PHYSIO-CONTROL, INC. Patent applications |
Patent application number | Title | Published |
20160121133 | MEDICAL MONITOR-DEFIBRILLATOR WITH DEFIBRILLATOR AND DATA OPERATIONS PROCESSORS - A defibrillator is provided with two processors for enhancing the defibrillation process. A first processor is dedicated to controlling when an electrical charge is applied to a patient. A second processor is dedicated to data operations for enhancing the coaching of the defibrillation process. The second data processor is in communication with one or more external devices for transmission and receipt of network data for further enhancing the coaching process. The second data processor allows both the defibrillator to be maintained with updated network data and software and the one or more external devices to be maintained with updated defibrillator data. Independent controllers provide multiple processing paths on critical charge and coaching functions; with the second data processor further providing redundancy control in the event of any malfunction of the first charge processor. | 05-05-2016 |
20160117496 | INTELLIGENT ACCESSORIES FOR MEDICAL DEVICES - An accessory for a host medical device that is capable of authenticating itself to the host medical device. The accessory includes an onboard facility for authenticating the accessory to the host medical device. Various embodiments of the accessory enable it to validate itself to the host medical device without the host medical device reading any stored information from the accessory. | 04-28-2016 |
20160067140 | CPR CHEST COMPRESSION MACHINE STOPPING TO DETECT PATIENT RECOVERY - Embodiments of the present concept are directed to CPR chest compression machines that include a sensor to detect a parameter about a patient, such as an indication of patient recovery, and include a processor that determines whether to cease series of successive compressions on the patient in response to the detected parameter. | 03-10-2016 |
20150283391 | PRESSURE RESISTANT CONDUCTIVE FLUID CONTAINMENT - A conductive fluid reservoir can be used to dispense conductive fluid to increase electrical connectivity between an electrode of a defibrillator and a patient. The reservoir includes a container that holds the conductive fluid, one or more outlets on the container, and an inflatable pouch located at least partially within the container. The inflatable pouch is capable of being inflated from a deflated state to an inflated state. In the deflated state, a free end of the inflatable pouch covers the one or more outlets. In the inflated state, the free end of the inflatable pouch is removed from the one or more outlets such that the conductive fluid is allowed to flow out of the container via the one or more outlets. Inflating the inflatable pouch causes the conductive fluid to be dispensed from the reservoir. | 10-08-2015 |
20150256140 | VARIABLE SOUND SYSTEM FOR MEDICAL DEVICES - A system capable of self-adjusting both sound level and spectral content to improve audibility and intelligibility of medical device audible cues. Audible cues are stored as sound files. Ambient noise is detected, and the output of the audible cues is altered based on the ambient noise. Various embodiments include processed sound files that are more robust in noisy environments. | 09-10-2015 |
20150148855 | ANTENNA SYSTEM FOR SIGNAL-ATTENUATING CONTAINERS - A system can include a container that includes a cabinet capable of attenuating or blocking wireless signals, an AED located within the cabinet, an internal patch antenna removably mounted to an internal surface of the cabinet, an external patch antenna removably mounted to an external surface of the cabinet, and an electrical connection between the internal patch antenna and the external patch antenna. The internal and external patch antennas can be configured to transmit wireless signals at a particular frequency and to receive wireless signals at the particular frequency. The system can be configured such that the internal patch antenna is operative to receive a first wireless signal from the AED, a first electrical signal based on the first wireless signal is provided via the electrical connection to the external patch antenna, and a second wireless signal based on the first electrical signal is radiated by the external patch antenna. | 05-28-2015 |
20150073490 | SYSTEM AND METHOD FOR USING DIAGNOSTIC PULSES IN CONNECTION WITH DEFIBRILLATION THERAPY - An external defibrillator system is disclosed that generates and applies a diagnostic signal to the patient in conjunction with defibrillation therapy. The diagnostic signal is designed to elicit a physiologic response from the patient's heart, namely, mechanical cardiac response and electrical cardiac response, electrical cardiac response only, or no cardiac response. Depending upon the type of cardiac response detected, the system selects an appropriate resuscitation protocol that considers the likely responsiveness of the patient to defibrillation therapy. In one practical embodiment, a stimulus signal is applied to patients that show mechanical and electrical capture in response to the diagnostic signal. The stimulus signal maintains the mechanical capture (and, therefore, perfusion) for a period of time prior to the delivery of a defibrillation pulse. | 03-12-2015 |
20140358048 | SELECTIVE POST-SHOCK TRANSTHORACIC PACING - A medical device can include a housing, an energy storage module within the housing to store an electrical charge, and a defibrillation port to guide via electrodes the stored electrical charge to a person in need of medical assistance. The medical device can also include a processor to perform a patient signal analysis on an electrocardiogram (ECG) signal corresponding to the person and further determine, based on a result of the patient signal analysis, whether post-shock transcutaneous pacing should be performed on the person. | 12-04-2014 |
20140336546 | TIME-VARYING CHEST COMPRESSIONS - Various types of chest compressions may be performed on a patient during a single resuscitation event. In embodiments one or more compression time parameters may be changed during the event, potentially optimizing blood flow for one side of the patient's heart, then the other. In some embodiments the event includes one or more prolonged compressions interposed between other compressions, potentially enabling the blood to reach to more remote locations than otherwise. In embodiments, a CPR chest compression machine includes a compression mechanism configured to perform successive compressions to the patient's chest, and a driver configured to drive the compression mechanism accordingly. In embodiments, a CPR metronome issues prompts for compressions accordingly. | 11-13-2014 |
20140303530 | CPR APPARATUS AND METHOD - A CPR apparatus comprises a chest compression unit and a means for mounting the chest compression unit on a patient. The chest compression unit comprises a plunger disposed in a housing. At its one end extending from the housing the plunger has a compression member. The plunger is driven in a reciprocating manner by a reversible electromotor via a mechanical means for translating rotational motion to linear motion or by a linear induction electromotor. The chest compression unit comprises an electromotor control unit including a microprocessor, a first monitoring means for monitoring the position of the plunger in respect of the housing and a second monitoring means for monitoring the position of the plunger in respect of the mechanical means for translating rotational motion to linear motion or the rotor of the linear induction electromotor. The monitored positions are communicated to the electromotor control unit. Also disclosed is a corresponding CPR method. | 10-09-2014 |
20140278463 | CLINICAL DASHBOARD FOR MEDICAL DEVICE - A clinical dashboard device, system, method for providing clinical data for clinical dashboard display on a device is disclosed. The system includes a server for providing clinical dashboard data, which may include data from one or more defibrillators, and further includes a clinical dashboard device. The clinical dashboard device includes a processor, a communication module configured for enabling communication between the processor and the server for receiving the clinical dashboard data from the server, and a clinical dashboard client. The clinical dashboard client includes a clinical dashboard data manager module including an instance of a clinical dashboard data manager service that provides managed clinical dashboard data between one or more clinical dashboard applications and the server. The instance of the clinical dashboard data manager service further provides managed display of managed clinical dashboard data on the display of the clinical dashboard device. The processor is configured to execute the instance. | 09-18-2014 |
20140277227 | MEDICAL MONITOR-DEFIBRILLATOR WITH DEFIBRILLATOR AND DATA OPERATIONS PROCESSORS - A defibrillator is provided with two processors for enhancing the defibrillation process. A first processor is dedicated to controlling when an electrical charge is applied to a patient. A second processor is dedicated to data operations for enhancing the coaching of the defibrillation process. The second data processor is in communication with one or more external devices for transmission and receipt of network data for further enhancing the coaching process. The second data processor allows both the defibrillator to be maintained with updated network data and software and the one or more external devices to be maintained with updated defibrillator data. Independent controllers provide multiple processing paths on critical charge and coaching functions; with the second data processor further providing redundancy control in the event of any malfunction of the first charge processor. | 09-18-2014 |
20140272860 | DECISION SUPPORT TOOL FOR USE WITH A MEDICAL MONITOR-DEFIBRILLATOR - Work flows are modeled as a graph of interdependent tasks to be performed. The tasks to be performed are set by a task file module configured to enable interactions between tasks and including modules for event viewing, protocol assistance, smart messaging, smart indices, reference material lookup. A decision support manager module is configured to construct data and model profiles for storage in a data and model profile bank, events for storage in a decision support events bank, and protocols for storage in a decision support protocol bank. Configuration files are provided to specify a configuration for execution of one of the tasks. Data entered through a user interface or from a network via a wireless or wired communication module may define task files in the task files module, configuration files in the configuration files module, as well as data, events, and protocols to be used for a defibrillation procedure. A decision support manager module is configured to construct a dependency graph of tasks as specified in at least one of the configuration files and to execute the dependency graph. | 09-18-2014 |
20140243918 | Wearable Defibrillator With A Multivector Shock Waveform - A transthoracic defibrillator for external defibrillation comprises at least three electrodes configured to be attached to the thorax of a patient to establish at least two electrical paths across the thoracic cavity and through the heart of the patient. In addition, a defibrillator circuit contained in a defibrillator housing has the capability to deliver a different defibrillation waveform across each of the at least two electrical paths. | 08-28-2014 |
