and inspiration at a flow rate sensor 5210-3 may be determined by producing a measure of maximum flow rate and a measure of minimum flow rate over a breath cycle.

The difference in flow rates may then be calculated as the difference between the measure of maximum flow rate and the e of minimum flow rate over a breath cycle. The water level may then be determined by correlation to, for example, the difference between flow rate between expiration and inspiration.

In one arrangement of the present technology, the central controller 4230 of the RPT device 4000 may be configured to maintain the blower 4142 at a fixed speed for 505787DIV4/73 each target therapy pressure. ing to this arrangement, a change in flow impedance of the reservoir 5110 may affect the flow rate of air through the air circuit, as the blower 4142 operates at a constant speed.

Fig. 9b shows one arrangement of a system that may be suitable for determining the quantity of liquid in the reservoir 5110 using a flow rate sensor 5210-3 when such a constant-speed blower is used. The flow rate sensor 5210-3 may produce a measure of the flow rate Fm3, which would vary as the flow impedance of the reservoir 5110 varies. Accordingly, the measure of the flow rate Fm3, as well as a speed of the blower 4142 may be ated to determine the quantity of water in the reservoir 5110 using a mensional p table or a two-variable function. In some cases, other characteristics, such as motor current or altitude may be added as independent dimensions or variables to the p table and/or the function to further improve accuracy of the look-up table of the function.

According to a yet another aspect of the present technology, noise may be a le indicative characteristic from which the quantity of water may be determined. For example, a sensor may be placed to determine a measure of noise at a location where the noise may be affected by the quantity of water in the reservoir 5110. Suitable locations may include: in the reservoir 5110 or downstream of the reservoir 5110 such as in the humidifier 5000, in the air circuit 4170 or the patient interface 3000. The resulting noise may be used to determine the quantity of water remaining in the reservoir 5110, for example by a comparison to a measured or estimated reference noise.

In some cases, the reference noise may be a noise output by a reference generator, which may be a ent of the RPT device 4000 and/or the humidifier 5000. For example, noise d by the blower 4142 as a by-product of generating a pressured flow of air may be used as the reference noise. In this case, the level and frequency characteristics of the reference noise may therefore vary (e.g. according to a pressure or flow rate delivered by the blower 4142), and may need to be measured (or estimated) in conjunction with the resulting noise to establish a relationship etween.

Alternatively, or additionally, the reference noise input may e a known noise output from a component such as a speaker or a buzzer. According to r e of the present technology, the measure of the resulting noise may include a filter to exclude or 505787DIV4/73 reduce the effects of other noise sources, such as snoring by the t 1000 or background noise near the patient 1000.

According to an exemplary arrangement shown in Fig. 6b, a first microphone 5215-1 may be placed upstream of the reservoir 5110 to measure a reference noise, and a second hone 5215-2 may be placed downstream of the oir 5110 to measure a resulting noise. The reference noise and ing noise measures may be correlated to a water quantity by, for example, calculating the attenuation in noise levels between the first microphone 5215-1 and the second microphone 5215-2. The attenuation in noise levels may be correlated to a quantity of water using similar methods to those described above (e.g. via a look-up table or a function).

Alternatively, in some forms, the reference noise may be estimated (e.g. according to r measure) rather than measured. In one example, where the reference noise es a known noise output (e.g. from a ent such as speaker or a buzzer) the reference noise may be estimated as a predetermined noise. In some forms, the reference noise may be estimated based on another ter such as motor speed or motor current. For example, a noise output of a RPT device 4000 and/or a humidifier 5000 or a component thereof (e.g. of the blower 4142) may be characterised by its manufacturer, from which a predetermined look-up table of reference noise may be saved onto a memory of the RPT device 4000 and/or a humidifier 5000.

In an arrangement shown in Fig. 9c, one or more measures from a microphone 5215-3 may be used to determine the water quantity in the reservoir 5110. The microphone 5215-3 may produce a measure of the resulting noise level Nm3, which may be used to determine the water quantity in this case using a look-up table or a function. In one example, a function may use as inputs the resulting noise level Nm3, as well as a predetermined reference noise to output (i.e. determine) the water quantity. In r example, a look-up table may be multi-dimensional, such that a look-up table may receive as inputs a motor speed, and the resulting noise level Nm3 to determine the water quantity.

