Respiratory apparatus with multiple power supplies

JP2025041606AActive Publication Date: 2025-03-26RESMED PTY LTD

Patent Information

Application Number
JP2024204840
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Priority Date
2017-10-18
Filing Date
2024-11-25
Publication Date
2025-03-26
Estimated Expiration
2038-10-08

AI Technical Summary

Benefits of technology

【0014】 技術の簡単な説明 本技術は、呼吸器病状の検出、診断、改善、治療および/または予防において用いられ 得る医療機器、あるいはそのコンポーネントの提供に関連し、これらは、向上した快適性 、コスト、有効性、使い易さおよび製造可能性のうち1つ以上を有する。

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Abstract

To provide a medical instrument that can be used in detection, diagnosis, improvement, treatment and / or prevention of respiratory pathologies.SOLUTION: A respiratory apparatus includes components to permit different operations of the apparatus with different power supplies. For example, a respiratory therapy apparatus for controlling a respiratory therapy may include a power input circuit to receive a first power or a second power. The first power may be provided by a connectable low-power power supply and the second power may be provided by a connectable high-power power supply. A controller of the respiratory apparatus coupled to the power input circuit may be configured to detect one of the power supplies, and based on the detection, selectively activate one of a first mode of operation and a second mode of operation. The first mode of operation may be a non-therapy mode with the first power such as for a data setup or data transfer with the respiratory therapy apparatus and the second mode of operation may be a therapy mode with the second power.SELECTED DRAWING: Figure 10
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Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application is a joint venture of U.S. Provisional Patent Application No. 62 / 574,019 (filed October 18, 2017). No. 60 / 339,993, filed on Oct. 23, 2003, the entire contents of which are incorporated herein by reference.

[0002] Technology Background (1) Technology field The technology provides a means for diagnosing, treating, and / or improving respiratory diseases, and for preventing respiratory diseases. In particular, the present technology relates to medical devices and their components, e.g., respiratory disease Such techniques are directed to the prevention of respiratory diseases and the treatment of respiratory diseases. Controlling or setting up devices for convenience in operation or setup using different power sources It may relate to components (eg, power supply circuits) that improve operation. [Background technology]

[0003] (2) Description of related technology The body's respiratory system facilitates gas exchange. The nose and oral cavity form the entrance to the patient's airways. Complete.

[0004] These airways contain a series of branching tubes that narrow as they progress deeper into the lungs. The primary function of the lungs is gas exchange, taking oxygen from the air into the venous blood. The trachea divides into the right and left main bronchi, which The main bronchi divide further and finally become the terminal bronchioles. The airways are divided into respiratory tracts and do not participate in gas exchange. The alveolar regions of the lungs where gas exchange occurs are called respiratory regions. See West's Respiratory Physiology: Essentials.

[0005] Obstructive sleep apnea (OSA), Cheyne-Stokes respiration (CSR), obesity hyperventilation syndrome (OHS), chronic obstructive pulmonary disease (COPD), neuromuscular disease (NMD), chest wall disease and There are various respiratory diseases, including bronchial asthma and associated respiratory failure.

[0006] Meanwhile, healthy individuals can utilize the system and device to prevent the onset of respiratory diseases. Summary of the Invention [Problem to be solved by the invention]

[0007] Systems One known product used to treat sleep-disordered breathing is the S 9 Sleep Therapy System. , an RPT device, a humidifier, a patient interface, and an air circuit.

[0008] treatment Multiple therapies (e.g., nasal continuous positive airway pressure (CPAP), noninvasive ventilation (NIV), high-flow High-frequency therapy (HFT) may be used to treat one or more respiratory disorders.

[0009] Patient Interface To deliver supply air at positive pressure to the entrance of the patient's airway, a nasal mask, a full-face mask, This is done using a patient interface such as a nasal pillow. Although support devices are known, many of them are difficult to use, especially when worn for long periods of time or when the patient is not comfortable with the system. If you are unfamiliar with it, it may seem intrusive, aesthetically unpleasing, or unusable. suffer from one or more problems, such as difficulty in use, discomfort, or other inconveniences. Airman's masks or anesthesia administration masks designed as part of the However, they may still be undesirably uncomfortable when worn for extended periods, for example while sleeping. be.

[0010] RPT Devices Respiratory therapy devices such as positive airway pressure (PAP) machines or devices with motor-driven blowers The RPT device allows the delivery of positive pressure or high flow of air to the patient's airway. As noted above, the outlet of the blower is connected to the patient interface via a flexible delivery conduit. It is connected to the source.

[0011] Such devices have a significant power demand during therapeutic operation. For example, powering a therapeutic blower motor typically requires a significant amount of electrical power ( For example, power in excess of 20, 30 or 40 watts may be required. In such devices, the flow or pressurized air provided by the flow generator is adjusted to a comfortable level. These may include accessory components that form a complete system. For example, The collected air is then applied to a humidifier that humidifies and heats the therapeutic gas before delivery to the patient. The humidifier typically includes a heating element. Similarly, the supply unit or humidifier to assist in maintaining a particular temperature of the supply gas being delivered to the patient from A variety of heating elements may be connected to the delivery conduit. Microcontrollers or digital processors and devices used in such devices This requires a significant amount of power compared to the power requirements of the memory to provide the therapy. For therapeutic systems for 100 W or even more power (over 120 Watts).

[0012] In some circumstances, a therapy system may be configured by someone other than the user of the therapy system. For example, a clinician or home medical equipment (HME) provider may provide a In some circumstances, the initial settings may be changed or A HME may perform the procedure multiple times (e.g., to personalize settings for multiple patients) .

[0013] Therefore, if the setting can be simplified even a little, it may be useful for patients. It can also be useful for those who set things up multiple times, and the benefits will be just as great. . [Means for solving the problem]

[0014] A brief description of the technology The technology may be used in the detection, diagnosis, amelioration, treatment and / or prevention of respiratory conditions. This relates to the provision of medical equipment, or components thereof, that provides improved comfort or , one or more of cost, effectiveness, ease of use and manufacturability.

[0015] Some embodiments of the present technology are useful for detecting, diagnosing, ameliorating, treating or preventing respiratory disorders. Relates to the equipment used.

[0016] Some embodiments of the present technology include a respiratory apparatus or RPT device. The blower may include a blower configured to generate a flow of gas. a power bus that may be connected to a power source sufficient to power the fan and another power source insufficient to power the fan. The blower is powered on the power bus or power rail of the device. It may include a motor.

[0017] The ventilator or RPT device may be configured to use a low-power source without initiating therapy. The device may be configured to be powered on in a "low power mode" that enables The device is also configured to be powered on in a "high power" mode for treatment using a high power source. This allows, for example, devices to be By plugging it into a tablet computer or smartphone, For example, users or healthcare / equipment providers can easily configure devices in low power modes. This allows the device to be connected to different power sources. and to allow different operation depending on the type of power supply installed. , which can be configured to detect a low power condition (e.g., a low battery condition) of a single power source. and change operation using a single power source based on the state of the single power source (low battery) This can be contrasted with a device.

[0018] Some versions of the technology include a respiratory treatment device that provides treatment for respiratory disorders. The respiratory treatment device includes a power input for receiving one or more of the first power and the second power. The first power may be provided from a low power power source adapted to interface with the respiratory treatment device. The second power source may be a high power source adapted to connect to the respiratory treatment device. The respiratory treatment device may include a controller, the controller including a power input. a power supply connected to the circuit and configured to detect at least one of a low power source and a high power source; The controller may be configured to determine whether the power supply is at a low level or at a high level based on the detection of one of the low power supply and the high power supply. Selectively activating a first mode of operation of a respiratory treatment device and a second mode of operation of a respiratory treatment device The first mode of operation may be a non-therapeutic mode, and the second mode of operation may be a non-therapeutic mode. The mode may be a therapeutic mode.

[0019] In some versions, the power input circuit includes a first supply interface and a second supply interface. The first supply interface may be connected to a low-power power source. The second supply interface may be configured to connect to a high power power source. In some cases, the first supply interface and the second supply interface may be configured as At least one of the power supply interfaces is a connection for a detachable power cable. In some versions, the first supply interface and the second At least one of the supply interfaces may include a wireless power interface. Optionally, the first supply interface and the second supply interface are Each of the first and second supply interfaces may include a connector for a removable power cable. and at least one of the second supply interfaces is a removable power and A connector for a data communication cable may be included. The power input circuitry includes a low power supply and a high power supply. The first supply interface may include a first supply interface configured to connect to a source. The interface may include a connector for a removable power cable. The interface may be configured for data communication over a detachable power cable. The receptacle may be a USB connector (eg, a USB Type-C connector).

[0020] In some versions, the first mode of operation is to The communication modes may include communication modes for transmitting and / or receiving data communications. and a setting operation that causes one or more operational control settings to be transferred into the memory of the respiratory treatment device. A mode can be used to store one or more of the following: operational control settings, diagnostic data, and / or operational data. The therapy mode may include a download operation to retrieve the therapy mode from the memory of the therapy device. A motor for powering a blower to generate gas flow to a respiratory interface for a user. Optionally, the input power circuit may include a detection circuit. The detection circuit may include: A voltage detector may be included that detects a voltage indicative of the power received by the power input circuit. The controller may be configured to detect one of the low power supply and the high power supply. The controller may be connected to the detection circuit to receive a signal indicative of either one of the following: A detection circuit is connected to sample the voltage signal generated by the voltage detector. obtain.

[0021] In some versions, the controller compares the detected voltage to a predetermined threshold. and configuring one of the first and second operating modes to compare the first and second operating modes. The detected voltage may be configured to trigger a low power supply and a high power supply based on the comparison. The second mode of operation may be selected by the controller to indicate power from any of the power sources. Activation causes a gas flow to be generated for the user to the respiratory interface. The power supply may include a switching circuit configured to route the power supply to a motor circuit of the fan. The circuitry may be connected to a controller. The switching circuitry may include a semiconductor switch.

[0022] In some versions, the input power circuitry has a first mode of operation and a second mode of operation. The respiratory treatment device may include a voltage regulator for powering the controller in the mode. The motor may further include a blower including a controller to regulate the speed of the motor. The motor may include a motor control circuit connected to the controller. may further be connected to the power supply line of the input power circuit via a switch activated by the controller. The controller may include a processor and a memory. The processor may be configured to: and a second operating mode. obtain.

[0023] In some versions of the respiratory treatment device, the low power source is approximately 5 watts to 20 watts. The high power supplies produce power in the range of approximately 20 watts to 110 watts. The low power power source may include a Universal Serial Bus (USB) power source. The source may include a Qi power source. In some cases, such as in the case of high flow therapy Much higher powers, up to 300W, can be used by respiratory treatment devices.

[0024] Some versions of the present technology include respiratory therapy systems for treating respiratory disorders. The respiratory treatment system may include a first set of components including a memory. The stem may include a second set of components. The second set of components may be and / or a pressure generator configured to provide an air flow delivered to the heater. The respiratory treatment system may include a power interface. The controller may include a power interface. and selectively (a) determining an available power based on the determined available power. A first set of components is adapted to receive power and / or operate in a non-therapeutic mode. (b) to transmit data to the first set of computers to operate in a therapeutic mode; Both the first set of components and the second set of components receive power and / or transmit data. and enabling the controller to perform the , if the determined available power is above a threshold, the first set of components and the second set of components are The components may be configured to allow both to receive electrical power.

[0025] In some versions, the first set of components further includes a display. The first set of components may further include a communication circuit. Optionally, a power interface. The interface may be configured to receive a cable. The cable may be connected to a USB port. The power interface may be an external power interface for a respiratory treatment system. There may be a single power interface so that only the power supply can be provided.

