We provide a respiratory therapy system comprising: a flow generator; a humidifier; a respiratory conduit a patient interface coupled to the respiratory conduit to deliver a gases flow to a patient; a sensor configured to determine pressure or flow of the gases flow; a controller configured to control the flow generator to generate the gases flow; and the controller configured to: a) retrieve at least one first signal associated with or indicative of a gases flow and/or pressure in the respiratory conduit; b) determine a measure of at least one first parameter associated with gases flow perturbations and/or pressure perturbations for at least one portion of the retrieved at least one first signal; and c) determine the presence of liquid in the respiratory conduit based at least in part on the measure(s) of the at least one first parameter meeting a first threshold.

The system can be used to reduce or alleviate condensation in a respiratory gas deliver conduit.

A method of treatment and delivery device for mixed carbon dioxide, carbonic acid, saline and optional active additives for treating head ailments includes delivery of dosage of the treatment at specified flow rates, using a) main housing having a hollow central area containing the dosage; b) a dosage dispenser head located at the distal end of the main housing, and having at least one flow channel for movement of the dosage from the main housing through the dosage dispenser head and to external of the dosage dispenser head; c) a dosage release control component located between the main housing and the dosage dispenser head to permit flow of the dosage through the dosage dispenser head in response to increased pressure against the dosage; and d) a pressure-changing moveable component on the main housing.

This disclosure relates to methods and apparatus for treating diseases and conditions of the colon and alimentary canal which are associated with obligate anaerobic microorganisms, and particularly, for treating Clostridioides difficile infection. The method and apparatus provide for continuous administration of intraluminal oxygen to the rectum, colon, and cecum to maintain oxygen in those environments at levels toxic to obligate anaerobic microorganisms such as Clostridioides difficile.

A gas delivery system supplying a body cavity with a given gas includes a first guide pipe for supplying the given gas into the body cavity and a second guide pipe installed in the first guide pipe for supplying the given gas into the body cavity at a flow velocity that differs from that of the first guide pipe. A flow velocity of the given gas that is supplied from a first conduit which is formed by the first guide pipe and the second guide pipe is faster than a flow velocity of the given gas that is supplied from a second conduit which is formed in the second guide pipe.

Disclosed is a system to generate bubbles. The bubbles may be formed to include a substantially or medically pure gas. The bubbles may be formed on demand and in a selected small size.

A surgical access apparatus is presented including a cannula having a housing and a cannula shaft, the cannula shaft defining an internal lumen and a slot in communication with the internal lumen and an obturator insertable through the internal lumen of the cannula. The obturator includes an obturator shaft having a proximal end and a distal end and a tip member disposed at the distal end of the obturator shaft, the tip member configured to form an incision through tissue. An outer surface of the obturator shaft and the tip member defines a channel for receiving and directing insufflation fluid into a body cavity, a portion of the same channel also configured to guide a surgical instrument, such as a suture passer/grasper for closing an incision, towards and through the slot. In this way, the cannula and obturator can be employed both for forming an incision at the beginning of a surgical procedure and for closing the same incision at the conclusion of the surgical procedure.

The disclosed system includes a probe for mechanically cutting tissue Other components of the system include a luminally protective sheath, a microscopic end cauterizing probe, a surgical console, an identification-sensitive self-sealed cassette, and a plurality of flexible tubing lines with pinch valves thereon.

A pressure regulating or pressure relief device comprises an inlet and an outlet chamber with an outlet. The inlet is in fluid communication with the outlet chamber. A valve seat is located between the inlet and the outlet. A valve member is biased to seal against the valve seat, and displaces from the valve seat by an inlet pressure at the inlet increasing above a pressure threshold to allow a flow of gases from the inlet to the outlet via the outlet chamber. The flow of gases through the outlet causes an outlet pressure in the outlet chamber to act on the valve member together with the inlet pressure to displace the valve member from the valve seat.

An apparatus and method is provided for reducing middle ear fluid and equalizing middle ear pressure in infants and toddlers. The apparatus coordinates the act of swallowing and the forcing of air into the nostril of the child. The coordinated actions allow air forced into the nostril to traverse the Eustachian tube when in its open state. A flexible member and a main flexible tube, connected accordingly, are both adapted to be inserted into the child's mouth and nostril, respectively, to achieve such coordination and allow air to enter the Eustachian tube when in its open state, ultimately allowing air to reach the middle ear.

Described herein are introducer devices and methods for using an introducer device to facilitate passing an endoluminal instrument to a target region of a body cavity. An introducer device may include a tubular member having an inner wall that defines a channel configured to receive the endoluminal instrument and a plurality of projections disposed in the channel at perimetrically spaced apart locations around the inner wall, where the projections extend inward and are configured to offset the endoluminal instrument from the inner wall, thereby creating a space between the endoluminal instrument and the inner wall. A method for using an introducer device may include passing the endoluminal instrument to a first instrument insertion depth within the introducer device, advancing the introducer device in the body cavity, and advancing the endoluminal instrument to a second instrument insertion depth within the introducer device.