Abstract: Defibrillator assemblies and methods to wirelessly transfer energy from an external source to a battery or other rechargeable power source within the defibrillator assembly. The transfer of energy may be through a non-contact interface on a defibrillator cradle or a docking station that mounts the defibrillator. The rate of energy transfer may be equal to the energy drain caused by self-discharge and automated self-testing. Accordingly, since the rate of energy transfer is lower than that required to run the defibrillator system continuously, several wireless methods of energy transfer may be used. In addition, the defibrillator assembly may communicate diagnostic and non-diagnostic data to the external source.

Abstract: A pulse detection apparatus, software, and method that uses signal data obtained from an accelerometer placed on a patient's body to detect the presence of a cardiac pulse. The accelerometer is adapted to sense movement due to a cardiac pulse and produce accelerometer signal data in response thereto. Processing circuitry analyzes the accelerometer signal data for a feature indicative of a cardiac pulse and determines whether a cardiac pulse is present in the patient based on the feature. In one aspect, the feature may be a temporal energy feature, such as a relative change in energy. In another aspect, the feature may be a spectral energy feature such as the energy or frequency of a peak in the energy spectrum of the signal. In yet another aspect, the feature may be obtained by comparing the accelerometer signal data with a previously-identified pattern known to predict the presence of a cardiac pulse. Multiple features may also be obtained and classified to determine the presence of a cardiac pulse.

Abstract: Signal data obtained from a piezoelectric sensor placed on a patient's body is used to detect the presence of a cardiac pulse. The piezoelectric sensor has a transducing element adapted to sense movement due to a cardiac pulse and produce piezoelectric signal data in response thereto. Processing circuitry analyzes the piezoelectric signal data for a feature indicative of a cardiac pulse and determines whether a cardiac pulse is present in the patient based on the feature. In one aspect, the feature may be a temporal feature such as a relative change in energy. In another aspect, the feature may be a spectral feature such as the energy or frequency of a peak in the energy spectrum of the signal. In yet another aspect, the feature may be obtained by comparing the piezoelectric signal data with a previously-identified pattern known to predict the presence of a cardiac pulse. Multiple features may also be obtained from the piezoelectric signal data and classified to determine the presence of a cardiac pulse.

Abstract: A method and apparatus for performing self-tests on defibrillation and pacing circuits including a patient isolation switch is disclosed. Following a test of the defibrillation and pacing circuitry, the isolation switch is tested by closing certain switches within the defibrillation circuitry so as to create a circuit path, and then opening and closing the isolation switch. Alternative tests may be performed depending on whether the impedance at the output of the defibrillator is determined to be an open circuit or a short circuit. If the output is determined to be an open circuit, then the test monitors the voltage across the output of the defibrillator as indicated by the voltage of a DC offset of a preamplifier coupled to the output of the defibrillator. For the short circuit test, the voltage on the energy storage capacitor is monitored.

Abstract: A method and apparatus for performing self-tests on defibrillation and pacing circuits including a patient isolation switch is disclosed. Tests are provided for the defibrillation and pacing circuitry as well as the isolation switch. For testing the defibrillation circuitry, the impedance drive circuits and preamplifier may be utilized such that the energy storage capacitor is not required to be charged and discharged during the test, thus conserving energy. For testing the pacing circuitry and the isolation switch, the defibrillation circuitry is utilized. For certain of the tests, the test stimulus is the output voltage on the energy storage capacitor, while for other tests the test stimulus may be the pace current as indicated by the voltage across the input to the preamplifier. Alternative tests may be performed depending on whether the impedance at the output of the defibrillator is determined to be an open circuit or a short circuit.

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 present invention pertains to a method for efficiently introducing exogenous genes into stem cells, particularly human stem cells. The method optionally includes the steps of inducing the proliferation of target cells by pre-stimulation with cytokines and/or growth factors, followed by incubating these cells with RD114-pseudotyped vector particles. In a specific embodiment, the vector particles are retronectin-immobilized or ultracentrifugation-concentrated retroviral vector particles pseudotyped with the feline endogenous retrovirus (RD114) envelope protein. The present invention further discloses a method for somatic gene therapy, which can be used for various therapeutic applications and involves introducing a gene of interest contained within the retroviral genome into human repopulating stem cells followed by introducing these cells into a human host.