Noise may be characterised in a number of ways, for example by a noise level (indicating amplitude, typically sed in ls or dB), as described above.

Alternatively, or additionally, noise may be characterised by frequency domain data. For example, noise may be characterised such that for a noise level may be measured for one 505787DIV4/73 or more of a plurality of frequencies (or frequency bands). In the ement shown in Fig. 6b, a first noise spectrum may be determined at the first sensor 5215-1 and ed to a second noise spectrum determined at the second sensor 5215-2. Such a comparison may indicate how the first noise spectrum correlates to the second noise spectrum. For example, the ison may evaluate changes in noise levels at a frequency and/or a frequency band in the first noise spectrum to the second noise spectrum. In one form, the first noise spectrum may be ed to a second noise spectrum, for example to determine a noise attenuation spectrum for correlation to a water quantity.

Measures of noise may not be limited to those of audible frequency ranges. In some forms, measures of inaudible vibrations of the flow of air, such as ultrasounds, may be used to determine a quantity of water in the reservoir 5110.

In another aspect of the t ion, a time lag between two locations in the pneumatic path may be used to determine the quantity of water. A change to the quantity of water in the reservoir 5110 may affect a length of time taken for the flow of air to travel through the humidifier reservoir 5110. Accordingly, the length of time taken, or the time lag, for the flow of air to travel through the humidifier reservoir 5110 may be correlated to the quantity of water in the reservoir 5110 by way of a look-up table or a on similarly to those described above.

Fig. 6 shows an exemplary arrangement of the present technology suitable for determining a time lag between two locations. In the arrangement shown in Fig. 6, the first sensor 5202-1 may determine a reference measure set, which may be a ity (e.g. a ) of measures or a single measure of the flow of air, where the reference measure is associated with a first time T1 (e.g. a time at the start of the end of the reference measure). The second sensor 5202-2 may measure a resulting measure set associated with a second time T2, wherein the resulting measure set correlates to the reference e set. A difference in time ∆T may be ined (e.g. using an equation ∆T= T2- T1) and may be correlated to the ty of water. In some forms, where the resulting measure set and the reference measure set each comprise a waveform (e.g. a plurality of measures made over a time period), the two waveforms may be compared for equivalence in the waveform shape to determine that the resulting measure correlates to the reference measure. 505787DIV4/73 The determination of water quantity using any of the above methods may be made using a look-up table or a on. The particular look-up table and/or the function may vary between implementations of the present technology as the correlation may vary for a number of factors, for example locations of the sensor(s) or the geometry of the humidifier 5000. The number of variables used to create the look-up table and/or the function may be varied while taking advantage of the present technology. For example, as described above, introducing additional les may improve the accuracy of the lookup table and/or the function, however in some forms, a p table or a function that uses one or two indicative characteristics as variables may be utilised.

It should be noted that the number of s employed towards determination of water quantity may be varied from the specific examples disclosed herewithin while still taking advantage of the present technology. .5.3.4.4 Measures of the humidifier 5000 According to another aspect of the present technology, the quantity of water in the reservoir 5110 may be determined from one or more measures of teristics of the humidifier 5000, such as its vibratory characteristics or mechanical characteristics. .5.3.4.4.1 Vibration As the quantity of water in the reservoir 5110 varies, vibration characteristics of the reservoir 5110, and/or the humidifier 5000 may vary ingly. For example, vibratory characteristics such as the damping ratio, natural frequencies and/or ission loss of an object or a system (e.g. humidifier reservoir 5110 or humidifier 5000) may depend on one or more aspects of the object or the , for example the mass, density, material damping rate or stiffness among others. Further examples of vibration characteristics that may be affected e ion attenuation through the humidifier reservoir 5110 (overall or ing on ncy), and natural vibration frequencies of the oir 5110. Thus one or more measurements of vibration characteristics (e.g. of the reservoir 5110 and/or the humidifier 5000) may be used to determine a quantity of water in the reservoir 5110.

