Embodiments of the present invention provide systems and methods for delivering respiratory treatment to a patient. For example, a treatment system may include a mechanism for delivering a positive pressure breath to a patient, and one or more limb flow control assemblies which modulate gas flow to and from the patient. Exemplary treatment techniques are embodied in anesthesia machines, mechanical ventilators, and manual ventilators.

A therapy of oxygen pulses delivered through the pulmonary system of human patient for treating neurodegenerative disorders such as Parkinson Disease (PD), Alzheimer's Disease (AD), Amiotrophic Lateral Sclerosis (ALS) or Motor Neuron Disease (MND) and other dementias, and Lymphedema, Arthritis and Depression is provided. Aspects of the methods including administering to the subjects an effective amount of oxygen as pulses through the respiratory tract are included. Also provided are methods of assessing severity of the disease, mild, moderate, severe, or critical, and oxygen doses and frequencies. The method can be applied to human patient for treating neurodegenerative disorders such as Parkinson Disease (PD), Alzheimer's Disease (AD) Amiotrophic Lateral Sclerosis (ALS) or Motor Neuron Disease (MND) and other dementias, and Lymphedema, arthritis and depression.

A medical system comprises an operation console, a support platform configured to support a catheter, a driving unit moveably coupled to the support platform, the driving unit being configured to advance or retract the catheter based on an instruction from the operation console, a support platform configured to support a catheter, a separator device including: a first end, a second end opposite the first end, and a fixed length portion between the first end and the second end, and a medical tube adaptor including: a first end, and a second end opposite the first end and mateable with a medical tube. The medical tube is insertable into a mouth of a patient. The second end of the separator device is mateable with or attached to the first end of the medical tube adapter.

A suction assembly is described. The suction assembly includes a therapy unit with a body that can apply a supplemental therapy to a skin surface. The suction assembly also includes a cup that can be removably connected to the therapy unit and that can interface with a skin surface to define a chamber within the cup. A pump of the therapy unit can reduce a pressure within the chamber to draw the skin surface into the chamber in a cupping therapy. In response to the skin surface being drawn into the chamber, the body can move in a longitudinal direction to maintain contact with the skin surface. A wall of the cup is translucent and the suction assembly is dimensioned to provide a user with a view into the chamber through the wall of the cup that is substantially unobstructed by the housing.

Methods and systems are provided for aerosolization of individual building blocks of medical microrobots and subsequent in situ assembly into microrobots capable of medical intervention deep within lung tissues of a subject. The methods and systems of the disclosure may allow for microrobot-based therapy of pulmonary diseases that have previously been difficult to effectively treat using conventional therapeutic approaches.

A method and system of sleep maintenance includes configuring a stimulation device comprising a transducer to emit a transcutaneous vibratory output to a body part of a subject, receiving physiological data of the subject from at least one sensor at a processor, providing a stimulation pattern for the transcutaneous vibratory output to be emitted by the transducer, the stimulation pattern comprising a perceived pitch, a perceived beat, and an intensity of the transcutaneous vibratory output, causing the transducer to emit the transcutaneous vibratory output in the stimulation pattern, determining a sleep state of the subject based on the physiological data, and altering the stimulation pattern based on the sleep state, wherein altering comprises at least one of (i) reducing a frequency of the perceived pitch, (ii) increasing an interval of the perceived beat, or (iii) reducing the intensity.

The invention relates to a method of controlling a respiratory assistance apparatus delivering a flow of gas, particularly a flow of air, comprising the steps of measuring at least one parameter indicative of said flow of gas; converting said at least one parameter indicative of said flow of gas into at least one signal indicative of said flow of gas; processing said at least one signal indicative of the flow of gas in order therefrom to deduce at least one item of information relating to cardiac massage being performed on a patient in cardiac arrest; on the basis of said at least one deduced item of information, automatically selecting a given ventilation mode from among a number of stored ventilation modes, and controlling the respiratory assistance apparatus by applying the selected ventilation mode. Respiratory assistance apparatus capable of implementing said control method.

Provided is a medical handpiece having liquid spray and suction functions and capable of being replaced with a drill. The medical handpiece includes a handpiece body having an accommodation space therein, a spray unit receiving liquid from an outside to spray the liquid onto a target to be treated, a pump unit transmitting air pressure to the spray unit to increase a spray speed of liquid sprayed by the spray unit, a drive unit converting a rotary motion into a reciprocating motion to transmit power to the pump unit, and a suction unit sucking liquid and foreign matter from the target to be treated.

An implantable medical device for transcatheter delivery, which includes an anchor unit (100) configured to be anchored at an annulus of a cardiac valve of a patient, at least one coupling unit (200) that extends along a first length radially from said anchor unit (100) towards a coaptation line of said valve and including an extension unit (400) extending along a second length. The extension unit (400) is configured to cross between the leaflets of the cardiac valve in order to fill out for an insufficient closing of the valve leaflets of said cardiac valve.

The wound treatment apparatus combines an internal negative pressure (vacuum) pump and an internal positive pressure (compressor) pump connectable to an external oxygen supply for providing both negative pressure wound therapy and hyperbaric oxygen wound therapy to a wound site. The apparatus also includes a user interface operatively connected to an electronic controller that monitors and actuates the vacuum and compressor pumps. The user interface and controller enables the apparatus to provide multiple modes of operation and the ability to selectively change between negative pressure therapy operational modes and hyperbaric oxygen operational modes.