WO2011035366A1 - Dispositif de secours et procédé pour indiquer des informations de fréquence - Google Patents

Dispositif de secours et procédé pour indiquer des informations de fréquence Download PDF

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Publication number
WO2011035366A1
WO2011035366A1 PCT/AU2010/001224 AU2010001224W WO2011035366A1 WO 2011035366 A1 WO2011035366 A1 WO 2011035366A1 AU 2010001224 W AU2010001224 W AU 2010001224W WO 2011035366 A1 WO2011035366 A1 WO 2011035366A1
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WO
WIPO (PCT)
Prior art keywords
user
patient
indicative
emergency device
response
Prior art date
Application number
PCT/AU2010/001224
Other languages
English (en)
Inventor
David Hua Wang
Original Assignee
Dhw Family Pty Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from AU2009904648A external-priority patent/AU2009904648A0/en
Application filed by Dhw Family Pty Ltd filed Critical Dhw Family Pty Ltd
Publication of WO2011035366A1 publication Critical patent/WO2011035366A1/fr

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Classifications

    • 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
    • G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
    • G16H10/20—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for electronic clinical trials or questionnaires
    • 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
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/30—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to physical therapies or activities, e.g. physiotherapy, acupressure or exercising
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H31/00—Artificial respiration or heart stimulation, e.g. heart massage
    • A61H31/004—Heart stimulation
    • A61H31/005—Heart stimulation with feedback for the user
    • 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
    • G16H50/00—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/20—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems

Definitions

  • the present invention relates to emergency devices and in particular to emergency devices for indicating a procedural operation.
  • the invention has been developed primarily for use as an emergency device to indicate the procedural operation of performing cardio pulmonary resuscitation and will be described hereinafter with reference to this application. However, it will be appreciated that the invention is not limited to this particular field of use.
  • Known devices for indicating the procedural operation of performing cardio pulmonary resuscitation typically include instructional aids in the form of documentation or signage.
  • instructional aids in the form of documentation or signage.
  • the carer can be incapable of reading, comprehending and implementing written instructions.
  • an emergency device for indicating rate timing information to a user in performing an emergence response, the device comprising:
  • processor module is adapted to receive data indicative of the patient condition and in response to the receive data controls the output element to indicate the rate timing information.
  • the processor prompts the user to provide data indicative of the patient though a series of predetermined questions, the data being provided by the user.
  • the processor prompts the user by illuminating a selections set including one or more key selections indicative of acceptable answers.
  • a first selection set is preferably indicative of the patient being an adult or child.
  • the first selection set can alternatively indicate the patient being selected from any two or more of the set comprising adult, child and infant.
  • a second selection set is preferably indicative of the number of emergency response providers being one or two.
  • a third selection set is preferably indicative of the patient airway being clear or not clear.
  • a fourth selection set is preferably indicative of the patient breathing or not breathing.
  • a fifth selection set is preferably indicative of the patient presetting with a pulse or without a pulse.
  • the output element preferably includes one or more observable indicators for indicating rate timing information to a user for performing cardio pulmonary resuscitation.
  • a first observable indicator is preferably indicative of the rate timing for providing cardiac compressions.
  • a second observable indicator is preferably indicative of the rate timing for providing lung inflation.
  • the first observable indicator further alerts of timing of a pending lung inflation relative to a sequence of cardiac compressions.
  • One or more observable indicators are preferably illuminated representations.
  • one or more observable indicators can be auditory representations.
  • a first representation is preferably indicative of the rate and timing of a cardiac compression.
  • a second representation is preferably indicative of the rate and timing of lung inflation.
  • a third representation can preferably indicate the rate and timing of a cardiac compression preceding the next lung inflation.
  • the method further comprises the step of activating a device as previously described.
  • the method further comprises the step of prompting the user to provide data indicative of the patient though a series of predetermined questions, the data being provided by the user.
  • the method comprises the step of prompting the user to provide data indicative of the patient being an adult or child, and receiving response data provided by the user. More preferably, the method comprises the step of prompting the user to provide data indicative of the patient being selected from any two or more of the set comprising adult, child and infant and receiving response data provided by the user.
  • the method comprises the step of prompting the user to provide data indicative of the number of emergency response providers being one or two, and receiving response data provided by the user.
  • the method comprises the step of prompting the user to provide data indicative of any one or more of the set including: the patient airway being clear or not clear, the patient being breathing or not breathing, patient presetting with a pulse or without a pulse; and receiving response data provided by the user.
  • the controlling at least one output element coupled to the processor module to indicate the rate timing information preferably comprises indicating rate timing information to a user for performing cardio pulmonary resuscitation.
  • a first observable indicator is preferably indicative of the rate timing for providing cardiac compressions.
  • a second observable indicator is preferably indicative of the rate timing for providing lung inflation.
  • the first observable indicator further alerts of timing of a pending lung inflation relative to a sequence of cardiac compressions.
  • a computer program product for implementing a method for indicating rate timing information to a user in performing an emergence response.
  • computer-readable carrier medium carrying a set of instructions that when executed by one or more processors cause the one or more processors to carry out a method for indicating rate timing information to a user in performing an emergence response.
  • FIG. 1 is an example schematic view of an emergency device according to the
  • FIG. 2A is an example flowchart of a method performed by the device of FIG. 1, for indicating the procedural operation of performing cardio pulmonary resuscitation according to the invention
  • FIG. 2B is an example flowchart of a method performed by the device of FIG. 1, for indicating the procedural operation of performing cardio pulmonary resuscitation according to the invention
  • FIG. 3 is an example schematic view of an emergency device according to the
  • FIG. 4 is an example flowchart of a method performed by the device of FIG. 3, for indicating the procedural operation of performing cardio pulmonary resuscitation according to the invention
  • FIG. 5 is an example schematic view of an emergency device of FIG. 3, show having a cover
  • FIG. 6 is an example schematic view of an emergency device according to the
  • an emergency response provider would then be typically expected to check if:
  • the patient has a clear airway
  • the patient is breathing normally;
  • the patient has blood circulation.
