According to one example of the present disclosure an infusion device is configured to control a medication delivery apparatus to intravenously deliver a pharmaceutical preparation to a patient. The infusion device comprises a processor and a memory storing instructions executable by the processor to cause the medication delivery apparatus to deliver the pharmaceutical preparation to the patient according to a predetermined dose profile. The predetermined dose profile is designed to deliver a therapeutic dose of the pharmaceutical preparation to the patient over a predetermined infusion time in a manner which facilitates safe detection of an adverse reaction of the patient to the pharmaceutical preparation, or desensitization the patient to the pharmaceutical preparation, during a first stage of administering the therapeutic dose.

A humidification control system comprises a ventilation therapy apparatus main body, a respiratory humidifier, a heating pipeline and a nasal oxygen cannula, wherein the ventilation therapy apparatus main body comprises a fan and a first controller, the respiratory humidifier comprises a water tank, a heating plate, a water tank air inlet temperature sensor and a heating plate temperature sensor, an air outlet of the fan is connected to an air inlet of the water tank; an air outlet of the water tank is connected to an air inlet of the heating pipeline; an air outlet of the water tank is connected to an input port of the nasal oxygen cannula; the heating pipeline comprises a heating pipeline air inlet temperature sensor and a heating pipeline heating control module; and the first controller makes the relative humidity of the current first mixed airflow.

The disclosure provides for an isovolumetric pump system for the removal of a thrombus and a method of use thereof. The isovolumetric pump system includes at least one inflow container connected to an output of the treatment region, at least one outflow container connected to an input of the treatment region, and a drawbar connecting the inflow container and the outflow container. As the drawbar is drawn back, the same quantity of fluid is drawn from the treatment region into the inflow container and injected into the treatment region from the outflow container.

Devices for delivering a controlled concentration of an agent are provided. The device includes a reservoir for the agent and a flow control portion operably connected to the reservoir. The device also includes a valve for releasing the agent from the flow control portion and a pump for flowing air to mix with the agent released by the valve and for flowing the agent and air mixture out of the device. Methods of delivering a vaporized agent to a subject are also provided. The methods include storing a liquid agent in a reservoir of a device and flowing the agent into a flow control chamber to change the agent to a gas. The methods also include mixing the agent in gas form with air and flowing the agent and air mixture out of the device to be delivered to a subject.

A negative pressure wound therapy device can include a negative pressure source configured to be connected, via a fluid flow path, to a wound, a valve positioned in the fluid flow path and configured to, in an open state, permit supply of negative pressure from the negative pressure source upstream of the valve and, in a closed state, block supply of negative pressure from the negative pressure source upstream of the valve, a flow restrictor positioned in the fluid flow path, and a pressure sensor configured to measure a pressure differential across the flow restrictor. The device can include control circuitry configured to, in a normal operational mode, cause the valve to be in the open state and, in a test mode, perform at least one of a leak test, a flow test, or an excessive pressure test.

The present application provides a device (100) for transferring a fluid from a surgical site, comprising an elongate body portion (102) defining a proximal end region (106) connectable to a source of negative pressure; an elongate neck portion (104) defining a distal end region (108) of the device locatable at a surgical site; a through bore (118) extending from the distal end region to the proximal end region; and a control member (116) for selectively controlling a negative pressure at the distal end region, wherein the control member comprises a valve portion (124) configured to at least partially restrict a fluid flowing along the through bore when moved from an open position towards a closed position. A system including the device for transferring a fluid from a surgical site is also provided.

Supplying therapeutic gas based on inhalation duration. At least some of the example embodiments are methods including: sensing a current inhalation of the patient; providing a flow of therapeutic gas to the patient based on the sensing; and ceasing the flow of therapeutic gas to the patient based on a value indicative of previous inhalation duration.

A ventilation treatment device and a ventilation-control method are provided. During use, when a headband contacts a headrest, a first valve assembly contacts a second valve assembly to open first air holes and second air holes, thereby communicating a first chamber with a second chamber, such that air from an air source into the first chamber enters the second chamber and further enters a respiratory chamber of a patient connecting apparatus for inhalation by a patient; and when the headband is separated from the headrest, the first valve assembly and the second value assembly are separated to close the first air holes and the second air holes, thereby preventing the air in the first chamber and the second chamber from flowing out through the first air holes and the second air holes, respectively.

System for assisting a patient in speaking, comprising at least one ventilation apparatus and a patient interface, the ventilation apparatus comprising at least one controllable respiratory gas source and being designed to identify two or more respiratory phases, at least inspiration and expiration, of the patient, and the patient interface having at least one speaking tube and a respiratory tube and being configured to conduct speaking gas to the patient via the speaking tube and to conduct respiratory gas to and/or from the patient via the respiratory tube. The system is configured to provide speaking gas to the patient at least temporarily in a speaking mode in order to enable speaking.

A ventilation device comprising a controllable respiratory gas source and a programmable control unit being configured to perform the following: determining the respiratory gas flow, which is used to determine whether an inspiration or an expiration is present, regulating the pressure for an inspiration (IPAP) and an expiration (EPAP), wherein the control unit determines a typical expiration time over n breaths, the control unit lowers the pressure from the IPAP to the EPAP taking into account the typical expiration time in such a way that the pressure drop to the EPAP is already reached to the extent of at least 85% after a proportion of the typical expiration time in the range of 40-60% of the typical expiration time, the EPAP after completion of the pressure drop being predefined until the end of the typical expiration time.