[0026] Some versions of this technology use Universal Serial Bus cables and A respiratory therapy device comprising: a respiratory treatment device including a respiratory treatment method and a method for treating a respiratory disorder including powering an operating mode of a respiratory treatment device using a monkey serial bus power source; A method for a respiratory treatment device includes: The Universal Serial Bus power supply may include a low The mode of operation may be a non-therapeutic mode of operation. In one embodiment, a method for a respiratory treatment device includes: The method may further include powering the device using a universal serial bus cable. The generating mode of operation may include operating a flow generator of a respiratory treatment device.

[0027] Some versions of the present technology may utilize a low power source for non-therapeutic operation of a respiratory treatment device. The method may include powering a respiratory treatment device in a non-therapeutic mode of operation. includes accessing and / or downloading data from a respiratory treatment device. In some versions, access to low-power power is provided via the Universal Serial Bus This can be done using a cable.

[0028] Some versions of this technology use Universal Serial Bus cables and A respiratory treatment device configured to be powered in an operational mode by a monkey serial bus power supply. The operational mode may include accessing and / or downloading the memory of the respiratory treatment device. The universal serial bus power source may be a low power power source, The device is connected to a Universal Serial Bus power supply and a Universal Serial Bus cable. The mode of operation may include a non-therapeutic mode of operation. could be.

[0029] Some versions of the technology are powered in a non-therapeutic mode of operation by a low power source. The non-therapeutic mode of operation may include a respiratory treatment device configured to: access to and / or downloading data from the memory of the respiratory treatment device. In some versions, the low-power power supply may include a Universal Serial Bus The cable allows for external interfacing with respiratory treatment equipment.

[0030] Some versions of the present technology include a method for a respiratory treatment device, the method comprising: The method may include powering the respiratory treatment device in an operational mode using a wireless power transfer device. The operational mode may include accessing data from a respiratory treatment device.

[0031] Some versions of the technology are powered in their operational mode by a wireless power transmission device. The respiratory treatment device includes a respiratory treatment device configured to: This may include:

[0032] Headings used in the detailed description are for the convenience of the reader and are intended to guide the reader through the present disclosure or should not be used to limit what may appear in the claims as a whole. These headings should not be used to interpret the scope of a claim or a claim limitation. should not be used interchangeably.

[0033] Various aspects of the exemplary embodiments described above may be combined with aspects of other specific exemplary embodiments. Further embodiments may be embodied by combining one or more of any one of the examples. It is understood that features may be combined with one or more features of other embodiments. In addition, any single example or any of the examples may be Any single feature or combination of features may constitute patentable subject matter.

[0034] Other features of the present technology will become apparent in light of the information contained within the following detailed description. do.

[0035] Brief Description of Several Drawings The present technology is illustrated by way of example and not by way of limitation in the accompanying drawings, in which like reference characters refer to: contains the following similar elements: [Brief description of the drawings]

[0036] [Figure 1A] 1 shows an exemplary treatment system. A patient 1000 wears a patient interface 3000 and receives a positive pressure air supply from an RPT device 4000. Air from the RPT device is humidified by a humidifier 5000 and travels along an air circuit 4170 to the patient 1000. [Figure 1B] Shown is the RPT device in use on a patient wearing a nasal mask. [Figure 1C] Shown is the RPT device in use on a patient wearing a full face mask. [Figure 2A] An outline of the human respiratory system is shown, including the nasal and oral cavities, larynx, vocal folds, esophagus, trachea, bronchi, lungs, alveolar sacs, heart and diaphragm. [Diagram 3] 1 illustrates an exemplary patient interface. [Figure 4A] 1 illustrates an exemplary RPT device. [Figure 4B] 1 is a schematic diagram of an exemplary pneumatic circuit for an RPT device, with upstream and downstream directions indicated. [Figure 4C] FIG. 1 is a schematic diagram of some example electrical components of an RPT device. [Figure 4D]1 is a schematic diagram of an example process (e.g., algorithm) that may be embodied in a processor or central controller of an RPT device, in which solid arrows indicate the actual flow of information, e.g., via electronic signals. [Diagram 5] 1 shows a humidifier according to an aspect of the present technology. [Figure 6] FIG. 1 is a schematic diagram of an embodiment of an RPT device illustrating a configuration with input power circuits for different power sources operating with a common power input interface, in accordance with an embodiment of the present technology. [Figure 7] FIG. 13 is another schematic diagram of an embodiment of an RPT device showing a configuration with input power circuits for different power supply operations with multiple power input interfaces, in accordance with an embodiment of the present technology. [Figure 8] FIG. 13 is another schematic diagram of an embodiment of an RPT device showing configurations with input power circuits for different power source operations including a wireless power input interface, in accordance with an embodiment of the present technology. [Figure 9] 1A-1C are another schematic diagrams of an embodiment of an RPT device illustrating configurations of the input power circuit for different power supply operations in accordance with an embodiment of the present technology. [Figure 10] FIG. 11 is a flow diagram illustrating an example mode selection method, eg, for a controller, in some versions of the present technology. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0037] Detailed Description of the Preferred Embodiments of the Invention Before describing the present technology in more detail, it is important to understand that the present technology is It should be understood that the present invention is not limited to the specific embodiments that may be used. The terminology used herein is for the purpose of describing the specific embodiments described herein. It should also be understood that this is not limiting.

[0038] As mentioned above, the setting up of the treatment system requires multiple steps (such as repeating the process multiple times a day, or working a week) by a third party (e.g., HME provider or clinician) Therefore, for the person who sets it up, even a small improvement in efficiency is a It is extremely valuable.

[0039] By way of background, the breathing apparatus of the present technology (e.g., RPT devices) requires electrical power to operate. Typically, RPT devices require a variety of outputs (i.e. A power supply with a maximum power (e.g., about 20 to 120 W) is used. For AirSense® 10 devices from d Corporation, It operates on a 90 watt power supply (either from a power source or a battery). In some cases, smaller For powering a portable RPT device, a 20 watt power supply is sufficient. In some cases, a 65 watt power supply is used to power the RPT device. It is possible.

[0040] So for such a power supply, for example, a 100W DC converter is needed to convert the mains power to 90W DC power. May require AC / DC converters, which can typically be bulky and cumbersome Therefore, the provider may not use the power supply unit with the user's power supply unit solely for the purpose of performing the setup procedure. It may be necessary to remove the device from its packaging and then repackage it. It may be necessary to set power settings independently of the patient's device, e.g. A production run may require multiple sets of power supplies, and each of these multiple runs may require multiple This may not be desirable as product variations may exist.

[0041] Advantageously, the breathing apparatus of the present technology can be powered by different types of power sources that can provide different power levels. The breathing apparatus may be configured for use with different power connections. Such operating mode selection may be performed by input power circuits (e.g., Such an operating mode may be implemented with a detection circuit as described in more detail herein. Mode selection allows, for example, a user / healthcare equipment provider to quickly match a breathing device to a patient. Such an arrangement may be implemented to facilitate easy and convenient configuration. Low power levels are required for implementation (compared to the power required to deliver effective respiratory therapy) This is achieved by not having

[0042] For example, the connected power source must provide sufficient power to power the therapeutic operation of the RPT device. The RPT device is not configured to start therapy because the power is not sufficient to initiate therapy. The RPT device can be configured to be powered in a "low power mode" that allows for The device is responsible for detecting connected power from such an external source and for determining the operating mode and power and determining which subsystems should be powered on. In the example, the power supply is a universal serial bus that is insufficient to power all the components of the RPT. All components of the RPT or computing device (e.g., Enough to power a tablet computer, laptop or smartphone Dedicated modules (e.g., ResMed AirSense® 10 device) ResMed 90W power supply.

[0043] For example, a power supply designed to provide sufficient power for full operation (e.g., 90W supply) If power is detected, the RPT device may choose to operate in "therapy mode" and A power source that is not designed to be sufficient for operation (e.g., low-power 5 or 10 W available) If a fault condition is detected, the RPT may operate in a "low power mode."

[0044] In such a low power mode, the RPT device operates a first set of subsystems (e.g. , its controller(s) and memory, and in some cases, its The user can then power only the display and / or input / output devices. , one or more settings of the RPT device, for example by accessing the device's memory Or, operating parameters may be set or changed. can be achieved by using the RPT display / input device itself or by using an external device (e.g. For example, by implementing changes in the user interface of a tablet computer, In the latter case, the external device may be able to respond to the parameter change(s). The RPT's communication device and external devices (e.g. wired data connection or wireless device) The communication is made to the RPT via a data connection. Therefore, in low power mode, the controller will not (b) not initiate the operation(s) on the

[0045] For example, if a power source designed to be sufficient for such power operation is detected, it is selected. When operating in a selected therapy mode, the RPT device uses Required subsystems (e.g., pressure system, humidifier and heater(s)) For example, the heating tube) may be further powered on. Typically, a high power supply is connected If the device can provide power, it may operate / function in non-therapeutic (or low power) mode as well as in therapeutic mode. available in the device (e.g., access to the device's memory and Transfer of data to or from your device, data from your device (e.g. RPT by downloading doses, operations (e.g., errors, diagnostics) or other data Setting or changing one or more configuration or operating parameters of the device). The mode may be a data transfer mode or a data access mode.

[0046] Powers the RPT device when operating in a selected non-therapeutic (or low-power) mode. Simply connect it to a power transfer medium (e.g. USB cable, Lightning cable, Enables non-therapeutic operation with RPT devices through wireless protocols (e.g., Qi) It is possible.

[0047] Such low-power operation is particularly beneficial for clinicians from home medical equipment (HME) providers. These operations simplify the configuration of RPT devices without the need for a specific power supply. This operation allows for faster RPT for maintenance, for example. Downloading data from devices is also easier and faster, without the need for a specific power source For example, in the case of a hardware failure, the therapy component may not be activated at low power. This allows technicians to diagnose RPT devices without risking further damage to the device. For example, software can be transmitted over a low-power data cable without the need for a high-power power supply. Uploading may also allow for software upgrades of the RPT.

[0048] As described in more detail herein, in some versions, the connected The source detection may be realized through detection of the voltage of the connected power source.

[0049] Treatment System Thus, in one form, the present technology includes an apparatus for treating respiratory disorders. A flow of pressurized expiratory gas (e.g., air) is directed through an air delivery tube to the patient interface 3000. The device may include a blower or flow generator for delivering the air to the patient 1000.

[0050] treatment In one form, the present technology includes a method of treating a respiratory disorder. This involves applying positive pressure or high flow to the entrance of the airway.

[0051] Nasal CPAP for OSA In one form, the technology provides for the administration of nasal continuous positive airway pressure or high flow therapy to a patient. The present invention includes a method of treating obstructive sleep apnea in a patient by

[0052] In certain embodiments of the present technology, a supply of air at positive pressure is delivered through one or both nostrils. and delivered to the patient's nasal passages.

[0053] Patient Interface 3000 Referring to FIG. 3, a non-invasive patient interface 3000 according to one aspect of the present technology includes: The following functional features are included: a seal-forming structure 3100, a plenum chamber 3200, a positioning and and stabilizing structure 3300, and connection ports for connection to air circuit 4170. In some embodiments, functionality may be provided by one or more physical components. In some embodiments, a single physical component provides more than one functional aspect. In use, the seal-forming structure 3100 may facilitate the delivery of air at positive pressure to the airway. The patient interface 30 is disposed to surround the entrance of the patient's airway so as to 00 is a ventilation device constructed and arranged to allow for the expulsion of exhaled carbon dioxide. The patient interface 3000 may include a forehead support 3700. Other types of patient interfaces may also be implemented (e.g., high-flow therapy interfaces). interface (e.g., nasal cannula).

[0054] RPT Device 4000 Referring to FIG. 4A, a respiratory treatment apparatus such as an RPT device 4000 includes mechanical components. 4100, pneumatic components, and electrical components 4200, The device may be programmed to execute algorithm 4300 (shown in FIG. 4D). As shown in the figure, the RPT device has an outer housing 4010. The housing 4010 includes an upper portion 4012 of the outer housing 4010 and an outer housing 4010 The lower part 4014 is formed of two parts. In an alternative embodiment, the outer housing 4010 may be formed of one or more panel(s). 4015. The RPT device 4000 may include one or more The system includes a chassis 4016 that supports the internal components. The bracket 4020 is supported by or is part of the chassis 4016. The RPT device 4000 may include a handle 4018.

