WO2012068568A2 - Self-contained patient monitor - Google Patents
Self-contained patient monitor Download PDFInfo
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- WO2012068568A2 WO2012068568A2 PCT/US2011/061558 US2011061558W WO2012068568A2 WO 2012068568 A2 WO2012068568 A2 WO 2012068568A2 US 2011061558 W US2011061558 W US 2011061558W WO 2012068568 A2 WO2012068568 A2 WO 2012068568A2
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- WIPO (PCT)
- Prior art keywords
- pwh
- patient
- monitor
- self
- portable
- Prior art date
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Classifications
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- G—PHYSICS
- G08—SIGNALLING
- G08B—SIGNALLING OR CALLING SYSTEMS; ORDER TELEGRAPHS; ALARM SYSTEMS
- G08B25/00—Alarm systems in which the location of the alarm condition is signalled to a central station, e.g. fire or police telegraphic systems
- G08B25/005—Alarm destination chosen according to a hierarchy of available destinations, e.g. if hospital does not answer send to police station
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- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/0002—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
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- A61B5/0002—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network
- A61B5/0015—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network characterised by features of the telemetry system
- A61B5/002—Monitoring the patient using a local or closed circuit, e.g. in a room or building
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- A—HUMAN NECESSITIES
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- A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
- A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
- A61B5/6813—Specially adapted to be attached to a specific body part
- A61B5/6824—Arm or wrist
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- A—HUMAN NECESSITIES
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- A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
- A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
- A61B5/683—Means for maintaining contact with the body
- A61B5/6831—Straps, bands or harnesses
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- A—HUMAN NECESSITIES
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- A61B5/74—Details of notification to user or communication with user or patient ; user input means
- A61B5/746—Alarms related to a physiological condition, e.g. details of setting alarm thresholds or avoiding false alarms
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
- G16H40/67—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
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- H01R13/46—Bases; Cases
- H01R13/516—Means for holding or embracing insulating body, e.g. casing, hoods
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R31/00—Coupling parts supported only by co-operation with counterpart
- H01R31/06—Intermediate parts for linking two coupling parts, e.g. adapter
- H01R31/065—Intermediate parts for linking two coupling parts, e.g. adapter with built-in electric apparatus
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- A—HUMAN NECESSITIES
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- A61B2560/04—Constructional details of apparatus
- A61B2560/0431—Portable apparatus, e.g. comprising a handle or case
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- A—HUMAN NECESSITIES
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- A61B2560/04—Constructional details of apparatus
- A61B2560/0456—Apparatus provided with a docking unit
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- A—HUMAN NECESSITIES
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- A61B5/02—Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
- A61B5/0205—Simultaneously evaluating both cardiovascular conditions and different types of body conditions, e.g. heart and respiratory condition
Definitions
- the present specification relates generally to patient monitoring systems.
- the present specification relates to a portable, wearable patient monitor for monitoring patient parameters.
- the present specification relates to a self-contained patient monitor designed to remain with the patient for the duration of care that can communicate with both a bedside patient monitor and a patient monitoring network, either wired or wirelessly, and thus, continuously monitor the patient without interruption.
- a patient monitoring system is an electronic medical device that measures a patient's various vital signs, collects and processes all measurements as data, and then displays the data graphically and/or numerically on a viewing screen. Graphical data is displayed continuously as data channels on a time axis (waveforms).
- Patient monitoring systems are positioned near hospital beds, typically in critical care units, where they continually monitor patient status via measuring devices attached to the patient and can be viewed by hospital personnel. The systems are typically on a shelf, attached to the bed, or attached to a wall. Some patient monitoring systems can only be viewed on a local display, whereas others can be joined to a network and thereby display data at other locations, such as central monitoring or nurses' stations.
- Portable patient monitoring systems are available for use by emergency medical services (EMS) personnel. These systems typically include a defibrillator along with the monitor. Other portable units, such as Holier monitors, are worn by patients for a particular time period and then returned to the physician for evaluation of the measured and collected data.
- Current patient monitoring systems are able to measure and display a variety of vital signs, including, pulse oximetry (Sp0 2 ), electrocardiograph (ECG), invasive blood pressure (IBP), non-invasive blood pressure (NIBP), electroencephalograph (EEG), body temperature, cardiac output, capnography (C0 2 ), and respiration.
- ECG pulse oximetry
- IBP invasive blood pressure
- NIBP non-invasive blood pressure
- EEG electroencephalograph
- body temperature C0 2
- C0 2 capnography
- respiration respiration.
- Patient monitoring systems are capable of measuring and displaying maximum, minimum, and average values and frequencies, such as pulse and respiratory rates.
- Data collected can be transmitted through fixed wire connections or wireless data communication.
- Power to patient monitoring systems can be supplied through a main power line or by batteries. While current patient monitoring systems are effective in monitoring patient conditions and notifying medical personnel of changes, they are not without certain drawbacks and limitations.
- Such a device will also require a uniform system for connecting parameter sensing devices.
- Mechanical enclosures meant for electrical medical devices need to be robust and meet regulatory requirements.
- Typical electrical medical devices include printed circuit boards (PCBs), connectors, cables and gaskets, which are all rigidly mounted inside the enclosure by means of mechanical components. Normally this may require three to four individual components to achieve. Multiple components call for a specific and careful assembly procedure, more inventories, and more maintenance and risk.
- devices used in medical applications have restrictions in material and process of manufacture and assembly. Hence, considering the complexities involved, manufacturers prefer conventional design and assembly methods.
- electrical medical devices must be able to function reliably in hospital environments where the risk of water damage is high. Therefore, what is needed is a uniform adapter device which includes a mechanical enclosure that accepts a multitude of original equipment manufacturer (OEM) components that is simple to assemble and, in addition, prevents liquid ingress.
- OEM original equipment manufacturer
- the present specification is directed toward a portable, self-contained device used to monitor patient parameters, comprising an internal battery, at least one connection for a parameter measuring instrument, and at least one connection assembly for connection of a third party measuring instrument, said connection assembly comprising printed circuit boards, a plug, and an enclosure, wherein said device: provides continuous, uninterrupted monitoring of at least one patient parameter; is capable of communicating with a bedside monitor and a patient monitoring network; is worn by and remains with an assigned patient for the duration of care; and, is designed in a compact and lightweight manner to enhance portability.
- the portable, self-contained device used to monitor patient parameters further comprises a connector for docking of said device within a docking station, wherein said docking station provides operating and battery charging power to said device, and wherein said docking station receives power from an external power supply.
- the patient parameters capable of being measured by the device include, but are not limited to, electrocardiograph (ECG)/respiration, pulse oximetry (Sp0 2 ), temperature, invasive blood pressure (IBP), non-invasive blood pressure (NIBP), cardiac output, capnography, mixed venous oxygen saturation (Sv0 2 ) and central venous oxygen saturation (Svc0 2 ), multi-gas analysis, bispectral index (BISx), neuromuscular transmission (NMT), transcutaneous oxygen (Tcp0 2 ) & transcutaneous carbon dioxide (TcpC0 2 ), spirometry, blood glucose, pulmonary mechanics, electroencephalograph (EEG) and resultant entropy characteristics, auditory evoked potential (AEP), hemodialysis, hemo filtration, and 16-lead ECG.
- ECG electrocardiograph
- Sp0 2 pulse oximetry
- IBP invasive blood pressure
- NIBP non-invasive blood pressure
- cardiac output capnography
- mixed venous oxygen saturation Sv
- the portable, self-contained device used to monitor patient parameters further comprises an integrated touchscreen display. In one embodiment, the portable, self-contained device used to monitor patient parameters further comprises alarm annunciation capabilities.
- the portable, self-contained device used to monitor patient parameters further comprises an integrated NIBP measuring instrument.
- the portable, self-contained device used to monitor patient parameters further comprises internal memory capable of storing measured patient parameter data.