  • Checking for a clear airway typically involves placing the patient on their back, tilting the head back (not for infants or injured), removing foreign matter from mouth (and nose of baby); place the patient on side if there is a lot of foreign matter.
  • a mini-touch can be either fixedly or releasablly attached to the device for checking the patients airway, if the patient is breathing normally, and/or if there is any foreign matter in a dark environment. This can be particularly useful if the emergency occurs at night).
  • Checking for breathing typically involves listening and feeling for breathing, and watch for chest movement (for example using the mini-touch when in the dark). If the patient is breathing normally, the patient is typically left on their side. If the patient is not breathing normally, the patient is typically placed on their back with their head tilted back (not for infants or injured). Two breaths at often provided whilst watching rise and fall of chest.
  • Checking for a circulation typically involves feeling for the presence of a pulse. If there is not detected circulation, the emergency response provider may be required to perform cardio pulmonary resuscitation.
  • the specifications for performing cardio pulmonary resuscitation can vary from time to time, and is often dependent on the age of the patient and the number of emergency response providers in attendance.
  • the recommended rate of compressions is typically about one hundred compressions per minute and the ratio of compression to breaths is 30: 1 for one response provider and 15: 1 for two response providers.
  • FIG. 1 shows an example embodiment of an emergency device 100 for indicating rate timing information to a user in performing an emergence response.
  • the device comprises an input element 110 and an output element 120.
  • a processor module 130 is coupled to both the input and output elements, and is adapted to receive data indicative of the patient condition from the input element.
  • the processor module is further adapted to control the output element, in response to the receive data, to indicate the rate timing information.
  • the rate timing for cardio pulmonary resuscitation can be dictated by the age of the patient (adult, child and infant) and the number of emergency response providers.
  • the processor prompts the user to provide data indicative of the patient though a series of predetermined questions, the data being provided by the user.
  • FIG. 2 A shows an example embodiment of a flow chart of a method 200 for indicating rate timing information to a user in performing an emergence response, the method comprising:
  • STEP 220 receiving data, at a processor module, indicative of the patient condition;
  • STEP 230 determining, in response to the receive data, appropriate rate timing
  • STEP 240 controlling at least one output element, coupled to the processor module, to indicate the rate timing information.
  • the method can comprise STEP 210 of activating a device.
  • the power source typically in the form of a battery
  • Activation can be achieved by removing an insulator placed between a battery terminal and a battery connector.
  • activation can be achieved by having an isolation switch.
  • the isolation switch can be operatively associated with removing a cover from the device.
  • STEP 230 can determine appropriate rate timing information, in response to the receive data, in which:
  • compression rate and compression:breath ratio is determined by various medical bodies and change from time to time. Further the compression:breath ratio may require 'n' compressions followed by one or more breaths, as set by the advisory body.
  • FIG. 2B shows an example embodiment flow chart of a method 200 for indicating rate timing information to a user in performing an emergence response.
  • the method comprises the steps of:
  • STEP 241 determining if a breath (or lung inflation) is required based on the
  • STEP 242 if appropriate, indicating a breath is required
  • STEP 243 determining if a compression is required based on the determined
  • one or more observable indicators for indicating a compression and/or lung inflation are illuminated representations, typically in the form of flashing lights, graphical displays, or text.
  • one or more observable indicators can be auditory representations, including set sounds, signals or voice commands (synthesised or recorded).
  • a first representation is indicative of the rate and timing of cardiac compressions and a second representation is preferably indicative of the rate and timing of lung inflation.
  • a compression:breath ratio should also be maintained, and therefore, a third representation can be provided to indicate the rate and timing of a cardiac compression preceding the next breath (or lung inflation).
  • an observable indicators for indicating a compression can comprise a plurality of individual indicators that, while indicating the timing for compression, further alerts to the timing of a pending lung inflation relative to a sequence of cardiac compressions.
  • an observable indicator for indicating lung inflation can comprise a plurality of individual indicators that further alerts of timing of a pending lung inflation relative to a sequence of cardiac compressions.
  • a sequence can be indicated visually (for example by flashing lights, graphical displays, or text) or audibly (set sounds, signals or voice commands), or a combination of visual and auditory cues.
  • FIG. 3 is an example embodiment of an emergency device 100 for indicating rate timing information to a user in performing an emergence response.
  • the device comprises an input element 110 and an output element 120.
  • a processor module 130 is coupled to both the input and output elements, and is adapted to receive data indicative of the patient condition from the input element.
  • the processor module is further adapted to control the output element, in response to the receive data, to indicate the rate timing information.
  • the rate timing for cardio pulmonary resuscitation can be dictated by the age of the patient (adult, child or baby and new born) and the number of emergency response providers.
  • the processor prompts the user to provide data indicative of the patient though a series of predetermined questions, the data being provided by the user.
  • the processor prompts the user by highlighting/illuminating a selections set including one or more key selections indicative of acceptable answers.
