(19)
(11)EP 3 370 598 B1

(12)EUROPEAN PATENT SPECIFICATION

(45)Mention of the grant of the patent:
20.05.2020 Bulletin 2020/21

(21)Application number: 16759698.0

(22)Date of filing:  17.08.2016
(51)International Patent Classification (IPC): 
A61B 5/00(2006.01)
A61B 5/0205(2006.01)
A61B 5/11(2006.01)
A61B 5/0408(2006.01)
A61B 5/024(2006.01)
(86)International application number:
PCT/EP2016/069546
(87)International publication number:
WO 2017/108215 (29.06.2017 Gazette  2017/26)

(54)

A HEALTH-MONITOR PATCH

GESUNDHEITSMONITOR-PFLASTER

TIMBRE DE SURVEILLANCE DE SANTÉ


(84)Designated Contracting States:
AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

(30)Priority: 23.12.2015 US 201514757584

(43)Date of publication of application:
12.09.2018 Bulletin 2018/37

(73)Proprietor: LUMIRADX UK LTD
London SE1 2AQ (GB)

(72)Inventors:
  • QUINLAN, Thomas
    Stow Massachusetts 01775 (US)
  • GAUDET, Paul
    Dracut Massachusetts 01826 (US)
  • OHLENBUSCH, Norbert
    Andover Massachusetts 01810 (US)
  • ZHANG, Jianwei
    Westborough Massachusetts 01581 (US)
  • OLIVER, Steven
    Attleboro Massachusetts 02703 (US)
  • BLACKADAR, Thomas
    Hanson, MA 02341 (US)
  • MONAHAN, David
    West Chester Pennsylvania 19382 (US)

(74)Representative: HGF Limited 
Cavendish House 39-41 Waterloo Street
Birmingham, West Midlands B2 5PP
Birmingham, West Midlands B2 5PP (GB)


(56)References cited: : 
US-A1- 2007 191 728
US-A1- 2013 261 422
US-A1- 2015 073 231
US-A1- 2013 060 115
US-A1- 2014 206 976
US-A1- 2015 148 637
  
      
    Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention).


    Description

    FIELD



    [0001] The technology relates to wearable devices that are configured to monitor physiological parameters (heart rate, heart rate variability, respiratory rate, etc.) of a subject and/or physical activity performed by the subject.

    BACKGROUND



    [0002] There currently exist small sensing devices that can be worn by a user to monitor physical activity performed by the user. As an example, the FitLinxx® ActiPed+ (available from FitLinxx, Shelton, CT, USA) is a small device that can be clipped to a shoe and used to monitor walking and running activities by the user. When a user walks or runs, an on-board accelerometer outputs data that is stored on the device for subsequent transmission to a computer system. The computer system can analyze the data to determine activity type, and calculate various activity parameters (e.g., duration of activity, total steps, distance traveled, and calories burned). Results of the data analysis may be presented on the computer's display, so that a user may review details of his or her activity. The results may be stored, so that the user can maintain a record of exercise regimens and track progress toward exercise goals, or so that the data may be used by medical personnel to track recovery from an illness or injury. Other modern activity monitors perform similar functions with varying degrees of accuracy. US 2015/0073231 discloses a sensor system comprising a plane member, a plurality of electrodes within the plane member, adapted to contact the human body to detect and monitor human generated voltages. US 2015/0148637 discloses systems, methods and devices for reducing noise in health monitoring.

    [0003] Most activity monitors are configured to be attached to a subject's clothing or strapped to a subject's limb. For example, some activity monitors may clip on clothing, or be configured to clip on or lace in a shoe. Activity monitors that attach to clothing are generally not adapted to sense a physiological parameter of the subject. Some activity monitors that may be worn on the wrist or ankle of a subject may be adapted to sense heart rate, but these monitors generally cannot measure details of cardiac waveform to obtain information such as heart-rate variability (HRV) or cardiac abnormalities such as arrhythmias.

    SUMMARY OF EXAMPLE EMBODIMENTS



    [0004] An adhesive, health-monitor patch that can be adhered to the skin of a subject in the vicinity of the heart is described. In some embodiments, the health-monitor patch comprises a flexible and waterproof strip, and is designed to be worn for extended periods of time. Two monitoring electrodes on the strip may contact the skin of the subject and be used to collect cardiac waveform data. At least a third electrode may be included to suppress electrical noise and improve the quality of data collected by the health-monitor patch. The cardiac waveform data may be analyzed to determine various physiological parameters of a subject, such as heart rate, heart-rate variability, caloric burn, resting heart rate, recovery from a workout, respiratory rate, etc. The health-monitor patch may further include an accelerometer from which acceleration data may be analyzed to determine parameters associated with motion of the subject (e.g., body orientation of the subject, type of activity performed by the subject, intensity of activity performed by the subject, etc.).

    [0005] Some examples of a health-monitor patch may comprise a flexible strip assembly, which may house electrical components of the health-monitor patch, and a replaceable electrode strip that adheres to the flexible strip assembly. The replaceable electrode strip may provide replaceable adhesion and electrical connections between the subject and the flexible strip assembly. Other embodiments of the health-monitor patch may be single-use, disposable strips that include electronics and adhesive layers for attaching to a subject's skin. A disposable health-monitor patch may be a low-cost device suitable for single-use applications, such as for out-patient health monitoring.

    [0006] A health-monitor patch may include an accelerometer, processor, and machine-readable instructions that adapt the health-monitor patch to perform a variety of different functions and data analyses as described, for example, in U.S. Patent Application Pub. No. 2015-0119728 and in U.S. Patent Application Pub. No. 2013-021 7979.

    [0007] According to some examples, a health-monitor patch may comprise a cardiac sensor comprising two monitor electrodes that are configured to receive two signals from two locations on the skin of the subject. A health-monitor patch may further include a noise electrode configured to receive a signal from the skin of the subject at a location separate from the two locations of the two monitor electrodes. A health-monitor patch may further include an electronic assembly comprising a processor configured to process signals from the two monitor electrodes.

    [0008] Some examples relate to methods for operating a health-monitor patch. Some methods of operation may include acts of receiving two electrical signals at two monitor electrodes of the health-monitor patch, wherein the two monitor electrodes contact the skin of a subject and are separated by a distance, conducting electrical signals from the two monitor electrodes over two conductive paths to two signal inputs of an electronic circuit mounted within the health-monitor patch, receiving an electrical signal from a noise electrode that contacts the skin of the subject and is located between the two monitor electrodes, and conducting the electrical signal from the noise electrode to a conductive shield, such as an ESD shield, that extends at least part way over the two conductive paths. The conductive shield may also extend over the electronic circuit.

    [0009] The foregoing and other aspects, embodiments, and features of the present teachings can be more fully understood from the following description in conjunction with the accompanying drawings. The invention is defined by appended claims 1-15.

    BRIEF DESCRIPTION OF THE DRAWINGS



    [0010] The skilled artisan will understand that the figures, described herein, are for illustration purposes only. It is to be understood that in some instances various aspects of the invention may be shown exaggerated or enlarged to facilitate an understanding of the invention. In the drawings, like reference characters generally refer to like features, functionally similar and/or structurally similar elements throughout the various figures. The drawings are not necessarily to scale, emphasis instead being placed upon illustrating the principles of the teachings. The drawings are not intended to limit the scope of the present teachings in any way. The invention is defined by appended claims 1-15.

    FIG. 1A depicts a plan view of a health-monitor patch, according to some examples;

    FIG. 1B depicts an elevation view of a health-monitor patch, according to some examples;

    FIG. 1C depicts an underside view of a health-monitor patch, according to some examples;

    FIG. 2A depicts a plan view of a disposable health-monitor patch, according to some examples;

    FIG. 2B depicts an elevation view of a disposable health-monitor patch, according to some examples;

    FIG. 2C depicts an underside view of a disposable health-monitor patch, according to some examples;

    FIG. 3 illustrates electronic components that may be included in a health-monitor patch, according to some examples;

    FIG. 4 depicts an exploded view of a disposable health-monitor patch, according to some examples;

    FIG. 5 illustrates a noise suppression configuration and conductive adhesive in a circuit of a health-monitor patch, according to some examples;

    FIG. 6 illustrates infused conductors in a flexible strip assembly, according to some examples;

    FIG. 7A depicts an exploded view of components for a replaceable electrode strip, according to some examples;

    FIG. 7B depicts a cross section of a replaceable electrode strip, according to some examples;

    FIG. 8 illustrates a cardiac waveform; and

    FIG. 9 illustrates a cardiac waveform obtained with a health-monitor patch.



    [0011] The features and advantages of the present invention, which is defined by appended claims 1-15, will become more apparent from the detailed description set forth below when taken in conjunction with the drawings.

    DETAILED DESCRIPTION OF EXAMPLE EMBODIMENTS



    [0012] An example embodiment of a health-monitor patch 100 is depicted in FIG. 1A. According to some examples, a health-monitor patch may be formed from flexible materials and configured to adhere to the skin of a person. A health-monitor patch may include at least one accelerometer for sensing motion and/or activities of a subject, and/or may include electrodes, one or more lasers, one or more light-emitting diodes, one or more photodiodes, one or more temperature sensors and/or other sensors for sensing one or more physiological parameters of a subject. The inventors have recognized and appreciated that a flexible patch-type device that having electrodes and/or other sensors that can directly contact a subject's skin can provide more accurate information about a subject's biophysical parameters (such as cardiac waveform, body temperature, respiratory rate, blood oxygenation level, blood glucose level, etc.), which conventional pedometers may not be able to provide. To obtain a reliable cardiac waveform signal, such a patch device is preferably located in the vicinity of a subject's heart and includes two or more electrodes spaced a distance apart. Accordingly, a health-monitor patch is preferably flexible so that it's sensing electrodes can remain in contact with the skin of the subject as the subject moves.