Vibration characteristics of the humidifier reservoir 5110 may be determined by one or more of a number of ways known to those skilled in the art. In one example, a DIV4/73 measure of vibration response may be compared t a vibration reference to determine vibration characteristics of the humidifier reservoir 5110. ing to one exemplary ement as shown in Fig. 10, a vibration source 5232 located on, for example, the RPT device 4000 and/or the humidifier 5000 may be configured to provide a reference vibration input such as a vibration impulse of a ermined magnitude or a periodic vibration to the humidifier reservoir 5110. In some forms, a vibration source 5232 may provide a varying reference vibration input, for example where the blower 4142 is used as a vibration source 5232. A nce vibration from the blower 4142 may vary for example according to a pressure and/or flow rate delivered by the blower 4142. The reference vibration input may be, for example, in an audible ncy range, or an inaudible frequency range (i.e. subsonic or ultrasonic). The reference vibration input may also be predominantly transmitted to the reservoir 5110 via a gas, liquid, solid or any ation thereof, such as the flow of air, the water, or the structure of, for example, the RPT device 4000 and/or the humidifier 5000.

A vibration sensor 5234 as shown in Fig. 10 may be used to produce a e of a ion response, for example of the humidifier reservoir 5110, ing the water contained therein. A le example of a vibration sensor 5234 may be a piezoelectric accelerometer or a velocity sensor. The measure of the vibration response may then be used to determine the quantity of water in the reservoir 5110. For instance, a natural frequency of the reservoir 5110 may typically increase as a quantity of water is reduced in the reservoir 5110, and may typically decrease as a quantity of water increases.

Alternatively, or additionally, a plurality of measures of vibrations may be used to determine the quantity of water. For example, vibration may be measured at a plurality of locations, wherein the reservoir 5110 is located at least partially therebetween the two location. A difference in the two measures of vibration may be also referred to as vibration attenuation, and may depend on a quantity of water in the reservoir 5110. Thus a measure of any number of vibration characteristics, such as the l frequency of the reservoir, the overall magnitude of vibration at the reservoir 5110, or the vibration attenuation between the vibration nce and at the reservoir 5110 may also be used to determine the quantity of water.

DIV4/73 As previously discussed, it may be preferable to arrange any s or sensors to be discrete from a disposable component such as the reservoir 5110. Therefore, in some forms, the vibration sensor 5234 may be removably coupled to the reservoir 5110 to measure its vibration characteristic(s), or measure vibration characteristic(s) of the reservoir 5110 indirectly. Thus, in one form, the vibration sensor 5234 may be configured to determine ion characteristics of the oir 5110 such as by measuring a ion response of the humidifier 5000. .5.3.4.4.2 Mechanical In another aspect of the present technology, a mechanical property or a mechanical response of the fier 5000 and/or the reservoir 5110 may be measured to determine the quantity of water in the reservoir 5110.

According to one arrangement, a strain sensor/gauge (or a deformation sensor) may be placed at a base of the humidifier reservoir 5110 to measure a strain (or deformation) of a base of the reservoir 5110. The deformation of the base of the humidifier reservoir 5110 may be dependent on the quantity of water, thus the measure of the ation or strain may be correlated to determine to the quantity of water in the reservoir 5110. Alternatively, or additionally, the strain sensor may also be d at a number of other locations such as the side of the reservoir 5110, or on humidifier 5000 where it may be deformed according to a varying ty of water in the reservoir 5110.

Any number of other sensors such as tilt sensors or load cells may also produce a measure that may be suitable indicative characteristics of the quantity of water. Yet further, similarly to above, a look-up table or a on may be used to determine the quantity of water from the measure of the mechanical property produced by a sensor. .5.3.4.5 Measures of inertial mass According to another aspect of the present technology, the quantity of water in the reservoir 5110 may be determined by a measure of an inertial mass of the water in the reservoir 5110. In one example, the inertial mass of the water in the reservoir 5110 may be ined by imparting a force to the water in the reservoir 5110 and measuring a response such as a resulting acceleration of the water or the reservoir 5110. The force may be ed to the body of water in the reservoir 5110 in a number of ways, and a 505787DIV4/73 resulting acceleration of the water may be measured to ine to the inertial mass of the water.