  • a first selection set (311 , 312) is indicative of the patient being an adult or child respectively. It will be appreciated that the first selection set can alternatively indicate the patient being selected from any two or more of the set comprising adult, child and infant.
  • a second selection set (313, 314) is indicative of the number of emergency response providers being one or two respectively.
  • a third selection set 315 is preferably indicative of the patient airway being clear or not clear.
  • a fourth selection set 316 is preferably indicative of the patient breathing or not breathing.
  • a fifth selection set 317 is preferably indicative of the patient presetting with a pulse or without a pulse.
  • the selections sets 315, 316 and 317 may only highlight to a user (or an emergency response provider) to check the airway, breathing and circulation respectively, thereby only requiring the highlighting and/or confirming that an action should-be and/or has-been conducted.
  • the output element 120 includes a plurality of observable indicators (321, 325, 326, 327, 328 and 329) for indicating rate timing information to a user performing cardio pulmonary resuscitation.
  • Observable indicators 325, 326, 327, 328 and 329 are indicative of the rate timing for providing cardiac compressions, and indicator 321 is indicative of the rate timing for providing lung inflation.
  • observable indicators 325, 326, 327, 328 and 329 are individually illuminated in time with a cardiac compressions being required. If a compression:breath ratio of 30: 1 is required then, by way of example only, indicator 325 can be illuminated five times, followed by indicator 326 being illuminated five times, followed by indicator 327 being illuminated five times, followed by indicator 328 being illuminated five times, followed by indicator 329 being illuminated five times. After the completion of this sequence, indicator 321 can be illuminated to indicate a lung inflation is now required. As the illuminated compression indicator is successively closer to the indicator 321, this can further alert an emergency response provider of the timing of pending lung inflation relative to a sequence of cardiac compressions.
  • one or more observable indicators can comprise auditory representations as provided by a speaker or piezoelectric 340.
  • the auditory representation may be provided in combination with the visual representation discussed herein.
  • Auditory cues can, by way of example, include set sounds, signals or voice (synthesised or recorded).
  • a timing module 350 is provided for indicating (recording or displaying) any one or more of the following:
  • a power source 331 (typically in the form of a battery) for powering the processor module 130 can be isolated to preserve the life of the power source.
  • the power source is connected to the processor module.
  • Activation can be achieved by removing an insulator placed between a battery terminal and a battery connector.
  • activation can be achieved by having an isolation switch 131. The isolation switch can be operatively associated with removing the cover from the device (as shown in FIG. 5).
  • an attachment element 360, and/or torch 370 can be included.
  • the torch can be separable and have an independent power source.
  • the device can be manufactured to a size suitable for attaching to a key ring.
  • the device having a detachable mini-touch can provide light assistance in an emergency or non emergency situation.
  • FIG. 4 is an example flowchart of a method 400 for indicating the procedural operation of performing cardio pulmonary resuscitation. This method comprises the steps of prompting the user to provide data indicative of the patient though a series of predetermined questions, the data being provided by the user.
  • This method comprises:
  • STEP 421 receiving data indicative of the patient being an adult and/or child and/or infant.
  • STEP 422 receiving data indicative of the number of emergency response providers being one or two.
  • STEP 423 receiving data indicative of the state being that the patient's airway had been checked
  • STEP 424 receiving data indicative of the state being that the patient's breathing had been checked
  • STEP 425 receiving data indicative of the state being that the patient's circulation had been checked
  • STEP 430 determining, in response to the receive data, appropriate rate timing
  • STEP 451 displaying current time
  • STEP 452 displaying duration of emergency response
  • STEP 441 determining if a breath (or lung inflation) is required based on the
  • STEP 442 if appropriate, indicating a breath required (returning to STEP 441);
  • STEP 443 determining if a compression is required based on the determined
  • STEP 444 if appropriate, indicating a compression required (returning to STEP 443);
  • steps 433, 434, and 435 may prompt the user to provide data indicative of any one or more of the set including: the patient airway being clear or not clear, the patient being breathing or not breathing, patient presetting with a pulse or without a pulse; and receiving response data provided by the user.
  • steps 441, 442, 443, and 444 controls at least one output element coupled to the processor module to indicate the rate timing information to a user performing cardio pulmonary resuscitation.
  • a fist observable indicator is controlled at steps 443 and 444 to indicate the rate timing for providing cardiac compressions.
  • a second observable indicator is controlled at steps 441 and 442 to indicate the rate timing for providing lung inflation.
  • Step 443 can further alert of the timing of pending lung inflation relative to a sequence of cardiac compressions.
  • FIG. 5 is an example schematic view of an emergency device 100 having a cover 590.
  • the opening of the cover can activate the device by connecting the power source to the processor module. Activation can be achieved by removing an insulator place between a battery terminal and a battery connector or actuating an isolation switch 131.
  • the cover can also have a pocket 591 for retaining a safety mask (not shown).
  • FIG. 6 is an example schematic view of an emergency device 600 comprising a computer program product for implementing a method, as described herein, for indicating rate timing information to a user in performing an emergence response.
