AUTOMATED WEARABLE BELT CARDIAC DEFIBRILLATOR
20220355122 · 2022-11-10
Inventors
- Gera Strommer (Caesarea, IL)
- Avraham Broder (Caesarea, IL)
- Robert Fishel (Caesarea, IL)
- Itzik Shmarak (Caesarea, IL)
Cpc classification
A61N1/0476
HUMAN NECESSITIES
A61N1/0496
HUMAN NECESSITIES
A61N1/3993
HUMAN NECESSITIES
International classification
Abstract
An automated wearable belt cardiac defibrillator (BCD) for wearing by a subject, comprising: at least two patches adapted for adhering to the subject each comprising a defibrillation electrode and an ECG sensor; and a BCD controller connected to each of the patches, wherein the patches comprise an adhesive adapted for long-term adhering of the patches to the subject, wherein the adhesive is a biocompatible adhesive, wherein the patches and adhesive are adapted for movement of the subject while the patches are adhered to the subject, wherein the patches are replaceable, wherein the controller is housed in a belt for wearing by the subject, wherein the belt is adapted for being flexible, wherein the adaptation for being flexible comprises a plurality of compartments for housing components of the controller, wherein a method for usage of the BCD comprises: following completion of an operational period, positioning of the patches to alternative locations on the subject wherein each of the alternate locations represents an alternate shock vector.
Claims
1. A flexible automated wearable belt cardiac defibrillator (BCD) for wearing by a subject, the subject having a body, the BCD comprising: at least two disposable patches adapted for adhering to the body of the subject, each patch comprising a defibrillation electrode, wherein at least one patch includes an ECG sensor; and a controller that is separate from the patches and connected via a connection cable to each patch, wherein the patches comprise an adhesive adapted for long-term adhering of the patches to the body of the subject, wherein the patches and the adhesive are adapted for movement of the subject while the patches are adhered to the body of the subject, wherein the controller is housed in a flexible belt comprising a plurality of compartments for wearing by the subject, is adapted for being flexible, and is not required to be in contact with the body of the subject, and wherein the adaptation for being flexible comprises distributing components of the controller between the plurality of compartments.
2. The BCD of claim 1, wherein the controller components comprise a battery, at least one high voltage and high energy capacitor, and controller electronics, and wherein each of the controller components is housed in a separate one of the plurality of compartments.
3. (canceled)
4. The BCD of claim 1, wherein the long-term is between one day and 10 days.
5. (canceled)
6. The BCD of claim 1, wherein the patches comprise a gel for enhancing electrical contact.
7. The BCD of claim 1, wherein the adhesive is a biocompatible adhesive.
8. The BCD of claim 1, wherein at least one of the patches comprises a vibration element.
9. The BCD of claim 8, wherein the vibration element is adapted for vibrating to alert the subject prior to an impending shock delivery by the defibrillation electrode.
10. (canceled)
11. (canceled)
12. The BCD of claim 1, wherein the at least two patches include at least three patches for providing at least two defibrillation vectors.
13. The BCD of claim 1, wherein the controller comprises a controller vibration pad.
14. The BCD of claim 13, wherein the controller vibration pad is adapted to generate vibration to alert the subject of an impending shock to be delivered by the defibrillation electrode.
15. The BCD of claim 1, wherein the controller comprises an audio output device adapted to generate an alarm sound in case of an impending a shock about to be delivered by the defibrillation electrode.
16. The BCD of claim 15, wherein the audio output device is adapted to sound an alarm following administering of a defibrillating shock.
17. (canceled)
18. The BCD of claim 1, wherein the controller is adapted for storage and/or analysis of ECG sensor data sensed by the at least one ECG sensor.
19. The BCD of claim 18, wherein the controller comprises an ECG event button adapted to be pressed to create a time stamp in the collected ECG sensor data.
20. The BCD of claim 19, wherein pressing of the ECG event button initiates recording via a microphone.
21. The BCD of claim 1, wherein the controller is adapted to measure impedance between each patch and a body of the subject to determine strength of an electrical connection therebetween.
22. The BCD of claim 1, wherein the controller comprises an abort button adapted for aborting an impending shock from the defibrillation electrode.
23. (canceled)
24. The BCD of claim 1, wherein the controller comprises a controller motion sensor and/or the BCD comprises an ECG motion sensor.
25. The BCD of claim 24, wherein one or both of controller motion sensor and the ECG motion sensor are adapted for determining data related to movement of the subject.
26. (canceled)
27. The BCD of claim 1, wherein the patches comprise connectors for connecting or disconnecting interconnection cables between the patches and/or between the patches and the controller.