20140236053 | CPR QUALITY ASSESSMENT ACCOUNTING FOR PAUSE ASPECT - Devices, systems, software and methods for CPR quality assessment. Patient data is received, derived from a session of administering sets of CPR chest compressions to a patient. The sets can be separated by pauses. In some embodiments, a penalty value can be determined for at least one of the pauses, from at least one control factor unrelated to a constant linear dependence on the pause duration. An Indicative value can be derived from the penalty value. In some embodiments, at least some of the pauses are classified in one or more pause groups, depending on how well they meet one or more classification criteria. The indicative value can be derived for one of the pause groups. The indicative value can be output, and/or an alarm can be emitted if it exceeds a threshold. CPR quality assessment can be improved in real time, and provide feedback for training/ | 08-21-2014 |
20140221883 | FIXATION OF DEVICE TO BACK PLATE - A mechanical CPR device can include a back plate, a first tower, and a second tower. The back plate can have a first side and a second side. The first tower can include a first foot and the second tower can include a second foot. The first and second towers can be configured to securely hold a beam above the back plate. The first side of the back plate can be configured to be held to the first foot of the first tower and the second side of the back plate can be configured to be held to the second foot of the second tower when a distributed weight is placed on the back plate. | 08-07-2014 |
20140221882 | BEAM MECHANICAL COMPRESSION DEVICE - A mechanical CPR device includes a back plate, a first tower removably attached to the back plate, a second tower removably attached to the back plate, and a beam releasably connected to each of the first tower and the second tower. The first tower can include a first linear motion device. The second tower can include a second linear motion device. Each of the first and second linear motion devices can be configured to move one end of the beam toward and away from the back plate. The first and second linear motion devices can be configured to operate in concert such that, when the back plate is resting on a surface, the beam remains substantially parallel to the surface during movement of the beam toward and away from the back plate. | 08-07-2014 |
20140207201 | WEARABLE CARDIAC DEFIBRILLATOR SYSTEM CONTROLLING CONDUCTIVE FLUID DEPLOYMENT - In embodiments, a wearable cardiac defibrillator system includes an energy storage module configured to store a charge. Two electrodes can be configured to be applied to respective locations of a patient. One or more reservoirs can store one or more conductive fluids. Respective fluid deploying mechanisms can be configured to cause the fluids to be released from one or more of the reservoirs, which decreases the impedance at the patient location, and decreases discomfort for the patient. In some embodiments an impedance is sensed between the two electrodes, and the stored charge is delivered when the sensed impedance meets a discharge condition. In some embodiments, different fluids are released for different patient treatments. In some embodiments, fluid release is controlled to be in at least two doses, with an intervening pause. | 07-24-2014 |
20140207031 | SUPPORT STRUCTURE FOR ADMINISTERING CARDIOPULMONARY RESUSCITATION - The present invention relates generally to a support structure for fixating a patient to a treatment unit, and especially to a support structure for fixating the patient to a cardiopulmonary resuscitation unit. An embodiment of the support structure comprises a back plate for positioning behind said patient's back posterior to said patient's heart and a front part for positioning around said patient's chest anterior to said patient's heart. Further, the front part can comprise two legs, each leg having a first end pivotably connected to at least one hinge and a second end removably attachable to said back plate. Said front part can further be devised for comprising a compression/decompression unit arranged to automatically compress or decompress said patient's chest when said front part is attached to said back plate. | 07-24-2014 |
20140200464 | PATIENT TEMPERATURE CHANGE COMBINED WITH REMOTE ISCHEMIC CONDITIONING - A single system may provide to a patient: temperature change, remote ischemic conditioning, and sometimes both concurrently. The system may include a patient unit that includes an inflatable bladder, and a duct having a cavity. The patient unit is intended to be applied around a patient's limb. A temperature subsystem can force a flow of a first fluid through the cavity so that the first fluid can exchange heat with the patient's limb. The pressure subsystem may force a fluid into the bladder, to establish pressure against the limb. A controller may control both the temperature subsystem and the pressure subsystem, so as to control the treatment received by the patient. | 07-17-2014 |
20140188500 | CONTEXT-SENSITIVE CHEST COMPRESSION FRACTION MEASUREMENT FOR CPR QUALITY ASSESSMENT - Devices, systems, software and methods for CPR quality assessment. Patient data is received that may be derived from a session of administering sets of CPR chest compressions to a patient. The sets can be separated by pauses. Then a figure of merit (FOM) can be computed from the data in the computation, at least one pause can contribute a penalty to the FOM. The penalty has a value determined from at least one control factor, other than a constant linear dependence on the duration of the pause. This way, pauses can incur penalties to the FOM computation depending on their context, instead of merely their duration. For example, a penalty can escalate non-linearly if its pause becomes unduly long, or if it follows a set of chest compressions that was unduly short. As such, a better CPR quality assessment is achieved. | 07-03-2014 |
20140180180 | MECHANICAL CPR DEVICE WITH AUTOMATIC SUCTION CUP ATTACHMENT - A suction cup on the end of a piston of a mechanical CPR device can be automatically attached to a patient's torso. The mechanical CPR device can extend the piston until a first position at which the suction cup comes into contact with the patient's torso. The piston can be further extended to cause air to be forced out from an area between the suction cup and the patient's torso until a first threshold is reached. The piston can be retracted until the suction cup is at the first position. The piston can be further retracted from the first position until a second threshold is exceeded. The piston can then be extended to a second point at which the second threshold is no longer exceeded. | 06-26-2014 |
20140159904 | MEDICAL DEVICE INCLUDING SETUP OPTION REPORTING - A medical device for use with a patient is described. The medical device includes a component for administering a treatment to the patient or receiving data of the patient. The component is configured to operate according to an internal setting. The medical device also includes a user interface through which a user can modify the internal setting, as well as a settings signature generator for generating a settings signature that represents a present state of the internal setting. A gateway is also provided for communicating a version of the settings signature out of the medical device. | 06-12-2014 |
20140148869 | External Defibrillator Electrode, Method and System for Reducing ECG Artifact - An electrode for use with an external defibrillator for a patient includes a first combination circuit including a circuit node electrically coupled to an adapter for coupling to the defibrillator. The circuit node is further coupled to a monitoring node defined by a monitoring segment of a first pad of the electrode and to a therapy node defined by a therapy segment of the first pad of the electrode. The therapy segment is electrically insulated from the monitoring segment. The first combination circuit further includes a capacitor coupled between the circuit node and the therapy node. The electrode of this disclosure hence provides additional solutions for reducing ECG artifact during the operation of the electrode. | 05-29-2014 |
20140148718 | LINEAR DISPLAY OF ECG SIGNALS - An illustrative method and system for displaying ECG data of a patient includes the steps of: receiving an ECG waveform of a patient, determining at least a first attribute of the ECG waveform, and determining at least one data point from the first attribute of the ECG waveform. The first data point and associated first attribute of the ECG waveform are displayed on a linear scale. In an alternative method, the at least one data point is structured in a database of ECG data according to the Cabrera sequence; the display domain of the display is divided into several recurrent display slots; and a sequential one of the several recurrent display slots is associated with the at least one data point, which is displayed on the linear scale in the order in which the at least one data point appears in the Cabrera structured database of ECG data. | 05-29-2014 |
20140142647 | DEFIBRILLATOR PATIENT MONITORING POD - A patient parameter monitoring pod in embodiments of the teachings may include one or more of the following features: (a) portable housing containing a power supply, (b) a patient parameter module connectable to a patient via lead cables to collect patient data, the patient data including at least one vital sign, (c) a transceiver adapted to wirelessly transmit the patient data to a defibrillator, (d) a data port adapted to supply the patient data via a direct electrical connection to the defibrillator, and (e) a carrying handle extending from the housing proximate a patient lead cable port that permits connection of the lead cables to the pod, the carrying handle positioned to protect the patient lead cable port and the patient lead cables attached to the port from direct impact. | 05-22-2014 |
20140135667 | SYSTEM AND METHOD FOR DETERMINING DEPTH OF CHEST COMPRESSIONS - Systems and methods for determining depth of compressions of a chest of a patient receiving chest compressions. A field detector is used having at least two coils at a fixed distance from each other. | 05-15-2014 |
20140121576 | BACK PLATES FOR MECHANICAL CPR COMPRESSION - A back plate includes an upper portion, a lower surface defining a plane, a first side, a second side, a plurality of first static attachment elements configured to releasably connect to legs of the compression device, and a plurality of second static attachment elements configured to releasably connect to legs of the compression device. Each of the first and second sides can include one of the plurality of first static attachment elements and one of the plurality of second static attachment elements. The distance between one of the plurality of second static attachment elements on the first side and one of the plurality of second static attachment elements on the second side is greater than a distance between one of the plurality of first static attachment elements on the first side and one of the plurality of first static attachment elements on the second side. | 05-01-2014 |