    [0013] The inventors have also recognized and appreciated that a health-monitor patch attached to a subject's torso can provide more reliable information about a subject's position (lying, sitting, standing) than a conventional activity monitor that straps to a subject's wrist or ankle. Torso orientation can be helpful when identifying a type of activity that a subject is performing (e.g., distinguishing rowing from cycling or cycling from running) or identifying a resting state of a subject. Torso orientation can also be helpful when monitoring patients. For example, an increased heart rate accompanied by data indicating the patient has changed from a lying position to a vertical and/or walking orientation may be of no concern, whereas an increased heart rate while the patient remains in a lying position may require the attention of a caregiver.

    [0014] The inventors have further conceived of structures, circuits, processes, and combinations of materials that provide a waterproof health-monitor patch, according to some examples, and a low-cost disposable health-monitor patch, according to some examples. Further details of a health-monitor patch are described below.

    [0015] Referring again to FIG. 1A, a health-monitor patch 100 may include a first end region 110a and a second end region 110b. A health-monitor patch may comprise a flexible strip assembly 105 that may or may not have an open center 120. For examples that include an open center, one or more flexible ribs 107 may connect the first end region 110a and the second end region 110b. For examples that do not have an open center 120, a center portion of the flexible strip assembly 105 may be thin or otherwise configured to provide flexible bending and twisting between the first end region and the second end region. A width W of a health-monitor patch 100 may be between approximately 10 mm and approximately 50 mm, according to some embodiments.

    [0016] An elevation view of a health-monitor patch 100 is depicted in FIG. 1B. In some examples, a health-monitor patch may comprise enlarged lobes at the end regions 110a, 110b as shown in the drawing. Electronics of a health-monitor patch may be housed within the lobes. An overall length L of a health-monitor patch 100 may be between approximately 50 mm and approximately 150 mm. A height H of a health-monitor patch may be between approximately 3 mm and approximately 10 mm. The flexible strip assembly may comprise a flexible polymer such as, but not limited to, silicone.

    [0017] According to some examples, a replaceable electrode strip 150 may be adhered, temporarily, to a lower surface of a health-monitor patch 100, as depicted in FIG. 1B. The replaceable electrode strip may provide adhesion, electrical connections, and a waterproof seal between the flexible strip assembly and the skin of a subject. The replaceable electrode strip may be peeled off of the lower surface of the flexible strip assembly 105 and replaced with a new replaceable electrode strip 150. For example, a user may adhere a health-monitor patch 100 to their skin for a period of time (e.g., one or several days, a week, or more), and then remove the health-monitor patch, replace the replaceable electrode strip 150, and then re-adhere the health-monitor patch to their skin for continued monitoring of activity and physiological parameters.

    [0018] A bottom-side or skin-side view of a health-monitor patch having a replaceable electrode strip 150 is illustrated in FIG. 1C, according to some embodiments. The replaceable electrode strip may include an adhesion surface 152 configured to adhere to a subject's skin. The replaceable electrode strip may comprise two or more electrodes 160a, 160b that provide electrical contact to the subject's skin, and electrically connect with electronic circuitry inside the flexible strip assembly 105. In some examples, a first monitor electrode 160a is located at a first end of the replaceable electrode strip 150, and a second monitor electrode 160b is located at a second end of the replaceable electrode strip. A distance D between the first monitor electrode and second monitor electrode may be between approximately 50 mm and approximately 90 mm. The first monitor electrode 160a and second monitor electrode 160b may comprise hydrogel electrodes in examples, or may comprise other flexible electrodes for contacting a subject's skin. A width of the replaceable electrode strip 150 may be between approximately 10 mm and approximately 50 mm, according to some examples.

    [0019] In some cases, there may be one or more noise electrodes 170 located separately from the first monitor electrode 160a and the second monitor electrode 160b. As shown, in some examples, the noise electrode(s) 170 may be located between the monitor electrodes 160a, 160b. A noise electrode may also comprise a hydrogel electrode or other flexible electrode. For some implementations, a noise electrode 170 may be located approximately half-way between the first monitor electrode and the second monitor electrode. In other examples, one or more noise electrodes may be placed closer to one or the other of the first monitor electrode and second monitor electrode or at other locations on the strip 150. A noise electrode may provide an electrical contact to the skin of a subject and further connect electrically to noise cancellation circuitry within the flexible strip assembly 105.

    [0020] A second example embodiment of a health-monitor patch is depicted in FIG. 2A. As shown, in some embodiments, a disposable health-monitor patch 200 may comprise a flexible strip assembly 205 that includes a first end region 210a and a second and region 210b. The length L and width W of a disposable health-monitor patch 200 may be of approximately the same corresponding dimensions for a health-monitor patch 100 described above in connection with FIG. 1A. Referring to FIG. 2B, a disposable health-monitor patch 200 may have a lower profile, and a height that is between approximately 2 mm and approximately 8 mm. A flexible strip assembly 205 may be more uniform in height along its length, and formed from a plurality of flexible layers of materials. In some examples, it may include bulged end regions 210a, 210b that accommodate the device's electronics (e.g., a PCB assembly and battery).

    [0021] A disposable health-monitor patch 200 may not have a replaceable electrode strip 150, but may include an adhesion surface 252. A disposable health-monitor patch 200 may have a release liner (shown in FIG. 7A) located over the adhesion surface 252 that may be removed just prior to adhesion of the disposable health-monitor patch to the skin of a subject. A disposable health-monitor patch may operate between approximately one day and approximately 14 days on a subject, and then be removed and disposed.

    [0022] A plan-view illustration of an adhesion surface 252 of a disposable health-monitor patch 200 is depicted in FIG. 2C, according to some embodiments. The adhesion surface 252 may accommodate a first monitor electrode 260a and a second monitor electrode 260b. The monitor electrodes may be separated by a distance between approximately 50 mm and approximately 90 mm, according to some implementations. Between the monitor electrodes, or at some other location on the adhesion surface 252, there may be one or more noise electrodes 270. The monitor electrodes may provide an electrical connection to the patient's skin and to sensing and data analysis circuitry within the disposable health-monitor patch. The one or more noise electrodes may provide electrical connection to the subject's skin and to noise cancellation circuitry within the disposable health-monitor patch 200. In some examples, there may be one or more openings through the adhesion surface 252 for radiation to pass through from one or more light-emitting devices 286 (e.g., laser(s), LED(s)), and for backscattered light to pass through to one or more photodiodes 287.

    [0023] In operation, a health-monitor patch may collect physiological data (e.g., cardiac data, temperature data, blood oxygenation data, etc.) and/or motion data (e.g., accelerometer data) from one or more of its sensors. In some examples, some of the data may be processed or pre-processed by an on-board processor of the health-monitor patch. In some implementations, collected data may be offloaded to a remote device (e.g., a smart phone, a laptop, a tablet, a computer, etc.) which may process the collected data. Data accumulated on a health-monitor patch may be downloaded via a wireless connection. Examples of data processing and data transfer are described in further detail in U.S. Patent Application Pub. No. 2015-0119728.

    [0024] FIG. 3 depicts some components and an example circuit 300 that may be implemented in a health-monitor patch, according to some examples. As shown, a health-monitor patch's circuitry may, for example, comprise a source of power 305 (e.g., at least one battery or energy-scavenging chip and a wake-up and power-management circuit 350) that provide and manage power delivery to one or more of an accelerometer 330, a digital processor 310, memory 320, and a transceiver 340. The processor 310 may be coupled to one or more of the wake-up circuit, the accelerometer, memory, and the transceiver. The power source 305 and/or processor 310 may be coupled to additional components, such as one or more physiological sensors 354.

    [0025] The term "digital processor" or "processor" as used herein may refer to at least one microcontroller, microprocessor, digital signal processor (DSP), application-specific integrated circuit (ASIC), field-programmable gate array (FPGA), or data-processing logic circuitry. "Digital processor" or "processor" may also be used to refer to any combination of the foregoing digital processing devices, including more than one of a particular data processing device.

    [0026] The processor may be configured to receive and process data from one or more sensors on the health-monitor patch (e.g., from the accelerometer 330 and/or one or more physiological sensors 354). The processor 310 may further be configured to read and write data to memory 320, and to send and receive data from transceiver 340. The wake-up circuit 350 may be adapted to sense when the health-monitor patch is not in use, and in response, reduce power consumption of the internal circuit 300, according to some examples. The wake-up circuit may be further adapted to sense when the health-monitor patch is placed in use, and in response, activate one or more elements of the internal circuit 300.

    [0027] In some examples, the processor 310 may, for example, comprise a low-power, 8-bit processor configured to draw low power in sleep-mode operation, and capable of operating at multiple millions of instructions per second (MIPS) when activated. One example of a suitable processor is the 8051F931 processor available from Silicon Laboratories Inc. of Austin, Texas. Another example of a processor is the nRF51822 processor available from Nordic Semiconductor of Oslo, Norway, though any other suitable processor or microprocessor may alternatively be employed in other examples. In some implementations, the processor 310 may support radio-frequency communications with other devices. A balun (e.g., BAL-NRF02D3 available from ST Microelectronics of Geneva, Switzerland) may be used to match RF signals between an antenna and the processor, according to some examples.

    [0028] The processor 310 may, for example, include various types of on-board memory (e.g., flash memory, SRAM, and XRAM) for storing data and/or machine-readable instructions, and may be clocked by an internal oscillator or external oscillator. In some examples, the processor may be clocked by an internal high-frequency oscillator (e.g., an oscillator operating at about 25 MHz or higher) when the processor is active and processing data, and alternatively clocked by a low-frequency oscillator (external or internal to the processor) when the processor is substantially inactive and in sleep mode. The clocking of the processor at low frequency may reduce power consumption by the processor during sleep mode. The low-frequency clocking may be at a frequency that is less than 50% of the high-frequency clocking in some examples, less than 20% of the high-frequency clocking in some examples, less than 10% of the high-frequency clocking in some examples, less than 5% of the high-frequency clocking in some examples, less than 2% of the high-frequency clocking in some examples, less than 1% of the high-frequency clocking in some examples, and yet less than 0.1% in some examples .

