Abstract: A defibrillator is described which executes a resuscitation protocol having a CPR pause period. The CPR pause period may be interrupted for the acquisition of ECG signal data which is not contaminated by chest compression artifacts. Following the acquisition of ECG signal data, the CPR period resumes and continues for its full period. The ECG signal data acquired during the interruption of the CPR period is analyzed and, if a shockable rhythm is identified, a shock sequence is initiated immediately upon conclusion of the CPR period.

Abstract: An ECG monitoring device comprises an integral handheld device including a ECG electronic module and an electrode patch having a plurality of electrodes which contact a subject by conductive hydrogel. A release liner covers and protects the hydrogel prior to use and is removed to expose the hydrogel. A second release liner is removed to expose a pressure sensitive adhesive by means of which the device is attached to a subject. The first and second release liners may be parts of a single release liner layer. After use the electrode patch is disposable and the ECG electronic module is detached from the patch for reuse.

Abstract: A method for operating an automatic external defibrillator (AED) prompts an operator about proper operation of the automatic external defibrillator and placement of the electrodes to ensure rapid and proper operation. Depending upon a state of a pad storage compartment, upon activation the AED issues an initial prompt, pauses after the initial prompt and then issues a second prompt. The AED also determines whether the pads have been removed from a liner and if so, issues a pad application prompt. The AED next determines whether both pads have been placed and if so, analyzes an impedance signal and if the impedance signal is erratic, issues a pad correction prompt. The AED also issues the pad correction prompt if the pads are removed from the liner but never go on the patient.

Abstract: An ECG monitoring device comprises an integral handheld device including a ECG electronic module and an electrode patch having a plurality of electrodes which contact a subject by conductive hydrogel. A release liner covers and protects the hydrogel prior to use and is removed to expose the hydrogel. A second release liner is removed to expose a pressure sensitive adhesive by means of which the device is attached to a subject. The first and second release liners may be parts of a single release liner layer. After use the electrode patch is disposable and the ECG electronic module is detached from the patch for reuse.

Abstract: A defibrillator is described which executes a resuscitation protocol having a CPR pause period. The CPR pause period may be interrupted for the acquisition of ECG signal data which is not contaminated by chest compression artifacts. Following the acquisition of ECG signal data, the CPR period resumes and continues for its full period. The ECG signal data acquired during the interruption of the CPR period is analyzed and, if a shockable rhythm is identified, a shock sequence is initiated immediately upon conclusion of the CPR period.

Abstract: A circuit includes a sensor coupled to a processor. The sensor senses an electrical signal that is representative of a patient parameter, and the processor determines a condition of the patient by analyzing first and second overlapping portions of the sensed electrical signal. For example, a portable AED can include such a circuit to sense first and second overlapping sections of an ECG. By utilizing this overlapping-window technique, the AED can obtain and analyze multiple sections of ECG data, and thus can make a shock/no-shock decision, more quickly than an AED using contiguous-window analysis. Thus, the overlapping-window technique allows one to use both longer ECG sections (better accuracy per window) and more of these longer sections (better voting accuracy) over a given analysis time.

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: 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: A defibrillation system for patients of all ages may include an Automated External Defibrillator (AED) coupled to a set of universal electrodes. Universal electrodes may be reduced-size versions of adult electrodes, and may include an opening to lower effective impedance. The AED may include an adult/pediatric mode control or switch. Based upon the setting of the adult/pediatric switch, the AED may perform an adult defibrillation sequence or a pediatric defibrillation sequence. An adult defibrillation sequence may comprise delivery of one or more waveforms or shocks characterized by energies appropriate for adults, for example, 150 Joule biphasic waveforms. A pediatric defibrillation sequence may comprise delivery of one or more waveforms characterized by energies appropriate for children, for example, 50 Joule biphasic waveforms.

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: An electrotherapy device including at least one sensor operable to sense at least one physiological parameter of a patient. A controller is operably connected to the at least one sensor operable to receive signals from the at least one sensor corresponding to the at least one physiological parameter. Memory is operable to store computer-programming code executed by the controller. The programming code includes decision-making criteria operable to adapt a patient treatment in response changes to the detected at least one physiological parameter. At least one pair of electrodes is operably connected to the controller and operable to administer the treatment to the patient.

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 defibrillation system for patients of all ages may include an Automated External Defibrillator (AED) coupled to a set of universal electrodes. Universal electrodes may be reduced-size versions of adult electrodes, and may include an opening to lower effective impedance. The AED may include an adult/pediatric mode control or switch. Based upon the setting of the adult/pediatric switch, the AED may perform an adult defibrillation sequence or a pediatric defibrillation sequence. An adult defibrillation sequence may comprise delivery of one or more waveforms or shocks characterized by energies appropriate for adults, for example, 150 Joule biphasic waveforms. A pediatric defibrillation sequence may comprise delivery of one or more waveforms characterized by energies appropriate for children, for example, 50 Joule biphasic waveforms.

Abstract: An electrotherapy device including at least one sensor operable to sense at least one physiological parameter of a patient. A controller is operably connected to the at least one sensor operable to receive signals from the at least one sensor corresponding to the at least one physiological parameter. Memory is operable to store computer-programming code executed by the controller. The programming code includes decision-making criteria operable to adapt a patient treatment in response changes to the detected at least one physiological parameter. At least one pair of electrodes is operably connected to the controller and operable to administer the treatment to the patient.

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: 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: A defibrillator configurable for optimal behavior across a broad spectrum of patients, users, and circumstances is provided. A set of environmental characteristics that represent the patient population, the user population, and the possible circumstances are determined and then applied to a configure algorithm to determine an optimal behavior of the defibrillator as reflected through the set up parameters. The set of environmental characteristics can be entered manually or determined from dispatch data supplied by computerized dispatch systems. The optimal behavior can also be achieved using adaptation algorithms such as fuzzy logic and neural networks that allow the defibrillator to obtain measurements of the environmental characteristics and alter its behavior based on those measurements.

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: A novel apparatus for inactivating the AED prompting feature without inactivating the monitoring and analysis capability of the AED. AEDs are designed to be deployed by lay responders, such as flight attendants and police officers. As a result, in addition to a shock advisory algorithm which determines when a victim has a shockable rhythm, the devices also typically provide detailed prompts to the user. However, once a more advanced user arrives at the emergency (such as a paramedic) the detailed prompts are typically no longer required. The ability to silence the prompting feature without disabling the monitoring and analysis capability, as opposed to attaching the patient to another defibrillator, enables an advanced user to continue using the device.

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.