28. The BCD of claim 1, wherein the controller is adapted for data communication with a remote monitoring center (RMC).
29. The BCD of claim 28, wherein ECG data sensed by the ECG sensor is transmitted to the RMC for analysis and storage.
30. The BCD of claim 28, wherein detected arrhythmia events are transmitted to the RMC.
31. The BCD of claim 28, wherein the controller comprises a GPS receiver adapted for determining the geolocation of the BCD, and wherein the determined location is transmitted to the RMC.
32. The BCD of claim 28, wherein the controller comprises a microphone and an audio device and is adapted for initiating a voice call with the RMC.
33. The BCD of claim 1, wherein the controller is adapted for wireless communication with an external device.
34-50. (canceled)
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0033] Aspects, embodiments and features disclosed herein will become apparent from the following detailed description when considered in conjunction with the accompanying drawings. Like elements may be marked with like numerals in different figures, where:
[0034]
[0035]
[0036]
[0037]
[0038]
[0039]
[0040]
DETAILED DESCRIPTION
[0041] Exemplary embodiments disclosed herein relate to a wearable AED (BCD) and method of use.
[0042]
[0043] As shown in the plan view of
[0044]
[0045] In some embodiments, BCD 200 is adapted for use by a female subject. As shown in
[0046]
[0047]
[0048] Non-limiting examples of external device 422 are a smart watch or smartphone. External device 422 is in wireless communication with defibrillation patches 416, ECG sensors 418 and defibrillation controller 420. A non-limiting example of a wireless communication protocol is Bluetooth. External device 422 is a computing device and runs software to monitor the subject's heart using data received wirelessly from sensors 418, and triggers defibrillation patches 416 if required by communicating with controller 420 and/or defibrillation patches 416. In some embodiments, controller 420 is integrated into RPS 410 similarly to the way controller 320 is integrated into RPS 310.
[0049]
[0050] In some embodiments, each of patches 510 includes include three or more ECG sensors 518 for sensing simultaneous sensing vectors. Multiple sensing electrodes per EC sensor 518 provides better sensing and detection of VF and discrimination of non-VF arrhythmias.
[0051] In some embodiments, each of patches 510 includes three or more defibrillation electrodes 516 for providing multiple simultaneous shock vectors. for better coverage of the heart and reduction of defibrillation threshold energy.
[0052] Patches 510A, 510B are affixed to the body of the subject using a biocompatible adhesive that is non-irritating for skin, is adapted both for extended use and for ensuring adhesion while that the subject continues to be active and mobile. A non-limiting example of a suitable adhesive may be KM40C by Katecho LLC of Des Moines, Iowa. In some embodiments, extended use covers a period of over 7 days. In some embodiments, extended use covers a period of over 10 days.
[0053] In some embodiments, patches 510A, 510B comprise gel for enhancing electrical contact. In some embodiments, defibrillation electrode 516 performs ECG signal measurement and ECG sensor 518 is not required.
[0054] In some embodiments, replaceable patches 510A, 510B include a vibration element 530 used to alert the patient prior to shock delivery. In some embodiments, replaceable patches 510A, 510B are replaced periodically. In some embodiments, replaceable patches 510A, 510B are disposable. In some embodiments, BCD 500 comprises more than two patches 510. Cables 522 provide electrical connectivity between patches 510 and cables 524 provide electrical connectivity between patches 510 and controller belt 520. As shown in
[0055] Controller belt 520 has the form of a flexible belt. Belt 528 comprises a flexible material. Controller belt 520 is flexible and wearable and comprises an adjustment means 542 such a belt adjustment means known in the art in order to fit controller belt 520 comfortably around the waist or torso of the subject. Alternatively, belt 520 may be worn on another part of the body or may be carried.
[0056] Controller belt 520 contains all the components of a defibrillator controller (such as controller 720, high voltage capacitors, batteries, electronics, high voltage shock circuits, alarm system, communication system, operating software as well as detection algorithm software) embedded in a flexible manner. In the form of a flexible belt, controller 520 is portable and well suited for comfortable wearing by a patient on a daily basis and may be shifted around the waist of the subject (or worn elsewhere) for comfort. As shown in
[0057] Wiring (not shown) between compartments 526 provides for the electrical connections between the components of controller 520. In some embodiments, compartments 526 are cylindrical in shape. In some embodiments, compartments 526 have the form of a pocket. In some embodiments, compartments 526 are rectangular in shape. In some embodiments, belt 520 is a lightweight belt. In some embodiments, belt 520 including the patches 526 and cables 524 weighs less than 500 g.