    [0029] In various examples, the processor 310 may be configured to receive acceleration data from accelerometer 330 and process the received data according to preprogrammed machine-readable instructions that are loaded onto and execute on the processor. The processor 310 may be configured to receive analog and/or digital input data, and may include on-board analog-to-digital and digital-to-analog converters and on-board timers or clocks. According to some examples, the processor may also be configured to receive and analyze cardiac waveform data from electrodes in contact with a user's skin. In some examples, the processor may be further configured to receive power through wake-up and power management circuitry 350. The processor may, in some examples, cooperate with or comprise a portion or all of power management circuitry 350, and facilitate activating and deactivating one or more circuit elements within the health-monitor patch.

    [0030] In some examples, the processor 310 may be configured to operate at a number of different clock frequencies. When operating at a low clock frequency, the processor will typically consume less power than when operating at a high clock frequency. In some examples, the processor may be configured to be in a "sleep" mode and operating at a low clock frequency when there is no motion of health-monitor patch, and to be cycled through several operating states when motion of the health-monitor patch is detected. As one example, when in sleep mode, the processor may sample data at a rate less than 10 Hz and draw less than about 30 microamps.

    [0031] In some examples, accelerometer 330 may, for example, comprise a multi-axis accelerometer and/or gyroscopes configured to sense acceleration along at least two substantially orthogonal spatial directions. The accelerometer 330 may comprise a three-axis accelerometer based on micro-electro-mechanical systems (MEMS) technology. In some implementations, one or more single-axis accelerometers may additionally or alternatively be used. In some embodiments, the accelerometer 330 may be configured to provide one or more analog data-stream outputs (e.g., X, Y, Z data outputs corresponding to each axis of the accelerometer) that are each representative of a magnitude and direction of acceleration along a respective axis. One example of a suitable accelerometer is the Kionix model KXSC7 accelerometer available from Kionix Inc., Ithaca, New York. Another example of a suitable accelerometer is the LIS2DH accelerometer available from ST Microelectronics of Geneva, Switzerland. The accelerometer 330 may provide analog output data, that may later be converted to digital data, or may provide digital output data representative of acceleration values.

    [0032] The accelerometer 330 may be characterized by several parameters. Among these parameters may, for example, be a sensitivity value and a sampling rate value. The accelerometer's analog sensitivity may be between about 100 millivolts (mV) per gravitational value (100 mV/G) and about 200 mV/G in some examples, between about 200 mV/G and about 400 mV/G in some examples, between about 400 mV/G and about 800 mV/G in some examples, and yet between about 800 mV/G and about 1600 mV/G in some examples. When configured to provide a digital output, the sampling rate of the accelerometer may be between about 10 samples per second per axis (10 S/sec-A) and about 20 S/sec-A in some examples, between about 20 S/sec-A and about 40 S/sec-A in some examples, between about 40 S/sec-A and about 80 S/sec-A in some examples, between about 80 S/sec-A and about 160 S/sec-A in some examples between about 160 S/sec-A and about 320 S/sec-A in some examples, and yet between about 320 S/sec-A and about 640 S/sec-A in some examples. It will be appreciated that in some examples the higher sampling rates may improve the quality of the measured accelerations.

    [0033] It will be appreciated that, in some examples, an accelerometer 330 may be combined with one or more analog-to-digital converters to provide digital output data representative of acceleration values at sampling rates described above. When digital output data is provided by an accelerometer, the accelerometer's sensitivity may be expressed in units of bits per gravitational constant (b/G). As examples, an accelerometer providing digital output data may have a sensitivity of more than about 2 b/G in some examples, more than about 4 b/G in some examples, more than about 6 b/G in some examples, more than about 8 b/G in some examples, more than about 10 b/G in some examples, more than about 12 b/G in some examples, or even higher values in some examples.

    [0034] According to some examples, a health-monitor patch may include one or more sensors in addition to motion sensor 352 and accelerometer 330. For example, a health-monitor patch may include at least one physiological sensor 354 (e.g., cardiac sensor, temperature sensor, blood glucose sensor, blood oxygenation sensor, etc.) configured to sense at least one physiological parameter of a subject. A physiological sensor may comprise one or more electrodes configured to provide electrical connection to the skin of a subject in some examples. Other components that may be used in a physiological sensor include, but are not limited to, pressure transducers, acoustic transducers, temperature sensing elements (e.g., thermistors, infrared sensors), light sources (e.g., LEDs or laser diodes), and photodetectors.) One illustrative example of a physiological sensor comprises the AD8232 ECG chip available from Analog Devices, Inc. of Norwood, Massachusetts. Such a chip may be combined with electrodes arranged to contact the skin of a subject.

    [0035] A physiological sensor 354 may include various signal-processing electronics and associated circuitry. For example, a physiological sensor 354 may comprise input amplifiers and noise filters that process received signals from monitoring electrodes or other detectors. Input amplifiers may include low-noise amplifiers and differential amplifiers. A physiological sensor 354 may be disposed, at least in part, in a same package with a health-monitor patch in some implementations, or may be formed as a separate monitor to be attached to the subject at a separate location and wirelessly, or via a wired link, transmit data to the health-monitor patch according to a predetermined communication protocol. In some implementations, a portion (e.g., a signal processing portion) of a physiological sensor may be incorporated on a printed circuit board assembly of a health-monitor patch, whereas electrodes or detectors for the sensor may be located off the PCB assembly. In some cases, a central processor of a health-monitor patch may comprise a portion of a physiological sensor and process signals from electrodes or other detectors to determine one or more physiological parameters. Examples of physiological parameters that may be sensed by one or more physiological sensors 354 include, but are not limited to, cardiac waveform, heart rate, heart-rate variability, arrhythmia, skin temperature, core temperature, respiration rate, plethysmography waveform, EKG waveform, blood oxygenation level, blood glucose level, hydration, blood pressure, etc.

    [0036] In some examples, a health-monitor patch may include memory 320 that is external to and accessible to the processor 310. The memory 320 may be any one of or combination of the following types of memory: RAM, SRAM, DRAM, ROM, flash memory. The memory 320 may, for example, be used to store and/or buffer raw data from accelerometer 330 and/or physiological sensor 354, machine-readable instructions for processor 310, program data used by the processor for processing accelerometer data and/or physiological data, and/or activity data representative of an activity. In some embodiments, the memory 320 may additionally or alternatively be used to store diagnostic information about the health of the health-monitor patch, e.g., battery life, error status, etc., and/or technical information about the device, e.g., memory size, gravitational sensitivity, weight, battery model, processor speed, version of operating software, user interface requirements, etc. In some examples, the memory may also be used to store information pertinent to a user, e.g., user weight, height, gender, age, training goals, specific workout plans, activity-specific data for a user that may be used to identify an activity performed by the user or process data representative of an identified activity. According to some examples, the memory 320 may store tables of metabolic equivalents (METs), calibration values, and health guideline data that is used to determine health benefit levels for various activities.

    [0037] In some examples, the memory 320 may additionally or alternatively be used to store data structures and/or code received from an external device, e.g., via a wired or wireless link. The data structures and/or code may be used to update one or more data processing applications used by the health-monitor patch. For example, one type of data structure may be data representative of an activity data pattern that may be used to identify a specific type of activity not previously recognized by the health-monitor patch, e.g., a new activity or an activity that is specific to an individual user of the health-monitor patch. As another example, a data structure may comprise a membership function, described below, defined for a new activity or redefined for an identifiable activity. According to some examples, the data structure may include one or more sample accelerometer traces and physiological data obtained during performance of the activity and/or may comprise identification data (e.g., membership functions) resulting from the processing of the accelerometer traces that may be used in an algorithm executed by the health-monitor patch to identify the activity. Further, in some examples, the memory 320 may be used to store updates and/or replacements to algorithms executed by the health-monitor patch. The stored data structures and algorithms may be used to reprogram and/or expand the functionality of the health-monitor patch to identify new activities or activities not previously recognized by the health-monitor patch and/or improve the accuracy or confidence of results calculated for identified activities.

    [0038] In some examples, the memory 320 may also be used to store calibration and/or conversion data that is used by the processor 310 to characterize detected activities. Calibration data may be used to improve the accuracy of detected activity parameters (e.g., stride length, speed), and/or improve the accuracy of fitness metrics computed from detected activities. Conversion data may, for example, be used to convert a detected activity into an amount of expended human energy, e.g., calories burned, metabolic equivalents, etc.

    [0039] According to some examples, a health-monitor patch may include a transceiver 340 and/or one or more data communication ports (e.g., a USB port, an RF communication port, a Bluetooth port) for communicating data between the health-monitor patch and one or more external devices such as a computer, tablet, cell phone, portable communication device, data processor, a sensor, another intelligent sensor, or a versatile sensor, any of which may be configured to communicate with other similar devices in a network such as the world-wide web or a local area network. A health-monitor patch may, for example, be configured to communicate via the transceiver 340 through a wired or wireless port to any device or combination or devices selected from the following list: a personal computer, laptop computer, tablet computer, PDA, a watch, an MP3 player, an iPod, a mobile phone, a medical device such as a blood glucose meter, blood pressure monitor, or InR meter, an electronic interactive gaming apparatus, intelligent training equipment, and an automobile system. Data retrieved from the memory 320 or to be stored in memory may, for example, be communicated between the health-monitor patch and an external device via the transceiver 340. In some examples, data transmitted from the health-monitor patch may be configured for routing to a data service device adapted to process data received from a health-monitor patch.