  • a computer-readable carrier medium can carrying a set of instructions that when executed by one or more processors cause the one or more processors to carry out a method, as described herein, for indicating rate timing information to a user in performing an emergence response.
  • a touch screen based computing device has installed a computer program that when executed carries out a method, as described herein, by displaying the input element 110 and an output element 120, a timing device 350.
  • a processor module 130 is coupled to both the input and output elements, and is adapted to receive data indicative of the patient condition from the input element. In absence of a touch screen, input may be provided by made using buttons or a cursor based selection.
  • the processor module is further adapted to control the output element, in response to the receive data, to indicate the rate timing information.
  • the output element 120 includes a plurality of observable indicators (621,622 and 633) for indicating rate timing information to a user performing cardio pulmonary resuscitation.
  • Observable indicators 622 and 623 are indicative of the rate timing for providing cardiac compressions, and indicator 621 is indicative of the rate timing for providing lung inflation.
  • observable indicator 623 is displayed to provide a proximity timing of pending lung inflation relative to a sequence of cardiac
  • one or more observable indicators can comprise auditory
  • auditory representations as provided by a speaker (or piezoelectric element) 640.
  • the auditory representation may be provided in combination with the visual representation discussed herein. Auditory cues can, by way of example, include any one or more of set sounds, signals or voice (synthesised or recorded).
  • an emergency button 680 can be provided to automatically turn on the device and/or initiate execution of the computer program product.
  • pressing the emergency button can also initiate a call to emergency services for obtaining assistance, preferably automatically setting the device to speaker (hands free) mode.
  • the computer program product is an application installed on the device, which is selected for execution by the user of the device.
  • a second output element 690 can also be provided to further provide cues in providing an emergency response.
  • these cues for performing an emergency response can include any one or more of graphic images and/or graphic video and/or displayed text. This can be further combined with one or more observable indicators comprising auditory representations.
  • processing refers to the action and/or processes of a computer or computing system, or similar electronic computing device, that manipulate and/or transform data represented as physical, such as electronic, quantities into other data similarly represented as physical quantities.
  • processor may refer to any device or portion of a device that processes electronic data, e.g., from registers and/or memory to transform that electronic data into other electronic data that, e.g., may be stored in registers and/or memory.
  • a "computer” or a “computing machine” or a “computing platform” may include one or more processors.
  • the methodologies described herein are, in one embodiment, performable by one or more processors that accept computer-readable (also called machine-readable) code containing a set of instructions that when executed by one or more of the processors carry out at least one of the methods described herein.
  • Any processor capable of executing a set of instructions (sequential or otherwise) that specify actions to be taken are included.
  • a typical processing system that includes one or more processors.
  • Each processor may include one or more of a CPU, a graphics processing unit, and a programmable DSP unit.
  • the processing system further may include a memory subsystem including main RAM and/or a static RAM, and/or ROM.
  • a bus subsystem may be included for communicating between the components.
  • the processing system further may be a distributed processing system with processors coupled by a network. If the processing system requires a display, such a display may be included, e.g., a liquid crystal display (LCD). If manual data entry is required, the processing system also includes an input device such as one or more of an alphanumeric input unit such as a keyboard, a pointing control device such as a mouse, and so forth.
  • a display e.g., a liquid crystal display (LCD).
  • LCD liquid crystal display
  • the processing system also includes an input device such as one or more of an alphanumeric input unit such as a keyboard, a pointing control device such as a mouse, and so forth.
  • the term memory unit as used herein, if clear from the context and unless explicitly stated otherwise, also encompasses a storage system such as a disk drive unit.
  • the processing system in some configurations may include a sound output device, and a network interface device.
  • the memory subsystem thus includes a computer-readable carrier medium that carries computer-readable code (e.g., software) including a set of instructions to cause performing, when executed by one or more processors, one of more of the methods described herein.
  • computer-readable code e.g., software
  • the software may reside in the hard disk, or may also reside, completely or at least partially, within the RAM and/or within the processor during execution thereof by the computer system.
  • the memory and the processor also constitute computer-readable carrier medium carrying computer-readable code.
  • a computer-readable carrier medium may form, or be included in a computer program product.
  • the one or more processors operate as a stand alone device or may be connected, e.g., networked to other processor(s), in a networked deployment, the one or more processors may operate in the capacity of a server or a client machine in server-client network environment, or as a peer machine in a peer-to-peer or distributed network environment.
  • the one or more processors may form a personal computer (PC), a tablet PC, a set-top box (STB), a Personal Digital Assistant (PDA), a cellular telephone, a web appliance, a network router, switch or bridge, or any machine capable of executing a set of instructions (sequential or otherwise) that specify actions to be taken by that machine.
  • PC personal computer
  • PDA Personal Digital Assistant