[0055] Referring to FIG. 4B, the air pressure path of the RPT device 4000 includes an inlet air filter 411. 2. Inlet muffler 4122, capable of supplying air at positive pressure and controllable (flow rate or pressure) a blower 4142, and an outlet muffler 4124. One or more pressure and flow sensors are provided in the pneumatic path.

[0056] The pneumatic block 4020 is a part of the pneumatic path disposed within the outer housing 4010. may include.

[0057] Referring to FIG. 4C, the electronic components 4200 of the RPT device 4000 include a power supply 4 210, one or more input devices 4220, a central controller 4230, a treatment device controller The present invention relates to a treatment device 4245, a controller 4240, one or more protection circuits 4250, and a memory 42 60, a converter 4270, a data communication interface 4280, and one or more output devices. The electrical component 4200 may include a single-printer device 4290 as shown in FIG. 4202. , the RPT device 4000 may include more than one PCBA 4202.

[0058] Referring to FIG. 4D, the central controller 4230 of the RPT device 4000 includes one or more In one embodiment, the device is programmed to execute the algorithm module 4300 of The algorithm module 4300 includes an operation mode detection module 4309, a pre-processing module 4309, and a module 4310, treatment engine module 4320, pressure control module 4330, or the mode of the fault condition detection module 4340.

[0059] In accordance with some aspects of the present technology, the central controller 4230 may Module 4340 may be optionally omitted. Furthermore, fault detection may be performed by a central controller This may be accomplished by a disturbance mitigation integrated circuit, optionally added separately to 4230.

[0060] In one form, the RPT device 4000 may be referred to interchangeably as a ventilator. .

[0061] RPT Devices Mechanical and Pneumatic Components 4100 Air filter(s) 4110 Referring to FIG. 4B, an RPT device in accordance with one form of the present technology includes an air filter 4110. or multiple air filters 4110 (e.g., filters 4112 and 4114). do.

[0062] Muffler(singular or plural)4120 In one form of the present technology, the inlet muffler 4122 is disposed in the air pressure path of the blower 41 42. See FIG. 4B.

[0063] In one form of the present technology, the outlet muffler 4124 is disposed in the air pressure path to the blower 41 42 and the patient interface 3000. See Figure 4B.

[0064] Pressure Device 4140 Referring to FIG. 4B, in one form of the present technology, a flow of air is generated at a positive pressure. Alternatively, the pressure device 4140 is a controllable blower 4142. For example, the blower may be A brushless DC electric motor 414 with one or more impellers housed within a volute 4. The blower may provide delivery of the air supply at, for example, about 120 liters per minute, about 4 cm H 2 O~about 20cmH 2Positive pressure in the range of O2 or about 30 cmH2O2 or other forms 2 O This can be done.

[0065] The flow or pressure device 4140 is under the control of a treatment device controller 4240. do.

[0066] Transducer(s) 4270 With continued reference to FIG. 4B, in one form of the present technology, one or more transducers 4270 are One or more transducers 4270 may be disposed upstream of the force device 4140 in the pneumatic path. The airflow characteristics are constructed and arranged to measure the airflow characteristics at that point.

[0067] In one form of the present technology, one or more transducers 4270 are downstream of the pressure device 4140. , and may be located upstream of the air circuit 4170. One or more transducers 4270 may be constructed and arranged to measure respective characteristics of the airflow at respective points in the path .

[0068] In one form of the present technology, one or more transducers 4270 are connected to the patient interface 300. It is placed near 0.

[0069] Anti-spillback valve 4160 The anti-spillback valve is designed to reduce the risk of water spilling upstream from the Humidifier 5000. The device may be constructed and arranged as follows:

[0070] Air Circuit 4170 4B, an air circuit 4170 according to one aspect of the present technology is configured to supply air or breathable Gas flow travels between the pneumatic block 4020 and the patient interface 3000. It is constructed and positioned so that

[0071] Oxygen Delivery With continued reference to FIG. 4B, in one form of the present technology, supplemental oxygen 4180 is provided via a pneumatic It can be delivered to any point in the path.

[0072] RPT Device Electrical Parts 4200 RPT Devices One or more power supplies 4210 4C and 6 to 10, power from power supply 4210 (PS1) is typically Other components of the RPT device 4000 (e.g., input device 4220, A central controller 4230, a treatment device 4245, and an output device 4290, a heater The inputs are supplied to the data processor (singular or plural).

[0073] In one form of the present technology, the power supply 4210 powers the RPT device 4000 without a humidifier. In another embodiment of the present technology, power is supplied to the RPT device 4210 from a power source 4210. In yet another embodiment, the power supply 4210 is provided to both the power supply 4210 and the humidifier 5000. Power from the RPT device 4000, the humidifier 5000 and the air circuit 4170 is provided. The air circuit 4170 includes a heating element.

[0074] In one form of the present technology, the power supply 4210 is integrated into the external housing of the RPT device 4000. In another form of the present technology, the power supply 4210 is internal to the RPT device. The outer housing 4010 of the chair 4000 (sometimes referred to herein as the RPT) It's outside.

[0075] However, as shown in Figures 6-9, the RPT can be configured to operate with different power sources. For example, the RPT may be connected to two different power sources (e.g., fluctuating or different power outputs). The RPT may be configured to operate with two power sources with different power levels. The RPT may be configured to provide different operation in response to different power sources connected to it. In some versions, the operating mode of the device, as described in more detail herein, The controller controls the RPT according to the type (or power level) of power source attached to the RPT. The time may be determined by the controller or a processor.

[0076] For example, power supply 4210 (PS1) has a main power switching module that can block negative regenerative current. In some versions, the power supply 4210 may be rated to produce more than 20 watts. configured to provide a maximum power of approximately 20 to 120 watts The power source may be a high power source (e.g., an internal or external power source) that is connected to the , 100 watt power supply, 65 watt power supply or 20 watt power supply). In the present invention, such a power source may be used, for example, to provide a treatment using such a power source. For smaller, more portable RPT devices (which can be In some versions, such a device may be used for the treatment mode of the RPT device. A suitable power supply may be a 65 watt power supply. An external power supply may be, for example, a cable that connects the power supply to the RPT. The cable allows the RPT's interface 6711 (e.g. wireless for data and power) Wire-powered with wires or integrated data / power interface 6711B only The power supply 6711 may be plugged into a power interface 6711A having a power supply (single or multiple Optionally, the interface 6711 is a single interface, e.g. for power supply. other external power interfaces (connectors or ports) may be The RPT device is not provided with a T device operation. For example, the interface 6711 (e.g., USB interface (e.g., USB type C interface)) can function as a power and / or data interface. , for example, low power (e.g., less than about 20 watts (e.g., 5 watts)) or high It can receive power (e.g., power in the range of about 20 watts to 100 watts or more). An external power supply (or internal power supply) may also be plugged into the mains power outlet. , connect the cable to the mains outlet so that the AC input of the internal power supply is connected to the mains outlet. It can be plugged in and is more directly integrated with the RPT's power bus. Internal or external The external power supply is an AC / DC converter that converts the AC mains input to a DC output for powering the RPT. It may be a converter.

[0077] Such external or internal power supplies convert the power supply's input into an output DC signal (e.g., 12 volts, 24 volts or 30 volts), but preferably is approximately 24 volts. In some versions, the external power source is a DC / DC converter. (e.g., accepts 12 volt and / or 24 volt DC input and supplies this to the RPT (A converter capable of converting a 12 or 24 volt DC power signal for use in a 12V or 24V DC power supply.) Thus, the output DC power signal from the external power supply may be a 24 volt signal.

[0078] Such a power source may be connected to a blower motor (e.g., the treatment device controller 424 4245) including the power supply 4240 and any necessary sensor(s). For example, when providing a flow of pressurized breathable gas from a device, Providing sufficient power to operate the RPT in treatment mode(s); Thus, such a power source may be considered as a power source that produces high power. 5 includes humidification (e.g., humidity controller 5250 and heater 5240) and / or Other heater devices (e.g., tube heaters) may be optionally included. Typically, Such a high power supply is sufficient for powering all operations of the RPT as a system.

[0079] However, in some versions, as described in more detail herein, other A power source may optionally be used with the RPT of the present technology. For example, the RPT may be It may be configured to connect to an alternative power source 4210-ALT (PS2) via an interface. Such alternative power sources may generate insufficient power to power all of the RPT's operations and may cause It may be considered a low or reduced power source because it is particularly inefficient at powering medical operations. Such external low power sources may range in power (e.g., from about 5 watts to 15 watts) (e.g., For example, the maximum power may be about 10 watts or 5 watts. In the embodiment, the output DC power signal from such a low power external power supply may be a 5 volt signal. Typically, such a low-power external power source provides power to the controller and memory (e.g., The power supply is sufficient to power the RPT's communication circuits (e.g., data communication In some cases, such low The external power source supplies power to one or more output devices 4290 (e.g., a display) and a RP It may also be sufficient to power one or more input devices 4220 (e.g., a keypad) of T. do.

[0080] A low-power external power supply may be used, for example, with a cable connecting the power supply to the RPT. 6711 (e.g., by connecting wires for data and power to the RPT) Wires (single or multiple) dedicated to power or integrated data / power interface 6711B In some such cases, In this case, the low power external power source may be configured similarly to the high power external power source (e.g., using the same cable). or coupler interface), so plug the former and latter into the same interface (e.g., either one at a time into a single interface 6711) (Can be plugged in at any time). Interface 6711 or integrated data / electricity The power interface 6711B is, for example, a Universal Serial Bus (USB) connector. It can be a port (e.g., Type A, Type B or Type C connector port, Micro USB connector connector port, Lightning connector port, or other suitable connector port). In some cases, such cable connections serve as power transfer conduits for RPTs. It can also function as a data transfer conduit / bus as well as a power supply. For example, Universal Serial Bus (USB) hubs, USB port power adapters, Management devices (e.g., desktop computers, laptop computers, tablets, computer) has a USB port. Therefore, connect it to a USB cable or a Lightning cable. The cable can be used to connect an RPT device and an alternative power source 4210-ALT.

[0081] In some versions, the RPT is interfaced to accept wireless power. 8. Alternatively, the power supply 6711 may be connected to the power source 6711 via the wireless power interface 6711C shown in FIG. In such a case, the alternate power source 421 The 0-ALT may be a wireless power source. For example, such an interface may be electromagnetic induction. Power can be received by resonant inductive coupling, magnetic resonance, or inductive power transfer (IPT). In such cases, the interface may include a receiving coil and a receiving circuit. The transmit coil and receive circuit receive the magnetic field from the transmit coil of the alternative power source 4210-ALT. The transmitter coil generates DC power within the RPT by connecting the As described above, if an alternative power source is located near the RPT device 4211, Operated by an alternative power source so that it can function as a power source or a power saving source In some such versions, the Alternative Power Supply 4210-ALT may be In some versions, the coil is a planar Thus, the RPT may be configured with, for example, a pair of flat surfaces on the lower housing of the RPT. A receiving coil may be included, which may transmit power via a wireless alternative power source via a planar coil for power transfer. As mentioned above, such a wireless external power source can be configured, for example, by a controller (e.g. For example, it may be sufficient to power a memory (e.g., central controller 4230) and the RPT It may also power communication circuits (e.g., data communication interface 4280). A wireless external power source such as a It may also be optionally configured.

[0082] In some configurations, the RPT device may include multiple power sources 42, as shown, for example, in FIG. 10 at the same time (e.g., power supplies 4210 (PS1) and 42 In such an arrangement, the RPT device is The power supply may be configured to prioritize one power source over another (e.g., a power source capable of higher power may be configured to prioritize one power source over another). (if preferred).