In one example (see Fig. 12a), a reservoir 5110 may comprise a movable paddle 5112 that extends along a vertical direction of the reservoir 5110, and at least partially exposed to the flow of air. In one form, the paddle 5112 may be rotatably fixed to the reservoir 5110 about a paddle axis 5114 (e.g. vertical axis) within the reservoir 5110. The flow of air in the reservoir 5110 may act on d surface areas of the paddle 5112 to motivate the paddle 5112 to turn. sely, the quantity of water in the reservoir 5110 may resist a movement of the s 5112.

Furthermore, as the quantity of water in the reservoir 5110 changes, the area of the paddle 5112 exposed to the flow of air may change. This may have the effect of ng the force imparted into the paddle 5112 by the flow of air. At the same time, as the quantity of water changes the resistance of the body of water to the paddles 5112 turning within the reservoir 5110 may also vary. Therefore, a measure of movement of the paddle 5112 may be a suitable indicative characteristic from which the quantity of water may be inferred.

In another arrangement of the present technology, a sensor may be configured to determine measure of torque produced by the humidifier reservoir 5110. The flow of air may impart force and/or a torque to the reservoir 5110 as it travels therethrough. In some cases, the force and/or the torque imparted may be dependent on the quantity of water present in the reservoir 5110, as the internal volume of the reservoir 5110 that is exposed to the flow of air changes. For e, as the water quantity in the reservoir 5110 is reduced, the total e area exposed to the flow of air may increase. Thus the measure of torque may depend on the quantity of water in the humidifier reservoir 5110, and may be also a suitable tive characteristic. The force and/or the torque may be measured by any number of sensors such as a load cell, force gauge, strain gauge or others known to those skilled in the art. .5.3.4.6 Movable water level indicator In one arrangement, the humidifier oir 5110 may comprise a movable n configured to move as the quantity of water in the reservoir 5110 changes, for example by following the height of the quantity of water in the reservoir 5110. In one 505787DIV4/73 form, the movable portion may be a float located on the inside of the reservoir 5110, or it may be a part of the exterior of the reservoir 5110 such as a concertina n that is configured to move as the water level in the reservoir 5110 changes. The humidifier 5000 may comprise a sensor configured to determine the position or the height of the e n. The sensor may be, among others, an optical sensor configured to determine a position of the movable portion as shown in Fig. 11a, an angular sensor configured as shown in Fig. 11b to determine an angular position a pivotably coupled component ured to move with the movable n, or a proximity sensor configured as shown in Fig. 11c to determine a distance between it and the humidifier movable portion.

According to the exemplary arrangement shown in Fig. 11a, the movable portion 5233 is coupled to the reservoir 5110 and configured to move according to a change in height of the water level (e.g. to be positioned at or near a top surface of the . In Fig. 11a, where the top surface of the water is at a water level of WL-2, the movable portion 5233 may be positioned as shown, and for water levels of WL-1 or WL- 3, the movable portion 5233 may be re-positioned accordingly. In this arrangement, the humidifier 5000 may comprise an optical sensor 5235 configured to determine the position of the movable portion 5233. In some forms, the optical sensor 5235 may comprise a field of view which spans ons of the e portion 5233 for a maximum and a minimum allowable quantity of water, for example up to a first boundary of view 5235-1 and up to a second boundary of view 5235-2. The optical sensor 5235 may then produce a signal to te the position of the movable portion 5233 and/or the quantity of water in the reservoir 5110.

In another arrangement, shown in Fig. 11b, an angular sensor 5236 may be coupled to the movable portion 5233 using a connecting portion 5238. As the movable portion 5233 moves ing to the quantity of water in the reservoir 5110, an angle α n the angular sensor 5236 and the connecting portion 5238 may be varied. The angular sensor 5236 may be configured to determine the angle α to produce a signal to indicate the position of the movable portion 5233 and/or the quantity of water in the reservoir 5110.

According to a yet another arrangement as shown in Fig. 11c, the humidifier 5000 may comprise a ity sensor 5237 to determine a position of the movable portion 5233. In one example, the proximity sensor 5237 may be located toward the 505787DIV4/73 bottom of the humidifier 5000 and configured to detect proximity of the movable portion 5233. In such a configuration, as the movable portion 5233 moves according to the quantity of water in the reservoir 5110, the proximity sensor 5237 may produce a signal to indicate the on of the movable portion 5233 and/or the quantity of water in the reservoir 5110. .5.3.4.7 Electrical properties According to another aspect of the present technology, measures of electrical properties of the body of water in the reservoir 5110 may be used to determine the quantity of water. For example, capacitance and/or resistance of the volume of water may be measured by one or more s. The electrical properties of the body of water in the reservoir 5110 may vary according to the quantity of the body of water. For e, the capacitance of the water may increase as the quantity of the body of water is increased.

