A system for measuring cardiovascular data includes an elongate member having a channel, a first expandable member carried by the elongate member and movable between a collapsed state and an expanded state by adjustment initiated externally of a subject, a first sensor disposed on a surface of the elongate member, second and third sensors disposed on a surface of the first expandable, a first optical sensor located at a first location in relation to the distal end of the elongate member and configured for obtaining photoplethysmographic data, and wherein the first expandable member in its expanded state is configured to interface with the subject's larynx for delivery of at least oxygen gas into the respiratory system of the subject, and the second and third sensors are configured to contact tissue in proximity to the larynx when the first expandable member is in its expanded state.

The present invention provides improved medical devices, including oral airway devices, equipped with a visualization device for intubation, extubation, ventilation, drug delivery, feeding and continuous remote monitoring of a patient. The present invention also provides methods for rapid and accurate placement of a medical device in a patient and continuous real time monitoring, including a remote monitoring, of the patient after the placement.

The present invention provides medical devices comprising a camera combined with a second device selected from an endotracheal tube, oral airway, supraglottic airway, tracheostomy tube, suction catheter, tubeless intubating device, tool tube and/or stylet. The present invention also provides methods for rapid and accurate placement of a medical device in a patient with a guidance of a bougie and continuous real-time monitoring, including a remote monitoring, of the patient after the placement.

A neonatal laryngeal mask airway (NLMA) can be used for airway management in the neonate in emergent situations, e.g., respiratory distress syndrome after premature birth, and nonemergent situations, e.g., elective surgery. The NLMA includes a back plate and a cuff. The back plate provides a shelf, a back plate opening, and a wall, which is perpendicular to the shelf, that surrounds a portion of the back plate opening. The cuff is coupled completely around a perimeter of the back plate. The cuff is configured for inflation from an uninflated state to an inflated state in a patient with a pharynx, a larynx with a laryngeal inlet, and a trachea. In the inflated state, the cuff forms a seal around the laryngeal inlet to isolate the larynx from the pharynx, and the back plate is configured to guide a catheter inserted through the back plate opening into the trachea.

A ventilator conduit for a reversible airway device (RAD) is provided. The RAD can include a supra-glottic support member connected to a tubular guide (TG) having oppositely disposed proximal and distal end portions and TG lumen, which extends between the ends and is defined by an inner surface. The RAD can be physically free of an endotracheal tube. The ventilator conduit can include a hollow tube having first and second ends, and a ventilator conduit lumen extending between the ends. The first and second ends can be adapted for connection to a ventilator circuit and insertion into the TG lumen, respectively. At least the second end of the hollow tube can be sized and dimensioned so that, upon insertion into the TG, an outer surface of the second end is brought into direct contact with a portion of the inner surface to form an air-tight seal therebetween.

There are provided herein methods, devices, kits and systems utilizing respiratory mask for delivering pressurized fluid to a subject via inhalation in an efficient manner. The fluid may include gas and/or drug and by utilizing the methods, devices, kits and systems provided, efficient drug delivery to the subject's airways is achieved. The systems, devices, kits and methods further allow inducing insufflation/exsufflation in particular in subjects having impaired suffering from low neuromotor capacity, such as spinal cord injuries (SCI) patients.

A laryngeal mask includes a housing having a neck part and a head part extending from a first end of the neck part. The head part further includes a sealing face and an opposing face, the sealing face and the opposing face being connected by an enclosing wall extending upwardly from the sealing face. The sealing face has a peripheral seal for forming a seal around a larynx and having an opening arranged to be positioned over a laryngeal opening. An airway tube is positioned within the housing and extends from a second end of the neck part to the opening in the peripheral seal, wherein the head part includes a resiliently deformable portion positioned between the sealing face and the opposing face. The resiliently deformable portion is a deformable portion of the head part. The resiliently deformable portion has a protrusion and protrudes upwardly from the opposing face.

A laryngeal mask includes a housing having a neck part and a head part extending from the neck part. The head part includes a sealing face and an opposing face, the sealing face and the opposing face being connected by an enclosing wall extending upwardly from the sealing face. The sealing face has a peripheral seal for forming a seal around a larynx and having an opening arranged to be positioned over a laryngeal opening. The mask further includes an airway tube positioned within the housing and extending from the neck part to the opening in the peripheral seal. The mask further includes a first drain tube extending from the neck part to an aperture located in a distal tip of the head part, and a second drain tube extending from the neck part to a position within the head part that is proximal to the distal tip.

A laryngeal mask apparatus includes a mask portion, a breathing tube and a suction tube. The suction tube is adapted for connection to a suction-producing device. The suction tube further includes suction ports that suck fluids and secretions from the patient's hypopharyngeal region when suction is created within the interior of the suction tube. The breathing tube is adapted for connection to a ventilating system. Air flows through the breathing tube and into the mask portion. A capillary tube is positioned within the interior of the suction tube. When the mask portion is positioned within a patient's throat and suction is created within interior of the suction tube, the suction ports suck the fluids and secretions in the patient's hypopharyngeal region. At the same time, the suction tube and capillary tube cooperate to provide a stream of air that decreases the direct suction forces on the mucosa of the patient's throat that are caused by the suction ports. The laryngeal mask apparatus includes a scope tube having an interior and an inner tube disposed within the interior of the scope tube. The inner tube is sized for receiving a gastric tube.

A sanitary device for securing a breathing tube to a patient during anesthesia administration, which also prevents leaking anesthetic gases from entering the operating room environment. The novel design allows rapid application by the user and prevents potential transmission of infectious agents to the patient while securing the breathing tube. A unique, integrated suction system efficiently evacuates leaking anesthetic gases. The device may be manufactured inexpensively and is provided in sanitary packaging. It is intended for single use.