- the internal memory is capable of storing up to 24 hours of continuous patient data and up to 96 hours of trend data.
- the portable, self-contained device used to monitor patient parameters further comprises an internal real-time clock (RTC).
- RTC real-time clock
- the portable, self-contained device used to monitor patient parameters communicates through a wired connection with the bedside monitor via detachable cables.
- the device comprises an internal wireless network card and is capable of communicating wirelessly with the bedside monitor, a parameter transceiver, and a hospital network.
- measured data is transmitted from the device to the bedside monitor and then presented in numerical and graphical form on an external display.
- the parameter measuring instrument is connected to the device via a Dual Serial Bus (DSB) connection.
- DSP Dual Serial Bus
- the portable, self-contained device used to monitor patient parameters further comprises a securing band or similar structure for securing the device to the patient during transport and ambulation.
- the portable, self-contained device used to monitor patient parameters comprises an internal battery, an integrated NIBP measuring instrument, an integrated Sp0 2 measuring instrument, an integrated ECG/respiration instrument, at least one connection for a parameter measuring instrument, and at least one connection assembly for connection of a third party measuring instrument, said connection assembly comprising printed circuit boards, a plug, and an enclosure.
- the device comprises the same components as the device described directly above, plus, an integrated touchscreen display, alarm annunciation, and limited data storage capability.
- connection assembly used to translate electronic information from a first protocol to a second protocol, comprising: a plug at a first end of said assembly for connecting a first device cable from a first device, said first device operating on said first protocol; at least one first connector at a second end of said assembly opposite said first end of said assembly, for connecting at least one printed circuit board; at least one second connector at said second end of said assembly opposite said first end of said assembly, for connecting at least one second device cable from a second device, said second device operating on said second protocol; at least one printed circuit board capable of translating said electronic information from said first protocol to said second protocol, said printed circuit board connected to said at least one first connector at said second end of said assembly; and, at least one movable elongate member attached to said plug along an exterior edge of said plug, said at least one movable elongate member movable from a first position to a second position wherein said movable elongate member forms an enclosure at least partially encompassing said at least one printed circuit board and said
- the plug includes a gasket around the outer edge of said plug to prevent liquid ingress into the assembly.
- the present specification is also directed toward a system for providing continuous patient monitoring, comprising: a portable, self-contained device used to monitor patient parameters, comprising an internal battery, at least one connection for a parameter measuring instrument, and at least one connection assembly for connection of a third party measuring instrument, said connection assembly comprising printed circuit boards, a plug, and an enclosure, wherein; said device provides continuous, uninterrupted monitoring of at least one patient parameter; said device is capable of communicating with a bedside monitor and a patient monitoring network; said device is worn by and remains with an assigned patient for the duration of care; and, said device is designed in a compact and lightweight manner to enhance portability; at least one patient parameter measuring instrument connected to the device; a bedside monitor in communication with the device; at least one external display connected to the bedside monitor; and, a hospital network in communication with the bedside monitor.
- portable, self-contained device included in the system described above comprises an integrated wireless network card, wherein the device is capable of direct communication with the hospital network.
- FIG. 1 is an oblique front view illustration of one embodiment of the Patient Worn Hub (PWH) of the present invention
- FIG. 2 is an oblique front view illustration of another embodiment of the Patient Worn Hub (PWH) including an optional securing band;
- PWH Patient Worn Hub
- FIG. 3 A is an oblique front view illustration of one embodiment of the Patient Worn Hub docking unit of the present invention
- FIG. 3B is an oblique front view illustration of one embodiment of the Patient Worn Hub docking unit depicting the PWH placed into the docking unit;
- FIG. 4 is an illustration of a multitude of possible embodiments of the Patient Worn Hub connected to a hospital network
- FIG. 5A is an oblique front view illustration of one embodiment of the hinge connector assembly in the open position prior to assembly;
- FIG. 5B is a side view illustration of one embodiment of the hinge connector assembly in the open position prior to assembly
- FIG. 6 is an oblique front view illustration of one embodiment of the hinge connector assembly in the open position with a DSB device cable in place;
- FIG. 7A is an oblique front view illustration of one embodiment of the hinge connector assembly fully assembled with a DSB device cable attached;
- FIG. 7B is a side view illustration of one embodiment of the hinge connector assembly fully assembled with a DSB device cable attached;
- FIG. 8 is a block diagram illustrating the components included in one embodiment of the Patient Worn Hub;
- FIG. 9 is a block diagram illustrating one embodiment of the design of the electrical architecture of the PWH;
- FIG. 10 is a block diagram illustrating one embodiment of an exemplary processor included in the electrical architecture of the PWH;
- FIG. 11 is a block diagram illustrating one embodiment of an upstream USB port of the
- FIG. 12 is a block diagram illustrating one embodiment of the power section of the PWH.
- the present specification is directed toward a Patient Worn Hub (PWH) device for monitoring patient parameters.
- the PWH is a self-contained patient monitoring device designed to remain with the patient for the duration of care.
- the PWH is assigned to each patient and will remain with that patient across multiple departments throughout the care process, thus eliminating the need for re-cabling patients.
- the PWH is designed in a compact and lightweight manner making it easily portable.
- the PWH is able to communicate with the bedside monitor of the patient monitoring system and provides continuous, uninterrupted patient monitoring.
- the PWH is capable of communicating with the monitor of the patient monitoring system described in copending United States Patent Application Number 13/300,462, entitled “Configurable Patient Monitoring System", filed on November 18, 2011 and assigned to the Applicant of the present invention, which is hereby incorporated by reference.
- the PWH communicates with the monitor via wired cables.
- the PWH communicates with the monitor wirelessly, allowing the patient to be transferred to a different location while the monitor remains in the patient room.
- the PWH connects to the monitor and the parameter measuring devices of a patient monitoring system via Dual Serial Bus (DSB) connectors and cables.
- the DSB interface comprises a first serial protocol and a second serial protocol, wherein the first protocol is a USB, Firewire, or Ethernet protocol and the second serial protocol is a Low Power Serial (LPS) protocol.
- LPS Low Power Serial
- each component of the patient monitoring system is a DSB Host, DSB Device, or, both a DSB Host and DSB Device.
- a DSB Host is in communication with and can supply operating and battery charging power to a connected DSB Device and also contains a switched Auxiliary Voltage Supply (AVS) which can provide up to 15 W of power to attached DSB Devices for battery charging or other high power needs.
- ADSB interface is presented in greater detail in co-pending United States Patent Application number 13/300,478, entitled “Dual Serial Bus Interface", filed on November 18, 2011 and assigned to the Applicant of the present invention, which is hereby incorporated by reference.
- PWH Patient Worn Hub
- PT refers to a Parameter Transceiver, which is a wireless transceiver that will send patient parameter data to a central system for processing. In one embodiment, the PT has two DSB Host interfaces.
- DSB is a Dual Serial Bus, an interface of the present invention that supports communication and power transfer via both USB and LPS protocols.
- the DSB interface includes at least six conductors which physically connect a DSB Host to a DSB Device.
- the six conductors comprise: a virtual bus (VBUS) conductor for power transfer, two data transmission conductors, a ground conductor, an auxiliary voltage supply (AVS) conductor to provide greater power for battery charging and higher power needs, and a spare conductor reserved for future use.
- VBUS virtual bus
- AVS auxiliary voltage supply
- LPS Low Power Serial
- DSB Host refers to a system device that controls the DSB interface, which can be a Patient Worn Hub (PWH) or Smart Display (SD), or a Parameter Transceiver (PT).
- DSB Device refers to a system device that is controlled by a DSB Host through a DSB interface, such as a FED or PWH.
- FED refers to a front end device, which is a device for collecting patient parameter data.
- SD refers to a Smart Display and is a patient monitor with an integrated display that acts as a DSB Host and runs the algorithms needed for patient parameter processing.
