Abstract: A method and article for storing an automatic external defibrillator for use without a prescription are described. The hermetically sealed electrode pads of the OTC AED are electrically coupled to the OTC AED base unit where they are constantly accessible to self-test circuitry inside the base unit for periodic, automatic self-test. In one embodiment the self-test is designed to determine whether the conductive gel of the electrode pads has dried out. In another embodiment self-test circuitry also tests the battery while the OTC AED is being stored prior to use.

Abstract: Systems and methods for transferring medical information from a first medical monitoring device to a second device are provided. Medical information from the first medical monitoring device is encoded as an ECG waveform and the ECG waveform having the encoded medical information is provided to the second device as an input ECG waveform.

Abstract: A system and method are described for delivering electrotherapy to a patient that includes delivering electrotherapy to defibrillate the patient and providing at least one non-interruptible time period for administration of CPR prior to entering a monitor mode during which a patent cardiac signal is monitored for indication of a shockable rhythm.

Abstract: A defibrillator, equipped with a battery power source, is described which is arranged to operate in any one of both a first mode and a second mode, the battery power source comprising at least two voltage sources. The voltage sources are arranged to be connected in parallel to each other when the defibrillator is operating in a first mode, and in series with each other when the defibrillator is operating in a second mode. The invention can be implemented by a battery pack for a defibrillator. This arrangement allows both voltage sources to be drawn down at the same rate which lengthens the overall life of the batteries. A more efficient use of battery power is thereby obtained. The invention ultimately extends the projected life of the batteries and when applied to an automatic external defibrillator increases the shelf life of the defibrillator.

Abstract: A defibrillator capable of delivering a damped biphasic truncated (DBT) defibrillation pulse is provided. An energy storage circuit is coupled across a high voltage switch such as an H-bridge for delivering a defibrillation pulse to the patient through a pair of electrodes. A controller operates to control the entire defibrillation process and detects shockable rhythms from the patient via an ECG front end. The energy storage circuit consists of an energy storage capacitor, a series inductor, a shunt diode, and optionally a resistor in series with the inductor. The controller measures as the patient dependent parameter the time interval between the initial delivery of the defibrillation pulse and the occurrence of the peak current or voltage to determine the first and second phases of the defibrillation pulse to provide for compensation for patient impedance.

Abstract: An automated or semi-automated defibrillator (AED) system includes an AED and a cartridge attachable to the AED. The cartridge includes electrode pads and a power source such as a battery or fuel cell, which may recharge a defibrillator battery, power defibrillator circuitry, or both. Because the cartridge includes both a power source and electrode pads, one can replace the power source and the pads at the same time by replacing a single cartridge. Furthermore, in defibrillator systems where the power source charges the defibrillator battery, the power source can be selected to have the same life as the pads, thus making it practical to replace the power source and pads at the same time. In addition, maintenance for such a charging defibrillator system typically costs less than for a non-charging system because it often costs less to replace the power source than to replace the defibrillator battery.

Abstract: A novel apparatus and method for recording and replaying patient treatment and response data that occurs during the course of an emergency response on a defibrillator. The data and events of an emergency response may be recorded automatically by the defibrillator. Incidents may then be randomly accessible (i.e. “scrollable”) by medical personnel on the defibrillator by placing the defibrillator into an incident review mode. The ability to quickly review critical ECG and event data on the scene. This provides medical personnel with a reliable and efficient alternative to paper based recording systems.

Abstract: An automated or semi-automated external defibrillator (AED) is provided with a plurality of power sources. The AED includes a first power source that powers circuitry creating a defibrillation electrical shock, and a second power source for powering other circuitry. By including a separate power source for the low-power needs of the AED, the high-power source will typically last longer than if the low-power source were omitted. This reduces maintenance costs, particularly where the high-power source is more expensive to replace than the low-power source. Furthermore, one may use the high-power source as a backup to the low-power source so the AED can still operate even if the low-power source fails.

Abstract: A modular automated external defibrillator (AED) system includes a base unit and at least one interconnected module. The base unit typically includes a functional circuit and includes an interface that couples the functional circuit to the module. Likewise, the module includes an interface that couples the module to the base unit By manufacturing such modular AED models instead of one-piece, i.e., integrated, AED models, a manufacturer can reduce the cost and complexity of its manufacturing process. Furthermore, the manufacturer may be able to bring such a modular AED to market more quickly than it could bring an integrated model of the AED to market. Moreover, a modular AED allows the manufacturer and customer flexibility in respectively providing and selecting feature sets. In addition, a customer can obtain replacements for broken modules, and the manufacturer can provide cheaper upgrades by upgrading a module or base unit instead of upgrading the entire AED.

Abstract: A device such as an electrotherapy device implementing the invention includes multiple power module receptacles each of which is configured to received at least one type of power module, and a power management system that selectively routes power provided by one or more installed power modules to the device components and, preferably, to other power module receptacles. The types of power modules that operate in the power module receptacles include, for example, rechargeable battery packs, non-rechargeable battery packs and AC power packs. Preferably these power modules are each fully integrated, functionally self-contained power modules. For example, the rechargeable battery pack includes a charge controller specifically designed to charge the battery pack in which it is implemented.