Accordingly, electrical properties of the body of water in the reservoir 5110 may also be suitable indicative characteristics to be used to determine the quantity of water in the reservoir 5110. 4.8 Image processing A yet another aspect of the present technology may be use of image sing to determine the quantity of water in the reservoir 5110. According to one arrangement, the humidifier 5000 may comprise a camera configured to capture an image of the water in the reservoir 5110. The image may be processed by a controller such as the humidifier controller 5250, and analysed to identify features that could be used to determine the quantity of water (such as the water level).

In some cases, the captured image may be digitised, and then ed to uate features such as any boundaries such as an open surface of the water or boundaries between the water and the reservoir. Then the controller may execute image processing thms to extract and classify the features and any patterns so as to enable the quantity of water to be determined.

According to one arrangement of the present technology, the humidifier oir 5110 may be ured to enhance distinction between water and air in the captured image, such as by ing a visual st between air, water and the reservoir for instance. In one instance, the reservoir may require a clear ‘window’ to allow 505787DIV4/73 the water to be clearly seen therethrough, or visual markers such as high-contrast surfaces or marked lines to improve identification of es by the image processing algorithm.

Yet further, as the humidifier 5000 may often be in ion in a dark environment such as a bedroom during evening, the humidifier 5000 may comprise a lighting element to provide illumination to the oir 5110, the camera and/or the water. .5.3.4.9 Look-up tables or Functions In any of above methods that may be used to determine, estimate, or infer, water quantity, it should be understood that one or more look-up tables, one or more functions, or a combination of any numbers both may be used to relate the measured teristics to the quantity of water in the reservoir 5110.

Yet further, it should be noted that indicative characteristics, or les, that are used in the p tables or functions need not be measured directly by a sensor. An indicative characteristic may be determined or inferred from measures of one or more other properties. For e, a flow rate of a gas may be ed from other characteristics such as motor speed and electrical current, similarly to as disclosed in United States Patent US 6,237,593, the entire contents of which is included herewithin. .5.3.4.10 ng/Calibration mode According to r aspect of the present technology, a fier 5000 may comprise an algorithm for a learning or calibration mode. A learning mode may modify, populate, or ine a look-up table and/or a function correlates the one or more indicative characteristics with the water quantity.

For instance, on a learning mode the controller may determine a rate at which water is consumed during a therapy session, for example until the reservoir 5110 is empty, or until the end of a session. Then, if appropriate, the controller may update the look-up table and/or the function based on the determined water consumption rates and measures of the one or more relevant indicative characteristics.

Alternatively, the humidifier 5000 may comprise an algorithm for a calibration mode. In one exemplary arrangement of a calibration mode, a known, predetermined amount of water is entered into the humidifier reservoir 5110 and the controller tests how the look-up table or the function performs in determining the water 505787DIV4/73 quantity based on measures of the indicative teristics against the known, predetermined amount of water. One such test may be referred to as a calibration cycle. In some cases, a calibration mode may comprise multiple such calibration cycles for improved accuracy, in some cases with varying amounts of water. For example, the humidifier 5000 may instruct its user, such as the patient 1000 or the caregiver to fill the reservoir 5110 to a ular, known amount of water, to undertake calibration. Therefore use of such a calibration mode may improve accuracy of the look-up table and/or the function, and may also compensate for any racies that may develop in the system over its lifetime.

