Provided are a mask, a sample collecting tube, and a pathogen collecting apparatus. The mask includes a mask body, a breather valve fixed on the mask body, and a sampling structure including a pathogen adsorption portion. The pathogen adsorption portion is disposed on an inner side of the breather valve and is adapted to adsorb pathogens in exhaled gas. The pathogen adsorption portion is adapted to enter the sample collecting tube to be in contact with a sample preservation solution in the sample collecting tube.

Provided herein is a capnography fitting for use in a capnography system wherein the capnography fitting is configured to fit inhalation masks of various sizes and shapes so that viable carbon dioxide readings can be obtained from an air sample obtained from a patient's exhaled gas. The fitting includes a rigid tube having a proximal end inlet configured to receive an inhalation gas and to slidably engage a mixed gas fitting, and a distal end outlet configured to slidably engage directly to an inlet of an inhalation mask configured to cover a nose and/or mouth. The tube also includes an angled port in fluid communication with and disposed adjacent to the proximal end inlet or the distal end outlet. Methods and kits are also provided.

A gas delivery system, for providing gas to a wearer, includes a first body having a first cavity. The first body is supportable to a side of a nose and mouth of the wearer. A first adapter receives gas from a gas supply and provide the gas to the first cavity. A plurality of first openings in the first body to create a bolus of gas about the nostrils of the nose and the mouth. The first body, and a second similar body may be supported by an adjustable bridge on opposite sides of the nose and mouth of the wearer.

A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient includes a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface; wherein flow rate of the respiratory gas is controlled by a microprocessor, a mixing area for mixing a first gas and a second gas in the respiratory gas flow pathway, a humidification area downstream of the mixing area and configured for humidifying respiratory gas in the respiratory gas flow pathway, and a heated delivery conduit for minimizing condensation of humidified respiratory gas.

A diagnostic device is disclosed for characterisation of particles from a patient's airways, such as a lung, when ventilated by a ventilator, and/or for control thereof, comprising a particle detecting unit configured to be connected to a conduit for passing expiration fluid from said patient, for obtaining data related to particles being exhaled from said patient's airways.

In an embodiment, a connector or connector assembly for attaching a nasal cannula with a gas delivery hose includes a sensor port for a sensor probe positioned near an end of a nasal cannula, which can allow the sensor probe to be placed closer to the patient's nostrils than previous connector parts allowed. The connector can be configured to advantageously allow the nasal cannula to rotate relative to the gas delivery hose, thereby allowing a patient or healthcare provider to untangle or otherwise straighten the hose or the cannula. The connector assembly can be configured to automatically align locking protrusions on a first component with locking recesses on a second component, where insertion of the second component within the first component causes the second component to rotate relative to the first component, thereby aligning the locking protrusions with associated locking recesses.

A respiration device (1) supports cardio-pulmonary resuscitation (CPR) and a method for operating a respiration device (1) supports cardio-pulmonary resuscitation (CPR). The respiration device (1) has a control and regulation unit (7) in order to actuate an expiratory metering unit (3), and an inspiratory metering unit (2) such that, in a first phase, a current value of pressure is increased relative to a first pre-defined value (16) and such that, in a second phase, the current value of the pressure is reduced relative to the first pre-defined value (16).

A method of treating a human subject which is effected by inhalation of gaseous nitric oxide, the method comprising a first treatment period comprising administering gNO by inhalation over a period of about at least 5 days, wherein the first treatment period is followed by a second treatment period comprising administering gNO by inhalation over a period of at least 3 months. The method can be utilized for treating a human subject suffering from, or prone to suffer from, a disease or disorder that is manifested in the respiratory tract, or from a disease or disorder that can be treated via the respiratory tract.

A detection device for detecting characteristics of a mixed fluid containing different types of substances with different thermal properties within a prescribed range, includes: one or a plurality of heaters for heating the mixed fluid; a plurality of temperature detectors for detecting the temperature of the mixed fluid heated; a flow rate calculation unit for calculating the flow rate of the mixed fluid using the output from at least a portion of the plurality of temperature detectors; a correspondence relation storage unit that stores the correspondence relation between the output from the temperature detectors for a prescribed flow rate and the mixture ratio of the substances in the mixed fluid; and a mixture ratio calculation unit for calculating the mixture ratio of the substances in the mixed fluid on the basis of the output from the temperature detectors and the correspondence relation.

In some implementations, a low dead space airway adapter for sampling fluid flowing through a ventilation assembly includes an outer wall configured to couple to an endotracheal (ET) tube adapter and an internal projection positioned at least partially within an internal cavity defined by the outer wall and configured to extend within an internal cavity of the ET tube adapter when the airway adapter is in use. The internal projection can include a fluid passageway configured for fluid communication with at least a portion of the internal cavity of the ET tube adapter and a free end comprising an opening in fluid communication with the fluid passageway. At least a portion of the free end can be chamfered around the opening and configured to contact an inner surface of the ET tube adapter when the outer wall is coupled to the ET tube adapter.