Patent classifications
A61H2230/40
Systems and Methods to Increase Survival With Favorable Neurological Function After Cardiac Arrest
A system includes a guidance device that provides feedback to a user to compress a patient's chest at a rate of between about 90 and 110 compressions per minute and at a depth of between about 4.5 centimeters to about 6 centimeters. The system includes a pressure regulation system having a pressure-responsive valve that is configured to be coupled to a patient's airway. The pressure-responsive valve is configured to remain closed during successive chest compressions in order to permit removal at least about 200 ml from the lungs in order to lower intracranial pressure to improve survival with favorable neurological function. The pressure-responsive valve is configured to remain closed until the negative pressure within the patient's airway reaches about −7 cm H.sub.2O, at which time the pressure-responsive valve is configured to open to provide respiratory gases to flow to the lungs through the pressure-responsive valve.
INTEGRATED RESUSCITATION
An example of a CPR data recording system includes a hand-held chest compression measurement device and an external computing device communicatively coupled to the hand-held chest compression measurement device. The hand-held chest compression measurement device includes a housing, a motion sensor, a communication device, a memory disposed within the housing, and a processor disposed within the housing. The processor is configured to process a signal output from the motion sensor, calculate chest compression data from the processed signal output, evaluate the chest compression data after a delay from a start of the chest compressions to identify chest compressions that satisfy a pre-determined quality criterion, record the chest compression data in the memory, and send the recorded chest compression data to the external computing device via the communication device. The external computing device is configured to enable a review of the chest compression data.
RESUSCITATION SYSTEM
A resuscitation system for use in the resuscitation of a subject includes a computing device configured to input subject information and use the subject information to create a subject resuscitation strategy, a sensor configured to detect subject biosignals and use the subject biosignals to monitor for a subject cardiac arrest event, and a defibrillator configured to determine and deliver a subject resuscitation treatment. On determination of a subject cardiac arrest event, the sensor outputs sensor subject biosignals to the computing device. The computing device uses the sensor subject biosignals to adapt the subject resuscitation strategy and output the subject resuscitation strategy to the defibrillator. The defibrillator measures subject biodata and uses the subject biodata and the subject resuscitation strategy to determine and deliver a subject resuscitation treatment. During subject resuscitation treatment, the defibrillator repeatedly uses measured subject biodata and the subject resuscitation strategy to adapt the subject resuscitation treatment.
Use of Muscle Oxygen Saturation and PH in Clinical Decision Support
Embodiments of the present invention include a system having at least one sensor configured to monitor a muscle oxygen saturation (SmO2) level of a patient who is undergoing cardiac arrest and to generate a signal representing SmO2 level; a user interface device; a processor communicably coupled to the user interface device, the processor configured to cause the user interface device to present an array of two or more possible nodes of a clinical decision support tree, wherein at least one of the nodes indicates cardiopulmonary resuscitation (CPR) treatment of the patient with no ventilation, and wherein at least another of the nodes indicates CPR treatment of the patient with active ventilation; determine which of the two or more possible nodes should be emphasized based on the SmO2 level; and update the array of the two or more possible nodes based on the determination.
DYNAMIC SAUNA
Systems and methods are provided for controlling infrared radiation (IR) sources of a sauna including tuning IR wavelength-ranges and radiated power-levels of IR sources, and directing IR to locations on a user's body. In one illustrative embodiment, a sauna may be provided having adjustable IR emitters to emit IR at any wavelength resulting in a desirable radiation treatment for the sauna user. In another illustrative embodiment, a method is provided for tuning IR emitters in a sauna.
Vacuum and Positive Pressure Ventilation Systems and Methods for Intrathoracic Pressure Regulation
Medical techniques include systems and methods for administering a positive pressure ventilation, a positive end expiratory pressure, and a vacuum to a person. Approaches also include treating a person with an intrathoracic pressure regulator so as to modulate or upregulate the autonomic system of the person, and treating a person with a combination of an intrathoracic pressure regulation treatment and an intra-aortic balloon pump treatment.
Wearable Devices, Systems, Methods and Architectures for Sensory Stimulation and Manipulation and Physiological Data Acquisition
A garment with prepositioned, definite sensory stimulating devices attached. The sensory stimulating devices include, but are not limited to, electrical stimulation, audio and physical stimulation such as localized force generation, compression, constriction, vibration, and surround sound. Predetermined and defined actuators allow the wearer to receive tissue, nerve and/or muscle stimulation and/or contraction so that the stimulation is precise as determined by its ability to conform to the scientific methodology of repeatability, reproducibility and reliability; this being due to consistency of actuator positioning in one or multiple locals on the human body. A personal surround sound can also be integrated to the garment to ensure the wearer is always in the optimal position relative to the speakers. These actuators can be force generators within the garment for the wearer to feel impact or apparatus or electrodes included in the garment to locally constrict and increase pressure to the wearer.
Dynamic sauna
Systems and methods are provided for controlling infrared radiation (IR) sources of a sauna including tuning IR wavelength-ranges and radiated power-levels of IR sources, and directing IR to locations on a user's body. In one illustrative embodiment, a sauna may be provided having adjustable IR emitters to emit IR at any wavelength resulting in a desirable radiation treatment for the sauna user. In another illustrative embodiment, a method is provided for tuning IR emitters in a sauna.
Apparatus and Method for Tactile Stimulation of Human Skin
It is disclosed an apparatus (100) for tactile stimulation of C-Tactile afferents comprising a casing (10) configured to be positioned onto a user's skin and at least one tactile stimulation element (21) carried by the casing (10) and operated by a motor (30) at a controlled velocity for generating at least one tactile stimulation. The apparatus (100) further comprises an electronic control unit (40) and at least one pressure sensor (50) in electrical communication with the electronic control unit (40) to control the pressure force exerted by the tactile stimulation element (21) onto the user's skin by adjusting the position of the tactile stimulation element (21) with respect to the user's skin, based on a feedback signal transmitted by said at least one pressure sensor (50). A method of generating at least one tactile stimulation of C-Tactile afferents carried out by using the aforesaid apparatus (100) is also disclosed.
SYSTEMS AND METHODS FOR ASSISTING PATIENT AIRWAY MANAGEMENT
A medical system for assisting with an intubation procedure for a patient. The system comprising airflow sensors configured to obtain data indicative of airflow in the patient's airway and physiological sensors configured to obtain information regarding airflow in the patient's lungs. The system further including a monitoring device communicatively coupled to the airflow sensors and the physiological sensors. The patient monitoring device comprising at least one processor coupled to memory and configured to: provide a user interface on a display and assist the rescuer in determining proper placement of an endotracheal tube, receive the data indicative of the airflow in the patient's airway, receive the physiological information regarding the airflow in the patient's lungs, and determine whether the tube is properly placed based on the received physiological information, and present an output of the determination of whether the ET tube was properly placed.