[0083] Additionally, the RPT device receives power from the first power source while transmitting power through the second power source. The RPT device may be configured to communicate with connected external devices. Power (e.g. mains switching mode) and low power (e.g. tablet computer) power sources In this configuration, the RPT device can be connected simultaneously to It may be configured to receive power from a high power power source and communicate with a tablet computer. For example, a user may use a tablet computer while the RPT device is powered by a high-power source. The RPT device may use the power supply to perform the configuration procedure, for example, when a high-power source is disconnected. It may be further configured to begin receiving power from the low-power power source.

[0084] Input device(s) 4220 An input device 4220 (shown in FIG. 4C) allows a human to interact with the RPT device 4000. The device may include one or more buttons, switches, or dials to enable the following: A switch or dial is a physical control that can be accessed via the touch screen. The button, switch or dial may be a device or a software device. In one embodiment, it may be physically connected to the outer housing 4010 or may be a separate In some embodiments, the central controller 4230 may communicate wirelessly with a receiver electrically connected thereto.

[0085] In one form, the input device 4220 allows a human to enter values ​​and / or menu selections. The present invention may be constructed and arranged to allow for the selection of

[0086] Central Controller 4230 In one form of the present technology, the central controller 4230 (shown in FIG. 4C) is a dedicated electronic circuit 4220, receiving an input signal(s) from an input device 4220, and The force signal(s) may be transmitted to the output device 4290 and / or the treatment device controller. and providing the signal to the humidifier controller 4240 and / or the humidifier controller. do.

[0087] In one form, the central controller 4230 is an application specific integrated circuit. In an embodiment, the central controller 4230 may be formed of discrete electronic components.

[0088] In one form of the present technology, a central controller 4230 (shown in FIG. 4C) A processor 4230 suitable for controlling an RPT device 4000, such as an NTEL processor It may be a P or a microprocessor.

[0089] A central controller 42 suitable for controlling an RPT device 4000 according to another aspect of the present technology. 30 is based on the ARM Cortex-M processor from ARM Holdings. Processors include, for example, STM32 from ST MICROELECTRONICS A series of microcontrollers may be used.

[0090] In a further alternative embodiment of the present technology, the central controller 4230 is an ARM9 based It may include a member selected from the family of 32-bit RISC CPUs. For example, The STR9 series of microcontrollers from MICROELECTRONICS are used. It is possible.

[0091] In a particular alternative embodiment of the present technology, a 16-bit RISC CPU is 4000 as a central controller 4230. For example, From Troller's MSP430 family (manufacturer: TEXAS INSTRUMENTS) A processor of the type may be used.

[0092] The central controller 4230 controls one or more converters 4270 and one or more input devices. The central control 4220 is configured to receive an input signal or signals from the central control 4220. The controller 4230 may, for example, be configured to operate in conjunction with the operation of the input power circuit 6710 as an operating mode detection module. To implement module 4309, one or more digital or analog inputs as described above may be used. It may also be configured with a force port.

[0093] The central controller 4230 controls the output device 4290, the treatment device controller 42 40, data communication interface 4280 and humidifier controller 5250 The central control unit is configured to provide an output signal or signals to one or more of the central control units. The controller 4230 controls the operation of the input power circuit 6710, for example, in conjunction with the switching operation of the input power circuit 6710. To implement the code detection module 4309, one or more digital or may also be configured with an analog output port.

[0094] The central controller 4230, or a number of such processors, may be any of the processors described herein. The method may be configured (e.g., configured to implement one or more of the methods of As a computer program recorded in a recording medium (e.g., memory 4260) One or more algorithms 4300 (shown in FIG. 4D) expressed as As previously mentioned, such processor(s) may be implemented in the RPT device 4000. However, in some devices, the processor(s) ) for the purpose of performing, for example, any of the methods described herein without direct control of respiratory therapy delivery. etc., may be implemented separately from the flow generation components of the RPT device. For example, Such a processor may analyze stored data, such as from any of the sensors described herein. For purposes of determining control settings for ventilators or other respiratory-related events through analysis: Such a processor may perform any of the methods described herein. The method relates to different operating modes for different types of power supplies as described in more detail below. Either one can be done.

[0095] Therapeutic Devices 4245 In one form of the present technology, a treatment device 4245 (shown in FIG. 4C) is The therapy device 4230 is configured to deliver therapy to the patient 1000 under the control of the therapy driver 4230. The device 4245 may include a controllable flow or pressure device 4140 (e.g., a positive pressure device 4140). Such a device may be a blower (e.g., a servo-controlled blower). Such a blower may be implemented with a motor having an impeller in a volute. It can be implemented in

[0096] Therapeutic Device Controller 4240 In one form of the present technology, a therapy device controller 4240 (shown in FIG. 4C) A control module 4330 (shown in FIG. 4D ) that is controlled by the central controller 4230. or embodies the functionality of algorithm 4300 executed in conjunction therewith. In some cases, the therapy device controller 4240 may be implemented with a motor drive.

[0097] In one form of the present technology, the therapy device controller 4240 includes a dedicated motor control integrated For example, in one form, the MC33035 manufactured by ONSEMI A brushless DC motor controller is used.

[0098] protection circuit 4250 Preferably, the RPT device 4000 according to the present technology includes one or more protection circuits 4250 (FIG. 4C).

[0099] One form of protection circuit 4250 according to the present technology is an electrical protection circuit.

[0100] One form of protection circuit 4250 in accordance with the present technology is a temperature or pressure safety circuit.

[0101] In some versions of the technology, the protection circuit 4250 may be a transient absorbing diode circuit. The circuit may include a circuit 4400. The circuit may include a circuit 4400 that generates rotational kinetic energy from, for example, a blower motor. Alternatively, the device may be configured to absorb the converted energy. , the protection circuitry 4250 may include a disturbance mitigation integrated circuit.

[0102] Memory 4260 In accordance with one aspect of the present technology, the RPT device 4000 includes a memory 4260 (shown in FIG. 4C ). ) (preferably non-volatile memory). In some embodiments, the memory 4260 includes: In some forms, the memory 4260 may include volatile The memory may include nonvolatile RAM (eg, DRAM, SRAM, or FRAM).

[0103] Preferably, memory 4260 is located on PCBA 4202 (shown in FIG. 4A). Memory 4260 may take the form of an EEPROM or NAND flash.

[0104] Additionally or alternatively, the RPT device 4000 may include a removable memory 4260. (e.g., memory cards made according to the Secure Digital (SD) standard).

[0105] In one embodiment of the present technology, the memory 4260 is a computer-readable recording medium. The recording medium includes a computer program that implements one or more of the methods described herein. The data program instructions (eg, one or more algorithms 4300) are recorded.

[0106] Transmitter 4270 The converter 4270 (shown in FIG. 4C) may be internal to the device or may be The external transducer may be external to the T device. The external transducer may be located, for example, on the air circuit. or may form part of the air delivery circuit and / or the patient interface. The external transducer may take the form of a non-contact sensor (e.g., a data transmitter RPT device). (Doppler radar moving sensor that is fixed or moved).

[0107] flow A flow transducer 4274 according to the present technology (shown in FIG. 4C) may be a differential pressure transducer (e.g., SENS The differential pressure transducers can be based on pneumatic Each of the pressure transducers is in fluid communication with the circuit and is connected to a respective first point within the flow restricting element. and connected to a second point.

[0108] In use, a signal indicative of the total flow rate Qt from the flow transducer 4274 is However, the generation of such a flow signal or the estimation of flow may be For example, in some embodiments, a mass flow meter may be implemented. A sensor (e.g., a hot wire mass flow sensor) is implemented to generate a flow signal. Optionally, one of the methods described in, for example, U.S. Patent Application No. 12 / 192,247 may be used. Flow may be estimated from the signals of one or more of the other sensors mentioned above, as described elsewhere herein. The same document is incorporated herein by reference.

[0109] pressure A pressure transducer 4272 (shown in FIG. 4C) according to the present technology is disposed in fluid communication with the pneumatic circuit. One example of a suitable pressure transducer is the HONEYWELL ASDX series. Another suitable pressure transducer is the GENERAL ELECTRIC There are sensors from the NPA series.

[0110] In use, the signal from the pressure transducer 4272 is controlled by the central controller 4230. In one form, the signal from the pressure transducer 4272 may be filtered. After being processed, it is received by the central controller 4230.

[0111] Motor Speed In one form of the present technology, the motor speed from a motor speed converter 4276 (shown in FIG. 4C) The motor speed signal is preferably transmitted to the therapy device controller 4240. The motor speed is provided, for example, by a speed sensor (e.g., a Hall effect sensor). It can be generated by:

[0112] temperature A temperature transducer 4278 (shown in FIG. 4C) may measure the temperature of the gas in the pneumatic circuit. An example of a temperature converter 4278 is a thermocouple or a resistance temperature detector (RTD).

[0113] Data Communication Systems In a preferred embodiment of the present technology, a data communication interface 4280 (shown in FIG. 4C) ) is provided and connected to the central controller 4230. 280 is preferably connectable to a remote external communications network 4282. The interface 4280 is preferably connectable to a local external communications network 4284. Preferably, the remote external communication network 4282 is Preferably, the local external communication network 4284 is a local external device. The data communication interface is a data / power interface. interface 6711B and / or wireless communication interface (e.g. wireless protocol (e.g. Bluetooth, WIFI, Bluetooth LE) In some versions, the data communication interface The interface is, for example, a cellular wireless protocol (e.g., GSM, CDMA and LTE In accordance with the present invention, cellular or mobile communication may be embodied.

[0114] In one embodiment, the data communication interface 4280 is connected to the central controller 4230. In another embodiment, the data communication interface 4280 is part of a central control It is an integrated circuit separate from the controller 4230.

[0115] In one embodiment, the remote external communications network 4282 is the Internet. The communication interface 4280 is a It may use wired communication (via the Internet or optical fiber) or it may use wireless protocols. do.

[0116] In one embodiment, the local external communication network 4284 is compliant with one or more communication standards (e.g. For example, using Bluetooth or consumer infrared protocols.

[0117] In one embodiment, the remote external device 4286 may include one or more computers (e.g., In one embodiment, the remote external device 42 86 may be a virtual computer rather than a physical computer. A remote external device 4286, such as Access may be possible from

[0118] Preferably, the local external device 4288 is a personal computer, a mobile phone, a tablet, a touch screen or remote control.

[0119] Optional display and output devices including alarms Output device 4290 (shown in FIG. 4C) according to the present technology includes visual, audio and tactile units. The visual display may take the form of one or more of a Liquid Crystal Display (LCD) Or it may be a light emitting diode (LED) display.

[0120] Display Driver 4292 A display driver 4292 (shown in FIG. 4C) controls the display 4294. It receives as input the characters, symbols or images to be displayed and displays these characters on the display 4294. Converts the text into a command to display letters, symbols, or images.

[0121] Display 4294 A display 4294 (shown in FIG. 4C) receives signals from a display driver 4292. The display is configured to visually display characters, symbols or images in response to commands received from the display. For example, the display 4294 may be an eight-segment display, in which case the The play driver 4292 plays each character or symbol (for example, the number "0") as a specific character or Eight logic signals indicating whether each of the eight segments should be activated to display a symbol or a symbol. Convert to number.

[0122] Input power circuit 6710 To accommodate the above mentioned different power sources, the RPT is The input power circuit 6710 typically includes a power supply (PS1 and / or 6711 for the PS2) (e.g., power interface 6711A, Data / Power Interface 6711B and / or Wireless Power Interface 67 11C). The input power circuit 6710 supplies power to one or more power sources in response to the power source. A circuit connector for receiving and routing some or all of the components of the RPT. For example, the circuitry 6710 may include a power routing component, such as a power level This can be done from a power supply 4210 via a power supply 4220, for example a high power supply (PS1 ) is connected to the RPT, the RPT's components (e.g., treatment generation components) ) It will be possible to power everything.