    [0040] In some examples, power for the internal electronics of a health-monitor patch may be provided by at least one battery 305 and managed by a wake-up and power-management circuit 350. The battery may be small, e.g, a button-cell type, and may, for example, comprise one or more lithium-type batteries that may be rechargeable or replaceable. As just one example, a single lithium coin or button-cell, 3-volt battery having a capacity of about 230 mAh may be used (model CR2032 available from Renata SA of Itingen, Switzerland). Another example of a health-monitor patch may include one or more model CR1616 batteries, though any suitable type of battery may alternatively be used in various examples. In some examples, a health-monitor patch may include power-generation or energy-harvesting hardware (e.g., a piezo-electric material or electric generator configured to convert mechanical motion into electric current, a solar cell, an RF or thermal converter). Power that is generated on board may be stored in a battery or charge-storage component such as a super capacitor. In some implementations, generated electrical current may be provided to a storage component via a diode bridge. One example of a suitable energy harvesting device is a microenergy cell MEC225 available from Infinite Power Solutions, Inc. of Littleton, Colorado. In some examples, power generation components may be used in combination with a rechargeable battery as a source of power for a health-monitor patch. A voltage regulator chip (e.g., TPS78001 available from Texas Instruments of Dallas, Texas) may be used to condition power from at least one power source before delivering the power to components of a health-monitor patch, according to some embodiments.

    [0041] According to some examples, a battery 305 of a health-monitor patch may be recharged wirelessly. For example, a health-monitor patch may include a conductive coil that can inductively couple electromagnetic energy from an alternating magnetic field. Current from the coil may be provided to a rectifying circuit that converts the alternating current into a direct current that can be used to charge a battery 305.

    [0042] In some implementations, wake-up and power-management circuitry 350 may include a motion sensor 352 that, in combination with the wake-up and power-management circuitry 350, identifies when a health-monitor patch is being moved in a manner that may be representative of an activity to be monitored. The wake-up and power-management circuitry 350 may, for example, comprise logic and control circuitry to enable, disable, reduce and/or increase power to various circuit elements shown in FIG. 3. Logic and control circuitry for the wake-up and power-management circuitry may, for example, comprise machine-readable instructions and utilized hardware of the processor 310, or may comprise machine-readable instructions and utilized hardware of an application specific integrated circuit.

    [0043] In some examples, the motion sensor 352 may comprise one or more force sensitive switches, e.g., a piezo element configured to generate an electric signal representative of an amount of acceleration that a health-monitor patch experiences. In other examples, the motion sensor 352 may additionally or alternatively comprise one or more contact switches that close a circuit, or open a circuit, when the health-monitor patch is subjected to an acceleration, e.g., a "ball-in-tube" switch. Wake-up may, for example, be initiated when a frequency of switch closures exceeds a pre-selected value. In other examples, the sensor 352 may additionally or alternatively comprise one or more force-sensitive contact switches that close only when a health-monitor patch undergoes acceleration in excess of a pre-selected value.

    [0044] According to some examples, a health-monitor patch may include an electro-optic display (e.g., a liquid-crystal display, an OLED display, one or more LEDs) and be configured to recognize one or more tapping sequences and/or motion gestures (e.g., moving the device in a figure-8 pattern, a circle pattern, a back-and-forth linear pattern). Responsive to recognition of a tapping sequence or gesture, a health-monitor patch may activate the display to communicate information or a summary of information stored on the patch. A tapping sequence or gesture may correspond to a particular information query, to which the health-monitor patch may respond by indicating with the display relevant information. According to one example, the health-monitor patch may be tapped in a particular manner, and in response activate a number of LEDs to indicate that a user has reached an approximate percentage of an activity goal (e.g., illuminating 8 of 10 LEDs to signal approximately 80%). An activity goal may be preprogrammed into the health-monitor patch by a user of physician using another electronic device such as a computer or smart phone that can communicate wirelessly with the health-monitor patch. Information about progress toward one or more activity goals can be communicated by the device (e.g., walked 30% of a goal of 3 miles, ran 60% of a goal of 8 miles, swam 90% of a goal of 60 laps, achieved 70% of creditable health-beneficial activity for the day, achieved 50% of a recommended number of health credits for a week, etc.) A display may also be used to communicate other information responsive to particular tapping sequences or gestures, e.g., battery life, pace comparison (ahead of, or behind, best pace for an activity), heart rate, calories burned, etc.

    [0045] Data may also be communicated to and from a health-monitor patch using a wireless communication protocol (e.g., Bluetooth, BluetoothLE, Bluetooth Smart, a modified Bluetooth protocol, Wi-Fi, etc.). For example, a wireless transceiver and antenna may be included with a health-monitor patch and used to transmit and receive data to and from a remote device such as a smart phone, smart watch, computer, tablet, etc.

    [0046] According to some examples, a health-monitor patch may include at least one light source 286 and at least one photodetector 287. The at least one light source and photodetector may be used, for example, for sensing one or more physiological parameters of a subject, e.g., blood oxygenation level, plethysmography waveforms, blood glucose level, blood flow rate, etc. In some examples, the light source 286 may comprise a high-brightness infrared (IR) photodiode and a shorter wavelength photodiode. In recent years, progress in indium-gallium-nitride LED technology has yielded devices with both lowered junction voltage and increased radiated intensity. Using InGaN technology, and applying power management techniques described in U. S. patent application No. 13/840,098, to which this application claims priority, may provide a health-monitor patch capable of measuring heart rate and/or other physiological parameters that can run for a week or more on one or more coin-cell silver-oxide batteries. The photodetector 287 may be any suitable photodetector (e.g., one or more silicon photodiodes that may include a wavelength filter), and may be mounted to detect light from the light source that is scattered or reflected from the subject.

    [0047] FIG. 4 depicts an exploded view of a disposable health-monitor patch 400, according to some examples. A flexible strip assembly of a disposable health-monitor patch may include a first PCB assembly 405, a battery 305, and a plurality of flexible materials. At least some of the flexible materials or layers may comprise a sheet formed from solid material (e.g., a plymer film, cloth, polymer or cloth mesh, etc.) that provides tensile strength and shape retention for a health-monitor patch. For example, one or more layers may comprise flexible adhesive tape or films. Some layers may be deposited as a liquid or gel, according to some examples. In some cases, the PCB assembly may comprise a flexible PCB.

    [0048] According to some examples, a battery strap 445 may provide a connection between a first terminal of the battery 305 (e.g., the positive terminal) and a battery conductor 480. The battery strap and conductor may be formed from a conductive metal and/or conductive polymer (e.g., a conductive carbon vinyl film which may or may not be coated with a film comprising silver. The battery 305 may be a coin-cell type battery having a diameter between about 10 mm and about 20 mm, and may be located adjacent to an insulating ring 410 that helps to electrically isolate the two terminals of the battery. A second terminal of the battery may electrically connect to a noise/ground conductor 470. The noise/ground conductor may also connect to a noise electrode 270 on the disposable health-monitor patch 400. According to some implementations, the noise/ground conductor 470 may further connect to a ground contact (not shown) located on the PCB assembly 405.

    [0049] There may be additional conductors that connect to the monitor electrodes of a disposable health-monitor patch. For example a first monitor conductor 460a may provide electrical connection between a first monitor electrode 260a and a first signal input pad (not shown) of the PCB assembly 405. A second monitor conductor 460b may provide electrical connection between a second monitor electrode 260b and a second signal input pad (not shown) on the PCB assembly 405. The first monitor conductor 460a, the second monitor conductor 460b, the battery conductor 480, and the noise/ground conductor 470 may be formed from a conductive polymer which may or may not be adhesive. In some examples these conductors may be formed from a carbon vinyl polymer or coated vinyl polymer. An example of a coated vinyl polymer that may be used for a flexible conductor is model 6355, available from Coveris Advanced Coatings of Matthews, North Carolina. In some implementations, one or more of the conductors may be formed from a flexible PCB. In some examples, the first monitor conductor 460a, the second monitor conductor 460b, the battery conductor 480, and the noise/ground conductor 470 may be cut or punched from a film of the conductive polymer.

    [0050] Below the conductors may be a conductor adhesion layer 425 to which the conductors may be adhered. The conductor adhesion layer 425 may retain the conductors in place as the disposable health-monitor patch flexes on a subject. In some examples, the conductor adhesion layer 425 may be a silicone adhesive layer that is electrically insulating. According to some implementations, the conductor adhesion layer 425 may have adhesive surfaces on opposing sides (e.g., double-sided adhesive). An example of a conductor adhesion layer 425 is model 96022 silicone adhesive, available from 3M Corporation of St. Paul, Minnesota. According to some examples, the conductor adhesion layer 425 may be cut and/or punched from a film of the adhesive material.

    [0051] According to some examples, there may be conductive adhesive elements 415 located above the battery and signal conductors. The conductive adhesive elements may have adhesion surfaces on opposing sides. These elements may be formed in a similar shape to the conductors 460a, 460b, 470, 480 from a flexible conductive adhesive film. The conductive adhesive elements 415 can provide electrical connection between the underlying conductors and contact pads on the PCB assembly and terminals on the battery 305. The conductive adhesive elements 415 can also adhere the underlying conductors, PCB assembly, and battery together into a flexible assembly. A conductive adhesive element may be formed from adhesive film, model 9719, available from 3M Corporation of St. Paul, Minnesota, according to some examples. The conductive adhesive elements 415 may be cut or punched from a film of conducting adhesive.

    [0052] In some cases, an insulating layer 430 may be located below the conductor adhesion layer 425. The insulating layer 430 may provide some stiffness to the lower layers and help retain the monitor electrodes 260a, 260b and the noise electrode 270. In some cases, insulating layer 430 may comprise a foam material having an adhesive surface on one side, an example of which is model 1774W, available from 3M Corporation of St. Paul, Minnesota. The adhesive surface may be facing the conductors 460a, 460b, 470, 480, for example. The insulating layer 430 may be cut or punched from a film of the material.

    [0053] In some examples, there may be a surface adhesion layer 435 that adheres to the insulating layer 430. An example of a surface adhesion layer 430 is model 96022 silicone adhesive, available from 3M Corporation of St. Paul, Minnesota, though other suitable adhesion layers may be used. According to some embodiments, the surface adhesion layer 430 may be cut and/or punched from a film of the adhesive material.

