An intubating device is provided for use with an endotracheal tube. In some embodiments, the intubating device includes a sheath having a distal end and a proximal end, and the sheath is configured to be introduced into a body cavity. The sheath has a rigid section, and the sheath has a flexible section at the distal end. The flexible section is selectively bendable. A control housing is located at the proximal end. The control housing includes a deflector for selectively bending the flexible section of the sheath. In some embodiments, an intubating device includes a sheath having a malleable first section and a second section that is selectively bendable located at a distal end of the sheath.

A system for obtaining signals related to electrical activity of the heart of a subject includes a sensing device including an elongate member having a distal end configured for placement within a body lumen of a subject, and a proximal end configured to extend from the subject, an actuation portion carried by the elongate member and configured for placement within the body lumen, the actuation portion having a low-profile state for delivery within the body lumen and an expanded state, and one or more sensors disposed on the actuation portion, each including a contact surface configured to contact an interior wall of the body lumen, wherein the actuation portion is configured to cause the contact surface of each of the one or more sensors to contact a location on the interior wall of the body lumen to provide a signal component for producing one or more electrocardiogram signals.

A patient tube securement apparatus is disclosed that may be used for oral or nasal intubation of a patient. The apparatus may comprise an endotracheal tube securement apparatus for securing an endotracheal tube to a patient, the apparatus comprising a dermal patch arranged to be positioned on the skin of the patient, and at least one tube holder on the dermal patch. The apparatus may comprise a patient tube securement apparatus for securing a patient tube to a patient, the apparatus comprising a dermal patch arranged to be positioned on the skin of the patient, and at least one tube holder on the dermal patch. Examples are provided in which the tube holder is adjustably mounted on the dermal patch such that the position of the tube holder on the dermal patch can be adjusted without removing the dermal patch from the skin of the patient.

An example nasal airway tube includes a tubular body having a distal end and a proximal end. A surface at the distal end including an opening. The tubular body having an overall curvature with a radius of curvature defined relative to a longitudinal axis of the tube. An X-axis is defined by the longitudinal axis of the tube, and a Y-axis extends perpendicularly from the longitudinal axis and has a positive direction defined outwardly relative to the radius of curvature. At least a portion of the opening faces outwardly relative to the radius of curvature. A vector normal to a plane defined by the opening includes a positive Y-coordinate.

A continuous positive airway pressure system comprises an inspiratory portion, an expiratory portion, and a controller. The inspiratory portion is coupled to a patient interface to provide an airflow with positive pressure to a patient. The inspiratory portion includes a first sensor to measure a pressure and/or a flow rate of the airflow at the inspiratory portion. The expiratory portion is coupled to the patient interface to receive air exhaled from the patient. The expiratory portion includes a second sensor for measuring a pressure and/or a flow rate of the air exhaled at the expiratory portion. The controller (i) determines a pressure at the patient interface based on the measured pressures and/or the flow rates of the airflow at the inspiratory portion and the air exhaled at the expiratory portion and (ii) modifies the airflow provided by the inspiratory portion based on the determined pressure.

A nasopharyngeal airway device for receiving a nasal cannula is provided. The device has a flexible tube having first and second open ends and a flexible receptacle open at its upper end and integral with the flexible tube first open end. The flexible receptacle has a diameter greater than a diameter of the flexible tube and contains a lower end opening that communicates with the flexible tube first open end and opposed recesses arranged at an upper edge thereof and configured to receive and retain a nasal cannula. Preferably, the receptacle further includes a bottom wall containing the lower end opening and side wall containing the recesses. When the flexible tube second open end is inserted into a nasal passage of a patient, tubing of a nasal cannula is arranged in the recesses to deliver oxygen to the patient via the receptacle and the flexible tube.

A method of using nanoparticle (NP) spray to treat an infection in the respiratory system and far infrared radiation (FIR) to treat inflammation. The method uses a spray probe inserted into the airway of a patient to apply mSiO.sub.2 and FIR to a target site in the upper respiratory tract. FIR applied may be in the 3-10 μm range. The mSiO.sub.2 spray kills any organisms, including COVID-19 and FIR reduces inflammation resulting from infection. The treatment may be applied to intubated or spontaneously breathing patients and via the oral or nasal passages.

An apparatus for selectively coupling a first tube and a second tube allows easy separation and connection of tubing in cases of accidental or forceful removal of the tube. A first connecting member and a second connecting member can be easily connected and disconnected as needed to prevent and allow fluid flow to and from a patient. The apparatus can be applied to prevent the accidental removal of patients undergoing extended treatments involving tubes entering the body in the clinical, geriatric, or other care settings. The apparatus also allows for the purposeful detachment and sealing of tubes entering the body to allow for increased patient mobility.

Systems, methods, and apparatus for securing nasal tubes are disclosed. An exemplary system includes a bridle, a magnetic portion connected to the bridle, a delivery probe, a retrieval probe, and a clamp. The delivery probe includes an elongated member having proximal and distal ends, the distal end configured to deliver the magnetic portion, and a bridle lock configured to release the bridle upon actuation of an actuator. The retrieval probe includes an elongated member having proximal and distal ends, the distal end including a magnetic portion configured to magnetically couple with the other magnetic portion, and a magnetic coupling indicator configured to provide an indication in response to a magnetic coupling. The clamp includes a channel portion with an inside diameter larger than an outside diameter of a nasal tube. The clamp is configured to secure the nasal tube following placement of the bridle by the delivery and retrieval probes.

A system for obtaining signals related to electrical activity of the heart of a subject includes a sensing device including an elongate member having a distal end configured for placement within a body lumen of a subject, and a proximal end configured to extend from the subject, an actuation portion carried by the elongate member and configured for placement within the body lumen, the actuation portion having a low-profile state for delivery within the body lumen and an expanded state, and one or more sensors disposed on the actuation portion, each including a contact surface configured to contact an interior wall of the body lumen, wherein the actuation portion is configured to cause the contact surface of each of the one or more sensors to contact a location on the interior wall of the body lumen to provide a signal component for producing one or more electrocardiogram signals.