[0123] Circuit 6710 allows the use of an alternative power supply to power only a subset of the RPT's components. Power from the 4210-ALT (PS2) power supply can be connected to the RPT via the power rail. It is also possible to route to a subset of the components of a network. Such a subset is called an RPT. For example, a subset of components may include: Controller (e.g., Central Controller 4230 or other processor component of the RPT) Such a subset may be, for example, a wired connection for sending and receiving data to and from an RPT. A communication circuit (e.g., a communication interface 4280) for communication or wireless communication. From such a subset, typically a therapeutic or therapeutic device and / or The higher power consumption of the RPT is used in other operations with heating components. Components (e.g., therapeutic devices) are excluded (e.g., motor inverter bridges, etc. motors and / or therapy device controllers) and heating components (e.g. (e.g. humidifier heater, tube heater).

[0124] As shown in FIG. 9, in some cases, the input power circuit 6710 may include one or more detectors. The detection circuit 9002 may typically include a controller in the RPT (e.g., The detection circuit 9002 is connected to the input power circuit. For example, in some cases, the input The power circuit may include a voltage detector or voltage sensor circuit. The sensor is configured to detect a voltage associated with or specific to the power source connected to the RPT. Thus, the voltage detector detects the identification voltage generated by the connected power supply. For example, in the case of an exemplary 24 volt power supply (PS1) connection, The voltage detector detects a proportional voltage indicative of the 24 volt supply and produces a signal indicative of such voltage. The controller of the RPT (e.g., the central controller 4230) may (e.g., digital or analog input port) and extracts high power from this signal. In the case of a 5 volt power supply (PS2) connection, the voltage detector detects the 5 volt A proportional voltage indicative of the power supply may be sensed and a signal indicative of such voltage may be generated. A controller (e.g., central controller 4230) may then route this signal to the same or another input port. (e.g., a digital or analog input port) and The connection may be determined.

[0125] In one embodiment, the detector / sensor may be implemented with an operational amplifier. , configured as a comparator, and comparing the voltage associated with a power supply or input voltage with a different power supply (e.g. For example, a 6 volt threshold or a 7 volt threshold or other value) The output signal from the comparator is then compared to a suitable threshold voltage level. A power source may be indicated by an input to an input port of the controller 4230. For example, When a high (true) output signal is obtained from the comparator, this indicates that a voltage above the threshold (e.g., This indicates that a low voltage (higher than the low voltage of a power source, such as a power supply voltage) has been detected. Then, take such a (high true) output signal and use it as a digital input for a controller, for example. It is possible to indicate to the controller that a high-power power supply is connected at the port. The low output signal from the comparator represents a voltage lower than the threshold (e.g., lower than the high voltage of a high power supply voltage). Such a low (false) signal can then be used to, for example, This can be taken out at the input port to indicate to the controller that a low power supply is connected. A comparator can be used to generate a signal to the controller for such a decision. Any other suitable comparison may be implemented.

[0126] In some versions, the voltage detector / sensor detects the voltage of the connected power source (e.g., P Such a voltage can be generated proportional to the voltage supplied from the is sampled by the controller's sampler or sampling circuitry to obtain the controller's analog It may then be sampled at an input port (e.g., central controller 4230). The controller then compares the sampled values ​​with one or more programmed The power supply may be digitally compared to a threshold value to determine which power supply is connected.

[0127] In some versions, the input power circuit 6710 determines the detected power source type or One or more switching circuits 9 that actively route power based on the detected power level. Such a switch may also include a power / voltage rail for one or more of the RPTs and The RPT controller can be connected to, for example, a particular power supply to detect when it is connected to the Based on what the controller detects, the controller activates one or more switches. By selectively allowing power from a connected source through the voltage rails, the current can be controlled to a specific It can be supplied to a component or a subset of components in an RPT. Regarding the point, the output signal from the output port of the controller (e.g., digital output signal) activating one or more transistors (e.g., semiconductor type transistors) to generate a Power on the T rail(s) can be sent or initiated from a power source For example, one or more of these switches may allow an alternative power source to be connected to the RPT4000 interface. When connected to the 6711 interface, the supply line from the Alternate Power Supply 4210-ALT (PS2) This will prevent the power supply from being connected to the RPT treatment and / or heating device. Similarly, such one or more of such switches may cause the power supply to When connected to the interface 6711 at 0, the supply line from the power supply 4210 (PS1) Allows the ins to be connected to treatment and / or RPT heating devices do.

[0128] In some cases, the input power circuit 6710 may be a controller for an RPT (e.g., One or more voltage regulator modules (single or multiple) that may power the central controller 4230 Multiple) 9006 or VRM (PPM (Processor Power Module) (e.g., step-down Such a voltage regulator module (or modules) may include a The number of power supplies (PS1 and PS2) determines whether the component is powered by one or both of the power supplies. The input and / or input power circuit traces may be receptively connected. Such a voltage regulator module or modules are used to regulate other low voltage The voltage regulator may then be connected to the power component 4210 or an alternative Regardless of whether the power supply 4210-ALT is connected or coupled to the RPT4000, a controller (e.g., a central controller 4230) and optionally a communication circuit (e.g., , and may provide power to the data communication interface 4280). In some versions, such a voltage regulator module or modules may be A display / splay driver (e.g., output device 4290) and an input device For purposes of illustrating the present technology, a simplified version of FIG. Although not shown, one or more of the voltage regulators may be powered by either or both sources. It will be appreciated that additional circuit components may be provided to enable this.

[0129] RPT Device Algorithm As described above, the central controller executes programs for carrying out the functions of the respiratory treatment device. The following exemplary process modules may be implemented with the algorithm: Any one or more of these may be included.

[0130] Operation Mode Detection Module 4309 As shown with reference to FIG. 10, a controller of the RPT (e.g., a central controller 42 30) is when the power supplies connected to the RPT are different (e.g. PS1 or PS2). The device may be configured to select different operation modes depending on whether the device is a Such mode selection is performed by the input power circuit 6710 (e.g., its detection circuit 9002 as described above). ) The execution of such an operation mode selection may be embodied by a controller in conjunction with: The user / healthcare equipment provider may choose to Quickly and easily set up a patient breathing device with a readily available power connection; Support downloading data, uploading software, etc. This can be done as follows.

[0131] For example, a controller of the RPT device 4000 (e.g., a central controller 4230 ) may embody a mode selection method as shown in the flow chart of FIG. The initial power supply to the controller is provided by, for example, the power supply (PS1) or the alternative power supply ( Optionally, RPT is started after power connection. A button may be provided on the RPT to turn it on. As mentioned above, this The input power supply 6710 may be powered by the voltage regulator module 9006 of the input power circuit 6710.

[0132] Next, at 10004, the controller may detect a power source connected to the RPT. For example, as described above, the controller may determine whether the power supply ( Such detection may be performed by a detection circuit 9002. Such detection may be performed by voltage detection (e.g., by a voltage detector / sensor). The comparison may be based on a comparison between a predetermined reference voltage and the sensed voltage. A power source is connected (e.g., sufficient power for therapeutic action) or a low-power power source is connected ( For example, it may function to determine whether there is insufficient power for therapy operation.

[0133] Thus, at 10006, the controller initiates a particular mode of operation based on the detection. For example, if a high power source is detected, the controller may initiate a therapy action (e.g., , a pre-processing module 4310 and a treatment engine module 4320 and a control module Similarly, the high power supply may be capable of detecting or performing the operations described above in connection with the control circuit 4330. If issued, the controller may (e.g. motor controllers and blower motors) and / or heating controllers and heating components (e.g., for humidifiers 5000 and heating tubes (singular or Such activation may result in the input power circuit for such components being turned on. This may include activating one or more switches in the switching circuit 9004 of the path 6710. The RPT controller detects available power from the external power source and and determining which of the subsystems to turn on. The decision as to which system or systems to turn on is based on a given set of subsystem priorities. The hierarchy may be based on the determined power output of the connected power sources.

[0134] If a low power source is detected, the controller may choose to disable non-therapy operations (e.g., certain high power therapy operations). Such low power devices may permit or perform certain operations (operations without the use of medical components). In the mode(s), the RPT device configures a first set of subsystems (e.g. , the controller(s) and memory and in some cases the data In such mode or modes, the The controller(s) may operate solely for data access (e.g., Download and upload operations (e.g. parameter settings, software updates) (Upgrade, diagnostic access). Such startups include low-power components such as Switching circuitry for the input power circuit 6710 for an input device (e.g., a display or input device) There is activation of one or more switches of 9004. Thus, the operating mode of the respiratory treatment device The board is powered by a Universal Serial Bus cable and Universal Serial Bus power supply. The operating mode may be to access data or memory of the respiratory treatment device. Alternatively, the operating mode of the respiratory treatment device may include using a wireless power transmission device. The operating mode may be to access data or memory of the respiratory treatment device. may include.

[0135] In such a low-power operating mode, the user may then, for example, use the built-in display to for data communication (wired or wireless) with the RPT device 4000 The RPT device can be accessed through an external device (e.g., a tablet computer) connected to the device. change one or more settings on the device or access data on the RPT device This can be done.

[0136] Pre-processing module 4310 With reference to FIG. 4D, for example, a therapy mode may be activated based on the operation mode detection module. After the measurement, the pre-processing module 4310 of the present technology performs a pre-processing of the transducer (e.g., pressure transducer 42 72 or flow transducer 4274) as input, and preferably one or more The system performs one or more process steps to calculate the output values ​​listed above. These output values ​​are then are used as input to modules (eg, treatment engine module 4320).

[0137] In one form of the present technology, the output values ​​are the interface or mask pressure Pm, respiratory flow Includes quantity Qr and leakage flow rate Ql.

[0138] In various forms of the present technology, the pre-processing module 4310 performs the following algorithm: Contains one or more of: Pressure Compensation Algorithm 4312, Airflow Algorithm 4314, Leakage flow algorithm 4316, respiratory flow algorithm 4318, and jamming detection Algorithm 4319.

[0139] Pressure Compensation In one form of the present technology, a pressure compensation algorithm 4312 (shown in FIG. 4D) A signal indicative of the pressure in the pneumatic path proximal to the outlet of the block is received as an input. The algorithm 4312 estimates the pressure drop in the air circuit 4170 and The estimated pressure Pm in the interface 3000 is provided as an output.

[0140] Ventilation flow In one form of the present technology, an airflow algorithm 4314 (FIG. 4) for calculating airflow 3D) receives as input the estimated pressure Pm in the patient interface 3000 and The ventilation flow rate Qv of air from the ventilation hole 3400 in the user interface 3000 is estimated.

[0141] Leakage flow In one form of the present technology, a leak flow algorithm 4316 (shown in FIG. 4D) calculates the total flow It takes Qt and the ventilation flow Qv as inputs and is long enough to include many respiratory cycles. The leak rate Q is calculated by calculating the average of Qt-Qv over a period (e.g., 10 seconds). Provide l as output.

[0142] In one form, the leak rate algorithm 4316 provides the leak rate Ql as an output. Calculate the leakage conductance and calculate the leakage flow rate Ql from the leakage conductance and in The patient interface pressure Pm is determined as a function of the patient interface pressure Pm. The total flow rate Qt, the ventilation flow rate Qv, and the estimated pressure Pm in 3000 are received as inputs. In the embodiment, the leakage conductance is calculated by the low-pass filtered non-ventilation flow rate Qv-Qt It is calculated as the low-pass filtered square root of the quotient of The filter time constant should have a value large enough to include several respiratory cycles (e.g., about 10 seconds). do.

[0143] Respiratory flow In one form of the present technology, the respiratory flow algorithm 4318 calculates the total flow Qt, the ventilation flow Q v and leakage flow rate Ql are received as input, and the ventilation flow rate Qv and leakage flow rate Ql are calculated as the total flow rate Q By subtracting from t, the respiratory flow to the patient, Qr, is estimated.