- An SD can extend the functionality of a Patient Worn Hub (PWH) and provides a larger local display.
- PWH Patient Worn Hub
- HD refers to a Headless Display and is equivalent to a Smart Display (SD) except that it uses an external display rather than having an integrated display.
- the PWH does not include a display and transmits its data to the monitor which in turn presents said data on the full-screen external display.
- the PWH is connected to a Smart Display (SD) which provides a larger screen size and additional front end device (FED) ports.
- the PWH is connected to the SD via a cable.
- the PWH communicates wirelessly with the SD.
- the PWH docks to the SD using a docking port.
- the SD is a transport type smart display.
- the SD is a portable type smart display.
- the SD is a fixed type smart display, such as a bedside monitor.
- the connection to the SD allows the PWH to connect to a hospital network at large so the PWH can publish and archive patient data as well as interact with other devices on the network in real time. Most maintenance (such as software updating) and configuration operations are initiated through the SD user interface using this connection.
- the PWH itself contains an internal 802.11 wireless network card so that it can connect to a hospital network.
- the PWH includes an integrated display.
- the integrated display is a color touchscreen display.
- the PWH contains an internal NIBP measurement device.
- up to five external Front End Devices (FEDs) can be connected to the PWH, allowing the PWH to act both as a system host and as a system device.
- caregivers can decrease or increase the number of parameters being monitored as a patient's acuity changes. This is accomplished simply by removing or plugging in more FEDs, creating a "plug and play" environment.
- the PWH contains its own internal battery for up to 6 hours run-time and is designed to function as a standalone monitoring device.
- the PWH can be connected to a monitor or external display to expand its monitoring and display capabilities.
- the PWH weighs less than 1.2 lbs, in accordance with the current weight standard for handheld devices. The dimensions of the PWH are maintained to ensure easy portability. In one embodiment, the PWH measures less than 5 inches wide by 3.5 inches high by 1.5 inches deep. The PWH is designed to fit comfortably in the hand representative of the largest stature user class and the smallest stature user class, and, in one embodiment, includes a securing band that wraps around the wrist of the user. In one embodiment, the PWH is designed such that the controls which have the potential to interrupt or prevent proper function are not susceptible to accidental operation. For example, the power on/off interface is designed in such a way to prevent accidental power down while in use.
- the power on/off switch is placed within a recess on the surface of the PWH. In one embodiment, the power on/off switch requires a certain amount of force to actuate. In one embodiment, once the power on/off switch is depressed while the unit is in use, the PWH displays a confirmation screen requiring user acceptance before the unit is powered down.
- the PWH is designed as a robust device and is capable of operating in hot, cold, dry, and humid environments.
- the PWH is capable of surviving a wash cycle in a hospital laundry.
- the PWH is capable of being submerged in a liquid tank (e.g., a toilet) for a maximum period of one hour while still retaining functionality.
- the PWH can be mounted directly onto installation mounts on the patient monitoring system.
- the PWH can be propped up on a flat, horizontal surface, such as a countertop.
- the present specification includes a docking unit for the PWH.
- the docking unit provides power to and charges the PWH while the PWH is placed in the docking unit.
- the docking unit provides power to and charges the PWH via a cable connected between the docking unit and the PWH.
- the docking unit includes its own external power supply.
- the PWH is responsible for storing data collected via directly connected FED's. In another embodiment, the PWH is responsible for storing data collected via directly connected FED's and all data collected from any other FED associated with that patient as well. In one embodiment, the PWH is capable of non-volatile storage of 24 hours of continuous patient data, including waveforms, as well as additional storage for trend data ranging from 24 to 96 hours. In another embodiment, the PWH can connect to a central monitoring system to sync stored patient date, including backfilling any gaps in the patient record.
- a real-time clock is integrated into the PWH design to support time stamping of logging and communications. This time-keeping function of the PWH maintains its ability to keep time even when the system battery is not operational.
- the PWH is capable of exporting filtered & time synchronized historical data, which includes time-stamped printed tabular trends.
- the PWH supports a plurality of parameter measurements using at least one Front End Device (FED) that is connected into an available FED port located on the PWH.
- FED Front End Device
- the PWH includes five FED ports and can therefore support up to five FED's, either proprietary to the applicant or third party.
- the measurable parameters include, but are not limited to: ECG/respiration (3-lead, 6-lead, and 10-lead); pulse oximetry (Sp0 2 ); temperature (oral, tympanic, and continuous); invasive blood pressure (single channel and 4-channel); cardiac output (thermodilution, continuous, and non-invasive); capnography (mainstream, sidestream, and fraction of inspired oxygen (Fi0 2 )); mixed venous oxygen saturation (Sv0 2 ) and central venous oxygen saturation (Svc0 2 ); multi-gas analysis (including anesthetic agent nitrous oxide (N 2 0) and 0 2 ); bispectral index (BISx); neuromuscular transmission (NMT); transcutaneous oxygen (Tcp0 2 ) & transcutaneous carbon dioxide (TcpC0 2 ); spirometry; blood glucose; pulmonary mechanics; electroencephalograph (EEG) and resultant entropy characteristics; auditory evoked potential (AEP) hemodialysis
- the PWH of the present invention can be connected to third party devices via the use of a 'living hinge' connection device, which shall be referred to as a living hinge, hinge connector assembly, or, more generally, as a connection device.
- the hinge connector assembly comprises device-specific transition connectors.
- a third party parameter sensor connection is enabled through the use of a hinge connector assembly, which translates the output of the third party device to the protocol utilized by the PWH or monitor.
- the hinge connector assembly has a first form when in an unconnected state and then adopts a new form when it is connected to or integrated with other components. This is accomplished by means of a flexible hinge.
- the hinge connector assembly is manufactured using a conventional injection molding process.
- the hinge connector assembly becomes a device interface cable.
- the device interface cable has a DSB connector at one end and a cable connector at the other end to interface with the host and the third party device respectively.
- the device interface cable includes a mechanical enclosure that includes printed circuit boards, required cabling with the DSB connector, and the connector to connect with the third party device. The printed circuit boards translate the data provided by the connector of the third party device to the DSB protocol.
- the mechanical enclosure serves to hold and guide the DSB cable that connects to the PWH or monitor.
- the hinge connector assembly includes a groove along the outer circumference of the connector end. The groove holds a gasket which acts to prevent liquid ingress. This simplifies the assembly method by eliminating a secondary operation for assembly of the gasket.
- the hinge connector assembly is designed for single use. Once integrated with the third party device, the hinge connector assembly cannot be disassembled for further use.
- the PWH can be connected to critical care ventilators, anesthesia delivery systems, hemodynamic devices, infusion pumps, and other devices via the use of the hinge connector assembly.
- the PWH can be connected to a plurality of monitoring peripherals to enhance device functionality, including but not limited to, a mouse, a keyboard (in supported languages), a keyboard with integrated navigation (touchpad or trackball), a barcode scanner, remote control devices, biometric devices, bedside printing devices, and a network laser printer.
- a mouse a keyboard (in supported languages), a keyboard with integrated navigation (touchpad or trackball), a barcode scanner, remote control devices, biometric devices, bedside printing devices, and a network laser printer.
- the electrical architecture of the PWH is based upon a single board processor.
- the PWH electrical design also includes a companion chip.
- the companion chip integrates a number of common system functions into a single chip to allow for compact designs.
- the present invention is directed toward a Patient Worn Hublet device for monitoring patient parameters.
- the Hublet is a lighter version of the PWH and contains fewer features.
- the Hublet includes dedicated hardware and parameter processing for Sp0 2 and ECG/Respiration, as well as for NIBP, as these parameters are typically most desired in a monitoring context.
- the Hublet is designed based upon an absolute minimum set of features and is named a Level 1 Hublet.
- the Level 1 Hublet includes the following features: internal NIBP; internal Sp02; internal ECG/respiration; and minimal FED based parameter support.