20140100622 | EXTERNAL DEFIBRILLATION WITH AUTOMATIC POST-SHOCK ANTI-TACHYCARDIA (APSAT) PACING - A medical device such as an external defibrillator delivers electrical therapy using a special pulse sequence. The special pulse sequence includes a defibrillation shock that is automatically followed by a quick succession of automatic post-shock anti-tachycardia (APSAT) pacing pulses. Because of the pacing pulses, the defibrillation shock can be of lesser energy than an equivalent defibrillation shock of a larger energy. Accordingly, the external defibrillator can be made physically smaller and weigh less, without sacrificing the therapeutic effect of a larger external defibrillator that would deliver a defibrillation shock of higher energy. As such, the defibrillator is easier to configure for transporting, handling, and even wearing. | 04-10-2014 |
20140100496 | DEVICES AND METHODS FOR PERFORMING CPR WHILE STANDING UP - In one embodiment, a manual CPR device, also known as a CPR derrick, includes a frame that is put close to a patient who is on the ground. The device also includes a piston that can be moved up and down, and is aligned to be over the patient's chest. The device also has an actuator that the rescuer can operate manually so as to move the piston up and down, which will deliver compressions to the patient's chest. A bottom stop prevents the compressions from being too deep. In some embodiments, proper dimensioning of the CPR derrick permits the rescuer to perform CPR chest compressions while standing up, i.e. without kneeling. The rescuer may be able to perform higher quality CPR, and for a longer time, giving more opportunity to a life-saving team to arrive in time. | 04-10-2014 |
20140094869 | PREVENTING USE OF SYNC MODE DURING CARDIOVERSION AND DEFIBRILLATION - An external defibrillator may have a controller to set the defibrillator in a synchronous shock operating mode or an asynchronous shock operating mode, a shock module to cause the defibrillator to deliver shock therapy to a patient according to the present operating mode of the defibrillator, and a heart rhythm detector to detect a heart rhythm of the patient. The defibrillator may also have a mode assessment module to determine whether the present operating mode or selected defibrillation energy of the defibrillator is appropriate based on the detected heart rhythm of the patient. | 04-03-2014 |
20140094867 | DEFIBRILLATOR WITH SYNC MODE ASSISTING SELECTION OF FEATURE TO LOCK-ON - An external defibrillator, such as a wearable defibrillator can have a heart rhythm detector to detect the heart rhythm of a patient. The defibrillator can also have a synchronous shock operating mode and an asynchronous shock operating mode. A controller can set the defibrillator in the synchronous shock operating mode or the asynchronous shock operating mode. The defibrillator can also include a shock module to cause the defibrillator to deliver shock therapy to the patient according to the operating mode of the defibrillator and a sync module configured to identify a first portion of the heart rhythm detected from a first ECG lead with which to time the delivery of the shock therapy to the patient when the operating mode of the defibrillator is in synchronous shock operating mode. A comparator module can compare timing of a QRS complex detected from the first ECG lead with the timing of the QRS complex detected by the second EGG lead. | 04-03-2014 |
20140094866 | INTELLIGENT SYNC MODE FOR DEFIBRILLATION - The defibrillator may include a heart rhythm detector to detect the heart rhythm of a patient, a manual mode controller structured to set the defibrillator in a synchronous shock operating mode or an asynchronous shock operating mode depending on an input from a human operator, a shock module to cause the defibrillator to deliver a shock to the patient according to the operating mode, and an automatic mode controller structured to, after the shock module has delivered the shock to the patient, set the external defibrillator to the synchronous shock operating mode or the asynchronous shock operating mode depending on the detected heart rhythm of the patient and without input from the human operator. | 04-03-2014 |
20140094865 | DEFIBRILLATOR WARNING OF SYNC MODE SETTING AFTER DELIVERY OF SHOCK - An external defibrillator can have a synchronous shock operating mode and an asynchronous shock operating mode and include a controller to set the defibrillator in the synchronous shock operating mode or the asynchronous shock operating mode. The defibrillator can also include a shock module to cause the defibrillator to deliver shock therapy to the patient according to the operating mode of the defibrillator, and a prompt module to transmit a prompt, after delivery of the shock therapy, that includes the operating mode of the defibrillator. | 04-03-2014 |
20140088660 | WEARABLE CARDIAC DEFIBRILLATOR SYSTEM WITH ANTI-BRADYARRHYTHMIA PACING & METHODS - In one embodiment, a wearable defibrillation system may sense whether its wearer meets an unconscious bradyarrhythmia condition that can be associated with becoming unconscious. Even though such a condition might not be helped with a defibrillation pulse, the wearable-defibrillation system may still administer pacing pulses to prevent the bradycardia from becoming worse, such as a sudden cardiac arrest. In some embodiments, the pacing pulses are administered at a frequency too slow for the patient to regain consciousness. An advantage is that, because the patient remains unconscious, he does not experience the sometimes severe discomfort due to the pacing pulses. | 03-27-2014 |
20140088374 | FILTERING PATIENT SIGNAL ALSO FOR VENTILATION ARTIFACTS - In embodiments, an external medical device is intended to care for a patient. If it receives an input that signifies that ventilation artifact is present in a signal of the patient, it transmits a corrective signal responsive to the received input. In further embodiments, a patient signal is received, which is generated from a patient while the patient is or was receiving chest compressions at a frequency Fc, and also receiving ventilations at frequency Fv. At least one filter mechanism may be applied to the patient signal to substantially remove artifacts at a) frequency Fc, b) a higher harmonic of frequency Fc, and c) a third frequency substantially equaling frequency Fc plus or minus frequency Fv, while substantially passing other frequencies between them. As a result, the patient signal can be cleaner, for diagnosing the patient's state more accurately. | 03-27-2014 |
20140087762 | DEFIBRILLATOR LOCATION TRACKING DEVICE - A defibrillator is disclosed for communication with a transmitter associated with a location. The defibrillator is configured to generate an electronic signature for determining a position of the defibrillator within the location. The electronic signature includes electronic data correlating the position of the defibrillator to the transmitter. The electronic data may include GPS data. The defibrillator is configured to generate the electronic signature during a first and a second window of time to define a first and a second electronic signature. A differential between the first and the second electronic signatures corresponds to a positional state of the defibrillator, indicating movement within or between two locations. In a disclosed system, the first electronic signature is stored in a database and a server is configured to generate the differential and to communicate the positional state of the defibrillator to a stakeholder. Methods of use are also disclosed. | 03-27-2014 |
20140085082 | PATIENT MONITORING DEVICE WITH REMOTE ALERT - A remote patient monitoring system provides patient physiological data and alerts/alarms from a main patient monitor to a remote patient monitor worn by a medical professional. The medical professional is alerted as to physiological data of the monitored patient, and provided alerts or alarms when predetermined levels are reached. The medical professional is able to reset the alert or alarms at the remote patient monitor. | 03-27-2014 |
20140085081 | WEARABLE CARDIAC DEFIBRILLATOR RECEIVING INPUTS BY BEING DELIBERATELY TAPPED & METHODS - A wearable defibrillation system includes an output device and a motion sensor. The output device emits a sound or a vibration for the patient, who responds by deliberately tapping the system. The motion sensor registers the tapping, and interprets it as a reply from the patient. The reply can be that the patient is conscious, or convey data that the patient enters by tapping the right number of times, or that the patient wants attention, and so on. Since the patient does not need direct access to the wearable defibrillation system for tapping it, he or she can wear it under their other garments, which helps preserve their dignity and privacy. | 03-27-2014 |
20140066823 | Mechanical CPR Device with Variable Resuscitation Protocol - Methods to control the delivery of CPR to a patient through a mechanical CPR device are described. The method generally allows for a gradual increase in the frequency of CPR cycles. The gradual increase can be regulated by protocols programmed within the CPR device such as intermittently starting and stopping the delivery of CPR accelerating the delivery of CPR, stepping up the CPR frequency, increasing the force of CPR, and adjusting the ratio of compression and decompression in a CPR cycle. Combinations of each of these forms may also be used to control the delivery of CPR. This manner of gradually accelerating artificial blood flow during the first minutes of mechanical CPR delivery can serve to lessen the potential for ischemia/reperfusion injury in the patient who receives mechanical CPR treatment. | 03-06-2014 |
20140058469 | PULSE DETECTION USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates optical characteristics of light transmitted into a patient to ascertain physiological signals, such as pulsatile changes in general blood volume proximate a light detector module. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 02-27-2014 |
20140052202 | MEDICAL DEVICE WITH SCREEN, AND DOOR COVERING THE SCREEN - Medical devices and methods of operating medical devices that treat and monitor patients include a housing and a module located within the housing. The module is configured to perform the treating and monitoring parameters of the patient. A screen is also attached to the housing. The screen is viewable by the user outside of the housing. The medical device also includes a door that is coupled with the housing. The door is movable between a closed position that covers at least some portion of the coverable portion of the screen so as to prevent the coverable portion of the screen from being viewed and an open position that does not cover the coverable portion of the screen. | 02-20-2014 |
20140052201 | MEDICAL DEVICE WITH INTERACTIVE CONTROL PANEL - Medical devices and methods in which a user can treat a patient or monitor a parameter of the patient or both may include a housing, a patient module located within the housing that is used for treating the patient, monitoring the patient or both, and a control panel. The control panel is attached to the housing and has a first surface and a second surface and is positionable between a first position and a second position with respect to the housing. The first position exposes a user to a first surface of the control panel and the second position exposes the user to a second surface of the control panel. A first set of user controls are located on one or the other of the first surface and the second surface and are structured to allow the user to interact with the patient module. | 02-20-2014 |