A ation mode may be configured to run at a predetermined interval, such as every six , and/or at a predetermined time or event, such as after a treatment period, during an initial set-up process of the humidifier 5000, during or after manufacturing or prior to sale of the humidifier 5000. In some instances, the calibration cycle may be performed by r party than the patient 1000, such as by a clinician, a caregiver or a home medical equipment provider. Alternatively, as described, it may be run during therapy in what may be a learn mode, or it may be arranged to prompt the user at a predetermined interval such as every month. .5.3.5 Humidity delivery algorithms Another aspect of the present logy may relate to management of delivery of humidity to the flow of air, such as according to the ty of water present in the humidifier reservoir 5110. For instance, a controller may ascertain an average length of a therapy session for the patient 1000 based on a predetermined l length, or based on usage data of the patient 1000. Based on the determined average length of the therapy session, and the quantity of water present in the reservoir 5110, the controller may then be able to determine the humidity profile delivered to the flow of air for the duration of the therapy n. In one example, the ller may determine a maximum output humidity that the patient 1000 may be able to set, so as to be able to deliver a humidified flow of air to the patient 1000 hout a therapy session without running out of water.

According to another aspect, a rate of water usage may be determined based on one or more measures of the quantity of water. For es, rates of water usage may be determined at various times throughout a therapy session by a controller. In some forms, the controller may determine a historical profile of water usage throughout the 505787DIV4/73 therapy session based on a plurality of measured rates of water usage. In one form, the controller may adjust one or more humidification settings based on the determined historical water usage profile. For example, if the water usage rate is above a threshold value, the controller may reduce fication output or a maximum humidifier output, and conversely the controller may increase humidification or a maximum humidifier output if the water usage rate is below a threshold value.

As illustrative examples, PCT patent ation publication number WO/2006/015416 discloses, among others, methods of providing profiling delivery of humidified gas to a patient, potentially to e breathing comfort or to maximise efficient use of water. US patent application publication number WO/2006/015416 discloses, among others, methods of providing humidity to a flow of air using a humidifier, controlling the te or relative ty of the air to be provided to the patient. Materials disclosed in either application, by themselves or in combination with each other, may be suitable for use in combination with the present sure. The entire contents of both patent applications WO/2006/015416 and WO/2006/015416 are incorporated herein by reference. .6 GLOSSARY For the purposes of the present logy sure, in certain forms of the present technology, one or more of the following definitions may apply. In other forms of the present technology, alternative definitions may apply. .6.1 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. heric air enriched with oxygen.

Ambient: In certain forms of the present technology, the term t 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 surrounding the humidifier, e.g. the humidity in the room 505787DIV4/73 where a patient is sleeping. 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 al 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 d, other than for e, noise generated by a RPT device or emanating from a mask or patient interface. Ambient noise may be generated by sources outside the room.

Continuous Positive Airway Pressure (CPAP) therapy: CPAP therapy will be taken to mean the application of a supply of air to an entrance to the airways at a pressure that is continuously positive with respect to atmosphere. The pressure may be approximately nt through a respiratory cycle of a patient. In some forms, the pressure at the entrance to the s will be slightly higher during exhalation, and slightly lower during tion. In some forms, the re will vary between different respiratory cycles of the patient, for example, being increased in response to detection of indications of partial upper airway obstruction, and decreased in the absence of indications of partial upper airway obstruction.

Patient: A person, whether or not they are suffering from a respiratory disease. .7 OTHER REMARKS A portion of the disclosure of this patent document contains al 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 ever.

Unless the context clearly dictates ise and where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit, between the upper and lower limit of that range, and any other stated or intervening value in that stated range is encompassed within the technology. The upper and lower limits of these intervening ranges, which may be independently included in the 505787DIV4/73 intervening ranges, are also encompassed within the logy, 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. rmore, where a value or values are stated herein as being implemented as part of the technology, it is understood that such values may be approximated, unless otherwise stated, and such values may be utilized to any suitable significant digit to the extent that a practical technical implementation may permit or require it.

Unless defined ise, all technical and scientific terms used herein have the same g as commonly understood by one of ordinary skill in the art to which this technology belongs. Although any methods and materials similar or lent to those described herein can also be used in the practice or testing of the present technology, a limited number of the exemplary s and materials are described herein.

When a particular material is identified as being used to construct a component, obvious alternative als 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 e of being manufactured and, as such, may be manufactured er or separately.

It must be noted that as used herein and in the appended claims, the singular forms "a", "an", and "the" e their plural equivalents, unless the context clearly dictates ise.