[0058] Cables 524 enables removal of controller belt 520 from the subject for placing proximal to the patient while patches 510 remain attached to the subject to enable, for example, sleeping. In some embodiments, cables 524 are extendable for placing controller belt 520 further away from the subject. In some embodiments, compartments 526 are attached to controller belt 520 using flexible spacers (not shown).
[0059] In some embodiments, replaceable patches 510A, 510B can be placed in alternate locations to eliminate skin damage which may occur due to long-term usage of the patch in one position. A method for overcoming skin irritations which may be caused by patches and adhesives is shown in
[0060] In
[0061] Alternating the sides for patches 510 enables use of relatively large patches compared to standard AED patches (desirable for conductivity) while reducing potential discomfort of subjects.
[0062] In the embodiment of
[0063]
[0064] To enable sufficient energy to be conveyed by defibrillation electrodes 616 to the heart of a subject during a shock, more than two patches 610 are affixed to the subject. Multiple defibrillation electrodes 616 provide multiple shock vectors between the affixed defibrillation electrodes 616. As shown in
[0065] In some embodiments, patches 610 comprise gel for enhancing electrical contact. In some embodiments, replaceable patches 610 are replaced periodically. Cables 622 provide electrical connectivity between patches 610 via connectors 644 and cables 624 provide electrical connectivity between patches 610 (via connector 644) and controller belt 620 as described above with reference to
[0066]
[0067] It should be appreciated that the components of controller 720 as described below may be provided in a single housing (such as but not limited to the housings of controllers 120 or 420) or alternatively may be distributed into multiple housings such as but not limited to the embodiment of
[0068] In some embodiments, the ECG sensors 718 and controller are adapted for sensing simultaneous sensing vectors. The adaptation includes sensing from three or more sensing electrodes placed on two or more patches for better sensing and detection of VF and discrimination of non-VF arrhythmias.
[0069] In some embodiments, defibrillation electrodes 716 are adapted for providing multiple simultaneous shock vectors. The adaptation includes providing three or more shock electrodes each placed on a patch 715 for better coverage of the heart and reduction of defibrillation threshold energy.
[0070] In some embodiments, controller 720 comprises an activation switch 728 to turn BCD 700 ON once the patches are in place. In some embodiments, controller 720 comprises an audio output device 726 to generate an alarm sound such as beeping or buzzing to alert the patient in case VT or VF was detected and a shock is about to be delivered. Additionally, audio device 726 may play audio messages from RMC 724, or messages related to the BCD 700 status. In some embodiments, controller 720 also comprises a microphone 730 for hearing comments from the subject. In some embodiments, audio output device 726 sounds an audible alarm following administering a defibrillating shock to warn/notify passers-by.
[0071] In some embodiments, ECG data as sensed by sensor patch 718 is collected for storage by controller 720, analysis by controller 720 and/or transmission to RMC 724 for analysis and storage. In some embodiments, controller 720 includes an ECG event button 752 for creating a time stamp in the collected ECG data such as but not limited to when a patient feels an arrythmia or other sensation the patient wishes to record. In some embodiments, ECG event button 752 initiates recording via microphone 730 such that the patient can state the reason for pressing ECG event button 752. In some embodiments, ECG data is continually buffered but only stored/recorded by controller 720 when ECG event button 752 is pressed including recording a time period before ECG event button 752 was pressed.
[0072] In some embodiments, controller 720 comprises visual indication means such as a display 732 and/or status lights 734 for displaying the status of BCD 700 and/or displaying messages related to BCD 700 and use thereof. In some embodiments, controller 720 measures impedance of patches 716, 718 to the body of the subject to determine the strength of the electrical connection therebetween. In some embodiments, controller 720 displays the measured strength of the electrical connection of a patch 716 and/or 718 to the skin of the subject. In some embodiments, controller 720 indicates the level of connection of patches 716 and/or 718 with the skin of the subject. In some embodiments, controller 720 indicates a suggested period for replacement or movement of patches 716, 718.
[0073] In some embodiments, controller 720 comprises a vibration device 736 to generate vibration to alert the patient in case VF was detected and a shock is about to be delivered. Additionally or alternatively, in some embodiments, a vibration alert is delivered to the subject via vibration patch 714.
[0074] In some embodiments, controller 720 comprises an abort button 738 used to abort a shock in a case the patient feels fine but the BCD 700 is alerting that a shock is about to be delivered. In some embodiments, controller 720 comprises an emergency call button 740. In some embodiments, safety switch 754 electrically disconnects controller 720 from defibrillation patch 716. In some embodiments, safety switch 754 is activated by abort button 738.