20140051962 | DETECTING LOSS OF FULL SKIN CONTACT IN PATIENT ELECTRODES - Patient electrodes, patient monitors, defibrillators, wearable defibrillators, software and methods may warn when an electrode stops being fully attached to the patient's skin. A patient electrode includes a pad for attaching to the skin of a patient, a lead coupled to the pad, and a contact detector that can change state, when the pad does not contact fully the skin of the patient. When the detector changes state, an output device may emit an alert, for notifying a rescuer or even the patient. | 02-20-2014 |
20140049377 | RFID-BASED SENSING OF CHANGED CONDITION - RFID-based sensors, RFID readers and software sense a changed condition. In one embodiment, an RFID-based sensor includes a base that may be placed at a location where a condition may change. The sensor includes an RFID tag that is coupled to the base. The sensor also includes a detector that can be electrically coupled to the RFID tag. If the condition changes, an electrical property of the detector also changes, impacting an operation of the RFID tag. The impacted operation can be detected by an RFID reader/interrogator so as to provide a notification. An advantage over the prior art is that the condition change can be sensed wirelessly over a domain that can be laborious or hazardous to access otherwise. Moreover, RFID based sensors can be made by modifying common RFID tags. | 02-20-2014 |
20140047314 | AUTOMATICALLY EVALUATING LIKELY ACCURACY OF EVENT ANNOTATIONS IN FIELD DATA - Embodiments operate in contexts where field data have been generated from a field event, and annotations have been generated from the field data, which purport to identify events within the field data, such as CPR compressions and ventilations. Metrics are generated from the annotations, which are used in training. In such contexts, a grade may be assigned that reflects how well the annotations meet one or more accuracy criteria. The grade may be used in a number of ways. Reviewers may opt to disregard field data and metrics that have a low grade. Expert annotators may be guided as to precisely which annotations to revise, saving time. A low grade may decide that the results are not emailed to reviewers, but to annotators. A learning medical device can use the grade internally to adjust its own internal parameters so as to improve its annotating algorithms. | 02-13-2014 |
20140046393 | SEQUENTIAL STACKED CAPACITOR DEFIBRILLATOR AND WAVEFORM GENERATED THEREFROM - A medical device such as an external defibrillator delivers electrical therapy using a special ascending, biphasic waveform. The special waveform is characterized by a set of at least two peaks. The amplitude of the second peak is greater than the amplitude of the first peak. The waveform is generated by switching capacitance configuration in the defibrillator from a parallel configuration to a series configuration while the defibrillator is delivering the defibrillation shock to the patient. Because of the switching capacitances and/or the waveform, the external defibrillator can be made physically smaller and weigh less, without sacrificing the therapeutic effect of a larger external defibrillator that would deliver a defibrillation shock of higher energy. As such, the defibrillator is easier to configure for transporting, handling, and even wearing. | 02-13-2014 |
20140046391 | WEARABLE DEFIBRILLATOR SYSTEM COMMUNICATING VIA MOBILE COMMUNICATION DEVICE - A wearable defibrillation system can establish a local comlink with a mobile communication device, such as a smartphone, tablet-type computer and the like. The mobile communication device can in turn establish a remote comlink with other devices in a network such as the internet. Accordingly, communication tasks relating to the wearable defibrillation system can be performed via the local and the remote comlinks, with or without the participation of the patient, who is wearing the system. The wearer can thus use the familiar interface of a mobile communication device for interacting with his defibrillator system. Moreover, he can do so while keeping on his regular clothes, which could conceal completely the wearable defibrillator system. The patient can thus preserve his dignity and privacy. | 02-13-2014 |
20140046228 | Mechanical Chest Compression Device with Tilt Sensor - A medical device such as an external cardiopulmonary resuscitation (CPR) device delivers chest compressions to a patient. The patient may shift and/or slide within the CPR chest compression structure if the CPR chest compression structure is tilted from the horizontal, however. A tilt module is used to sense a tilt event, report it to a user of the CPR chest compression machine, and cause the CPR chest compression machine, user, or tilt module to respond to the tilt event. Response can be pausing the CPR chest compression machine, having the user reposition the CPR chest compression machine, or the like. | 02-13-2014 |
20140043149 | MOBILE COMMUNICATION DEVICE & APP FOR WEARABLE DEFIBRILLATOR SYSTEM - A mobile communication device such as a smartphone or a tablet-type computer, can establish a local comlink with a wearable defibrillation system. At the same time, the mobile communication device can establish a remote comlink with other devices in a network such as the internet. Accordingly, communication tasks relating to the wearable defibrillation system can be performed via the local and the remote comlinks, with or without the participation of the patient, who is wearing the system. The patient can thus use the familiar interface of a mobile communication device for interacting with his defibrillator system. Moreover, he can do so while keeping on his regular clothes, which could conceal completely the wearable defibrillator system. The patient can thus preserve his dignity and privacy. | 02-13-2014 |
20140025131 | WEARABLE DEFIBRILLATOR WITH VOICE PROMPTS AND VOICE RECOGNITION - An external medical device such as a wearable defibrillator can include a housing, an energy storage module within the housing for storing an electrical charge, and a defibrillation port within the housing for guiding via electrodes the stored electrical charge to a person. The medical device can also include a processor within the housing configured to control a voice prompt customization module, in which the voice prompt customization module allows a programmer to customize voice prompts, and a user interface configured to deliver at least one voice prompt customized by the programmer | 01-23-2014 |
20140025129 | MEDICAL DEVICE WITH PROTOCOL LOCALIZATION - An external medical device can include a housing, an energy storage module within the housing for storing an electrical charge, and a defibrillation port for guiding via electrodes the stored electrical charge to a person. The device can also include a user interface to deliver prompts to a user during a defibrillation session and a locale detector in the housing to determine a present locale of the device. The prompts delivered by the user interface to the user during the defibrillation session can be in accordance with a protocol that is selected based on the present locale. | 01-23-2014 |
20140025128 | MEDICAL DEVICE WITH LANGUAGE LOCALIZATION - An external medical device can include a housing, an energy storage module within the housing for storing an electrical charge, and a defibrillation port for guiding via electrodes the stored electrical charge to a person. The device can also include a user interface to deliver prompts to a user during a defibrillation session and a language detector in the housing to determine a vicinity language. The prompts can be in a language that is selected based on the determined vicinity language. | 01-23-2014 |
20140005735 | DEFIBRILLATOR WITH IMPLANTABLE MEDICAL DEVICE DETECTION | 01-02-2014 |
20130345769 | USER INTERFACE METHOD AND APPARATUS FOR A MEDICAL DEVICE - A user interface method and apparatus is described for use with a defibrillator ( | 12-26-2013 |
20130338724 | PULSE DETECTION APPARATUS, SOFTWARE, AND METHODS USING PATIENT PHYSIOLOGICAL SIGNALS - A cardiac pulse in a patient is determined by evaluating physiological signals in the patient. A medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. The medical devices, or any portion thereof, can be worn by the patient or may be attached to the patient. | 12-19-2013 |
20130333054 | POST-DOWNLOAD PATIENT DATA PROTECTION IN A MEDICAL DEVICE - Patient data is stored in a medical device, such as an external defibrillator, and may be transferred, or downloaded, from the medical device to a computing device for storage or analysis. In response to the transfer, the medical device protects the patient data so that at least a subset of users cannot access the patient data from the medical device. The other device to which patient data is transferred from the medical device may be remote from the medical device or may be configured to be part of the medical device. The device to which the patient data is transferred from the medical device can be a remote computing device like a computer or server and/or may include or may be an intermediary data management device (DMD). The medical device may be a wearable medical device, such as a wearable defibrillator or a wearable automatic external defibrillator (AED). | 12-12-2013 |
20130331899 | DEFIBRILLATOR/MONITOR SYSTEM HAVING A POD WITH LEADS CAPABLE OF WIRELESSLY COMMUNICATING - A modular external defibrillator system in embodiments of the teachings may include one or more of the following features: a base containing a defibrillator to deliver a defibrillation shock to a patient, (b) one or more pods each connectable to a patient via patient lead cables to collect at least one patient vital sign, the pods operable at a distance from the base, (c) a wireless communications link between the base and a selected one of the two or more pods to carry the at least one vital sign from the selected pod to the base, the selection being based on which pod is associated with the base. | 12-12-2013 |
20130317560 | MEDICAL DEVICE WITH LACK-OF-READINESS ALARM - A medical device for caring for a patient includes a patient utility for measuring a patient parameter or administering a therapy to the patient and an alarm system that has a receiver to accept status information about the medical device. A use detector of the alarm system is structured to determine when the medical device is being prepared for use and a status detector of the alarm system is adapted to determine from the status information that the medical device is in a ready state. The alarm system further includes an alarm that is activated when the medical device is both being prepared for use and not in the ready state. This description also includes methods of generating an alarm when the medical device is both being prepared for use and not in the ready state. | 11-28-2013 |
20130304147 | DEFIBRILLATOR NETWORK SYSTEM - A defibrillator system optimizes the timing and manner of applying a defibrillator charge to a patient based upon data provided to the defibrillator from a utility module or one or more external devices. A parameter module on the utility module provides the defibrillator with patient parameter information. Devices external to the utility module may provide the utility module with coaching data that the utility module may pass through to the defibrillator as a proxy to the external devices. The utility module may also provide external devices with patient data that the utility module may pass through to the external devices as a proxy to the defibrillator on a scheduled or other basis. The utility module may additionally provide a reserve of power to enable defibrillators to be used where power is unavailable and to enable defibrillators to deliver multiple charges more readily anywhere, anytime. | 11-14-2013 |