- the Level 1 Hublet does not include any of the following features: integrated display (interfaces via DSB to monitor display); alarm annunciation; stand-alone monitor functionality; or network connectivity.
- the Hublet is designed on a limited features concept and is named a Level 2 Hublet.
- the Level 2 Hublet includes, but is not limited to, the following features: integrated display with touchscreen; internal NIBP; internal Sp0 2 ; internal ECG/respiration; moderate FED-based parameter support; alarm annunciation; some stand-alone monitor functionality; and limited data storage capability.
- FIG. 1 is an oblique front view illustration of one embodiment of the Patient Worn Hub (PWH) 100.
- the on/off switch 106 is positioned in a recess on the surface of the PWH 100 so that inadvertent actuation of said switch becomes less likely. This feature helps prevent accidental shut off during use.
- the PWH 100 includes an integrated touchscreen display 108.
- the display 108 features waveform and numerical data and a multitude of touchscreen commands.
- the on/off switch and touchscreen can be sized and located in different configurations in various embodiments.
- FIG. 2 is an oblique front view illustration of another embodiment of the Patient Worn
- PWH 200 including an optional securing band 204.
- the securing band 204 is adjustable depending on the arm size of the patient and is used to secure the PWH 200 to the patient during transport and ambulation.
- This embodiment also includes a recessed on/off switch 206 and an integrated touchscreen display 208.
- FIG. 3A is an oblique front view illustration of one embodiment of the Patient Worn Hub docking unit 305 of the present invention.
- the docking unit 305 contains a cradle 307 for holding the PWH and a connector 309 for powering and charging the PWH.
- the docking unit 305 receives its power directly via an attached power cord 311.
- FIG. 3B is an oblique front view illustration of one embodiment of the Patient Worn Hub docking unit 305 depicting the PWH 300 placed into said docking unit 305.
- the PWH 300 fits snugly into the docking unit 305 and receives power and charging while placed into the docking unit 305.
- FIG. 4 is an illustration of a multitude of possible embodiments of the Patient Worn Hub 400, 401, 402 connected to a hospital network 450.
- the hospital network 450 includes legacy systems 452, a central data store (DB) 454, a printer 456, and a central station (CS) 458 with a multitude of displays 459.
- the PWH 400 is connected to a Smart Display (SD) 410 which is in turn connected to the hospital network 450.
- An FED 412 is connected to the PWH 400, via a hinge connector assembly as described above, to measure patient parameters.
- a third party device 414 is connected to the SD 410 via a device interface (DI) 416, which also includes a hinge connector assembly as described above.
- An additional display 418 is also connected to the SD 410.
- DI device interface
- the PWH 401 is connected to a Headless Display (HD) 420 which is in turn connected to the hospital network 450.
- An FED 422 is connected to the PWH 401 to measure patient parameters.
- Additional displays 428 are connected to the HD 420.
- the PWH 402 communicates wirelessly with a wireless access point 430 which is in turn connected to the hospital network 450.
- An FED 432 is connected to the PWH 402 to measure patient parameters.
- a Parameter Transceiver (PT) 434 also communicates wirelessly with the IPAP 430.
- An additional FED 436 is connected to the PT 434 to measure patient parameters.
- a Parameter Transceiver (PT) 444 communicates wirelessly with a wireless medical device access point (MDAP) 440 which is in turn connected to the hospital network 450.
- An FED 442 is connected to the PT 444 to measure patient parameters.
- FIG.'s 5 A and 5B depict oblique front view and side view illustrations, respectively, of one embodiment of the hinge connector assembly 500 in the open position prior to assembly.
- the hinge connector assembly 500 includes an elevated plug member 507, to which are attached an upper wing member 510 and a lower wing member 511.
- the elevated plug member 507 is formed in the shape of an oval.
- a connector 505 is set into the face of the elevated plug member 507 for connection of a third party device.
- the connector 505 is formed in a circular shape with six inserts.
- the elevated plug member and connector can take any shape that facilitates connection to a desired third party device.
- a gasket 515 is included around the end of the elevated plug member 507 for protection against liquid ingress.
- the upper wing member 510 is movable downward and away from the front of the plug member 507 about an upper hinge 520 in the range of 90 degrees from its depicted fully extended and open configuration to a closed, operable configuration as seen in FIG.'s 7A and 7B.
- the lower wing member 511 is movable upward and away from the front of the plug member 507 about a lower hinge 521 in the range of 90 degrees from its depicted fully extended and open configuration to a closed, operable configuration as seen in FIG.'s 7A and 7B.
- FIG. 6 is an oblique front view illustration of one embodiment of the hinge connector assembly 600 in the open position with a DSB device cable 625 in place. Also depicted are the printed circuit boards (PCB) 630 required to translate the output of the third party device to the protocol embedded within the PWH.
- the PCBs 630 are oriented perpendicular to the plane of the wings 610, 611 and attach to the elevated plug member 607 on the side opposite the connector 605.
- the DSB cable 625 interfaces with a connector within the enclosure formed by the PCBs 630 and the wings 610, 611.
- the wings 610, 611 fold in 90 degrees toward the PCB's 630 and the DSB device cable 625 to complete assemblage of the hinge connector assembly.
- a circular shaped cutout 635 with holes on either side that interfaces with a similarly shaped cutout 636 with pins on either side located at the end of the lower wing 611 to form a DSB device cable 625 holding feature when fully assembled.
- FIG.'s 7A and 7B are oblique front view and side view illustrations, respectively, of one embodiment of the hinge connector assembly fully assembled with a DSB device cable 725 attached.
- the folded wings 710, 711 form an enclosure, like a chassis, around the PCB's 730 and DSB device cable 725. This enclosure acts to guide and securely fix the PCB's 730 and the DSB device cable 725 in place.
- the ends of the wings 710, 711 include cutouts 735, 736 respectively that interface to hold the DSB device cable 725 in place. In one embodiment, these cutouts 735, 736 include a set of pins and holes on either side which interface when the wings 710, 711 are in the assembled position.
- the PWH 800 comprises at its core a processor 802 which is coupled with a storage module 804, a user interface 810, a DSB device port interface 820, a DSB host port interface 822, a power management module 824, a wireless Ethernet 824, a battery charger/battery gas gauge 828, and a serial port interface 818.
- the core processor 802 processes, stores, and displays all the data supplied by the associated FEDs.
- the processor core 802 is not active more than 50% of the time as averaged over a one second interval in a worst case configuration.
- the PWH 800 processor 802 manages its power utilization effectively, moving to lower power modes when possible.
- the processor 802 operates under the Windows® CE operating system.
- the storage module 804 comprises non-volatile storage, such as FlashTM memory, which is used to store all collected and processed patient data as well as programs (including boot code), back-up programs, and all information related to those programs.
- the processor 802 is capable of booting from the non-volatile memory.
- the storage module 804 also comprises volatile (RAM) storage large enough to accommodate the runtime memory requirements of the processor 802. This includes space for uncompressed executable operating system and application code.
- the nonvolatile memory storage is capable of storing complete clinical history data including all waveform and numeric physiological data for a minimum of 24 hours as well as additional storage of numeric trend data only for a minimum of 96 hours. Further, the non- volatile memory storage stores duplicate software images, including supporting non-volatile databases, languages, and configuration information.
- the user interface module 810 comprises a display module 811, a touchscreen module 812, an audio module 813, and an alarm LED module 814.
- the display module 811 in one embodiment, is a full color display which operates primarily in landscape mode and can operate in portrait mode.
- the core processor 802 interfaces to this display 811 through an internal image processing unit (IPU), while a graphics processing unit (GPU) provides hardware support for image rendering.
- the PWH 800 is provided with a backlight. This backlight driver circuit supports adjustable brightness so the display screen 811 may be read easily in any hospital environment.
- user interaction is primarily accomplished using the touchscreen module 812 on the PWH 800.