[0144] Jamming Detection The leakage has recently been changed and the leakage flow algorithm 4316 is now fully compensated for this change. If the above is not the case, a state called "jamming" exists. , U.S. Patent No. 6,532,957, U.S. Patent No. 6,810,876 or U.S. Patent No. It can be determined based on the method described in the application Published Application No. 2010 / 0101574A1. In a jamming condition, the respiratory flow baseline is There is usually some degree of inaccuracy due to distortion of flow geometry and limitations in flow detection. Jamming is taken out to show the extent of uncompensated leakage. and calculated by the jamming detection algorithm 4319 (shown in FIG. 4D).

[0145] Treatment Engine Module 4320 In one form of the present technology, a therapy engine module 4320 (shown in FIG. 4D) Pressure in the interface 3000 Pm, air flow rate to the patient Qr, leakage flow rate Ql, The system receives as input one or more of the camera variables and outputs one or more treatment parameters. and provide it.

[0146] In some versions of the technology, the treatment parameters are the CPAP treatment pressure Pt or two-level pressure therapy.

[0147] In one form of the present technology, the treatment parameters include the level of pressure support and the target ventilation rate. There is at least one of them.

[0148] Phase Decision In one form of the present technology, the RPT device 4000 does not determine the phase.

[0149] In one form of the present technology, a phase determination algorithm 4321 (shown in FIG. 4D) A signal indicative of the inhalation flow rate Qr is received as an input and an estimate of the phase of the respiratory cycle of the patient 1000 is provided. The rate of phase change indicates the respiratory rate.

[0150] Waveform determination In one form of the present technology, a therapy control module 4330 controls the therapy device 4245. The device controls the positive airway pressure to provide a nearly constant positive airway pressure throughout the patient's respiratory cycle.

[0151] In one form of the present technology, a therapy control module 4330 controls a predetermined pressure waveform for the phase. The treatment device 4245 is controlled so as to obtain a positive airway pressure according to the In one embodiment, the waveform is square. It is a wave, where at some values ​​of the phase the values ​​are higher and at other values ​​of the phase the values ​​are lower. In some cases, the treatment device is controlled to provide high flow treatment. It is possible.

[0152] In one form of the present technology, a waveform determination algorithm 4322 (shown in FIG. 4D) determines the current Receives a value indicating patient ventilation Vent as an input and provides a pressure vs. phase waveform as an output do.

[0153] In one form, the waveform is a square wave with a value of 1 at the early value of the phase corresponding to inspiration. In other forms, the waveform is more A "smooth and comfortable" waveform that rises gradually to 1 at early phase values ​​and Then it gradually decreases to 0.

[0154] Ventilation decision In one form of the present technology, a ventilation decision algorithm 4323 (shown in FIG. 4D) determines the respiratory flow. A quantity Qr is received as input and a measurement indicative of patient ventilation Vent is determined.

[0155] In one form, the ventilation decision algorithm 4323 loads the current value of the patient ventilation, Vent. It is determined as 1 / 2 the pass-filtered absolute respiratory flow value Qr.

[0156] Determining Inspiratory Flow Limitation In one form of the present technology, a processor is configured to detect one or more inspiratory flow limitations. Executes the flow limiting algorithm 4324 (shown in FIG. 4D).

[0157] In one form, the inspiratory flow limitation algorithm 4324 receives the respiratory flow signal Qr as an input and and providing as an output a metric of the extent to which the inspiratory portion of the breath exhibits inspiratory flow limitation.

[0158] The inspiratory flow limitation algorithm 4324 detects at least one of the following three types of inspiratory flow limitation: Calculate the measures of: normal flat, M-shape and "inverted chair" shape.

[0159] Apnea and hypopnea detection In one form of the present technology, a central controller 4230 detects apnea and / or hypopnea. One or more apnea and / or hypopnea algorithms 4325 for detection of hypopnea (Figure 4 D).

[0160] Snoring Detection In one form of the present technology, a central controller 4230 includes one or more Run the above snore algorithm 4326 (shown in FIG. 4D).

[0161] EPAP Decision In one form of the present technology, when multiple distinct characteristics of upper airway obstruction ("UAO") are present, If the EPAP exceeds the preset minimum value, minimum EPAP, the upper It increases to a degree that is largely proportional to the severity of the airway obstruction. In the absence of features indicative of UAO, E The PAP is gradually decreased to a preset minimum EPAP. This tends to minimize the amount of EPAP delivered. At any given time, EPAP is It is a balance between the forces that increase EPAP and the forces that decrease EPAP. When near-equilibrium is reached, EPAP may be affected due to occasional indicators of moderate UAO. The upward movement is due to the decline that occurs in the absence of the UAO indicator. A balance is struck.

[0162] When the EPAP adjustment algorithm 4327 (shown in FIG. 4D) prescribes an increase in EPAP However, this increase cannot occur instantly. Such an increase in EPAP is caused by the central controller 4 230, and the period during which the RPT device 4000 is considered to be in an inhalation state. Examples of such techniques are shown in U.S. Pat. No. 2011 / 0203588A1, which is incorporated herein by reference. do.

[0163] Determination of target ventilation 4328 In some cases, the target ventilation is a percentage of typical recent ventilation ( For example, it can be set to 90%. Typical modern ventilation has a time constant of 3 minutes (the ventilation filter). It is calculated as the output of a one-dimensional low-pass filter by applying a 1D low-pass filter (VL) to the instantaneous ventilation.

[0164] Determining treatment parameters The central controller 4230 may include one or more algorithms for determining treatment parameters. Execute 4329 (shown in FIG. 4D).

[0165] Control Module 4330 A therapy control module 4330 according to one form of the present technology receives a target therapy pressure Pt as input. and controls the treatment device 4245 to deliver that pressure.

[0166] A therapy control module 4330 in accordance with another form of the present technology may be configured to measure EPAP, waveform values ​​and pressure The assist level is received as an input, a target treatment pressure Pt is calculated, and a treatment device 424 5 is controlled to deliver this pressure.

[0167] A therapy control module 4330 according to another form of the present technology may be configured to control EPAP, waveform values, target It receives pressure support from target ventilation and instantaneous ventilation as input. Calculates levels and calculates target therapy pressure Pt using EPAP, waveform values ​​and pressure assistance The pressure controller 4245 calculates the pressure in the blood vessel 4242 and controls the treatment device 4245 to deliver this pressure.

[0168] Detecting fault conditions In one form of the present technology, the central controller 4230 may include one A fault condition detected by one or more of the methods may be determined by at least one of the following: May contain at least one of: ● Power outage (no power or insufficient power) ● Converter failure detection ● Unable to detect the presence of a component ● Operating parameters are outside the recommended range (e.g., pressure, flow, temperature, PaO 2 ) • Failure of a test alert to produce a detectable warning signal.

[0169] When a fault condition is detected, the corresponding algorithm signal is generated by one or more of the following: Signaling the presence of a fault: ● Initiating audible, visual and / or kinetic (e.g. vibration) warnings. ● Sending messages to external devices Incident logging

[0170] In accordance with another aspect of the present technology, the central controller 4230 includes software to detect fault conditions. Instead, the detection of fault conditions may be performed by a central controller, as described above. This can be handled exclusively by the controller 4230 and another fault mitigation integrated circuit. In some cases, the fault mitigation integrated circuit is also processed within the central controller. Serves as a redundant backup for the algorithmic fault detection / mitigation module obtain.

[0171] Therapeutic Devices 4245 In a preferred form of the present technology, a treatment device 4245 (shown in FIG. 4C) is 0 is under the control of the therapy control module 4330.

[0172] Preferably, the treatment device 4245 is a positive air pressure device 4140 .

[0173] humidifier 5000 In one form of the present technology, a humidifier 5000 (shown in FIG. 5) includes a water reservoir and a heating plate. (shown in FIG. 1) is provided.

[0174] Example RPT Device Use Case(s) The exemplary apparatus implementations described herein may then, for example, perform device configuration or diagnostics. Relatedly, improved RPT device operation can be obtained. For example, a user can Connect the computer to the RPT device, for example via a USB cable. Therefore, if power is only available from the tablet, the RPT device can A tablet cable that provides power to the RPT device (using the tablet's USB power source) This cable can be used with a USB Type-C connector, for example. The RPT device can then be connected to a single power interface (port) of the RPT device. RPT devices provide low or high power on a single power interface (interface Is the power available via the power line(s) / pin(s) of the and operates according to this power detection in the selected mode. In low power mode, the RPT device typically detects the low power mode. The device is connected via a single power interface (the data lines of the interface ( data communication with the tablet via the serial number or numbers / pin(s) For example, RPT devices, patient settings, and configuration data for RPT devices can be uploaded to a tablet. or to load tablet error logs, usage logs, or diagnostic data onto the RPT device. Currently, USB Type-C cables can only support 5 watts (low power devices). It can provide up to 100 watts (high power mode). If you plug the cable into a single power port / interface, e.g. a tablet High power from an appropriate higher power source that is connected to a single interface when the power is disconnected. Therefore, RPT devices can be powered using the same cable coupler and interface. With the interface configuration, it can operate in a high power mode that can exceed 20 watts. For CPAP-type RPT devices, 100 watts may be sufficient to provide therapy, but R The PT device can also provide therapeutic operation at about 65 watts or about 90 watts. RPT device power consumption is typically measured based on the number of sleep disordered breathing events detected (e.g., The pressure RPT device provides depends on the delivered therapy pressure, which may depend on the apnea / hypopnea index. Events such as these and the humidity generated by humidifiers should be avoided. The humidity generated by the air depends on the ambient humidity and temperature (cold air requires much more humidification). For high-flow therapeutic RPT devices, power sources up to 300 watts of power may be required. may be necessary.

[0175] As mentioned above, the RPT device must be configured so that different power sources are connected to the RPT device at different times. configured to connect to multiple power sources through a single power interface when Thus, different power sources typically have a single power interface. The power supply can be connected to one of these power sources via a single power interface. (at different times) so that it can be connected to other power sources via the same port (i.e., the same port). Alternatively, more than one power source may be used in a single power interface. or can be connected in parallel simultaneously via dual interfaces. A logic controller may be used to determine which one to use. For example, a computing device (e.g., a tablet) may be connected to a USB cable. The RPT device can be connected to the high power computing device through a single interface. The computing device (e.g., The tablet may then be connected to a high-power power source (e.g., the mains). determines the possible actions to take given power available from a single interface. Similarly, connect the cable from the high-power supply to the first input of the dual interface (e.g. power and / or data) and at the same time can be connected to a low-power source. Connect another cable to the second input of the dual interface (e.g., power and / or device Thus, as mentioned above, it is possible to connect more than one power source (e.g. For example, both power sources can be connected to the power interface(s) at the same time. A power interface may be implemented as multiple power interfaces so that Next, the controller of the RPT device can provide a These possible operations may be determined based on at least one of the connected power sources. Some or all of the treatment modes of operation when one has a sufficiently high maximum power Examples of separate power interfaces on RPT devices include Wired interfaces for USB (e.g. USB Type-C) and wireless power interfaces for wireless power sources There is a face.

[0176] Glossary For purposes of this disclosure, in certain embodiments of the present technology, one or more of the following definitions may be used: In other aspects of the technology, other definitions may also apply.

[0177] general Air: In certain forms of the present technology, the air supplied to the patient may be atmospheric air, In other forms of the technology, the atmosphere may be supplemented with oxygen.

[0178] Continuous Positive Airway Pressure (CPAP): CPAP therapy provides a supply of air or breathable gas to Continuously at a positive pressure relative to atmosphere, preferably at a substantially constant pressure throughout the patient's respiratory cycle. This is taken to mean attaching the catheter to the entrance of the airway. The pressure at the airway entrance varies by a few centimetres of water during a single respiratory cycle. In some forms, the airway The pressure at the inlet of the pleura increases slightly during exhalation and decreases slightly during inhalation. In some embodiments, the pressure varies during different respiratory cycles of the patient (e.g., Increased in response to detection of signs of partial upper airway obstruction and absence of notice of partial upper airway obstruction (sometimes reduced).

