MULTI-RESOLUTION GRAPHICAL DISPLAY FOR FEEDBACK ON CHEST COMPRESSION DEPTH
    1.
    发明申请
    MULTI-RESOLUTION GRAPHICAL DISPLAY FOR FEEDBACK ON CHEST COMPRESSION DEPTH 审中-公开
    用于反馈压缩深度的多分辨率图形显示

    公开(公告)号:WO2012075044A3

    公开(公告)日:2012-11-22

    申请号:PCT/US2011062463

    申请日:2011-11-29

    Abstract: Embodiments of the present concept are directed to medical devices. For example, a medical device including a display for providing feedback to a rescuer who is performing Cardio Pulmonary Resuscitation (CPR) chest compressions to a patient. The display is structured to graphically indicate an instantaneous value of a measured compression depth of the chest of the patient. The display includes an indicator range that corresponds at least in part to a compression depth range of some of the measured compression depths. An indicator is represented as progressing along the indicator range as the depth changes within the compression depth range to represent a value of the measured compression depth in relation to the indicator range. Depending on the measured compression depth, the indicator progresses at a variable rate relative to a difference in the measured compression depth.

    Abstract translation: 本概念的实施例涉及医疗装置。 例如,医疗设备包括用于向正在对患者执行心肺复苏(CPR)胸部按压的救援者提供反馈的显示器。 显示器被构造成图形地指示患者胸部的测量的压缩深度的瞬时值。 显示器包括至少部分地对应于一些测量的压缩深度的压缩深度范围的指示器范围。 随着深度在压缩深度范围内变化以指示相对于指示器范围的测量的压缩深度的值,指示符被表示为沿指示器范围的前进。 根据测量的压缩深度,指示器以相对于测量的压缩深度的差异的可变速率进行。

    DEFIBRILLATOR BATTERY AUTHENTICATION SYSTEM
    2.
    发明申请
    DEFIBRILLATOR BATTERY AUTHENTICATION SYSTEM 审中-公开
    减震器电池认证系统

    公开(公告)号:WO2009149065A2

    公开(公告)日:2009-12-10

    申请号:PCT/US2009045943

    申请日:2009-06-02

    Abstract: A method for operating an external medical device such as a defibrillator includes obtaining a data set from a battery pack and examining the data set to determine whether the battery pack is authenticated for use in the external medical device. If the examination does not confirm the authentication, the method includes causing the device to follow a non- authenticated battery pack protocol. The non- authenticated battery pack protocol may include drawing power from the non- authenticated battery pack only if it is the only available source of power for the external medical device. It may include limiting functionality of the external medical device. It may include modifying the battery status information display for the non- authenticated battery pack. A power system for an external medical device may include a power source external to the medical device and including a memory which stores data indicative of an authorized status of the power source and a processor in the medical device configured to analyze the data and to control a function of the medical device based at least in part on the authorization status.

    Abstract translation: 用于操作诸如除颤器的外部医疗设备的方法包括从电池组获得数据集并检查数据集以确定电池组是否被认证用于外部医疗装置。 如果检查未确认认证,则该方法包括使设备遵循非认证的电池组协议。 未经认证的电池组协议可以包括仅当其是用于外部医疗设备的唯一可用电源时才从未认证的电池组中抽取功率。 它可以包括限制外部医疗设备的功能。 它可能包括修改非认证电池组的电池状态信息显示。 用于外部医疗设备的电力系统可以包括医疗设备外部的电源,并且包括存储器,其存储指示电源的授权状态的数据,以及处理器,被配置为分析数据并控制 至少部分地基于授权状态的医疗设备的功能。