- the touchscreen 812 can be locked to prevent accidental interaction by selecting the appropriate function through the touchscreen interface.
- the touchscreen 812 does not require a special device, such as a stylus, to operate and can be operated by finger contact.
- the touchscreen 812 includes a multitude of control and status functions.
- the control of an attached non-invasive blood pressure measurement module of the PWH 800 is through the touchscreen 812.
- the PWH 800 provides status information such as battery condition and charge state through the touchscreen 812 interface enabling the user to determine the amount of time remaining while operating on batteries or the charge state when plugged into an upstream or charging device.
- the PWH 800 alerts the user when the battery level is too low or when the battery needs to be replaced.
- the alert is an audio-visual alarm that is displayed on the screen to give an indication that the battery life is nearing end.
- the audio module 813 comprises an audio output section that is used for alarm annunciation and user feedback (such as a tone to indicate acknowledgement of a user action).
- the audio output supports an adjustable volume.
- the audio module 813 is also capable of emitting distinct audible tones based upon the source of the alarm. It is possible to control the volume and to mute the alarm from the touchscreen user interface 812. It is also possible to adjust alarm volumes and alarm status using a touchscreen interface 812. In one embodiment, high, medium and low priority alarms all have distinct alarm tones associated therewith to yield a clear distinction between alarms.
- the PWH 800 also provides visual indicators during an alarm situation. In addition to showing alarm information on the display module 811, the PWH 800 will provide visual indications on the case so an alarm will be evident in a situation where the PWH 800 is resting with the display module 811 face down.
- the alarm LED module 814 comprises an array of LEDs. In one embodiment, the LED's support red, green, and blue colors. In multiple embodiments, various alarm situations can be represented by various combinations of colors. The LED's emit light through a semi-transparent section of the enclosure, such that the sides of the PWH 800 are illuminated when the LED's are active.
- the PWH 800 includes an upstream port 820 and a downstream port 822.
- the upstream port 820 is a DSB connection to Host devices 830 such as a Smart Display and is not Low Power Serial (LPS) compatible.
- the downstream port 822 connects to the external devices 832 such as FED's, and is LPS compatible.
- the upstream ports are designed to conform to the DSB specification and are LPS capable.
- the DSB device port interface 820 provides an upstream DSB port for connection to Smart Displays or other similar types of monitoring devices, either by cable or by docking the PWH 800 into the Smart Display.
- This DSB device port 820 is compliant with the USB high speed and the DSB specifications (excluding the LPS portion).
- the Smart Display or similar device may reset the PWH 800 without intervention from the PWH processor 802.
- the PWH 800 also may be charged through the upstream DSB device port 820.
- the DSB host port interface 822 contains multiple downstream DSB ports for connection of external devices 832 such as FED's.
- the DSB ports allow for connection and disconnection of FED's regardless of the operational state of the PWH 800. Since each DSB port supports USB (full and low speed), any USB device may be plugged in as long as it conforms to the DSB specification and interface control specifications.
- the USB subsystem in the PWH core processor 802 initiates contact with the FED 832.
- the FED 832 will then request power (if necessary), and the PWH 800 will respond by either denying the request or by enabling either the higher current USB or by enabling an Auxiliary Voltage Supply (AVS) line.
- Auxiliary Voltage Supply Auxiliary Voltage Supply
- the PWH 800 design accommodates the appropriate line filtering and/or isolation to allow plugging and unplugging of DSB devices without affecting other unrelated functions.
- the PWH 800 can support external user interface devices (such as a barcode reader) via the downstream ports.
- the PWH 800 provides a method of uniquely authenticating users through (but not limited to) fingerprint (biometric) identification, radio frequency ID tags, bar-code readers, or user passwords.
- the USB host port interface 822 supports a full speed/low speed connection to externally connected FED's.
- an internal 7 port hub provides the expansion out to the 5 DSB ports. This hub provides power control for each DSB port, limiting the power to 500 niA per port. Over current detection is provided for each port through this internal hub.
- each port has on/off control, which provides the PWH 800 the ability to reset a connected FED.
- the PWH 800 additionally provides AVS power to each DSB port.
- the AVS supply is initially off, but can be enabled on a port-by-port basis.
- the PWH 800 limits the AVS output power per port. Over current detection for the AVS line is provided for each port.
- the PWH 800 is self-powered so it may continuously monitor a patient in any normal hospital situation. When connected to the Smart Display, the PWH 800 uses the SD's AVS line to power the PWH functions and uses any extra available AVS power to charge the batteries. In one embodiment, the PWH 800 may be powered from the AVS supply of the upstream port 820, from which it will supply power to all internal PWH functions as well as the external DSB functions. The PWH 800 is also provided an internal battery, from which it can supply power to all internal PWH functions as well as the external DSB functions.
- the power management module 824 provides the functionality of conserving power, including but not limited to, temporarily decreasing or turning off the backlight for the display and disabling clocks to idle interior devices.
- the PWH 800 when connected to an SD, or stand-alone charger, may remain in an operational state while charging.
- the internal battery may be charged from a fully discharged state to a fully charged state in 1.5 hours or less when the PWH 800 is connected to a suitable external power source.
- a battery gauge module 828 enables the PWH 800 to accurately track battery life and charge state.
- the PWH 800 Unlike a standard laptop computer or a cell phone, which operate infrequently and spend much of their time in an idle state, the PWH 800 will spend much of its time collecting and processing data.
- the PWH 800 powers down any unused function (as much as is feasible), including the display.
- the core processor 802 In cases where the core processor 802 is in a powered on but extended idle state, the core processor 802 is placed in a standby mode. In this mode, any interaction from an FED 832 or a user interface such as the touchscreen 812 places the PWH 800 back into an operational state.
- the PWH 800 provides a wireless Ethernet radio 826. This enables wireless connection to a main control system via a wireless access point.
- the PWH 800 provides an internal antenna for this radio.
- the PWH 800 additionally provides capability for a wired Ethernet connection.
- a non-invasive blood pressure measurement (NIBP) FED 819 is housed within the PWH enclosure.
- the NIBP FED 819 is controlled by a separate microcontroller that communicates with the PWH core processor 802 via an internal serial port 818 connection. Control information, data, and maintenance messaging to and from the NIBP 819 processor is all funneled through the serial port 818.
- the PWH 800 supports adult, pediatric, and neonatal patients.
- NIBP 819 Configuration of the NIBP 819 for functions such as sample interval and patient type (adult, pediatric, etc.) are made through the PWH display 811 /touchscreen 812 interface.
- the PWH processor 802 is used to provide the "safety processor" functions for the NIBP 819 sub-system.
- the PWH processor 802 monitors the secondary pressure port and can override and deflate the external NIBP cuff if it detects an error condition.
- the processor 802 assures that communication with the NIBP 819 is active, and if not, an alarm is signaled and the NIBP 819 pump and valve control are overridden. This insures that the NIBP 819 does not fall into a harmful situation in the event of a problem with any part of the NIBP 819 system.
- the PWH 800 may reset the internal modules such as DSB hubs
- the PWH 800 may be reset by a command from the display interface 811, from the ON/OFF button, or from a Smart Display device.
- the PWH 800 is provided with latch circuitry, which may be accessed by the core processor 802 to determine if the reset was initiated via a reset line or from a power condition.
- the core processor 802 upon initialization, will change the state of the latch from its default setting. Upon recovery from a reset, if the core processor 802 notes that this latch is in its default state, then the latch itself must have reset due to a power condition.
- the reset mechanism for the Smart Display operates even in cases where the core processor 802 is non-functional, by detecting the case where the upstream AVS line is powered and the BUS line goes low. This low period must extend long enough to avoid false triggering.
- the PWH 800 In order to reset a connected FED 832, the PWH 800 simply drops the BUS line out to the FED 832 for a period of time, and then re- enables this line.
- reset information may be retrieved for diagnostic purposes. The reset information may be accessible via the user interface 810.
