Abstract: A system and method is provided for a wearable robotic upper body garment. In an embodiment, an upper body garment or apparatus comprises a shoulder saddle, one or more actuators, one or more flexible tendons, back torso section, front, torso section, torso wrap, and upper arm cuff. The shoulder saddle may be comprised of a yoke and one or more elevated shoulder sections. The one or more elevated shoulder sections may be comprised of a first elevated shoulder section. In an embodiment, the back torso and front torso sections may be structurally connected to the yoke. In an embodiment, the one or more actuators may be structurally connected to either said back torso section or front torso section. In an embodiment, the one or more flexible tendons may be operationally connected to a predetermined one or more actuators and an upper arm cuff.

Abstract: The invention relates to a respiratory mask with an interface for the connection of at least two components, wherein the interface is round or oval and has a maximum diameter, and the components each make available at least one subregion of the interface. The component has a grip part which extends radially outward from the subregion and which is configured as a pressing surface or gripping means for fingers or the hand of an operator, wherein the component has two grip parts, wherein the subregions are in form-fit engagement with each other in an assembled state and are movable about a rotation axis (DA), for which purpose the grip part is rotatable to different rotation positions relative to the two grip parts.

Abstract: The invention relates to a respiratory mask of modular construction. The main components are reduced to four parts and are provided by the mask body, the forehead support, the mask cushion and the attachment piece. The design, according to the invention, of the outflow structure between mask body and forehead support makes apertures in the mask body unnecessary for this purpose.

Abstract: Devices and methods for allowing for improved assisted ventilation of a patient. The methods and devices provide a number of benefits over conventional approaches for assisted ventilation. For example, the methods and devices described herein permit blind insertion of a device that can allow ventilation regardless of whether the device is positioned within a trachea or an esophagus. In addition, the methods and device allow for timed delivery of ventilations based on a condition of a thoracic cavity to increase the amount and efficiency of blood flow during a resuscitation procedure.

Abstract: A face mask uses a neck hanger with axillary oxygen to facilitate the flow of filtered fresh air inside the face mask for inhaling. Neck hanger filters the fresh air from the environment mixes with oxygen that is stored in the neck hanger before releasing inside the face mask for inhaling. The neck hanger is a lightweight tube that houses fans, HEPA or ULPA filters, compressed oxygen, a regulator, and a battery with a control circuit. One fan sucks the air from the environment that after being filtered and mixed with oxygen is blown into the face mask through an air pipe that is attached to both the neck hanger and face mask. The exhaled air from interior of the mask is sucked by a second fan through another air pipe, then filtered and released into the environment.

Abstract: A detachable cap for measuring usage of an inhaler includes a hollow receiving portion adapted to removably receive the inhaler. A vent is formed in a roof portion of the cap to allow airflow through the cap to the inhaler. An extension portion is provided for containing electronic components, including an electronic circuit provided in the extension portion, the electronic circuit including a controller coupled to a storage device and a power source. A pressure sensor is provided adjacent to the vent, the pressure sensor communicatively coupled to the controller and adapted to detect an air pressure within the cap. The controller is programmed to calculate an air flow rate through the cap based on the detected air pressure and to store the calculated air flow rate in the storage device.

Abstract: A CPR chest compression system includes a retention structure that retains the body of a patient, and a motor and a compressor that can perform CPR compressions to the chest of the patient. The motor is powered by a battery that is located on the retention structure but away from the motor, and is electrically connected to the motor via one or more wires. Accordingly the weight and volume of the battery can be located away from a top portion of the retention structure. This renders the CPR system is less heavy at the top, and therefore less likely to tilt and start compressing the chest at a different point. Moreover, this permits X-Rays of a larger footprint to go through the CPR system and reach the patient, in example configurations where the components are transparent to X-Rays.

Abstract: An integrated oxygen supply device that is configured to generate oxygen continuously and release the oxygen non-continuously is provided. In some embodiments, the oxygen generated by the integrated oxygen supply device is stored in a porous material with the integrated oxygen supply device. The delivery of the oxygen produced by integrated oxygen supply device to a patient, in those embodiments, is controlled. In some embodiments, the control of the delivering oxygen is according one or more breathing patterns. The breathing pattern(s) may or may not be a current breathing pattern of the patient. For example, in one embodiment, the breathing pattern is a predetermined breathing pattern with a specified inspiration period followed by a specified expiration period.

Abstract: A massaging device (100) with a massaging surface and a plurality of massaging elements (101, 102, 103) moveable relative to each other; characterized in that the massaging surface is adapted such that when applying the massaging surface to a skin surface (111) and moving the massaging elements (101, 102, 103) relative to each other, two differently directed forces are simultaneously exercised by the massaging elements (101, 102, 103) on the skin surface (111) thereby causing simultaneous pinching and stretching of the skin surface (111) present in between the massaging elements (101, 102, 103).

Abstract: A stand-alone chamber or multi-chamber inhalation system has at least two alternative vaporized test liquid supply systems for passive or self-administered delivery of vaporized test fluid and air to one or more test chambers, which can be passive or restraint chambers, based on operator selection of delivery on and off times in a passive mode or actuation of an actuator in the chamber by a test animal in a self-administered mode. In one case, a multiple inhalation chamber system has two or more separate test fluid delivery systems and provides options for selective passive uniform drug delivery to multiple chambers or selective delivery of two or more different drugs to different groups of chambers from different delivery systems so that two different drugs or different concentrations of delivered drugs can be tested simultaneously.