All publications mentioned herein are incorporated herein by reference in their entirety to disclose and describe the methods and/or materials which are the subject of those publications. The publications discussed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the present technology is not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided may be different from the actual publication dates, which may need to be independently confirmed. 505787DIV4/73 The terms "comprises" and ising" should be interpreted as referring to elements, components, or steps in a non-exclusive manner, indicating that the referenced elements, components, or steps may be t, or utilized, or combined with other elements, components, or steps that are not sly referenced.

The subject headings used in the detailed description are included only for the ease of reference of the reader and should not be used to limit the subject matter found throughout the disclosure or the claims. The subject headings should not be used in construing the scope of the claims or the claim limitations.

Although the technology herein has been described with reference to particular examples, it is to be understood that these examples are merely illustrative of the principles and applications of the technology. In some instances, the terminology and symbols may imply specific details that are not required to practice the technology. For example, gh 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 n distinct elements. Furthermore, although process steps in the ologies may be described or illustrated in an order, such an ordering is not required. Those skilled in the art will recognize that such ordering may be modified and/or s thereof may be conducted concurrently or even onously.

It is therefore to be understood that numerous modifications may be made to the illustrative examples and that other arrangements may be devised without departing from the spirit and scope of the technology. .8 NCE SIGNS LIST Item Reference patient interface 3000 seal-forming ure 3100 plenum chamber 3200 positioning and stabilising structure 3300 vent 3400 decoupling ure 3500 connection port 3600 forehead support 3700 505787DIV4/73 RPT device 4000 external housing 4010 upper portion 4012 lower portion 4014 panel 4015 chassis 4016 handle 4018 pneumatic block 4020 ical and pneumatic components 4100 air filter 4110 inlet air filter 4112 outlet air filter 4114 inlet muffler 4122 outlet muffler 4124 pressure tor 4140 blower 4142 motor 4144 anti-spill back valve 4160 air circuit 4170 supplemental oxygen 4180 electrical components 4200 PCBA 4202 power supply 4210 input device 4220 central controller 4230 clock 4232 therapy device controller 4240 protection circuit 4250 memory 4260 sensor 4270 pressure sensor 4272 flow rate sensor 4274 motor speed sensor 4276 505787DIV4/73 data communication interface 4280 remote external communication k 4282 local external communication network 4284 remote external device 4286 local external device 4288 output device 4290 display driver 4292 display 4294 humidifier 5000 humidifier inlet 5002 humidifier outlet 5004 humidifier base 5006 fier reservoir 5110 paddle 5112 paddle axis 5114 reservoir inlet 5118 heating plate 5120 reservoir outlet 5122 reservoir dock 5130 locking lever 5135 water level reference 5150 conductive portion 5152 humidifier sensor 5202 pressure sensor 5205 flow rate sensor 5210 ty sensor 5218 temperature sensor 5220 vibration source 5232 movable portion 5233 vibration sensor 5234 optical sensor 5235 angular sensor 5236 proximity sensor 5237 505787DIV4/73 connecting portion 5238 g element 5240 humidifier controller 5250 central humidifier controller 5251 heating element controller 5252 air circuit controller 5254 505787DIV4/73 6.

Claims

1. Apparatus for humidifying a flow of air to be delivered to a patient, the apparatus comprising: an inlet to receive the flow of air; an outlet to emit a humidified flow of air; a humidifier reservoir configured to contain a body of water for humidifying the flow of air, the fier reservoir being in fluid communication with the inlet and outlet; at least one sensor configured to generate a signal indicative of quantity of the body of water in the humidifier oir; and a controller configured to: determine the quantity of the body of water in the humidifier reservoir, based on the signal, control a change to humidification output based on the determined oir water quantity so as to be able to r a humidified flow of air throughout a therapy session without running out of water, ine a rate of water usage based on the signal or determined reservoir water quantity, and control at least one of (i) a decrease in the humidification output if the determined rate of water usage is above a threshold value, and (ii) an increase in the fication output if the ined rate of water usage is below the threshold value.

2. The apparatus of claim 1, wherein the controller is configured to decrease the humidification output if the determined rate of water usage is above a threshold value.

3. The apparatus of any one of claims 1 to 2 wherein the controller is configured to increase the humidification output if the determined rate of water usage is below the threshold value. 505787DIV