- the companion chip 902 includes the following components: a power management component 951 controlled by the core voltage/frequency controller 913 of the micro-controller central processing unit (CPU) 901; a backlight power supply 952 which provides power to the display backlights 965; a real-time clock (RTC) 953; a touchscreen controller 954 which communicates with the touchscreen 974; an audio out 955 which sends signals to the amp 970 which in turn sends signals to the speaker 971; a codec 956; and, a CPU interface 957 which communicates with the serial peripheral interface (SPI) 914 of the microcontroller CPU 901.
- a power management component 951 controlled by the core voltage/frequency controller 913 of the micro-controller central processing unit (CPU) 901
- a backlight power supply 952 which provides power to the display backlights 965
- RTC real-time clock
- touchscreen controller 954 which communicates with the touchscreen 974
- an audio out 955 which sends signals to the amp 970 which in turn sends signals to
- the power management component 951 controls the power supply 960 which determines a range of power output 963 (1.2-1.65, 1.8, 3.3, 5, and 18 V).
- a battery charger 962 charges a lithium ion (Li-Ion) battery 961 which in turn supplies power to the power supply 960.
- FIG. 10 is a block diagram illustrating one embodiment of the processor 1000 included in the electrical architecture of the PWH.
- the processor 1000 is based upon a core 1001 architecture, which supports the Windows® CE operating system.
- the CPU core 1002 is augmented with a co-processor 1004.
- the processor 1000 has memory interfaces for synchronous dynamic random access memory (SDRAM)/double data rate random access memory (DDR RAM) 1016, pseudostatic random access memory (PSRAM) 1018, and SmartMedia 1019, as well as a built in NAND flash controller 1017.
- the PWH is provided with two separate Flash memory devices: a NAND Flash and a NOR Flash.
- the 1GB NAND flash contains all information associated with the patient including the trend and historical data. No other external devices are needed for the NAND Flash since the micro-controller contains a NAND flash controller. The micro-controller 1000 cannot boot from the NAND Flash due to its page access interface, so a NOR Flash is required.
- the Flash memory contains the boot software image, main software image, and backup software image for the PWH.
- the NOR Flash is available with a 1.8V interface, so no external devices are needed to interface this to the CPU.
- the micro-controller processor 1000 also provides a Dual Data Rate (DDR) interface. This interface provides data on both edges of a clock cycle. Since many of the Mobile DDR devices are available with a 1.8V interface, no additional hardware is necessary to connect the DDR to the processor.
- DDR Dual Data Rate
- the display support included in the processor 1000 consists of a multimedia and human interface 1020 and an Image Processing Unit (IPU) 1022.
- the multimedia and human interface 1020 comprises an internal Graphics Processing Unit (GPU) which provides hardware acceleration for many graphics functions, an MPEG-4 Encoder, and a Keypad interface.
- the IPU 1022 handles image manipulation (inversion, rotation, blending, scaling, etc.), Pre- and Post-Processing, and a Camera interface, as well as image output to the display via a Display/TV Controller.
- the processor 1000 provides internal connectivity interfaces 1024 for connecting internal devices as well as external connectivity interfaces 1026 for connecting external devices.
- the internal connectivity interfaces 1024 include three
- the external connectivity interfaces 1026 include five UART interfaces, one USB OTG HS interface, two USB Host interfaces, one 1-Wire interface, and one Fast IrDA interface. Higher throughput devices can be connected via expansion interfaces 1028 through one PCMCIA/CF port, two MMC/SD ports, two Memory Stick Pro ports, one SIM port, and one ATA port. Two of the three USB ports are host-only ports supporting USB high speed connections, while one of the high speed ports can be configured as a device (for connection to upstream USB devices). Supporting the interfaces 1024, 1026 are an array of DMA controllers and a 5 input, 6 output crossbar connection smart speed switch 1030 which allows simultaneous access to multiple devices.
- the processor 1000 has built in security hardware support 1032 for high assurance boot (HAB), runtime integrity checking (RTIC), and tamper detection.
- HAB high assurance boot
- RTIC runtime integrity checking
- tamper detection The HAB authenticates the boot code, preventing booting from unauthorized code.
- the RTIC checks sections of memory during execution. If the contents fail to match the original hash signature, the security monitor is triggered.
- the tamper protection allows the change of an external IO pin (selectable) on the processor to trigger the security monitor.
- the processor 1000 supports standard system control functions 1034 including joint tag action group (JTAG), electronic token meter (ETM), bootstrap, system reset, and phase-locked loop (PLL) and power management.
- the processor 1000 supports standard system input/output (I/O) functions 1036 including direct memory access (DMA), three timers, pulse-width modulation (PWM), watchdog (WD) Timer, real time clock (RTC), general purpose input/output (GPIO), and random access memory (RAM)/read-only memory (ROM).
- JTAG joint tag action group
- ETM electronic token meter
- PLL phase-locked loop
- I/O system input/output
- DMA direct memory access
- PWM pulse-width modulation
- WD watchdog
- Timer Real time clock
- GPIO general purpose input/output
- RAM random access memory
- ROM read-only memory
- FIG. 11 is a block diagram illustrating one embodiment of an upstream USB port of the PWH.
- the upstream USB port 1102 of the PWH provides a USB compliant high speed connection to upstream devices 1104.
- the port on the micro-controller CPU is connected via a multiplexer (MUX) 1106 either to a standard DSB connection or to a set of contacts that provide connection when the PWH is docked in a Smart Display (SD) type of device.
- the port MUX 1106 switches to the connected port when it senses that port's VBUS line. If both the standard DSB connection and the SD contacts are active, the standard DSB port is selected.
- the VBUS lines of each port are connected through diodes to prevent feedback of the VBUS supply in the case of a dual connection.
- USB High Speed hub 1108 is inserted in between the MUX 1106 and the USB port 1102 on the micro-controller so that it may enumerate even when the rest of the PWH is powered off.
- An electrically-erasable programmable read-only memory (EEPROM) connected to the Hub provides the vendor identification (VID)/product information (PID) for proper enumeration.
- VIP vendor identification
- PID product information
- This transceiver 1110 changes the data from a serial stream to a byte wide stream that operates at a lower rate.
- the transceiver 1110 also combines the CPUs transmit and receive paths into a single differential output.
- the USB port 1102 and transceiver 1110 are internally powered and the USB Hub 1108, MUX 1106, and upstream devices 1104 are all input VBUS powered.
- FIG. 12 is a block diagram illustrating one embodiment of the power section of the PWH.
- the power section of the PWH requires a number of voltage levels for the external devices while the core processor itself requires the power be segmented into banks.
- the main power source for the PWH emanates from the upstream DSB port's AVS line 1202, or from the internal PWH battery pack 1204.
- the battery pack 1204 comprises a 2-cell lithium ion (Li- Ion) battery pack.
- the batteries are connected in series, providing a maximum voltage of 8.4 V and a minimum working voltage of 6 V.
- the battery pack 1204 contains a safety circuit as well as a highly accurate gas gauge.
- This gas gauge communicates with a battery charger 1206 through a system management bus (SMBUS) connection.
- SMBUS system management bus
- the battery charger 1206 is an SMBUS compliant "smart charger". This charger 1206 is automatic from a user point of view.
- the core processor detects when the batteries need to be charged and enables the charger if running on external power. Charge profiles are programmable via the SMBUS interface. In order to keep the PWH operational while charging, the battery charger 1206 gets only the remaining current above what is necessary for operation.
- the PWH has the ability to reduce power consumption to the lowest possible levels in order to minimize battery size and maximize run-time. Based upon processor activity, the PWH core processor automatically manages the core power in conjunction with the micro-controllers companion chip 1208.
- the CPU may turn off external devices (such as the Flash memory, Display, USB Hubs, etc.) when not in use.
- the core processor possesses the ability to power down each voltage regulator, except those regulators on which it will depend for operation.