[0179] RPT Device Aspects Air Circuit: A circuit that connects air or breathable gas between the RPT device and the patient interface. A conduit or tube constructed and arranged in use to deliver a supply of gas. The pneumatic circuit may be fluidly connected to the outlet of the pneumatic block and to the patient interface. The air circuit may be referred to as an air delivery tube. In some cases, In some cases, there may be separate legs of the circuit. In other cases, a single leg is used.

[0180] APAP: Automatic Positive Airway Pressure. Lower and upper limits depending on the presence or absence of signs of SDB onset. Continuously adjustable positive airway pressure between

[0181] Blower or flow generator: A device that delivers a flow of air at pressures above ambient pressure. vinegar.

[0182] Controller: A device or part of a device that regulates an output based on an input. For example, ,One form of controller is the control variables under ,control that constitute the input to the device (i.e. The output of the device is the current value of the controlled variable and the set point of this variable. is a function. A servo ventilator has ventilation as an input and target ventilation as a setpoint. , a controller having as an output the pressure assist level. Other forms of inputs include: It can be one or more of: oxygen saturation (SaO2), partial pressure of carbon dioxide (PCO2) Force, movement, photoplethysmography signals, and peak flow. Controller design A fixed point can be one or more of the following: a fixed point, a variable point, or a learned point. For example, , the set point in the ventilator may be the long-term average of the patient's measured ventilation. The device may have a ventilation set point that changes over time. The pressure controller controls the air pressure to a specific pressure. The controller may be configured to control a blower or pump to deliver the fluid at a The controller may include a microcontroller, a microprocessor, or a processor. It may be a microcontroller, a microprocessor or a processor.

[0183] Treatment: Treatment in this context can be one or more of the following: positive pressure therapy, high flow therapy , oxygen therapy, carbon dioxide therapy, dead space control, and drug administration.

[0184] Motor: A device that converts electrical power into rotary motion of a member. In this context, the rotating member is an impeller, which rotates around a fixed axis at a predetermined position and moves along the axis of rotation This applies an increase in pressure to the air passing through it.

[0185] Positive Airway Pressure (PAP) Device: A device that delivers a supply of air at positive pressure to the airways.

[0186] Transducer: a device that converts one form of energy or signal into another. A transducer is , a sensor or detector that converts mechanical energy (e.g., motion) into an electrical signal. Examples of transducers include pressure sensors, flow sensors, and carbon dioxide (CO 2 ) sensor, oxygen (O 2 ) sensors, exertion sensors, motion sensors, noise sensors, plethysmographs and cameras There is a la.

[0187] Volute: The casing of a centrifugal pump through which the air is being pumped by the impeller. The cross section of the volute is the diameter of the outlet port. increases as it approaches

[0188] Aspects of the Breathing Cycle Apnea: An apnea is a period of flow below a given threshold, for example for a duration of 10 seconds. Obstructive apnea is said to have occurred when the breathing continues for a period of time that is not controlled by the patient's efforts. However, it is said to occur when some airway obstruction does not allow air to flow. Central apnea is when apnea is detected due to reduced or absent respiratory effort. It is said to refer to a state in which

[0189] Respiratory Rate: The patient's spontaneous breathing rate, usually measured in breaths per minute.

[0190] Duty Cycle: The ratio of inspiration time Ti to total breathing time Ttot.

[0191] Effort (breathing): Preferably, the effort of breathing is achieved by the spontaneous breathing of a person trying to breathe. It is said to refer to the movement that is carried out.

[0192] Expiratory portion of the respiratory cycle: the period from the start of the expiratory flow to the start of the inspiratory flow.

[0193] Flow restriction: Preferably, flow restriction occurs when an increase in effort by the patient leads to a corresponding increase in flow. This is interpreted as the situation in which a patient does not wake up during the inspiratory portion of the respiratory cycle. When flow limitation occurs due to breathing difficulties, the flow limitation can be referred to as inspiratory flow limitation. When flow limitation occurs in the expiratory portion of the cycle, the flow limitation is called expiratory flow limitation. It is possible.

[0194] Flow-limited inspiration waveform types: (i) Flattening: An upswing followed by a relatively flat area and then a downswing. (ii) M-shape: two local regions, one on the rising edge and one on the falling edge The spectrum has two peaks, with a relatively flat region between these two peaks. (iii) Chair-shaped: A single local peak occurs at the rising part. This is followed by a relatively flat section. (iv) Inverted chair: A relatively flat area followed by a single local peak. It occurs on the falling edge.

[0195] Hypopnea: Preferably, hypopnea refers to a reduction in flow, not an interruption in flow. In this condition, hypopnea is defined as a state in which a reduction in flow rate below the threshold continues for a sustained period of time. Respiratory dysfunction is said to have occurred in adults if any of the following occurs: Could be considered a decline: (i) A 30% decrease in patient respiration for at least 10 seconds plus an associated 4% desaturation, or (ii) A reduction in patient respiration (less than 50%) lasting for at least 10 seconds and associated desaturation is at least 3% or awakening occurs.

[0196] Inhalation portion of the breathing cycle: preferably the period from the start of the inhalation flow to the start of the exhalation flow is , taken as the inhalation portion of the respiratory cycle.

[0197] Patency (airway): The degree to which the airway is open or the extent to which the airway is open. Airway patency and The quantification of airway patency can be done, for example, by dividing the airway patency value (1) into patency and closure value (2). This can be done together with (0).

[0198] Positive end-expiratory pressure (PEEP): The pressure above atmosphere in the lungs that exists at the end of expiration.

[0199] Peak flow (Qpeak): The maximum value of flow during the inspiratory portion of the respiratory flow waveform.

[0200] Respiratory airflow, airflow, patient airflow, respiratory airflow (Qr): these synonyms are , may be understood to refer to an estimate of the respiratory airflow of an RPT device, typically liters / minute This is contrasted with the "true respiratory flow" or "true respiratory airflow," which is the actual respiratory flow of the patient, expressed as It is used for reference.

[0201] Tidal volume (Vt): The amount of air inhaled or exhaled during normal breathing without extra effort is the amount of air that is sucked in.

[0202] (Inspiration) Time (Ti): The duration of the inspiratory portion of the respiratory flow waveform.

[0203] (Expiratory) Time (Te): The duration of the expiratory portion of the respiratory flow waveform.

[0204] (Total) Time (Ttot): The time between the start of one inspiratory portion of the respiratory flow waveform and the next The total duration between the start of the inhalation portion of the

[0205] Typical recent ventilation: ventilation values ​​that tend to cluster together over a given time scale (i.e., the degree of central tendency of the most recent ventilation values).

[0206] Upper Airway Obstruction (UAO): Includes both partial and total upper airway obstruction. As the pressure difference in the upper airway increases (Starling resistor behavior), the flow rate increases slightly. The present invention may be associated with a condition of flow limitation that may increase or decrease.

[0207] Vent: The gas exchange carried out by a patient's respiratory system (the amount of air taken in per unit of time) When expressed as volume per minute, this is a measure of the total volume of air that is expelled (including both inhalation and exhalation flow). The amount of ventilation is often referred to as "minute ventilation". Minute ventilation is also sometimes given simply as volume. and is understood as volume per minute.

[0208] RPT Device Parameters Flow Rate: The instantaneous volume (or mass) of air delivered per unit time. Flow Rate and Ventilation Rate have the same order of magnitude of volume or mass per unit time, but the flow rate is much shorter. The flow rate may be nominally positive for the inspiratory portion of the patient's breathing cycle. Therefore, it may be negative for the expiratory portion of the patient's breathing cycle. When referring to a quantity, it refers to a scalar quantity (i.e., a quantity that has only a magnitude). In the above, when referring to flow rate, we refer to vector quantities (i.e., quantities that have both magnitude and direction). The total flow rate, Qt, is the amount of air exiting the RPT device. The vent flow rate Qv is the amount of air that must be removed from the vent to allow the exhaled gas to escape. The leakage flow rate, Ql, is the flow rate of unintentional air leaking from the patient interface system. The respiratory flow Qr is the flow rate of air received into the patient's respiratory system. be.

[0209] Leakage: Preferably, the term "leakage" is taken as air flow to the surroundings. CO 2 A leak may be intentionally provided to allow for the washout of For example, there may be unintentional causes, such as an incomplete seal between the mask and the patient's face. It is possible.

[0210] Pressure: force per unit area. Pressure can be measured in a variety of units (e.g., cmH 2 O , gf / cm 2 , and hectopascals). 1cmH 2 O is 1g-f / cm 2 Equal to , approximately 0.98 hectopascals. In this specification, unless otherwise specified, pressure is cmH 2 In the case of nasal CPAP treatment for OSA, the therapeutic pressure is referred to. When this is done, it is about 4 to 20 cmH. 2 O or approx. 4-30cmH 2 This refers to pressures in the range of 100. The pressure in the interface is given the symbol Pm.

[0211] Sound power: The energy carried by a sound wave per unit time. Sound power is the Sound power is proportional to the square of the pressure multiplied by the wavefront area. Sound power is usually expressed in decibels (SWL). That is, 10 -12 It is expressed in decibels relative to a reference power taken as watts.

[0212] Sound pressure: local pressure difference from the ambient pressure at a given time that results from the passage of a sound wave through a medium Sound power is usually measured in decibels SPL (i.e., taken as the threshold of human hearing). Usually it is 20×10 -6 Relative to a reference power taken as pascals (Pa) It is expressed in decibels.

[0213] Ventilator Terminology Adaptive servo-ventilator: A ventilator that does not have a fixed target ventilation but can be changed. The variable target ventilation may be learned from some characteristics of the patient (e.g., the patient's breathing characteristics). .

[0214] Backup Rate: The ventilator parameter that determines how much the ventilator will Establish the minimum respiratory rate (typically the number of breaths per minute) that can be delivered to the patient from the ventilator. Can.

[0215] Cycle: The end of the inspiratory phase of the ventilator. When delivering a breath from a ventilator, at the end of the inspiratory portion of the breathing cycle, the ventilator: It is said to be cycled to stop breath delivery.

[0216] EPAP (or EEP): The desired mask pressure that the ventilator attempts to achieve at a given time. A base pressure to which varying pressures are added within a breath to generate pressure.

[0217] IPAP: The desired mask pressure that the ventilator attempts to achieve during the inspiratory portion of the breath.

[0218] Pressure Support: A number indicating the increase in pressure during ventilator inhalation compared to the ventilator exhalation and mainly refers to the pressure difference between the maximum value during inspiration and the minimum value during expiration (e.g., P S=IPAP-EPAP). In some contexts, pressure support means This refers to the difference that the ventilator attempts to achieve (rather than the difference it actually achieves).

[0219] Servo ventilator: A ventilator that has both patient ventilation and target ventilation, and Adjust the level of pressure support to approach target ventilation.

[0220] Spontaneous / Timed (S / T): Attempts to detect the onset of breathing in spontaneously breathing patients , a mode of a ventilator or other device, but the device does not detect a breath for a period of time. If not, the device will automatically begin breath delivery.

[0221] Swing: A term equivalent to pressure assistance.

[0222] Trigger: When a ventilator delivers a breath of air to a spontaneously breathing patient, the patient begins to breathe. When the breath portion of the cycle begins, the ventilator is triggered to deliver a breath. He says.

[0223] Ventilator: A mechanical device that provides pressure support to a patient while performing some or all of the work of breathing. Vice.

[0224] Ventilator inhalation and ventilator exhalation: The ventilation that is appropriate for the patient's inhalation and exhalation, respectively. The period during which the ventilator considers it necessary to deliver pressure from the inspiratory system. Depending on the quality and upper airway obstruction, these may correspond to actual patient inspiration or expiration. However, it does not have to be compatible.

[0225] Respiratory System Anatomy diaphragm sheet of muscle that runs over the lower rib cage. It protects the heart, lungs, and ribs It separates the thoracic cavity, which contains the lungs, from the abdominal cavity. When the diaphragm contracts, the volume of the thoracic cavity increases, allowing air to enter the lungs. It draws you in.