    Defibrillator, der hörbare Aufforderungen an eine Hörmuschel liefert

    公开(公告)号:DE112011103648B4

    公开(公告)日:2018-06-14

    申请号:DE112011103648

    申请日:2011-10-31

    Abstract: Defibrillator (100, 300, 400, 500, 600), um für eine Person (82) zu sorgen, wobei der Defibrillator (100, 300, 400, 500, 600) mit wenigstens einem externen persönlichen Tongerät (410, 420, 431, 612, 622) Verwendung findet, welches dazu eingerichtet ist, unhörbare Audio-Information zu empfangen, welche einer hörbaren Angabe entspricht, und die hörbare Angabe in Reaktion auf ein Empfangen der Audio-Information an einen Nutzer (380, 381, 414, 424, 434, 616, 626) zu liefern, welcher für die Person (82) sorgt, wobei der Defibrillator (100, 300, 400, 500, 600) umfasst:ein Gehäuse (501, 601), welches ein Energiespeichermodul (350) zum Speichern von elektrischer Ladung enthält;einen Defibrillationsanschluss zum Leiten der gespeicherten elektrischen Ladung über Elektroden (104, 108, 304, 308) an die Person (82);einen Prozessor (330, 430), der dazu eingerichtet ist, zu bestimmen, ob die hörbare Angabe an den Nutzer (380, 381, 414, 424, 434, 616, 626) auszugeben ist;eine erste Buchse (510, 610) in dem Gehäuse (501, 601), wobei die erste Buchse (510, 610) dazu eingerichtet ist, einen Stecker zu empfangen, der dem wenigstens einen externen persönlichen Tongerät (410, 420, 431, 612, 622) zugeordnet ist;eine zweite Buchse (520, 620) in dem Gehäuse (501, 601), wobei die zweite Buchse (520, 620) ebenfalls dazu eingerichtet ist, den Stecker zu empfangen, der dem wenigstens einen externen persönlichen Tongerät (410, 420, 431, 612, 622) zugeordnet ist; undein Kommunikationsmodul (490), das dazu eingerichtet ist, in Reaktion auf eine Bestimmung durch den Prozessor (330, 430), dass die hörbare Angabe auszugeben ist, die unhörbare Audio-Information, welche der hörbaren Angabe entspricht, an das wenigstens eine externe persönliche Tongerät (410, 420, 431, 612, 622) zu übertragen, wobei die übertragene Audio-Information für den Nutzer (380, 381, 414, 424, 434, 616, 626) unhörbar ist,in welchem das Kommunikationsmodul (490) ferner dazu eingerichtet ist, unhörbare Audio-Informationen unter Verwendung der ersten Buchse zu übertragen, die verschieden sind von unhörbaren Audio-Informationen, die unter Verwendung der zweiten Buchse übertragen werden.

    5.
    发明专利
    未知

    公开(公告)号:DK1986739T3

    公开(公告)日:2009-12-07

    申请号:DK06733999

    申请日:2006-01-31

    Abstract: Methods and apparatus are provided for determining a defibrillation treatment protocol in an external defibrillator whereby a user may override a CPR-first default protocol. The method includes following steps configured in a defibrillator controller of issuing an inquiry; waiting for a response to the inquiry for a set time; ordering a CPR treatment protocol if no response is received within the set time; analyzing a response; ordering a CPR treatment protocol upon receiving a non-affirmative response to the inquiry; and ordering a shock treatment protocol upon receiving an affirmative response to the inquiry. Upon selecting a shock treatment protocol, the defibrillator performs a shock analysis under the shock treatment protocol, and either orders a CPR treatment protocol if shock treatment is not indicated by the shock analysis or provides a defibrillation shock if shock treatment is indicated by the shock analysis. Queries may be presented to a user in visual, audible, or both visual and audible format.