    [0054] According to some aspects, a skin adhesion layer 490 may be attached to the insulator layer 430. The skin adhesion layer 490 may include an adhesion surface 252 that provides a durable adhesion to the skin of the subject. Any suitable skin adhesive material may be used for the skin adhesion layer 490. According to some examples, a suitable acrylic skin adhesive available from Avery Dennison of Glendale, California may be used as a skin adhesion layer 490. One example of a skin adhesion layer 490 is a Tegaderm adhesive, model 1626W, available from 3M Corporation of St. Paul, Minnesota, though other biocompatible adhesion layers may be used. In some implementations, a hydrocolloid adhesive, model H011, available from Adhesive R&D of Eau Claire, Wisconsin may be used for the skin adhesion layer. A skin adhesion layer 490 may include a release liner (not shown) over the adhesion surface, that is removed prior to adhering the disposable health-monitor patch 400 to a subject. An example release liner is model 1361 liner, available from 3M Corporation of St. Paul, Minnesota. In some implementations, a skin adhesion layer 490 may be cut and/or punched from a film of the material.

    [0055] Upper layers of a disposable health-monitor patch 400 may include an insulating adhesive layer 450 and an electrostatic discharge (ESD) shield 455 that extend over the battery 305, the PCB assembly 405, and a majority of the conductive adhesive elements 415. In some cases, there may be a hole or notch in the insulating adhesive layer 450 that allows the noise/ground conductor 470 to electrically connect to the ESD shield 455, which may be located adjacent to the insulating adhesion layer 450. The insulating adhesive layer 450 may have adhesive surfaces on opposing sides, or may have a single adhesive surface. An example insulating adhesive layer is adhesive model 9474LE, available from 3M Corporation of St. Paul, Minnesota, though other insulating adhesive layers may be used in other examples. An example double-sided, insulating, adhesive layer aving different adhesion properties on opposing sides (e.g., a differential adhesive) include adhesive model 9425, available from 3M Corporation of St. Paul, Minnesota. The insulating adhesive layer 450 may be cut and/or punched from a film of the adhesive material.

    [0056] In some examples, an ESD shield 455 may extend over at least a portion of the first monitor conductor 460a and at least a portion of the second monitor conductor 460b. The ESD shield may further electrically connect to the noise electrode 270 via the noise/ground conductor 470. The ESD shield may be insulated from the first monitor conductor and the second monitor conductor, but be located in close proximity (e.g., less than about 2 mm) to the two conductors (e.g., arranged as parallel plates in some locations). The ESD shield may be formed from a conductive polymer, according to some examples. An example conductive polymer is coated carbon vinyl film, model 6355, available from Coveris Advanced Coatings of Matthews, North Carolina, though uncoated conductive films may be used.

    [0057] According to some examples electrical noise transmitted across the skin of the subject may be picked up by the noise electrode 270 and conducted to the ESD shield 455. This noise may then couple into the first monitor conductor 460a and the second monitor conductor 460b from the ESD shield due to the close proximity of the ESD overlying the first monitor conductor 460a and second monitor conductor 460b. In some examples, the amount of signal coupled to each monitor electrode may have similar amplitudes (e.g., within about ± 15 %). A differential amplifier may be arranged at a signal input of the PCB assembly 405 to amplify signals received from the first monitor electrode 260a and second monitor electrode 260b. Since the noise is coupled into the two conductors and inputs of the differential amplifier, it may be reduced or cancelled via common-mode rejection.

    [0058] According to some examples, there may be an adhesive cover layer 402 attached over the ESD shield 455 that covers the disposable health-monitor patch 400. The adhesive cover layer 402 may comprise cloth, foam, a flexible polymer (such as silicone), or any other suitably flexible material. In some examples, a cover layer 402 may comprise a second layer of the same material used for the insulating layer 430. The cover layer may be cut or punched from a film of the material. In some instances, the cover layer 402 and insulating layer 430 may comprise sealed foam or a suitable water resistant or waterproof material to reduce ingress of water to the PCB assembly 405 and battery 305.

    [0059] Some components of a disposable health-monitor patch are depicted in the elevation view of FIG. 5, according to some examples. The depiction shows a PCB assembly 405 that connects to the first monitor electrode 260a via a conductive adhesive element (depicted as a gray line) and the first monitor conductor 460a. The PCB assembly 405 also electrically connects to the second monitor electrode 260b via a conductive adhesive element (gray line) and the second monitor conductor 460b. The battery 305 and its conductors are not depicted in FIG. 5 to simplify the drawing.

    [0060] In some implementations, the ESD shield 455 is disposed over the PCB assembly 405, the first monitor conductor 460a, and the second monitor conductor 460b. There may be an insulating adhesion layer 450 between the ESD shield 455 and the conductive adhesive elements. The insulating layer may include an opening 452 (also depicted in FIG. 4) between the ESD shield 455 and the conductive adhesive element 415 that is located over the noise/ground conductor 470. The opening allows an electrical connection to be made between the ESD shield 455 and the noise electrode 270 when the layers of the health-monitor patch are all pressed together.

    [0061] Further details of a repeated-use health-monitor patch 100 are depicted in the elevation view of FIG. 6, for some implementations. The illustration shows an arrangement of components for the device illustrated in FIGS. 1A-1C, according to some examples. Within the flexible strip assembly 105, there may be a PCB assembly 405 and a battery 305. The flexible strip assembly 105 may further include conductive elements (not all shown) that provide electrical connection between terminals of the battery and power/ground pads on the PCB assembly and one or more noise electrodes or sensing components, and between signal inputs on the PCB assembly and monitor electrodes 160a, 160 b. The noise electrode and monitor electrodes may be located on the replaceable electrode strip 150, which is shown separated from the flexible strip assembly.

    [0062] According to some 2. examples, there may be electrical onnections between various components of a health-monitor patch. For example, a patterned flexible PCB may be used to form electrical connections between a monitor electrode and a PCB assembly 405. The inventors have recognized and appreciated that linkages between a flexible conductor (e.g., a flexible PCB) and a more rigid electrical component (e.g., a PCB assembly 405) can be improved by adding strain-relief material at an interface of the flexible conductor. For example, silicone, polyimide, or a thermal set adhesive may be added to reinforce and provide strain relief at a junction between a flexible conductor and a more rigid electrical component.

    [0063] In some examples, the flexible strip assembly 105 may be formed in part from flexible silicone. For example, the silicone may be applied in gel or liquid form into a mold to cover electronic components of a health-monitor patch. The resulting silicone casing 605 may extend entirely around the battery 305, the PCB assembly 405, and the associated conductors. The silicone may then be cured, so that the assembly 105 can be highly flexible and completely waterproof. A waterproof enclosure may allow the health-monitor patch to be worn on a subject and immersed in water. Further, adhesives used for the replaceable electrode strip 150 form watertight seals with the silicone casing 605 and skin of a subject. The inventors have recognized and appreciated that conventional activity monitors that sense heart rate do not perform well or at all when immersed in water. The silicone enclosure may allow the health-monitor patch to monitor activity and physiological parameters of a swimmer, surfer, windsurfer, kiteboarder, etc.

    [0064] Since, in some implementations, the on-board battery may be fully encased in silicone, wireless charging may be used to recharge the on-board battery. In some examples, a coil and rectifying circuit may be included in a health-monitor patch so that electromagnetic energy may be wirelessly coupled to the coil from a wireless charger. Energy coupled to the coil may be rectified and used to charge the battery.

    [0065] Although silicone provides a flexible and robust environmental seal, it is an electrical insulator. The inventors have conceived of locally modifying the silicone so that electrical connection through the silicone to the monitor and noise electrodes of the replaceable electrode strip 150 can be achieved. According to some examples, the electrical connections do not require metal wires or inflexible metal pads at the surface of the silicone casing 605.

    [0066] According to some examples, the silicone casing may be infused with carbon or other conductive materials at surface locations that correspond to locations of the monitor electrodes 160a, 160b and noise electrode(s) 170 on the replaceable electrode strip 150. For example, the flexible strip assembly 105 may include a first infused monitor electrode 660a and a second infused monitor electrode 660b. The flexible strip assembly may further include one or more infused noise electrodes 670.

    [0067] The carbon-infused electrodes may be formed, according to some examples, using a double-injection process. For example, a first injection of uncured, carbon-infused silicone may be used to form the infused electrodes 660a, 660b, 670 at the correct locations. Conductive carbon powder may be premixed into the silicon to make the silicone conductive. A second silicone injection may then be used to form the remaining casing 605 of the flexible strip assembly. The second silicone injection may comprise insulating silicone. The first injection may be uncured, partially cured, or fully cured prior to the second injection.

    [0068] Internal conductors 672 (e.g., conductors on a flexible PCB or conductors made from a flexible conductive film) may electrically connect to a corresponding infused electrode. (Not all conductors are shown in FIG. 6.) For example, the carbon-infused silicone may be injected around an exposed end of a conductor. The conductor may then provide an electrical connection to a signal input on the PCB assembly 405 or to the ESD shield 455. The infused electrode may provide electrical conduction between a conductor and another conductive element on the replaceable electrode strip.

    [0069] An example showing further details of a replaceable electrode strip 150 is illustrated in FIG. 7A. The components are shown in an exploded elevation view in FIG. 7A and depicted in an assembled elevation view in FIG. 7B. In some implementations, a replaceable electrode strip may comprise a first release liner 710 sealing a top adhesive surface of the replaceable electrode strip and a second release liner 712 covering a skin adhesion surface 152 of the replaceable electrode strip. In some implementations, the first and second release liners may be release liner model 1361, available from 3M Corporation of St. Paul, Minnesota, though other liners may be used in other examples. The first release liner may be removed prior to adhering the replaceable electrode strip 150 to the bottom (skin-side) surface of the flexible strip assembly 105. The second release liner may be removed prior to adhering the flexible strip assembly and replaceable electrode strip to the skin of a subject.