20130304146 | UTILITY MODULE INTERFACE - A defibrillator system optimizes the timing and manner of applying a defibrillator charge to a patient based upon data provided to the defibrillator from a utility module or one or more external devices. A parameter module on the utility module provides the defibrillator with patient parameter information. Devices external to the utility module may provide the utility module with coaching data that the utility module may pass through to the defibrillator as a proxy to the external devices. The utility module may also provide external devices with patient data that the utility module may pass through to the external devices as a proxy to the defibrillator on a scheduled or other basis. The utility module may additionally provide a reserve of power to enable defibrillators to be used where power is unavailable and to enable defibrillators to deliver multiple charges more readily anywhere, anytime. | 11-14-2013 |
20130304145 | UTILITY MODULE SYSTEM - A defibrillator system optimizes the timing and manner of applying a defibrillator charge to a patient based upon data provided to the defibrillator from a utility module or one or more external devices. A parameter module on the utility module provides the defibrillator with patient parameter information. Devices external to the utility module may provide the utility module with coaching data that the utility module may pass through to the defibrillator as a proxy to the external devices. The utility module may also provide external devices with patient data that the utility module may pass through to the external devices as a proxy to the defibrillator on a scheduled or other basis. The utility module may additionally provide a reserve of power to enable defibrillators to be used where power is unavailable and to enable defibrillators to deliver multiple charges more readily anywhere, anytime. | 11-14-2013 |
20130304143 | MEDICAL DATA STORAGE AND COMMUNICATION SYSTEM - An external medical device can include a medical data collection port for collecting medical data corresponding to a person using the external medical device, a radio frequency identification (RFID) communication module, and a processor configured to cause the RFID communication module to provide the medical data to an RFID device that is external to the external medical device. | 11-14-2013 |
20130304142 | UTILITY MODULE - A defibrillator system optimizes the timing and manner of applying a defibrillator charge to a patient based upon data provided to the defibrillator from a utility module or one or more external devices. A parameter module on the utility module provides the defibrillator with patient parameter information. Devices external to the utility module may provide the utility module with coaching data that the utility module may pass through to the defibrillator as a proxy to the external devices. The utility module may also provide external devices with patient data that the utility module may pass through to the external devices as a proxy to the defibrillator on a scheduled or other basis. The utility module may additionally provide a reserve of power to enable defibrillators to be used where power is unavailable and to enable defibrillators to deliver multiple charges more readily anywhere, anytime. | 11-14-2013 |
20130296747 | RFID-BASED DETERMINATION OF COMPRESSION AND MOTION DURING CPR CHEST COMPRESSION - During cardiopulmonary resuscitation (CPR), compressions are delivered to a patient. The CPR compression includes a depth of compression. A medical device uses radio frequency identification (RFID) technology to determine the depth of compression. | 11-07-2013 |
20130296727 | FILTER MECHANISM FOR REMOVING ECG ARTIFACT FROM MECHANICAL CHEST COMPRESSIONS - An external medical device can include a housing and a processor within the housing. The processor can be configured to receive an input signal for a patient receiving chest compressions from a mechanical chest compression device. The processor can also be configured to select at least one filter mechanism, the mechanical chest compression device having a chest compression frequency f. The processor can be further configured to apply the at least one filter mechanism to the signal to at least substantially remove chest compression artifacts from the signal, wherein the chest compression artifacts correspond to the chest compressions being delivered to the patient by the mechanical chest compression device, and wherein the at least one filter mechanism substantially rejects content in the frequency f plus content in at least one more frequency that is a higher harmonic to the frequency f. | 11-07-2013 |
20130292283 | DEFIBRILLATOR CABINET WITH VIBRATION ISOLATION - An apparatus for storing a defibrillator, such as an AED, on a host structure includes a container shell mountable to the host structure. The container shell may be used to store the defibrillator within it. Also included in the container shell is a vibration-dampening material disposed between the host structure and the housing of the defibrillator. The vibration-dampening material is configured to reduce an amount of vibration of the host structure imparted to the defibrillator. This is especially useful for storing AEDs on means of transportation, i.e. where the traveling host structure is a bus, an airplane, a ship, or an elevator, and where the vibration sources from its propulsion system. | 11-07-2013 |
20130253600 | INTERNET SUPPORTED SOFTWARE UPDATES FOR MEDICAL DEVICES - A computer can include a first communication port for establishing a first connection with a medical device, a second communication port for establishing a second connection with a network, and an agent configured to query a collection of device records within the network to determine whether a device record specific to the medical device exists. The computer can also include a processor configured to receive over the second connection a message from the network responsive to the query, the message including an upgrade link specific to a device type corresponding to the device. The processor can also be configured to send to the medical device over the first connection an upgrade of a software application on the medical device responsive to a user selecting the upgrade link, where the software application is structured to cause the device to operate. | 09-26-2013 |
20130226255 | DEFIBRILLATOR THAT MONITORS CPR TREATMENT AND ADJUSTS PROTOCOL - An apparatus and method is provided for a defibrillator that specifies treatment protocols in terms of number of chest compressions instead of time intervals. The defibrillator includes a connection port that is configured to attach with a plurality of electrodes that are capable of delivery of a defibrillation shock and/or sensing one or more physical parameters. An energy storage device capable of storing a charge is attached to the plurality of electrodes. A controller is coupled to the plurality of electrodes and the energy storage device, the controller is configured to provide CPR chest compression instructions in terms of the numbers of CPR chest compressions. | 08-29-2013 |
20130225972 | ALERTING USERS OF CPR FEEDBACK DEVICE OF DETECTED MAGNETIC INTERFERENCE - A medical device and/or a method are used by a rescuer who is caring for a patient. The depth of CPR chest compressions is determined, by detecting magnetic fields. An interference is sensed, which is not associated with the CPR chest compressions, but which is superimposed on the detected magnetic fields. Appropriate countermeasures may be taken, if the sensed interference is larger than a threshold. | 08-29-2013 |
20130218220 | DEFIBRILLATORS DETECTING ORIENTATION OF ELECTRODE CONNECTION TO ADJUST ENERGY DOSAGE - Embodiments of the present concept are directed to external defibrillators that include an electrode connection port having multiple connection options, and include a detection device to determine an electrode connection configuration so as to provide an appropriate electrical shock to a patient. The detection device detects the electrode connection configuration of a plug connector for connected electrodes to determine if the plug connector is in an adult orientation or a pediatric orientation. The external defibrillator is configured to a deliver an electrical shock with less energy when the pediatric orientation is detected rather than the adult orientation. | 08-22-2013 |
20130218218 | VARIABLE FREQUENCY IMPEDANCE MEASUREMENT - When a defibrillator selects a dosage of energy or current to be delivered to a patient, the defibrillator selects an excitation current frequency and applies the excitation current at the selected frequency to the patient. The frequency of the excitation current is selected as a function of the dosage to be delivered. The patient's response to the excitation current at the selected frequency will accurately reflect the impedance that the defibrillator will “see” when delivering the selected dosage of energy or current. | 08-22-2013 |
20130172951 | DEFIBRILLATOR WITH UTILITY LIGHT - Embodiments of the present concept are directed to external defibrillators that include a utility light for use by one or more rescuers using the defibrillator. In one implementation, an external defibrillator has a housing, an energy storage module for storing an electrical charge, a defibrillation port for guiding the stored electrical charge to a person, and a processor for determining when to guide the electrical charge. The defibrillator also includes a user interface that includes a screen showing indications by light, and a separate utility light coupled to the housing via a light-coupling structure. The utility light is structured to generate and cast a beam of light with a beam divergence angle of no more than 160 degrees in order to illuminate a certain point of the local environment. This illumination capability may help rescuers reach a person in need of medical attention and apply medical assistance to the person. | 07-04-2013 |
20130127624 | POWER CONSERVING ALERT FOR MEDICAL DEVICES - Techniques are provided for alerting a person to check a medical device while conserving battery power. The medical device initiates a status alert if a readiness condition of the medical device is no longer being met. The status alert includes notification periods during which an audible sound is emitted alternating with off periods during which substantially no audible sound is emitted. The audible sounds may include certain tones or at least one spoken word. At least one of the duration of successive notification periods or the duration of successive off periods may be varied. In this manner, the medical device may provide audible sound at different times during the day in an attempt to get the attention of a person. In addition, the medical device may sense an activity to determine when to provide the audible sound. | 05-23-2013 |
20130060148 | PULSE DETECTION USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates optical characteristics of light transmitted into a patient to ascertain physiological signals, such as pulsatile changes in general blood volume proximate a light detector module. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 03-07-2013 |