Abstract: A data card drawer for installing a data card, such as a compact flash card, into a device that uses data cards. Devices that use data cards include, for example, medical devices, and more particularly defibrillators. The data card drawer electrically isolates the data card from the user when the user is installing or removing the data card from the device. The data card drawer may also be formed to provide a closure to the opening in the device housing provided to receive the data card. Further, the data card drawer may be formed to prevent damaging pins located on a pin connector within the receiving device which communicate data with the data card. The data card drawer preferably mates with the device to prevent ingress and egress of foreign matter and moisture.

Abstract: A battery system including a main battery cell having a first capacity; a sense battery cell connected in series with the main battery cell, the sense battery cell having a second capacity less than the first capacity; and a battery capacity indicator monitoring a parameter of the sense battery cell. A method of determining a battery condition in a battery operated device, the method including providing a battery system, the battery system comprising a main battery cell having a first capacity and a sense battery cell, the sense battery cell having a second capacity less than the first capacity, the main battery cell and the sense battery cell being coupled in series; monitoring a parameter of the sense battery cell; and determining a condition of the main battery cell from the monitored sense battery cell parameter.

Abstract: An electrode includes a conductive adhesive layer and a conductive foil layer having a void therein. One such electrode may be mounted in conjunction with another electrode upon a release liner having one or more openings therein to facilitate electrical signal exchange between electrodes. A release liner may include a moisture permeable and/or moisture absorbent membrane. A release liner may alternatively include a conductive backing layer. A release liner may also include an insulating swatch covering an opening. A release liner may be implemented as a foldable sheet, such that multiple electrodes may be mounted upon the same side of the foldable sheet. A medical device to which the mounted electrodes are coupled may characterize the electrical path between the electrodes. The medical device may perform a variety of electrical measurements, including real and/or complex impedance measurements.

Abstract: A device such as an electrotherapy device implementing the invention includes multiple power module receptacles each of which is configured to received at least one type of power module, and a power management system that selectively routes power provided by one or more installed power modules to the device components and, preferably, to other power module receptacles. The types of power modules that operate in the power module receptacles include, for example, rechargeable battery packs, non-rechargeable battery packs and AC power packs. Preferably these power modules are each fully integrated, functionally self-contained power modules. For example, the rechargeable battery pack includes a charge controller specifically designed to charge the battery pack in which it is implemented.

Abstract: An electrotherapy apparatus includes a connecting mechanism coupled between an energy source and a pair of electrodes for contacting a patient. A controller coupled to the energy source configures the energy source to provide a selected one of a plurality of energy levels. The controller actuates the connecting mechanism to couple the energy source to the electrodes. A sensor coupled to the controller measures a parameter or parameters related to the energy delivered to the patient through the electrodes. The controller performs an operation using the output received from the sensor. Based upon the operation, the controller actuates the connecting mechanism to decouple the energy source from the electrodes. In an embodiment of the electrotherapy apparatus, the energy source includes a high voltage power supply for charging a capacitor to a selected one of a plurality of initial voltages.

Abstract: An automated or semi-automated external defibrillator (AED) is provided with a plurality of power sources. The AED includes a first power source that powers circuitry creating a defibrillation electrical shock, and a second power source for powering other circuitry. By including a separate power source for the low-power needs of the AED, the high-power source will typically last longer than if the low-power source were omitted. This reduces maintenance costs, particularly where the high-power source is more expensive to replace than the low-power source. Furthermore, one may use the high-power source as a backup to the low-power source so the AED can still operate even if the low-power source fails.

Abstract: A defibrillator having infrared communication capability is provided. The wireless communications capability is implemented using infrared light or RF communications and standardized communications protocols such as the IRDA protocol to allow for ready communication between defibrillators such as during handoffs of patient along the Chain of Survival. The wireless communications network also allows for communications between a defibrillator and a host computer such as a palmtop for incident report generation after each handoff. Another embodiment of the present invention provides for a defibrillator having an infrared mode switch to allow for restricted access to advanced cardiac life support (ACLS) features of the defibrillator. A further embodiment of the present invention provides for a defibrillator having a remote training mode that is implemented via wireless communications.

Abstract: A device such as an electrotherapy device implementing the invention includes multiple power module receptacles each of which is configured to received at least one type of power module, and a power management system that selectively routes power provided by one or more installed power modules to the device components and, preferably, to other power module receptacles. The types of power modules that operate in the power module receptacles include, for example, rechargeable battery packs, non-rechargeable battery packs and AC power packs. Preferably these power modules are each fully integrated, functionally self-contained power modules. For example, the rechargeable battery pack includes a charge controller specifically designed to charge the battery pack in which it is implemented.

Abstract: An apparatus for delivering defibrillation therapy to a patient. Specifically, an external defibrillators or automatic or semi-automatic external defibrillator (AEDs) is described. The defibrillator is automatically activated or inactivated by, for example, inserting or removing an object, such as a plug or a pin, into a receptacle within the defibrillator housing.

Abstract: An electrode includes a conductive adhesive layer and a conductive foil layer having a void therein. One such electrode may be mounted in conjunction with another electrode upon a release liner having one or more openings therein to facilitate electrical signal exchange between electrodes. A release liner may include a moisture permeable and/or moisture absorbent membrane. A release liner may alternatively include a conductive backing layer. A release liner may also include an insulating swatch covering an opening. A release liner may be implemented as a foldable sheet, such that multiple electrodes may be mounted upon the same side of the foldable sheet. A medical device to which the mounted electrodes are coupled may characterize the electrical path between the electrodes. The medical device may perform a variety of electrical measurements, including real and/or complex impedance measurements.