    [0070] A replaceable electrode strip 150 may further include a patch adhesion layer 720 that provides adhesion of the replaceable electrode strip to the flexible strip assembly 105 (e.g., to the silicone casing 605). The patch adhesion layer may comprise adhesive surfaces 722, 726 on opposing sides in some cases. In some implementations, the adhesive surfaces may be formed of a same material. In other examples, the adhesive surfaces may be formed of a different material. Examples of double-sided adhesives formed of same materials may include adhesive models 96042 or 9474LE, available from 3M Corporation of St. Paul, Minnesota. An example double-sided adhesive having different adhesion properties on opposing sides (e.g., a differential adhesive) include adhesive model 9425, available from 3M Corporation of St. Paul, Minnesota. The patch adhesion layer may be configured to adhere to silicone on a first adhesive side 722 and an underlying layer of the replaceable electrode strip on a second adhesive side 726.

    [0071] In some examples, the patch adhesion layer 720 may include vias 725 that expose conductive adhesive disks 730 when the first release liner 710 is removed. The vias 725 may have a diameter between about 5 mm and about 20 mm, according to some examples. The conductive adhesive disks 730 may have a diameter approximately 2 mm to approximately 6 mm larger than the diameter of the vias 725.

    [0072] In some implementations, the conductive adhesive disks 730 may be formed from conductive adhesive model 9713, available from 3M Corporation of St. Paul, Minnesota, though other conductive adhesives may be used in some cases. The conductive adhesive disks 730 may adhere to infused silicone electrodes 660a, 660b, 670 on one side and to conductive disks 740 on an opposing side and provide electrical connections between the infused electrodes and conductive disks. The conductive adhesive disks 730 may also adhere to the patch adhesion layer 720 and retain the conductive disks 740 in a desired location (e.g., aligned to electrodes 160a, 160b, 170). The flexible conductive disks 740 may be formed from a conductive polymer, such as a carbon vinyl film model 6355, available from Coveris Advanced Coatings of Matthews, North Carolina, though other conductive films may be used in some cases. A diameter of the conductive disks 740 may be between approximately 1 mm and approximately 6 mm smaller than the diameter of the conductive adhesive disks 730, according to some examples. In some examples, a diameter of the conductive disks 740 may be equal to or larger than the diameter of the conductive adhesive disks 730.

    [0073] A replaceable electrode strip 150 may further include a skin adhesion layer 750. The skin adhesion layer 750 may be electrically insulating and include vias 745 that expose the conductive disks 740 to underlying electrodes 160a, 160b, 170. The diameter of the vias 745 may be less than or greater than the diameter of the conductive disks 740. An example of a skin adhesion layer 750 is a Tegaderm adhesive, model 1626W, available from 3M Corporation of St. Paul, Minnesota, though other biocompatible adhesive layers may be used. In some implementations, a hydrocolloid adhesive, model H011, available from Adhesive R&D of Eau Claire, Wisconsin may be used for the skin adhesion layer 750.

    [0074] The vias 745 of the skin adhesion layer 750 may accommodate the monitor electrodes 160a, 160b and the noise electrode(s) 170, according to some examples. These electrodes may be formed from a hydrogel, e.g., X863 Hydrogel available from Adhesive R&D of Eau Claire, Wisconsin, though any other suitable hydrogel may be used. The diameter of the electrodes may be between approximately 5 mm and approximately 20 mm, in some cases. In some examples, the diameter of the electrodes may be between approximately 8 mm and approximately 16 mm.

    [0075] In some implementations, one or more of the electrodes 160a, 160b, 170 may be surrounded laterally by an adhesive ring 765. The adhesive ring may be insulating, according to some examples. The adhesive rings may be formed from adhesive model 1774W, available from 3M Corporation of St. Paul, Minnesota, though other adhesives may be used to form adhesive rings 765.

    [0076] FIG. 7B shows components of a replaceable electrode assembly 150 pressed together to bond the different layers and components into an assembly. In some examples, the hydrogel may be injected after pressing the layers and other components together and prior to applying the second release liner 712. According to some examples, the flexible layers and components of the replaceable electrode assembly 150 (apart from the hydrogel electrodes) may be cut and/or punched to a suitable shape when manufacturing the assembly. Referring again to FIG. 4, flexible layers and components of a disposable health-monitor patch 400 (apart from the hydrogel electrodes, PCB assembly, and battery) may be cut and/or punched to a suitable shape when manufacturing the assembly. The inventors have recognized and appreciated that multiple layers and components of a replaceable electrode assembly 150 and a disposable health-monitor patch 400 may be formed and assembled using reel-to-reel or "converter" manufacturing processes. This can greatly reduce manufacturing costs for producing a health-monitor patch or replaceable electrode strip.

    [0077] In some examples, two or more "levels" of a disposable health-monitor patch or replaceable electrode strip may be assembled using a converter process to form a first composite. Separately, two or more additional levels may be assembled using a converter process to form a second composite. Then, the two composites may be assemble using a converter process.

    [0078] For example and referring to FIG. 7A, a first composite may be assembled in a converter process by unrolling a release liner 710 from a first roll (level 1), punching vias 725 in a sheet from a second roll comprising patch adhesion layer 720 (level 2), and perforating conductive adhesive disks 730 from a third roll comprising a conductive adhesive (level 3). Perforating a layer may allow the disks 730 (or other component) to be weakly retained in the sheet of material, and subsequently broken or torn free from the sheet when bonding to another layer.

    [0079] The three levels may then be pressed together to form a first composite, and excess material from the conductive adhesive roll may be removed. Similar processing may be used to assemble the conductive disks 740 (level 4), skin adhesion layer 750 (level 5), and adhesive rings 765 (level 6) to form a second composite. The first and second composites may then be aligned and pressed together in a converter process. Subsequently, the hydrogel electrodes 160a, 160b, 170 may be injected and the second release liner 712 applied. Finally, the replaceable electrode assembly 150 may be punched from the assembled composites and packaged. Other suitable manufacturing processes may be used in other examples.

    [0080] When placed in operation, a health-monitor patch (repeated-use or disposable) may detect full PQRST waveform profiles or portions of PQRST waveform profiles of a subject continuously or intermittently, according to some implementations. An illustration of a PQRST waveform profile is depicted in FIG. 8. The detected waveforms may be processed (e.g., by processor 310, digital signal processing circuitry, or any suitable signal processing circuitry) to determine one or more physiological parameters. Physiological parameters that may be determined by a health-monitor patch from cardiac waveforms may include heart rate, inter-beat interval (IBI), heart rate variability (HRV), arrhythmia, and respiration rate, for example.

    [0081] According to some examples, electronic filtering may be used to pre-process a cardiac waveform. For example, filtering may be used to reduce noise, pass or block certain frequency components, or emphasize aspects of a PQRST waveform so that a particular parameter (e.g., heart rate, HRV, arrhythmia, etc.) may be determined by a processor 310 more accurately, for example. A cardiac waveform 910 recorded by a health-monitor patch of an example embodiment is plotted in FIG. 9. The signal has been pre-processed by on-board circuitry to emphasize aspects of the R wave, so that heart rate may be determined more accurately. According to some examples, different signal processing schemes may be employed to emphasize selected aspects of a cardiac waveform, so that a recorded or analyzed waveform may be different from those shown in FIG. 8 and FIG. 9.

    [0082] According to some implementations, power conservation for a health-monitor patch may, at least in part, be based on cardiac data received from a cardiac sensor and/or motion data received from an accelerometer. Power conservation methods based on cardiac data may run in parallel with or in combination with power conservation methods based on motion data. In some cases, a power conservation mode of operation may be determined in part based upon a health condition of the subject. For example, recovering patients or individuals presenting a health impairment may need more continuous and/or full monitoring of cardiac waveform and/or activity/motion data, whereas less monitoring of cardiac waveforms and activity data may be needed for fit individuals. Selection or setting of power-conservation mode options may be made via wireless communication with the health-monitor patch or via a tapping sequence or gesture recognizable by the health-monitor patch.

    [0083] To extend battery life, a health-monitor patch may cycle through one or more operational modes that consume different amounts of power depending on the state of the subject. As just one illustrative example of power conservation, motion data may be analyzed by a system processor to determine that a subject is in an inactive state (e.g., sitting, lying, riding in a vehicle, etc.). A health-monitor patch may then determine that at least power to an accelerometer may be reduced. In some examples, circuitry and processing algorithms associated with the accelerometer may enter a sleep or reduced-power mode. In some examples, a cardiac sensor of the same health-monitor patch may also enter a sleep mode in which a full cardiac waveform is not recorded. Instead, portions of a cardiac waveform (e.g., only R-wave portions), or none of a cardiac waveform, may be recorded and/or processed. In some implementations, portions of the cardiac waveform may be recorded and processed intermittently (e.g., skipping one or more beats between recordings). In other examples, a cardiac sensor may continue to sense a full cardiac waveform while an inactive state of the subject has been detected (e.g., to monitor a cardiac parameter for a patient).

    [0084] In some examples, a full-power continuous detection mode may be automatically activated when the health-monitor patch determines that the subject is active based on data from the accelerometer. In some implementations, a power management circuit of a health-monitor patch may place a cardiac sensor in a power-conserving state when a subject is active. For example, a health-monitor patch may determine that a subject's heart rate is stable during an activity, and may then place the cardiac sensor in a power-conserving state in which portions of the cardiac cycle are monitored continuously or intermittently.