20130041421 | ELECTROCARDIOGRAM MONITORING - Techniques for determining whether one or more leads are not adequately connected to a patient, e.g., for ECG monitoring, are described. The techniques involve injection of an integrated signal (which includes a test signal) into one lead, and monitoring the driven lead and the response at the other leads, including the common mode and the difference between the other leads. These “lead-off” detection techniques may be provided by an external defibrillator that provides three-wire ECG monitoring. Techniques for determining a type of a cable coupled to a defibrillator are also described. The cable-type identification may allow a defibrillator to, for example, operate in either a three-wire ECG monitoring mode or a therapy mode, based on whether a three-wire ECG cable or a defibrillation cable is coupled to the defibrillator. | 02-14-2013 |
20120302896 | PULSE DETECTION APPARATUS, SOFTWARE, AND METHODS USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 11-29-2012 |
20120296384 | MEDICAL DEVICES ALERTING USER ABOUT POTENTIAL INTERRUPTION OF WIRELESS PATIENT DATA TRANSFER - An external defibrillator can receive wirelessly a data signal transmitted by a transmitting device over a communication link. The defibrillator can include a processor configured to monitor a reception parameter of the communication link while the data signal is being received and to set an alert flag if the processor determines from the reception parameter that reception of the data signal may be discontinued prematurely. The defibrillator can also include a user interface capable of outputting an alerting user notification responsive to the alert flag being set. | 11-22-2012 |
20120283608 | DRIVING CONTROL OF A RECIPROCATING CPR APPARATUS - A method of controlling the amount of compressed gas used for driving a reciprocating apparatus for cardio-pulmonary resuscitation (CPR) comprising a valve means for controlling the provision of driving gas comprises operation of the valve means during the compression phase to stop provision of driving gas, which operation is separated in time from the venting of the driving gas from the apparatus at the end of the compression phase. Also disclosed are; a CPR apparatus operated by the method; a method of compression depth sensing. | 11-08-2012 |
20120197665 | SELECTIVELY ROUTING PATIENT DATA BETWEEN FIELD DEVICES AND TREATMENT CENTER DESTINATIONS - Techniques for routing event data from a field device, such as an external defibrillator, to a selected subset of a plurality of possible destinations are described. The event data may include physiological data of the patient, such as a 12-lead electrocardiogram (ECG). The destinations may be associated with one of a plurality of patient treatment centers, and may include, as examples, computing device, printers, displays, personal digital assistants, or web-accessible accounts. In some examples, a server maintains user-configurable information or rules for at least some of the destinations, and uses the information or rules for determining whether event data received from a field device is routed to the destination. In some examples, the server may also make the routing determination based on an analysis of event data, such as a determination as to whether the event data indicates that the patient is suspected to be experiencing an acute myocardial infarction. | 08-02-2012 |
20120197324 | MEDICAL DEVICE ADJUSTING OPERATION WHEN USED WITH NON-AUTHENTICATED PATIENT PARAMETER COLLECTING ACCESSORY - Embodiments are directed to a medical device, such as a defibrillator, for use with an accessory capable of collecting a parameter of a patient. The medical device is capable of at least performing a basic functionality, an advanced functionality, and of defibrillating the patient. The medical device includes an energy storage module within a housing for storing an electrical charge that is to be delivered to the patient for the defibrillating. The medical device includes a processor structured to determine whether a data set received from the accessory confirms or not a preset authentication criterion about the accessory. Although when the accessory is coupled to the housing the medical device is capable of the defibrillating and the basic functionality, the medical device is capable of the advanced functionality only when the accessory is coupled to the housing and it is determined that the preset authentication criterion is confirmed. Embodiments also include methods of operation and a programmed solution. | 08-02-2012 |
20120185006 | DEFIBRILLATORS DETECTING ORIENTATION OF ELECTRODE CONNECTION TO ADJUST ENERGY DOSAGE - Embodiments of the present concept are directed to external defibrillators that include an electrode connection port having multiple connection options, and include a detection device to determine an electrode connection configuration so as to provide an appropriate electrical shock to a patient. The detection device detects the electrode connection configuration of a plug connector for connected electrodes to determine if the plug connector is in an adult orientation or a pediatric orientation. The external defibrillator is configured to a deliver an electrical shock with less energy when the pediatric orientation is detected rather than the adult orientation. | 07-19-2012 |
20120157818 | ECG ELECTRODE AND ELECTRODE SUPPORT - An electrically non-conductive back plate for supporting the back of a patient in a supine position comprises on its front face facing the back of the patient a pair or more of ECG electrodes capable of maintaining electrically conductive skin contact with the patient's back. The pair of ECG electrodes is disposed at a sharp angle with the mean heart vector, in particular so as to form an angle β of about 45°±25° with the projection S of the patient's spine on the back plate. Also disclosed is an ECG electrode for mounting in a recess of the back plate and an apparatus for treating cardiac arrest by compression of the sternum comprising the back plate. | 06-21-2012 |
20120136404 | MEDICAL DEVICE INCLUDING SETUP OPTION REPORTING - A medical device for use with a patient is described. The medical device includes a component for administering a treatment to the patient or receiving data of the patient. The component is configured to operate according to an internal setting. The medical device also includes a user interface through which a user can modify the internal setting, as well as a settings signature generator for generating a settings signature that represents a present state of the internal setting. A gateway is also provided for communicating a version of the settings signature out of the medical device. | 05-31-2012 |
20120136286 | MULTI-RESOLUTION GRAPHICAL DISPLAY FOR FEEDBACK ON CHEST COMPRESSION DEPTH - 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. | 05-31-2012 |
20120123504 | MANUALLY INITIATING WIRELESS RECEPTION OF RESUSCITATION EVENT DATA FROM MEDICAL DEVICE - An external defibrillator can include a bump sensor for generating motion information and a bump detector for determining whether the external defibrillator has been subjected to a local bump event. The external defibrillator can transmit wirelessly a data signal encoding resuscitation event data to a second external defibrillator over a wireless communication link between the two devices. | 05-17-2012 |
20120123490 | MANUALLY INITIATING WIRELESS TRANSMISSION OF RESUSCITATION EVENT DATA TO MEDICAL DEVICE - An external defibrillator can include a bump sensor for generating motion information and a bump detector for determining whether the external defibrillator has been subjected to a local bump event. The external defibrillator can transmit wirelessly a data signal encoding resuscitation event data to a second external defibrillator over a wireless communication link between the two devices. | 05-17-2012 |
20120123242 | EXTERNAL MEDICAL DEVICE REACTING TO WARNING FROM OTHER MEDICAL DEVICE ABOUT IMPENDING INDEPENDENT ADMINISTRATION OF TREATMENT - In one embodiment, an external second medical device is capable of being attached to a patient. The second medical device includes an operation module that is capable of operating at different capacities, such as at a first capacity and a second capacity. The second medical device also includes a receiver for receiving a warning about an impending administration of a first treatment to the patient, by a first medical device that does not know about the second medical device being attached to the patient. In response to receiving the warning, the second medical device undertakes a defensive action, whereby the operation of the operation module is capable of being performed at the second capacity. This way, the first treatment, when administered, will impact the second medical device less or not at all. | 05-17-2012 |
20120123241 | EXTERNAL MEDICAL DEVICE WARNING OTHER MEDICAL DEVICE OF IMPENDING ADMINISTRATION OF TREATMENT - In one embodiment, an external first medical device includes a treatment module for administering a first treatment. The first medical device also includes a warning module for transmitting, before the first treatment is administered, a warning about the impending administration of the first treatment. The warning is suitable for receipt by a second medical device that could be attached to the patient unbeknownst to the first device, and which could be impacted by the first treatment. As such, the second medical device is given the opportunity to take a defensive action. | 05-17-2012 |
20120116272 | COOPERATING DEFIBRILLATORS AND EXTERNAL CHEST COMPRESSION DEVICES - Devices, methods, and software implementing those methods for providing communicating external chest compression (ECC) devices and defibrillation (DF) devices, where the ECC and DF devices can be physically separate from each other. Both ECC and DF devices are able to operate autonomously, yet able to communicate with and cooperate with another device when present. Some ECC and DF devices are adapted to be physically and/or electrically coupled to each other. One ECC device includes a backboard, a chest compression member, a communication module, controller, and at least one sensor, electrode lead or electrode. One DF device includes a defibrillator module, a controller, and a communication module that can communicate with the ECC communication module. The communicating ECC and DF devices may deliver ECC, pacing, defibrillation, ventilation, and cooling therapies, and may deliver instructions to human assistants, in a coordinated and cooperative fashion. | 05-10-2012 |
20120109239 | DEFIBRILLATOR WITH MUTABLE SOUND PROMPTS - Defibrillators, software and methods are provided, for issued verbal prompts to rescuers. A defibrillator may receive a muting input and, responsive thereto, cause a verbal prompt to not be issued or to be issued less loudly relative another verbal prompt. | 05-03-2012 |
20120105238 | DEFIBRILLATOR DELIVERING AUDIBLE PROMPTS TO EARPIECE - Defibrillators, software and methods are provided, for transmitting inaudible audio information to one or more external personal sound devices. The audio information may encode an audible indication, which can thus be played by an external personal sound device to a user such as a rescuer. | 05-03-2012 |
20120083720 | REFERENCE SENSOR FOR CPR FEEDBACK DEVICE - Embodiments of the present concept are directed to medical devices for use by a rescuer who is caring for a patient and includes a bottom device for use with a top device to measure the depth of Cardio Pulmonary Resuscitation (CPR) chest compressions delivered to the chest of a patient. The top device is intended for placement on the chest of the patient and has a top mechanism that is moveable up and down as the chest compressions are delivered to the patient. The bottom device includes a generally elongate member having a handle at one end and a bottom mechanism near the opposite end. The elongate member is structured to be placed under the patient during delivery of CPR. The top mechanism and the bottom mechanism cooperate to generate a value for a net depth of the compressions of the patient chest with reference to each other. | 04-05-2012 |
