A paediatric closed system suction catheter assembly has a patient end fitting (20) through which a suction catheter (24) is advanced into the tracheal tube (1). The patient end fitting comprises two parts: a machine end portion (30) including a wiper seal (32) and a ventilation side port (37), and a patient end portion (31) with a tapered spigot (42) inserted directly into the machine end (12) of the tube (1) without any intervening connector. The machine end and patient end portions (30) and (31) are connected together by a rotatable joint (43) formed by part-spherical surfaces (39) and (41) on the two portions.

The present invention relates to a tracheal ventilation apparatus, in particular a tracheostomy cannula or an endotracheal tube, having a cannula tube, which from a point of view from a gas supply, has a proximal tube portion with a proximal opening and a distal tube portion with a distal opening. In order to provide an easy-to-handle tracheal ventilation apparatus that can easily be inserted and that impedes a swallowing process as little as possible, the proximal tube portion and the distal tube portion are connected to one another by way of an axially air-permeable joint that facilitates at least restricted mobility and, in particular, pivotability of a longitudinal axis of the distal tube portion with respect to a longitudinal axis of the proximal tube portion.

A gases flow rate sensing system may be configured to operate in at least two different target temperature modes, based upon a measured temperature of the gases flow. In some embodiments, the gases flow sensing system may have a voltage divider containing a thermistor. The gases flow rate may be determined based upon a voltage output indicating an amount of power needed to maintain the thermistor at a target temperature as specified by the target temperature mode, and a measured temperature of the gases flow.

Systems and methods can determine whether a patient is attached to a respiratory device (such as to via a patient interface) by analyzing a flow parameter signal in the time domain. Additionally, the processes can classify the patient attachment status into one of the four categories: detached, attaching, attached, or detaching. The system can include a non-sealed patient interface, such as a nasal cannula in a nasal high flow therapy, or any other patient interfaces. Data of the patient's use of the respiratory system can provide therapy compliance and long-term trend of use information and/or progress in the patient's respiratory functions and/or other physiological functions.

The present invention provides an improved percutaneous dilation tracheostomy device. The device is configured to include all of the required components to perform a percutaneous tracheotomy. The device includes a retractable needle and an extendable j-wire rather than having separate components as in typical percutaneous tracheostomy devices. The device includes a dilator section to expand the diameter of a patient's stoma. The device is further configured to allow an operator to perform a bubble test to alert the user that the tube is in the trachea. In addition, the device is generally more compact than typical emergency tracheostomy devices.

An irrigating intraluminal suction inner cannula system for a tracheostomy tube may be a suction-powered system that may be used for suction alone or a combination of rinse and intraluminal suction for tracheostomy tubes in place of conventional catheter-based intraluminal suction. An inner cannula includes chambers, or regions, and holes that facilitate intraluminal suction and cleaning at multiple locations within the tracheostomy tube. It may be applied/actuated by a patient, healthcare worker, caretaker, or via an electronic system either on-demand or on regular or triggered intervals, in either inpatient/hospital or outpatient/ambulatory care setting.

Embodiments of the invention relate to a ventilation device comprising: a. a ventilation tube having proximal and distal ends; and b. an inflatable cuff having a proximal bulge portion and a distal neck portion disposed distal to the bulge portion, the inflatable cuff being mounted around the ventilation tube to define proximal and distal cuff attachment locations which are both fixed on an outer surface of the ventilation tube.

A respiratory ventilation apparatus configured to deliver a respiratory gas to a patient interface is provided. The apparatus may include a gas pressurization unit configured to generate a pressurized respiratory gas, a gas inlet port configured to introduce the respiratory gas into the respiratory ventilation apparatus, a gas outlet port configured to discharge the pressurized respiratory gas to a respiration tube, a detection module configured to detect the pressure of the pressurized respiratory gas, at least one non-volatile memory configured to store a plurality of parameters and a plurality of programs, and one or more controllers. The one or more controllers may be configured to initiate the respiratory ventilation apparatus upon a boot operation, and/or initiate a program that constantly reads information from the detection module, and controls the pressure of the pressurized respiratory gas using the information read from the detection module and at least one parameter.

Systems and methods for classifying breathing disorders of subjects are based on the respiratory response to a change in a pressure level of a pressurized flow of breathable gas. The change presents a breathing challenge to a subject. The challenge may be limited to the inspiratory breathing phase. The inspiratory pressure level may be lower than the expiratory pressure level during challenges.

An instrument for accessing and visualizing hollow organs is provided. The instrument includes a mouthpiece having a perforated mask and a sleeve having a generally cylindrical or ovoid shape extending from the perforated mask substantially perpendicularly thereto and defining a channel. The instrument further includes sucking means having a suction chamber or closed volume that is restrained to the mask on the side where the sleeve is formed. The suction chamber has a plurality of through openings adapted to allow fluid communication with a surrounding environment, an intake opening communicating with the suction chamber formed on the mask, wherein the through openings are formed on the skirt of a dome-shaped member which delimits the suction chamber.