    [0085] Additional examples of power-conserving modes include, but are not limited to, a beat-detect mode, a QRS-detect mode, and a full-wave mode. In a beat-detect mode, a heart monitor may sleep for a period of time between each heartbeat of a subject and awake in time only to determine a point or timing in the cardiac waveform that is sufficient to indicate an inter-beat interval (IBI). For example, the cardiac sensor may awake in time to detect a portion of the cardiac waveform corresponding to an R wave. In some implementations, the cardiac signal may be fed to a comparator or processor configured to detect a threshold crossing or change in slope (e.g., location of a peak) of the R wave. A comparator may require less power to operate than circuitry needed to capture and analyze a portion of the cardiac waveform.

    [0086] In a QRS-detect mode, a cardiac sensor may sleep for a period of time between each heartbeat of a subject and "awake" in time to capture a QRS waveform for subsequent analysis. The QRS waveform may, for example, be analyzed by a processor for arrhythmia, heart rate variability, and/or respiration rate, according to some implementations. In some examples, respiration rate may be determined from an envelope of the R-wave over multiple cardiac cycles.

    [0087] In a full-wave mode of operation, a heart monitor may operate continuously to capture a full cardiac waveform for multiple beats. A full-wave mode of operation may be executed periodically to ascertain the timing of P or R waves, for example, and determine an interval of sleep for a cardiac monitor between heartbeats. In some implementations, a full-wave mode of operation may be executed when a subject becomes active, or may be executed when a subject's activity is found to be moderate and/or vigorous. In some implementations, a user may command continuous monitoring of a cardiac waveform and/or other physiological parameters irrespective of the user's activity by communicating wirelessly with, or tapping a sequence on, the health-monitor patch that can be detected by the motion sensor, processed, and recognized by the health-monitor patch's processor as a command to record full-wave, continuous data.

    [0088] Additional examples of power-conserving modes and processing cardiac signals are described in U.S. Patent Application Pub. No. 2015-0119728.

    [0089] The invention is defined by appended claims 1-15.


    Claims

    1. A health-monitor patch (400) configured to be adhered to the skin of a subject, the health-monitor patch (400) comprising:

    a cardiac sensor (354) comprising a first monitor electrode (260a), which is configured to receive a first signal from a first location on the skin of the subject, and a second monitor electrode (260b), which is configured to receive a second signal from a second location on the skin of the subject;

    a third, noise electrode (270) configured to receive a third signal from the skin of the subject at a third location, separate from the first and second locations;

    an electronic circuit comprising a processor (310) configured to process signals from the first and second monitor electrodes (260a, 260b);

    a battery (305) configured to provide power to the processor (310);

    a first conductive path between the first monitor electrode (260a) and the electronic circuit;

    a second conductive path between the second monitor electrode (260b) and the electronic circuit; and

    a conductive shield (455) that extends over at least a portion of the first and second conductive paths, wherein the conductive shield (455) is electrically connected to each of the third, noise electrode (270) and a terminal of the battery (305).


     
    2. The health-monitor patch (400) of claim 1, wherein the third electrode (270) is configured to receive the third signal from the skin of the subject at a third location between the first and second locations.
     
    3. The health-monitor patch (400) of claim 1 or claim 2, wherein the conductive shield extends over the electronic assembly.
     
    4. The health-monitor patch (400) of any preceding claim, wherein the conductive shield and first and second conductive paths are arranged such that noise detected by the third electrode (270) couples from the conductive shield (455) to the first and second conductive paths.
     
    5. The health-monitor patch (400) of any preceding claim, wherein the processor (310) is disposed on a printed circuit board (PCB) assembly (405) and the conductive shield comprises an electrostatic discharge (ESD) shield (455) that extends over the PCB assembly (405).
     
    6. The health-monitor patch (400) of claim 5, wherein the ESD shield (455) is insulated from and located less than about two millimeters from the first and second conductive paths (460a, 460b).
     
    7. The health-monitor patch (400) of claim 5 or 6, wherein the health-monitor patch (400) is formed as a flexible strip (105) and the ESD shield (455) comprises a conductive polymer film.
     
    8. The health-monitor patch (400) of any preceding claim, further comprising a silicone casing (605) surrounding the processor (310), wherein the first and second monitor electrodes (260a, 260b) and the third electrode (270) comprise conductive silicone regions at a surface of the silicone casing (605) that are infused with a conductive material.
     
    9. A method for detecting a cardiac waveform with a wearable health-monitor patch (400), the method comprising:

    receiving a first electrical signal at a first monitor electrode (260a) of the health-monitor patch (400), the first monitor electrode (260a) contacting the skin of a subject at a first location;

    receiving a second electrical signal at a second monitor electrode (260b) of the health-monitor patch (400), the second monitor electrode (260b) contacting the skin of the subject at a second location that is separated from the first location by a distance;

    conducting the first electrical signal from the first monitor electrode (260a) over a first conductive path to a first signal input of an electronic circuit mounted within the health-monitor patch (400), the electronic circuit comprising a battery (305) and a processor (310) configured to process signals from the first and second monitor electrodes (260a, 260b);

    conducting the second electrical signal from the second monitor electrode (260b) over a second conductive path to a second signal input of an electronic circuit mounted within the health-monitor patch (400);

    receiving a third electrical signal from a third, noise electrode (270) of the health-monitor patch (400), the third electrode (270) contacting the skin of the subject at a third location that is separate from the first and second locations;

    conducting the electrical signal from the third, noise electrode (270) to a conductive shield (455) which is electrically connected to each of the third, noise electrode and a terminal of the battery (305), wherein the conductive shield (455) extends over at least portions of the first and second conductive paths.


     
    10. The method of claim 9, wherein the conductive shield extends over the electronic circuit.
     
    11. The method of claim 9 or 10, wherein the third electrode (270) is contacts the skin of the subject at a location between the first and second monitor electrodes (260a, 260b).
     
    12. The method of claim 9 or claim 10, further comprising coupling the third electrical signal from the conductive shield to the first and second conductive paths.
     
    13. The method of any one of claims 9 to 12, wherein the processor (310) is disposed on a printed circuit board (PCB) assembly (405) and the conductive shield comprises an electrostatic (ESD) shield (455) that extends over the PCB assembly (405).
     
    14. The method of claim 13, wherein the ESD shield (455) is less than two millimeters from the portions of the first and second conductive paths.
     
    15. The method of clam 13 or 14, wherein the wearable health-monitor patch (400) is formed as a flexible strip (105) and the ESD shield (455) comprises a conductive polymer film.
     


    Ansprüche

    1. Gesundheitsüberwachungspflaster (400), das dazu konfiguriert ist, an die Haut einer Person geklebt zu werden, wobei das Gesundheitsüberwachungspflaster (400) umfasst:

    einen Herzsensor (354), der eine erste Überwachungselektrode (260a), die dazu konfiguriert ist, ein erstes Signal von einer ersten Stelle auf der Haut der Person zu empfangen, und eine zweite Überwachungselektrode (260b), die dazu konfiguriert ist, ein zweites Signal von einer zweiten Stelle auf der Haut der Person zu empfangen, umfasst;

    eine dritte Rauschelektrode (270), die dazu konfiguriert ist, ein drittes Signal von der Haut der Person an einer dritten Stelle zu empfangen, die von der ersten und der zweiten Stelle getrennt ist;

    ein elektronischer Schaltkreis, umfassend:

    einen Prozessor (310), der dazu konfiguriert ist, Signale von der ersten und der zweiten Überwachungselektrode (260a, 260b) zu verarbeiten;

    eine Batterie (305), die dazu konfiguriert ist, dem Prozessor (310) Energie bereitzustellen;

    eine erste Leiterbahn zwischen der ersten Überwachungselektrode (260a) und dem elektronischen Schaltkreis;

    eine zweite Leiterbahn zwischen der zweiten Überwachungselektrode (260b) und dem elektronischen Schaltkreis und

    eine leitende Abschirmung (455), die sich über mindestens einem Abschnitt der ersten und der zweiten Leiterbahn erstreckt, wobei die leitende Abschirmung (455) mit jeder von der dritten Rauschelektrode (270) und einer Klemme der Batterie (305) elektrisch verbunden ist.


     
    2. Gesundheitsüberwachungspflaster (400) nach Anspruch 1, wobei die dritte Elektrode (270) dazu konfiguriert ist, das dritte Signal von der Haut der Person an einer dritten Stelle zwischen der ersten und der zweiten Stelle zu empfangen.
     
    3. Gesundheitsüberwachungspflaster (400) nach Anspruch 1 oder 2, wobei sich die leitende Abschirmung über der elektronischen Baugruppe erstreckt.
     
    4. Gesundheitsüberwachungspflaster (400) nach einem vorhergehenden Anspruch, wobei die leitende Abschirmung und die erste und die zweite Leiterbahn derart eingerichtet sind, dass sich Rauschen, das von der dritten Elektrode (270) erkannt wird, von der leitenden Abschirmung (455) zu der ersten und der zweiten Leiterbahn koppelt.
     
    5. Gesundheitsüberwachungspflaster (400) nach einem vorhergehenden Anspruch, wobei der Prozessor (310) auf einer Leiterplattenbaugruppe (PCB-Baugruppe) (405) angeordnet ist und die leitende Abschirmung eine Abschirmung gegen elektrostatische Entladungen (ESD-Abschirmung) (455) umfasst, die sich über der PCB-Baugruppe (405) erstreckt.
     
    6. Gesundheitsüberwachungspflaster (400) nach Anspruch 5, wobei die ESD-Abschirmung (455) von der ersten und der zweiten Leiterbahn (460a, 460b) isoliert ist und sich weniger als etwa zwei Millimeter davon befindet.
     
    7. Gesundheitsüberwachungspflaster (400) nach Anspruch 5 oder 6, wobei das Gesundheitsüberwachungspflaster (400) als ein flexibler Streifen (105) geformt ist und die ESD-Abschirmung (455) eine leitende Polymerfolie umfasst.
     