- the PWH also uses the AVS input 1202 to drive the AVS outputs to the FEDs. If the input AVS 1202 is not available, then a boost converter 1210 is used to boost the battery supply voltage up to the level required for the AVS outputs. To do this, the battery pack supply is fed into a boost-style switching regulator to boost the voltage. The cutover to this regulator is automatic, based upon the presence of the AVS input. Additionally, when this input is available, the voltage regulator is disabled to save power.
- a switching type regulator 1212 Due to the wide input range a switching type regulator 1212, is provided.
- the output primarily supplies the VBUS lines for the downstream USB ports as well as any components that require 5 V supplies, such as the audio amp.
- the 3.3 V regulator supplies all 3.3 V components as well as providing the input for the micro-controller companion chip 1208.
- the companion chip 1208 provides a plurality of integrated linear and switching style regulators.
- Regulator 1214 provides the 1.8 V required for the PWH as well as supplies the core processor's I/O pins.
- Regulator 1216 is a dynamically controlled regulator, which provides the 1.2 to 1.6 V output which is used to power the core processor.
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- Measuring And Recording Apparatus For Diagnosis (AREA)
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11841530.6A EP2641151A4 (en) | 2010-11-19 | 2011-11-18 | Self-contained patient monitor |
CN201180065517.3A CN103313651B (en) | 2010-11-19 | 2011-11-18 | Self-sustaining patient monitor |
PCT/US2011/061558 WO2012068568A2 (en) | 2010-11-19 | 2011-11-18 | Self-contained patient monitor |
US13/300,526 US20120130204A1 (en) | 2010-11-19 | 2011-11-18 | Self-contained patient monitor |
BR112013012315A BR112013012315A2 (en) | 2011-11-18 | 2011-11-18 | standalone patient monitor |
GB1310778.4A GB2499174B (en) | 2010-11-19 | 2011-11-18 | Self-contained patient monitor |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US41579910P | 2010-11-19 | 2010-11-19 | |
US61/415,799 | 2010-11-19 | ||
PCT/US2011/061558 WO2012068568A2 (en) | 2010-11-19 | 2011-11-18 | Self-contained patient monitor |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2012068568A2 true WO2012068568A2 (en) | 2012-05-24 |
WO2012068568A3 WO2012068568A3 (en) | 2012-10-11 |
Family
ID=47359478
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2011/061558 WO2012068568A2 (en) | 2010-11-19 | 2011-11-18 | Self-contained patient monitor |
Country Status (5)
Country | Link |
---|---|
US (1) | US20120130204A1 (en) |
EP (1) | EP2641151A4 (en) |
CN (1) | CN103313651B (en) |
GB (1) | GB2499174B (en) |
WO (1) | WO2012068568A2 (en) |
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US9152765B2 (en) | 2010-03-21 | 2015-10-06 | Spacelabs Healthcare Llc | Multi-display bedside monitoring system |
US9298889B2 (en) | 2007-03-09 | 2016-03-29 | Spacelabs Healthcare Llc | Health data collection tool |
US9384652B2 (en) | 2010-11-19 | 2016-07-05 | Spacelabs Healthcare, Llc | System and method for transfer of primary alarm notification on patient monitoring systems |
US9604020B2 (en) | 2009-10-16 | 2017-03-28 | Spacelabs Healthcare Llc | Integrated, extendable anesthesia system |
WO2017089319A1 (en) * | 2015-11-24 | 2017-06-01 | Koninklijke Philips N.V. | Portable device case for pulse oximetry measurements |
US9797764B2 (en) | 2009-10-16 | 2017-10-24 | Spacelabs Healthcare, Llc | Light enhanced flow tube |
US10699811B2 (en) | 2011-03-11 | 2020-06-30 | Spacelabs Healthcare L.L.C. | Methods and systems to determine multi-parameter managed alarm hierarchy during patient monitoring |
US10987026B2 (en) | 2013-05-30 | 2021-04-27 | Spacelabs Healthcare Llc | Capnography module with automatic switching between mainstream and sidestream monitoring |
US12102416B2 (en) | 2019-06-26 | 2024-10-01 | Spacelabs Healthcare L.L.C. | Using data from a body worn sensor to modify monitored physiological data |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8133197B2 (en) | 2008-05-02 | 2012-03-13 | Smiths Medical Asd, Inc. | Display for pump |
USD733727S1 (en) * | 2011-10-11 | 2015-07-07 | Proteus Digital Health, Inc. | Display screen portion having a graphical user interface for patient monitoring |
US9335910B2 (en) * | 2012-04-23 | 2016-05-10 | Tandem Diabetes Care, Inc. | System and method for reduction of inadvertent activation of medical device during manipulation |
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US10911891B2 (en) | 2014-12-18 | 2021-02-02 | Drägerwerk AG & Co. KGaA | Alarm routing optimization strategies in targeted alarm system |
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US10541987B2 (en) | 2016-02-26 | 2020-01-21 | Tandem Diabetes Care, Inc. | Web browser-based device communication workflow |
US20170273597A1 (en) * | 2016-03-24 | 2017-09-28 | Eresearchtechnology, Inc. | Methods and systems for collecting spirometry data |
US10849541B2 (en) * | 2016-08-08 | 2020-12-01 | Hexacheck Inc. | Portable complex sensor device for measuring multiple items of biometric information, and measurement method |
CN106308777A (en) * | 2016-08-16 | 2017-01-11 | 成都市和平科技有限责任公司 | Portable electronic doctor equipment and portable electronic doctor system |
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US11364361B2 (en) | 2018-04-20 | 2022-06-21 | Neuroenhancement Lab, LLC | System and method for inducing sleep by transplanting mental states |
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5375604A (en) | 1992-12-11 | 1994-12-27 | Siemens Medical Electronics, Inc. | Transportable modular patient monitor |
US20100261979A1 (en) | 2006-09-22 | 2010-10-14 | Masimo Corporation | Modular patient monitor |
Family Cites Families (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US39233A (en) * | 1863-07-14 | Improved machine for making cement pipes | ||
US5353793A (en) * | 1991-11-25 | 1994-10-11 | Oishi-Kogyo Company | Sensor apparatus |
GB2288922B (en) * | 1994-04-25 | 1998-04-01 | John Edward Mcgrath | Patient monitoring apparatus |
US5520191A (en) * | 1994-10-07 | 1996-05-28 | Ortivus Medical Ab | Myocardial ischemia and infarction analysis and monitoring method and apparatus |
US6050940A (en) * | 1996-06-17 | 2000-04-18 | Cybernet Systems Corporation | General-purpose medical instrumentation |
US6364834B1 (en) * | 1996-11-13 | 2002-04-02 | Criticare Systems, Inc. | Method and system for remotely monitoring multiple medical parameters in an integrated medical monitoring system |
US6042548A (en) * | 1997-11-14 | 2000-03-28 | Hypervigilant Technologies | Virtual neurological monitor and method |
US6398727B1 (en) * | 1998-12-23 | 2002-06-04 | Baxter International Inc. | Method and apparatus for providing patient care |
US20020140675A1 (en) * | 1999-01-25 | 2002-10-03 | Ali Ammar Al | System and method for altering a display mode based on a gravity-responsive sensor |
US6770028B1 (en) * | 1999-01-25 | 2004-08-03 | Masimo Corporation | Dual-mode pulse oximeter |
US6416471B1 (en) * | 1999-04-15 | 2002-07-09 | Nexan Limited | Portable remote patient telemonitoring system |
