The inventive concepts disclosed and claimed herein are generally directed to an improved assisted walking device, such as a cane, walker or wheelchair, that includes an integrated oxygen concentrator housed within the assisted walking device. In some embodiments, for example, the improved assisted walking device includes a handle, a control pad, an elongated housing having an interior chamber, an oxygen concentrator, a leg member and a foot member. The oxygen concentrator detachably positioned within the interior chamber of the elongated housing and including an adsorption system configured to generate a flow of oxygen enriched gas, a compressor that includes a motor, a battery, a plurality of sieve beds configured to extract oxygen-enriched gas from ambient air, and a controller in communication with the control pad.

A cardiopulmonary resuscitation system capable of avoiding fighting in an asynchronous mode in which sternum compression and artificial respiration are performed independently and continuously. The cardiopulmonary resuscitation system includes: a sternum compressor that includes an impact hammer for compressing the chest of a patient and repeats a sternum compression cycle having, as one cycle, a compression period in which the impact hammer is pressed against the chest and a recoil period in which the impact hammer is separated from the chest; an artificial respirator that repeats an artificial respiration cycle having, as one cycle, an inhalation period in which respiratory gas is supplied to the patient and an exhalation period in which supply of the respiratory gas is stopped; and a controller that controls the artificial respirator and the sternum compressor, the controller executes the artificial respiration cycle a predetermined number of times per unit time while executing the sternum compression cycle a predetermined number of times per unit time, and stops pressing the impact hammer against the chest during the compression period overlapping with the inhalation period.

An ozone and contrast therapy system including an enclosure defining an interior volume, a steam system having a steam dispenser for releasing steam within the interior volume, a cold shower system having a shower head for releasing cold water within the interior volume over a user, and an ozone system having a nozzle for releasing ozone into the interior volume.

A patient-coupled resuscitation device for use with a plurality of medical devices is provided. The resuscitation device includes a portion configured to provide treatment, a connector configured to connect the resuscitation device to one of a first medical device and a second medical device, and a housing including a memory and associated circuitry. The memory and associated circuitry is configured to store a device identifier to identify the resuscitation device; receive medical treatment information from the first medical device, the medical treatment information including at least one of: patient physiological data, patient characteristic data, and rescuer performance data; receive timing information of the medical treatment information from the first medical device; record the medical treatment information and the timing information; and transfer, upon detecting a connection to the second medical device, the medical treatment information and the timing information to the second medical device.

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.

A system of delivering multi-frequency acoustic vibrations into the body of a user for increasing a voltage of the cells of the user's body is provided. The system including: a base assembly including a space defined by a top plate and a bottom plate including voice coils, magnets and springs, wherein each voice coil is aligned with a magnet and the springs maintain a predefined thrust between the top and bottom plate, each voice coil lying within a magnetic flux of a magnet for producing acoustic waves of predefined frequencies for deliverance into the user's body through the user's feet when the user is standing on the base assembly; and a tower assembly tethered with the base assembly, and including at least one speaker, and one or more cell exciter pads for attaching with a portion of the user's body, the speaker and pads producing acoustic waves of predefined frequencies for deliverance into the user's body.

The invention relates to an anteroposterior thoracic restriction device comprising holding means intended to surround a patient's chest, a compressible fluid bag, intended to be held against the patient's sternum by said holding means, and reversible bilateral tightening means, arranged on either side of the fluid bag and capable of reversibly tightening the holding means around the patient's chest.

A defibrillation system may include a cardiac arrest detector detecting whether cardiac arrest of a passenger has occurred in a state of taking a seat of a self-driving vehicle and fastening a seatbelt of the vehicle; a passenger posture detection device detecting a posture of the passenger; a seat driving device changing the posture of the passenger into another posture in which the passenger lies down based on a detection signal of the passenger posture detection device when the cardiac arrest of the passenger occurs; a heart position detector configured to search for a position of a heart of the passenger; a defibrillation robot to perform a CPR method or a method using an AED on the heart of the passenger; and a controller controlling operation of the seat driving device, the heart position detector, and the defibrillation robot based on detection signals of the cardiac arrest detector and the passenger posture detection device.

The present invention is directed to a system and method of use for an operational halotherapy enclosure system sufficiently sized to retain therein an exercise machine for a person to do physical exercise and includes a red light panel and a thermal heating light panel. The halotherapy enclosure system also includes a salt aerosol dispersing device configured to disperse salt particles inside of the enclosed space, and a controller configured to control the emission of red light waves from the red light panel, thermal energy from the thermal heating light panel, and air salination emissions from the aerosol dispersing device within the enclosed space. The combination of aerosolized salt, red light waves, and thermal energy produces an enhanced beneficial result when a person inside of the halotherapy enclosure is exercising and inhaling the aerosolized salt under the red light and thermal energy conditions.

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.