An add-on device and method for an Endo-Tracheal Tube (ETT), the add-on device including a lengthy body having a major arc-shaped cross section sized and shaped to tightly fit over an ETT, at least one longitudinal cavity passing along the lengthy body, including a distal suction cavity ending with a suction inlet at a distal end of the lengthy body; and a distal suction outlet channel extending from a proximal end of the lengthy body, the channel is a continuous extension of the distal suction cavity and configured to provide suction to the distal suction cavity. The add-on device senses moisture at a distal end of the add-on device, and in case of detection of excessive wetness, provides suction to the distal end of the device through a cavity passing along the device, the suction is provided via a suction outlet channel extending from a proximal end of the device.

A laryngeal mask airway device (LMA) is disclosed comprising a ventilation conduit having operatively upper and lower ends, and a mask at the operatively lower end of the ventilation conduit. The mask has an inner surface forming a receptacle that is in fluid communication with the ventilation conduit, and an outer oropharyngeal surface facing away from the receptacle. The device includes a separate oropharyngeal suction conduit having an operatively lower end forming a collector defining a plurality of suction openings that extends across the oropharyngeal surface of the mask. In use secretions may be drawn through the suction openings into the oropharyngeal suction conduit for removal from the patient through the oropharyngeal suction conduit.

The endotracheal tube system (10) includes an endotracheal tube (12), an auxiliary sterilizing tube (20), and a sterilizing agent source (28) for sterilization of the endotracheal tube (12) while it is in use. The endotracheal tube (12) is an elongated, hollow tube having a distal end (14) and a proximal end (16). An inflatable cuff (18) is disposed on the elongated hollow tube (12), adjacent the distal end (14). The sterilizing tube (20) has a closed distal end (24) and an open proximal end (22). The closed distal end (24) is secured to the elongated hollow tube (12) adjacent the inflatable cuff (18), and a plurality of pores (26) are formed through at least a portion of the sterilizing tube (20). The sterilizing agent source (28) injects chlorhexidine into the sterilizing tube (20), which is distributed to the elongated hollow tube (12) through pores (26).

An improved endotracheal tube or patient ventilation tube which prevents the leakage of proximal secretions to the distal airways of the patient.

Disclosed is a suction device. The suction device includes a sensor unit configured to measure breathing condition of a patient, a tube unit configured to move into a bronchus of the patient so as to suck foreign material generated in the bronchus of the patient when a measured value measured by the sensor unit exceeds a predetermined reference value, and a control unit configured to control an operation of the tube unit based on the measured value measured by the sensor unit. According to the present invention, there is provided the suction device which is automatically operated by directly determining whether foreign material is generated in the bronchus of the patient.

A system comprising a nasogastric tube comprising a nasogastric location element, a feeding mechanism, a suction mechanism configured to sealingly draw an inner wall of an esophagus against said nasogastric tube, and a gastric decompression mechanism.

A cleaning device, system and method for use with an ETT or tracheostomy ventilation tube 60, a ventilator machine 900, a source(s) 602 of fluid (for example, pressurized or unpressurized) and a source(s) of suctioning 603 is disclosed. In some embodiments, the cleaning device is useful for cleaning an inner surface of the ventilation tube 60 and/or for preventing or hindering the accumulation of biofilm thereon. In some embodiments, it is possible to clean biofilm or any other material on the inner surface 201 by delivering fluid into an interior of the ventilation tube, wiping the tube interior with a width-expanded wiping element (e.g. an inflated balloon) by longitudinal motion of the wiping element, and suctioning material out of the ventilation tube ventilation tube.

A catheter body (210) defines a distal-most suction orifice (444) and an outer lateral wall (592), which defines a lateral opening (448) therethrough into a suction lumen (530). An inflatable-element outer wall (590) of an inflatable element (588) is mounted to the catheter body (210). An inner membrane (589) is positioned within the inflatable element (588) and is mounted to the catheter body (210) around the lateral opening (448) along a seal perimeter (583) around the lateral opening (448), so as to define a collapsible membrane portion (596) that (a) covers the lateral opening (448), and (b) together with the inflatable-element outer wall (590), defines an inflatable chamber (587) between the inflatable-element outer wall (590) and the collapsible membrane portion (596). The inner membrane (589) entirely surrounds the catheter body (210).

A system for controlling and monitoring flow in a cuffed endotracheal tube device is disclosed. The system comprises: a connector panel having at least three connectors adapted for establishing fluid communication with proximal ends of at least a first fluid line, a second fluid line and a cuff inflation line of the endotracheal tube device. The system can further comprise a processing unit and a control unit, wherein the processing unit is configured to instruct the control unit to execute various operations, including at least a rinsing procedure, a suctioning procedure, a cuff inflation procedure, a leak detection procedure and a venting procedure, and to select any of the first and the second fluid lines for any of the rinsing, suctioning, leak detection and venting procedures. In some embodiments, the system exploits the cuff as sensor to sense pulmonary data.

Methods, systems, and devices are disclosed for providing selective and non-selective cooling and warming of a patient. Multiple embodiments of devices are disclosed for performing rapid induction and maintenance of therapeutic hypothermia either in a hospital setting or in the field so that hypothermic treatment can be quickly instituted before significant tissue damage occurs. Methods are also disclosed for targeting brain cooling by irrigating the upper airway, aerodigestive tract, and/or more generalized cooling by irrigating the esophagus and/or stomach.