20120081230 | POWER CONSERVING ALERT FOR MEDICAL DEVICES - Techniques are provided for alerting a person to check a medical device while conserving battery power. The medical device initiates a status alert if a readiness condition of the medical device is no longer being met. The status alert includes notification periods during which an audible sound is emitted alternating with off periods during which substantially no audible sound is emitted. The audible sounds may include certain tones or at least one spoken word. At least one of the duration of successive notification periods or the duration of successive off periods may be varied. In this manner, the medical device may provide audible sound at different times during the day in an attempt to get the attention of a person. In addition, the medical device may sense an activity to determine when to provide the audible sound. | 04-05-2012 |
20120071940 | DEFIBRILLATOR WITH UTILITY LIGHT - Embodiments of the present concept are directed to external defibrillators that include a utility light for use by one or more rescuers using the defibrillator. In one implementation, an external defibrillator has a housing, an energy storage module for storing an electrical charge, a defibrillation port for guiding the stored electrical charge to a person, and a processor for determining when to guide the electrical charge. The defibrillator also includes a user interface that includes a screen showing indications by light, and a separate utility light coupled to the housing via a light-coupling structure. The utility light is structured to generate and cast a beam of light with a beam divergence angle of no more than 160 degrees in order to illuminate a certain point of the local environment. This illumination capability may help rescuers reach a person in need of medical attention and apply medical assistance to the person. | 03-22-2012 |
20120071939 | MEDICAL DEVICE WITH SPEAKER HAVING EXTERIOR DIAPHRAGM - Embodiments of the present concept are directed to medical devices having features that prevent contaminants from infiltrating the housing of the device while providing a mechanism to provide clear auditory sounds to aid a rescuer in providing care to a patient. In one example, a medical device includes a housing having a transmission area associated with an enclosed voice coil. An exterior diaphragm formed integrally with the housing surrounds the transmission area and provides a watertight seal of the transmission area. In addition, the diaphragm is structured to generate a sound that can be heard by the rescuer from the voice coil. | 03-22-2012 |
20120035678 | PULSE DETECTION APPARATUS, SOFTWARE, AND METHODS USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 02-09-2012 |
20120035676 | PULSE DETECTION USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates optical characteristics of light transmitted into a patient to ascertain physiological signals, such as pulsatile changes in general blood volume proximate a light detector module. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 02-09-2012 |
20120035675 | EXTERNAL DEFIBRILLATOR WITH ADAPTIVE CPR DURATION - A method and apparatus for a defibrillating system is disclosed that monitors the patient during treatment and then uses the information it gathers to adjust treatment protocols during treatment based on the patient's response. The protocols may include adaptive rhythm analysis intervals, adaptive CPR intervals, and adaptive shock stacks. A method of operating a defibrillator may include the steps of: obtaining a data set on at least one physiological parameter of a patient in a first data gathering interval; performing an analysis of the data set; and determining a time interval between the analysis of the first data set and a second data set, or the duration of a CPR interval, or the number of shocks in a shock stack, based on the result of the analysis of the data set. | 02-09-2012 |
20120035485 | PULSE DETECTION USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates optical characteristics of light transmitted into a patient to ascertain physiological signals, such as pulsatile changes in general blood volume proximate a light detector module. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 02-09-2012 |
20120029584 | PULSE DETECTION APPARATUS, SOFTWARE, AND METHODS USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 02-02-2012 |
20120029583 | PULSE DETECTION APPARATUS, SOFTWARE, AND METHODS USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 02-02-2012 |
20120029368 | PULSE DETECTION APPARATUS, SOFTWARE, AND METHODS USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 02-02-2012 |
20120022606 | CPR TIME INDICATOR FOR VENTILATIONS FOR A DEFIBRILLATOR DATA MANAGEMENT SYSTEM - A system is disclosed wherein patient data, such as an electrocardiogram (“ECG”) signal or a chest impedance measurement signal, collected by a defibrillator device during a resuscitation event is analyzed and processed by a computing device to provide an assessment of CPR administered during the event. The CPR assessment results in one or more CPR figures of merit that relate to temporal characteristics of the CPR relative to the duration of the event. In one embodiment, the CPR figure of merit represents a percentage of the event period during which chest compressions were administered to the patient. | 01-26-2012 |
20120022339 | PULSE DETECTION APPARATUS, SOFTWARE, AND METHODS USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 01-26-2012 |
20110319797 | SUPPORT STRUCTURE - The present invention relates generally to a support structure for fixating a patient to a treatment unit, and especially to a support structure for fixating the patient to a cardiopulmonary resuscitation unit. An embodiment of the support structure comprises a back plate for positioning behind said patient's back posterior to said patient's heart and a front part for positioning around said patient's chest anterior to said patient's heart. Further, the front part can comprise two legs, each leg having a first end pivotably connected to at least one hinge and a second end removably attachable to said back plate. Said front part can further be devised for comprising a compression/decompression unit arranged to automatically compress or decompress said patient's chest when said front part is attached to said back plate. | 12-29-2011 |
20110308534 | SUPPORT STRUCTURE - The present invention relates generally to a support structure for fixating a patient to a treatment unit, and especially to a support structure for fixating the patient to a cardiopulmonary resuscitation unit. An embodiment of the support | 12-22-2011 |
20110236867 | PROMPTING SYSTEM FOR CPR DELIVERY - A method of providing instruction on the performance of chest compressions includes providing a series of signals of a first type corresponding to the desired rhythm of delivery of chest compressions in a chest compression series, and providing signals of a second type which indicate a desired point in the first series. The desired point may be a point near the end of the chest compression series. The signals of the second type may be a voiced countdown to the end of the compression series. The signals of the first type may be a series of identical sounds delivered in the desired rhythm for chest compressions, and the signals of the second type may be sounds distinct from those of the first type which correspond to the rhythm of the last N compressions in the series. The desired point in the first series may include a first point at a desired interval from the first compression, where the interval is measured in number of compressions or elapsed time. A protocol may be chosen between a protocol for a patient with a secured airway and one for a patient with an unsecured airway. | 09-29-2011 |
20110208259 | DEFIBRILLATOR/MONITOR SYSTEM HAVING A POD WITH LEADS CAPABLE OF WIRELESSLY COMMUNICATING - A modular external defibrillator system in embodiments of the teachings may include one or more of the following features: a base containing a defibrillator to deliver a defibrillation shock to a patient, (b) one or more pods each connectable to a patient via patient lead cables to collect at least one patient vital sign, the pods operable at a distance from the base, (c) a wireless communications link between the base and a selected one of the two or more pods to carry the at least one vital sign from the selected pod to the base, the selection being based on which pod is associated with the base. | 08-25-2011 |
20110190836 | DEFIBRILLATOR WITH OVERRIDABLE CPR-FIRST PROTOCOL - 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. | 08-04-2011 |
20110167009 | CONTROLLED-VENDOR MANUFACTURING METHODS - Embodiments of the invention are directed to manufacturing a medical device in a way that minimizes the possibility of defects. Because of the general increasing desire to eliminate lead from the environment, electronic producers are removing lead from their manufacturing processes. The lead had beneficial qualities, however, in that it prevented other metals, in particular tin, from developing “whiskers,” believed to be caused from thermal and mechanical stress of the tin parts or components. Removing the lead has caused an increasing incidence of failure in electronic devices. Many vendors, believing that lead-free devices are universally desirable, routinely substitute lead-free components for components that previously contained lead. Oftentimes these substitutions are made without knowledge of the buyer. Some devices, in particular life-saving devices, may be adversely affected by such a substitution. Embodiments of the invention prevent non-specified goods from being assembled into the medical device by generating evidence or requiring that vendors generate evidence of component composition for particular components that may be at risk for premature failure in the medical device. | 07-07-2011 |
20110166888 | SIMPLIFIED LAUNCHING OF ELECTRONIC MESSAGES IN CENTER FOR TREATING PATIENT - Devices, systems, software and methods facilitate launching protocol in a treatment center for an incoming patient. When a patient characterization is input, one or more draft messages become prepared at least in part for different functions, departments and people of the treatment center. | 07-07-2011 |
20110166615 | EXTERNAL DEFIBRILLATOR AND METHODS FOR OPERATING THE EXTERNAL DEFIBRILLATOR - Methods and apparatus are provided for minimizing the inherent time delays within external defibrillators. The methods and apparatuses utilize timing schemes for initiation and completion of charging of an energy storage device of an external defibrillator, measuring one or physical parameters of the patient and conducting a physiology analysis of the patient. The initiation and completion of one or more of these activities are arranged so that the energy storage device is charged to a desired level and available for a defibrillation shock to the patient with minimal delay after activation of the external defibrillator. | 07-07-2011 |
20110144708 | PULSE DETECTION APPARATUS, SOFTWARE, AND METHODS USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 06-16-2011 |