    USER INTERFACE METHOD AND APPARATUS FOR A MEDICAL DEVICE

    公开(公告)号:CA2828141A1

    公开(公告)日:2003-11-27

    申请号:CA2828141

    申请日:2003-05-08

    Abstract: A user interface method and apparatus is described for use with a defibrillator (100) such as an automated external defibrillator (AED). The user interface comprises a plurality of layered user interface components which become available to the operator of the defibrillator (100) as they become necessary or appropriate during the operation of the defibrillator (100) and treatment of the patient. In one embodiment, the layered user interface components comprise an on/off actuator (108), a lid (104), an electrode package (120) containing defibrillation electrodes (142, 144), and a shock key (170), as well as accompanying visual and aural instructions for operating the defibrillator (100) and for treating the patient.

    7.
    发明专利
    未知

    公开(公告)号:DE602006008992D1

    公开(公告)日:2009-10-15

    申请号:DE602006008992

    申请日:2006-01-31

    Abstract: Methods and apparatus are provided for determining a defibrillation treatment protocol in an external defibrillator whereby a user may override a CPR-first default protocol. The method includes following steps configured in a defibrillator controller of issuing an inquiry; waiting for a response to the inquiry for a set time; ordering a CPR treatment protocol if no response is received within the set time; analyzing a response; ordering a CPR treatment protocol upon receiving a non-affirmative response to the inquiry; and ordering a shock treatment protocol upon receiving an affirmative response to the inquiry. Upon selecting a shock treatment protocol, the defibrillator performs a shock analysis under the shock treatment protocol, and either orders a CPR treatment protocol if shock treatment is not indicated by the shock analysis or provides a defibrillation shock if shock treatment is indicated by the shock analysis. Queries may be presented to a user in visual, audible, or both visual and audible format.

    Multi-resolution graphical display for feedback on chest compression depth

    公开(公告)号:AU2011336723B2

    公开(公告)日:2017-02-23

    申请号:AU2011336723

    申请日:2011-11-29

    Abstract: Embodiments of the present concept are directed to medical devices. For example, a medical device including a display for providing feedback to a rescuer who is performing Cardio Pulmonary Resuscitation (CPR) chest compressions to a patient. The display is structured to graphically indicate an instantaneous value of a measured compression depth of the chest of the patient. The display includes an indicator range that corresponds at least in part to a compression depth range of some of the measured compression depths. An indicator is represented as progressing along the indicator range as the depth changes within the compression depth range to represent a value of the measured compression depth in relation to the indicator range. Depending on the measured compression depth, the indicator progresses at a variable rate relative to a difference in the measured compression depth.

    Multi-resolution graphical display for feedback on chest compression depth

    公开(公告)号:AU2011336723A1

    公开(公告)日:2013-06-20

    申请号:AU2011336723

    申请日:2011-11-29

    Abstract: Embodiments of the present concept are directed to medical devices. For example, a medical device including a display for providing feedback to a rescuer who is performing Cardio Pulmonary Resuscitation (CPR) chest compressions to a patient. The display is structured to graphically indicate an instantaneous value of a measured compression depth of the chest of the patient. The display includes an indicator range that corresponds at least in part to a compression depth range of some of the measured compression depths. An indicator is represented as progressing along the indicator range as the depth changes within the compression depth range to represent a value of the measured compression depth in relation to the indicator range. Depending on the measured compression depth, the indicator progresses at a variable rate relative to a difference in the measured compression depth.

    USER INTERFACE METHOD AND APPARATUS FOR A MEDICAL DEVICE

    公开(公告)号:CA2828141C

    公开(公告)日:2015-12-08

    申请号:CA2828141

    申请日:2003-05-08

    Abstract: A user interface method and apparatus is described for use with a defibrillator (100) such as an automated external defibrillator (AED). The user interface comprises a plurality of layered user interface components which become available to the operator of the defibrillator (100) as they become necessary or appropriate during the operation of the defibrillator (100) and treatment of the patient. In one embodiment, the layered user interface components comprise an on/off actuator (108), a lid (104), an electrode package (120) containing defibrillation electrodes (142, 144), and a shock key (170), as well as accompanying visual and aural instructions for operating the defibrillator (100) and for treating the patient.

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