    8. Gesundheitsüberwachungspflaster (400) nach einem vorhergehenden Anspruch, weiterhin umfassend eine Silikonumhüllung (605), die den Prozessor (310) umgibt, wobei die erste und die zweite Überwachungselektrode (260a, 260b) und die dritte Elektrode (270) leitende Silikonregionen an einer Oberfläche der Silikonumhüllung (605) umfassen, die mit einem leitenden Material infundiert sind.
     
    9. Verfahren zur Erkennung einer Herzwellenform mit einem tragbaren Gesundheitsüberwachungspflaster (400), wobei das Verfahren umfasst:

    Empfangen eines ersten elektrischen Signals an einer ersten Überwachungselektrode (260a) des Gesundheitsüberwachungspflasters (400), wobei die erste Überwachungselektrode (260a) die Haut einer Person an einer ersten Stelle berührt;

    Empfangen eines zweiten elektrischen Signals an einer zweiten Überwachungselektrode (260b) des Gesundheitsüberwachungspflasters (400), wobei die zweite Überwachungselektrode (260b) die Haut der Person an einer zweiten Stelle berührt, die um einen Abstand von der ersten Stelle getrennt ist;

    Leiten des ersten elektrischen Signals von der ersten Überwachungselektrode (260a) über eine erste Leiterbahn zu einem ersten Signaleingang eines elektronischen Schaltkreises, der innerhalb des Gesundheitsüberwachungspflasters (400) montiert ist, wobei der elektronische Schaltkreis eine Batterie (305) und einen Prozessor (310) umfasst, der dazu konfiguriert ist, Signale von der ersten und der zweiten Überwachungselektrode (260a, 260b) zu verarbeiten;

    Leiten des zweiten elektrischen Signals von der zweiten Überwachungselektrode (260b) über eine zweite Leiterbahn zu einem zweiten Signaleingang eines elektronischen Schaltkreises, der innerhalb des Gesundheitsüberwachungspflasters (400) montiert ist;

    Empfangen eines dritten elektrischen Signals von einer dritten Rauschelektrode (270) des Gesundheitsüberwachungspflasters (400), wobei die dritte Elektrode (270) die Haut der Person an einer dritten Stelle berührt, die von der ersten und der zweiten Stelle getrennt ist;

    Leiten des elektrischen Signals von der dritten Rauschelektrode (270) zu einer leitenden Abschirmung (455), die mit jeder von der dritten Rauschelektrode und einer Klemme der Batterie (305) elektrisch verbunden ist, wobei sich die leitende Abschirmung (455) über mindestens Abschnitte der ersten und der zweiten Leiterbahn erstreckt.


     
    10. Verfahren nach Anspruch 9, wobei sich die leitende Abschirmung über dem elektronischen Schaltkreis erstreckt.
     
    11. Verfahren nach Anspruch 9 oder 10, wobei die dritte Elektrode (270) die Haut der Person an einer Stelle zwischen der ersten und der zweiten Überwachungselektrode (260a, 260b) berührt.
     
    12. Verfahren nach Anspruch 9 oder 10, weiterhin umfassend ein Koppeln des dritten elektrischen Signals von der leitenden Abschirmung zu der ersten und der zweiten Leiterbahn.
     
    13. Verfahren nach einem der Ansprüche 9 bis 12, wobei der Prozessor (310) auf einer Leiterplattenbaugruppe (PCB-Baugruppe) (405) angeordnet ist und die leitende Abschirmung eine elektrostatische Abschirmung (ESD-Abschirmung) (455) umfasst, die sich über der PCB-Baugruppe (405) erstreckt.
     
    14. Verfahren nach Anspruch 13, wobei die ESD-Abschirmung (455) weniger als zwei Millimeter von den Abschnitten der ersten und der zweiten Leiterbahn ist.
     
    15. Verfahren nach Anspruch 13 oder 14, wobei das tragbare Gesundheitsüberwachungspflaster (400) als ein flexibler Streifen (105) geformt ist und die ESD-Abschirmung (455) eine leitende Polymerfolie umfasst.
     


    Revendications

    1. Patch de contrôle de santé (400) configuré pour adhérer à la peau du sujet, le patch de contrôle de santé (400) comprenant :

    un capteur cardiaque (354) comprenant une première électrode de contrôle (260a), configurée pour recevoir un premier signal d'un premier emplacement sur la peau du sujet, et une deuxième électrode de contrôle (260b) configurée pour recevoir un deuxième signal d'un deuxième emplacement sur la peau du sujet ;

    une troisième électrode de bruit (270) configurée pour recevoir un troisième signal de la peau du sujet, sur un troisième emplacement, distinct des premier et deuxième emplacements ;

    un circuit électronique comprenant un processeur (310) configuré pour traiter des signaux provenant des première et deuxième électrodes de contrôle (260a, 260b) ;

    une batterie (305) configurée pour fournir de l'énergie au processeur (310) ;

    un premier trajet conducteur entre la première électrode de contrôle (260a) et le circuit électronique ;

    un deuxième trajet conducteur entre la deuxième électrode de contrôle (260b) et le circuit électronique ; et

    un écran conducteur (455) s'étendant sur au moins une partie des premier et deuxième trajets conducteurs, l'écran conducteur (455) étant connecté électriquement à chacune de la troisième électrode de bruit (270) et d'une borne de la batterie (305).


     
    2. Patch de contrôle de santé (400) selon la revendication 1, la troisième électrode (270) étant configurée pour recevoir le troisième signal de la peau du sujet en un troisième emplacement situé entre les premier et deuxième emplacements.
     
    3. Patch de contrôle de santé (400) selon la revendication 1 ou la revendication 2, l'écran conducteur s'étendant au-dessus du module électronique.
     
    4. Patch de contrôle de santé (400) selon une quelconque des revendications précédentes, l'écran conducteur ainsi que les premier et deuxième trajets conducteurs étant agencés de sorte que le bruit détecté par la troisième électrode (270) couple de l'écran conducteur (455) aux premier et deuxième trajets conducteurs.
     
    5. Patch de contrôle de santé (400) selon une quelconque des revendications précédentes, le processeur (310) étant disposé sur un ensemble de carte de circuit imprimé (PCB) (405), et l'écran conducteur comprenant un écran de décharge électrostatique (ESD) (455) s'étendant au-dessus de l'ensemble PCB (405).
     
    6. Patch de contrôle de santé (400) selon la revendication 5, l'écran ESD (455) étant isolé des premier et deuxième trajets conducteurs (460a, 460b), et situés à moins d'environ deux millimètres de ces derniers.
     
    7. Patch de contrôle de santé (400) selon la revendication 5 ou 6, le patch de contrôle de santé (400) étant composé d'une bande flexible (105), et l'écran ESD (455) comprenant un film polymère conducteur.
     
    8. Patch de contrôle de santé (400) selon une quelconque des revendications précédentes, comprenant en outre une boîtier de silicone (605) entourant le processeur (310), les première et deuxième électrodes de contrôle (260a, 260b) et la troisième électrode (270) comprenant des zones de silicone conducteur sur une surface du boîtier de silicone (605), infusées avec une matière conductrice.
     
    9. Méthode pour la détection d'une forme d'onde cardiaque à l'aide d'un patch de contrôle de santé (400) portable, la méthode comprenant :

    la réception d'un premier signal électrique à une première électrode de contrôle (260a) du patch de contrôle de santé (400), la première électrode de contrôle (260a) étant au contact de la peau d'un sujet en un premier emplacement ;

    la réception d'un deuxième signal électrique à une deuxième électrode de contrôle (260b) du patch de contrôle de santé (400), la deuxième électrode de contrôle (260b) étant au contact de la peau d'un sujet en un deuxième emplacement, séparé du premier emplacement par une distance ;

    la conduction du premier signal électrique depuis la première électrode de contrôle (260a) sur un premier trajet conducteur jusqu'à une première entrée de signal d'un circuit électronique monté dans le patch de contrôle de santé (400), le circuit électronique comprenant une batterie (305) et un processeur (310) configurés pour traiter des signaux provenant des première et deuxième électrodes de contrôle (260a, 260b) ;

    conduction du deuxième signal électrique depuis la deuxième électrode de contrôle (260b) sur un deuxième trajet conducteur jusqu'à une deuxième entrée de signal d'un circuit électronique monté dans le patch de contrôle de santé (400) ;

    la réception d'un troisième signal électrique depuis une troisième électrode de bruit (270) du patch de contrôle de santé (400), la troisième électrode (270) étant au contact de la peau d'un sujet en un troisième emplacement séparé des premier et deuxième emplacements ;

    la conduction du signal électrique de la troisième électrode de bruit (270) à un écran conducteur (455) connecté électriquement à chacune de la troisième électrode de bruit et d'une borne de la batterie (305), l'écran conducteur (455) s'étendant sur au moins des parties des premier et deuxième trajets conducteurs.


     
    10. Méthode selon la revendication 9, l'écran conducteur s'étendant au-dessus du circuit électronique.
     
    11. Méthode selon la revendication 9 ou 10, la troisième électrode (270) étant au contact de la peau du sujet en un emplacement situé entre les première et deuxième électrodes de contrôle (260a, 260b).
     
    12. Méthode selon la revendication 9 ou la revendication 10, comprenant le couplage du troisième signal électrique de l'écran conducteur aux premier et deuxième trajets conducteurs.
     
    13. Méthode selon une quelconque des revendications 9 à 12, le processeur (310) étant disposé sur un ensemble de carte de circuit imprimé (PCB) (405), et l'écran conducteur comprenant un écran électrostatique (ESD) (455) s'étendant au-dessus de l'ensemble PCB (405).
     
    14. Méthode selon la revendication 13, l'écran ESD (455) étant situé à moins de deux millimètres des parties des premier et deuxième trajets conducteurs.
     
    15. Méthode selon la revendication 13 ou 14, le patch de contrôle de santé (400) portable étant composé d'une bande flexible (105), et l'écran ESD (455) comprenant un film polymère conducteur.
     




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    Cited references

    REFERENCES CITED IN THE DESCRIPTION



    This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.

    Patent documents cited in the description