Abstract: A dosage for electrotherapy delivered to a patient, such as a defibrillation pulse delivered by an external defibrillator, is selected based on an age-related classification, such as adult or child, and a measured electrical parameter, such as the transthoracic impedance, of the patient. For example, a nominal voltage level for an energy storage circuit may be determined based on a nominal dosage. The nominal voltage level may be adjusted by applying a function that relates voltage level adjustment to impedance to the measured impedance. The function may be selected based on the age-related classification of the patient. The dosage of the defibrillation pulse delivered based on the adjusted voltage level, i.e., the selected dosage, may have a substantially equivalent probability of success for the patient as the nominal dosage would provide for a reference patient with an average transthoracic impedance for the class of which the patient is a member.

Abstract: Delivery of energy by a defibrillator or other medical device is inhibited when the processor or software that controls a module of the medical device operates abnormally. A windowed watchdog timer (WWDT) incorporated into one module of the medical device is used to control the operation of other modules of the medical device via a software-based extension technique. As a result, the risk of harm to the patient is reduced compared to medical devices that incorporate over-limit type watchdog timers. In addition, costs associated with implementing WDTs in multiple modules of the defibrillator are avoided, thereby lowering the overall cost of implementation.

Abstract: An automated external defibrillator automatically determines the type of patient to which it is attached based on patient-specific information entered by the user. The defibrillator includes electrodes that are adapted for placement on a patient, a pulse generator connected to the electrodes, and processing circuitry that controls the defibrillation pulse delivery from the pulse generator. The automated external defibrillator causes a defibrillation pulse to be delivered to the patient in accordance with the determined patient type. A user interface having a user input connected to the processing circuitry enables the user of the defibrillator to enter patient-specific information. The user may enter the patient-specific information by interacting with the user input during a time period in relation to a prompt from the defibrillator. In another aspect, data pertaining to identification of the type of patient connected to the electrodes may be recorded with event data in a memory.

Abstract: 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.

Abstract: A system is described that comprises a medical device on which is installed a version of software and a software agent communicatively coupled to the medical device without regard to the version of software installed on the medical device. An example of the medical device includes a defibrillator. The software agent may reside in a personal digital assistant and can be operated to communicate with the defibrillator to access the data stored in the defibrillator irrespective of the version of software of the defibrillator.

Abstract: Delivery of energy by a defibrillator or other medical device is inhibited when the processor or software that controls a module of the medical device operates abnormally. A windowed watchdog timer (WWDT) incorporated into one module of the medical device is used to control the operation of other modules of the medical device via a software-based extension technique. As a result, the risk of harm to the patient is reduced compared to medical devices that incorporate over-limit type watchdog timers. In addition, costs associated with implementing WWDTs in multiple modules of the defibrillator are avoided, thereby lowering the overall cost of implementation.

Abstract: The invention provides an elevator cab equipped with an emergency medical device, such as an automated external defibrillator (AED). The elevator cab equipped with the emergency medical device may be controlled in order to deliver the emergency medical device to a floor of a building on which an emergency medical situation occurred. In response to emergency medical input identifying the emergency medical situation, an elevator control unit overrides regular operation of the elevator cab in response to receiving emergency medical input, and directs the elevator cab to a floor on which an emergency medical situation occurs. For example, the elevator control unit may cancel active floor calls made by passengers within the elevator cab or individuals on one or more floors of the building and direct the elevator cab to the floor of the emergency situation.