[0226] Larynx: The larynx or voice box that contains the vocal folds and connects the lower part of the pharynx (hypopharynx) to the trachea. Continue.

[0227] Lung: respiratory organ in humans. The conductive zones of the lungs are the trachea, bronchi, bronchioles, and terminalis. The respiratory region includes the respiratory bronchioles, the alveolar ducts and the alveoli.

[0228] Nasal Cavity: The nasal cavity (or nasal fossa) is a large, air-filled cavity in the center of the face above and behind the nose. The nasal cavity is divided into two by a vertical fin called the nasal septum. On the sides there are three horizontal extensions called nasal conchae or nasal turbinates. Posteriorly it connects to the nasopharynx via the choanal cavity.

[0229] pharynx throat located directly below (inferior to) the nasal cavity and above the esophagus and larynx The pharynx is traditionally divided into three parts: the nasopharynx (the upper part of the pharynx) part), the oropharynx (mid-pharynx) (oral part of the pharynx), and the pharynx (hypopharynx).

[0230] Other notes A portion of the disclosure of this patent document contains material which is subject to copyright protection. The copyright owners reserve the right to make, distribute, and use of the material in any form whatsoever. The reproduction by facsimile of this patent document or this patent disclosure by any person shall not be deemed to be a copy of the patent or disclosure of this patent document or disclosure of this patent document by facsimile. If it is stated in the patent file or records, there is no objection if it is for a purpose. All other purposes copyright reserved.

[0231] Unless otherwise clearly indicated by the context and unless a range of values ​​is provided, the lower limit 1 / 10 of a unit, between the upper and lower limits of the range, and any other stated value in the stated range. It is understood that each intervening value for any one or more of the above ranges is encompassed by the present technology. The upper and lower limits of these intervening ranges specifically exceed the limits of the stated range. If the range described includes one or both of these limits, In this case, ranges exceeding either or both of these stated limits are also encompassed by the present technology.

[0232] Furthermore, when a value or values ​​are embodied herein as part of the technology, other Unless otherwise specified, such values ​​may be approximated and may vary as practical technical practice permits or requires. It is understood that such values ​​may be used to any appropriate degree of significance.

[0233] Unless otherwise stated, all technical and scientific terms used herein belong to the art. The term has the same meaning as commonly understood by those skilled in the art. and any methods and materials similar or equivalent to the materials used in the practice or testing of this technology. Although a limited number of exemplary methods and materials can be used in the present invention, It will be published.

[0234] Certain materials are described as being suitable for use in the construction of the components, but the properties Similar and obvious alternative materials may be used as substitutes. Insofar as any and all components described herein are manufacturable, they should be understood as such. Therefore, they can be manufactured collectively or separately.

[0235] As used herein and in the appended claims, the singular form "a" "an" and "the" are used interchangeably unless the context clearly indicates otherwise. Please note that the present invention includes multiple equivalents of:

[0236] All publications mentioned herein are incorporated by reference in their entirety for all purposes, including, but not limited to, the methods and / or methods that are the subject of these publications. or incorporated by reference for disclosure and description of the materials. The references herein are provided solely for their disclosure prior to the filing date of the present application. None of the content is intended to be construed as a declaration that the present technology did not antedate such publication by virtue of prior patents. Further, the dates of publication provided should not be construed as representing the actual publication dates. Dates may vary from those shown and should be independently verified.

[0237] Moreover, in interpreting this disclosure, all terms shall be interpreted broadly and reasonably in accordance with the context. For details, see the words "comprises" and "comprising" and The term "component" shall be interpreted in a non-exclusive sense as referring to any element, component, or step. other elements, components or steps not specifically described, Indicates that it may be present, utilized, or combined with a component or step.

[0238] Headings used in the detailed description are for the convenience of the reader and are intended to guide the reader through the present disclosure or should not be used to limit what may appear in the claims as a whole. These headings should not be used to interpret the scope of a claim or a claim limitation. should not be used in any manner whatsoever.

[0239] Although the technology herein has been described with reference to specific embodiments, these embodiments It should be understood that the above embodiments are merely illustrative of the principles and applications of the present technology. In some cases, the terms and symbols may indicate specific details that are not necessary for the practice of the present technology. For example, "first" and "second" (etc.) Although terms are used, unless otherwise specified, these terms are not intended to denote any order. The terms "process step" and "process sequence" are used to distinguish between separate elements. Although the steps may be described or illustrated in a sequential order, such order is not essential. Those skilled in the art will recognize that such sequences can be changed and / or that aspects can be implemented in the same manner. It will be appreciated that this can be done simultaneously or even synchronously.

[0240] Thus, without departing from the spirit and scope of the present technology, in an exemplary embodiment: It should be understood that numerous variations are possible and other arrangements may be devised. It is.

Claims

1. 1. A respiratory treatment device for providing treatment for a respiratory disorder, comprising: A power input circuit for receiving one or more of a first power and a second power, The first power source is derived from a low power source adapted to connect to a respiratory treatment device, and the second power source is adapted to connect to a respiratory treatment device. The power for the power input is derived from a high power power source adapted to connect to the respiratory treatment device. The circuit, a power supply connected to the power input circuit and configured to detect at least one of a low power supply and a high power supply; a controller configured to control a low power supply and a high power supply; and determining a first operating mode of the respiratory treatment device based on the detection of one of the power sources. and selectively activating a second mode of operation of the first mode of operation being a non-therapeutic mode. a first mode of operation and a second mode of operation is a therapy mode; and Respiratory treatment equipment.

2. The power input circuit includes a first supply interface and a second supply interface. and at least one of the first supply interface and the second supply interface. The respiratory treatment device of claim 1 , further comprising a wireless power interface.

3. The power input circuit is a single power supply configured to connect to a low power source and a high power source.

10. The respiratory treatment device of claim 1, including a supply interface.

4. the single supply interface includes a connector for a detachable power cable; 4. The respiratory treatment device of claim 3.

5. The single supply interface provides data communication through a removable power cable. The respiratory treatment device of claim 4 further configured for:

6. 6. The method of claim 5, wherein the connector is a Universal Serial Bus (USB) connector. Respiratory treatment equipment.

7. The first mode of operation includes transmitting data communications to a processor of a respiratory treatment device; A respiratory treatment according to any one of claims 1 to 6, comprising a communication mode for transmitting and / or receiving Device.

8. The communication mode may be configured to transfer one or more operational control settings into the memory of the respiratory treatment device.

8. The respiratory treatment device of claim 7, comprising a constant operation.

9. The communication mode may include operational control settings, diagnostic data, usage data, and / or operational A download operation is included to retrieve one or more of the data from the memory of the respiratory treatment device.

9. A respiratory treatment device as claimed in claim 7 or 8.

10. The therapy mode is for generating a gas flow to a respiratory interface for a user. The respiratory treatment method according to any one of claims 1 to 9, further comprising: Device.

11. 2. The method of claim 1, wherein the input power circuit includes a detection circuit, the detection circuit including a voltage detector. A respiratory treatment device as described in any one of claims 1 to 10.

12. The voltage detector is adapted to detect a voltage indicative of power received by the power input circuit.

12. The respiratory treatment device of claim 11, configured as follows:

13. The controller receives a signal indicative of one of a low power supply and a high power supply.

12. The respiratory treatment device of claim 11, wherein the respiratory treatment device is connected to a detection circuit so as to receive a signal from the detection circuit.

14. The controller is configured to sample a voltage signal generated by a voltage detector.

12. The respiratory treatment device of claim 11, wherein the sensing circuit is connected to the

15. The controller is adapted to compare the detected voltage with a predetermined threshold and to perform a first operation. and a second operating mode based on the comparison. The detected voltage is determined based on the power from either a low power supply or a high power supply.

15. A respiratory treatment device according to any one of claims 1 to 14.

16. Activating the second mode of operation by the controller reduces the gas flow for the user. to the respiratory interface. a switching circuit configured to switch the input / output signals of the input / output terminals of the first and second input / output terminals of the second and second ... second and second input / output terminals of the second and second input / output terminals of the second and second input / output terminal 16. A respiratory treatment device according to any one of claims 1 to 15.

17. 17. The respiratory treatment device of claim 16, wherein the switching circuitry includes a solid-state switch.

18. The input power circuit includes a controller in a first operating mode and a second operating mode. A respiratory treatment apparatus according to any one of claims 1 to 15, comprising a voltage regulator for powering 。

19. The blower further includes a motor, the motor being configured to be controlled by a controller to regulate the speed of the motor. a motor control circuit connected to the motor controller, the motor being configured to It is further connected to the power line of the input power circuit through a switch activated by the controller. A respiratory treatment device according to any one of claims 1 to 18.

20. The controller includes a processor and a memory, the processor executing a first operating mode. and programmed to control operation of the respiratory treatment device in a first mode and a second mode of operation.

20. A respiratory treatment device according to any one of claims 1 to 19.

21. The low power supply produces power in the range of about 5 watts to 20 watts, and the high power supply produces 21. Any one of claims 1 to 20, generating a power in the range of about 20 watts to 110 watts.

2. A respiratory treatment device as described in claim 1.

22. 20. The method according to claim 1, wherein the low power source comprises a Universal Serial Bus (USB) power source.

2. A respiratory treatment device as described in any one of claims 1 to 11.

23. Respiratory therapy according to any one of claims 1 to 20, wherein the low power power source comprises a Qi power source. Device.

24. 1. A respiratory treatment system for treating a respiratory disorder, the respiratory treatment system comprising: a first set of components including a memory; A pressure generating device configured to provide an air flow delivered to a patient and / or a heater. a second set of components including a vessel; A power interface; Determining available power available from a power interface; selectively (a) operate in a non-therapeutic mode based on the determined available power; The first set of components is configured to receive power; or (b) to operate in a treatment mode. Both the first and second sets of components receive power such that and enabling the device to: If the determined available power is above a threshold, the controller to enable both the first and second set of components to receive electrical power. ,A respiratory treatment system comprising:

25. 25. The respiratory system of claim 24, wherein the first set of components further includes a display. Treatment system.

26. Any of claims 24 to 25, wherein the first set of components further comprises a communication circuit.

13. A respiratory treatment system as described in claim 1.

27. The power interface is configured to receive a cable.

7. A respiratory treatment system as described in any one of claims 6.

28. 28. The respiratory treatment system of claim 27, wherein the cable is connectable to a USB port. Hmm.

29. The power interface only provides an external power interface for the respiratory treatment system. According to any one of claims 26 to 28, a single power interface is provided. Respiratory treatment systems.

30. Breathing with Universal Serial Bus cable and Universal Serial Bus power supply 1. A method for a respiratory treatment device comprising powering an operating mode of the treatment device. The operational mode includes accessing and / or downloading data from a respiratory treatment device. The method includes:

31. 31. The method of claim 30, wherein the Universal Serial Bus power source is a low power power source.

32. 32. The method according to claim 30, wherein the mode of operation is a non-therapeutic mode of operation. A method for a respiratory treatment device.

33. Powered by Universal Serial Bus cable and Universal Serial Bus power supply A respiratory treatment device configured to be powered in a respiratory treatment mode, the operating mode being accessing and / or downloading data from the memory of the medical device; Includes, a method.

34. The Universal Serial Bus power supply is a low power power supply and the respiratory treatment device is Universal Serial Bus power supply and connection to the Universal Serial Bus cable 34. The respiratory treatment device of claim 33, comprising an external interface for

35. 35. The method according to claim 33, wherein the mode of operation is a non-therapeutic mode of operation. Respiratory treatment equipment.

36. A respiratory treatment method comprising: powering an operating mode of a respiratory treatment device using a wireless power transmission device.

11. A method for a respiratory treatment device, the operating mode comprising: accessing data from a respiratory treatment device; The method includes:

37. A respiratory treatment device configured to be powered in an operational mode by a wireless power transmission device. wherein the mode of operation includes accessing a memory of a respiratory treatment device.

Citation Information

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