  • machine shall also be taken to include any collection of machines that individually or jointly execute a set (or multiple sets) of instructions to perform any one or more of the methodologies discussed herein.
  • each of the methods described herein is in the form of a computer-readable carrier medium carrying a set of instructions, e.g., a computer program that are for execution on one or more processors, e.g., one or more processors that are part of whatever the device is.
  • a computer-readable carrier medium carrying computer readable code including a set of instructions that when executed on one or more processors cause the processor or processors to implement a method.
  • aspects of the present invention may take the form of a method, an entirely hardware embodiment, an entirely software embodiment or an embodiment combining software and hardware aspects.
  • the present invention may take the form of carrier medium (e.g., a computer program product on a computer-readable storage medium) carrying computer-readable program code embodied in the medium.
  • the software may further be transmitted or received over a network via a network interface device.
  • the carrier medium is shown in an exemplary embodiment to be a single medium, the term “carrier medium” should be taken to include a single medium or multiple media (e.g., a centralized or distributed database, and/or associated caches and servers) that store the one or more sets of instructions.
  • the term “carrier medium” shall also be taken to include any medium that is capable of storing, encoding or carrying a set of instructions for execution by one or more of the processors and that cause the one or more processors to perform any one or more of the methodologies of the present invention.
  • a carrier medium may take many forms, including but not limited to, non- volatile media, volatile media, and transmission media.
  • Non- volatile media includes, for example, optical, magnetic disks, and magneto-optical disks.
  • Volatile media includes dynamic memory, such as main memory.
  • Transmission media includes coaxial cables, copper wire and optics fibre, including the wires that comprise a bus subsystem. Transmission media also may also take the form of acoustic or light waves, such as those generated during radio wave and infrared data communications.
  • carrier medium shall accordingly be taken to included, but not be limited to, solid-state memories, a computer product embodied in optical and magnetic media, a medium bearing a propagated signal detectable by at least one processor of one or more processors and representing a set of instructions that when executed implement a method, a carrier wave bearing a propagated signal detectable by at least one processor of the one or more processors and representing the set of instructions a propagated signal and representing the set of instructions, and a transmission medium in a network bearing a propagated signal detectable by at least one processor of the one or more processors and representing the set of instructions.
  • any one of the terms comprising, comprised of or which comprises is an open term that means including at least the elements/features that follow, but not excluding others.
  • the term comprising, when used in the claims should not be interpreted as being limitative to the means or elements or steps listed thereafter.
  • the scope of the expression a device comprising A and B should not be limited to devices consisting only of elements A and B.
  • Any one of the terms including or which includes or that includes as used herein is also an open term that also means including at least the elements/features that follow the term, but not excluding others. Thus, including is synonymous with and means comprising.
  • Coupled should not be interpreted as being limitative to direct connections only.
  • the terms “coupled” and “connected,” along with their derivatives, may be used. It should be understood that these terms are not intended as synonyms for each other.
  • the scope of the expression a device A coupled to a device B should not be limited to devices or systems wherein an output of device A is directly connected to an input of device B. It means that there exists a path between an output of A and an input of B which may be a path including other devices or means.
  • Coupled may mean that two or more elements are either in direct physical or electrical contact or that two or more elements are not in direct contact with each other but yet still co-operate or interact with each other.
  • an embodiment of the invention can consist essentially of features disclosed herein.
  • an embodiment of the invention can consist of features disclosed herein.
  • the invention illustratively disclosed herein suitably may be practiced in the absence of any element which is not specifically disclosed herein.

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  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medical Informatics (AREA)
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  • Life Sciences & Earth Sciences (AREA)
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  • Percussion Or Vibration Massage (AREA)

Abstract

L'invention concerne un dispositif de secours et un procédé pour indiquer des informations de fréquence à un utilisateur lorsqu'il effectue une intervention d'urgence. Le dispositif comprend un module de processeur, au moins un élément d'entrée couplé au module de processeur et au moins un élément de sortie couplé au module de processeur. Ledit module de processeur est conçu pour recevoir des données indiquant l'état du patient et, en réponse aux données reçues, commander l'élément de sortie afin qu'il indique les informations de fréquence.
PCT/AU2010/001224 2009-09-24 2010-09-20 Dispositif de secours et procédé pour indiquer des informations de fréquence WO2011035366A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AU2009904648 2009-09-24
AU2009904648A AU2009904648A0 (en) 2009-09-24 Emergency Device and Method

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Publication Number Publication Date
WO2011035366A1 true WO2011035366A1 (fr) 2011-03-31

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Citations (4)

* Cited by examiner, † Cited by third party
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US5088037A (en) * 1990-03-23 1992-02-11 Anthony Battaglia Portable rescue administration aid device
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