EP1217942A1 (en) * | 1999-09-24 | 2002-07-03 | Healthetech, Inc. | Physiological monitor and associated computation, display and communication unit |
ATE502567T1 (en) * | 2000-05-19 | 2011-04-15 | Welch Allyn Protocol Inc | DEVICE FOR MONITORING PATIENTS |
GB0014854D0 (en) * | 2000-06-16 | 2000-08-09 | Isis Innovation | System and method for acquiring data |
DK1309270T3 (en) * | 2000-08-18 | 2009-08-03 | Masimo Corp | Pulse oximeter with two modes |
US20090182204A1 (en) * | 2001-10-04 | 2009-07-16 | Semler Herbert J | Body composition, circulation, and vital signs monitor and method |
US6726634B2 (en) * | 2002-01-25 | 2004-04-27 | Koninklijke Philips Electronics N.V. | System and method for determining a condition of a patient |
US20050288571A1 (en) * | 2002-08-20 | 2005-12-29 | Welch Allyn, Inc. | Mobile medical workstation |
US20040147818A1 (en) * | 2002-11-18 | 2004-07-29 | Andrew Levy | Portable system for monitoring and processing patient parameters in multiple oprational modes |
US20040162510A1 (en) * | 2003-02-14 | 2004-08-19 | Medtronic Physio-Control Corp | Integrated external chest compression and defibrillation devices and methods of operation |
CA2517880C (en) * | 2003-03-04 | 2013-01-22 | Ethicon Endo-Surgery, Inc. | Patient monitoring and drug delivery system and method of use |
US7316648B2 (en) * | 2003-06-11 | 2008-01-08 | Draegers Medical Systems Inc | Portable patient monitoring system including location identification capability |
US20050113704A1 (en) * | 2003-11-26 | 2005-05-26 | Lawson Corey J. | Patient monitoring system that incorporates memory into patient parameter cables |
US20050146431A1 (en) * | 2003-12-31 | 2005-07-07 | Ge Medical Systems Information Technologies, Inc. | Alarm notification system, receiver, and methods for providing live data |
CN100581444C (en) * | 2004-11-15 | 2010-01-20 | 皇家飞利浦电子股份有限公司 | Ambulatory medical telemetry device having an audio indicator |
JP2008526443A (en) * | 2005-01-13 | 2008-07-24 | ウェルチ・アリン・インコーポレーテッド | Vital signs monitor |
US20070060869A1 (en) * | 2005-08-16 | 2007-03-15 | Tolle Mike C V | Controller device for an infusion pump |
US20070255126A1 (en) * | 2006-04-28 | 2007-11-01 | Moberg Sheldon B | Data communication in networked fluid infusion systems |
US7539532B2 (en) * | 2006-05-12 | 2009-05-26 | Bao Tran | Cuffless blood pressure monitoring appliance |
US9131892B2 (en) * | 2006-07-25 | 2015-09-15 | Gal Markel | Wearable items providing physiological, environmental and situational parameter monitoring |
US7396762B2 (en) * | 2006-08-30 | 2008-07-08 | International Business Machines Corporation | Interconnect structures with linear repair layers and methods for forming such interconnection structures |
AU2008247319B2 (en) * | 2007-05-02 | 2013-07-18 | Sensitive Pty Ltd | Non-invasive measurement of blood oxygen saturation |
US8412293B2 (en) * | 2007-07-16 | 2013-04-02 | Optiscan Biomedical Corporation | Systems and methods for determining physiological parameters using measured analyte values |
JP5079423B2 (en) * | 2007-08-24 | 2012-11-21 | フクダ電子株式会社 | Flexible board connection device |
WO2009036150A2 (en) * | 2007-09-11 | 2009-03-19 | Aid Networks, Llc | Wearable wireless electronic patient data communications and physiological monitoring device |
US20090192541A1 (en) * | 2008-01-28 | 2009-07-30 | Ethicon Endo-Surgery, Inc. | Methods and devices for predicting performance of a gastric restriction system |
EP2358266A4 (en) * | 2008-11-20 | 2012-10-03 | Bodymedia Inc | Method and apparatus for determining critical care parameters |
EP2424433A4 (en) * | 2009-04-27 | 2014-05-07 | Spacelabs Healthcare Llc | Multiple mode, portable patient monitoring system |
US8909330B2 (en) * | 2009-05-20 | 2014-12-09 | Sotera Wireless, Inc. | Body-worn device and associated system for alarms/alerts based on vital signs and motion |
WO2011001302A1 (en) * | 2009-06-29 | 2011-01-06 | Koninklijke Philips Electronics, N.V. | Patient monitoring with automatic resizing of display sectors |
US8744875B2 (en) * | 2009-12-23 | 2014-06-03 | Mindray Ds Usa, Inc. | Systems and methods for synchronizing data of a patient monitor and a portable sensor module |
DE102010010610A1 (en) * | 2010-03-08 | 2011-09-08 | Pulsion Medical Systems Ag | Portable sensor device and patient monitor |
US8888700B2 (en) * | 2010-04-19 | 2014-11-18 | Sotera Wireless, Inc. | Body-worn monitor for measuring respiratory rate |
US20140275873A1 (en) * | 2013-03-14 | 2014-09-18 | Covidien Lp | Sensor connector |
-
2011
- 2011-11-18 EP EP11841530.6A patent/EP2641151A4/en not_active Withdrawn
- 2011-11-18 GB GB1310778.4A patent/GB2499174B/en not_active Expired - Fee Related
- 2011-11-18 US US13/300,526 patent/US20120130204A1/en not_active Abandoned
- 2011-11-18 WO PCT/US2011/061558 patent/WO2012068568A2/en active Application Filing
- 2011-11-18 CN CN201180065517.3A patent/CN103313651B/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5375604A (en) | 1992-12-11 | 1994-12-27 | Siemens Medical Electronics, Inc. | Transportable modular patient monitor |
US20100261979A1 (en) | 2006-09-22 | 2010-10-14 | Masimo Corporation | Modular patient monitor |
Non-Patent Citations (1)
Title |
---|
See also references of EP2641151A4 |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9298889B2 (en) | 2007-03-09 | 2016-03-29 | Spacelabs Healthcare Llc | Health data collection tool |
US9604020B2 (en) | 2009-10-16 | 2017-03-28 | Spacelabs Healthcare Llc | Integrated, extendable anesthesia system |
US9797764B2 (en) | 2009-10-16 | 2017-10-24 | Spacelabs Healthcare, Llc | Light enhanced flow tube |
US9152765B2 (en) | 2010-03-21 | 2015-10-06 | Spacelabs Healthcare Llc | Multi-display bedside monitoring system |
US9384652B2 (en) | 2010-11-19 | 2016-07-05 | Spacelabs Healthcare, Llc | System and method for transfer of primary alarm notification on patient monitoring systems |
US10699811B2 (en) | 2011-03-11 | 2020-06-30 | Spacelabs Healthcare L.L.C. | Methods and systems to determine multi-parameter managed alarm hierarchy during patient monitoring |
US11562825B2 (en) | 2011-03-11 | 2023-01-24 | Spacelabs Healthcare L.L.C. | Methods and systems to determine multi-parameter managed alarm hierarchy during patient monitoring |
US10987026B2 (en) | 2013-05-30 | 2021-04-27 | Spacelabs Healthcare Llc | Capnography module with automatic switching between mainstream and sidestream monitoring |
WO2017089319A1 (en) * | 2015-11-24 | 2017-06-01 | Koninklijke Philips N.V. | Portable device case for pulse oximetry measurements |
US12102416B2 (en) | 2019-06-26 | 2024-10-01 | Spacelabs Healthcare L.L.C. | Using data from a body worn sensor to modify monitored physiological data |
Also Published As
Publication number | Publication date |
---|---|
EP2641151A2 (en) | 2013-09-25 |
EP2641151A4 (en) | 2018-04-18 |
GB2499174A (en) | 2013-08-07 |
CN103313651B (en) | 2016-06-08 |
WO2012068568A3 (en) | 2012-10-11 |
GB201310778D0 (en) | 2013-07-31 |
GB2499174B (en) | 2017-06-14 |
US20120130204A1 (en) | 2012-05-24 |
CN103313651A (en) | 2013-09-18 |
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