20110144707 | EXTERNAL DEFIBRILLATOR WITH CHARGE ADVISORY ALGORITHM - An external defibrillator includes a therapy delivery circuit, a sensor, and a processor. The therapy delivery circuit is configured to be electrically charged and to deliver electrical therapy to a patient. The sensor is configured to sense a physiological condition of the patient and generate data indicative of a probability that therapy will be delivered to the patient. The processor is configured to analyze data generated by the sensor to determine whether there is a threshold level of the probability that the therapy delivery will be delivered to the patient, if the probability is at least at the threshold level, charge the therapy delivery circuit, and determine whether therapy delivery is advisable based on the physiological condition of the patient after determining whether the probability is at least at the threshold level. | 06-16-2011 |
20110118800 | ECG ANALYSIS THAT RELATIVELY DISCOUNTS ECG DATA OF CPR PERIOD TRANSITIONS - Medical devices, software and methods are provided, for making a decision as to whether to administer electric shock therapy to a patient. The decision is made with respect to ECG data that is discounted at least partially, and sometimes even completely, if it occurs during a transition between chest compression group and a pause for ventilation. | 05-19-2011 |
20110112423 | INCREASING CPR EFFECTIVENESS USING PHONOCARDIOGRAM ANALYSIS - Embodiments of the invention include a system and methods for providing status information about resuscitation efforts of a person receiving chest compressions as part of Cardiopulmonary Resuscitation (CPR). A microphone generates a soundtrack by sampling sounds within or around the body of the person receiving CPR. The soundtrack is gated in one or more various ways to eliminate portions of the soundtrack, and analysis performed on the remaining portions. By evaluating the remaining portions of the soundtrack, the system can determine a cardiovascular effect of the compressions and provide status information to the rescuer about the determined cardiovascular effect. | 05-12-2011 |
20110082510 | DECIDING ON PATIENT ELECTRIC SHOCK THERAPY - Systems, devices, software and methods are provided, for making a decision as to whether to administer an electric shock to a patient. The decision can be made differently, depending on whether the patient has already been shocked or not. | 04-07-2011 |
20110082379 | ANALYZING ECG DATA IN DECIDING ON PATIENT CHEST COMPRESSION TREATMENT - Medical devices, software and methods are provided, for making a decision as to whether to pause patient chest compression treatment in connection with administering electric shock therapy to the patient. The decision is made depending whether signal spikes identified in the ECG data are determined to be QRS complexes, or merely likely impulsive artifact caused by the chest compressions. | 04-07-2011 |
20100318145 | DEFIBRILLATORS CUSTOMIZED FOR ANTICIPATED PATIENTS - An external defibrillator is customized for at least one person, i.e., an anticipated patient, through creation of a profile for the anticipated patient that allows the defibrillator and users of the defibrillator to provide customized treatment to the patient. The profile may include treatment parameters for the anticipated patient, such as defibrillation therapy parameters selected for the patient. The profile may also include a baseline recording of a physiological parameter of the patient, and medical history and personal information regarding the patient. In some embodiments, the external defibrillator stores a profile for each of one or more anticipated patients within a memory. In other embodiments, a profile for an anticipated patient is stored within a medium associated with that anticipated patient. The medium may, for example, be a removable medium for external defibrillators. | 12-16-2010 |
20100318144 | DEFIBRILLATORS CUSTOMIZED FOR ANTICIPATED PATIENTS - An external defibrillator is customized for at least one person, i.e., an anticipated patient, through creation of a profile for the anticipated patient that allows the defibrillator and users of the defibrillator to provide customized treatment to the patient. The profile may include treatment parameters for the anticipated patient, such as defibrillation therapy parameters selected for the patient. The profile may also include a baseline recording of a physiological parameter of the patient, and medical history and personal information regarding the patient. In some embodiments, the external defibrillator stores a profile for each of one or more anticipated patients within a memory. In other embodiments, a profile for an anticipated patient is stored within a medium associated with that anticipated patient. The medium may, for example, be a removable medium for external defibrillators. | 12-16-2010 |
20100318143 | DEFIBRILLATORS CUSTOMIZED FOR ANTICIPATED PATIENTS - An external defibrillator is customized for at least one person, i.e., an anticipated patient, through creation of a profile for the anticipated patient that allows the defibrillator and users of the defibrillator to provide customized treatment to the patient. The profile may include treatment parameters for the anticipated patient, such as defibrillation therapy parameters selected for the patient. The profile may also include a baseline recording of a physiological parameter of the patient, and medical history and personal information regarding the patient. In some embodiments, the external defibrillator stores a profile for each of one or more anticipated patients within a memory. In other embodiments, a profile for an anticipated patient is stored within a medium associated with that anticipated patient. The medium may, for example, be a removable medium for external defibrillators. | 12-16-2010 |
20100297594 | INTERACTIVE FIRST AID INFORMATION SYSTEM - In general, the invention is directed to techniques for determining appropriate first aid and applying first aid that is appropriate. A first aid system receives patient status information from an input device or a sensor, and presents first aid information as a function of the received patient status information. The first aid system may be incorporated with an external defibrillator. The first aid system may acquire patient status information through an interaction with an operator, in which the first aid system asks the operator to supply patient status information. In one embodiment of the invention, the operator may supply patient status information by touching a diagram representing at least a portion of a human body. | 11-25-2010 |
20100198287 | SELECTIVE RECHARGING OF MEDICAL DEVICE DEPENDING ON AUTHENTICATION OF POWER ADAPTER SYSTEM - In an embodiment, a medical device can be used with a power adapter system. In addition, it can receive a data set from the power adapter system, and examine the data set to determine whether the data set confirms or not an authentication of the power adapter for use with the medical device. If the authentication is not confirmed, the external medical device can operate differently than otherwise. For example, power can be drawn more slowly from the power adapter system. | 08-05-2010 |
20100198286 | SELECTIVE POWERING OF MEDICAL DEVICE DEPENDING ON AUTHENTICATION OF POWER ADAPTER SYSTEM - In an embodiment, a medical device can be used with a power adapter system. In addition, it can receive a data set from the power adapter system, and examine the data set to determine whether the data set confirms or not an authentication of the power adapter for use with the medical device. If the authentication is not confirmed, the external medical device can operate differently than otherwise. For example, power can be drawn from the power adapter system only if an inside battery is not charged. | 08-05-2010 |
20100194425 | METHOD AND APPARATUS FOR TESTING AN ALTERNATING CURRENT POWER SOURCE FOR DEFIBRILLATION COMPATIBILITY - A device tests a circuit that is a source of alternating current by measuring at least one electrical parameter of the circuit to determine whether the circuit is able to provide adequate energy for defibrillation by an external defibrillator. The device may test the circuit by applying a load to the circuit, and measuring one or more electrical parameters when the load is applied to the circuit. The device may be the external defibrillator itself, or a separate testing device. In some embodiments in which an external defibrillator tests a circuit, the defibrillator modifies a value of at least one therapy delivery parameter for a subsequent delivery of one or more defibrillation pulses based on the measured electrical parameter value measured. By modifying a therapy delivery parameter, the defibrillator may deliver defibrillation pulses at an energy level that is supportable by the circuit. | 08-05-2010 |
20100152800 | CPR TIME INDICATOR FOR A DEFIBRILLATOR DATA MANAGEMENT SYSTEM - A system is disclosed wherein patient data, such as an electrocardiogram (“ECG”) signal or a chest impedance measurement signal, collected by a defibrillator device during a resuscitation event is analyzed and processed by a computing device to provide an assessment of CPR administered during the event. The CPR assessment results in one or more CPR figures of merit that relate to temporal characteristics of the CPR relative to the duration of the event. In one embodiment, the CPR figure of merit represents a percentage of the event period during which chest compressions were administered to the patient. | 06-17-2010 |
20090295326 | Defibrillator Battery Authentication System - 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 authentications 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. | 12-03-2009 |
20090270930 | External Defibrillator With Adaptive Protocols - A method and apparatus for a defibrillating system is disclosed that monitors the patient during treatment and then uses the information it gathers to adjust treatment protocols during treatment based on the patient's response. The protocols may include adaptive rhythm analysis intervals, adaptive CPR intervals, and adaptive shock stacks. A method of operating a defibrillator may include the steps of: obtaining a data set on at least one physiological parameter of a patient in a first data gathering interval; performing an analysis of the data set; and determining a time interval between the analysis of the first data set and a second data set, or the duration of a CPR interval, or the number of shocks in a shock stack, based on the result of the analysis of the data set. | 10-29-2009 |
20080250166 | Medical Device Status Information System - In general, the invention is directed to management of status information from a plurality of external medical devices, such as AEDs. A system may include one or more medical devices associated with one or more docking stations. The medical devices and docking stations may communicate with one another and with a remote unit. A medical device or a docking station in the system may acquire status information and may communicate the status information to the remote unit, which may serve as a central point for collecting and aggregating status information pertaining to medical devices and docking stations in the system. The remote unit may present the status information to a person via an input/output device, may maintain a status log for the devices in the system, and may interrogate the devices in the system for status information. | 10-09-2008 |