[0075] In some embodiments, controller 720 is in wireless communications with an RMC 724. In some embodiments, controller 720 notifies RMC 724 of an administered defibrillation shock. In some embodiments, controller 720 continuously analyzes the signal from ECG patch 718 to determine whether an arrhythmia has occurred. In some embodiments, detected arrhythmia events are stored by controller 720. In some embodiments, detected arrhythmia events are transmitted to RMC 724. In some embodiments, controller 720 comprises a GPS receiver 742, and the location of controller 720 is transmitted along with any information transmitted to RMC 724. In some embodiments, a patient can initiate a voice call with medical staff at the RMC 724 using microphone 730 and audio output 726.
[0076] In some embodiments, controller 720 includes a motion sensor 748. Motion sensor 748 may include one or more of a gravity sensor, linear acceleration sensor, rotation vector sensor, step counter, step detector, accelerometer and/or gyroscope. In some embodiments, sensor patch 718 includes a motion sensor 750. Motion sensor 750 may include one or more of a gravity sensor, linear acceleration sensor, rotation vector sensor, step counter, step detector, accelerometer and/or gyroscope. In some embodiments, one or both of motion sensors 748, and 750 may determine data related to movement of the patient. In some embodiments, movement data is collected by controller and combined with the ECG data provided sensor patch 718. In some embodiments, motion sensor data, indicative of the movement of the patient, is used as part of monitoring of syncope by controller 720 and/or by RMC 724.
[0077] In some embodiments, controller 720 comprises batteries 744 that can be replaceable and/or rechargeable. In some embodiments, rechargeable batteries 744 use either wireless charging or are charged using a cable (not shown) connected to the controllers from a power source.
[0078] In some embodiments, controller 720 is in wireless communication with external device 722. Non-limiting examples of external device 722 include a smartphone or smart watch. External device 722 comprises a software application (app) 746 for running on the external device. In some embodiments, app 746 presents the status of BCD 700 using the display of the external device such as, for example, to indicate a need for charging of BCD 700 or to indicate an error in the functioning of BCD 700. In some embodiments, the audible, visual and/or vibrating indication of an impending shock is provided by app 746 using the display, audio, and/or vibrating functions of external device 722. In some embodiments, an abort button is provided by app 746 and the touchscreen capability for activating the abort button is provided by external device 722. In some embodiments, an indication of the impending shock or activation of a shock is transmitted from controller 720 to external device 722 for further transmission by external device 722 using the built-in data communication functionality of external device 722 to a RMC 724, such as for emergency response. In some embodiments, app 746 provides BCD 700 status information. In some embodiments, app 746 provides guided instructions for patch placement and rotation. In some embodiments, data from ECG patch 718 is provided to app 746 for analyzing of the signal from ECG patch 718 to determine whether an arrhythmia has occurred. In some embodiments, detected arrhythmia events are stored by app 746 on device 722. In some embodiments, detected arrhythmia events are transmitted by app 746 to RMC 724 using the communication features of device 722. In some embodiments, event button 752 is activated via app 746.
[0079] In some embodiments, when BCD 700 detects asystole after delivering a shock, BCD 700 delivers high voltage temporary external percutaneous heart pacing via patches 716. In some embodiments, the pacing is ventricular demand pacing (VVI). In some embodiments, the pacing is provided at a rate of 35 BPM.
[0080] In some embodiments, each patch 716, 718 comprises multiple perforations throughout the patch allowing for breathing of the skin while the patch is applied.
[0081] In the claims or specification of the present application, unless otherwise stated, adjectives such as “substantially” and “about” modifying a condition or relationship characteristic of a feature or features of an embodiment, are understood to mean that the condition or characteristic is defined to within tolerances that are acceptable for operation of the embodiment for an application for which it is intended.
[0082] It should be understood that where the claims or specification refer to “a” or “an” element, such reference is not to be construed as there being only one of that element.
[0083] In the description and claims of the present application, each of the verbs, “comprise” “include” and “have”, and conjugates thereof, are used to indicate that the object or objects of the verb are not necessarily a complete listing of components, elements or parts of the subject or subjects of the verb.
[0084] While this disclosure describes a limited number of embodiments, it will be appreciated that many variations, modifications and other applications of such embodiments may be made. The disclosure is to be understood as not limited by the specific embodiments described herein, but only by the scope of the appended claims.