Abstract: A method for performing cardiopulmonary resuscitation (CPR) includes elevating the head, heart and shoulders of an individual from a starting elevation angle to a final elevation angle greater than zero degrees relative to horizontal while performing CPR by repeatedly compressing the chest. The method includes elevating the brain within a time period selected to be slow enough to permit a sufficient amount of blood to flow to the brain throughout the elevation time period. The method also includes regulating the intrathoracic pressure of the individual while performing CPR. The performance of chest compressions is stopped and after stopping the performance of chest compressions, the head, heart, and shoulders are promptly from the final elevation angle within a timeframe selected to prevent significant drainage of blood from the brain until the head, heart and shoulders are lowered.

Abstract: Disclosed herein are modules for performing hyperbaric oxygen therapy (“HBOT”) on a patient submerged in pressurized water where substantially no gas is present in the module. The modules generally have an entry, a fluid inlet for introducing water into the module, first and second fluid outlets positioned substantially at a base and a top of the module respectively, and a utilities inlet and outlet in part for transferring breathing air to and from the patient. The module permits HBOT treatment on a patient submerged in water with no air in the module, thus reducing the risk of fire or explosion. Methods and systems are also contemplated. Disclosed herein are methods of filling a module with water until there is substantially no gas in the module, and providing the patient in the module with treatment air during HBOT treatment.

Abstract: Patient interface components and/or associated head gear and adjustment systems improve sealing and/or patient comfort and/or ease of use. The interface comprising an inflating or ballooning seal. The headgear assembly can be connected to the interface with an elastic component and an inelastic component. The elastic component enabling a course fitting of the interface to the patient and the inelastic component enabling a final fitting of the interface to the patient.

Abstract: A method for performing cardiopulmonary resuscitation (CPR) includes elevating the heart of an individual to a first height relative to a lower body of the individual. The lower body may be in a substantially horizontal plane. The method may also include elevating the head of the individual to a second height relative to the lower body of the individual. The second height may be greater than the first height. The method may further include performing one or more of a type of CPR or a type of intrathoracic pressure regulation while elevating the heart and the head. The first height and the second height may be determined based on one or both of the type of CPR or the type of intrathoracic pressure regulation.

Abstract: A method for performing cardiopulmonary resuscitation (CPR) includes elevating the heart of an individual to a first height relative to a lower body of the individual. The lower body may be in a substantially horizontal plane. The method may also include elevating the head of the individual to a second height relative to the lower body of the individual. The second height may be greater than the first height. The method may further include performing one or more of a type of CPR or a type of intrathoracic pressure regulation while elevating the heart and the head. The first height and the second height may be determined based on one or both of the type of CPR or the type of intrathoracic pressure regulation.

Abstract: A method to improve neurologically-intact survival rates after cardiac arrest may include performing CPR on an individual in cardiac arrest while the individual is in a supine position in general alignment with a horizontal plane. The method may include elevating the individual's head, shoulders, and heart relative to the individual's lower body while the individual's lower body remains generally aligned with the horizontal plane to cause blood to actively drain venous blood from the brain to reduce intracranial pressure. The method may include performing chest compressions on the individual and actively decompressing the individual's chest while the individual's head, shoulders, and heart are elevated.

Abstract: An ambulatory respiratory assist device utilizes a cuirass worn on the chest and/or abdomen and supported by a hip belt so that it does not place a load on the patient's shoulders. The belt also supports a ventilator that includes a pump and its power supply, valving, controls and auxiliary equipment. The device is optionally integrated with auxiliary features such as chest wall vibration, which can be achieved by utilizing cuirass pressure modulation, with shoulder or upper arm supports for simulating the “tripod position”, with positive pressure ventilation apparatus, or with patient monitoring. Shoulder or upper arm supports can extend directly from the belt to the shoulders or upper arms, utilized independently of the cuirass, and optionally integrated with one or more of the above-mentioned auxiliary features.

Abstract: A spatially sensitive augmented reality system for providing resuscitative feedback in a mixed reality environment to an acute care provider during occurrence of a cardiac event in a patient includes a wearable augmented reality device having at least one three-dimensional sensor, a visual display for viewing by the acute care provider, and at least one processor. The at least one processor is configured to receive and process three-dimensional information of a scene of the cardiac event; produce a three-dimensional representation of a field of view of the acute care provider based on the processed three-dimensional information; identify one or more physical objects associated with the cardiac event in the three-dimensional representation; generate at least one virtual three-dimensional object within the three-dimensional representation; and generate an image of the virtual three-dimensional object within the three-dimensional representation on the visual display.

Abstract: A robotic joint comprises a first link, a middle link, a torque generator, a second link, and a locking mechanism. Different ends of the middle link are rotatably coupled to the first link and the second link. The torque generator is coupled to the first link and the middle link and is configured to produce torque between these links. The locking mechanism is switchable between a locking state and an unlocking state. In the unlocking state, the locking mechanism allows free rotation of the second link relative to the middle link in the first and second rotation directions. In the locking state, the locking mechanism is configured to impede rotation of the second link relative to the middle link in the first rotation direction and to allow rotation of the second link relative to the middle link in the second rotation direction opposite of the first rotation direction.

Abstract: The CPAP enclosure is for use in treating sleep apnea in a patient. The CPAP enclosure creates a protected space that contains atmospheric gases at an increased pressure. The increased pressure created within the protected space of the CPAP enclosure prevents the narrowing of the patient's breathing airways during sleep. The CPAP enclosure includes a tent, a valve structure, and a CPAP machine. The tent forms the protected space of the CPAP enclosure. The CPAP machine generates a flow of atmospheric gas under pressure that is pumped into the protected space of the CPAP enclosure. The valve structure controls the flow of atmospheric gas under pressure from the CPAP machine into the protected space of the CPAP enclosure. The valve structure controls the pressure of the atmospheric gas contained within the protected space of the CPAP enclosure.